Classification, Labelling and Packaging Regulation

02008R1272-20150101 → 02008R1272-20150601

Article 14 Specific rules for the classification of mixtures 1. The classification of a mixture shall not be affected where the evaluation of the information indicates any of the following: (a) that the substances in the mixture react slowly with atmospheric gases, in particular oxygen, carbon dioxide, water vapour, to form different substances at low concentration; (b) that the substances in the mixture react very slowly with other substances in the mixture to form different substances at low concentration; (c) that the substances in the mixture may self-polymerise to form oligomers or polymers, at low concentration. 2. A mixture need not be classified for explosive, oxidising, or flammable properties as referred to in Part 2 of Annex I provided that any of the following requirements are met: (a) none of the substances in the mixture possesses any of those properties and, on the basis of the information available to the supplier, the mixture is unlikely to present hazards of this kind; (b) in the event of a change in the composition of a mixture, scientific evidence indicates that an evaluation of the information on the mixture will not lead to a change in classification; classification. (c) where a mixture is placed on the market in the form of an aerosol dispenser, it satisfies Article 8(1a) of Council Directive 75/324/EEC of 20 May 1975 on the approximation of the laws of the Member States relating to aerosol dispensersOJ L 147, 9.6.1975, p. 40..

02008R1272-20150101 → 02008R1272-20150601

Article 23 Derogations from labelling requirements for special cases The specific provisions on labelling laid down in section 1.3 of Annex I shall apply in respect of the following: (a) transportable gas cylinders; (b) gas containers intended for propane, butane or liquefied petroleum gas; (c) aerosols and containers fitted with a sealed spray attachment and containing substances or mixtures classified as presenting an aspiration hazard; (d) metals in massive form, alloys, mixtures containing polymers, mixtures containing elastomers; (e) explosives, as referred to in section 2.1 of Annex I, placed on the market with a view to obtaining an explosive or pyrotechnic effect. effect; (f) substances or mixtures classified as corrosive to metals but not corrosive to skin and/or eyes.

02008R1272-20150101 → 02008R1272-20150601

Article 35 Packaging 1. Packaging containing hazardous substances or mixtures shall satisfy the following requirements: (a) the packaging shall be designed and constructed so that its contents cannot escape, except in cases where other more specific safety devices are prescribed; (b) the materials constituting the packaging and fastenings shall not be susceptible to damage by the contents, or liable to form hazardous compounds with the contents; (c) the packaging and fastenings shall be strong and solid throughout to ensure that they will not loosen and will safely meet the normal stresses and strains of handling; (d) packaging fitted with replaceable fastening devices shall be designed so that it can be refastened repeatedly without the contents escaping. 2. Packaging containing a hazardous substance or a mixture supplied to the general public shall not have either a shape or design likely to attract or arouse the active curiosity of children or to mislead consumers, or have a similar presentation or a design used for foodstuff or animal feeding stuff or medicinal or cosmetic products, which would mislead consumers. Where the packaging contains a substance or mixture which meets the requirements in section 3.1.1 of Annex II it shall have a child-resistant fastening in accordance with sections 3.1.2, 3.1.3 and 3.1.4.2 of Annex II. Where the packaging contains a substance or mixture which meets the requirements in section 3.2.1 of Annex II it shall bear a tactile warning of danger in accordance with section 3.2.2 of Annex II. Where a liquid consumer laundry detergent, as defined in Article 2(1a) of Regulation (EC) No 648/2004 of the European Parliament and of the CouncilRegulation (EC) No 648/2004 of the European Parliament and of the Council of 31 March 2004 on detergents (OJ L 104, 8.4.2004, p. 1)., is contained in a soluble packaging for single use, the additional requirements of section 3.3 of Annex II shall apply. 3. The packaging of substances and mixtures shall be deemed to satisfy the requirements of paragraph 1(a), (b) and (c) if it complies with the requirements of the rules on the transport of dangerous goods by air, sea, road, rail or inland waterways.

02008R1272-20150101 → 02008R1272-20150601

compared line by line: this provision is too large to compare word by word, so a marked line is a line that changed somewhere

ANNEX I CLASSIFICATION AND LABELLING REQUIREMENTS FOR HAZARDOUS SUBSTANCES AND MIXTURES This annex sets out the criteria for classification in hazard classes and in their differentiations and sets out additional provisions on how the criteria may be met. … 48 unchanged lines … 1.1.3. Bridging principles for the classification of mixtures where test data are not available for the complete mixture Where the mixture itself has not been tested to determine its hazardous properties, but there are sufficient data on similar tested mixtures and individual hazardous ingredient substances to adequately characterise the hazards of the mixture, these data shall be used in accordance with the following bridging rules referred to in Article 9(4) for each individual hazard class in Part 3 and Part 4 of this Annex, subject to any specific provisions for mixtures in each hazard class. 1.1.3.1. Dilution If a tested mixture is diluted with a substance (diluent) which has an equivalent or lower hazard category classification than the least hazardous original ingredient substance and which is not expected to affect the hazard classification of other ingredient substances, then one of the following shall be applied: If a tested mixture is diluted with a substance (diluent) which has an equivalent or lower hazard category classification than the least hazardous original ingredient substance and which is not expected to affect the hazard classification of other ingredient substances, then one of the following shall be applied: the new mixture shall be classified as equivalent to the original mixture; the method explained in each section of Part 3 and in Part 4 for classification of mixtures when data are available for all components or only some components of the mixture; in the case of acute toxicity, the method for classification of mixtures based on ingredients of the mixture (additivity formula). 1.1.3.2. Batching The hazard category of a tested production batch of a mixture can be assumed to be substantially equivalent to that of another untested production batch of the same commercial product, when produced by or under the control of the same supplier, unless there is reason to believe there is significant variation such that the hazard classification of the untested batch has changed. If the latter occurs, a new evaluation is necessary. 1.1.3.3. Concentration of highly hazardous mixtures In the case of the classification of mixtures covered by sections 3.1, 3.2, 3.3, 3.8, 3.9, 3.10 and 4.1, if a tested mixture is classified in the highest hazard category or sub-category, and the concentration of the components of the tested mixture that are in that category or sub-category is increased, the resulting untested mixture shall be classified in that category or sub-category without additional testing. In the case of the classification of mixtures covered by sections 3.1, 3.2, 3.3, 3.8, 3.9, 3.10 and 4.1, if a tested mixture is classified in the highest hazard category or sub-category, and the concentration of the components of the tested mixture that are in that category or sub-category is increased, the resulting untested mixture shall be classified in that category or sub-category without additional testing. 1.1.3.4. Interpolation within one toxicity category In the case of the classification of mixtures covered by sections 3.1, 3.2, 3.3, 3.8, 3.9, 3.10 and 4.1, for three mixtures (A, B and C) with identical components, where mixtures A and B have been tested and are in the same hazard category, and where untested mixture C has the same hazardous components as mixture A and B but has concentrations of those hazardous components intermediate to the concentrations in mixtures A and B, then mixture C is assumed to be in the same hazard category as A and B. In the case of the classification of mixtures covered by sections 3.1, 3.2, 3.3, 3.8, 3.9, 3.10 and 4.1, for three mixtures (A, B and C) with identical components, where mixtures A and B have been tested and are in the same hazard category, and where untested mixture C has the same hazardous components as mixture A and B but has concentrations of those hazardous components intermediate to the concentrations in mixtures A and B, then mixture C is assumed to be in the same hazard category as A and B. 1.1.3.5. Substantially similar mixtures Given the following: (a) two mixtures each containing two ingredients: (i) A + B (ii) C + B; (b) the concentration of ingredient B is essentially the same in both mixtures; (c) the concentration of ingredient A in mixture (i) equals that of ingredient C in mixture (ii); (d) hazard data for A and C are available and substantially equivalent, i.e. they are in the same hazard category and are not expected to affect the hazard classification of B. If mixture (i) or (ii) is already classified based on test data, then the other mixture shall be assigned the same hazard category. If mixture (i) or (ii) is already classified based on test data, then the other mixture shall be assigned the same hazard category. 1.1.3.6. Review of classification where the composition of a mixture has changed The following variations in initial concentration are defined for the application of Article 15(2)(a): Table 1.2 Bridging Principle for changes in the composition of a mixture Initial concentration range of the constituent Permitted variation in initial concentration of the constituent ≤ 2,5 % ± 30 % 2,5 < C ≤ 10 % ± 20 % 10 < C ≤ 25 % ± 10 % 25 < C ≤ 100 % ± 5 % 1.1.3.7. Aerosols In the case of the classification of mixtures covered by sections 3.1, 3.2, 3.3, 3.4, 3.8 and 3.9, an aerosol form of a mixture shall be classified in the same hazard category as the non-aerosolised form of the mixture, provided that the added propellant does not affect the hazardous properties of the mixture upon spraying and scientific evidence is available demonstrating that the aerosolised form is not more hazardous than the nonaerosolised form. 1.2. Labelling 1.2.1. General rules for the application of labels required by Article 31 1.2.1. General rules for the application of labels required by Article 31 1.2.1.1. Hazard pictograms shall be in the shape of a square set at a point. 1.2.1.2. Hazard pictograms as laid down in Annex V shall have a black symbol on a white background with a red frame sufficiently wide to be clearly visible. 1.2.1.3. Each hazard pictogram shall cover at least one fifteenth of the minimum surface area of the label dedicated to the information required by Article 17. The minimum area of each hazard pictogram shall not be less than 1 cm2. 1.2.1.2. Hazard pictograms as laid down in Annex V shall have a black symbol on a white background with a red frame sufficiently wide to be clearly visible. 1.2.1.3. Each hazard pictogram shall cover at least one fifteenth of the minimum surface area of the label dedicated to the information required by Article 17. The minimum area of each hazard pictogram shall not be less than 1 cm2. 1.2.1.4. The dimensions of the label and of each pictogram shall be as follows: Table 1.3 Minimum dimensions of labels and pictograms Capacity of the package Dimensions of the label (in millimetres) for the information required by Article 17 Dimensions of each pictogram (in millimetres) Not exceeding 3 litres: If possible, at least 52 × 74 Not smaller than 10 × 10 Capacity of the package Dimensions of the label (in millimetres) for the information required by Article 17 Dimensions of each pictogram (in millimetres) Not exceeding 3 litres: If possible, at least 52 × 74 Not smaller than 10 × 10 If possible, at least 16 × 16 Greater than 3 litres but not exceeding 50 litres: At least 74 × 105 At least 23 × 23 Greater than 50 litres but not exceeding 500 litres: At least 105 × 148 At least 32 × 32 Greater than 500 litres: At least 148 × 210 At least 46 × 46 Greater than 3 litres but not exceeding 50 litres: At least 74 × 105 At least 23 × 23 Greater than 50 litres but not exceeding 500 litres: At least 105 × 148 At least 32 × 32 Greater than 500 litres: At least 148 × 210 At least 46 × 46 1.3. Derogations from labelling requirements for special cases In accordance with Article 23 the following derogations shall apply: 1.3.1. Transportable gas cylinders For transportable gas cylinders, one of the following shall be permitted to be used for gas cylinders with a water capacity of less than or equal to 150 litres: (a) A format and dimensions following the prescriptions of the current edition of Standard ISO 7225 relating to Gas cylinders — Precautionary labels. In this case, the label can bear the generic name or industrial or commercial name of the substance or mixture provided that the hazardous substances in a mixture are shown on the body of the gas cylinder in a clear and indelible way. (b) The information specified in Article 17 provided on a durable information disc or label held captive on the cylinder. 1.3.2. Gas containers intended for propane, butane or liquefied petroleum gas (LPG) 1.3.2.1. If propane, butane and liquefied petroleum gas or a mixture containing these substances classified in accordance with the criteria of this Annex, is placed on the market in closed refillable cylinders or in non-refillable cartridges within the scope of EN 417 as fuel gases which are only released for combustion (current edition of EN 417, relating to Non-refillable metallic gas cartridges for liquefied petroleum gases, with or without a valve, for use with portable appliances; construction, inspection, testing and marking), these cylinders or cartridges shall only be labelled with the appropriate pictogram and the hazard and precautionary statements concerning flammability. 1.3.2.2. No information concerning the effects on human health and the environment is required on the label. Instead the supplier shall provide the information concerning effects on human health and the environment to downstream users or distributors by means of the safety data sheet (SDS). 1.3.2.3. For consumers, sufficient information shall be transmitted to enable them to take all necessary measures for health and safety. 1.3.3. Aerosols and containers fitted with a sealed spray attachment and containing substances or mixtures classified as presenting an aspiration hazard With regard to the application of section 3.10.4, substances or mixtures classified in accordance with the criteria of sections 3.10.2 and 3.10.3 need not be labelled for this hazard when placed on the market in aerosol containers or in containers fitted with a sealed spray attachment. 1.3.4. Metals in massive form, alloys, mixtures containing polymers, mixtures containing elastomers 1.3.4.1. Metals in massive form, alloys, mixtures containing polymers and mixtures containing elastomers do not require a label according to this Annex, if they do not present a hazard to human health by inhalation, ingestion or contact with skin or to the aquatic environment in the form in which they are placed on the market, although classified as hazardous in accordance with the criteria of this Annex. 1.3.4.2. Instead, the supplier shall provide the information to downstream users or distributors by means of the SDS. 1.3.5. Explosives placed on the market with a view to obtaining an explosive or pyrotechnic effect Explosives, as referred to in section 2.1, placed on the market with a view to obtaining an explosive or pyrotechnic effect shall be labelled and packaged in accordance with the requirements for explosives only. 1.3.6. Substances or mixtures classified as corrosive to metals but not corrosive to skin and/or eyes Substances or mixtures classified as corrosive to metals but not corrosive to skin and/or eyes which are in the finished state as packaged for consumer use do not require on the label the hazard pictogram GHS05. 1.4. Request for use of an alternative chemical name 1.4.1. Requests for use of an alternative chemical name under Article 24 may be granted only where (I) the substance has not been assigned a Community workplace exposure limit; and … 44 unchanged lines … 1) Flammable gases of category 2; 2) Reproductive toxicity: effects on or via lactation; 3) Hazardous to the aquatic environment — Chronic of category 3 or 4. 1.5.2.1.3. The pictogram, the signal word, the hazard statement, and the precautionary statement linked to the hazard categories listed below may be omitted from the label elements required by Article 17 where: 1.5.2.1.3. The pictogram, the signal word, the hazard statement, and the precautionary statement linked to the hazard categories listed below may be omitted from the label elements required by Article 17 where: (a) the contents of the package do not exceed 125 ml; and (b) the substance or mixture is classified in one or more of the following hazard categories: 1) Corrosive to metals. 1.5.2.2. Labelling of soluble packaging for single use The label elements required by Article 17 may be omitted from soluble packaging intended for single use where: (a) The content of each soluble packaging does not exceed a volume of 25 ml; (b) The classification of the contents of the soluble packaging is exclusively one or more of the hazard categories in 1.5.2.1.1 (b), 1.5.2.1.2 (b) or 1.5.2.1.3 (b); and (b) The classification of the contents of the soluble packaging is exclusively one or more of the hazard categories in 1.5.2.1.1 (b), 1.5.2.1.2 (b) or 1.5.2.1.3 (b); and (c) The soluble packaging is contained within outer packaging that fully meets the requirements of Article 17. 1.5.2.3. Section 1.5.2.2 shall not apply to substances or mixtures within the scope of Directives 91/414/EEC or 98/8/EC. 1.5.2.4. Labelling of inner packaging where the contents do not exceed 10 ml 1.5.2.4.1. The label elements required by Article 17 may be omitted from the inner packaging where: (a) the contents of the inner packaging do not exceed 10 ml; (b) the substance or mixture is placed on the market for supply to a distributor or downstream user for scientific research and development or quality control analysis; and (c) the inner packaging is contained within outer packaging that meets the requirements of Article 17. 1.5.2.4.2. Notwithstanding sections 1.5.1.2 and 1.5.2.4.1, the label on the inner packaging shall contain the product identifier and, where appropriate, the hazard pictograms GHS01, GHS05, GHS06 and/or GHS08. Where more than two pictograms are assigned, GHS06 and GHS08 may take precedence over GHS01 and GHS05. 1.5.2.5. Section 1.5.2.4 shall not apply to substances or mixtures within the scope of Regulation (EC) No 1107/2009 or (EU) No 528/2012. 2. PART 2: PHYSICAL HAZARDS 2.1. Explosives 2.1.1. Definitions 2.1.1.1. The class of explosives comprises (a) explosive substances and mixtures; (b) explosive articles, except devices containing explosive substances or mixtures in such quantity or of such a character that their inadvertent or accidental ignition or initiation shall not cause any effect external to the device either by projection, fire, smoke, heat or loud noise; and (c) substances, mixtures and articles not mentioned in points (a) and (b) which are manufactured with a view to producing a practical, explosive or pyrotechnic effect. 2.1.1.2. For the purposes of this Regulation the following definitions shall apply: An explosive substance or mixture is a solid or liquid substance or mixture of substances which is in itself capable by chemical reaction of producing gas at such a temperature and pressure and at such a speed as to cause damage to the surroundings. Pyrotechnic substances are included even when they do not evolve gases. A pyrotechnic substance or mixture is a substance or mixture of substances designed to produce an effect by heat, light, sound, gas or smoke or a combination of these as the result of non-detonative self-sustaining exothermic chemical reactions. An unstable explosive is an explosive substance or mixture which is thermally unstable and/or too sensitive for normal handling, transport and use. An explosive article is an article containing one or more explosive substances or mixtures. A pyrotechnic article is an article containing one or more pyrotechnic substances or mixtures. An intentional explosive is a substance, mixture or article which is manufactured with a view to producing a practical, explosive or pyrotechnic effect. 2.1.2. Classification criteria 2.1.2.1. Substances, mixtures and articles of this class are classified as an unstable explosive on the basis of the flowchart in Figure 2.1.2. The test methods are described in Part I of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria. 2.1.2.1. Substances, mixtures and articles of this class are classified as an unstable explosive on the basis of the flowchart in Figure 2.1.2. The test methods are described in Part I of the UN RTDG, Manual of Tests and Criteria. 2.1.2.2. Substances, mixtures and articles of this class, which are not classified as an unstable explosive, shall be assigned to one of the following six divisions depending on the type of hazard they present: (a) Division 1.1 Substances, mixtures and articles which have a mass explosion hazard (a mass explosion is one which affects almost the entire quantity present virtually instantaneously); (b) Division 1.2 Substances, mixtures and articles which have a projection hazard but not a mass explosion hazard; (c) Division 1.3 Substances, mixtures and articles which have a fire hazard and either a minor blast hazard or a minor projection hazard or both, but not a mass explosion hazard: (i) combustion of which gives rise to considerable radiant heat; or (ii) which burn one after another, producing minor blast or projection effects or both; (d) Division 1.4 Substances, mixtures and articles which present no significant hazard: substances, mixtures and articles which present only a small hazard in the event of ignition or initiation. The effects are largely confined to the package and no projection of fragments of appreciable size or range is to be expected. An external fire shall not cause virtually instantaneous explosion of almost the entire contents of the package; (e) Division 1.5 Very insensitive substances or mixtures which have a mass explosion hazard: substances and mixtures which have a mass explosion hazard but are so insensitive that there is very little probability of initiation or of transition from burning to detonation under normal conditions; (f) Division 1.6 Extremely insensitive articles which do not have a mass explosion hazard: articles which contain only extremely insensitive detonating substances or mixtures and which demonstrate a negligible probability of accidental initiation or propagation. articles which contain only extremely insensitive detonating substances or mixtures and which demonstrate a negligible probability of accidental initiation or propagation. 2.1.2.3. Explosives, which are not classified as an unstable explosive, shall be classified in one of the six divisions referred to in paragraph 2.1.2.2 of this Annex based on Test Series 2 to 8 in Part I of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria according to the results of the tests laid down in Table 2.1.1: Table 2.1.1 Criteria for explosives This comprises substances, mixtures and articles which are manufactured with a view to producing a practical, explosive or pyrotechnic effect. Category Criteria Unstable explosives or explosives of Divisions 1.1 to 1.6 For explosives of Divisions 1.1 to 1.6, the following are the core set of tests that need to be performed: Explosibility: according to UN Test Series 2 (section 12 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria). Intentional explosives shall not be subject to UN Test Series 2. Sensitiveness: according to UN Test Series 3 (section 13 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria). Thermal stability: according to UN Test 3(c) (sub-section 13.6.1 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria). Explosibility: according to UN Test Series 2 (section 12 of the UN RTDG, Manual of Tests and Criteria). Intentional explosives shall not be subject to UN Test Series 2. Sensitiveness: according to UN Test Series 3 (section 13 of the UN RTDG, Manual of Tests and Criteria). Thermal stability: according to UN Test 3(c) (sub-section 13.6.1 of the UN RTDG, Manual of Tests and Criteria). Further tests are necessary to allocate the correct Division. 2.1.2.4. If explosives are unpackaged or repacked in packaging other than the original or similar packaging, they shall be retested. 2.1.3. Hazard Communication Label elements shall be used for substances, mixtures or articles meeting the criteria for classification in this hazard class in accordance with Table 2.1.2. NOTE to Table 2.1.2: Unpackaged explosives or explosives repacked in packaging other than the original or similar packaging shall include all of the following label elements: (a) the pictogram: exploding bomb; (b) the signal word: Danger; and (c) the hazard statement: explosive; mass explosion hazard unless the hazard is shown to correspond to one of the hazard categories in Table 2.1.2, in which case the corresponding symbol, the signal word and/or the hazard statement shall be assigned. Table 2.1.2 Label elements for explosives Classification Unstable Explosive Division 1.1 Division 1.2 Division 1.3 Division 1.4 Division 1.5 Division 1.6 GHS Pictograms Signal Word Danger Danger Danger Danger Warning Danger No signal word Hazard Statement H200: Unstable Explosive H201: Explosive; mass explosion hazard H202: Explosive; severe projection hazard H203: Explosive; fire, blast or projection hazard H204: Fire or projection hazard H205: May mass explode in fire No hazard statement Precautionary Statement Prevention P201 P202 P281 P210 P280 P210 P230 P240 P250 … 150 unchanged lines … No ANE substance/mixture shall be classified as a Category 2 oxidising liquid or a Category 2 oxidising solid (sections 2.13 and 2.14) 2.1.4.2. Screening procedure Explosive properties are associated with the presence of certain chemical groups in a molecule which can react to produce very rapid increases in temperature or pressure. The screening procedure is aimed at identifying the presence of such reactive groups and the potential for rapid energy release. If the screening procedure identifies the substance or mixture to be a potential explosive, the acceptance procedure (see section 10.3 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria) has to be performed. Explosive properties are associated with the presence of certain chemical groups in a molecule which can react to produce very rapid increases in temperature or pressure. The screening procedure is aimed at identifying the presence of such reactive groups and the potential for rapid energy release. If the screening procedure identifies the substance or mixture to be a potential explosive, the acceptance procedure (see section 10.3 of the UN RTDG, Manual of Tests and Criteria) has to be performed. Note: Neither a series 1 type (a) propagation of detonation test nor a series 2 type (a) test of sensitivity to detonative shock is required if the exothermic decomposition energy of organic materials is less than 800 J/g. For organic substances and mixtures of organic substances with a decomposition energy of 800 J/g or more, tests 1 (a) and 2 (a) need not be performed if the outcome of the ballistic mortar Mk.IIId test (F.1), or the ballistic mortar test (F.2) or the BAM Trauzl test (F.3) with initiation by a standard No 8 detonator (see Appendix 1 to the UN RTDG, Manual of Tests and Criteria) is no. In this case, the results of test 1 (a) and 2 (a) are deemed to be -. Neither a series 1 type (a) propagation of detonation test nor a series 2 type (a) test of sensitivity to detonative shock is required if the exothermic decomposition energy of organic materials is less than 800 J/g. For organic substances and mixtures of organic substances with a decomposition energy of 800 J/g or more, tests 1 (a) and 2 (a) need not be performed if the outcome of the ballistic mortar Mk.IIId test (F.1), or the ballistic mortar test (F.2) or the BAM Trauzl test (F.3) with initiation by a standard No 8 detonator (see Appendix 1 to the UN RTDG, Manual of Tests and Criteria) is no. In this case, the results of test 1 (a) and 2 (a) are deemed to be -. 2.1.4.3. A substance or mixture shall not be classified as explosive if: (a) There are no chemical groups associated with explosive properties present in the molecule. Examples of groups which may indicate explosive properties are given in Table A6.1 in Appendix 6 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria; or (a) There are no chemical groups associated with explosive properties present in the molecule. Examples of groups which may indicate explosive properties are given in Table A6.1 in Appendix 6 of the UN RTDG, Manual of Tests and Criteria; or (b) The substance contains chemical groups associated with explosive properties which include oxygen and the calculated oxygen balance is less than - 200; The oxygen balance is calculated for the chemical reaction: CxHyOz+ [x+ (y/4)-(z/2)] O2 → x CO2 + (y/2) H2O Using the formula: Oxygen balance = -1600 [2x + (y/2)-z]/molecular weight; (c) When the organic substance or a homogenous mixture of organic substances contains chemical groups associated with explosive properties but the exothermic decomposition energy is less than 500 J/g and the onset of exothermic decomposition is below 500 oC. The exothermic decomposition energy can be determined using a suitable calorimetric technique; or (d) For mixtures of inorganic oxidising substances with organic material(s), the concentration of the inorganic oxidising substance is: less than 15 % by mass, if the oxidising substance is assigned to Categories 1 or 2; less than 30 % by mass, if the oxidising substance is assigned to Category 3. 2.1.4.4. In the case of mixtures containing any known explosives, the acceptance procedure has to be performed. 2.2. Flammable gases 2.2.1. Definition Flammable gas means a gas or gas mixture having a flammable range with air at 20 oC and a standard pressure of 101,3 kPa. 2.2. Flammable gases (including chemically unstable gases) 2.2.1. Definitions 2.2.1.1. Flammable gas means a gas or gas mixture having a flammable range with air at 20 °C and a standard pressure of 101,3 kPa. 2.2.1.2. A chemically unstable gas means a flammable gas that is able to react explosively even in the absence of air or oxygen. 2.2.2. Classification criteria 2.2.2.1. A flammable gas shall be classified in this class in accordance with Table 2.2.1: Table 2.2.1 Criteria for flammable gases Note: Aerosols shall not be classified as flammable gases; see section 2.3. Category Criteria 1 Gases, which at 20 oC and a standard pressure of 101,3 kPa: 1 Gases, which at 20 °C and a standard pressure of 101,3 kPa: (a) are ignitable when in a mixture of 13 % or less by volume in air; or (b) have a flammable range with air of at least 12 percentage points regardless of the lower flammable limit. 2 Gases, other than those of Category 1, which, at 20 oC and a standard pressure of 101,3 kPa, have a flammable range while mixed in air. Note: Aerosols shall not be classified as flammable gases; see section 2.3. 2 Gases, other than those of Category 1, which, at 20 °C and a standard pressure of 101,3 kPa, have a flammable range while mixed in air. 2.2.2.2. A flammable gas that is also chemically unstable shall additionally be classified in one of the two categories for chemically unstable gases using the methods described in Part III of the UN RTDG, Manual of Tests and Criteria according to the following table: Table 2.2.2 Criteria for chemically unstable gases Category Criteria A Flammable gases which are chemically unstable at 20 °C and a standard pressure of 101,3 kPa B Flammable gases which are chemically unstable at a temperature greater than 20 °C and/or a pressure greater than 101,3 kPa 2.2.3. Hazard Communication Label elements shall be used for substances and mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.2.2. Table 2.2.2 Label elements for flammable gases Classification Category 1 Category 2 GHS Pictogram No pictogram Signal Word Danger Warning Hazard Statement H220: Extremely flammable gas H221: Flammable gas Precautionary Statement Prevention P210 P210 Precautionary Statement Response P377 Label elements shall be used for substances and mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.2.3. Table 2.2.3 Label elements for flammable gases (including chemically unstable gases) Classification Flammable gas Chemically unstable gas Category 1 Category 2 Category A Category B GHS Pictogram No pictogram No additional pictogram No additional pictogram Signal Word Danger Warning No additional signal word No additional signal word Hazard Statement H220: Extremely flammable gas H221: Flammable gas H230: May react explosively even in the absence of air H231: May react explosively even in the absence of air at elevated pressure and/or temperature Precautionary Statement Prevention P210 P210 P202 P202 Precautionary Statement Response P377 P381 P377 P381 Precautionary Statement Storage P403 P403 Precautionary Statement Disposal 2.2.4. Additional Classification Considerations 2.2.4.1. Flammability shall be determined by tests or, for mixtures where there are sufficient data available, by calculation in accordance with the methods adopted by ISO (see ISO 10156 as amended, Gases and gas mixtures — Determination of fire potential and oxidising ability for the selection of cylinder valve outlet). Where insufficient data are available to use these methods, test method EN 1839 as amended (Determination of explosion limits of gases and vapours) can be used. 2.3. Flammable aerosols P381 Precautionary Statement Storage P403 P403 Precautionary Statement Disposal The classification procedure is set out in the following decision logic (see Figures 2.2.1 to 2.2.2). Figure 2.2.1 Flammable gases Gaseous substance or mixture of gases Does it have a flammable rage with air at 20 °C and a standard pressure of 101,3 kPa? NO Not classified YES At 20 °C and a standard pressure of 101 kPa, does it: (a) ignite when in a mixture of 13 % or less by volume in air; or (b) have a flammable range with air of at least 12 percentage points regardless of the lower flammable limit? YES Category 1 Danger NO Category 2 No pictogram Warning Figure 2.2.2 Chemically unstable gases Flammable gas or gas mixture Is it chemically unstable at 20 °C temperature and a standard pressure of 101,3 kPa? YES Category A (chemically unstable gas) No additional pictogram No additional signal word NO Is it chemically unstable at a temperature greater than 20 °C and/or a pressure greater than 101,3 kPa? YES Category B (chemically unstable gas) No additional pictogram No additional signal word NO Not classified as chemically unstable 2.2.4. Additional Classification Considerations 2.2.4.1. Flammability shall be determined by tests or, for mixtures where there are sufficient data available, by calculation in accordance with the methods adopted by ISO (see ISO 10156 as amended, Gases and gas mixtures — Determination of fire potential and oxidising ability for the selection of cylinder valve outlet). Where insufficient data are available to use these methods, test method EN 1839 as amended (Determination of explosion limits of gases and vapours) may be used. 2.2.4.2. Chemical instability shall be determined in accordance with the method described in Part III of the UN RTDG, Manual of Tests and Criteria. If the calculations in accordance with ISO 10156 as amended show that a gas mixture is not flammable it is not necessary to carry out the tests for determining chemical instability for classification purposes. 2.3. Aerosols 2.3.1. Definitions Aerosols, this means aerosol dispensers, are any non-refillable receptacles made of metal, glass or plastics and containing a gas compressed, liquefied or dissolved under pressure, with or without a liquid, paste or powder, and fitted with a release device allowing the contents to be ejected as solid or liquid particles in suspension in a gas, as a foam, paste or powder or in a liquid state or in a gaseous state. 2.3.2. Classification criteria 2.3.2.1. Aerosols shall be considered for classification as flammable in accordance with 2.3.2.2 if they contain any component which is classified as flammable according to the criteria contained in this Part, i.e.: Liquids with a flash point ≤ 93 oC, which includes Flammable Liquids according to section 2.6; Flammable gases (see 2.2); Flammable solids (see 2.7). 2.3.2.1. Aerosols shall be considered for classification as flammable in accordance with section 2.3.2.2 if they contain any component which is classified as flammable according to the following criteria set out in this Part: Liquids with a flash point ≤ 93 °C, which includes Flammable Liquids according to section 2.6; Flammable gases (see section 2.2); Flammable solids (see section 2.7). Note 1: Flammable components do not cover pyrophoric, self-heating or water-reactive substances and mixtures because such components are never used as aerosol contents. Note 2: Flammable aerosols do not fall additionally within the scope of sections 2.2 (flammable gases), 2.6 (flammable liquids) or 2.7 (flammable solids). 2.3.2.2. A flammable aerosol shall be classified in one of the two categories for this Class on the basis of its components, of its chemical heat of combustion and, if applicable, of the results of the foam test (for foam aerosols) and of the ignition distance test and enclosed space test (for spray aerosols) in accordance with Figure 2.3.1 and the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, Part III, sub-sections 31.4, 31.5 and 31.6. Figure 2.3.1 Figure 2.3.1(a) for flammable aerosols Aerosols do not fall additionally within the scope of sections 2.2 (flammable gases), 2.5 (gases under pressure), 2.6 (flammable liquids) and 2.7 (flammable solids). Depending on their contents, aerosols may however fall within the scope of other hazard classes, including their labelling elements. 2.3.2.2. An aerosol shall be classified in one of the three categories for this Class on the basis of its components, of its chemical heat of combustion and, if applicable, of the results of the foam test (for foam aerosols) and of the ignition distance test and enclosed space test (for spray aerosols) in accordance with Figures 2.3.1(a) to 2.3.1(c) of this Annex and subsections 31.4, 31.5 and 31.6 of Part III of the UN RTDG, Manual of Tests and Criteria. Aerosols which do not meet the criteria for inclusion in Category 1 or Category 2 shall be classified in Category 3. Note: Aerosols containing more than 1 % flammable components or with a heat of combustion of at least 20 kJ/g, which are not submitted to the flammability classification procedures in this section shall be classified as aerosols, Category 1. Figure 2.3.1 (a) Aerosols AEROSOL Does it contain ≤ 1% flammable components and does it have a heat of combustion < 20 kJ/g? Does it contain ≤ 1 % flammable components and does it have a heat of combustion < 20 kJ/g? YES NOT CLASSIFIED Category 3 No pictogram Warning NO Does it contain ≥ 85% flammable components and does it have a heat of combustion ≥ 30 kJ/g? Does it contain ≥ 85 % flammable components and does it have a heat of combustion ≥ 30 kJ/g? YES Category 1 Danger NO Danger For spray aerosols, go to decision logic 2.3.1 (b); For foam aerosols, got to decision logic 2.3.1 (c). Figure 2.3.1(b) for spray aerosols For spray aerosols, go to decision logic 2.3.1(b) For foam aerosols, go to decision logic 2.3.1(c) Figure 2.3.1 (b) Spray aerosols SPRAY AEROSOL In the ignition distance test, does ignition occur at a distance ≥ 75 cm? YES Category 1 Danger NO Does it have a heat of combustion < 20 kJ/g? NO Category 2 Warning YES In the ignition distance test, does ignition occur at a distance ≥ 15 cm? YES Category 2 Warning NO In the enclosed space ignition test; is: a) the time equivalent ≤ 300 s/m3 or b) the deflagration density ≤ 300 g/m3? (a) the time equivalent ≤ 300 s/m3; or (b) the deflagration density ≤ 300 g/m3? YES Category 2 Warning NO NOT CLASSIFIED Danger Category 3 No pictogram Warning Warning Warning Figure 2.3.1(c) for foam aerosols Figure 2.3.1 (c) Foam aerosols FOAM AEROSOL In the foam test, is: a) the flame height ≥ 20 cm and the flame duration ≥ 2 s; or b) the flame height ≥ 4 cm and the flame duration ≥ 7 s? In the foam test, is: (a) the flame height ≥ 20 cm and the flame duration ≥ 2 s; or (b) the flame height ≥ 4 cm and the flame duration ≥ 7s? YES Category 1 Danger NO In the foam test; is the flame height ≥ 4 cm and the flame duration ≥ 2 s? In the foam test, is the flame height ≥ 4 cm and the flame duration ≥ 2 s? YES Category 2 Warning NO NOT CLASSIFIED Danger Category 3 No pictogram Warning Note: Aerosols not submitted to the flammability classification procedures in this section shall be classified as flammable aerosols, Category 1. 2.3.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.3.2. Table 2.3.2 Label elements for flammable aerosols Classification Category 1 Category 2 GHS Pictograms Signal Word Danger Warning Hazard Statement H222: Extremely flammable aerosol H223: Flammable aerosol Precautionary Statement Prevention P210 Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.3.1. Table 2.3.1 Label elements for flammable and non-flammable aerosols Classification Category 1 Category 2 Category 3 GHS Pictograms No pictogram Signal Word Danger Warning Warning Hazard Statement H222: Extremely flammable aerosol H229: Pressurised container: May burst if heated H223: Flammable aerosol H229: Pressurised container: May burst if heated H229: Pressurised container: May burst if heated Precautionary Statement Prevention P210 P211 P251 P210 P211 P251 P210 P251 Precautionary Statement Response Precautionary Statement Storage P410 + P412 P410 + P412 Precautionary Statement Disposal 2.3.4. Additional Classification Considerations 2.3.4.1. The chemical heat of combustion (ΔHc), in kilojoules per gram (kJ/g), is the product of the theoretical heat of combustion (ΔHcomb), and a combustion efficiency, usually less than 1,0 (a typical combustion efficiency is 0,95 or 95 %). Precautionary Statement Response Precautionary Statement Storage P410 + P412 P410 + P412 P410 + P412 Precautionary Statement Disposal 2.3.4. Additional Classification Considerations 2.3.4.1. The chemical heat of combustion (ΔΗc), in kilojoules per gram (kJ/g), is the product of the theoretical heat of combustion (ΔΗcomb), and a combustion efficiency, usually less than 1,0 (a typical combustion efficiency is 0,95 or 95 %). For a composite aerosol formulation, the chemical heat of combustion is the summation of the weighted heats of combustion for the individual components, as follows: ΔHc productniwi %ΔHci where: ΔHc ΔΗc chemical heat of combustion (kJ/g); wi % mass fraction of component i in the product; ΔHc(i) ΔΗc(i) specific heat of combustion (kJ/g)of component i in the product. The chemical heats of combustion can be found in the literature, calculated or determined by tests (see ASTM D 240 as amended — Standard Test Methods for Heat of Combustion of Liquid Hydrocarbon Fuels by Bomb Calorimeter, EN/ISO 13943 as amended, 86.l to 86.3 — Fire safety — Vocabulary, and NFPA 30B as amended — Code for the Manufacture and Storage of Aerosol Products). 2.4. Oxidising gases 2.4.1. Definitions Oxidising gas means any gas or gas mixture which may, generally by providing oxygen, cause or contribute to the combustion of other material more than air does. 2.4.2. Classification criteria 2.4.2.1. An oxidising gas shall be classified in a single category for this class in accordance with Table 2.4.1.: Table 2.4.1 Criteria for oxidising gases Category Criteria 1 Any gas which may, generally by providing oxygen, cause or contribute to the combustion of other material more than air does. Note: Gases which cause or contribute to the combustion of other material more than air does mean pure gases or gas mixtures with an oxidising power greater than 23,5 % as determined by a method specified in ISO 10156 as amended or 10156-2 as amended. Gases which cause or contribute to the combustion of other material more than air does means pure gases or gas mixtures with an oxidising power greater than 23,5 % as determined by a method specified in ISO 10156 as amended. 2.4.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.4.2. Table 2.4.2 Label elements for oxidising gases Classification Category 1 GHS Pictogram Signal Word Danger Hazard Statement H270: May cause or intensify fire; oxidiser Precautionary Statement Prevention P220 P244 Precautionary Statement Response P370 + P376 Precautionary Statement Storage P403 Precautionary Statement Disposal 2.4.4. Additional Classification Considerations To classify an oxidising gas, tests or calculation methods as described in ISO 10156 as amended, gases and gas mixtures — Determination of fire potential and oxidising ability for the selection of cylinder valve outlet and ISO 10156-2 as amended, gas cylinders — gases and gas mixtures — Determination of oxidising ability of toxic and corrosive gases and gas mixtures — shall be performed. To classify an oxidising gas, tests or calculation methods as described in ISO 10156 as amended, Gases and gas mixtures — Determination of fire potential and oxidising ability for the selection of cylinder valve outlet shall be performed. 2.5. Gases under pressure 2.5.1. Definition 2.5.1.1. Gases under pressure are gases which are contained in a receptacle at a pressure of 200 kPa (gauge) or more, or which are liquefied or liquefied and refrigerated. 2.5.1.1. Gases under pressure are gases which are contained in a receptacle at a pressure of 200 kPa (gauge) or more at 20 °C, or which are liquefied or liquefied and refrigerated. They comprise compressed gases, liquefied gases, dissolved gases and refrigerated liquefied gases. 2.5.1.2. The critical temperature is the temperature above which a pure gas cannot be liquefied, regardless of the degree of compression. 2.5.2. Classification criteria Gases shall be classified, according to their physical state when packaged, in one of four groups in accordance with Table 2.5.1: 2.5.2.1. Gases under pressure shall be classified, according to their physical state when packaged, in one of four groups in accordance with Table 2.5.1: Table 2.5.1 Criteria for gases under pressure Note: Aerosols shall not be classified as gases under pressure. See section 2.3. Group Criteria Compressed gas A gas which when packaged under pressure is entirely gaseous at - 50 oC; including all gases with a critical temperature ≤ - 50 oC. Liquefied gas A gas which, when packaged under pressure, is partially liquid at temperatures above - 50 oC. A distinction is made between: (i) high pressure liquefied gas: a gas with a critical temperature between - 50 oC and + 65 oC; and (ii) low pressure liquefied gas: a gas with a critical temperature above + 65 oC. Compressed gas A gas which when packaged under pressure is entirely gaseous at – 50 °C; including all gases with a critical temperature ≤ – 50 °C. Liquefied gas A gas which, when packaged under pressure, is partially liquid at temperatures above – 50 °C. A distinction is made between: (i) high pressure liquefied gas: a gas with a critical temperature between – 50 °C and + 65 °C; and (ii) low pressure liquefied gas: a gas with a critical temperature above + 65 °C. Refrigerated liquefied gas A gas which when packaged is made partially liquid because of its low temperature. Dissolved gas A gas which when packaged under pressure is dissolved in a liquid phase solvent. 2.5.3. Hazard Communication … 16 unchanged lines … the vapour pressure at 50 oC; the physical state at 20 oC at standard ambient pressure; the critical temperature. Data can be found in the literature, calculated or determined by testing. Most pure gases are already classified in the UN Recommendations on the Transport of Dangerous Goods, Model Regulations. Data can be found in the literature, calculated or determined by testing. Most pure gases are already classified in the UN RTDG, Model Regulations. 2.6. Flammable liquids 2.6.1. Definition Flammable liquid means a liquid having a flash point of not more than 60 oC. 2.6.2. Classification criteria 2.6.2.1. A flammable liquid shall be classified in one of the three categories for this class in accordance with Table 2.6.1: Table 2.6.1 Criteria for flammable liquids For the purpose of this Regulation gas oils, diesel and light heating oils having a flash point between ≥ 55 oC and ≤ 75 oC may be regarded as Category 3. Category Criteria 1 Flash point < 23 oC and initial boiling point ≤ 35 oC 2 Flash point < 23 oC and initial boiling point > 35 oC 3 Flash point ≥ 23 oC and ≤ 60 oC Note: Aerosols shall not be classified as flammable liquids; see section 2.3. Aerosols shall not be classified as flammable liquids; see section 2.3. 2.6.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.6.2. Table 2.6.2 … 32 unchanged lines … Disposal P501 P501 P501 2.6.4. Additional Classification Considerations 2.6.4.1. For the classification of flammable liquids data on flash point and initial boiling point are needed. Data can be determined by testing, found in literature or calculated. If data are not available, the flash point and the initial boiling point shall be determined through testing. For flash point determination a closed-cup method shall be used. 2.6.4.2. In the case of mixturesTo date, the calculation method has been validated for mixtures containing up to 6 volatile components. These components may be flammable liquids like hydrocarbons, ethers, alcohols, esters (except acrylates), and water. It is however not yet validated for mixtures containing halogenated sulphurous, and/or phosphoric compounds as well as reactive acrylates. containing known flammable liquids in defined concentrations, although they may contain non-volatile components e.g. polymers, additives, the flash point need not be determined experimentally if the calculated flash point of the mixture, using the method given in 2.6.4.3, is at least 5 °CIf the calculated flash point is less than 5 °C greater than the relevant classification criterion, the calculation method may not be used and the flash point should be determined experimentally. greater than the relevant classification criterion (23 °C and 60 °C, respectively) and provided that: 2.6.4.2. In the case of mixturesTo date, the calculation method has been validated for mixtures containing up to 6 volatile components. These components may be flammable liquids like hydrocarbons, ethers, alcohols, esters (except acrylates), and water. It is however not yet validated for mixtures containing halogenated sulphurous, and/or phosphoric compounds as well as reactive acrylates. containing known flammable liquids in defined concentrations, although they may contain non-volatile components e.g. polymers, additives, the flash point need not be determined experimentally if the calculated flash point of the mixture, using the method given in 2.6.4.3, is at least 5 °CIf the calculated flash point is less than 5 °C greater than the relevant classification criterion, the calculation method may not be used and the flash point should be determined experimentally. greater than the relevant classification criterion (23 °C and 60 °C, respectively) and provided that: (a) the composition of the mixture is accurately known (if the material has a specified range of composition, the composition with the lowest calculated flash point shall be selected for assessment); (b) the lower explosion limit of each component is known (an appropriate correlation has to be applied when these data are extrapolated to other temperatures than test conditions) as well as a method for calculating the lower explosion limit of the mixture; (c) the temperature dependence of the saturated vapour pressure and of the activity coefficient is known for each component as present in the mixture; … 22 unchanged lines … (identical to EN ISO 13736) Deutsches Institut für Normung DIN 51755 (flash points below 65 C) as amended Prüfung von Mineralölen und anderen brennbaren Flüssigkeiten; Bestimmung des Flammpunktes im geschlossenen Tiegel, nach Abel-Pensky (identical to NF M07-036) 2.6.4.5 Liquids with a flash point of more than 35 °C and not more than 60 °C need not be classified in Category 3 if negative results have been obtained in the sustained combustibility test L.2, Part III, section 32 of the UN RTDG, Manual of Tests and Criteria. 2.6.4.5 Liquids with a flash point of more than 35 °C and not more than 60 °C need not be classified in Category 3 if negative results have been obtained in the sustained combustibility test L.2, Part III, section 32 of the UN RTDG, Manual of Tests and Criteria. 2.6.4.6. Possible test methods for determining the initial boiling point of flammable liquids are listed in Table 2.6.4. Table 2.6.4 Methods for determining the initial boiling point of flammable liquids OJ L 142, 31.5.2008, p. 1. OJ L 142, 31.5.2008, p. 1. European standards: EN ISO 3405 as amended Petroleum products — Determination of distillation characteristics at atmospheric pressure EN ISO 3924 as amended Petroleum products — Determination of boiling range distribution — Gas chromatography method EN ISO 4626 as amended Volatile organic liquids — Determination of boiling range of organic solvents used as raw materials Regulation (EC) No 440/2008 Method A.2 as described in Part A of the Annex to Regulation (EC) No 440/2008 Regulation (EC) No 440/2008 Method A.2 as described in Part A of the Annex to Regulation (EC) No 440/2008 2.7. Flammable solids 2.7.1. Definition 2.7.1.1. A flammable solid means a solid which is readily combustible, or may cause or contribute to fire through friction. Readily combustible solids are powdered, granular, or pasty substances or mixtures which are dangerous if they can be easily ignited by brief contact with an ignition source, such as a burning match, and if the flame spreads rapidly. 2.7.2. Classification criteria 2.7.2.1. Powdered, granular or pasty substances or mixtures (except powders of metals or metal alloys — see 2.7.2.2) shall be classified as readily combustible solids when the time of burning of one or more of the test runs, performed in accordance with the test method described in Part III, sub-section 33.2.1, of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, is less than 45 seconds or the rate of burning is more than 2,2 mm/s. 2.7.2.1. Powdered, granular or pasty substances or mixtures (except powders of metals or metal alloys — see 2.7.2.2) shall be classified as readily combustible solids when the time of burning of one or more of the test runs, performed in accordance with the test method described in Part III, sub-section 33.2.1, of the UN RTDG, Manual of Tests and Criteria, is less than 45 seconds or the rate of burning is more than 2,2 mm/s. 2.7.2.2. Powders of metals or metal alloys shall be classified as flammable solids when they can be ignited and the reaction spreads over the whole length of the sample in 10 minutes or less. 2.7.2.3. A flammable solid shall be classified in one of the two categories for this class using Method N.1 as described in 33.2.1 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria in accordance with Table 2.7.1: 2.7.2.3. A flammable solid shall be classified in one of the two categories for this class using Method N.1 as described in 33.2.1 of the UN RTDG, Manual of Tests and Criteria in accordance with Table 2.7.1: Table 2.7.1 Criteria for flammable solids Category Criteria 1 Burning rate test Substances and mixtures other than metal powders: (a) wetted zone does not stop fire and (b) burning time < 45 seconds or burning rate > 2,2 mm/s Metal powders burning time ≤ 5 minutes 2 Burning rate test Substances and mixtures other than metal powders: (a) wetted zone stops the fire for at least 4 minutes and (b) burning time < 45 seconds or burning rate > 2,2 mm/s Metal powders burning time > 5 minutes and ≤ 10 minutes Note 1: The test shall be performed on the substance or mixture in its physical form as presented. If, for example, for the purposes of supply or transport, the same chemical is to be presented in a physical form different from that which was tested and which is considered likely to materially alter its performance in a classification test, the substance shall also be tested in the new form. Note 2: Aerosols shall not be classified as flammable solids; see section 2.3. Aerosols shall not be classified as flammable solids; see section 2.3. 2.7.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.7.2. Table 2.7.2 … 23 unchanged lines … (b) they are oxidising liquids or solids, according to the criteria given in 2.13 or 2.14, except that mixtures of oxidising substances, which contain 5 % or more of combustible organic substances shall be classified as self-reactive substances according to the procedure defined in 2.8.2.2; (c) they are organic peroxides, according to the criteria given in 2.15; (d) their heat of decomposition is less than 300 J/g; or (e) their self-accelerating decomposition temperature (SADT) is greater than 75 oC for a 50 kg packageSee UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, sub-sections 28.1, 28.2, 28.3 and Table 28.3.. (e) their self-accelerating decomposition temperature (SADT) is greater than 75 oC for a 50 kg packageSee UN RTDG, Manual of Tests and Criteria, subsections 28.1, 28.2, 28.3 and Table 28.3.. 2.8.2.2. Mixtures of oxidising substances, meeting the criteria for classification as oxidising substances, which contain 5 % or more of combustible organic substances and which do not meet the criteria mentioned in (a), (c), (d) or (e) in 2.8.2.1, shall be subjected to the self-reactive substances classification procedure; Such a mixture showing the properties of a self-reactive substance type B to F (see 2.8.2.3) shall be classified as a self-reactive substance. Where the test is conducted in the package form and the packaging is changed, a further test shall be conducted where it is considered that the change in packaging will affect the outcome of the test. 2.8.2.3. Self-reactive substances and mixtures shall be classified in one of the seven categories of types A to G for this class, according to the following principles: (a) any self-reactive substance or mixture which can detonate or deflagrate rapidly, as packaged, shall be defined as self-reactive substance TYPE A; (b) any self-reactive substance or mixture possessing explosive properties and which, as packaged, neither detonates nor deflagrates rapidly, but is liable to undergo a thermal explosion in that package shall be defined as self-reactive substance TYPE B; (c) any self-reactive substance or mixture possessing explosive properties when the substance or mixture as packaged cannot detonate or deflagrate rapidly or undergo a thermal explosion shall be defined as self-reactive substance TYPE C; (d) any self-reactive substance or mixture which in laboratory testing: (i) detonates partially, does not deflagrate rapidly and shows no violent effect when heated under confinement; or (ii) does not detonate at all, deflagrates slowly and shows no violent effect when heated under confinement; or (iii) does not detonate or deflagrate at all and shows a medium effect when heated under confinement; shall be defined as self-reactive substance TYPE D; (e) any self-reactive substance or mixture which, in laboratory testing, neither detonates nor deflagrates at all and shows low or no effect when heated under confinement shall be defined as self-reactive substance TYPE E; (f) any self-reactive substance or mixture which, in laboratory testing, neither detonates in the cavitated state nor deflagrates at all and shows only a low or no effect when heated under confinement as well as low or no explosive power shall be defined as self-reactive substance TYPE F; (g) any self-reactive substance or mixture which, in laboratory testing, neither detonates in the cavitated state nor deflagrates at all and shows no effect when heated under confinement nor any explosive power, provided that it is thermally stable (SADT is 60 oC to 75 oC for a 50 kg package), and, for liquid mixtures, a diluent having a boiling point not less than 150 oC is used for desensitisation shall be defined as self-reactive substance TYPE G. If the mixture is not thermally stable or a diluent having a boiling point less than 150 oC is used for desensitisation, the mixture shall be defined as self-reactive substance TYPE F. Where the test is conducted in the package form and the packaging is changed, a further test shall be conducted where it is considered that the change in packaging will affect the outcome of the test. 2.8.2.4. Criteria for temperature control Self-reactive substances need to be subjected to temperature control if their SADT is less than or equal to 55 oC. Test methods for determining the SADT as well as the derivation of control and emergency temperatures are given in, Part II, section 28 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria. The test selected shall be conducted in a manner which is representative, both in size and material, of the package. Self-reactive substances need to be subjected to temperature control if their SADT is less than or equal to 55 oC. Test methods for determining the SADT as well as the derivation of control and emergency temperatures are given in, Part II, section 28 of the UN RTDG, Manual of Tests and Criteria. The test selected shall be conducted in a manner which is representative, both in size and material, of the package. 2.8.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.8.1. Table 2.8.1 … 30 unchanged lines … P420 Precautionary Statement Disposal P501 P501 P501 P501 Type G has no hazard communication elements assigned but shall be considered for properties belonging to other hazard classes. 2.8.4. Additional Classification Considerations 2.8.4.1. The properties of self-reactive substances or mixtures which are decisive for their classification shall be determined experimentally. The classification of a self reactive substance or mixture shall be performed in accordance with test series A to H as described in Part II of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria. The procedure for classification is described in Figure 2.8.1. 2.8.4.1. The properties of self-reactive substances or mixtures which are decisive for their classification shall be determined experimentally. The classification of a self reactive substance or mixture shall be performed in accordance with test series A to H as described in Part II of the UN RTDG, Manual of Tests and Criteria. The procedure for classification is described in Figure 2.8.1. 2.8.4.2. The classification procedures for self-reactive substances and mixtures need not be applied if: (a) There are no chemical groups present in the molecule associated with explosive or self reactive properties. Examples of such groups are given in Tables A6.1 and A6.2 in Appendix 6 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria; or (b) For a single organic substance or a homogeneous mixture of organic substances, the estimated SADT for a 50 kg package is greater than 75 oC or the exothermic decomposition energy is less than 300J/g. The onset temperature and decomposition energy can be estimated using a suitable calorimetric technique (see Part II, sub-section 20.3.3.3 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria). (a) There are no chemical groups present in the molecule associated with explosive or self reactive properties. Examples of such groups are given in Tables A6.1 and A6.2 in Appendix 6 of the UN RTDG, Manual of Tests and Criteria; or (b) For a single organic substance or a homogeneous mixture of organic substances, the estimated SADT for a 50 kg package is greater than 75 oC or the exothermic decomposition energy is less than 300J/g. The onset temperature and decomposition energy can be estimated using a suitable calorimetric technique (see Part II, sub-section 20.3.3.3 of the UN RTDG, Manual of Tests and Criteria). Figure 2.8.1 Self-reactive substances and mixtures SUBSTANCE/MIXTURE … 84 unchanged lines … 2.9.1. Definition Pyrophoric liquid means a liquid substance or mixture which, even in small quantities, is liable to ignite within five minutes after coming into contact with air. 2.9.2. Classification criteria 2.9.2.1. A pyrophoric liquid shall be classified in a single category for this class using test N.3 in Part III, sub-section 33.3.1.5 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria according to Table 2.9.1: 2.9.2.1. A pyrophoric liquid shall be classified in a single category for this class using test N.3 in Part III, sub-section 33.3.1.5 of the UN RTDG, Manual of Tests and Criteria according to Table 2.9.1: Table 2.9.1 Criteria for pyrophoric liquids Category Criteria … 21 unchanged lines … 2.10.1. Definition Pyrophoric solid means a solid substance or mixture which, even in small quantities, is liable to ignite within five minutes after coming into contact with air. 2.10.2. Classification criteria 2.10.2.1. A pyrophoric solid shall be classified in a single category for this class using test N.2 in Part III, sub-section 33.3.1.4 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria in accordance with Table 2.10.1: 2.10.2.1. A pyrophoric solid shall be classified in a single category for this class using test N.2 in Part III, sub-section 33.3.1.4 of the UN RTDG, Manual of Tests and Criteria in accordance with Table 2.10.1: Table 2.10.1 Criteria for pyrophoric solids Category Criteria … 24 unchanged lines … 2.11.1.1. A self-heating substance or mixture is a liquid or solid substance or mixture, other than a pyrophoric liquid or solid, which, by reaction with air and without energy supply, is liable to self-heat; this substance or mixture differs from a pyrophoric liquid or solid in that it will ignite only when in large amounts (kilograms) and after long periods of time (hours or days). 2.11.1.2. Self-heating of a substance or a mixture is a process where the gradual reaction of that substance or mixture with oxygen (in the air) generates heat. If the rate of heat production exceeds the rate of heat loss, then the temperature of the substance or mixture will rise which, after an induction time, may lead to self-ignition and combustion. 2.11.2. Classification criteria 2.11.2.1. A substance or mixture shall be classified as a self-heating substance or mixture of this class, if in the tests performed in accordance with the test method given in the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, Part III, sub-section 33.3.1.6: 2.11.2.1. A substance or mixture shall be classified as a self-heating substance or mixture of this class, if in the tests performed in accordance with the test method given in the UN RTDG, Manual of Tests and Criteria, Part III, sub-section 33.3.1.6: (a) a positive result is obtained using a 25 mm cube sample at 140 oC; (b) a positive result is obtained in a test using a 100 mm sample cube at 140 oC and a negative result is obtained in a test using a 100 mm cube sample at 120 oC and the substance or mixture is to be packed in packages with a volume of more than 3 m3; (c) a positive result is obtained in a test using a 100 mm sample cube at 140 oC and a negative result is obtained in a test using a 100 mm cube sample at 100 oC and the substance or mixture is to be packed in packages with a volume of more than 450 litres; (d) a positive result is obtained in a test using a 100 mm sample cube at 140 oC and a positive result is obtained in a test using a 100 mm cube sample at 100 oC. 2.11.2.2. A self-heating substance or mixture shall be classified in one of the two categories for this class if, in a test performed in accordance with test method N.4 in Part III, sub-section 33.3.1.6 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, the result meets the criteria according to Table 2.11.1: 2.11.2.2. A self-heating substance or mixture shall be classified in one of the two categories for this class if, in a test performed in accordance with test method N.4 in Part III, sub-section 33.3.1.6 of the UN RTDG, Manual of Tests and Criteria, the result meets the criteria according to Table 2.11.1: Table 2.11.1 Criteria for self-heating substances and mixtures Category Criteria … 65 unchanged lines … 2.12.1. Definition Substances or mixtures which, in contact with water, emit flammable gases means solid or liquid substances or mixtures which, by interaction with water, are liable to become spontaneously flammable or to give off flammable gases in dangerous quantities. 2.12.2. Classification criteria 2.12.2.1. A substance or mixture which, in contact with water, emits flammable gases shall be classified in one of the three categories for this class, using test N.5 in Part III, sub-section 33.4.1.4 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, in accordance with Table 2.12.1: 2.12.2.1. A substance or mixture which, in contact with water, emits flammable gases shall be classified in one of the three categories for this class, using test N.5 in Part III, sub-section 33.4.1.4 of the UN RTDG, Manual of Tests and Criteria, in accordance with Table 2.12.1: Table 2.12.1 Criteria for substances or mixtures which in contact with water emit flammable gases Category Criteria … 34 unchanged lines … 2.13.1. Definition Oxidising liquid means a liquid substance or mixture which, while in itself not necessarily combustible, may, generally by yielding oxygen, cause, or contribute to, the combustion of other material. 2.13.2. Classification criteria 2.13.2.1. An oxidising liquid shall be classified in one of the three categories for this class using test O.2 in Part III, sub-section 34.4.2 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria in accordance with Table 2.13.1: 2.13.2.1. An oxidising liquid shall be classified in one of the three categories for this class using test O.2 in Part III, sub-section 34.4.2 of the UN RTDG, Manual of Tests and Criteria in accordance with Table 2.13.1: Table 2.13.1 Criteria for oxidising liquids Category Criteria … 32 unchanged lines … (b) the substance or mixture contains oxygen, fluorine or chlorine and these elements are chemically bonded only to carbon or hydrogen. 2.13.4.2. For inorganic substances or mixtures the classification procedure for this class shall not apply if they do not contain oxygen or halogen atoms. 2.13.4.3. In the event of divergence between test results and known experience in the handling and use of substances or mixtures which shows them to be oxidising, judgments based on known experience shall take precedence over test results. 2.13.4.4. In cases where substances or mixtures generate a pressure rise (too high or too low), caused by chemical reactions not characterising the oxidising properties of the substance or mixture, the test described in Part III, sub-section 34.4.2 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria shall be repeated with an inert substance, e.g. diatomite (kieselguhr), in place of the cellulose in order to clarify the nature of the reaction and to check for a false positive result. 2.13.4.4. In cases where substances or mixtures generate a pressure rise (too high or too low), caused by chemical reactions not characterising the oxidising properties of the substance or mixture, the test described in Part III, sub-section 34.4.2 of the UN RTDG, Manual of Tests and Criteria shall be repeated with an inert substance, e.g. diatomite (kieselguhr), in place of the cellulose in order to clarify the nature of the reaction and to check for a false positive result. 2.14. Oxidising solids 2.14.1. Definition Oxidising solid means a solid substance or mixture which, while in itself is not necessarily combustible, may, generally by yielding oxygen, cause, or contribute to, the combustion of other material. 2.14.2. Classification criteria 2.14.2.1. An oxidising solid shall be classified in one of the three categories for this class using test O.1 in Part III, sub-section 34.4.1 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria in accordance with Table 2.14.1: 2.14.2.1. An oxidising solid shall be classified in one of the three categories for this class using test O.1 in Part III, sub-section 34.4.1 of the UN RTDG, Manual of Tests and Criteria in accordance with Table 2.14.1: Table 2.14.1 Criteria for oxidising solids Category Criteria … 69 unchanged lines … shall be defined as organic peroxide TYPE D; (e) any organic peroxide which, in laboratory testing, neither detonates nor deflagrates at all and shows low or no effect when heated under confinement shall be defined as organic peroxide TYPE E; (f) any organic peroxide which, in laboratory testing, neither detonates in the cavitated state nor deflagrates at all and shows only a low or no effect when heated under confinement as well as low or no explosive power shall be defined as organic peroxide TYPE F; (g) any organic peroxide which, in laboratory testing, neither detonates in the cavitated state nor deflagrates at all and shows no effect when heated under confinement nor any explosive power, provided that it is thermally stable, i.e. the SADT is 60 oC or higher for a 50 kg packageSee UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, sub-sections 28.1, 28.2, 28.3 and Table 28.3., and, for liquid mixtures, a diluent having a boiling point of not less than 150 oC is used for desensitisation, shall be defined as organic peroxide TYPE G. If the organic peroxide is not thermally stable or a diluent having a boiling point less than 150 oC is used for desensitisation, the organic peroxide shall be defined as organic peroxide TYPE F. (g) any organic peroxide which, in laboratory testing, neither detonates in the cavitated state nor deflagrates at all and shows no effect when heated under confinement nor any explosive power, provided that it is thermally stable, i.e. the SADT is 60 oC or higher for a 50 kg packageSee UN RTDG, Manual of Tests and Criteria, subsections 28.1, 28.2, 28.3 and Table 28.3., and, for liquid mixtures, a diluent having a boiling point of not less than 150 oC is used for desensitisation, shall be defined as organic peroxide TYPE G. If the organic peroxide is not thermally stable or a diluent having a boiling point less than 150 oC is used for desensitisation, the organic peroxide shall be defined as organic peroxide TYPE F. Where the test is conducted in the package form and the packaging is changed, a further test shall be conducted where it is considered that the change in packaging will affect the outcome of the test. 2.15.2.3. Criteria for temperature control The following organic peroxides need to be subjected to temperature control: (a) Organic peroxide types B and C with an SADT ≤ 50 C; (b) Organic peroxide type D showing a medium effect when heated under confinementAs determined by test series E as prescribed in UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, Part II. with an SADT ≤ 50 oC or showing a low or no effect when heated under confinement with an SADT ≤ 45 oC; and (b) Organic peroxide type D showing a medium effect when heated under confinementAs determined by test series E as prescribed in UN RTDG, Manual of Tests and Criteria, Part II. with an SADT ≤ 50 oC or showing a low or no effect when heated under confinement with an SADT ≤ 45 oC; and (c) Organic peroxide types E and F with an SADT ≤ 45 oC. Test methods for determining the SADT as well as the derivation of control and emergency temperatures are given in the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, Part II, section 28. The test selected shall be conducted in a manner which is representative, both in size and material, of the package. Test methods for determining the SADT as well as the derivation of control and emergency temperatures are given in the UN RTDG, Manual of Tests and Criteria, Part II, section 28. The test selected shall be conducted in a manner which is representative, both in size and material, of the package. 2.15.3. Hazard Communication Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.15.1. Table 2.15.1 … 29 unchanged lines … P420 Precautionary Statement Disposal P501 P501 P501 P501 Type G has no hazard communication elements assigned but shall be considered for properties belonging to other hazard classes. 2.15.4. Additional Classification Considerations 2.15.4.1. Organic peroxides are classified by definition based on their chemical structure and on the available oxygen and hydrogen peroxide contents of the mixture (see 2.15.2.1). The properties of organic peroxides which are necessary for their classification shall be determined experimentally. The classification of organic peroxides shall be performed in accordance with test series A to H as described in Part II of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria. The procedure for classification is described in Figure 2.15.1. 2.15.4.1. Organic peroxides are classified by definition based on their chemical structure and on the available oxygen and hydrogen peroxide contents of the mixture (see 2.15.2.1). The properties of organic peroxides which are necessary for their classification shall be determined experimentally. The classification of organic peroxides shall be performed in accordance with test series A to H as described in Part II of the UN RTDG, Manual of Tests and Criteria. The procedure for classification is described in Figure 2.15.1. 2.15.4.2. Mixtures of already classified organic peroxides may be classified as the same type of organic peroxide as that of the most dangerous component. However, as two stable components can form a thermally less stable mixture, the SADT of the mixture shall be determined. Note: The sum of the individual parts can be more hazardous than the individual components. Figure 2.15.1 … 75 unchanged lines … 2.16.1. Definition A substance or a mixture that is corrosive to metals means a substance or a mixture which by chemical action will materially damage, or even destroy, metals. 2.16.2. Classification criteria 2.16.2.1. A substance or a mixture which is corrosive to metals is classified in a single category for this class, using the test in Part III, sub-section 37.4 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria, in accordance with Table 2.16.1: 2.16.2.1. A substance or a mixture which is corrosive to metals is classified in a single category for this class, using the test in Part III, sub-section 37.4 of the UN RTDG, Manual of Tests and Criteria, in accordance with Table 2.16.1: Table 2.16.1 Criteria for substances and mixtures corrosive to metals Category Criteria 1 Corrosion rate on either steel or aluminium surfaces exceeding 6,25 mm per year at a test temperature of 55 oC when tested on both materials. Note Where an initial test on either steel or aluminium indicates the substance or mixture being tested is corrosive the follow up test on the other metal is not required. 2.16.3. Hazard Communication Label elements shall be used for substances and mixtures meeting the criteria for classification in this hazard class in accordance with Table 2.16.2. Table 2.16.2 Label elements for substances and mixtures corrosive to metals Classification Category 1 GHS Pictogram Signal Word Warning Hazard Statement H290: May be corrosive to metals Precautionary Statement Prevention P234 Precautionary Statement Response P390 Precautionary Statement Storage P406 Precautionary Statement Disposal 2.16.4. Additional Classification Considerations 2.16.4.1. The corrosion rate can be measured according to the test method of Part III sub-section 37.4 of the UN Recommendations on the Transport of Dangerous Goods, Manual of Tests and Criteria. The specimen to be used for the test shall be made of the following materials: Disposal Note: Where a substance or mixture is classified as corrosive to metals but not corrosive to skin and/or eyes, the labelling provisions set out in section 1.3.6 shall be used. 2.16.4. Additional Classification Considerations 2.16.4.1. The corrosion rate can be measured according to the test method of Part III sub-section 37.4 of the UN RTDG, Manual of Tests and Criteria. The specimen to be used for the test shall be made of the following materials: (a) for the purposes of testing steel, steel types S235JR+CR (1.0037 resp.St 37-2), S275J2G3+CR (1.0144 resp.St 44-3), ISO 3574 as amended, Unified Numbering System (UNS) G 10200, or SAE 1020; (b) for the purposes of testing aluminium: non-clad types 7075-T6 or AZ5GU-T6. 3. PART 3: HEALTH HAZARDS 3.1. Acute toxicity 3.1.1. Definitions 3.1.1.1. Acute toxicity means those adverse effects occurring following oral or dermal administration of a single dose of a substance or a mixture, or multiple doses given within 24 hours, or an inhalation exposure of 4 hours. 3.1.1.2. The hazard class Acute Toxicity is differentiated into: Acute oral toxicity; Acute dermal toxicity; Acute inhalation toxicity. 3.1.2. Criteria for classification of substances as acutely toxic 3.1.2.1. Substances can be allocated to one of four toxicity categories based on acute toxicity by the oral, dermal or inhalation route according to the numeric criteria shown in Table 3.1.1. Acute toxicity values are expressed as (approximate) LD50 (oral, dermal) or LC50 (inhalation) values or as acute toxicity estimates (ATE). Explanatory notes are shown following Table 3.1.1. Table 3.1.1 Acute toxicity hazard categories and acute toxicity estimates (ATE) defining the respective categories Gas concentrations are expressed in parts per million per volume (ppmV). Exposure route Category 1 Category 2 Category 3 Category 4 Oral (mg/kg bodyweight) ATE ≤ 5 5 < ATE ≤ 50 50 < ATE ≤ 300 300 < ATE ≤ 2000 Gas concentrations are expressed in parts per million per volume (ppmV). Exposure route Category 1 Category 2 Category 3 Category 4 Oral (mg/kg bodyweight) ATE ≤ 5 5 < ATE ≤ 50 50 < ATE ≤ 300 300 < ATE ≤ 2000 See: Note (a) Note (b) Dermal (mg/kg bodyweight) ATE ≤ 50 50 < ATE ≤ 200 200 < ATE ≤ 1000 1000 < ATE ≤ 2000 Dermal (mg/kg bodyweight) ATE ≤ 50 50 < ATE ≤ 200 200 < ATE ≤ 1000 1000 < ATE ≤ 2000 See: Note (a) Note (b) Gases (ppmV) ATE ≤ 100 100 < ATE ≤ 500 500 < ATE ≤ 2500 2500 < ATE ≤ 20000 Gases (ppmV) ATE ≤ 100 100 < ATE ≤ 500 500 < ATE ≤ 2500 2500 < ATE ≤ 20000 see: Note (a) Note (b) Note (c) Vapours (mg/l) ATE ≤ 0,5 0,5 < ATE ≤ 2,0 2,0 < ATE ≤ 10,0 10,0 < ATE ≤ 20,0 Vapours (mg/l) ATE ≤ 0,5 0,5 < ATE ≤ 2,0 2,0 < ATE ≤ 10,0 10,0 < ATE ≤ 20,0 see: Note (a) Note (b) Note (c) Note (d) Dusts and mists (mg/l) ATE ≤ 0,05 0,05 < ATE ≤ 0,5 0,5 < ATE ≤ 1,0 1,0 < ATE ≤ 5,0 Dusts and mists (mg/l) ATE ≤ 0,05 0,05 < ATE ≤ 0,5 0,5 < ATE ≤ 1,0 1,0 < ATE ≤ 5,0 see: Note (a) Note (b) Note (c) Notes to Table 3.1.1: (a) The acute toxicity estimate (ATE) for the classification of a substance is derived using the LD50/LC50 where available. (b) The acute toxicity estimate (ATE) for the classification of a substance in a mixture is derived using: the LD50/LC50 where available, the appropriate conversion value from Table 3.1.2 that relates to the results of a range test, or the appropriate conversion value from Table 3.1.2 that relates to a classification category. (c) Generic concentration limits for inhalation toxicity in the table are based on 4-hour testing exposures. Conversion of existing inhalation toxicity data which have been generated using a 1-hour exposure can be carried out by dividing by a factor of 2 for gases and vapours and 4 for dusts and mists. (d) For some substances the test atmosphere will not just be a vapour but will consist of a mixture of liquid and vapour phases. For other substances the test atmosphere may consist of a vapour which is near the gaseous phase. In these latter cases, classification shall be based on ppmV as follows: Category 1 (100 ppmV), Category 2 (500 ppmV), Category 3 (2500 ppmV), Category 4 (20000 ppmV). (c) The ranges of the acute toxicity estimates (ATE) for inhalation toxicity used in the Table are based on 4-hour testing exposures. Conversion of existing inhalation toxicity data which have been generated using a 1-hour exposure can be carried out by dividing by a factor of 2 for gases and vapours and 4 for dusts and mists. (d) For some substances the test atmosphere will not just be a vapour but will consist of a mixture of liquid and vapour phases. For other substances the test atmosphere may consist of a vapour which is near the gaseous phase. In these latter cases, classification shall be based on ppmV as follows: Category 1 (100 ppmV), Category 2 (500 ppmV), Category 3 (2500 ppmV), Category 4 (20000 ppmV). The terms dust, mist and vapour are defined as follows: dust: solid particles of a substance or mixture suspended in a gas (usually air), mist: liquid droplets of a substance or mixture suspended in a gas (usually air), vapour: the gaseous form of a substance or mixture released from its liquid or solid state. Dust is generally formed by mechanical processes. Mist is generally formed by condensation of supersaturated vapours or by physical shearing of liquids. Dusts and mists generally have sizes ranging from less than 1 to about 100 μm. Dust is generally formed by mechanical processes. Mist is generally formed by condensation of supersaturated vapours or by physical shearing of liquids. Dusts and mists generally have sizes ranging from less than 1 to about 100 μm. 3.1.2.2. Specific considerations for classification of substances as acutely toxic 3.1.2.2.1. The preferred test species for evaluation of acute toxicity by the oral and inhalation routes is the rat, while the rat or rabbit are preferred for evaluation of acute dermal toxicity. When experimental data for acute toxicity are available in several animal species, scientific judgement shall be used in selecting the most appropriate LD50 value from among valid, well-performed tests. 3.1.2.3. Specific considerations for classification of substances as acutely toxic by the inhalation route 3.1.2.3.1. Units for inhalation toxicity are a function of the form of the inhaled material. Values for dusts and mists are expressed in mg/l. Values for gases are expressed in ppmV. Acknowledging the difficulties in testing vapours, some of which consist of mixtures of liquid and vapour phases, the table provides values in units of mg/l. However, for those vapours which are near the gaseous phase, classification shall be based on ppmV. 3.1.2.3.2. Of particular importance in classifying for inhalation toxicity is the use of well articulated values in the high toxicity categories for dusts and mists. Inhaled particles between 1 and 4 microns mean mass aerodynamic diameter (MMAD) will deposit in all regions of the rat respiratory tract. This particle size range corresponds to a maximum dose of about 2 mg/l. In order to achieve applicability of animal experiments to human exposure, dusts and mists would ideally be tested in this range in rats. 3.1.2.3.3. In addition to classification for inhalation toxicity, if data are available that indicates that the mechanism of toxicity was corrosivity, the substance or mixture shall also be labelled as corrosive to the respiratory tract (see note 1 in 3.1.4.1). Corrosion of the respiratory tract is defined by destruction of the respiratory tract tissue after a single, limited period of exposure analogous to skin corrosion; this includes destruction of the mucosa. The corrosivity evaluation can be based on expert judgment using such evidence as: human and animal experience, existing (in vitro) data, pH values, information from similar substances or any other pertinent data. 3.1.3. Criteria for classification of mixtures as acutely toxic 3.1.3.1. The criteria for classification of substances for acute toxicity as outlined in section 3.1.2 are based on lethal dose data (tested or derived). For mixtures, it is necessary to obtain or derive information that allows the criteria to be applied to the mixture for the purpose of classification. The approach to classification for acute toxicity is tiered, and is dependent upon the amount of information available for the mixture itself and for its ingredients. The flow chart of Figure 3.1.1 outlines the process to be followed. 3.1.3.2. For acute toxicity each route of exposure shall be considered for the classification of mixtures, but only one route of exposure is needed as long as this route is followed (estimated or tested) for all components and there is no relevant evidence to suggest acute toxicity by multiple routes. When there is relevant evidence of toxicity by multiple routes of exposure, classification is to be conducted for all appropriate routes of exposure. All available information shall be considered. The pictogram and signal word used shall reflect the most severe hazard category and all relevant hazard statements shall be used. 3.1.3.2. For acute toxicity each route of exposure shall be considered for the classification of mixtures, but only one route of exposure is needed as long as this route is followed (estimated or tested) for all components and there is no relevant evidence to suggest acute toxicity by multiple routes. When there is relevant evidence of toxicity by multiple routes of exposure, classification is to be conducted for all appropriate routes of exposure. All available information shall be considered. The pictogram and signal word used shall reflect the most severe hazard category and all relevant hazard statements shall be used. 3.1.3.3. In order to make use of all available data for purposes of classifying the hazards of the mixtures, certain assumptions have been made and are applied where appropriate in the tiered approach: (a) the relevant ingredients of a mixture are those which are present in concentrations of 1 % (w/w for solids, liquids, dusts, mists and vapours and v/v for gases) or greater, unless there is a reason to suspect that an ingredient present at a concentration of less than 1 % is still relevant for classifying the mixture for acute toxicity (see Table 1.1). (b) where a classified mixture is used as an ingredient of another mixture, the actual or derived acute toxicity estimate (ATE) for that mixture may be used, when calculating the classification of the new mixture using the formulas in section 3.1.3.6.1 and paragraph 3.1.3.6.2.3. (c) If the converted acute toxicity point estimates for all components of a mixture are within the same category, then the mixture should be classified in that category. (d) When only range data (or acute toxicity hazard category information) are available for components in a mixture, they may be converted to point estimates in accordance with Table 3.1.2 when calculating the classification of the new mixture using the formulas in sections 3.1.3.6.1 and 3.1.3.6.2.3. (d) When only range data (or acute toxicity hazard category information) are available for components in a mixture, they may be converted to point estimates in accordance with Table 3.1.2 when calculating the classification of the new mixture using the formulas in sections 3.1.3.6.1 and 3.1.3.6.2.3. Figure 3.1.1 Tiered approach to classification of mixtures for acute toxicity Test data on the mixture as a whole … 22 unchanged lines … 3.1.3.4.1. Where the mixture itself has been tested to determine its acute toxicity, it shall be classified according to the same criteria as those used for substances, presented in Table 3.1.1. If test data for the mixture are not available, the procedures presented under sections 3.1.3.5 and 3.1.3.6 shall be followed. 3.1.3.5. Classification of mixtures where acute toxicity data are available for the complete mixture: bridging principles 3.1.3.5.1. Where the mixture itself has not been tested to determine its acute toxicity, but there are sufficient data on the individual ingredients and similar tested mixtures to adequately characterise the hazards of the mixture, these data shall be used in accordance with the bridging rules set out in section 1.1.3. 3.1.3.5.2. If a tested mixture is diluted with a diluent that has an equivalent or lower toxicity classification than the least toxic original components, and which is not expected to affect the toxicity of other components, then the new diluted mixture may be classified as equivalent to the original tested mixture. Alternatively, the formula explained in section 3.1.3.6.1 can be applied. 3.1.3.5.2. If a tested mixture is diluted with a diluent that has an equivalent or lower toxicity classification than the least toxic original components, and which is not expected to affect the toxicity of other components, then the new diluted mixture may be classified as equivalent to the original tested mixture. Alternatively, the formula explained in section 3.1.3.6.1 can be applied. 3.1.3.6. Classification of mixtures based on ingredients of the mixture (Additivity formula) 3.1.3.6.1. Data available for all ingredients In order to ensure that classification of the mixture is accurate, and that the calculation need only be performed once for all systems, sectors, and categories, the acute toxicity estimate (ATE) of ingredients shall be considered as follows: (a) include ingredients with a known acute toxicity, which fall into any of the acute toxicity categories shown in Table 3.1.1; (b) ignore ingredients that are presumed not acutely toxic (e.g., water, sugar); (c) ignore components if the data available are from a limit dose test (at the upper threshold for Category 4 for the appropriate route of exposure as provided in Table 3.1.1) and do not show acute toxicity. Components that fall within the scope of this section are considered to be components with a known acute toxicity estimate (ATE). See note (b) to Table 3.1.1 and section 3.1.3.3 for appropriate application of available data to the equation below, and section 3.1.3.6.2.3. (c) ignore components if the data available are from a limit dose test (at the upper threshold for Category 4 for the appropriate route of exposure as provided in Table 3.1.1) and do not show acute toxicity. Components that fall within the scope of this section are considered to be components with a known acute toxicity estimate (ATE). See note (b) to Table 3.1.1 and section 3.1.3.3 for appropriate application of available data to the equation below, and section 3.1.3.6.2.3. The ATE of the mixture is determined by calculation from the ATE values for all relevant ingredients according to the following formula for Oral, Dermal or Inhalation Toxicity:100ATEmixnCiATEi where: Ci concentration of ingredient i ( % w/w or % v/v) i the individual ingredient from 1 to n n the number of ingredients ATEi Acute Toxicity Estimate of ingredient i. 3.1.3.6.2. Classification of mixtures when data are not available for all components 3.1.3.6.2.1. Where an ATE is not available for an individual ingredient of the mixture, but available information, such as that listed below, can provide a derived conversion value such as those laid out in Table 3.1.2, the formula in section 3.1.3.6.1 shall be applied. This includes evaluation of: (a) extrapolation between oral, dermal and inhalation acute toxicity estimatesWhen mixtures contain components that do not have acute toxicity data for each route of exposure, acute toxicity estimates may be extrapolated from the available data and applied to the appropriate routes (see section 3.1.3.2). However, specific legislation may require testing for a specific route. In those cases, classification shall be performed for that route based upon the legal requirements.. Such an evaluation could require appropriate pharmacodynamic and pharmacokinetic data; (a) extrapolation between oral, dermal and inhalation acute toxicity estimatesWhen mixtures contain components that do not have acute toxicity data for each route of exposure, acute toxicity estimates may be extrapolated from the available data and applied to the appropriate routes (see section 3.1.3.2). However, specific legislation may require testing for a specific route. In those cases, classification shall be performed for that route based upon the legal requirements.. Such an evaluation could require appropriate pharmacodynamic and pharmacokinetic data; (b) evidence from human exposure that indicates toxic effects but does not provide lethal dose data; (c) evidence from any other toxicity tests/assays available on the substance that indicates toxic acute effects but does not necessarily provide lethal dose data; or (d) data from closely analogous substances using structure/activity relationships. This approach generally requires substantial supplemental technical information, and a highly trained and experienced expert (expert judgement, see section 1.1.1), to reliably estimate acute toxicity. If such information is not available, proceed to paragraph 3.1.3.6.2.3. 3.1.3.6.2.2. In the event that a component without any useable information for classification is used in a mixture at a concentration of 1 % or greater, it is concluded that the mixture cannot be attributed a definitive acute toxicity estimate. In this situation the mixture shall be classified based on the known components only, with the additional statement on the label and in the SDS that: × percent of the mixture consists of component(s) of unknown toxicity. 3.1.3.6.2.3. If the total concentration of the ingredient(s) with unknown acute toxicity is ≤ 10 % then the formula presented in section 3.1.3.6.1 shall be used. If the total concentration of the ingredient(s) with unknown toxicity is > 10 %, the formula presented in section 3.1.3.6.1 shall be corrected to adjust for the total percentage of the unknown ingredient(s) as follows: 100Cunknown if10%ETAmixnCiETAi 3.1.3.6.2.2. In the event that a component without any useable information for classification is used in a mixture at a concentration ≥ 1 %, it is concluded that the mixture cannot be attributed a definitive acute toxicity estimate. In this situation the mixture shall be classified based on the known components only, with the additional statement on the label and in the SDS that x per cent of the mixture consists of component(s) of unknown acute toxicity, taking into account the provisions set out in section 3.1.4.2. 3.1.3.6.2.3. If the total concentration of the relevant ingredient(s) with unknown acute toxicity is ≤ 10 % then the formula presented in section 3.1.3.6.1 shall be used. If the total concentration of the relevant ingredient(s) with unknown toxicity is > 10 %, the formula presented in section 3.1.3.6.1 shall be corrected to adjust for the percentage of the unknown ingredient(s) as follows: 100C unknown if10 %ATEmixnCiATEi Table 3.1.2 Conversion from experimentally obtained acute toxicity range values (or acute toxicity hazard categories) to acute toxicity point estimates for use in the formulas for the classification of mixtures Exposure routes Classification Category or experimentally obtained acute toxicity range estimate Converted acute toxicity point estimate … 41 unchanged lines … Note 1 These values are designed to be used in the calculation of the ATE for classification of a mixture based on its components and do not represent test results. 3.1.4. Hazard Communication 3.1.4.1. Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 3.1.3. Without prejudice to Article 27, combined hazard statements may be used in accordance with Annex III. 3.1.4.1. Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 3.1.3. Without prejudice to Article 27, combined hazard statements may be used in accordance with Annex III. Table 3.1.3 Acute toxicity label elements Classification Category 1 Category 2 Category 3 Category 4 GHS Pictograms Signal Word Danger Danger Danger Warning Hazard Statement: Oral H300: Fatal if swallowed H300: Fatal if swallowed H301: Toxic if swallowed H302: Harmful if swallowed Dermal H310:Fatal in contact with skin H310:Fatal in contact with skin H311: Toxic in contact with skin H312: Harmful in contact with skin Inhalation Oral H300: Fatal if swallowed H300: Fatal if swallowed H301: Toxic if swallowed H302: Harmful if swallowed — Dermal H310:Fatal in contact with skin H310:Fatal in contact with skin H311: Toxic in contact with skin H312: Harmful in contact with skin — Inhalation (see Note 1) H330:Fatal if inhaled H330: Fatal if inhaled H331: Toxic if inhaled H332: Harmful if inhaled Precautionary Statement Prevention (oral) P264 P270 P264 … 16 unchanged lines … P264 P270 P280 P280 P280 Precautionary Statement Response (dermal) P302 + P350 Precautionary Statement Response (dermal) P302 + P352 P310 P322 P361 P363 P302 + P350 P321 P361 + P364 P302 + P352 P310 P322 P361 P363 P302 + P352 P321 P361 + P364 P302 + P352 P312 P322 P361 P363 P302 + P352 P321 P361 + P364 P302 + P352 P312 P322 P363 P321 P362 + P364 Precautionary Statement Storage (dermal) P405 P405 P405 Precautionary Statement Disposal (dermal) P501 P501 P501 P501 Precautionary Statement Prevention (inhalation) P260 P271 … 17 unchanged lines … In addition to classification for inhalation toxicity, if data are available that indicates that the mechanism of toxicity is corrosivity, the substance or mixture shall also be labelled as EUH071: corrosive to the respiratory tract — see advice at 3.1.2.3.3. In addition to an appropriate acute toxicity pictogram, a corrosivity pictogram (used for skin and eye corrosivity) may be added together with the statement corrosive to the respiratory tract. Note 2 In the event that an ingredient without any useable information at all is used in a mixture at a concentration of 1 % or greater, the mixture shall be labelled with the additional statement that x percent of the mixture consists of ingredient(s) of unknown toxicity — see advice at 3.1.3.6.2.2. 3.1.4.2. The acute toxicity hazard statements differentiate the hazard based on the route of exposure. Communication of acute toxicity classification should also reflect this differentiation. If a substance or mixture is classified for more than one route of exposure then all relevant classifications should be communicated on the safety data sheet as specified in Annex II to Regulation (EC) No 1907/2006 and the relevant hazard communication elements included on the label as prescribed in section 3.1.3.2. If the statement x % of the mixture consists of ingredient(s) of unknown acute toxicity is communicated, as prescribed in section 3.1.3.6.2.2, then, in the information provided in the safety data sheet, it can also be differentiated based on the route of exposure. For example, x % of the mixture consists of ingredient(s) of unknown acute oral toxicity and x % of the mixture consists of ingredient(s) of unknown acute dermal toxicity. 3.2. Skin corrosion/irritation 3.2.1. Definitions 3.2.1.1. Skin Corrosion means the production of irreversible damage to the skin; namely, visible necrosis through the epidermis and into the dermis, following the application of a test substance for up to 4 hours. Corrosive reactions are typified by ulcers, bleeding, bloody scabs, and, by the end of observation at 14 days, by discolouration due to blanching of the skin, complete areas of alopecia, and scars. Histopathology shall be considered to evaluate questionable lesions. … 41 unchanged lines … 3.2.3.3.4.1. Particular care must be taken when classifying certain types of mixtures containing substances such as acids and bases, inorganic salts, aldehydes, phenols, and surfactants. The approach explained in paragraphs 3.2.3.3.1 and 3.2.3.3.2 may not be applicable given that many of such substances are corrosive or irritant at concentrations < 1 %. 3.2.3.3.4.2. For mixtures containing strong acids or bases the pH shall be used as a classification criterion (see paragraph 3.2.3.1.2) since pH is a better indicator of corrosion than the concentration limits of Table 3.2.3. 3.2.3.3.4.3. A mixture containing ingredients that are corrosive or irritant to the skin and that cannot be classified on the basis of the additivity approach (Table 3.2.3), due to chemical characteristics that make this approach unworkable, shall be classified as Skin Corrosive Category 1A, 1B or 1C if it contains ≥ 1 % of an ingredient classified in Category 1A, 1B or 1C respectively or as Category 2 when it contains ≥ 3 % of an irritant ingredient. Classification of mixtures with ingredients for which the approach in Table 3.2.3 does not apply is summarised in Table 3.2.4. 3.2.3.3.5. On occasion, reliable data may show that the skin corrosion/irritation hazard of an ingredient will not be evident when present at a level above the generic concentration limits mentioned in Tables 3.2.3 and 3.2.4. In these cases the mixture shall be classified according to that data (see also Articles 10 and 11). On other occasions, when it is expected that the skin corrosion/irritation hazard of an ingredient is not evident when present at a level above the generic concentration limits mentioned in Tables 3.2.3 and 3.2.4, testing of the mixture shall be considered. In those cases the tiered weight of evidence strategy shall be applied, as described in paragraph 3.2.2.5. 3.2.3.3.5. On occasion, reliable data may show that the skin corrosion/irritation hazard of an ingredient will not be evident when present at a level at or above the generic concentration limits mentioned in Tables 3.2.3 and 3.2.4 in section 3.2.3.3.6. In these cases the mixture shall be classified according to that data (see also Articles 10 and 11). On other occasions, when it is expected that the skin corrosion/irritation hazard of an ingredient is not evident when present at a level at or above the generic concentration limits mentioned in Tables 3.2.3 and 3.2.4, testing of the mixture shall be considered. In those cases the tiered weight of evidence strategy shall be applied, as set out in section 3.2.2.5. 3.2.3.3.6. If there are data showing that (an) ingredient(s) is/are corrosive or irritant at a concentration of < 1 % (corrosive) or < 3 % (irritant), the mixture shall be classified accordingly. Table 3.2.3 Generic concentration limits of ingredients classified for skin corrosive/irritant hazard (Category 1 or 2) that trigger classification of the mixture as corrosive/irritant to skin … 20 unchanged lines … Classification Category 1 A/1 B/1 C Category 2 GHS Pictograms Signal Word Danger Warning Hazard Statement H314: Causes severe skin burns and eye damage H315: Causes skin irritation Precautionary Statement Prevention P260 Precautionary Statement Prevention P260 P264 P280 P264 P280 Precautionary Statement Response P301 + P330 + P331 Precautionary Statement Response P301 + P330 + P331 P303 + P361 + P353 P363 P304 + P340 P310 P321 P305 + P351 + P338 P302 + P352 P321 P332 + P313 P362 Precautionary Statement Storage P405 Precautionary Statement Disposal P501 3.3. Serious eye damage/eye irritation P362 + P364 Precautionary Statement Storage P405 Precautionary Statement Disposal P501 3.3. Serious eye damage/eye irritation 3.3.1. Definitions 3.3.1.1. Serious eye damage means the production of tissue damage in the eye, or serious physical decay of vision, following application of a test substance to the anterior surface of the eye, which is not fully reversible within 21 days of application. Eye irritation means the production of changes in the eye following the application of test substance to the anterior surface of the eye, which are fully reversible within 21 days of application. … 44 unchanged lines … 3.3.3.3.4.1. Particular care must be taken when classifying certain types of mixtures containing substances such as acids and bases, inorganic salts, aldehydes, phenols, and surfactants. The approach explained in paragraphs 3.3.3.3.1 and 3.3.3.3.2 might not work given that many of such substances are corrosive or irritant at concentrations < 1 %. 3.3.3.3.4.2. For mixtures containing strong acids or bases the pH shall be used as classification criteria (see paragraph 3.3.2.3) since pH will be a better indicator of serious eye damage than the generic concentration limits of Table 3.3.3. 3.3.3.3.4.3. A mixture containing corrosive or irritant ingredients that cannot be classified based on the additivity approach (Table 3.3.3), due to chemical characteristics that make this approach unworkable, shall be classified as Category 1 for effects on the eye if it contains ≥ 1 % of a corrosive ingredient and as Category 2 when it contains ≥ 3 % of an irritant ingredient. Classification of mixtures with ingredients for which the approach in Table 3.3.3 does not apply is summarised in Table 3.3.4. 3.3.3.3.5. On occasion, reliable data may show that the reversible/irreversible eye effects of an ingredient will not be evident when present at a level above the generic concentration limits mentioned in Tables 3.3.3 and 3.3.4. In these cases the mixture shall be classified according to those data. On other occasions, when it is expected that the skin corrosion/irritation hazards or the reversible/irreversible eye effects of an ingredient will not be evident when present at a level above the generic concentration limits mentioned in Tables 3.3.3 and 3.3.4, testing of the mixture shall be considered. In those cases, the tiered weight of evidence strategy shall be applied. 3.3.3.3.5. On occasion, reliable data may show that the reversible/irreversible eye effects of an ingredient will not be evident when present at a level at or above the generic concentration limits mentioned in Tables 3.3.3 and 3.3.4 in section 3.3.3.3.6. In these cases the mixture shall be classified according to those data. On other occasions, when it is expected that the skin corrosion/irritation hazards or the reversible/irreversible eye effects of an ingredient will not be evident when present at a level at or above the generic concentration limits mentioned in Tables 3.3.3 and 3.3.4, testing of the mixture shall be considered. In those cases, the tiered weight of evidence strategy shall be applied. 3.3.3.3.6. If there are data showing that (an) ingredient(s) may be corrosive or irritant at a concentration of < 1 % (corrosive) or < 3 % (irritant), the mixture shall be classified accordingly. Table 3.3.3 Generic concentration limits of ingredients of a mixture classified as Skin corrosive Category 1 and/or eye Category 1 or 2 for effects on the eye that trigger classification of the mixture for effects on the eye (Category 1 or 2) … 34 unchanged lines … 3.4.1.2. Skin sensitiser means a substance that will lead to an allergic response following skin contact. 3.4.1.3. For the purpose of section 3.4, sensitisation includes two phases: the first phase is induction of specialised immunological memory in an individual by exposure to an allergen. The second phase is elicitation, i.e. production of a cell-mediated or antibody-mediated allergic response by exposure of a sensitised individual to an allergen. 3.4.1.4. For respiratory sensitisation, the pattern of induction followed by elicitation phases is shared in common with skin sensitisation. For skin sensitisation, an induction phase is required in which the immune system learns to react; clinical symptoms can then arise when subsequent exposure is sufficient to elicit a visible skin reaction (elicitation phase). As a consequence, predictive tests usually follow this pattern in which there is an induction phase, the response to which is measured by a standardised elicitation phase, typically involving a patch test. The local lymph node assay is the exception, directly measuring the induction response. Evidence of skin sensitisation in humans normally is assessed by a diagnostic patch test. 3.4.1.5. Usually, for both skin and respiratory sensitisation, lower levels are necessary for elicitation than are required for induction. Provisions for alerting sensitised individuals to the presence of a particular sensitiser in a mixture can be found in Annex II, section 2.8.. 3.4.1.5. Usually, for both skin and respiratory sensitisation, lower levels are necessary for elicitation than are required for induction. Provisions for alerting sensitised individuals to the presence of a particular sensitiser in a mixture can be found in Annex II, section 2.8.. 3.4.1.6. The hazard class Respiratory or Skin Sensitisation is differentiated into: Respiratory Sensitisation and; Skin Sensitisation. 3.4.2. Classification criteria for substances 3.4.2.1. Respiratory sensitisers 3.4.2.1.1. Hazard categories 3.4.2.1.1.1. Respiratory sensitisers shall be classified in Category 1 where data are not sufficient for sub-categorisation. 3.4.2.1.1.2. Where data are sufficient a refined evaluation according to 3.4.2.1.1.3 shall allow the allocation of respiratory sensitisers into sub-category 1A, strong sensitisers, or sub-category 1B for other respiratory sensitisers. 3.4.2.1.1.3. Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for respiratory sensitisers. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table 3.4.1 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals. 3.4.2.1.1.1. Respiratory sensitisers shall be classified in Category 1 where data are not sufficient for sub-categorisation. 3.4.2.1.1.2. Where data are sufficient a refined evaluation according to 3.4.2.1.1.3 shall allow the allocation of respiratory sensitisers into sub-category 1A, strong sensitisers, or sub-category 1B for other respiratory sensitisers. 3.4.2.1.1.3. Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for respiratory sensitisers. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table 3.4.1 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals. 3.4.2.1.1.4. Substances shall be classified as respiratory sensitisers in accordance with the criteria in Table 3.4.1: Table 3.4.1 Hazard category and sub-categories for respiratory sensitisers At present, recognised and validated animal models for the testing of respiratory hypersensitivity are not available. Under certain circumstances, data from animal studies may provide valuable information in a weight of evidence assessment. Category Criteria Category 1 Substances shall be classified as respiratory sensitisers (Category 1) where data are not sufficient for sub-categorisation in accordance with the following criteria: Category 1 Substances shall be classified as respiratory sensitisers (Category 1) where data are not sufficient for sub-categorisation in accordance with the following criteria: (a) if there is evidence in humans that the substance can lead to specific respiratory hypersensitivity; and/or (b) if there are positive results from an appropriate animal test. Sub-category 1A: Substances showing a high frequency of occurrence in humans; or a probability of occurrence of a high sensitisation rate in humans based on animal or other tests. Severity of reaction may also be considered. Sub-category 1B: Substances showing a low to moderate frequency of occurrence in humans; or a probability of occurrence of a low to moderate sensitisation rate in humans based on animal or other tests. Severity of reaction may also be considered. Sub-category 1A: Substances showing a high frequency of occurrence in humans; or a probability of occurrence of a high sensitisation rate in humans based on animal or other tests. Severity of reaction may also be considered. Sub-category 1B: Substances showing a low to moderate frequency of occurrence in humans; or a probability of occurrence of a low to moderate sensitisation rate in humans based on animal or other tests. Severity of reaction may also be considered. 3.4.2.1.2. Human evidence 3.4.2.1.2.1. Evidence that a substance can lead to specific respiratory hypersensitivity will normally be based on human experience. In this context, hypersensitivity is normally seen as asthma, but other hypersensitivity reactions such as rhinitis/conjunctivitis and alveolitis are also considered. The condition will have the clinical character of an allergic reaction. However, immunological mechanisms do not have to be demonstrated. 3.4.2.1.2.2. When considering the human evidence, it is necessary for a decision on classification to take into account, in addition to the evidence from the cases: (a) the size of the population exposed; (b) the extent of exposure. The use of human data is discussed in sections 1.1.1.3, 1.1.1.4 and 1.1.1.5. The use of human data is discussed in sections 1.1.1.3, 1.1.1.4 and 1.1.1.5. 3.4.2.1.2.3. The evidence referred to above could be: (a) clinical history and data from appropriate lung function tests related to exposure to the substance, confirmed by other supportive evidence which may include: (i) in vivo immunological test (e.g. skin prick test); (ii) in vitro immunological test (e.g. serological analysis); (iii) studies that indicate other specific hypersensitivity reactions where immunological mechanisms of action have not been proven, e.g. repeated low-level irritation, pharmacologically mediated effects; (iv) a chemical structure related to substances known to cause respiratory hypersensitivity; (b) data from one or more positive bronchial challenge tests with the substance conducted according to accepted guidelines for the determination of a specific hypersensitivity reaction. 3.4.2.1.2.4. Clinical history shall include both medical and occupational history to determine a relationship between exposure to a specific substance and development of respiratory hypersensitivity. Relevant information includes aggravating factors both in the home and workplace, the onset and progress of the disease, family history and medical history of the patient in question. The medical history shall also include a note of other allergic or airway disorders from childhood, and smoking history. 3.4.2.1.2.5. The results of positive bronchial challenge tests are considered to provide sufficient evidence for classification on their own. It is however recognised that in practice many of the examinations listed above will already have been carried out. 3.4.2.1.3. Animal studies 3.4.2.1.3.1. Data from appropriate animal studiesAt present, recognised and validated animal models for the testing of respiratory hypersensitivity are not available. Under certain circumstances, data from animal studies may provide valuable information in a weight of evidence assessment. which may be indicative of the potential of a substance to cause sensitisation by inhalation in humansThe mechanisms by which substances induce symptoms of asthma are not yet fully known. For preventative measures, these substances are considered respiratory sensitisers. However, if on the basis of the evidence, it can be demonstrated that these substances induce symptoms of asthma by irritation only in people with bronchial hyper reactivity, they should not be considered as respiratory sensitisers. may include: (a) measurements of Immunoglobulin E (IgE) and other specific immunological parameters in mice; (b) specific pulmonary responses in guinea pigs. 3.4.2.2. Skin sensitisers 3.4.2.2.1. Hazard categories 3.4.2.2.1.1. Skin sensitisers shall be classified in Category 1 where data are not sufficient for sub-categorisation. 3.4.2.2.1.2. Where data are sufficient a refined evaluation according to section 3.4.2.2.1.3 allows the allocation of skin sensitisers into sub-category 1A, strong sensitisers, or sub-category 1B for other skin sensitisers. 3.4.2.2.1.3. Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for skin sensitisers as described in section 3.4.2.2.2. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table 3.4.2 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals according to the guidance values provided in sections 3.4.2.2.2.1 and 3.4.2.2.3.2 for sub-category 1A and in sections 3.4.2.2.2.2 and 3.4.2.2.3.3 for sub-category 1B. 3.4.2.2.1.1. Skin sensitisers shall be classified in Category 1 where data are not sufficient for sub-categorisation. 3.4.2.2.1.2. Where data are sufficient a refined evaluation according to section 3.4.2.2.1.3 allows the allocation of skin sensitisers into sub-category 1A, strong sensitisers, or sub-category 1B for other skin sensitisers. 3.4.2.2.1.3. Effects seen in either humans or animals will normally justify classification in a weight of evidence approach for skin sensitisers as described in section 3.4.2.2.2. Substances may be allocated to one of the two sub-categories 1A or 1B using a weight of evidence approach in accordance with the criteria given in Table 3.4.2 and on the basis of reliable and good quality evidence from human cases or epidemiological studies and/or observations from appropriate studies in experimental animals according to the guidance values provided in sections 3.4.2.2.2.1 and 3.4.2.2.3.2 for sub-category 1A and in sections 3.4.2.2.2.2 and 3.4.2.2.3.3 for sub-category 1B. 3.4.2.2.1.4. Substances shall be classified as skin sensitisers in accordance with the criteria in Table 3.4.2: Table 3.4.2 Hazard category and sub-categories for skin sensitisers Category Criteria Category 1 Substances shall be classified as skin sensitisers (Category 1) where data are not sufficient for sub-categorisation in accordance with the following criteria: Category 1 Substances shall be classified as skin sensitisers (Category 1) where data are not sufficient for sub-categorisation in accordance with the following criteria: (a) if there is evidence in humans that the substance can lead to sensitisation by skin contact in a substantial number of persons; or (b) if there are positive results from an appropriate animal test (see specific criteria in section 3.4.2.2.4.1). Sub-category 1A: Substances showing a high frequency of occurrence in humans and/or a high potency in animals can be presumed to have the potential to produce significant sensitisation in humans. Severity of reaction may also be considered. Sub-category 1B: Substances showing a low to moderate frequency of occurrence in humans and/or a low to moderate potency in animals can be presumed to have the potential to produce sensitisation in humans. Severity of reaction may also be considered. (b) if there are positive results from an appropriate animal test (see specific criteria in section 3.4.2.2.4.1). Sub-category 1A: Substances showing a high frequency of occurrence in humans and/or a high potency in animals can be presumed to have the potential to produce significant sensitisation in humans. Severity of reaction may also be considered. Sub-category 1B: Substances showing a low to moderate frequency of occurrence in humans and/or a low to moderate potency in animals can be presumed to have the potential to produce sensitisation in humans. Severity of reaction may also be considered. 3.4.2.2.2. Human evidence 3.4.2.2.2.1. Human evidence for sub-category 1A can include: 3.4.2.2.2.1. Human evidence for sub-category 1A can include: (a) positive responses at ≤ 500 μg/cm2 (HRIPT, HMT — induction threshold); (b) diagnostic patch test data where there is a relatively high and substantial incidence of reactions in a defined population in relation to relatively low exposure; (c) other epidemiological evidence where there is a relatively high and substantial incidence of allergic contact dermatitis in relation to relatively low exposure. 3.4.2.2.2.2. Human evidence for sub-category 1B can include: 3.4.2.2.2.2. Human evidence for sub-category 1B can include: (a) positive responses at > 500 μg/cm2 (HRIPT, HMT — induction threshold); (b) diagnostic patch test data where there is a relatively low but substantial incidence of reactions in a defined population in relation to relatively high exposure; (c) other epidemiological evidence where there is a relatively low but substantial incidence of allergic contact dermatitis in relation to relatively high exposure. The use of human data is discussed in sections 1.1.1.3, 1.1.1.4 and 1.1.1.5. The use of human data is discussed in sections 1.1.1.3, 1.1.1.4 and 1.1.1.5. 3.4.2.2.3. Animal studies 3.4.2.2.3.1. For Category 1, when an adjuvant type test method for skin sensitisation is used, a response of at least 30 % of the animals is considered as positive. For a non-adjuvant Guinea pig test method a response of at least 15 % of the animals is considered positive. For Category 1, a stimulation index of three or more is considered a positive response in the local lymph node assay. Test methods for skin sensitisation are described in the OECD Guideline 406 (the Guinea Pig Maximisation test and the Buehler guinea pig test) and Guideline 429 (Local Lymph Node Assay). Other methods may be used provided that they are well-validated and scientific justification is given. For example, the mouse ear swelling test (MEST) could be a reliable screening test to detect moderate to strong sensitisers, and could be used as a first stage in the assessment of skin sensitisation potential. 3.4.2.2.3.2. Animal test results for sub-category 1A can include data with values indicated in Table 3.4.3 3.4.2.2.3.1. For Category 1, when an adjuvant type test method for skin sensitisation is used, a response of at least 30 % of the animals is considered as positive. For a non-adjuvant Guinea pig test method a response of at least 15 % of the animals is considered positive. For Category 1, a stimulation index of three or more is considered a positive response in the local lymph node assay. Test methods for skin sensitisation are described in the OECD Guideline 406 (the Guinea Pig Maximisation test and the Buehler guinea pig test) and Guideline 429 (Local Lymph Node Assay). Other methods may be used provided that they are well-validated and scientific justification is given. For example, the mouse ear swelling test (MEST) could be a reliable screening test to detect moderate to strong sensitisers, and could be used as a first stage in the assessment of skin sensitisation potential. 3.4.2.2.3.2. Animal test results for sub-category 1A can include data with values indicated in Table 3.4.3 Table 3.4.3 Animal test results for sub-category 1A Animal test results for sub-category 1A Assay Criteria Local lymph node assay EC3 value ≤ 2 % Guinea pig maximisation test ≥ 30 % responding at ≤ 0,1 % intradermal induction dose or ≥ 60 % responding at > 0,1 % to ≤ 1 % intradermal induction dose Buehler assay ≥ 15 % responding at ≤ 0,2 % topical induction dose or ≥ 60 % responding at > 0,2 % to ≤ 20 % topical induction dose 3.4.2.2.3.3. Animal test results for sub-category 1B can include data with values indicated in Table 3.4.4 below: Local lymph node assay EC3 value ≤ 2 % Guinea pig maximisation test ≥ 30 % responding at ≤ 0,1 % intradermal induction dose or ≥ 60 % responding at > 0,1 % to ≤ 1 % intradermal induction dose Buehler assay ≥ 15 % responding at ≤ 0,2 % topical induction dose or ≥ 60 % responding at > 0,2 % to ≤ 20 % topical induction dose 3.4.2.2.3.3. Animal test results for sub-category 1B can include data with values indicated in Table 3.4.4 below: Table 3.4.4 Animal test results for sub-category 1B Animal test results for sub-category 1B Assay Criteria Local lymph node assay EC3 value > 2 % Guinea pig maximisation test ≥ 30 % to < 60 % responding at > 0,1 % to ≤ 1 % intradermal induction dose or ≥ 30 % responding at > 1 % intradermal induction dose Buehler assay ≥ 15 % to < 60 % responding at > 0,2 % to ≤ 20 % topical induction dose or ≥ 15 % responding at > 20 % topical induction dose Local lymph node assay EC3 value > 2 % Guinea pig maximisation test ≥ 30 % to < 60 % responding at > 0,1 % to ≤ 1 % intradermal induction dose or ≥ 30 % responding at > 1 % intradermal induction dose Buehler assay ≥ 15 % to < 60 % responding at > 0,2 % to ≤ 20 % topical induction dose or ≥ 15 % responding at > 20 % topical induction dose 3.4.2.2.4. Specific considerations 3.4.2.2.4.1. For classification of a substance, evidence should include any or all of the following using a weight of evidence approach: (a) positive data from patch testing, normally obtained in more than one dermatology clinic; (b) epidemiological studies showing allergic contact dermatitis caused by the substance. Situations in which a high proportion of those exposed exhibit characteristic symptoms are to be looked at with special concern, even if the number of cases is small; (c) positive data from appropriate animal studies; (d) positive data from experimental studies in man (see section 1.3.2.4.7); (d) positive data from experimental studies in man (see section 1.3.2.4.7); (e) well documented episodes of allergic contact dermatitis, normally obtained in more than one dermatology clinic; (f) severity of reaction may also be considered. 3.4.2.2.4.2. Evidence from animal studies is usually much more reliable than evidence from human exposure. However, in cases where evidence is available from both sources, and there is conflict between the results, the quality and reliability of the evidence from both sources must be assessed in order to resolve the question of classification on a case-by-case basis. Normally, human data are not generated in controlled experiments with volunteers for the purpose of hazard classification but rather as part of risk assessment to confirm lack of effects seen in animal tests. Consequently, positive human data on skin sensitisation are usually derived from case-control or other, less defined studies. Evaluation of human data must therefore be carried out with caution as the frequency of cases reflect, in addition to the inherent properties of the substances, factors such as the exposure situation, bioavailability, individual predisposition and preventive measures taken. Negative human data should not normally be used to negate positive results from animal studies. For both animal and human data, consideration should be given to the impact of vehicle. 3.4.2.2.4.3. If none of the abovementioned conditions are met, the substance need not be classified as a skin sensitiser. However, a combination of two or more indicators of skin sensitisation as listed below may alter the decision. This shall be considered on a case-by-case basis. (a) Isolated episodes of allergic contact dermatitis; (b) epidemiological studies of limited power, e.g. where chance, bias or confounders have not been ruled out fully with reasonable confidence; (c) data from animal tests, performed according to existing guidelines, which do not meet the criteria for a positive result described in section 3.4.2.2.3, but which are sufficiently close to the limit to be considered significant; (c) data from animal tests, performed according to existing guidelines, which do not meet the criteria for a positive result described in section 3.4.2.2.3, but which are sufficiently close to the limit to be considered significant; (d) positive data from non-standard methods; (e) positive results from close structural analogues. 3.4.2.2.4.4. Immunological contact urticaria Substances meeting the criteria for classification as respiratory sensitisers may in addition cause immunological contact urticaria. Consideration should be given to classifying these substances also as skin sensitisers. Substances which cause immunological contact urticaria without meeting the criteria for respiratory sensitisers should also be considered for classification as skin sensitisers. There is no recognised animal model available to identify substances which cause immunological contact urticaria. Therefore, classification will normally be based on human evidence which will be similar to that for skin sensitisation. 3.4.3. Classification criteria for mixtures 3.4.3.1. Classification of mixtures when data are available for the complete mixture 3.4.3.1.1. When reliable and good quality evidence from human experience or appropriate studies in experimental animals, as described in the criteria for substances, is available for the mixture, then the mixture can be classified by weight of evidence evaluation of these data. Care shall be exercised in evaluating data on mixtures, that the dose used does not render the results inconclusive. 3.4.3.2. Classification of mixtures when data are not available for the complete mixture: bridging principles 3.4.3.2.1. Where the mixture itself has not been tested to determine its sensitising properties, but there are sufficient data on the individual ingredients and similar tested mixtures to adequately characterise the hazards of the mixture, these data shall be used in accordance with the bridging rules set out in section 1.1.3. 3.4.3.3. Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture 3.4.3.3.1. The mixture shall be classified as a respiratory or skin sensitiser when at least one ingredient has been classified as a respiratory or skin sensitiser and is present at or above the appropriate generic concentration limit as shown in Table 3.4.5 for solid/liquid and gas respectively. 3.4.3.3.2. Some substances that are classified as sensitisers may elicit a response, when present in a mixture in quantities below the concentrations established in Table 3.4.5, in individuals who are already sensitised to the substance or mixture (see Note 1 to Table 3.4.6). Table 3.4.5 Generic concentration limits of components of a mixture classified as either respiratory sensitisers or skin sensitisers that trigger classification of the mixture Component classified as: Generic concentration limits triggering classification of a mixture as: Respiratory sensitiser Category 1 Skin sensitiser Category 1 Category 1 Skin sensitiser Category 1 Solid/liquid Gas All physical states Respiratory sensitiser Category 1 ≥ 1,0 % ≥ 0,2 % Respiratory sensitiser Sub-category 1A ≥ 0,1 % ≥ 0,1 % Respiratory sensitiser Sub-category 1B ≥ 1,0 % ≥ 0,2 % Skin sensitiser Category 1 ≥ 1,0 % Category 1 ≥ 1,0 % ≥ 0,2 % Respiratory sensitiser Sub-category 1A ≥ 0,1 % ≥ 0,1 % Respiratory sensitiser Sub-category 1B ≥ 1,0 % ≥ 0,2 % Skin sensitiser Category 1 ≥ 1,0 % Skin sensitiser Sub-category 1A ≥ 0,1 % Sub-category 1A ≥ 0,1 % Skin sensitiser Sub-category 1B ≥ 1,0 % Sub-category 1B ≥ 1,0 % Table 3.4.6 Concentration limits for elicitation of components of a mixture Component classified as: Concentration limits for elicitation Respiratory sensitiser Category 1 Skin sensitiser Category 1 Category 1 Skin sensitiser Category 1 Solid/liquid Gas All physical states Respiratory sensitiser Category 1 ≥ 0,1 % (Note 1) ≥ 0,1 % (Note 1) Respiratory sensitiser Sub-category 1A ≥ 0,01 % (Note 1) ≥ 0,01 % (Note 1) Respiratory sensitiser Sub-category 1B ≥ 0,1 % (Note 1) ≥ 0,1 % (Note 1) Skin sensitiser Category 1 ≥ 0,1 % (Note 1) Category 1 ≥ 0,1 % (Note 1) ≥ 0,1 % (Note 1) Respiratory sensitiser Sub-category 1A ≥ 0,01 % (Note 1) ≥ 0,01 % (Note 1) Respiratory sensitiser Sub-category 1B ≥ 0,1 % (Note 1) ≥ 0,1 % (Note 1) Skin sensitiser Category 1 ≥ 0,1 % (Note 1) Skin sensitiser Sub-category 1A ≥ 0,01 % (Note 1) Sub-category 1A ≥ 0,01 % (Note 1) Skin sensitiser Sub-category 1B ≥ 0,1 % (Note 1) Sub-category 1B ≥ 0,1 % (Note 1) Note 1: This concentration limit for elicitation is used for the application of the special labelling requirements of Annex II section 2.8 to protect already sensitised individuals. A SDS is required for the mixture containing a component above this concentration. For sensitising substances with specific concentration limit lower than 0,1 %, the concentration limit for elicitation should be set at one tenth of the specific concentration limit. This concentration limit for elicitation is used for the application of the special labelling requirements of section 2.8 of Annex II to protect already sensitised individuals. A SDS is required for the mixture containing a component at or above this concentration. For sensitising substances with specific concentration limit lower than 0,1 %, the concentration limit for elicitation should be set at one tenth of the specific concentration limit. 3.4.4. Hazard communication 3.4.4.1. Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 3.4.7. Table 3.4.7 Respiratory or skin sensitisation label elements Classification Respiratory sensitisation Skin sensitisation Category 1 and sub-categories 1A and 1B Category 1 and sub-categories 1A and 1B GHS pictograms Signal word Danger Warning Hazard statement H334: May cause allergy or asthma symptoms or breathing difficulties if inhaled H317: May cause an allergic skin reaction Precautionary statement prevention P261 P285 P261 Category 1 and subcategories 1A and 1B Category 1 and subcategories 1A and 1B GHS Pictograms Signal Word Danger Warning Hazard Statement H334: May cause allergy or asthma symptoms or breathing difficulties if inhaled H317: May cause an allergic skin reaction Precautionary Statement Prevention P261 P284 P261 P272 P280 Precautionary statement response P304 + P341 P342 + P311 P302 + P352 P333 + P313 Precautionary Statement Response P304 + P340 P342 + P311 P302 + P352 P333 + P313 P321 P363 Precautionary statement storage Precautionary statement disposal P501 P501 P362 + P364 Precautionary Statement Storage Precautionary Statement Disposal P501 P501 3.5. Germ cell mutagenicity 3.5.1. Definitions and general considerations 3.5.1.1. A mutation means a permanent change in the amount or structure of the genetic material in a cell. The term mutation applies both to heritable genetic changes that may be manifested at the phenotypic level and to the underlying DNA modifications when known (including specific base pair changes and chromosomal translocations). The term mutagenic and mutagen will be used for agents giving rise to an increased occurrence of mutations in populations of cells and/or organisms. … 48 unchanged lines … 3.5.3.1. Classification of mixtures when data are available for all ingredients or only for some ingredients of the mixture 3.5.3.1.1. The mixture shall be classified as a mutagen when at least one ingredient has been classified as a Category 1A, Category 1B or Category 2 mutagen and is present at or above the appropriate generic concentration limit as shown in Table 3.5.2 for Category 1A, Category 1B and Category 2 respectively. Table 3.5.2 Generic concentration limits of ingredients of a mixture classified as germ cell mutagens that trigger classification of the mixture. Concentration limits triggering classification of a mixture as: Ingredient classified as: Category 1A mutagen Category 1B mutagen Category 2 mutagen Generic concentration limits of ingredients of a mixture classified as germ cell mutagens that trigger classification of the mixture Ingredient classified as: Concentration limits triggering classification of a mixture as: Category 1 mutagen Category 2 mutagen Category 1A Category 1B Category 1A mutagen ≥ 0,1 % — — Category 1B mutagen — ≥ 0,1 % — Category 2 mutagen — — ≥ 1,0 % Note The concentration limits in the table above apply to solids and liquids (w/w units) as well as gases (v/v units). 3.5.3.2. Classification of mixtures when data are available for the complete mixture 3.5.3.2.1. Classification of mixtures will be based on the available test data for the individual ingredients of the mixture using concentration limits for the ingredients classified as germ cell mutagens. On a case-by-case basis, test data on mixtures may be used for classification when demonstrating effects that have not been established from the evaluation based on the individual ingredients. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations, sensitivity and statistical analysis of germ cell mutagenicity test systems. Adequate documentation supporting the classification shall be retained and made available for review upon request. 3.5.3.3. Classification of mixtures when data are not available for the complete mixture: bridging principles 3.5.3.3.1. Where the mixture itself has not been tested to determine its germ cell mutagenicity hazard, but there are sufficient data on the individual ingredients and similar tested mixtures (subject to paragraph 3.5.3.2.1), to adequately characterise the hazards of the mixture, these data shall be used in accordance with the applicable bridging rules set out in section 1.1.3. 3.5.4. Hazard communication 3.5.4.1. Label elements shall be used in accordance with Table 3.5.3, for substances or mixtures meeting the criteria for classification in this hazard class. Table 3.5.3 Label elements of germ cell mutagenicity Classification Category 1A or Category 1B Category 2 Classification Category 1 (Category 1A, 1B) Category 2 GHS Pictograms Signal Word Danger Warning Hazard Statement H340: May cause genetic defects (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H341: Suspected of causing genetic defects (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) Precautionary Statement Prevention P201 Precautionary Statement Prevention P201 P202 P281 P201 P280 P201 P202 P281 Precautionary Statement Response P308 + P313 P308 + P313 Precautionary Statement Storage P405 P405 Precautionary Statement Disposal P501 P501 P280 Precautionary Statement Response P308 + P313 P308 + P313 Precautionary Statement Storage P405 P405 Precautionary Statement Disposal P501 P501 3.5.5. Additional classification considerations It is increasingly accepted that the process of chemical-induced tumorigenesis in humans and animals involves genetic changes for example in proto-oncogenes and/or tumour suppresser genes of somatic cells. Therefore, the demonstration of mutagenic properties of substances in somatic and/or germ cells of mammals in vivo may have implications for the potential classification of these substances as carcinogens (see also Carcinogenicity, section 3.6, paragraph 3.6.2.2.6). 3.6. Carcinogenicity … 51 unchanged lines … Table 3.6.2 Generic concentration limits of ingredients of a mixture classified as carcinogen that trigger classification of the mixture Ingredient classified as: Generic concentration limits triggering classification of a mixture as: Category 1A carcinogen Category 1B carcinogen Category 2 carcinogen Category 1 carcinogen Category 2 carcinogen Category 1A Category 1B Category 1A carcinogen ≥ 0,1 % — — Category 1B carcinogen — ≥ 0,1 % — Category 2 carcinogen — — ≥ 1,0 % [Note 1] Note The concentration limits in the table above apply to solids and liquids (w/w units) as well as gases (v/v units). Note 1 If a Category 2 carcinogen is present in the mixture as an ingredient at a concentration ≥ 0,1 % a SDS shall be available for the mixture upon request. 3.6.3.2. Classification of mixtures when data are available for the complete mixture 3.6.3.2.1. Classification of mixtures will be based on the available test data for the individual ingredients of the mixture using concentration limits for the ingredients classified as carcinogens. On a case-by-case basis, test data on mixtures may be used for classification when demonstrating effects that have not been established from the evaluation based on the individual ingredients. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations, sensitivity and statistical analysis of carcinogenicity test systems. Adequate documentation supporting the classification shall be retained and made available for review upon request. 3.6.3.3. Classification of mixtures when data are not available for the complete mixture: bridging principles 3.6.3.3.1. Where the mixture itself has not been tested to determine its carcinogenic hazard, but there are sufficient data on the individual ingredients and similar tested mixtures (subject to paragraph 3.6.3.2.1) to adequately characterise the hazards of the mixture, these data shall be used in accordance with the applicable bridging rules set out in section 1.1.3. 3.6.4. Hazard Communication 3.6.4.1. Label elements shall be used in accordance with Table 3.6.3, for substances or mixtures meeting the criteria for classification in this hazard class. Table 3.6.3 Label elements for carcinogenicity Classification Category 1A or Category 1B Category 2 Classification Category 1 (Category 1A, 1B) Category 2 GHS Pictograms Signal Word Danger Warning Hazard Statement H350: May cause cancer (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H351: Suspected of causing cancer (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) Precautionary Statement Prevention P201 Precautionary Statement Prevention P201 P202 P281 P201 P280 P201 P202 P281 Precautionary Statement Response P308 + P313 P308 + P313 Precautionary Statement Storage P405 P405 Precautionary Statement Disposal P501 P501 P280 Precautionary Statement Response P308 + P313 P308 + P313 Precautionary Statement Storage P405 P405 Precautionary Statement Disposal P501 P501 3.7. Reproductive toxicity 3.7.1. Definitions and general considerations 3.7.1.1. Reproductive toxicity includes adverse effects on sexual function and fertility in adult males and females, as well as developmental toxicity in the offspring. The definitions presented below are adapted from those agreed as working definitions in IPCS/EHC Document No 225, Principles for Evaluating Health Risks to Reproduction Associated with Exposure to Chemicals. For classification purposes, the known induction of genetically based heritable effects in the offspring is addressed in Germ Cell Mutagenicity (section 3.5), since in the present classification system it is considered more appropriate to address such effects under the separate hazard class of germ cell mutagenicity. … 81 unchanged lines … 3.7.3.1.2. The mixture shall be classified for effects on or via lactation when at least one ingredient has been classified for effects on or via lactation and is present at or above the appropriate generic concentration limit as shown in Table 3.7.2 for the additional category for effects on or via lactation. Table 3.7.2 Generic concentration limits of ingredients of a mixture classified as reproduction toxicants or for effects on or via lactation that trigger classification of the mixture Note: The concentration limits in Table 3.7.2 apply to solids and liquids (w/w units) as well as gases (v/v units). Note 1: If a Category 1 or Category 2 reproductive toxicant or a substance classified for effects on or via lactation is present in the mixture as an ingredient at a concentration at or above 0,1 %, a SDS shall be available for the mixture upon request. Ingredient classified as: Generic concentration limits triggering classification of a mixture as: Category 1A reproductive toxicant Category 1B reproductive toxicant Category 2 reproductive toxicant Additional category for effects on or via lactation Category 1 reproductive toxicant Category 2 reproductive toxicant Additional category for effects on or via lactation Category 1A Category 1B Category 1A reproductive toxicant ≥ 0,3 % [Note 1] Category 1B reproductive toxicant ≥ 0,3 % [Note 1] Category 2 reproductive toxicant ≥ 3,0 % [Note 1] Additional category for effects on or via lactation ≥ 0,3 % [Note 1] Note The concentration limits in the table above apply to solids and liquids (w/w units) as well as gases (v/v units). Note 1 If a Category 1 or Category 2 reproductive toxicant or a substance classified for effects on or via lactation is present in the mixture as an ingredient at a concentration above 0,1 %, a SDS shall be available for the mixture upon request. 3.7.3.2. Classification of mixtures when data are available for the complete mixture 3.7.3.2.1. Classification of mixtures will be based on the available test data for the individual ingredients of the mixture using concentration limits for the ingredients of the mixture. On a case-by-case basis, test data on mixtures may be used for classification when demonstrating effects that have not been established from the evaluation based on the individual components. In such cases, the test results for the mixture as a whole must be shown to be conclusive taking into account dose and other factors such as duration, observations, sensitivity and statistical analysis of reproduction test systems. Adequate documentation supporting the classification shall be retained and made available for review upon request. 3.7.3.3. Classification of mixtures when data are not available for the complete mixture: bridging principles 3.7.3.3.1. Subject to paragraph 3.7.3.2.1, where the mixture itself has not been tested to determine its reproductive toxicity, but there are sufficient data on the individual ingredients and similar tested mixtures to adequately characterise the hazards of the mixture, these data shall be used in accordance with the applicable bridging rules set out in section 1.1.3. 3.7.4. Hazard Communication 3.7.4.1. Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 3.7.3 Table 3.7.3 Label elements for reproductive toxicity Classification Category 1A or Category 1B Category 2 Additional category for effects on or via lactation Classification Category 1 (Category 1A, 1B) Category 2 Additional category for effects on or via lactation GHS Pictograms No pictogram Signal Word Danger Warning No signal word Hazard Statement H360: May damage fertility or the unborn child (state specific effect if known)(state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H361: Suspected of damaging fertility or the unborn child (state specific effect if known) (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H362: May cause harm to breast-fed children. Precautionary Statement Prevention P201 P202 P281 P201 P280 P201 P202 P281 P201 P280 P201 P260 P263 P264 … 115 unchanged lines … Note 1 If a Category 2 specific target organ toxicant is present in the mixture as an ingredient at a concentration ≥ 1,0 % a SDS shall be available for the mixture upon request. 3.8.3.4.4. Care shall be exercised when toxicants affecting more than one organ system are combined that the potentiation or synergistic interactions are considered, because certain substances can cause target organ toxicity at < 1 % concentration when other ingredients in the mixture are known to potentiate its toxic effect. 3.8.3.4.5. Care shall be exercised when extrapolating toxicity of a mixture that contains Category 3 ingredient(s). A generic concentration limit of 20 % is appropriate; however, it shall be recognised that this concentration limit may be higher or lower depending on the Category 3 ingredient(s) and that some effects such as respiratory tract irritation may not occur below a certain concentration while other effects such as narcotic effects may occur below this 20 % value. Expert judgement shall be exercised. Respiratory tract irritation and narcotic effects are to be evaluated separately in accordance with the criteria given in section 3.8.2.2. When conducting classifications for these hazards, the contribution of each component should be considered additive, unless there is evidence that the effects are not additive. 3.8.3.4.5. Care shall be exercised when extrapolating toxicity of a mixture that contains Category 3 ingredient(s). A generic concentration limit of 20 % is appropriate; however, it shall be recognised that this concentration limit may be higher or lower depending on the Category 3 ingredient(s) and that some effects such as respiratory tract irritation may not occur below a certain concentration while other effects such as narcotic effects may occur below this 20 % value. Expert judgement shall be exercised. Respiratory tract irritation and narcotic effects are to be evaluated separately in accordance with the criteria given in section 3.8.2.2. When conducting classifications for these hazards, the contribution of each component should be considered additive, unless there is evidence that the effects are not additive. 3.8.4. Hazard Communication 3.8.4.1 Label elements shall be used in accordance with Table 3.8.4., for substances or mixtures meeting the criteria for classification in this hazard class. Table 3.8.4 Label elements for specific target organ toxicity after single exposure Classification Category 1 Category 2 Category 3 GHS Pictograms Signal Word Danger Warning Warning Hazard Statement H370: Causes damage to organs (or state all organs affected, if known) (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H371: May cause damage to organs (or state all organs affected, if known) (state route of exposure if it is conclusively proven that no other routes of exposure cause the hazard) H335: May cause respiratory irritation; or H336: May cause drowsiness or dizziness Precautionary Statement Prevention P260 P264 P270 P260 P264 P270 P261 P271 Precautionary Statement Response P307 + P311 P321 P309 + P311 P304 + P340 Precautionary Statement Response P308 + P311 P321 P308 + P311 P304 + P340 P312 Precautionary Statement Storage P405 P405 P403 + P233 P405 … 72 unchanged lines … Inhalation (rat)vapour mg/litre/6h/day 0,2 < C ≤ 1,0 Inhalation (rat) dust/mist/fume mg/litre/6h/day 0,02 < C ≤ 0,2 3.9.2.9.8. The guidance values and ranges mentioned in paragraphs 3.9.2.9.6 and 3.9.2.9.7 are intended only for guidance purposes, i.e. to be used as part of the weight of evidence approach, and to assist with decisions about classification. They are not intended as strict demarcation values. 3.9.2.9.9. Thus it is feasible that a specific profile of toxicity occurs in repeat-dose animal studies at a dose/concentration below the guidance value, such as < 100 mg/kg bw/day by the oral route, however the nature of the effect, such as nephrotoxicity seen only in male rats of a particular strain known to be susceptible to this effect may result in the decision not to classify. Conversely, a specific profile of toxicity may be seen in animal studies occurring at above a guidance value, such as ≥ 100 mg/kg bw/day by the oral route, and in addition there is supplementary information from other sources, such as other long-term administration studies, or human case experience, which supports a conclusion that, in view of the weight of evidence, classification is the prudent action to take. 3.9.2.9.9. Thus it is feasible that a specific profile of toxicity occurs in repeat-dose animal studies at a dose/concentration below the guidance value, such as < 100 mg/kg bw/day by the oral route, however the nature of the effect, such as nephrotoxicity seen only in male rats of a particular strain known to be susceptible to this effect may result in the decision not to classify. Conversely, a specific profile of toxicity may be seen in animal studies occurring at or above a guidance value, such as ≥ 100 mg/kg bw/day by the oral route, and in addition there is supplementary information from other sources, such as other long-term administration studies, or human case experience, which supports a conclusion that, in view of the weight of evidence, classification is the prudent action to take. 3.9.2.10. Other considerations 3.9.2.10.1. When a substance is characterised only by use of animal data (typical of new substances, but also true for many existing substances), the classification process includes reference to dose/concentration guidance values as one of the elements that contribute to the weight of evidence approach. 3.9.2.10.2. When well-substantiated human data are available showing a specific target organ toxic effect that can be reliably attributed to repeated or prolonged exposure to a substance, the substance shall normally be classified. Positive human data, regardless of probable dose, predominates over animal data. Thus, if a substance is unclassified because no specific target organ toxicity was seen at or below the dose/concentration guidance value for animal testing, if subsequent human incident data become available showing a specific target organ toxic effect, the substance shall be classified. … 43 unchanged lines … 3.10.1.6.1. A review of the medical literature on chemical aspiration revealed that some hydrocarbons (petroleum distillates) and certain chlorinated hydrocarbons have been shown to pose an aspiration hazard in humans. 3.10.1.6.2. The classification criteria refer to kinematic viscosity. The following provides the conversion between dynamic and kinematic viscosity: Dynamic viscosity mPa sDensity gcm3Kinematic viscosity mm2s 3.10.1.6.2a Although the definition of aspiration in section 3.10.1.2 includes the entry of solids into the respiratory system, classification according to point (b) in Table 3.10.1 for Category 1 is intended to apply to liquid substances and mixtures only. 3.10.1.6.2a Although the definition of aspiration in section 3.10.1.2 includes the entry of solids into the respiratory system, classification according to point (b) in Table 3.10.1 for Category 1 is intended to apply to liquid substances and mixtures only. 3.10.1.6.3. Classification of aerosol/mist products Aerosol and mist forms of a substance or a mixture (product) are usually dispensed in containers such as self-pressurised containers, trigger and pump sprayers. The key to classifying these products is whether a pool of product is formed in the mouth, which then may be aspirated. If the mist or aerosol from a pressurised container is fine, a pool may not be formed. On the other hand, if a pressurised container dispenses product in a stream, a pool may be formed that may then be aspirated. Usually, the mist produced by trigger and pump sprayers is coarse and therefore, a pool may be formed that then may be aspirated. When the pump mechanism may be removed, and the contents are available to be swallowed then the classification of the substance or mixture shall be considered. 3.10.2. Classification criteria for substances … 39 unchanged lines … (b) acute (short-term) hazard means for classification purposes the hazard of a substance or mixture caused by its acute toxicity to an organism during short-term aquatic exposure to that substance or mixture. (c) availability of a substance means the extent to which this substance becomes a soluble or disaggregate species. For metal availability, the extent to which the metal ion portion of a metal (M°) compound can disaggregate from the rest of the compound (molecule). (d) bioavailability or biological availability means the extent to which a substance is taken up by an organism, and distributed to an area within the organism. It is dependent upon physico-chemical properties of the substance, anatomy and physiology of the organism, pharmacokinetics, and route of exposure. Availability is not a prerequisite for bioavailability. (e) bioaccumulation means the net result of uptake, transformation and elimination of a substance in an organism due to all routes of exposure (i.e. air, water, sediment/soil and food). (e) bioaccumulation means the net result of uptake, transformation and elimination of a substance in an organism due to all routes of exposure (i.e. air, water, sediment/soil and food). (f) bioconcentration means the net result of uptake, transformation and elimination of a substance in an organism due to waterborne exposure. (g) chronic aquatic toxicity means the intrinsic property of a substance to cause adverse effects to aquatic organisms during aquatic exposures which are determined in relation to the life-cycle of the organism. (h) degradation means the decomposition of organic molecules to smaller molecules and eventually to carbon dioxide, water and salts. (i) ECx means the effect concentration associated with x% response. (j) long-term hazard means for classification purposes the hazard of a substance or mixture caused by its chronic toxicity following long-term exposure in the aquatic environment. (k) no observed effect concentration (NOEC) means the test concentration immediately below the lowest tested concentration with statistically significant adverse effect. The NOEC has no statistically significant adverse effect compared to the control. 4.1.1.2. Basic elements 4.1.1.2.0. Hazardous to the aquatic environment is differentiated into: acute aquatic hazard, long-term aquatic hazard. 4.1.1.2.1. The basic elements used for classification for aquatic environmental hazards are: acute aquatic toxicity, chronic aquatic toxicity, potential for or actual bioaccumulation, and degradation (biotic or abiotic) for organic chemicals. 4.1.1.2.2. Preferably data shall be derived using the standardised test methods referred to in Article 8(3). In practice data from other standardised test methods such as national methods shall also be used where they are considered as equivalent. Where valid data are available from non-standard testing and from non-testing methods, these shall be considered in classification provided they fulfil the requirements specified in section 1 of Annex XI to Regulation (EC) No 1907/2006. In general, both freshwater and marine species toxicity data are considered suitable for use in classification provided the test methods used are equivalent. Where such data are not available classification shall be based on the best available data. See also Part 1 of Annex I to Regulation (EC) No 1272/2008. degradation (biotic or abiotic) for organic chemicals. 4.1.1.2.2. Preferably data shall be derived using the standardised test methods referred to in Article 8(3). In practice data from other standardised test methods such as national methods shall also be used where they are considered as equivalent. Where valid data are available from non-standard testing and from non-testing methods, these shall be considered in classification provided they fulfil the requirements specified in section 1 of Annex XI to Regulation (EC) No 1907/2006. In general, both freshwater and marine species toxicity data are considered suitable for use in classification provided the test methods used are equivalent. Where such data are not available classification shall be based on the best available data. See also Part 1 of Annex I to Regulation (EC) No 1272/2008. 4.1.1.3. Other considerations 4.1.1.3.1. Classification of substances and mixtures for environmental hazards requires the identification of the hazards they present to the aquatic environment. The aquatic environment is considered in terms of the aquatic organisms that live in the water, and the aquatic ecosystem of which they are part. The basis, therefore, of the identification of acute (short-term) and long-term hazards is the aquatic toxicity of the substance or mixture, although this shall be modified by taking account of further information on the degradation and bioaccumulation behaviour, if appropriate. 4.1.1.3.2. While the classification system applies to all substances and mixtures, it is recognised that for special cases (e.g. metals) the European Chemicals Agency has issued guidance. 4.1.2. Classification criteria for substances 4.1.2.1. The system for classification recognises that the intrinsic hazard to aquatic organisms is represented by both the acute and long-term hazard of a substance. For the long-term hazard, separate hazard categories are defined representing a gradation in the level of hazard identified. The lowest of the available toxicity values between and within the different trophic levels (fish, crustacean, algae/aquatic plants) shall normally be used to define the appropriate hazard category(ies). There are circumstances, however, when a weight of evidence approach is appropriate. 4.1.2.2. The core classification system for substances consists of one acute hazard classification category and three long-term hazard classification categories. The acute and the long-term hazard classification categories are applied independently. 4.1.2.3. The criteria for classification of a substance in category Acute 1 are defined on the basis of acute aquatic toxicity data only (EC50 or LC50). The criteria for classification of a substance into the categories Chronic 1 to 3 follow a tiered approach where the first step is to see if available information on chronic toxicity merits long-term hazard classification. In absence of adequate chronic toxicity data, the subsequent step is to combine two types of information, i.e. acute aquatic toxicity data and environmental fate data (degradability and bioaccumulation data) (see figure 4.1.1). 4.1.2.3. The criteria for classification of a substance in category Acute 1 are defined on the basis of acute aquatic toxicity data only (EC50 or LC50). The criteria for classification of a substance into the categories Chronic 1 to 3 follow a tiered approach where the first step is to see if available information on chronic toxicity merits long-term hazard classification. In absence of adequate chronic toxicity data, the subsequent step is to combine two types of information, i.e. acute aquatic toxicity data and environmental fate data (degradability and bioaccumulation data) (see figure 4.1.1). Figure 4.1.1 Categories for substances long-term hazardous to the aquatic environment Are there adequate chronic toxicity data available for all three trophic levels? Yes Classify according to the criteria given in Table 4.1.0(b) (i) or 4.1.0(b)(ii) depending on information on rapid degradation No Are there adequate chronic toxicity data available for one or two trophic levels? Yes Assess both: (a) according to the criteria given in Table 4.1.0(b)(i) or 4.1.0(b)(ii) (depending on information on rapid degradation), and (b) (if for the other trophic level(s) adequate acute toxicity data are available) according to the criteria given in Table 4.1.0(b) (iii), and classify according to the most stringent outcome No Are there adequate acute toxicity data available? Yes Classify according to the criteria given in Table 4.1.0(b) (iii) 4.1.2.4. The system also introduces a safety net classification (referred to as category Chronic 4) for use when the data available do not allow classification under the formal criteria for acute 1 or chronic 1 to 3 but there are nevertheless some grounds for concern (see example in Table 4.1.0). 4.1.2.5. Substances with acute toxicities below 1 mg/l or chronic toxicities below 0,1 mg/l (if non-rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute as components of a mixture to the toxicity of the mixture even at a low concentration and shall normally be given increased weight in applying the summation of classification approach (see note 1 of Table 4.1.0 and section 4.1.3.5.5). 4.1.2.4. The system also introduces a safety net classification (referred to as category Chronic 4) for use when the data available do not allow classification under the formal criteria for acute 1 or chronic 1 to 3 but there are nevertheless some grounds for concern (see example in Table 4.1.0). 4.1.2.5. Substances with acute toxicities below 1 mg/l or chronic toxicities below 0,1 mg/l (if non-rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute as components of a mixture to the toxicity of the mixture even at a low concentration and shall normally be given increased weight in applying the summation of classification approach (see note 1 of Table 4.1.0 and section 4.1.3.5.5). 4.1.2.6. The criteria for classifying and categorising substances as hazardous to the aquatic environment are summarised in Table 4.1.0. Table 4.1.0 Classification categories for hazardous to the aquatic environment (a) Acute (short-term) aquatic hazard Category Acute 1: (Note 1) 96 hr LC50 (for fish) ≤ 1 mg/l and/or 48 hr EC50 (for crustacea) ≤ 1 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) ≤ 1 mg/l. (Note 2) 96 hr LC50 (for fish) ≤ 1 mg/l and/or 48 hr EC50 (for crustacea) ≤ 1 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) ≤ 1 mg/l. (Note 2) (b) Long-term aquatic hazard (i) Non-rapidly degradable substances (Note 3) for which there are adequate chronic toxicity data available Category Chronic 1: (Note 1) Chronic NOEC or ECx (for fish) ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for crustacea) ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) ≤0,1 mg/l. Chronic NOEC or ECx (for fish) ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for crustacea) ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) ≤0,1 mg/l. Category Chronic 2: Chronic NOEC or ECx (for fish) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,1 to ≤ 1 mg/l. Chronic NOEC or ECx (for fish) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,1 to ≤ 1 mg/l. (ii) Rapidly degradable substances (Note 3) for which there are adequate chronic toxicity data available Category Chronic 1: (Note 1) Chronic NOEC or ECx (for fish) ≤ 0,01 mg/l and/or Chronic NOEC or ECx (for crustacea) ≤ 0,01 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) ≤ 0,01 mg/l. Chronic NOEC or ECx (for fish) ≤ 0,01 mg/l and/or Chronic NOEC or ECx (for crustacea) ≤ 0,01 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) ≤ 0,01 mg/l. Category Chronic 2: Chronic NOEC or ECx (for fish) > 0,01 to ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,01 to ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,01 to ≤ 0,1 mg/l. Chronic NOEC or ECx (for fish) > 0,01 to ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,01 to ≤ 0,1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,01 to ≤ 0,1 mg/l. Category Chronic 3: Chronic NOEC or ECx (for fish) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,1 to ≤ 1 mg/l. Chronic NOEC or ECx (for fish) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for crustacea) > 0,1 to ≤ 1 mg/l and/or Chronic NOEC or ECx (for algae or other aquatic plants) > 0,1 to ≤ 1 mg/l. (iii) Substances for which adequate chronic toxicity data are not available Category Chronic 1: (Note 1) 96 hr LC50 (for fish) ≤ 1 mg/l and/or 48 hr EC50 (for crustacea) ≤ 1 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) ≤ 1 mg/l. (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). 96 hr LC50 (for fish) ≤ 1 mg/l and/or 48 hr EC50 (for crustacea) ≤ 1 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) ≤ 1 mg/l. (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). Category Chronic 2: 96 hr LC50 (for fish) > 1 to ≤10 mg/l and/or 48 hr EC50 (for crustacea) > 1 to ≤10 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) > 1 to ≤10 mg/l (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). 96 hr LC50 (for fish) > 1 to ≤10 mg/l and/or 48 hr EC50 (for crustacea) > 1 to ≤10 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) > 1 to ≤10 mg/l (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). Category Chronic 3: 96 hr LC50 (for fish) > 10 to ≤ 100 mg/l and/or 48 hr EC50 (for crustacea) > 10 to ≤ 100 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) > 10 to ≤ 100 mg/l. (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). 96 hr LC50 (for fish) > 10 to ≤ 100 mg/l and/or 48 hr EC50 (for crustacea) > 10 to ≤ 100 mg/l and/or 72 or 96 hr ErC50 (for algae or other aquatic plants) > 10 to ≤ 100 mg/l. (Note 2) and the substance is not rapidly degradable and/or the experimentally determined BCF ≥ 500 (or, if absent, the log Kow≥ 4). (Note 3). Safety net classification Category Chronic 4 Cases when data do not allow classification under the above criteria but there are nevertheless some grounds for concern. This includes, for example, poorly soluble substances for which no acute toxicity is recorded at levels up to the water solubility (note 4), and which are not rapidly degradable in accordance with section 4.1.2.9.5 and have an experimentally determined BCF ≥ 500 (or, if absent, a log Kow ≥ 4), indicating a potential to bioaccumulate, which will be classified in this category unless other scientific evidence exists showing classification to be unnecessary. Such evidence includes chronic toxicity NOECs > water solubility or > 1 mg/l, or other evidence of rapid degradation in the environment than the ones provided by any of the methods listed in section 4.1.2.9.5. Cases when data do not allow classification under the above criteria but there are nevertheless some grounds for concern. This includes, for example, poorly soluble substances for which no acute toxicity is recorded at levels up to the water solubility (note 4), and which are not rapidly degradable in accordance with section 4.1.2.9.5 and have an experimentally determined BCF ≥ 500 (or, if absent, a log Kow ≥ 4), indicating a potential to bioaccumulate, which will be classified in this category unless other scientific evidence exists showing classification to be unnecessary. Such evidence includes chronic toxicity NOECs > water solubility or > 1 mg/l, or other evidence of rapid degradation in the environment than the ones provided by any of the methods listed in section 4.1.2.9.5. Note 1: When classifying substances as Acute Category 1 and/or Chronic Category 1 it is necessary at the same time to indicate the appropriate M-factor(s) (see Table 4.1.3). When classifying substances as Acute Category 1 and/or Chronic Category 1 it is necessary at the same time to indicate the appropriate M-factor(s) (see Table 4.1.3). Note 2: Classification shall be based on the ErC50 [= EC50 (growth rate)]. In circumstances where the basis of the EC50 is not specified or no ErC50 is recorded, classification shall be based on the lowest EC50 available. Note 3: When no useful data on degradability are available, either experimentally determined or estimated data, the substance should be regarded as not rapidly degradable. Note 4: No acute toxicity is taken to mean that the L(E)C50(s) is/are above the water solubility. Also for poorly soluble substances, (water solubility < 1 mg/l), where there is evidence that the acute test does not provide a true measure of the intrinsic toxicity. 4.1.2.7. Aquatic toxicity 4.1.2.7.1. Acute aquatic toxicity is normally determined using a fish 96-hour LC50, a crustacea species 48-hour EC50 and/or an algal species 72- or 96-hour EC50. These species cover a range of trophic levels and taxa and are considered as surrogate for all aquatic organisms. Data on other species (e.g. Lemna spp.) shall also be considered if the test methodology is suitable. The aquatic plant growth inhibition tests are normally considered as chronic tests but the EC50s are treated as acute values for classification purposes (see note 2). 4.1.2.7.2. For determining chronic aquatic toxicity for classification purposes data generated according to the standardised test methods referred to in Article 8(3) shall be accepted, as well as results obtained from other validated and internationally accepted test methods. The NOECs or other equivalent ECx (e.g. EC10) shall be used. 4.1.2.7.1. Acute aquatic toxicity is normally determined using a fish 96-hour LC50, a crustacea species 48-hour EC50 and/or an algal species 72- or 96-hour EC50. These species cover a range of trophic levels and taxa and are considered as surrogate for all aquatic organisms. Data on other species (e.g. Lemna spp.) shall also be considered if the test methodology is suitable. The aquatic plant growth inhibition tests are normally considered as chronic tests but the EC50s are treated as acute values for classification purposes (see note 2). 4.1.2.7.2. For determining chronic aquatic toxicity for classification purposes data generated according to the standardised test methods referred to in Article 8(3) shall be accepted, as well as results obtained from other validated and internationally accepted test methods. The NOECs or other equivalent ECx (e.g. EC10) shall be used. 4.1.2.8. Bioaccumulation 4.1.2.8.1. Bioaccumulation of substances within aquatic organisms can give rise to toxic effects over longer time scales even when actual water concentrations are low. For organic substances the potential for bioaccumulation shall normally be determined by using the octanol/water partition coefficient, usually reported as a log Kow. The relationship between the log Kow of an organic substance and its bioconcentration as measured by the bioconcentration factor (BCF) in fish has considerable scientific literature support. Using a cut-off value of log Kow ≥ 4 is intended to identify only those substances with a real potential to bioconcentrate. While this represents a potential to bioaccumulate, an experimentally determined BCF provides a better measure and shall be used in preference if available. A BCF in fish of ≥ 500 is indicative of the potential to bioconcentrate for classification purposes. Some relationships can be observed between chronic toxicity and bioaccumulation potential, as toxicity is related to the body burden. 4.1.2.9. Rapid degradability of organic substances 4.1.2.9.1. Substances that rapidly degrade can be quickly removed from the environment. While effects of such substances can occur, particularly in the event of a spillage or accident, they are localised and of short duration. In the absence of rapid degradation in the environment a substance in the water has the potential to exert toxicity over a wide temporal and spatial scale. 4.1.2.9.2. One way of demonstrating rapid degradation utilises the biodegradation screening tests designed to determine whether an organic substance is readily biodegradable. Where such data are not available, a BOD(5 days)/COD ratio ≥ 0,5 is considered as indicative of rapid degradation. Thus, a substance which passes this screening test is considered likely to biodegrade rapidly in the aquatic environment, and is thus unlikely to be persistent. However, a fail in the screening test does not necessarily mean that the substance will not degrade rapidly in the environment. Other evidence of rapid degradation in the environment may therefore also be considered and are of particular importance where the substances are inhibitory to microbial activity at the concentration levels used in standard testing. Thus, a further classification criterion is included which allows the use of data to show that the substance did actually degrade biotically or abiotically in the aquatic environment by > 70 % in 28 days. Thus, if degradation is demonstrated under environmentally realistic conditions, then the criterion of rapid degradability is met. 4.1.2.9.2. One way of demonstrating rapid degradation utilises the biodegradation screening tests designed to determine whether an organic substance is readily biodegradable. Where such data are not available, a BOD(5 days)/COD ratio ≥ 0,5 is considered as indicative of rapid degradation. Thus, a substance which passes this screening test is considered likely to biodegrade rapidly in the aquatic environment, and is thus unlikely to be persistent. However, a fail in the screening test does not necessarily mean that the substance will not degrade rapidly in the environment. Other evidence of rapid degradation in the environment may therefore also be considered and are of particular importance where the substances are inhibitory to microbial activity at the concentration levels used in standard testing. Thus, a further classification criterion is included which allows the use of data to show that the substance did actually degrade biotically or abiotically in the aquatic environment by > 70 % in 28 days. Thus, if degradation is demonstrated under environmentally realistic conditions, then the criterion of rapid degradability is met. 4.1.2.9.3. Many degradation data are available in the form of degradation half-lives and these can be used in defining rapid degradation provided that ultimate biodegradation of the substance, i.e. full mineralisation, is achieved. Primary biodegradation does not normally suffice in the assessment of rapid degradability unless it can be demonstrated that the degradation products do not fulfil the criteria for classification as hazardous to the aquatic environment. 4.1.2.9.4. The criteria used reflect the fact that environmental degradation may be biotic or abiotic. Hydrolysis can be considered if the hydrolysis products do not fulfil the criteria for classification as hazardous to the aquatic environment. 4.1.2.9.5. Substances are considered rapidly degradable in the environment if one of the following criteria holds true: (a) if, in 28-day ready biodegradation studies, at least the following levels of degradation are achieved: (i) tests based on dissolved organic carbon: 70 %; (ii) tests based on oxygen depletion or carbon dioxide generation: 60 % of theoretical maximum. These levels of biodegradation must be achieved within 10 days of the start of degradation which point is taken as the time when 10 % of the substance has been degraded, unless the substance is identified as an UVCB or as a complex, multi-constituent substance with structurally similar constituents. In this case, and where there is sufficient justification, the 10-day window condition may be waived and the pass level applied at 28 days; or (b) if, in those cases where only BOD and COD data are available, when the ratio of BOD5/COD is ≥ 0,5; or (c) if other convincing scientific evidence is available to demonstrate that the substance can be degraded (biotically and/or abiotically) in the aquatic environment to a level > 70 % within a 28-day period. (i) tests based on dissolved organic carbon: 70 %; (ii) tests based on oxygen depletion or carbon dioxide generation: 60 % of theoretical maximum. These levels of biodegradation must be achieved within 10 days of the start of degradation which point is taken as the time when 10 % of the substance has been degraded, unless the substance is identified as an UVCB or as a complex, multi-constituent substance with structurally similar constituents. In this case, and where there is sufficient justification, the 10-day window condition may be waived and the pass level applied at 28 days; or (b) if, in those cases where only BOD and COD data are available, when the ratio of BOD5/COD is ≥ 0,5; or (c) if other convincing scientific evidence is available to demonstrate that the substance can be degraded (biotically and/or abiotically) in the aquatic environment to a level > 70 % within a 28-day period. 4.1.2.10. Inorganic compounds and metals 4.1.2.10.1. For inorganic compounds and metals, the concept of degradability as applied to organic compounds has limited or no meaning. Rather, such substances may be transformed by normal environmental processes to either increase or decrease the bioavailability of the toxic species. Equally the use of bioaccumulation data shall be treated with careSpecific guidance has been issued by the European Chemicals Agency on how these data for such substances may be used in meeting the requirements of the classification criteria.. 4.1.2.10.2. Poorly soluble inorganic compounds and metals may be acutely or chronically toxic in the aquatic environment depending on the intrinsic toxicity of the bioavailable inorganic species and the rate and amount of this species which enter solution. All evidence must be weighed in a classification decision. This would be especially true for metals showing borderline results in the Transformation/Dissolution Protocol. 4.1.3. Classification criteria for mixtures 4.1.3.1. The classification system for mixtures covers all classification categories which are used for substances, i.e. categories Acute 1 and Chronic 1 to 4. In order to make use of all available data for purposes of classifying the aquatic environmental hazards of the mixture, the following is applied where appropriate: The relevant components of a mixture are those which are classified Acute 1or Chronic 1 and present in a concentration of 0,1 % (w/w) or greater, and those which are classified Chronic 2, Chronic 3 or Chronic 4 and present in a concentration of 1 % (w/w) or greater, unless there is a presumption (such as in the case of highly toxic components (see section 4.1.3.5.5.5)) that a component present in a lower concentration can still be relevant for classifying the mixture for aquatic environmental hazards. Generally, for substances classified as Acute 1 or Chronic 1 the concentration to be taken into account is (0,1/M) %. (For explanation M-factor see section 4.1.3.5.5.5.) 4.1.3.1. The classification system for mixtures covers all classification categories which are used for substances, i.e. categories Acute 1 and Chronic 1 to 4. In order to make use of all available data for purposes of classifying the aquatic environmental hazards of the mixture, the following is applied where appropriate: The relevant components of a mixture are those which are classified Acute 1or Chronic 1 and present in a concentration of 0,1 % (w/w) or greater, and those which are classified Chronic 2, Chronic 3 or Chronic 4 and present in a concentration of 1 % (w/w) or greater, unless there is a presumption (such as in the case of highly toxic components (see section 4.1.3.5.5.5)) that a component present in a lower concentration can still be relevant for classifying the mixture for aquatic environmental hazards. Generally, for substances classified as Acute 1 or Chronic 1 the concentration to be taken into account is (0,1/M) %. (For explanation M-factor see section 4.1.3.5.5.5.) 4.1.3.2. The approach for classification of aquatic environmental hazards is tiered, and is dependent upon the type of information available for the mixture itself and for its components. Figure 4.1.2 outlines the process to be followed. Elements of the tiered approach include: classification based on tested mixtures, … 26 unchanged lines … CLASSIFY for acute/long-term aquatic hazard 4.1.3.3. Classification of mixtures when toxicity data are available for the complete mixture 4.1.3.3.1. When the mixture as a whole has been tested to determine its aquatic toxicity, this information can be used for classifying the mixture according to the criteria that have been agreed for substances. The classification is normally based on the data for fish, crustacea and algae/plants (see sections 4.1.2.7.1 and 4.1.2.7.2). When adequate acute or chronic toxicity data for the mixture as a whole are lacking, bridging principles or summation method should be applied (see sections 4.1.3.4 and 4.1.3.5). 4.1.3.3.1. When the mixture as a whole has been tested to determine its aquatic toxicity, this information can be used for classifying the mixture according to the criteria that have been agreed for substances. The classification is normally based on the data for fish, crustacea and algae/plants (see sections 4.1.2.7.1 and 4.1.2.7.2). When adequate acute or chronic toxicity data for the mixture as a whole are lacking, bridging principles or summation method should be applied (see sections 4.1.3.4 and 4.1.3.5). 4.1.3.3.2. The long-term hazard classification of mixtures requires additional information on degradability and in certain cases bioaccumulation. Degradability and bioaccumulation tests for mixtures are not used as they are usually difficult to interpret, and such tests may be meaningful only for single substances. 4.1.3.3.3. Classification for category Acute 1 (a) When there are adequate acute toxicity test data (LC50 or EC50) available for the mixture as a whole showing L(E)C50 ≤ 1 mg/l: Classify mixture as Acute 1 in accordance with point (a) of Table 4.1.0. (a) When there are adequate acute toxicity test data (LC50 or EC50) available for the mixture as a whole showing L(E)C50 ≤ 1 mg/l: Classify mixture as Acute 1 in accordance with point (a) of Table 4.1.0. (b) When there are acute toxicity test data (LC50(s) or EC50(s)) available for the mixture as a whole showing L(E)C50(s) > 1 mg/l for normally all trophic levels: No need to classify for acute hazard. 4.1.3.3.4. Classification for categories Chronic 1, 2 and 3 (a) When there are adequate chronic toxicity data (ECxx or NOEC) available for the mixture as a whole showing ECx or NOEC of the tested mixture ≤ 1mg/l: (i) Classify the mixture as Chronic 1, 2 or 3 in accordance with point (b)(ii) of Table 4.1.0 as rapidly degradable if the available information allows the conclusion that all relevant components of the mixture are rapidly degradable; (ii) Classify the mixture as Chronic 1 or 2 in all other cases in accordance with point (b)(i) of Table 4.1.0 as non-rapidly degradable; (b) When there are adequate chronic toxicity data (ECx or NOEC) available for the mixture as a whole showing ECx(s) or NOEC(s) of the tested mixture > 1 mg/l for normally all trophic levels: No need to classify for long-term hazard in categories Chronic 1, 2 or 3. 4.1.3.3.4. Classification for categories Chronic 1, 2 and 3 (a) When there are adequate chronic toxicity data (ECxx or NOEC) available for the mixture as a whole showing ECx or NOEC of the tested mixture ≤ 1mg/l: (i) Classify the mixture as Chronic 1, 2 or 3 in accordance with point (b)(ii) of Table 4.1.0 as rapidly degradable if the available information allows the conclusion that all relevant components of the mixture are rapidly degradable; (ii) Classify the mixture as Chronic 1 or 2 in all other cases in accordance with point (b)(i) of Table 4.1.0 as non-rapidly degradable; (b) When there are adequate chronic toxicity data (ECx or NOEC) available for the mixture as a whole showing ECx(s) or NOEC(s) of the tested mixture > 1 mg/l for normally all trophic levels: No need to classify for long-term hazard in categories Chronic 1, 2 or 3. 4.1.3.3.5. Classification for category Chronic 4 If there are nevertheless reasons for concern: Classify the mixture as Chronic 4 (safety net classification) in accordance with Table 4.1.0. 4.1.3.4. Classification of mixtures when toxicity data are not available for the complete mixture: bridging principles 4.1.3.4.1. Where the mixture itself has not been tested to determine its aquatic environmental hazard, but there are sufficient data on the individual components and similar tested mixtures to adequately characterise the hazards of the mixture, this data shall be used in accordance with the bridging rules set out in section 1.1.3. However, in relation to application of the bridging rule for dilution, sections 4.1.3.4.2 and 4.1.3.4.3 shall be used. 4.1.3.4.2. Dilution: if a mixture is formed by diluting another tested mixture or a substance classified for its aquatic environmental hazard with a diluent which has an equivalent or lower aquatic hazard classification than the least toxic original component and which is not expected to affect the aquatic hazards of other components, then the resulting mixture may be classified as equivalent to the original tested mixture or substance. Alternatively, the method explained in section 4.1.3.5 may be applied. 4.1.3.4.3. If a mixture is formed by diluting another classified mixture or substance with water or other totally non-toxic material, the toxicity of the mixture can be calculated from the original mixture or substance. 4.1.3.4.1. Where the mixture itself has not been tested to determine its aquatic environmental hazard, but there are sufficient data on the individual components and similar tested mixtures to adequately characterise the hazards of the mixture, this data shall be used in accordance with the bridging rules set out in section 1.1.3. However, in relation to application of the bridging rule for dilution, sections 4.1.3.4.2 and 4.1.3.4.3 shall be used. 4.1.3.4.2. Dilution: if a mixture is formed by diluting another tested mixture or a substance classified for its aquatic environmental hazard with a diluent which has an equivalent or lower aquatic hazard classification than the least toxic original component and which is not expected to affect the aquatic hazards of other components, then the resulting mixture may be classified as equivalent to the original tested mixture or substance. Alternatively, the method explained in section 4.1.3.5 may be applied. 4.1.3.4.3. If a mixture is formed by diluting another tested mixture or substance with water or other totally non-toxic material, the toxicity of the mixture can be calculated from the original mixture or substance. 4.1.3.5. Classification of mixtures when toxicity data are available for some or all components of the mixture 4.1.3.5.1. The classification of a mixture is based on summation of the concentration of its classified components. The percentage of components classified as Acute or Chronic is fed straight in to the summation method. Details of the summation method are described in section 4.1.3.5.5. 4.1.3.5.2. Mixtures can be made of a combination of both components that are classified (as Acute 1 and/or Chronic 1, 2, 3, 4) and others for which adequate toxicity test data is available. When adequate toxicity data are available for more than one component in the mixture, the combined toxicity of those components is calculated using the following additivity formulas (a) or (b), depending on the nature of the toxicity data: 4.1.3.5.1. The classification of a mixture is based on summation of the concentration of its classified components. The percentage of components classified as Acute or Chronic is fed straight in to the summation method. Details of the summation method are described in section 4.1.3.5.5. 4.1.3.5.2. Mixtures can be made of a combination of both components that are classified (as Acute 1 and/or Chronic 1, 2, 3, 4) and others for which adequate toxicity test data is available. When adequate toxicity data are available for more than one component in the mixture, the combined toxicity of those components is calculated using the following additivity formulas (a) or (b), depending on the nature of the toxicity data: (a) Based on acute aquatic toxicity: CiLEC50mnCiLEC50i where: Ci concentration of component i (weight percentage); L(E)C50i (mg/l) LC50 or EC50 for component i; η number of components, and i is running from 1 to n; number of components, and i is running from 1 to n; L(E)C50m L(E) C50 of the part of the mixture with test data. The calculated toxicity may be used to assign that portion of the mixture an acute hazard category which is then subsequently used in applying the summation method; (b) Based on chronic aquatic toxicity: CiCjEqNOECmnCiNOECinCj0,1NOECj where: Ci concentration of component i (weight percentage) covering the rapidly degradable components; Cj concentration of component j (weight percentage) covering the non- rapidly degradable components; NOECi NOEC (or other recognised measures for chronic toxicity) for component i covering the rapidly degradable components, in mg/l; NOECj NOEC (or other recognised measures for chronic toxicity) for component j covering the non-rapidly degradable components, in mg/l; n number of components, and i and j are running from 1 to n; number of components, and i and j are running from 1 to n; EqNOECm Equivalent NOEC of the part of the mixture with test data. The equivalent toxicity thus reflects the fact that non-rapidly degrading substances are classified one hazard category level more severe than rapidly degrading substances. The calculated equivalent toxicity may be used to assign that portion of the mixture a long-term hazard category, in accordance with the criteria for rapidly degradable substances (point (b)(ii) of Table 4.1.0), which is then subsequently used in applying the summation method. 4.1.3.5.3. When applying the additivity formula for part of the mixture, it is preferable to calculate the toxicity of this part of the mixture using for each substance toxicity values that relate to the same taxonomic group (i.e. fish, crustacean, algae or equivalent) and then to use the highest toxicity (lowest value) obtained (i.e. use the most sensitive of the three taxonomic groups). However, when toxicity data for each component are not available in the same taxonomic group, the toxicity value of each component is selected in the same manner that toxicity values are selected for the classification of substances, i.e. the higher toxicity (from the most sensitive test organism) is used. The calculated acute and chronic toxicity is then used to assess whether this part of the mixture shall be classified as Acute 1 and/or Chronic 1, 2 or 3 using the same criteria described for substances. The calculated equivalent toxicity may be used to assign that portion of the mixture a long-term hazard category, in accordance with the criteria for rapidly degradable substances (point (b)(ii) of Table 4.1.0), which is then subsequently used in applying the summation method. 4.1.3.5.3. When applying the additivity formula for part of the mixture, it is preferable to calculate the toxicity of this part of the mixture using for each substance toxicity values that relate to the same taxonomic group (i.e. fish, crustacean, algae or equivalent) and then to use the highest toxicity (lowest value) obtained (i.e. use the most sensitive of the three taxonomic groups). However, when toxicity data for each component are not available in the same taxonomic group, the toxicity value of each component is selected in the same manner that toxicity values are selected for the classification of substances, i.e. the higher toxicity (from the most sensitive test organism) is used. The calculated acute and chronic toxicity is then used to assess whether this part of the mixture shall be classified as Acute 1 and/or Chronic 1, 2 or 3 using the same criteria described for substances. 4.1.3.5.4. If a mixture is classified in more than one way, the method yielding the more conservative result shall be used. 4.1.3.5.5. Summation method 4.1.3.5.5.1. Rationale 4.1.3.5.5.1.1. In case of the substance classification categories Chronic 1 to Chronic 3, the underlying toxicity criteria differ by a factor of 10 in moving from one category to another. Substances with a classification in a high toxicity band therefore contribute to the classification of a mixture in a lower band. The calculation of these classification categories therefore needs to consider the contribution of any substance classified as Chronic 1, 2 or 3. 4.1.3.5.5.1.2. When a mixture contains components classified as Acute 1 or Chronic 1, attention must be paid to the fact that such components, when their acute toxicity is below 1 mg/l and/or chronic toxicity is below 0,1 mg/l (if non rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute to the toxicity of the mixture even at a low concentration. Active ingredients in pesticides often possess such high aquatic toxicity but also some other substances like organometallic compounds. Under these circumstances the application of the normal generic concentration limits leads to an under-classification of the mixture. Therefore, multiplying factors shall be applied to account for highly toxic components, as described in section 4.1.3.5.5.5. 4.1.3.5.5.1.1. In case of the substance classification categories Chronic 1 to Chronic 3, the underlying toxicity criteria differ by a factor of 10 in moving from one category to another. Substances with a classification in a high toxicity band therefore contribute to the classification of a mixture in a lower band. The calculation of these classification categories therefore needs to consider the contribution of any substance classified as Chronic 1, 2 or 3. 4.1.3.5.5.1.2. When a mixture contains components classified as Acute 1 or Chronic 1, attention must be paid to the fact that such components, when their acute toxicity is below 1 mg/l and/or chronic toxicity is below 0,1 mg/l (if non rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute to the toxicity of the mixture even at a low concentration. Active ingredients in pesticides often possess such high aquatic toxicity but also some other substances like organometallic compounds. Under these circumstances the application of the normal generic concentration limits leads to an under-classification of the mixture. Therefore, multiplying factors shall be applied to account for highly toxic components, as described in section 4.1.3.5.5.5. 4.1.3.5.5.2. Classification procedure 4.1.3.5.5.2.1. In general a more severe classification for mixtures overrides a less severe classification, e.g. a classification with Chronic 1 overrides a classification with Chronic 2. As a consequence, in this example, the classification procedure is already completed if the result of the classification is Chronic 1. A more severe classification than Chronic 1 is not possible. Therefore it is not necessary to undergo the further classification procedure. 4.1.3.5.5.3. Classification for category Acute 1 4.1.3.5.5.3.1. First all components classified as Acute 1 are considered. If the sum of the concentrations (in %) of these components multiplied by their corresponding M-factors is greater than 25 % the whole mixture is classified as Acute 1. 4.1.3.5.5.3.1. First all components classified as Acute 1 are considered. If the sum of the concentrations (in %) of these components multiplied by their corresponding M-factors is greater than 25 % the whole mixture is classified as Acute 1. 4.1.3.5.5.3.2. The classification of mixtures for acute hazards based on this summation of classified components is summarised in Table 4.1.1. Table 4.1.1 Classification of a mixture for acute hazards, based on summation of classified components For explanation of the M-factor, see 4.1.3.5.5.5. Sum of components classified as: Mixture is classified as: Acute 1 × M ≥ 25 % Acute 1 4.1.3.5.5.4. Classification for the categories Chronic 1, 2, 3 and 4 4.1.3.5.5.4.1. First all components classified as Chronic 1 are considered. If the sum of the concentrations (in %) of these components multiplied by their corresponding M-factors is equal to or greater than 25 %, the mixture is classified as Chronic 1. If the result of the calculation is a classification of the mixture as Chronic 1, the classification procedure is completed. 4.1.3.5.5.4.2. In cases where the mixture is not classified as Chronic 1, classification of the mixture as Chronic 2 is considered. A mixture is classified as Chronic 2 if 10 times the sum of the concentrations (in %) of all components classified as Chronic 1 multiplied by their corresponding M-factors plus the sum of the concentrations (in %) of all components classified as Chronic 2 is equal to or greater than 25 %. If the result of the calculation is classification of the mixture as Chronic 2, the classification process is completed. 4.1.3.5.5.4.3. In cases where the mixture is not classified either as Chronic 1 or Chronic 2, classification of the mixture as Chronic 3 is considered. A mixture is classified as Chronic 3 if 100 times the sum of the concentrations (in %) of all components classified as Chronic 1 multiplied by their corresponding M-factors plus 10 times the sum of the concentrations (in %) of all components classified with Chronic 2 plus the sum of the concentrations (in %) of all components classified as Chronic 3 is ≥ 25 %. 4.1.3.5.5.4.4. If the mixture is still not classified in Chronic 1, 2 or 3, classification of the mixture as Chronic 4 shall be considered. A mixture is classified as Chronic 4 if the sum of the concentrations (in %) of components classified as Chronic 1, 2, 3 and 4 is equal to or greater than 25 %. Acute 1 × M ≥ 25 % Acute 1 4.1.3.5.5.4. Classification for the categories Chronic 1, 2, 3 and 4 4.1.3.5.5.4.1. First all components classified as Chronic 1 are considered. If the sum of the concentrations (in %) of these components multiplied by their corresponding M-factors is equal to or greater than 25 %, the mixture is classified as Chronic 1. If the result of the calculation is a classification of the mixture as Chronic 1, the classification procedure is completed. 4.1.3.5.5.4.2. In cases where the mixture is not classified as Chronic 1, classification of the mixture as Chronic 2 is considered. A mixture is classified as Chronic 2 if 10 times the sum of the concentrations (in %) of all components classified as Chronic 1 multiplied by their corresponding M-factors plus the sum of the concentrations (in %) of all components classified as Chronic 2 is equal to or greater than 25 %. If the result of the calculation is classification of the mixture as Chronic 2, the classification process is completed. 4.1.3.5.5.4.3. In cases where the mixture is not classified either as Chronic 1 or Chronic 2, classification of the mixture as Chronic 3 is considered. A mixture is classified as Chronic 3 if 100 times the sum of the concentrations (in %) of all components classified as Chronic 1 multiplied by their corresponding M-factors plus 10 times the sum of the concentrations (in %) of all components classified with Chronic 2 plus the sum of the concentrations (in %) of all components classified as Chronic 3 is ≥ 25 %. 4.1.3.5.5.4.4. If the mixture is still not classified in Chronic 1, 2 or 3, classification of the mixture as Chronic 4 shall be considered. A mixture is classified as Chronic 4 if the sum of the concentrations (in %) of components classified as Chronic 1, 2, 3 and 4 is equal to or greater than 25 %. 4.1.3.5.5.4.5. The classification of mixtures for long-term hazards, based on this summation of the concentrations of classified components, is summarised in Table 4.1.2. Table 4.1.2 Classification of a mixture for long-term hazards, based on summation of the concentrations of classified components For explanation of the M-factor, see 4.1.3.5.5.5. Sum of components classified as: Mixture is classified as: Chronic 1 × M ≥ 25 % Chronic 1 (M × 10 × Chronic 1) + Chronic 2 ≥ 25 % Chronic 2 (M × 100 × Chronic 1) + (10 × Chronic 2) + Chronic 3 ≥ 25 % Chronic 3 Chronic 1 + Chronic 2 + Chronic 3 + Chronic 4 ≥ 25 % Chronic 4 Chronic 1 × M ≥ 25 % Chronic 1 (M × 10 × Chronic 1) + Chronic 2 ≥ 25 % Chronic 2 (M × 100 × Chronic 1) + (10 × Chronic 2) + Chronic 3 ≥ 25 % Chronic 3 Chronic 1 + Chronic 2 + Chronic 3 + Chronic 4 ≥ 25 % Chronic 4 4.1.3.5.5.5. Mixtures with highly toxic components 4.1.3.5.5.5.1. Acute 1 and Chronic 1 components with toxicities below 1 mg/l and/or chronic toxicities below 0,1 mg/l (if non-rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute to the toxicity of the mixture even at a low concentration and shall normally be given increased weight in applying the summation of classification approach. When a mixture contains components classified as Acute or Chronic 1, one of the following shall be applied: the tiered approach described in sections 4.1.3.5.5.3 and 4.1.3.5.5.4 using a weighted sum by multiplying the concentrations of Acute 1 and Chronic 1 components by a factor, instead of merely adding up the percentages. This means that the concentration of Acute 1 in the left column of Table 4.1.1 and the concentration of Chronic 1 in the left column of Table 4.1.2 are multiplied by the appropriate multiplying factor. The multiplying factors to be applied to these components are defined using the toxicity value, as summarised in Table 4.1.3. Therefore, in order to classify a mixture containing Acute/Chronic 1 components, the classifier needs to be informed of the value of the M-factor in order to apply the summation method, the additivity formula (see section 4.1.3.5.2) provided that toxicity data are available for all highly toxic components in the mixture and there is convincing evidence that all other components, including those for which specific acute and/or chronic toxicity data are not available, are of low or no toxicity and do not significantly contribute to the environmental hazard of the mixture. 4.1.3.5.5.5.1. Acute 1 and Chronic 1 components with toxicities below 1 mg/l and/or chronic toxicities below 0,1 mg/l (if non-rapidly degradable) and 0,01 mg/l (if rapidly degradable) contribute to the toxicity of the mixture even at a low concentration and shall normally be given increased weight in applying the summation of classification approach. When a mixture contains components classified as Acute or Chronic 1, one of the following shall be applied: the tiered approach described in sections 4.1.3.5.5.3 and 4.1.3.5.5.4 using a weighted sum by multiplying the concentrations of Acute 1 and Chronic 1 components by a factor, instead of merely adding up the percentages. This means that the concentration of Acute 1 in the left column of Table 4.1.1 and the concentration of Chronic 1 in the left column of Table 4.1.2 are multiplied by the appropriate multiplying factor. The multiplying factors to be applied to these components are defined using the toxicity value, as summarised in Table 4.1.3. Therefore, in order to classify a mixture containing Acute/Chronic 1 components, the classifier needs to be informed of the value of the M-factor in order to apply the summation method, the additivity formula (see section 4.1.3.5.2) provided that toxicity data are available for all highly toxic components in the mixture and there is convincing evidence that all other components, including those for which specific acute and/or chronic toxicity data are not available, are of low or no toxicity and do not significantly contribute to the environmental hazard of the mixture. Table 4.1.3 Multiplying factors for highly toxic components of mixtures Non-rapidly degradable.Rapidly degradable. Acute toxicity M factor Chronic toxicity M factor L(E)C50 value mg/l NOEC value mg/l NRD components RD components L(E)C50 value (mg/l) NOEC value (mg/l) NRD components RD components 0,1 < L(E)C50 ≤ 1 1 0,01 < NOEC ≤ 0,1 1 — 0,01 < L(E)C50 ≤ 0,1 10 0,001 < NOEC ≤ 0,01 10 1 0,001 < L(E)C50 ≤ 0,01 100 0,0001 < NOEC ≤ 0,001 100 10 0,0001 < L(E)C50 ≤ 0,001 1000 0,00001 < NOEC ≤ 0,0001 1000 100 0,00001 < L(E)C50 ≤ 0,0001 10000 0,000001 < NOEC ≤ 0,00001 10000 1000 0,0001 < L(E)C50 ≤ 0,001 1000 0,00001 < NOEC ≤ 0,0001 1000 100 0,00001 < L(E)C50 ≤ 0,0001 10000 0,000001 < NOEC ≤ 0,00001 10000 1000 (continue in factor 10 intervals) (continue in factor 10 intervals) 4.1.3.6. Classification of mixtures with components without any useable information 4.1.3.6.1. In the event that no useable information on acute and/or long-term aquatic hazard is available for one or more relevant components, it is concluded that the mixture cannot be attributed to one or more definitive hazard category(ies). In this situation the mixture shall be classified based on the known components only, with the additional statement on the label and in the SDS that: Contains x % of components with unknown hazards to the aquatic environment. … 19 unchanged lines … 5.1. Hazardous to the ozone layer 5.1.1. Definitions and general considerations 5.1.1.1. Ozone depleting potential (ODP) is an integrative quantity, distinct for each halocarbon source species, that represents the extent of ozone depletion in the stratosphere expected from the halocarbon on a mass-for-mass basis relative to CFC-11. The formal definition of ODP is the ratio of integrated perturbations to total ozone, for a differential mass emission of a particular compound relative to an equal emission of CFC-11. Substance hazardous to the ozone layer means a substance which, on the basis of the available evidence concerning its properties and its predicted or observed environmental fate and behaviour may present a danger to the structure and/or the functioning of the stratospheric ozone layer. This includes substances which are listed in Annex I to Regulation (EC) No 1005/2009 of the European Parliament and of the Council of 16 September 2009 on substances that deplete the ozone layerOJ L 286, 31.10.2009, p. 1.. Substance hazardous to the ozone layer means a substance which, on the basis of the available evidence concerning its properties and its predicted or observed environmental fate and behaviour may present a danger to the structure and/or the functioning of the stratospheric ozone layer. This includes substances which are listed in Annex I to Regulation (EC) No 1005/2009 of the European Parliament and of the Council of 16 September 2009 on substances that deplete the ozone layerOJ L 286, 31.10.2009, p. 1.. 5.1.2. Classification criteria for substances 5.1.2.1. A substance shall be classified as hazardous to the ozone layer (Category 1) if the available evidence concerning its properties and its predicted or observed environmental fate and behaviour indicate that it may present a danger to the structure and/or the functioning of the stratospheric ozone layer. 5.1.2.1. A substance shall be classified as hazardous to the ozone layer (Category 1) if the available evidence concerning its properties and its predicted or observed environmental fate and behaviour indicate that it may present a danger to the structure and/or the functioning of the stratospheric ozone layer. 5.1.3. Classification criteria for mixtures 5.1.3.1. Mixtures shall be classified as hazardous to the ozone layer (Category 1) on the basis of the individual concentration of the substance(s) contained therein that are also classified as hazardous to the ozone layer (Category 1), in accordance with Table 5.1. 5.1.3.1. Mixtures shall be classified as hazardous to the ozone layer (Category 1) on the basis of the individual concentration of the substance(s) contained therein that are also classified as hazardous to the ozone layer (Category 1), in accordance with Table 5.1. Table 5.1 Generic concentration limits for substances (in a mixture), classified as hazardous to the ozone layer (Category 1), that trigger classification of the mixture as hazardous to the ozone layer (Category 1) Generic concentration limits for substances (in a mixture), classified as hazardous to the ozone layer (Category 1), that trigger classification of the mixture as hazardous to the ozone layer (Category 1) Classification of the substance Classification of the mixture Hazardous to the ozone layer (Category 1) C ≥ 0,1 % Hazardous to the ozone layer (Category 1) C ≥ 0,1 % 5.1.4. Hazard communication 5.1.4.1. Label elements shall be used for substances or mixtures meeting the criteria for classification in this hazard class in accordance with Table 5.2. Table 5.2 Label elements for hazardous to the ozone layer Symbol/pictogram Signal word Warning Hazard statement H420: Harms public health and the environment by destroying ozone in the upper atmosphere Precautionary statements P502

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ANNEX II SPECIAL RULES FOR LABELLING AND PACKAGING OF CERTAIN SUBSTANCES AND MIXTURES This Annex consists of 5 parts: Part 1 contains special rules for the labelling of certain classified substances and mixtures. Part 2 sets out rules for additional hazard statements to be … 1,849 unchanged words … that either: the type of closure is such that it is not necessary to perform the test referred to in section 3.1.2. or 3.1.3; or the closure has been tested and has been found to conform with the standards referred to above. 3.2. 3.2 Tactile warnings Warnings 3.2.1. Packaging to be fitted with a tactile warning 3.2.1.1. Where substances or mixtures are supplied to the general public and classified for acute toxicity, skin corrosion, germ cell mutagenicity category 2, carcinogenicity category 2, reproductive toxicity category 2, respiratory sensitisation, or Stot, STOT categories 1 and or 2, aspiration hazard, flammable gases, flammable liquids categories 1 or 2, or flammable gases, liquids and solids in categories 1 and 2, solids, the packaging of whatever capacity, shall be fitted with a tactile warning of danger. 3.2.2 3.2.1.2. Section 3.2.1.1 does not apply to transportable gas receptacles. Aerosols and containers fitted with a sealed spray attachment and containing substances or mixtures classified as presenting an aspiration hazard need not be fitted with a tactile warning unless they are classified for one or more of the other hazards in section 3.2.1.1. 3.2.2. Provisions relating to tactile warning 3.2.2.1. This provision does not apply to aerosols which are only classified and labelled as flammable aerosols, Category 1 or flammable aerosols, Category 2. It does not apply either to transportable gas receptacles. 3.2.2.2. The technical specifications for tactile warning devices shall conform to EN ISO standard 11683 as amended Packaging — Tactile warnings of danger-Requirements. danger — Requirements. 3.3 Liquid consumer laundry detergents in soluble packaging for single use Where a liquid consumer laundry detergent in dosages for single use is contained in a soluble packaging, the following additional provisions shall apply: 3.3.1. Liquid consumer laundry detergents contained in soluble packaging for single use shall be contained in an outer packaging. The outer packaging shall fulfil the requirements of section 3.3.2 and the soluble packaging shall fulfil the requirements of section 3.3.3. 3.3.2. The outer packaging shall: (i) be opaque or obscure so that it impedes the visibility of the product or individual doses; (ii) without prejudice to Article 32(3), bear the precautionary statement P102 Keep out of reach of children at a visible place and in a format that attracts attention; (iii) be an easily reclosable, self-standing container; (iv) without prejudice to the requirements of section 3.1, be fitted with a closure that: (a) impedes the ability of young children to open the packaging by requiring coordinated action of both hands with a strength that makes it difficult for young children to open it; (b) maintains its functionality under conditions of repeated opening and closing for the entire life span of the outer packaging. 3.3.3. The soluble packaging shall: (i) contain an aversive agent in a concentration which is safe, and which elicits oral repulsive behaviour within a maximum time of 6 seconds, in case of accidental oral exposure; (ii) retain its liquid content for at least 30 seconds when the soluble packaging is placed in water at 20 °C; (iii) resist mechanical compressive strength of at least 300 N under standard test conditions. 4. PART 4: SPECIAL RULE FOR LABELLING OF PLANT PROTECTION PRODUCTS Without prejudice to the information required in accordance with Article 16 of Directive 91/414/EEC and Annex V of that Directive, the labelling for plant protection products subject to Directive 91/414/EEC shall also include the following wording: EUH401 — To avoid risks to human health and the environment, comply with the instructions for use 5. PART 5: LIST OF HAZARDOUS SUBSTANCES AND MIXTURES TO WHICH ARTICLE 29(3) APPLIES Ready mixed cement and concrete in the wet state.

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compared line by line: this provision is too large to compare word by word, so a marked line is a line that changed somewhere

ANNEX III LIST OF HAZARD STATEMENTS, SUPPLEMENTAL HAZARD INFORMATION AND SUPPLEMENTAL LABEL ELEMENTS 1. Part 1: hazard statements The hazard statements shall be applied in accordance with Parts 2, 3, 4 and 5 of Annex I. In selecting the hazard statements in accordance with Articles 21 and 27, suppliers may use the combined hazard statements provided for in this Annex. In accordance with Article 27 the following principles of precedence for hazard statements may apply to labelling: The hazard statements shall be applied in accordance with Parts 2, 3, 4 and 5 of Annex I. In selecting the hazard statements in accordance with Articles 21 and 27, suppliers may use the combined hazard statements provided for in this Annex. In accordance with Article 27 the following principles of precedence for hazard statements may apply to labelling: (a) if the hazard statement H410 Very toxic to aquatic life with long lasting effects is assigned, the statement H400 Very toxic to aquatic life may be omitted; (b) if the statement H314 Causes severe skin burns and eye damage is assigned, the statement H318 Causes serious eye damage may be omitted. In order to indicate the route of administration or exposure the combined hazard statements in Table 1.2 may be used. In order to indicate the route of administration or exposure the combined hazard statements in Table 1.2 may be used. Table 1.1 Hazard statements for physical hazards The codification system for GHS hazard statements is still under discussion in the UN Committee of Experts and therefore amendments might be needed. … 197 unchanged lines … SL Vnetljiv plin. FI Syttyvä kaasu. SV Brandfarlig gas. H222 Language 2.3 — Flammable aerosols, Hazard Category 1 H222 Language 2.3 — Aerosols, Hazard Category 1 BG Изключително запалим аерозол. ES Aerosol extremadamente inflamable. CS Extrémně hořlavý aerosol. … 18 unchanged lines … SL Zelo lahko vnetljiv aerosol. FI Erittäin helposti syttyvä aerosoli. SV Extremt brandfarlig aerosol. H223 Language 2.3 — Flammable aerosols, Hazard Category 2 H223 Language 2.3 — Aerosols, Hazard Category 2 BG Запалим аерозол. ES Aerosol inflamable. CS Hořlavý aerosol. DA Brandfarlig aerosol. DE Entzündbares Aerosol. ET Tuleohtlik aerosool. EL Εύφλεκτο αερόλυμα. EN Flammable aerosol. FR Aérosol inflammable. GA Aerasól inadhainte. HR Zapaljivi aerosol. IT Aerosol infiammabile. LV Uzliesmojošs aerosols. LT Degus aerozolis. HU Tűzveszélyes aeroszol. MT Aerosol li jaqbad. NL Ontvlambare aerosol. PL Aerozol łatwopalny. NL Ontvlambaar aerosol. PL Łatwopalny aerozol. PT Aerossol inflamável. RO Aerosol inflamabil. SK Horľavý aerosól. … 100 unchanged lines … SL Vnetljiva trdna snov. FI Syttyvä kiinteä aine. SV Brandfarligt fast ämne. H229 Language 2.3 — Aerosols, Hazard Category 1, 2, 3 BG Съд под налягане: може да експлодира при нагряване. ES Recipiente a presión: Puede reventar si se calienta. CS Nádoba je pod tlakem: při zahřívání se může roztrhnout. DA Beholder under tryk. Kan sprænges ved opvarmning. DE Behälter steht unter Druck: Kann bei Erwärmung bersten. ET Mahuti on rõhu all: kuumenemisel võib lõhkeda. EL Δοχείο υπό πίεση. Κατά τη θέρμανση μπορεί να διαρραγεί. EN Pressurised container: May burst if heated. FR Récipient sous pression: peut éclater sous l’effet de la chaleur. GA Coimeádán brúchóirithe: D’fhéadfadh sé pléascadh, má théitear é. HR Spremnik pod tlakom: može se rasprsnuti ako se grije. IT Contenitore pressurizzato: può esplodere se riscaldato. LV Tvertne zem spiediena: karstumā var eksplodēt. LT Slėginė talpykla. Kaitinama gali sprogti. HU Az edényben túlnyomás uralkodik: hő hatására megrepedhet. MT Kontenitur taħt pressjoni. Jista jinfaqa meta jissaħħan. NL Houder onder druk: kan open barsten bij verhitting. PL Pojemnik pod ciśnieniem: Ogrzanie grozi wybuchem. PT Recipiente sob pressão: risco de explosão sob a ação do calor. RO Recipient sub presiune: Poate exploda daca este incalzit. SK Nádoba je pod tlakom: Pri zahriatí sa môže roztrhnúť. SL Posoda je pod tlakom: lahko eksplodira pri segrevanju. FI Painesäiliö: Voi revetä kuumennettaessa. SV Tryckbehållare: Kan sprängas vid uppvärmning. H230 Language 2.2 — Flammable gases (including chemically unstable gases), Hazard Category A BG Може да реагира експлозивно дори при отсъствие на въздух. ES Puede explotar incluso en ausencia de aire. CS Může reagovat výbušně i bez přítomnosti vzduchu. DA Kan reagere eksplosivt selv i fravær af luft. DE Kann auch in Abwesenheit von Luft explosionsartig reagieren. ET Võib reageerida plahvatuslikult isegi õhuga kokku puutumata. EL Δύναται να εκραγεί ακόμη και απουσία αέρος. EN May react explosively even in the absence of air. FR Peut exploser même en l’absence d’air. GA D’fhéadfadh sé imoibriú go pléascach fiú mura bhfuil aer ann. HR Može eksplozivno reagirati i bez prisustva zraka. IT Può esplodere anche in assenza di aria. LV Var eksplodēt pat bezgaisa vidē. LT Gali sprogti net ir nesant oro. HU Még levegő hiányában is robbanásszerű reakcióba léphet. MT Jista jisplodi anke fin-nuqqas ta’ l-arja. NL Kan explosief reageren zelfs in afwezigheid van lucht. PL Może reagować wybuchowo nawet bez dostępu powietrza. PT Pode reagir explosivamente mesmo na ausência de ar. RO Pericol de explozie, chiar si in absenta aerului. SK Môže reagovať výbušne aj bez prítomnosti vzduchu. SL Lahko reagira eksplozivno tudi v odsotnosti zraka. FI Voi reagoida räjähtäen jopa ilmattomassa tilassa. SV Kan reagera explosivt även i frånvaro av luft. H231 Language 2.2 — Flammable gases (including chemically unstable gases), Hazard Category B BG Може да реагира експлозивно дори при отсъствие на въздух при повишено налягане и/или температура. ES Puede explotar incluso en ausencia de aire, a presión y/o temperatura elevadas. CS Při zvýšeném tlaku a/nebo teplotě může reagovat výbušně i bez přítomnosti vzduchu. DA Kan reagere eksplosivt selv i fravær af luft ved forhøjet tryk og/eller temperatur. DE Kann auch in Abwesenheit von Luft bei erhöhtem Druck und/oder erhöhter Temperatur explosionsartig reagieren. ET Võib reageerida plahvatuslikult isegi õhuga kokku puutumata kõrgenenud rõhul ja/või temperatuuril. EL Δύναται να εκραγεί σε υψηλή θερμοκρασία και/ή πίεση ακόμη και απουσία αέρος. EN May react explosively even in the absence of air at elevated pressure and/or temperature. FR Peut exploser même en l’absence d’air à une pression et/ou température élevée(s). GA D’fhéadfadh sé imoibriú go pléascach fiú mura bhfuil aer ann ag brú ardaithe agus/nó ag teocht ardaithe. HR Može eksplozivno reagirati i bez prisustva zraka na povišenom tlaku i/ili temperaturi. IT Può esplodere anche in assenza di aria a pressione e/o temperatura elevata. LV Var eksplodēt pat bezgaisa vidē, paaugstinoties spiedienam un/vai temperatūrai. LT Gali sprogti net ir nesant oro, esant didesniam slėgiui ir (arba) temperatūrai. HU Magas nyomáson és/vagy hőmérsékleten még levegő hiányában is robbanásszerű reakcióba léphet. MT Jista jisplodi anke fin-nuqqas ta’ l-arja fi pressjoni għolja u/jew f’temperatura għolja. NL Kan explosief reageren zelfs in afwezigheid van lucht bij verhoogde druk en/of temperatuur. PL Może reagować wybuchowo nawet bez dostępu powietrza pod zwiększonym ciśnieniem i/lub po ogrzaniu. PT Pode reagir explosivamente mesmo na ausência de ar a alta pressão e/ou temperatura. RO Pericol de explozie, chiar și în absența aerului la presiune și/sau temperatură ridicată. SK Môže reagovať výbušne aj bez prítomnosti vzduchu pri zvýšenom tlaku a/alebo teplote. SL Lahko reagira eksplozivno tudi v odsotnosti zraka pri povišanem tlaku in/ali temperature. FI Voi reagoida räjähtäen jopa ilmattomassa tilassa kohonneessa paineessa ja/tai lämpötilassa. SV Kan reagera explosivt även i frånvaro av luft vid förhöjt tryck och/eller temperatur. H240 Language 2.8 — Self-Reactive Substances and Mixtures, Type A 2.1.5 — Organic Peroxides, Type A BG Може да предизвика експлозия при нагряване. … 580 unchanged lines … SL Povzroča draženje kože. FI Ärsyttää ihoa. SV Irriterar huden. H317 Language 3.4 — Sensitisation — Skin, hazard category 1, 1A, 1B H317 Language 3.4 — Sensitisation — Skin, hazard category 1, 1A, 1B BG Може да причини алергична кожна реакция. ES Puede provocar una reacción alérgica en la piel. CS Může vyvolat alergickou kožní reakci. … 143 unchanged lines … SL Zdravju škodljivo pri vdihavanju. FI Haitallista hengitettynä. SV Skadligt vid inandning. H334 Language 3.4 — Sensitisation — Respiratory, hazard category 1, 1A, 1B H334 Language 3.4 — Sensitisation — Respiratory, hazard category 1, 1A, 1B BG Може да причини алергични или астматични симптоми или затруднения в дишането при вдишване. ES Puede provocar síntomas de alergia o asma o dificultades respiratorias en caso de inhalación. CS Při vdechování může vyvolat příznaky alergie nebo astmatu nebo dýchací potíže. … 345 unchanged lines … SV Kan orsaka organskador <eller ange vilka organ som påverkas om detta är känt> genom lång eller upprepad exponering <ange exponeringsväg om det är definitivt bevisat att faran inte kan orsakas av några andra exponeringsvägar>. H300 + H310 Language 3.1 — Acute toxicity (oral) and acute toxicity (dermal), hazard category 1, 2 H310 Language 3.1 — Acutetoxicity (oral) and acute toxicity (dermal), hazard category 1, 2 BG Смъртоносен при поглъщане или при контакт с кожата ES Mortal en caso de ingestión o en contacto con la piel CS Při požití nebo při styku s kůží může způsobit smrt … 20 unchanged lines … SV Dödligt vid förtäring eller vid hudkontakt H300 + H330 Language 3.1 — Acute toxicity (oral) and acute toxicity (inhalation), hazard category 1, 2 H330 Language 3.1 — Acutetoxicity (oral) and acute toxicity (inhalation), hazard category 1, 2 BG Смъртоносен при поглъщане или при вдишване ES Mortal en caso de ingestión o inhalación CS Při požití nebo při vdechování může způsobit smrt … 20 unchanged lines … SV Dödligt vid förtäring eller inandning H310 + H330 Language 3.1 — Acute toxicity (dermal) and acute toxicity (inhalation), hazard category 1, 2 H330 Language 3.1 — Acutetoxicity (dermal) and acute toxicity (inhalation), hazard category 1, 2 BG Смъртоносен при контакт с кожата или при вдишване ES Mortal en contacto con la piel o si se inhala CS Při styku s kůží nebo při vdechování může způsobit smrt … 15 unchanged lines … PT Mortal por contacto com a pele ou inalação RO Mortal în contact cu pielea sau prin inhalare SK Pri styku s kožou alebo pri vdýchnutí môže spôsobiť smrť SL Smrtno v stiku s kožo ali pri vdihavanju SL Smrtno v stiku s kožo ali pri vdihavanju FI Tappavaa joutuessaan iholle tai hengitettynä SV Dödligt vid hudkontakt eller inandning H300 + H310 + H330 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 1, 2 H330 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 1, 2 BG Смъртоносен при поглъщане, при контакт с кожата или при вдишване ES Mortal en caso de ingestión, contacto con la piel o inhalación CS Při požití, při styku s kůží nebo při vdechování může způsobit smrt … 20 unchanged lines … SV Dödligt vid förtäring, hudkontakt eller inandning H301 + H311 Language 3.1 — Acute toxicity (oral) and acute toxicity (dermal), hazard category 3 H311 Language 3.1 — Acute toxicity (oral) and acute toxicity (dermal), hazard category 3 BG Токсичен при поглъщане или при контакт с кожата ES Tóxico en caso de ingestión o en contacto con la piel CS Toxický při požití a při styku s kůží … 20 unchanged lines … SV Giftigt vid förtäring eller hudkontakt H301 + H331 Language 3.1 — Acute toxicity (oral) and acute toxicity (inhalation), hazard category 3 H331 Language 3.1 — Acute toxicity (oral) and acute toxicity (inhalation), hazard category 3 BG Токсичен при поглъщане или при вдишване ES Tóxico en caso de ingestión o inhalación CS Toxický při požití a při vdechování … 20 unchanged lines … SV Giftigt vid förtäring eller inandning H311 + H331 Language 3.1 — Acute toxicity (dermal) and acute toxicity (inhalation), hazard category 3 H331 Language 3.1 — Acute toxicity (dermal) and acute toxicity (inhalation), hazard category 3 BG Токсичен при контакт с кожата или при вдишване ES Tóxico en contacto con la piel o si se inhala CS Toxický při styku s kůží a při vdechování … 15 unchanged lines … PT Tóxico em contacto com a pele ou por inalação RO Toxic în contact cu pielea sau prin inhalare SK Toxický pri styku s kožou alebo pri vdýchnutí SL Strupeno v stiku s kožo ali pri vdihavanju SL Strupeno v stiku s kožo ali pri vdihavanju FI Myrkyllistä joutuessaan iholle tai hengitettynä SV Giftigt vid hudkontakt eller förtäring H301 + H311 + H331 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 3 H331 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 3 BG Токсичен при поглъщане, при контакт с кожата или при вдишване ES Tóxico en caso de ingestión, contacto con la piel o inhalación CS Toxický při požití, při styku s kůží a při vdechování … 20 unchanged lines … SV Giftigt vid förtäring, hudkontakt eller inandning H302 + H312 Language 3.1 — Acute toxicity (oral) and acute toxicity (dermal), hazard category 4 H312 Language 3.1 — Acute toxicity (oral) and acute toxicity (dermal), hazard category 4 BG Вреден при поглъщане или при контакт с кожата ES Nocivo en caso de ingestión o en contacto con la piel CS Zdraví škodlivý při požití a při styku s kůží … 20 unchanged lines … SV Skadligt vid förtäring eller hudkontakt H302 + H332 Language 3.1 — Acute toxicity (oral) and acute toxicity (inhalation), hazard category 4 H332 Language 3.1 — Acute toxicity (oral) and acute toxicity (inhalation), hazard category 4 BG Вреден при поглъщане или при вдишване ES Nocivo en caso de ingestión o inhalación CS Zdraví škodlivý při požití a při vdechování … 20 unchanged lines … SV Skadligt vid förtäring eller inandning H312 + H332 Language 3.1 — Acute toxicity (dermal) and acute toxicity (inhalation), hazard category 4 H332 Language 3.1 — Acute toxicity (dermal) and acute toxicity (inhalation), hazard category 4 BG Вреден при контакт с кожата или при вдишване ES Nocivo en contacto con la piel o si se inhala CS Zdraví škodlivý při styku s kůží a při vdechování … 20 unchanged lines … SV Skadligt vid hudkontakt eller inandning H302 + H312 + H332 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 4 H332 Language 3.1 — Acute toxicity (oral), acute toxicity (dermal) and acute toxicity (inhalation), hazard category 4 BG Вреден при поглъщане, при контакт с кожата или при вдишване ES Nocivo en caso de ingestión, contacto con la piel o inhalación CS Zdraví škodlivý při požití, při styku s kůží a při vdechování … 145 unchanged lines … SL Lahko ima dolgotrajne škodljive učinke na vodne organizme. FI Voi aiheuttaa pitkäaikaisia haittavaikutuksia vesieliöille. SV Kan ge skadliga långtidseffekter på vattenlevande organismer. H420 Language 5.1 – Hazardous to the ozone layer — hazard category 1 H420 Language 5.1 – Hazardous to the ozone layer — hazard category 1 BG Вреди на общественото здраве и на околната среда, като разрушава озона във високите слоеве на атмосферата ES Causa daños a la salud pública y el medio ambiente al destruir el ozono en la atmósfera superior CS Poškozuje veřejné zdraví a životní prostředí tím, že ničí ozon ve svrchních vrstvách atmosféry … 337 unchanged lines … SL Nevarno za ozonski plašč. FI Vaarallista otsonikerrokselle. SV Farligt för ozonskiktet. 3. Part 3: supplemental label elements/information on certain certain substances and mixtures 3. Part 3: supplemental label elements/information on certain certain substances and mixtures EUH 201/ 201A Language 201 201A BG Съдържа олово. Да не се използва върху повърхност, която евентуално може да се дъвче или смуче от деца. Внимание! Съдържа олово. … 352 unchanged lines … SL Da bi se izognili tveganjem za ljudi in okolje, ravnajte v skladu z navodili za uporabo. FI Noudata käyttöohjeita ihmisen terveydelle ja ympäristölle aiheutuvien vaarojen välttämiseksi. SV För att undvika risker för människors hälsa och för miljön, följ bruksanvisningen.

02008R1272-20150101 → 02008R1272-20150601

compared line by line: this provision is too large to compare word by word, so a marked line is a line that changed somewhere

ANNEX IV LIST OF PRECAUTIONARY STATEMENTS In selecting the precautionary statements in accordance with Articles 22 and 28(3), suppliers may combine the Precautionary Statements in the table below, having regard to clarity and comprehensibility of the precautionary advice. Where square brackets […] appear around some text in a precautionary statement in column (2), this indicates that the text in square brackets is not appropriate in every case and should be used only in certain circumstances. In these cases, conditions for use explaining when the text should be used are given in column (5). When a backslash or diagonal mark [/] appears in a precautionary statement text in column (2), it indicates that a choice has to be made between the phrases they separate in accordance with the indications provided in column (5). When three full stops […] appear in a precautionary statement text in column (2), details on the information to be provided are indicated in column (5). 1. Part 1: Criteria for the selection of precautionary statements Table 6.1 Precautionary statements — General Code General precautionary statements Hazard class Hazard category Conditions for use (1) (2) (3) (4) (5) P101 If medical advice is needed, have product container or label at hand. as appropriate Consumer products P102 Keep out of reach of children. as appropriate Consumer products P103 Read label before use. as appropriate Consumer products Table 6.2 Precautionary statements — Prevention Code Prevention precautionary statements Hazard class Hazard category Conditions for use (1) (2) (3) (4) (5) P201 Obtain special instructions before use. Explosives (section 2.1) Unstable explosive Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P202 Do not handle until all safety precautions have been read and understood. Explosives (section 2.1) Unstable explosive Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Flammable gases (including chemically unstable gases) (section 2.2) A, B (chemically unstable gases) P210 Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 Flammable gases (section 2.2) 1, 2 Aerosols (section 2.3) 1, 2, 3 Flammable liquids (section 2.6) 1, 2, 3 Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 Organic peroxides (section 2.15) Types A, B, C, D, E, F P211 Do not spray on an open flame or other ignition source. Flammable aerosols (section 2.3) 1, 2 P220 Keep/Store away from clothing/…/combustible materials. Oxidising gases (section 2.4) 1 … Manufacturer/supplier to specify incompatible materials. P211 Do not spray on an open flame or other ignition source. Aerosols (section 2.3) 1, 2 P220 Keep/Store away from clothing/…/combustible materials. Oxidising gases (section 2.4) 1 …Manufacturer/supplier to specify other incompatible materials. Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Oxidising liquids (section 2.13) 1 … Manufacturer/supplier to specify incompatible materials. specify to keep away from clothing as well as other incompatible materials. 2, 3 … Manufacturer/supplier to specify incompatible materials. Oxidising solids (section 2.14) 1 … Manufacturer/supplier to specify incompatible materials. specify to keep away from clothing as well as other incompatible materials. 2, 3 … Manufacturer/supplier to specify incompatible materials. Oxidising liquids (section 2.13) 1 — specify to keep away from clothing and other combustible materials. 2, 3 …Manufacturer/supplier to specify other incompatible materials. Oxidising solids (section 2.14) 1 — specify to keep away from clothing and other combustible materials. 2, 3 …Manufacturer/supplier to specify other incompatible materials. Organic peroxides (section 2.15) Types A, B, C, D, E, F P221 Take any precaution to avoid mixing with combustibles/… Oxidising liquids (section 2.13) 1, 2, 3 … Manufacturer/supplier to specify incompatible materials. Oxidising solids (section 2.14) 1, 2, 3 P222 Do not allow contact with air. Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 P223 Keep away from any possible contact with water, because of violent reaction and possible flash fire. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P230 Keep wetted with … Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.5 … Manufacturer/supplier to specify appropriate material. P223 Do not allow contact with water. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P230 Keep wetted with … Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.5 … Manufacturer/supplier to specify appropriate material. if drying out increases explosion hazard, except as needed for manufacturing or operating processes (e.g. nitrocellulose). P231 Handle under inert gas. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 P232 Protect from moisture. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 P233 Keep container tightly closed. Flammable liquids (section 2.6) 1, 2, 3 Acute toxicity — inhalation (section 3.1) 1, 2, 3 if product is volatile so as to generate hazardous atmosphere. Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P234 Keep only in original container. Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Organic peroxides (section 2.15) Types A, B, C, D, E, F Corrosive to metals (section 2.16) 1 P235 Keep cool. Flammable liquids (section 2.6) 1, 2, 3 Self-reactive substances and mixtures (Section 2.8) Types A, B, C, D, E, F Self-heating substances and mixtures (section 2.11) 1, 2 Organic peroxides (section 2.15) Types A, B, C, D, E, F P240 Ground/bond container and receiving equipment. Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 if the explosive is electrostatically sensitive. Flammable liquids (section 2.6) 1, 2, 3 if electrostatically sensitive material is for reloading. if product is volatile so as to generate hazardous atmosphere. Flammable solids (section 2.7) 1, 2 if electrostatically sensitive material is for reloading. P241 Use explosion-proof electrical/ventilating/lighting/…/equipment. Flammable liquids (section 2.6) 1, 2, 3 … Manufacturer/supplier to specify other equipment. Flammable solids (section 2.7) 1, 2 … Manufacturer/supplier to specify other equipment. if dust clouds can occur. P242 Use only non-sparking tools. Flammable liquids (section 2.6) 1, 2, 3 P243 Take precautionary measures against static discharge. Flammable liquids (section 2.6) 1, 2, 3 P244 Keep reduction valves free from grease and oil. Oxidising gases (section 2.4) 1 P250 Do not subject to grinding/shock/…/friction. Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 … Manufacturer/supplier to specify applicable rough handling. P251 Pressurized container: Do not pierce or burn, even after use. Flammable aerosols (section 2.3) 1, 2 P260 Do not breathe dust/fume/gas/mist/vapours/spray. Acute toxicity — inhalation (section 3.1) 1, 2 Manufacturer/supplier to specify applicable conditions. P242 Use only non-sparking tools. Flammable liquids (section 2.6) 1, 2, 3 P243 Take precautionary measures against static discharge. Flammable liquids (section 2.6) 1, 2, 3 P244 Keep valves and fittings free from oil and grease. Oxidising gases (section 2.4) 1 P250 Do not subject to grinding/shock/…/friction. Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 … Manufacturer/supplier to specify applicable rough handling. P251 Do not pierce or burn, even after use. Aerosols (section 2.3) 1, 2, 3 P260 Do not breathe dust/fume/gas/mist/vapours/spray. Acute toxicity — inhalation (section 3.1) 1, 2 Manufacturer/supplier to specify applicable conditions. Specific target organ toxicity — single exposure (section 3.8) 1, 2 Specific target organ toxicity — repeated exposure (section 3.9) 1, 2 Skin corrosion (section 3.2) 1A, 1B, 1C Specify do not breathe dusts or mists. if inhalable particles of dusts or mists may occur during use. Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P261 Avoid breathing dust/fume/gas/mist/vapours/spray. Acute toxicity — inhalation (section 3.1) 3, 4 Manufacturer/supplier to specify applicable conditions. Respiratory sensitisation (section 3.4) 1, 1A, 1B Skin sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P261 Avoid breathing dust/fume/gas/mist/vapours/spray. Acute toxicity — inhalation (section 3.1) 3, 4 Manufacturer/supplier to specify applicable conditions. may be omitted if P260 is given on the label Respiratory sensitisation (section 3.4) 1, 1A, 1B Skin sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P262 Do not get in eyes, on skin, or on clothing. Acute toxicity — dermal (section 3.1) 1, 2 P263 Avoid contact during pregnancy/while nursing. Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P264 Wash … thoroughly after handling. Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Manufacturer/supplier to specify parts of the body to be washed after handling. Acute toxicity — dermal (section 3.1) 1, 2 Skin corrosion (section 3.2) 1A, 1B, 1C Skin irritation (section 3.2) 2 Eye irritation (section 3.3) 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category Specific target organ toxicity — single exposure (section 3.8) 1, 2 Specific target organ toxicity — repeated exposure (section 3.9) 1 P270 Do not eat, drink or smoke when using this product. Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Acute toxicity — dermal (section 3.1) 1, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category Specific target organ toxicity — single exposure (section 3.8) 1, 2 Specific target organ toxicity — repeated exposure (section 3.9) 1 P271 Use only outdoors or in a well-ventilated area. Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P272 Contaminated work clothing should not be allowed out of the workplace. Skin sensitisation (section 3.4) 1, 1A, 1B P273 Avoid release to the environment. Hazardous to the aquatic environment — acute aquatic hazard (section 4.1) 1 if this is not the intended use. Hazardous to the aquatic environment — long-term aquatic hazard (section 4.1) 1, 2, 3, 4 P272 Contaminated work clothing should not be allowed out of the workplace. Skin sensitisation (section 3.4) 1, 1A, 1B P273 Avoid release to the environment. Hazardous to the aquatic environment — acute aquatic hazard (section 4.1) 1 if this is not the intended use. Hazardous to the aquatic environment — long-term aquatic hazard (section 4.1) 1, 2, 3, 4 Hazardous to the ozone layer (section 5.1) 1 P280 Wear protective gloves/protective clothing/eye protection/face protection. Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 Manufacturer/supplier to specify type of equipment. P280 Wear protective gloves/protective clothing/eye protection/face protection. Explosives (section 2.1) Unstable explosives and divisions 1.1, 1.2, 1.3, 1.4, 1.5 Manufacturer/supplier to specify type of equipment. Specify face protection. Flammable liquids (section 2.6) 1, 2, 3 Manufacturer/supplier to specify type of equipment. Flammable liquids (section 2.6) 1, 2, 3 Manufacturer/supplier to specify type of equipment. Specify protective gloves and eye/face protection. Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Self-heating substances and mixtures (section 2.11) 1, 2 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 Organic peroxides (section 2.15) Types A, B, C, D, E, F Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Manufacturer/supplier to specify type of equipment. Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Self-heating substances and mixtures (section 2.11) 1, 2 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 Organic peroxides (section 2.15) Types A, B, C, D, E, F Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Manufacturer/supplier to specify type of equipment. Specify protective gloves/clothing. Skin corrosion (section 3.2) 1A, 1B, 1C Manufacturer/supplier to specify type of equipment. Skin corrosion (section 3.2) 1A, 1B, 1C Manufacturer/supplier to specify type of equipment. Specify protective gloves/clothing and eye/face protection. Skin irritation (section 3.2) 2 Manufacturer/supplier to specify type of equipment. Skin irritation (section 3.2) 2 Manufacturer/supplier to specify type of equipment. Specify protective gloves. Skin sensitisation (section 3.4) 1, 1A, 1B Severe eye damage (section 3.3) 1 Manufacturer/supplier to specify type of equipment. Skin sensitisation (section 3.4) 1, 1A, 1B Severe eye damage/(section 3.3) 1 Manufacturer/supplier to specify type of equipment. Specify eye/face protection. Eye irritation (section 3.3) 2 Eye irritation (section 3.3) 2 Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Manufacturer/supplier to specify type of equipment. Carcinogenicity (section 3.6) 1A, 1B, 2 Manufacturer/supplier to specify type of equipment. Reproductive toxicity (section 3.7) 1A, 1B, 2 Manufacturer/supplier to specify type of equipment. P281 Use personal protective equipment as required. Explosives (section 2.1) Unstable explosive Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 P282 Wear cold insulating gloves/face shield/eye protection. Gases under pressure (section 2.5) Refrigerated liquefied gas P283 Wear fire/flame resistant/retardant clothing. Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P284 Wear respiratory protection. Acute toxicity — inhalation (section 3.1) 1, 2 Manufacturer/supplier to specify equipment. P285 In case of inadequate ventilation wear respiratory protection. Respiratory sensitisation (section 3.4) 1, 1A, 1B Manufacturer/supplier to specify equipment. P284 [In case of inadequate ventilation] wear respiratory protection. Acute toxicity — inhalation (section 3.1) 1, 2 Manufacturer/supplier to specify equipment. text in square brackets may be used if additional information is provided with the chemical at the point of use that explains what type of ventilation would be adequate for safe use. Respiratory sensitisation (section 3.4) 1, 1A, 1B P285 In case of inadequate ventilation wear respiratory protection. Respiratory sensitisation (section 3.4) 1, 1A, 1B Manufacturer/supplier to specify equipment. P231 + P232 Handle under inert gas. Protect from moisture. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 P235 + P410 Keep cool. Protect from sunlight. Self-heating substances and mixtures (section 2.11) 1, 2 Table 6.3 Precautionary statements — Response Code Response precautionary statements Hazard class Hazard category Conditions for use (1) (2) (3) (4) (5) P301 IF SWALLOWED: Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Aspiration Hazard (section 3.10) 1 P302 IF ON SKIN: Pyrophoric liquids (section 2.9) 1 Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P302 IF ON SKIN: Pyrophoric liquids (section 2.9) 1 Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P303 IF ON SKIN (or hair): Flammable liquids (section 2.6) 1, 2, 3 Skin corrosion (section 3.2) 1A, 1B, 1C P304 IF INHALED: Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P304 IF INHALED: Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P305 IF IN EYES: Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 Eye irritation (section 3.3) 2 P306 IF ON CLOTHING: Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P307 IF exposed: Specific target organ toxicity — single exposure (section 3.8) 1 P308 IF exposed or concerned: Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P309 IF exposed or if you feel unwell: Specific target organ toxicity — single exposure (section 3.8) 2 P310 Immediately call a POISON CENTER or doctor/physician. Acute toxicity — oral (section 3.1) 1, 2, 3 Acute toxicity — dermal (section 3.1) 1, 2 Specific target organ toxicity, single exposure (section 3.8) 1, 2 P309 IF exposed or if you feel unwell: Specific target organ toxicity — single exposure (section 3.8) 2 P310 Immediately call a POISON CENTER/doctor/… Acute toxicity — oral (section 3.1) 1, 2, 3 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. Acute toxicity — dermal (section 3.1) 1, 2 Acute toxicity — inhalation (section 3.1) 1, 2 Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 Aspiration hazard (section 3.10) 1 P311 Call a POISON CENTRE or doctor/physician. Acute toxicity — inhalation (section 3.1) 3 Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure (section 3.8) 1, 2 P312 Call a POISON CENTER or doctor/physician if you feel unwell. Acute toxicity — oral (section 3.1) 4 Acute toxicity — dermal (section 3.1) 3, 4 P311 Call a POISON CENTER/doctor/… Acute toxicity — inhalation (section 3.1) 3 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure (section 3.8) 1, 2 P312 Call a POISON CENTER/doctor/…/if you feel unwell. Acute toxicity — oral (section 3.1) 4 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. Acute toxicity — dermal (section 3.1) 3, 4 Acute toxicity — inhalation (section 3.1) 4 Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P313 Get medical advice/attention. Skin irritation (section 3.2) 2, 3 Eye irritation (section 3.3) 2 Skin sensitisation (section 3.4) 1, 1A, 1B Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P313 Get medical advice/attention. Skin irritation (section 3.2) 2, 3 Eye irritation (section 3.3) 2 Skin sensitisation (section 3.4) 1, 1A, 1B Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P314 Get medical advice/attention if you feel unwell. Specific target organ toxicity — repeated exposure (section 3.9) 1, 2 P315 Get immediate medical advice/attention. Gases under pressure (section 2.5) Refrigerated liquefied gas P320 Specific treatment is urgent (see … on this label). Acute toxicity — inhalation (section 3.1) 1, 2 … Reference to supplemental first aid instruction. if immediate administration of antidote is required. P321 Specific treatment (see … on this label). Acute toxicity — oral (section 3.1) 1, 2, 3 … Reference to supplemental first aid instruction. — if immediate administration of antidote is required. Acute toxicity — inhalation (section 3.1) 3 … Reference to supplemental first aid instruction. — if immediate specific measures are required. Specific target organ toxicity — single exposure (section 3.8) 1 … Reference to supplemental first aid instruction. — if immediate measures are required. Skin sensitisation (section 3.4) 1, 1A, 1B … Reference to supplemental first aid instruction. — manufacturer/supplier may specify a cleansing agent if appropriate. Skin corrosion (section 3.2) 1A, 1B, 1C Skin irritation (section 3.2) 2 P321 Specific treatment (see … on this label). Acute toxicity — oral (section 3.1) 1, 2, 3 … Reference to supplemental first aid instruction. if immediate administration of antidote is required. Acute toxicity, dermal (section 3.1) 1, 2, 3, 4 … Reference to supplemental first aid instruction. if immediate measures, such as specific cleansing agent, are advised. Acute toxicity — inhalation (section 3.1) 3 … Reference to supplemental first aid instruction. if immediate specific measures are required. Skin corrosion (section 3.2) 1A, 1B, 1C … Reference to supplemental first aid instruction. manufacturer/supplier may specify a cleansing agent if appropriate. Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A,1B Specific target organ toxicity — single exposure (section 3.8) 1 … Reference to supplemental first aid instruction. if immediate measures are required. P322 Specific measures (see … on this label). Acute toxicity — dermal (section 3.1) 1, 2 … Reference to supplemental first aid instruction. if immediate measures such as specific cleansing agent is advised. Acute toxicity — dermal (section 3.1) 3, 4 … Reference to supplemental first aid instruction. if measures such as specific cleansing agent is advised. P330 Rinse mouth. Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C P331 Do NOT induce vomiting. Skin corrosion (section 3.2) 1A, 1B, 1C Aspiration hazard (section 3.10) 1 P332 If skin irritation occurs: Skin irritation (section 3.2) 2, 3 P333 If skin irritation or rash occurs: Skin sensitisation (section 3.4) 1, 1A, 1B P334 Immerse in cool water/wrap in wet bandages. Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 P332 If skin irritation occurs: Skin irritation (section 3.2) 2, 3 P333 If skin irritation or rash occurs: Skin sensitisation (section 3.4) 1, 1A, 1B P334 Immerse in cool water/wrap in wet bandages. Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P335 Brush off loose particles from skin. Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P336 Thaw frosted parts with lukewarm water. Do not rub affected area. Gases under pressure (section 2.5) Refrigerated liquefied gas P337 If eye irritation persists: Eye irritation (section 3.3) 2 P338 Remove contact lenses, if present and easy to do. Continue rinsing. Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 Eye irritation (section 3.3) 2 P340 Remove victim to fresh air and keep at rest in a position comfortable for breathing. Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C P340 Remove person to fresh air and keep comfortable for breathing. Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P341 If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. Respiratory sensitisation (section 3.4) 1, 1A, 1B P342 If experiencing respiratory symptoms: Respiratory sensitisation (section 3.4) 1, 1A, 1B P350 Gently wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 1, 2 P351 Rinse cautiously with water for several minutes. Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 P341 If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. Respiratory sensitisation (section 3.4) 1, 1A, 1B P342 If experiencing respiratory symptoms: Respiratory sensitisation (section 3.4) 1, 1A, 1B P350 Gently wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 1, 2 P351 Rinse cautiously with water for several minutes. Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 Eye irritation (section 3.3) 2 P352 Wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 3, 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P352 Wash with plenty of water/… Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 …Manufacturer/supplier may specify a cleansing agent if appropriate, or may recommend an alternative agent in exceptional cases if water is clearly inappropriate. Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P353 Rinse skin with water/shower. Flammable liquids (section 2.6) 1, 2, 3 Skin corrosion (section 3.2) 1A, 1B, 1C P360 Rinse immediately contaminated clothing and skin with plenty of water before removing clothes. Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P361 Remove/Take off immediately all contaminated clothing. Flammable liquids (section 2.6) 1, 2, 3 Acute toxicity — dermal (section 3.1) 1, 2, 3 P361 Take off immediately all contaminated clothing. Flammable liquids (section 2.6) 1, 2, 3 Acute toxicity — dermal (section 3.1) 1, 2, 3 Skin corrosion (section 3.2) 1A, 1B, 1C P362 Take off contaminated clothing and wash before reuse. Skin irritation (section 3.2) 2 P363 Wash contaminated clothing before reuse. Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Skin sensitisation (section 3.4) 1, 1A, 1B P370 In case of fire: Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 Oxidising gases (section 2.4) 1 P362 Take off contaminated clothing. Acute toxicity, dermal (section 3.1) 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P363 Wash contaminated clothing before reuse. Skin corrosion (section 3.2) 1A, 1B, 1C P364 And wash it before reuse. Acute toxicity, dermal (section 3.1) 1, 2, 3, 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P370 In case of fire: Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 Oxidising gases (section 2.4) 1 Flammable liquids (section 2.6) 1, 2, 3 Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 P371 In case of major fire and large quantities: Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P372 Explosion risk in case of fire. Explosives (section 2.1) Unstable explosives and Divisions 1.1, 1.2, 1.3, 1.4, 1.5 except if explosives are 1.4S AMMUNITION AND COMPONENTS THEREOF. P373 DO NOT fight fire when fire reaches explosives. Explosives (section 2.1) Unstable explosives and Divisions 1.1, 1.2, 1.3, 1.4, 1.5 P374 Fight fire with normal precautions from a reasonable distance. Explosives (section 2.1) Division 1.4 if explosives are 1.4S AMMUNITION AND COMPONENTS THEREOF. P375 Fight fire remotely due to the risk of explosion. Self-reactive substances and mixtures (section 2.8) Types A, B Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P376 Stop leak if safe to do so. Oxidising gases (section 2.4) 1 P377 Leaking gas fire: Do not extinguish, unless leak can be stopped safely. Flammable gases (section 2.2) 1, 2 P378 Use … for extinction. Flammable liquids (section 2.6) 1, 2, 3 … Manufacturer/supplier to specify appropriate media Do not extinguish, unless leak can be stopped safely. Flammable gases (section 2.2) 1, 2 P378 Use…to extinguish Flammable liquids (section 2.6) 1, 2, 3 … Manufacturer/supplier to specify appropriate media if water increases risk. Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Pyrophoric liquids (section 2.9) 1 Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 P380 Evacuate area. Explosives (section 2.1) Unstable explosives Explosives (section 2.1) Divisions 1.1, 1.2, 1.3, 1.4, 1.5 Self-reactive substances and mixtures (section 2.8) Types A, B Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P381 Eliminate all ignition sources if safe to do so. Flammable gases (section 2.2) 1, 2 P390 Absorb spillage to prevent material damage. Corrosive to metals (section 2.16) 1 P391 Collect spillage. Hazardous to the aquatic environment – acute aquatic hazard (section 4.1) 1 Hazardous to the aquatic environment – long-term aquatic hazard (section 4.1) 1, 2 P301 + P310 IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. Acute toxicity — oral (section 3.1) 1, 2, 3 Aspiration hazard (section 3.10) 1 P301 + P312 IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. Acute toxicity — oral (section 3.1) 4 P301 + P330 + P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. Skin corrosion (section 3.2) 1A, 1B, 1C P302 + P334 IF ON SKIN: Immerse in cool water/wrap in wet bandages. Pyrophoric liquids (section 2.9) 1 P302 + P350 IF ON SKIN: Gently wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 1, 2 P302 + P352 IF ON SKIN: Wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 3, 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P303 + P361 + P353 IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Flammable liquids (section 2.6) 1, 2, 3 Skin corrosion (section 3.2) 1A, 1B, 1C P304 + P340 IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C P381 Eliminate all ignition sources if safe to do so. Flammable gases (section 2.2) 1, 2 P390 Absorb spillage to prevent material damage. Corrosive to metals (section 2.16) 1 P391 Collect spillage. Hazardous to the aquatic environment – acute aquatic hazard (section 4.1) 1 Hazardous to the aquatic environment – long-term aquatic hazard (section 4.1) 1, 2 P301 + P310 IF SWALLOWED: Immediately call a POISON CENTER/doctor/… Acute toxicity — oral (section 3.1) 1, 2, 3 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. Aspiration hazard (section 3.10) 1 P301 + P312 IF SWALLOWED: Call a POISON CENTER/doctor/…/if you feel unwell. Acute toxicity — oral (section 3.1) 4 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. P301 + P330 + P331 IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. Skin corrosion (section 3.2) 1A, 1B, 1C P302 + P334 IF ON SKIN: Immerse in cool water/wrap in wet bandages. Pyrophoric liquids (section 2.9) 1 P302 + P350 IF ON SKIN: Gently wash with plenty of soap and water. Acute toxicity — dermal (section 3.1) 1, 2 P302 + P352 IF ON SKIN: Wash with plenty of water/… Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 …Manufacturer/supplier may specify a cleansing agent if appropriate, or may recommend an alternative agent in exceptional cases if water is clearly inappropriate. Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P303 + P361 + P353 IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. Flammable liquids (section 2.6) 1, 2, 3 Skin corrosion (section 3.2) 1A, 1B, 1C P304 + P340 IF INHALED: Remove person to fresh air and keep comfortable for breathing. Acute toxicity — inhalation (section 3.1) 1, 2, 3, 4 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P304 + P341 IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. Respiratory sensitisation (section 3.4) 1, 1A, 1B P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 P304 + P341 IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. Respiratory sensitisation (section 3.4) 1, 1A, 1B P305 + P351 + P338 IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. Skin corrosion (section 3.2) 1A, 1B, 1C Serious eye damage/eye irritation (section 3.3) 1 Eye irritation (section 3.3) 2 P306 + P360 IF ON CLOTHING: Rinse immediately contaminated clothing and skin with plenty of water before removing clothes. Oxidising liquids (section 2.13) 1 Oxidising solids (section 2.14) 1 P307 + P311 IF exposed: Call a POISON CENTER or doctor/physician. Specific target organ toxicity — single exposure (section 3.8) 1 P308 + P313 IF exposed or concerned: Get medical advice/attention. Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 P308 + P311 IF exposed or concerned: Call a POISON CENTER/doctor/… Specific target organ toxicity — single exposure (section 3.8) 1, 2 …Manufacturer/supplier to specify the appropriate source of emergency medical advice. P308 + P313 IF exposed or concerned: Get medical advice/attention. Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Reproductive toxicity — effects on or via lactation (section 3.7) Additional category P309 + P311 IF exposed or if you feel unwell: Call a POISON CENTER or doctor/physician. Specific target organ toxicity — single exposure (section 3.8) 2 P332 + P313 If skin irritation occurs: Get medical advice/attention. Skin irritation (section 3.2) 2 P333 + P313 If skin irritation or rash occurs: Get medical advice/attention. Skin sensitisation (section 3.4) 1, 1A, 1B P335 + P334 Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P337 + P313 If eye irritation persists: Get medical advice/attention. Eye irritation (section 3.3) 2 P342 + P311 If experiencing respiratory symptoms: Call a POISON CENTRE or doctor/physician. Respiratory sensitisation (section 3.4) 1, 1A, 1B P370 + P376 In case of fire: Stop leak if safe to do so. Oxidizing gases (section 2.4) 1 P370 + P378 In case of fire: Use … for extinction. Flammable liquids (section 2.6) 1, 2, 3 … Manufacturer/supplier to specify appropriate media. P309 + P311 IF exposed or if you feel unwell: Call a POISON CENTER or doctor/physician. Specific target organ toxicity — single exposure (section 3.8) 2 P332 + P313 If skin irritation occurs: Get medical advice/attention. Skin irritation (section 3.2) 2 P333 + P313 If skin irritation or rash occurs: Get medical advice/attention. Skin sensitisation (section 3.4) 1, 1A, 1B P335 + P334 Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. Pyrophoric solids (section 2.10) 1 Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2 P337 + P313 If eye irritation persists: Get medical advice/attention. Eye irritation (section 3.3) 2 P342 + P311 If experiencing respiratory symptoms: Call a POISON CENTER/doctor/… Respiratory sensitisation (section 3.4) 1, 1A, 1B …Manufacturer/supplier to specify the appropriate source of emergency medical advice. P361 + P364 Take off immediately all contaminated clothing and wash it before reuse. Acute toxicity, dermal (section 3.1) 1, 2, 3 P362 + P364 Take off contaminated clothing and wash it before reuse. Acute toxicity, dermal (section 3.1) 4 Skin irritation (section 3.2) 2 Skin sensitisation (section 3.4) 1, 1A, 1B P370 + P376 In case of fire: Stop leak if safe to do so. Oxidizing gases (section 2.4) 1 P370 + P378 In case of fire: Use … to extinguish. Flammable liquids (section 2.6) 1, 2, 3 …Manufacturer/supplier to specify appropriate media. if water increases risk. Flammable solids (section 2.7) 1, 2 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F … 30 unchanged lines … Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 Aspiration hazard (section 3.10) 1 P406 Store in corrosive resistant/… container with a resistant inner liner. Corrosive to metals (section 2.16) 1 … Manufacturer/supplier to specify other compatible materials. P407 Maintain air gap between stacks/pallets. Self-heating substances and mixtures (section 2.11) 1, 2 P410 Protect from sunlight. Flammable aerosols (section 2.3) 1, 2 Gases under pressure (section 2.5) Compressed gas P407 Maintain air gap between stacks/pallets. Self-heating substances and mixtures (section 2.11) 1, 2 P410 Protect from sunlight. Aerosols (section 2.3) 1,2, 3 Gases under pressure (section 2.5) Compressed gas Liquefied gas Dissolved gas Self-heating substances and mixtures (section 2.11) 1, 2 Dissolved gas — may be omitted for gases filled in transportable gas cylinders in accordance with packing instruction P200 of the UN RTDG, Model Regulations, unless those gases are subject to (slow) decomposition or polymerisation Self-heating substances and mixtures (section 2.11) 1, 2 Organic peroxides (section 2.15) Types A, B, C, D, E, F P411 Store at temperatures not exceeding … oC/…oF. Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F … Manufacturer/supplier to specify temperature Organic peroxides (section 2.15) Types A, B, C, D, E, F P411 Store at temperatures not exceeding … oC/…oF. Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F … Manufacturer/supplier to specify temperature Organic peroxides (section 2.15) Types A, B, C, D, E, F P412 Do not expose to temperatures exceeding 50 oC/122 oF. Flammable aerosols (section 2.3) 1, 2 P413 Store bulk masses greater than … kg/…lbs at temperatures not exceeding … oC/…oF. Self-heating substances and mixtures (section 2.11) 1, 2 … Manufacturer/supplier to specify mass and temperature. P412 Do not expose to temperatures exceeding 50 °C/122 °F. Aerosols (section 2.3) 1, 2, 3 P413 Store bulk masses greater than … kg/…lbs at temperatures not exceeding … oC/…oF. Self-heating substances and mixtures (section 2.11) 1, 2 … Manufacturer/supplier to specify mass and temperature. P420 Store away from other materials. Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Self-heating substances and mixtures (section 2.11) 1, 2 Organic peroxides (section 2.15) Types A, B, C, D, E, F P422 Store contents under … Pyrophoric liquids (section 2.9) 1 … Manufacturer/supplier to specify appropriate liquid or inert gas. Pyrophoric solids (section 2.10) 1 P402 + P404 Store in a dry place. Store in a closed container. Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 P403 + P233 Store in a well-ventilated place. Keep container tightly closed. Acute toxicity — inhalation (section 3.1) 1, 2, 3 if product is volatile so as to generate hazardous atmosphere. Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 P403 + P235 Store in a well-ventilated place. Keep cool. Flammable liquids (section 2.6) 1, 2, 3 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F P410 + P403 Protect from sunlight. Store in a well-ventilated place. Gases under pressure (section 2.5) Compressed gas Liquefied gas Dissolved gas P410 + P412 Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. Flammable aerosols (section 2.3) 1, 2 P411 + P235 Store at temperatures not exceeding … oC/…oF. Keep cool. Organic peroxides (section 2.15) Types A, B, C, D, E, F … Manufacturer/supplier to specify temperature. P410 + P403 Protect from sunlight. Store in a well-ventilated place. Gases under pressure (section 2.5) Compressed gas Liquefied gas Dissolved gas — may be omitted for gases filled in transportable gas cylinders in accordance with packing instruction P200 of the UN RTDG, Model Regulations, unless those gases are subject to (slow) decomposition or polymerisation P410 + P412 Protect from sunlight. Do not expose to temperatures exceeding 50 °C/122 °F. Aerosols (section 2.3) 1, 2, 3 P411 + P235 Store at temperatures not exceeding … oC/…oF. Keep cool. Organic peroxides (section 2.15) Types A, B, C, D, E, F … Manufacturer/supplier to specify temperature. Table 6.5 Precautionary statements — Disposal Code Disposal precautionary statements Hazard class Hazard category Conditions for use (1) (2) (3) (4) (5) P501 Dispose of contents/container to … Explosives (section 2.1) Unstable explosives and Divisions 1.1, 1.2, 1.3, 1.4, 1.5 … in accordance with local/regional/national/international regulation (to be specified). Flammable liquids (section 2.6) 1, 2, 3 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 Organic peroxides (section 2.15) Types A, B, C, D, E, F Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Acute toxicity — inhalation (section 3.1) 1, 2 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Skin sensitisation (section 3.4) 1, 1A, 1B Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Specific target organ toxicity — single exposure (section 3.8) 1, 2 Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 Specific target organ toxicity — repeated exposure (section 3.9) 1, 2 Aspiration hazard (section 3.10) 1 Hazardous to the aquatic environment — acute aquatic hazard(section 4.1) 1 Hazardous to the aquatic environment — long-term aquatic hazard (section 4.1) 1, 2, 3, 4 P502 Refer to manufacturer/supplier for information on recovery/recycling Hazardous to the ozone layer (section 5.1) 1 2. Part 2: precautionary statements P501 Dispose of contents/container to … Explosives (section 2.1) Unstable explosives and Divisions 1.1, 1.2, 1.3, 1.4, 1.5 … in accordance with local/regional/national/international regulation (to be specified). Flammable liquids (section 2.6) 1, 2, 3 Self-reactive substances and mixtures (section 2.8) Types A, B, C, D, E, F Substances and mixtures which, in contact with water, emit flammable gases (section 2.12) 1, 2, 3 Oxidising liquids (section 2.13) 1, 2, 3 Oxidising solids (section 2.14) 1, 2, 3 Organic peroxides (section 2.15) Types A, B, C, D, E, F Acute toxicity — oral (section 3.1) 1, 2, 3, 4 Acute toxicity — dermal (section 3.1) 1, 2, 3, 4 Acute toxicity — inhalation (section 3.1) 1, 2 Skin corrosion (section 3.2) 1A, 1B, 1C Respiratory sensitisation (section 3.4) 1, 1A, 1B Skin sensitisation (section 3.4) 1, 1A, 1B Germ cell mutagenicity (section 3.5) 1A, 1B, 2 Carcinogenicity (section 3.6) 1A, 1B, 2 Reproductive toxicity (section 3.7) 1A, 1B, 2 Specific target organ toxicity — single exposure (section 3.8) 1, 2 Specific target organ toxicity — single exposure; respiratory tract irritation (section 3.8) 3 Specific target organ toxicity — single exposure; narcosis (section 3.8) 3 Specific target organ toxicity — repeated exposure (section 3.9) 1, 2 Aspiration hazard (section 3.10) 1 Hazardous to the aquatic environment — acute aquatic hazard(section 4.1) 1 Hazardous to the aquatic environment — long-term aquatic hazard (section 4.1) 1, 2, 3, 4 P502 Refer to manufacturer/supplier for information on recovery/recycling Hazardous to the ozone layer (section 5.1) 1 2. Part 2: precautionary statements The precautionary statements shall be taken from this part of Annex IV and selected in accordance with Part 1. Table 1.1 Precautionary statements — General … 119 unchanged lines … SL Ne uporabljajte, dokler se ne seznanite z vsemi varnostnimi ukrepi. FI Lue varoitukset huolellisesti ennen käsittelyä. SV Använd inte produkten innan du har läst och förstått säkerhetsanvisningarna P210 Language BG Да се пази от топлина/искри/открит пламък/нагорещени повърхности. — Тютюнопушенето забранено. ES Mantener alejado de fuentes de calor, chispas, llama abierta o superficies calientes. — No fumar. CS Chraňte před teplem/jiskrami/otevřeným plamenem/horkými povrchy. — Zákaz kouření. DA Holdes væk fra varme/gnister/åben ild/varme overflader. Rygning forbudt. DE Von Hitze/Funken/offener Flamme/heißen Oberflächen fernhalten. Nicht rauchen. ET Hoida eemal soojusallikast/sädemetest/leekidest/kuumadest pindadest. — Mitte suitsetada. EL Μακριά από θερμότητα/σπινθήρες/γυμνές φλόγες/θερμές επιφάνειες. — Μην καπνίζετε. EN Keep away from heat/sparks/open flames/hot surfaces. — No smoking. FR Tenir à l’écart de la chaleur/des étincelles/des flammes nues/des surfaces chaudes. — Ne pas fumer. GA Coimeád ó theas/splancacha/lasair gan chosaint/dromchlaí te. — Ná caitear tobac. HR Čuvati odvojeno od topline/iskre/otvorenog plamena/vrućih površina. – Ne pušiti. IT Tenere lontano da fonti di calore/scintille/fiamme libere/superfici riscaldate. — Non fumare. LV Nelietot vietās, kur ir sastopams karstums/dzirksteles/atklāta uguns/…/karstas virsmas. Nesmēķēt. LT Laikyti atokiau nuo šilumos šaltinių/žiežirbų/atviros liepsnos/karštų paviršių. — Nerūkyti. HU Hőtől/szikrától/nyílt lángtól/…/forró felületektől távol tartandó. Tilos a dohányzás. MT Żomm ‘il bogħod mis-sħana/xrar tan-nar/fjammiet mikxufa/uċuħ jaħarqu. — Tpejjipx. NL Verwijderd houden van warmte/vonken/open vuur/hete oppervlakken. — Niet roken. PL Przechowywać z dala od źródeł ciepła/iskrzenia/otwartego ognia/gorących powierzchni. Palenie wzbronione. PT Manter afastado do calor/faísca/chama aberta/superfícies quentes. — Não fumar. RO A se păstra departe de surse de căldură/scântei/flăcări deschise/suprafețe încinse. — Fumatul interzis. SK Uchovávajte mimo dosahu tepla/iskier/otvoreného ohňa/horúcich povrchov. Nefajčite. SL Hraniti ločeno od vročine/isker/odprtega ognja/vročih površin. — Kajenje prepovedano. FI Suojaa lämmöltä/kipinöiltä/avotulelta/kuumilta pinnoilta. — Tupakointi kielletty. SV Får inte utsättas för värme/gnistor/öppen låga/heta ytor. — Rökning förbjuden. P210 Language BG Да се пази от топлина, нагорещени повърхности, искри, открит пламък, и други източници на запалване. Тютюнопушенето забранено. ES Mantener alejado del calor, de superficies calientes, de chispas, de llamas abiertas y de cualquier otra fuente de ignición. No fumar. CS Chraňte před teplem, horkými povrchy, jiskrami, otevřeným ohněm a jinými zdroji zapálení. Zákaz kouření. DA Holdes væk fra varme, varme overflader, gnister, åben ild og andre antændelseskilder. Rygning forbudt. DE Von Hitze, heißen Oberflächen, Funken, offenen Flammen sowie anderen Zündquellenarten fernhalten. Nicht rauchen. ET Hoida eemal soojusallikast, kuumadest pindadest, sädemetest, leekidest ja muudest süüteallikatest. Mitte suitsetada. EL Μακριά από θερμότητα, θερμές επιφάνειες, σπινθήρες, γυμνές φλόγες και άλλες πηγές ανάφλεξης. Μην καπνίζετε. EN Keep away from heat, hot surfaces, sparks, open flames and other ignition sources. No smoking. FR Tenir à l’écart de la chaleur, des surfaces chaudes, des étincelles, des flammes nues et de toute autre source d’inflammation. Ne pas fumer. GA Coimeád ó theas, dromchlaí te, splancacha, lasair gan chosaint agus foinsí eile adhainte. Ná caitear tobac. HR Čuvati odvojeno od topline, vrućih površina, iskri, otvorenih plamena i ostalih izvora paljenja. Ne pušiti. IT Tenere lontano da fonti di calore, superfici calde, scintille, fiamme libere o altre fonti di accensione. Non fumare. LV Sargāt no karstuma, karstām virsmām, dzirkstelēm, atklātas uguns un citiem aizdegšanās avotiem. Nesmēķēt. LT Laikyti atokiau nuo šilumos šaltinių, karštų paviršių, žiežirbų, atviros liepsnos arba kitų degimo šaltinių. Nerūkyti. HU Hőtől, forró felületektől, szikrától, nyílt lángtól és más gyújtóforrástól távol tartandó. Tilos a dohányzás. MT Biegħed mis-sħana, uċuħ jaħarqu, xrar tan-nar, fjammi miftuħa u sorsi oħra li jaqbdu. Tpejjipx. NL Verwijderd houden van warmte, hete oppervlakken, vonken, open vuur en andere ontstekingsbronnen. Niet roken. PL Przechowywać z dala od źródeł ciepła, gorących powierzchni, źródeł iskrzenia, otwartego ognia i innych źródeł zapłonu. Nie palić. PT Manter afastado do calor, superfícies quentes, faísca, chama aberta e outras fontes de ignição. Não fumar. RO A se păstra departe de surse de căldură, suprafețe fierbinți, scântei, flăcări și alte surse de aprindere. Fumatul interzis. SK Uchovávajte mimo dosahu tepla, horúcich povrchov, iskier, otvoreného ohňa a iných zdrojov zapálenia. Nefajčite. SL Hraniti ločeno od vročine, vročih površin, isker, odprtega ognja in drugih virov vžiga. Kajenje prepovedano. FI Suojaa lämmöltä, kuumilta pinnoilta, kipinöiltä, avotulelta ja muilta sytytyslähteiltä. Tupakointi kielletty. SV Får inte utsättas för värme, heta ytor, gnistor, öppen låga eller andra antändningskällor. Rökning förbjuden. P211 Language BG Да не се пръска към открит пламък или друг източник на запалване. ES No pulverizar sobre una llama abierta u otra fuente de ignición. CS Nestříkejte do otevřeného ohně nebo jiných zdrojů zapálení. … 90 unchanged lines … SL Preprečiti stik z zrakom. FI Ei saa joutua kosketuksiin ilman kanssa. SV Undvik kontakt med luft. P223 Language BG Да се избягва всякакъв възможен контакт с вода поради бурна реакция и възможно внезапно запалване. ES Mantener alejado de cualquier posible contacto con el agua, pues reacciona violentamente y puede provocar una llamarada. CS Chraňte před možným stykem s vodou kvůli prudké reakci a možnému náhlému vzplanutí. DA Undgå enhver kontakt med vand, da dette kan fremkalde voldsom reaktion og risiko for eksplosionsagtig brand. DE Kontakt mit Wasser wegen heftiger Reaktion und möglichem Aufflammen unbedingt verhindern. ET Hoida igasuguse kokkupuute eest veega, vastasel juhul reageerib ägedalt ja võib põhjustada hetkpõlemise. EL Αποφύγετε κάθε πιθανή επαφή με το νερό, διότι αντιδρά βίαια και μπορεί να προκληθεί ανάφλεξη. EN Keep away from any possible contact with water, because of violent reaction and possible flash fire. FR Éviter tout contact avec l’eau, à cause du risque de réaction violente et d’inflammation spontanée. GA Ná ceadaigh teagmháil de shaghas ar bith le huisce, mar gheall ar imoibriú foirtil agus splancthine a d’fhéadfadh a bheith ann. HR Spriječiti svaki dodir s vodom zbog burne reakcije i mogućeg zapaljenja. IT Evitare qualsiasi contatto con l’acqua: pericolo di reazione violenta e di infiammazione spontanea. LV Nepieļaut kontaktu ar ūdeni īpaši stipras reakcijas un iespējamas eksplozijas dēļ. LT Saugoti nuo bet kokio galimo kontakto su vandeniu, nes smarkiai reaguoja ir gali susidaryti ugnies pliūpsnis. HU Vízzel semmilyen formában nem érintkezhet, ellenkező esetben heves reakció és belobbanás fordulhat elő. MT Żomm ‘il bogħod minn kull kuntatt possibbli ma' l-ilma, minħabba li jirreaġġixxi bil-qawwa u jista’ jkun hemm fjamma nar. NL Contact met water vermijden in verband met een heftige reactie en een mogelijke wolkbrand. PL Chronić przed wszelkim kontaktem z wodą z powodu gwałtownej reakcji i możliwości wystąpienia błyskawicznego pożaru. PT Não deixar entrar em contacto com a água: risco de reacção violenta e possibilidade de formação de chama súbita. RO A se evita orice contact cu apa, din cauza reacției violente și a riscului de aprindere spontană. SK Zabráňte akémukoľvek kontaktu s vodou, aby nedošlo k prudkej reakcii a prípadnému zapáleniu. SL Hraniti ločeno od možnega stika z vodo zaradi burne reakcije in možnega bliskovitega požara. FI Ei saa joutua kosketuksiin veden kanssa voimakkaan reaktion ja mahdollisen leimahduksen takia. SV Undvik all kontakt med vatten eftersom det kan framkalla en våldsam reaktion och explosionsartad brand. P223 Language BG Не допускайте контакт с вода. ES Evitar el contacto con el agua. CS Zabraňte styku s vodou. DA Undgå kontakt med vand. DE Keinen Kontakt mit Wasser zulassen. ET Vältida kokkupuudet veega. EL Μην επιτρέπετε την επαφή με το νερό. EN Do not allow contact with water. FR Éviter tout contact avec l’eau. GA Ná bíodh aon teagmháil le huisce. HR Spriječiti dodir s vodom. IT Evitare qualunque contatto con l’acqua. LV Nepieļaut saskari ar ūdeni. LT Saugoti nuo sąlyčio su vandeniu. HU Nem érintkezhet vízzel. MT Tħallihx imiss mal-ilma. NL Contact met water vermijden. PL Nie dopuszczać do kontaktu z wodą. PT Não deixar entrar em contacto com a água. RO A nu se lăsa în contact cu apa. SK Zabráňte kontaktu s vodou. SL Preprečiti stik z vodo. FI Ei saa joutua kosketuksiin veden kanssa. SV Undvik all kontakt med vatten. P230 Language BG Да се държи навлажнен с… ES Mantener humedecido con… CS Uchovávejte ve zvlhčeném stavu… … 234 unchanged lines … SL Preprečiti statično naelektrenje. FI Estä staattisen sähkön aiheuttama kipinöinti. SV Vidta åtgärder mot statisk elektricitet. P244 Language BG Почиствайте редуциращите вентили от смазка и масло ES Mantener las válvulas de reducción limpias de grasa y aceite. CS Udržujte redukční ventily bez maziva a oleje. DA Reduktionsventilerne holdes fri for fedt og olie. DE Druckminderer frei von Fett und Öl halten. ET Hoida reduktsiooniklapid rasvast ja õlist puhtad. EL Να διατηρούνται καθαρές από γράσα και λάδια οι βαλβίδες μείωσης. EN Keep reduction valves free from grease and oil. FR S’assurer de l’absence de graisse ou d’huile sur les soupapes de réduction. GA Coimeád comhlaí brúlaghdaithe saor ó ghréisc agus ó ola. HR Spriječiti dodir redukcijskih ventila s masti i uljem. IT Mantenere le valvole di riduzione libere da grasso e olio. LV Turēt reducēšanās vārstus tīrus no taukiem un eļļas. LT Saugoti, kad ant redukcinių vožtuvų nepatektų riebalų ir tepalų. HU A nyomáscsökkentő szelepeket zsírtól és olajtól mentesen kell tartani. MT Żomm il-valvs ta' tnaqqis ħielsa mill-griż u ż-żejt. NL Reduceerventielen vrij van olie en vet houden. PL Chronić zawory redukcyjne przed tłuszczem i olejem. PT Manter as válvulas de redução isentas de óleo e massa lubrificantes. RO Protejați supapele reductoare de grăsimi și ulei. SK Redukčné ventily udržiavajte bez mazadiel a oleja. SL Preprečiti stik reducirnih ventilov z mastjo in oljem. FI Pidä paineenalennusventtiilit vapaana rasvasta ja öljystä. SV Reducerventilerna ska hållas fria från fett och olja. P244 Language BG Поддържайте вентилите и фитингите чисти от масло и смазка. ES Mantener las valvulas y los racores libres de aceite y grasa. CS Udržujte ventily i příslušenství čisté — bez olejů a maziv. DA Hold ventiler og tilslutninger frie for olie og fedt. DE Ventile und Ausrüstungsteile öl- und fettfrei halten. ET Hoida ventiilid ja liitmikud õlist ja rasvast puhtad. EL Διατηρείτε τα κλείστρα και τους συνδέσμους καθαρά από λάδια και γράσα. EN Keep valves and fittings free from oil and grease. FR Ni huile, ni graisse sur les robinets et raccords. GA Coinnigh comhlaí agus feistis saor ó ola agus ó ghréisc. HR Spriječiti dodir ventila i spojnica s uljem i masti. IT Mantenere le valvole e i raccordi liberi da olio e grasso. LV Uzturēt ventiļus un savienojumus tīrus no eļļas un taukvielām. LT Saugoti, kad ant vožtuvų ir jungiamųjų detalių nepatektų alyvos ir tepalų. HU A szelepeket és szerelvényeket zsírtól és olajtól mentesen kell tartani. MT Żomm il-valvi u fittings ħielsa miż-żejt u l-grease. NL Houd afsluiters en fittingen vrij van olie en vet. PL Chronić zawory i przyłącza przed olejem i tłuszczem. PT Manter válvulas e conexões isentas de óleo e gordura. RO Feriți valvele și racordurile de ulei și grăsime. SK Udržujte ventily a príslušenstvo čisté, bez olejov a mazív. SL Preprečiti stik ventilov in opreme z oljem in mastjo. FI Pidä venttiilit ja liittimet vapaana öljystä ja rasvasta. SV Håll ventiler och anslutningar fria från olja och fett. P250 Language BG Да не се подлага на стържене/удар/…/триене ES Evitar la abrasión/el choque/…/la fricción. CS Nevystavujte obrušování/nárazům/…/tření. … 18 unchanged lines … SL Ne izpostavljati drgnjenju/udarcem/…/trenju. FI Suojele rasitukselta/iskuilta/…/hankaukselta. SV Får inte utsättas för gnidning/stötar/…/friktion. P251 Language BG Съд под налягане: да не се пробива и изгаря дори след употреба. ES Recipiente a presión: no perforar ni quemar, aun después del uso. CS Tlakový obal: nepropichujte nebo nespalujte ani po použití. DA Beholder under tryk: Må ikke punkteres eller brændes, heller ikke efter brug. DE Behälter steht unter Druck: Nicht durchstechen oder verbrennen, auch nicht nach der Verwendung. ET Mahuti on rõhu all: mitte purustada ega põletada isegi pärast kasutamist. EL Περιέκτης υπό πίεση. Να μην τρυπηθεί ή καεί ακόμη και μετά τη χρήση. EN Pressurized container: Do not pierce or burn, even after use. FR Récipient sous pression: ne pas perforer, ni brûler, même après usage. GA Coimeádán brúchóirithe: Ná toll agus ná dóigh, fiú tar éis úsáide. HR Posuda je pod tlakom: ne bušiti, niti paliti čak niti nakon uporabe. IT Recipiente sotto pressione: non perforare né bruciare, neppure dopo l’uso. LV Tvertne zem spiediena: nedurt vai nededzināt, arī pēc izlietošanas. LT Slėginis indas. Nepradurti ir nedeginti net panaudoto. HU Nyomás alatti edény: ne lyukassza ki vagy égesse el, még használat után sem. MT Kontenitur taħt pressjoni: Ittaqqbux jew taħarqux, anki wara li tużah. NL Houder onder druk: ook na gebruik niet doorboren of verbranden. PL Pojemnik pod ciśnieniem. Nie przekłuwać ani nie spalać, nawet po zużyciu. PT Recipiente sob pressão. Não furar nem queimar, mesmo após utilização. RO Recipient sub presiune. Nu perforați sau ardeți, chiar și după utilizare. SK Nádoba je pod tlakom: neprepichujte alebo nespaľujte ju, a to ani po spotrebovaní obsahu. SL Posoda je pod tlakom: ne preluknjajte ali sežigajte je niti, ko je prazna. FI Painesäiliö: Ei saa puhkaista tai polttaa edes tyhjänä. SV Tryckbehållare: Får inte punkteras eller brännas, gäller även tömd behållare. P251 Language BG Да не се пробива и изгаря дори след употреба. ES No perforar ni quemar, incluso después de su uso. CS Nepropichujte nebo nespalujte ani po použití. DA Må ikke punkteres eller brændes, heller ikke efter brug. DE Nicht durchstechen oder verbrennen, auch nicht nach Gebrauch. ET Mitte purustada ega põletada isegi pärast kasutamist. EL Να μην τρυπηθεί ή καεί ακόμη και μετά τη χρήση. EN Do not pierce or burn, even after use. FR Ne pas perforer, ni brûler, même après usage. GA Ná toll agus ná dóigh, fiú tar éis úsáide. HR Ne bušiti, niti paliti čak niti nakon uporabe. IT Non perforare né bruciare, neppure dopo l’uso. LV Nedurt vai nededzināt, arī pēc izlietošanas. LT Nepradurti ir nedeginti net panaudoto. HU Ne lyukassza ki vagy égesse el, még használat után sem. MT Ittaqqbux u taħarqux, anki wara li tużah. NL Ook na gebruik niet doorboren of verbranden. PL Nie przekłuwać ani nie spalać, nawet po zużyciu. PT Não furar nem queimar, mesmo após utilização. RO Nu perforați sau ardeți, chiar și după utilizare. SK Neprepichujte alebo nespaľujte ju, a to ani po spotrebovaní obsahu. SL Ne preluknjajte ali sežigajte je niti, ko je prazna. FI Ei saa puhkaista tai polttaa edes tyhjänä. SV Får inte punkteras eller brännas, gäller även tömd behållare. P260 Language BG Не вдишвайте прах/пушек/газ/дим/изпарения/аерозоли ES No respirar el polvo/el humo/el gas/la niebla/los vapores/el aerosol. CS Nevdechujte prach/dým/plyn/mlhu/páry/aerosoly. … 306 unchanged lines … SL Nositi negorljiva oblačila in oblačila, odporna proti ognju. FI Käytä palosuojattua/paloturvallista vaatetusta. SV Använd brand-/flamsäkra eller brand-/flamhämmande kläder. P284 Language BG Носете респираторни предпазни средства. ES Llevar equipo de protección respiratoria. CS Používejte vybavení pro ochranu dýchacích cest. DA Anvend åndedrætsværn. DE Atemschutz tragen. ET Kanda hingamisteede kaitsevahendeid. EL Φοράτε μέσα ατομικής προστασίας της αναπνοής. EN Wear respiratory protection. FR Porter un équipement de protection respiratoire. GA Caith cosaint riospráide. HR Nositi sredstva za zaštitu dišnog sustava. IT Utilizzare un apparecchio respiratorio. LV Izmantot gāzmasku. LT Naudoti kvėpavimo takų apsaugos priemones. HU Légzésvédelem használata kötelező. MT Ilbes protezzjoni respiratorja. NL Adembescherming dragen. PL Stosować indywidualne środki ochrony dróg oddechowych. PT Usar protecção respiratória. RO Purtați echipament de protecție respiratorie. SK Používajte ochranu dýchacích ciest. SL Nositi opremo za zaščito dihal. FI Käytä hengityksensuojainta. SV Använd andningsskydd. P284 Language BG [При недостатъчна вентилация] носете средства за защита на дихателните пътища. ES [En caso de ventilación insuficiente,] llevar equipo de protección respiratoria. CS [V případě nedostatečného větrání] používejte vybavení pro ochranu dýchacích cest. DA [I tilfælde af utilstrækkelig ventilation], anvend åndedrætsværn. DE [Bei unzureichender Belüftung] Atemschutz tragen. ET [Ebapiisava ventilatsiooni korral] kanda hingamisteede kaitsevahendit. EL [Σε περίπτωση ανεπαρκούς αερισμού] χρησιμοποιείστε μέσα ατομικής προστασίας της αναπνοής. EN [In case of inadequate ventilation] wear respiratory protection. FR [Lorsque la ventilation du local est insuffisante] porter un équipement de protection respiratoire. GA [Mura leor an aeráil] caith cosaint riospráide. HR [U slučaju nedovoljne ventilacije] nositi sredstva za zaštitu dišnog sustava. IT [Quando la ventilazione del locale è insufficiente] indossare un apparecchio di protezione respiratoria. LV [Neatbilstošas ventilācijas gadījumā] lietot elpošanas orgānu aizsargierīces. LT [Esant nepakankamam vėdinimui] naudoti kvėpavimo takų apsaugos priemones. HU [Nem megfelelő szellőzés esetén] légzésvédelem kötelező. MT [F’każ ta’ ventilazzjoni inadegwata] ilbes protezzjoni respiratorja. NL [Bij ontoereikende ventilatie] adembescherming dragen. PL [W przypadku nieodpowiedniej wentylacji] stosować indywidualne środki ochrony dróg oddechowych. PT [Em caso de ventilação inadequada] usar proteção respiratória. RO [În cazul în care ventilarea este necorespunzătoare] purtați echipament de protecție respiratorie. SK [V prípade nedostatočného vetrania] používajte ochranu dýchacích ciest. SL [Ob nezadostnem prezračevanju] nositi opremo za zaščito dihal. FI Käytä hengityksensuojainta [jos ilmanvaihto on riittämätön]. SV [Vid otillräcklig ventilation], använd andningsskydd. P285 Language BG В случай на лоша вентилация носете респираторни предпазни средства. ES En caso de ventilación insuficiente, llevar equipo de protección respiratoria. CS V případě nedostatečného větrání používejte vybavení pro ochranu dýchacích cest. … 284 unchanged lines … SL PRI izpostavljenosti ali slabem počutju: FI Altistumisen tapahduttua tai jos ilmenee pahoinvointia: SV Vid exponering eller obehag: P310 Language BG Незабавно се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES Llamar inmediatamente a un CENTRO DE INFORMACION TOXICOLOGICA o a un médico. CS Okamžitě volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA Ring omgående til en GIFTINFORMATION eller en læge. DE Sofort GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET Võtta viivitamata ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL Καλέστε αμέσως το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό. EN Immediately call a POISON CENTER or doctor/physician. FR Appeler immédiatement un CENTRE ANTIPOISON ou un médecin. GA Cuir glao láithreach ar IONAD NIMHE nó ar dhoctúir/lia. HR Odmah nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT Contattare immediatamente un CENTRO ANTIVELENI o un medico. LV Nekavējoties sazinieties ar SAINDĒŠANĀS CENTRU vai ārstu. LT Nedelsiant skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU Azonnal forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib. NL Onmiddellijk een ANTIGIFCENTRUM of een arts raadplegen. PL Natychmiast skontaktować się z OŚRODKIEM ZATRUĆ lub lekarzem. PT Contacte imediatamente um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO Sunați imediat la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic. SK Okamžite volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL Takoj pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI Ota välittömästi yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin. SV Kontakta genast GIFTINFORMATIONSCENTRAL eller läkare. P311 Language BG Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES Llamar a un CENTRO DE INFORMACION TOXICOLOGICA o a un médico. CS Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA Ring til en GIFTINFORMATION eller en læge. DE GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET Võtta ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό. EN Call a POISON CENTER or doctor/physician. FR Appeler un CENTRE ANTIPOISON ou un médecin. GA Cuir glao ar IONAD NIMHE nó ar dhoctúir/lia. HR Nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT Contattare un CENTRO ANTIVELENI o un medico. LV Sazinieties ar SAINDĒŠANĀS CENTRU vai ārstu. LT Skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU Forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib. NL Een ANTIGIFCENTRUM of een arts raadplegen. PL Skontaktować się z OŚRODKIEM ZATRUĆ lub lekarzem. PT Contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO Sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic. SK Volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL Pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI Ota yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin. SV Kontakta GIFTINFORMATIONSCENTRAL eller läkare. P312 Language BG При неразположение се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES Llamar a un CENTRO DE INFORMACION TOXICOLOGICA o a un médico en caso de malestar. CS Necítíte-li se dobře, volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA I tilfælde af ubehag ring til en GIFTINFORMATION eller en læge. DE Bei Unwohlsein GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET Halva enesetunde korral võtta ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό εάν αισθανθείτε αδιαθεσία. EN Call a POISON CENTER or doctor/physician if you feel unwell. FR Appeler un CENTRE ANTIPOISON ou un médecin en cas de malaise. GA Cuir glao ar IONAD NIMHE nó ar dhoctúir/lia má bhraitheann tú tinn. HR U slučaju zdravstvenih tegoba nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT In caso di malessere, contattare un CENTRO ANTIVELENI o un medico. LV Sazinieties ar SAINDĒŠANĀS CENTRU vai ārstu, ja jums ir slikta pašsajūta. LT Pasijutus blogai, skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU Rosszullét esetén forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib jekk tħossok ma tiflaħx. NL Bij onwel voelen een ANTIGIFCENTRUM of een arts raadplegen. PL W przypadku złego samopoczucia skontaktować się z OŚRODKIEM ZATRUĆ lub z lekarzem. PT Caso sinta indisposição, contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO Sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic, dacă nu vă simțiți bine. SK Pri zdravotných problémoch, volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL Ob slabem počutju pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI Ota yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin, jos ilmenee pahoinvointia. SV Vid obehag, kontakta GIFTINFORMATIONSCENTRAL eller läkare. P310 Language BG Незабавно се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES Llamar inmediatamente a un CENTRO DE TOXICOLOGĺA/médico/… CS Okamžitě volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/… DA Ring omgående til en GIFTINFORMATION/læge/… DE Sofort GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET Võtta viivitamata ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL Καλέστε αμέσως το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/… EN Immediately call a POISON CENTER/doctor/… FR Appeler immédiatement un CENTRE ANTIPOISON/un médecin/… GA Cuir glao láithreach ar IONAD NIMHE/ar dhoctúir/… HR Odmah nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT Contattare immediatamente un CENTRO ANTIVELENI/un medico… LV Nekavējoties sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/… LT Nedelsiant skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/…. HU Azonnal forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT Sejjaħ minnufih ĊENTRU TAL-AVVELENAMENT/tabib/… NL Onmiddellijk een ANTIGIFCENTRUM/arts/… raadplegen. PL Natychmiast skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT Contacte imediatamente um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO Sunați imediat la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/… SK Okamžite volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL Takoj pokličite CENTER ZA ZASTRUPITVE/zdravnika/… FI Ota välittömästi yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/… SV Kontakta genast GIFTINFORMATIONSCENTRALEN/läkare… P311 Language BG Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES Llamar a un CENTRO DE TOXICOLOGĺA/médico/… CS Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/…. DA Ring til en GIFTINFORMATION/læge/… DE GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET Võtta ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/… EN Call a POISON CENTER/doctor/… FR Appeler un CENTRE ANTIPOISON/un médecin/… GA Cuir glao ar IONAD NIMHE/ar dhoctúir/… HR Nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT Contattare un CENTRO ANTIVELENI/un medico/… LV Sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/… LT Skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/…. HU Forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT Sejjaħ ĊENTRU TAL-AVVELENAMENT/tabib/… NL Een ANTIGIFCENTRUM/arts/… raadplegen. PL Skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT Contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO Sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic… SK Volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL Pokličite CENTER ZA ZASTRUPITVE/zdravnika/… FI Ota yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/… SV Kontakta GIFTINFORMATIONSCENTRALEN/läkare/… P312 Language BG При неразположение се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/…/. ES Llamar a un CENTRO DE TOXICOLOGĺA/médico/…/si la persona se encuentra mal. CS Necítíte-li se dobře, volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/… DA I tilfælde af ubehag, ring til en GIFTINFORMATION/læge/… DE Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET Halva enesetunde korral võtta ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/…εάν αισθανθείτε αδιαθεσία. EN Call a POISON CENTER/doctor/…/if you feel unwell. FR Appeler un CENTRE ANTIPOISON/un médecin/…/en cas de malaise. GA Cuir glao ar IONAD NIMHE/ar dhoctúir/…mura mbraitheann tú go maith. HR U slučaju zdravstvenih tegoba nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT Contattare un CENTRO ANTIVELENI/un medico/…./in caso di malessere. LV Sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/.., ja jums ir slikta pašsajūta. LT Pasijutus blogai, skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/…. HU Rosszullét esetén forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT Sejjaħ ĊENTRU TAL-AVVELENAMENT/tabib/…/jekk ma tħossokx f’sikktek. NL Bij onwel voelen een ANTIGIFCENTRUM/arts/… raadplegen. PL W przypadku złego samopoczucia skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT Caso sinta indisposição, contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO Sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/…/dacă nu vă simțiți bine. SK Pri zdravotných problémoch volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL Ob slabem počutju pokličite CENTER ZA ZASTRUPITVE/zdravnika/…/ FI Ota yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/…/jos ilmenee pahoinvointia. SV Vid obehag, kontakta GIFTINFORMATIONSCENTRALEN/läkare/… P313 Language BG Потърсете медицински съвет/помощ. ES Consultar a un médico. CS Vyhledejte lékařskou pomoc/ošetření. … 354 unchanged lines … SL Odstranite kontaktne leče, če jih imate in če to lahko storite brez težav. Nadaljujte z izpiranjem. FI Poista piilolinssit, jos sen voi tehdä helposti. Jatka huuhtomista. SV Ta ur eventuella kontaktlinser om det går lätt. Fortsätt att skölja. P340 Language BG Изведете пострадалия на чист въздух и го поставете в позиция, улесняваща дишането. ES Transportar a la víctima al exterior y mantenerla en reposo en una posición confortable para respirar. CS Přeneste postiženého na čerstvý vzduch a ponechte jej v klidu v poloze usnadňující dýchání. DA Flyt personen til et sted med frisk luft og sørg for, at vedkommende hviler i en stilling, som letter vejrtrækningen. DE Die betroffene Person an die frische Luft bringen und in einer Position ruhigstellen, die das Atmen erleichtert. ET Toimetada kannatanu värske õhu kätte ja asetada mugavasse puhkeasendisse, mis võimaldab kergesti hingata. P340 Language BG Изведете лицето на чист въздух и го поставете в позиция, улесняваща дишането. ES Transportar a la persona al aire libre y mantenerla en una posición que le facilite la respiración. CS Přeneste osobu na čerstvý vzduch a ponechte ji v poloze usnadňující dýchání. DA Flyt personen til et sted med frisk luft og sørg for, at vejrtrækningen lettes. DE Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen. ET Toimetada isik värske õhu kätte ja hoida asendis, mis võimaldab kergesti hingata. EL Μεταφέρετε τον παθόντα στον καθαρό αέρα και αφήστε τον να ξεκουραστεί σε στάση που διευκολύνει την αναπνοή. EN Remove victim to fresh air and keep at rest in a position comfortable for breathing. FR Transporter la victime à l'extérieur et la maintenir au repos dans une position où elle peut confortablement respirer. GA Tabhair amach faoin aer an duine agus coimeád socair é, i riocht ina bhféadfaidh sé anáil a tharraingt go réidh. HR Premjestiti unesrećenog na svježi zrak, umiriti ga i postaviti u položaj koji olakšava disanje. IT Trasportare l'infortunato all’aria aperta e mantenerlo a riposo in posizione che favorisca la respirazione. LV Izvest cietušo svaigā gaisā un turēt miera stāvoklī, lai būtu ērti elpot. LT Išnešti nukentėjusįjį į gryną orą; jam būtina ramybė ir padėtis, leidžianti laisvai kvėpuoti. HU Az érintett személyt friss levegőre kell vinni és olyan nyugalmi testhelyzetbe kell helyezni, hogy könnyen tudjon lélegezni. MT Esponi lill-vittma għall-arja friska u żommha mistrieħa f’pożizzjoni komda biex tkun tista’ tieħu n-nifs. NL Het slachtoffer in de frisse lucht brengen en laten rusten in een houding die het ademen vergemakkelijkt. PL Wyprowadzić lub wynieść poszkodowanego na świeże powietrze i zapewnić warunki do odpoczynku w pozycji umożliwiającej swobodne oddychanie. PT Retirar a vítima para uma zona ao ar livre e mantê-la em repouso numa posição que não dificulte a respiração. RO Transportați victima la aer liber și mențineți-o în stare de repaus într-o poziție confortabilă pentru respirație. SK Presuňte postihnutého na čerstvý vzduch a nechajte ho oddychovať v polohe, ktorá mu umožní pohodlné dýchanie. SL Prenesti žrtev na svež zrak in jo pustiti počivati v položaju, ki olajša dihanje. FI Siirrä henkilö raittiiseen ilmaan ja pidä lepoasennossa, jossa on helppo hengittää. SV Flytta personen till frisk luft och se till att han eller hon vilar i en ställning som underlättar andningen EN Remove person to fresh air and keep comfortable for breathing. FR Transporter la personne à l’extérieur et la maintenir dans une position où elle peut confortablement respirer. GA Tabhair an duine amach faoin aer úr agus coinnigh é i riocht ina bhféadfadh sé anáil a tharraingt go réidh. HR Premjestiti osobu na svježi zrak i postaviti ju u položaj koji olakšava disanje. IT Trasportare l’infortunato all’aria aperta e mantenerlo a riposo in posizione che favorisca la respirazione. LV Nogādāt cietušo svaigā gaisā un nodrošināt netraucētu elpošanu. LT Išnešti nukentėjusįjį į gryną orą; jam būtina patogi padėtis, leidžianti laisvai kvėpuoti. HU Az érintett személyt friss levegőre kell vinni, és olyan nyugalmi testhelyzetbe kell helyezni, hogy könnyen tudjon lélegezni. MT Qiegħed lill-persuna għall-arja friska f’pożizzjoni komda biex tieħu n-nifs. NL De persoon in de frisse lucht brengen en ervoor zorgen dat deze gemakkelijk kan ademen. PL Wyprowadzić lub wynieść poszkodowanego na świeże powietrze i zapewnić mu warunki do swobodnego oddychania. PT Retirar a pessoa para uma zona ao ar livre e mantê-la numa posição que não dificulte a respiração. RO Transportați persoana la aer liber și mențineți-o într-o poziție confortabilă pentru respirație. SK Presuňte osobu na čerstvý vzduch a umožnite jej pohodlne dýchať. SL Prenesti osebo na svež zrak in jo pustiti v udobnem položaju, ki olajša dihanje. FI Siirrä henkilö raittiiseen ilmaan ja varmista vaivaton hengitys. SV Flytta personen till frisk luft och se till att andningen underlättas. P341 Language BG При затруднено дишане изведете пострадалия на чист въздух и го поставете в позиция, улесняваща дишането. ES Si respira con dificultad, transportar a la víctima al exterior y mantenerla en reposo en una posición confortable para respirar. CS Při obtížném dýchání přeneste postiženého na čerstvý vzduch a ponechte jej v klidu v poloze usnadňující dýchání. … 90 unchanged lines … SL Previdno izpirati z vodo nekaj minut. FI Huuhdo huolellisesti vedellä usean minuutin ajan. SV Skölj försiktigt med vatten i flera minuter. P352 Language BG Измийте обилно със сапун и вода. ES Lavar con agua y jabón abundantes. CS Omyjte velkým množstvím vody a mýdla. DA Vask med rigeligt sæbe og vand. DE Mit viel Wasser und Seife waschen. ET Pesta rohke vee ja seebiga. EL Πλύνετε με άφθονο σαπούνι και νερό. EN Wash with plenty of soap and water. FR Laver abondamment à l’eau et au savon. GA Nigh le neart gallúnaí agus uisce. HR Oprati velikom količinom sapuna i vode. IT Lavare abbondantemente con acqua e sapone. LV Mazgāt ar lielu daudzmu ziepēm un ūdeni. LT Plauti dideliu kiekiu muilo ir vandens. HU Lemosás bő szappanos vízzel. MT Aħsel b’ħafna sapun u ilma. NL Met veel water en zeep wassen. PL Umyć dużą ilością wody z mydłem. PT Lavar com sabonete e água abundantes. RO Spălați cu multă apă și săpun. SK Umyte veľkým množstvom vody a mydla. SL Umiti z veliko mila in vode. FI Pese runsaalla vedellä ja saippualla. SV Tvätta med mycket tvål och vatten. P352 Language BG Измийте обилно с вода/… ES Lavar con abundante agua/… CS Omyjte velkým množstvím vody/… DA Vask med rigeligt vand/… DE Mit viel Wasser/…/waschen. ET Pesta rohke veega/… EL Πλύντε με άφθονο νερό/… EN Wash with plenty of water/… FR Laver abondamment à l’eau/… GA Nigh le neart uisce/… HR Oprati velikom količinom vode/… IT Lavare abbondantemente con acqua/… LV Nomazgāt ar lielu ūdens/.. daudzumu. LT Plauti dideliu vandens kiekiu/… HU Lemosás bő vízzel/…. MT Baħbaħ b’ħafna ilma/… NL Met veel water/… wassen. PL Umyć dużą ilością wody/… PT Lavar abundantemente com água/… RO Spălați cu multă apă/… SK Umyte veľkým množstvom vody/… SL Umiti z veliko vode/… FI Pese runsaalla vedellä/… SV Tvätta med mycket vatten/… P353 Language BG Облейте кожата с вода/вземете душ. ES Aclararse la piel con agua/ducharse. CS Opláchněte kůži vodou/osprchujte. … 43 unchanged lines … FI Huuhdo saastunut vaatetus ja iho välittömästi runsaalla vedellä ennen vaatetuksen riisumista. SV Skölj genast nedstänkta kläder och hud med mycket vatten innan du tar av dig kläderna. P361 Language BG Незабавно свалете цялото замърсено облекло. ES Quitarse inmediatamente las prendas contaminadas. ES Quitar inmediatamente todas las prendas contaminadas. CS Veškeré kontaminované části oděvu okamžitě svlékněte. DA Tilsmudset tøj tages straks af/fjernes. DA Alt tilsmudset tøj tages straks af. DE Alle kontaminierten Kleidungsstücke sofort ausziehen. ET Kõik saastunud rõivad viivitamata seljast võtta. EL Αφαιρέστε/Βγάλτε αμέσως όλα τα μολυσμένα ρούχα. EN Remove/Take off immediately all contaminated clothing. FR Enlever immédiatement les vêtements contaminés. ET Võtta viivitamata seljast kõik saastunud rõivad. EL Βγάλτε αμέσως όλα τα μολυσμένα ρούχα. EN Take off immediately all contaminated clothing. FR Enlever immédiatement tous les vêtements contaminés. GA Bain díot láithreach na héadaí éillithe go léir. HR Odmah ukloniti/skinuti svu zagađenu odjeću. IT Togliersi di dosso immediatamente tutti gli indumenti contaminati. LV Noņemt/Novilkt nekavējoties visu piesārņoto apģērbu. LT Nedelsiant nuvilkti/pašalinti visus užterštus drabužius. HU Az összes szennyezett ruhadarabot azonnal el kell távolítani/le kell vetni. MT Neħħi/Inża’ mall-ewwel l-ilbies ikkontaminat. HR Odmah skinuti svu zagađenu odjeću. IT Togliere immediatamente tutti gli indumenti contaminati. LV Novilkt nekavējoties visu piesārņoto apģērbu. LT Nedelsiant nuvilkti visus užterštus drabužius. HU Az összes szennyezett ruhadarabot azonnal le kell vetni. MT Neħħi minnufih il-ħwejjeg kontaminati kollha. NL Verontreinigde kleding onmiddellijk uittrekken. PL Natychmiast usunąć/zdjąć całą zanieczyszczoną odzież. PT Despir/retirar imediatamente toda a roupa contaminada. PL Natychmiast zdjąć całą zanieczyszczoną odzież. PT Retirar imediatamente toda a roupa contaminada. RO Scoateți imediat toată îmbrăcămintea contaminată. SK Ihneď odstráňte/vyzlečte všetky kontaminované časti odevu. SL Takoj odstraniti/sleči vsa kontaminirana oblačila. SK Všetky kontaminované časti odevu okamžite vyzlečte. SL Takoj sleči vsa kontaminirana oblačila. FI Riisu saastunut vaatetus välittömästi. SV Ta omedelbart av alla nedstänkta kläder. P362 Language BG Свалете замърсеното облекло и го изперете преди повторна употреба. ES Quitarse las prendas contaminadas y lavarlas antes de volver a usarlas. CS Kontaminovaný oděv svlékněte a před opětovným použitím ho vyperte. DA Forurenet tøj tages af og vaskes, før det bruges igen. DE Kontaminierte Kleidung ausziehen und vor erneutem Tragen waschen. ET Võtta saastunud rõivad seljast ja pesta neid enne järgmist kasutamist. EL Βγάλτε τα μολυσμένα ρούχα και πλύνετέ τα πριν τα ξαναχρησιμοποιήσετε. EN Take off contaminated clothing and wash before reuse. FR Enlever les vêtements contaminés et les laver avant réutilisation GA Bain díot láithreach na héadaí éillithe go léir agus nigh iad sula ndéanfar iad a athúsáid. HR Skinuti zagađenu odjeću i oprati prije ponovne uporabe. IT Togliersi di dosso gli indumenti contaminati e lavarli prima di indossarli nuovamente. LV Novilkt piesārņoto apģērbu un pirms atkārtotas lietošanas izmazgāt. LT Nusivilkti užterštus drabužius ir išskalbti prieš vėl juos apsivelkant. HU A szennyezett ruhát le kell vetni és az újbóli használat előtt ki kell mosni. MT Inża' l-ħwejjeġ kontaminati u aħsilhom qabel ma terġa' tużahom. NL Verontreinigde kleding uittrekken en wassen alvorens deze opnieuw te gebruiken. PL Zanieczyszczoną odzież zdjąć i wyprać przed ponownym użyciem. PT Retirar a roupa contaminada e lavá-la antes de a voltar a usar. RO Scoateți îmbrăcămintea contaminată și spălați-o înainte de reutilizare. SK Kontaminovaný odev vyzlečte a pred ďalším použitím vyperte. SL Sleči kontaminirana oblačila in jih oprati pred ponovno uporabo. FI Riisu ja pese saastunut vaatetus ennen uudelleenkäyttöä. SV Nedstänkta kläder tas av och tvättas innan de används igen. P362 Language BG Свалете замърсеното облекло. ES Quitar las prendas contaminadas. CS Kontaminovaný oděv svlékněte. DA Alt tilsmudset tøj tages af. DE Kontaminierte Kleidung ausziehen. ET Võtta saastunud rõivad seljast. EL Βγάλτε τα μολυσμένα ρούχα. EN Take off contaminated clothing. FR Enlever les vêtements contaminés. GA Bain díot aon éadaí éillithe. HR Skinuti zagađenu odjeću. IT Togliere gli indumenti contaminati. LV Novilkt piesārņoto apģērbu. LT Nuvilkti užterštus drabužius. HU A szennyezett ruhadarabot le kell vetni. MT Neħħi l-ħwejjeġ kontaminati. NL Verontreinigde kleding uittrekken. PL Zdjąć zanieczyszczoną odzież. PT Retirar a roupa contaminada. RO Scoateți îmbrăcămintea contaminată. SK Kontaminovaný odev vyzlečte. SL Sleči kontaminirana oblačila. FI Riisu saastunut vaatetus. SV Ta av nedstänkta kläder. P363 Language BG Изперете замърсеното облекло преди повторна употреба. ES Lavar las prendas contaminadas antes de volver a usarlas. CS Kontaminovaný oděv před opětovným použitím vyperte. … 18 unchanged lines … SL Kontaminirana oblačila oprati pred ponovno uporabo. FI Pese saastunut vaatetus ennen uudelleenkäyttöä. SV Nedstänkta kläder ska tvättas innan de används igen. P364 Language BG И го изперете преди повторна употреба. ES Y lavarlas antes de volver a usarlas. CS A před opětovným použitím vyperte. DA Og vaskes inden genanvendelse. DE Und vor erneutem Tragen waschen. ET Ja pesta enne korduskasutust. EL Και πλύντε τα πριν τα ξαναχρησιμοποιήσετε. EN And wash it before reuse. FR Et les laver avant réutilisation. GA Agus nigh iad sula ndéanfar iad a athúsáid. HR I oprati je prije ponovne uporabe. IT E lavarli prima di indossarli nuovamente. LV Un pirms atkārtotas lietošanas izmazgāt. LT Taip pat išskalbti prieš vėl apsivelkant. HU És újbóli használat előtt ki kell mosni. MT U aħslu qabel terġa’ tużah. NL En wassen alvorens deze opnieuw te gebruiken. PL I wyprać przed ponownym użyciem. PT E lavar antes de voltar a usar. RO Și spălați înainte de reutilizare. SK A pred ďalším použitím vyperte. SL In jih oprati pred ponovno uporabo. FI Ja pese ennen uudelleenkäyttöä. SV Och tvätta dem innan de används igen. P370 Language BG При пожар: ES En caso de incendio: CS V případě požáru: … 205 unchanged lines … Ei saa sammuttaa, jollei vuotoa voida pysäyttää turvallisesti. SV Läckande gas som brinner: Försök inte släcka branden om inte läckan kan stoppas på ett säkert sätt. P378 Language BG Използвайте … за гасене. ES Utilizar … para apagarlo. CS K hašení použijte … DA Anvend … til brandslukning. P378 Language BG Използвайте…, за да загасите. ES Utilizar… para la extinción. CS K uhašení použijte… DA Anvend…til brandslukning. DE … zum Löschen verwenden. ET Kustutamiseks kasutada … EL Χρησιμοποιήστε … για την κατάσβεση. EN Use … for extinction. FR Utiliser … pour l’extinction. ET Kustutamiseks kasutada… EL Χρησιμοποιείστε… για να κατασβήσετε. EN Use… to extinguish. FR Utiliser… pour l’extinction. GA Úsáid … le haghaidh múchta. HR Za gašenje rabiti … IT Estinguere con… LV Nodzēšanai izmantot… IT Utilizzare….per estinguere. LV Dzēšanai izmantojiet …. LT Gesinimui naudoti … HU Az oltáshoz … használandó. MT Uża’ … biex titfi. HU Oltásra …használandó. MT Uża… biex titfi. NL Blussen met … PL Użyć … do gaszenia. PT Para a extinção utilizar … RO Utilizați… pentru stingere. SK Na hasenie použite … SL Za gašenje uporabiti … FI Käytä palon sammuttamiseen … SV Släck branden med … PL Użyć… do gaszenia. PT Para extinguir utilizar…. RO A se utiliza… pentru a stinge. SK Na hasenie použite… SL Za gašenje se uporabi… FI Käytä palon sammuttamiseen… SV Släck med… P380 Language BG Евакуирайте зоната. ES Evacuar la zona. CS Vykliďte _roctor. … 90 unchanged lines … SL Prestreči razlito tekočino. FI Valumat on kerättävä. SV Samla upp spill. P301 + P310 Language BG ПРИ ПОГЛЪЩАНЕ: Незабавно се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES EN CASO DE INGESTIÓN: Llamar inmediatamente a un CENTRO DE INFORMACIÓN TOXICOLÓGICA o a un médico. CS PŘI POŽITÍ: Okamžitě volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA I TILFÆLDE AF INDTAGELSE: Ring omgående til en GIFTINFORMATION eller en læge. DE BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET ALLANEELAMISE KORRAL: võtta viivitamata ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΚΑΤΑΠΟΣΗΣ: Καλέστε αμέσως το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό. EN IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. FR EN CAS D’INGESTION: appeler immédiatement un CENTRE ANTIPOISON ou un médecin. GA MÁ SHLOGTAR: Cuir glao láithreach ar IONAD NIMHE nó ar dhoctúir/lia. HR AKO SE PROGUTA: odmah nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT IN CASO DI INGESTIONE: contattare immediatamente un CENTRO ANTIVELENI o un medico LV NORĪŠANAS GADĪJUMĀ: Nekavējoties sazināties ar SAINDĒŠANĀS CENTRU vai ārstu. LT PRARIJUS: Nedelsiant skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU LENYELÉS ESETÉN: azonnal forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT JEKK JINBELA’: Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib. NL NA INSLIKKEN: onmiddellijk een ANTIGIFCENTRUM of een arts raadplegen. PL W PRZYPADKU POŁKNIĘCIA: Natychmiast skontaktować się z OŚRODKIEM ZATRUĆ lub z lekarzem. PT EM CASO DE INGESTÃO: contacte imediatamente um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO ÎN CAZ DE ÎNGHIȚIRE: sunați imediat la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic. SK PO POŽITÍ: okamžite volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL PRI ZAUŽITJU: takoj pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI JOS KEMIKAALIA ON NIELTY: Ota välittömästi yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin. SV VID FÖRTÄRING: Kontakta genast GIFTINFORMATIONSCENTRAL eller läkare. P301 + P312 Language BG ПРИ ПОГЛЪЩАНЕ: Незабавно се обадете в ЦЕНТЪР ПО ТОСКИКОЛОГИЯ или на лекар при неразположение. ES EN CASO DE INGESTIÓN: Llamar a un CENTRO DE INFORMACIÓN TOXICOLÓGICA o a un médico si se encuentra mal. CS PŘI POŽITÍ: Necítíte-li s dobře, volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA I TILFÆLDE AF INDTAGELSE: I tilfælde af ubehag ring til en GIFTINFORMATION eller en læge. DE BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET ALLANEELAMISE KORRAL: halva enesetunde korral võtta ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΚΑΤΑΠΟΣΗΣ: Καλέστε αμέσως το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό, εάν αισθανθείτε αδιαθεσία. EN IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. FR EN CAS D’INGESTION: appeler un CENTRE ANTIPOISON ou un médecin en cas de malaise. GA MÁ SHLOGTAR: Cuir glao ar IONAD NIMHE nó ar dhoctúir/lia má bhraitheann tú tinn. HR AKO SE PROGUTA: u slučaju zdravstvenih tegoba nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT IN CASO DI INGESTIONE accompagnata da malessere: contattare un CENTRO ANTIVELENI o un medico. LV NORĪŠANAS GADĪJUMĀ: sazināties ar SAINDĒŠANĀS CENTRU vai ārstu, ja jums ir slikta pašsajūta. LT PRARIJUS: Pasijutus blogai, skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU LENYELÉS ESETÉN: rosszullét esetén azonnal forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT JEKK JINBELA’: Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib jekk tħossok ma tiflaħx. NL NA INSLIKKEN: bij onwel voelen een ANTIGIFCENTRUM of een arts raadplegen. PL W PRZYPADKU POŁKNIĘCIA: W przypadku złego samopoczucia skontaktować się z OŚRODKIEM ZATRUĆ lub z lekarzem. PT EM CASO DE INGESTÃO: caso sinta indisposição, contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO ÎN CAZ DE ÎNGHIȚIRE: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic, dacă nu vă simțiți bine. SK PO POŽITÍ: ak máte zdravotné problémy, okamžite volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL PRI ZAUŽITJU: ob slabem počutju pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI JOS KEMIKAALIA ON NIELTY: Ota yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin, jos ilmenee pahoinvointia. SV VID FÖRTÄRING: Kontakta GIFTINFORMATIONSCENTRAL eller läkare om du mår dåligt. P301 + P310 Language BG ПРИ ПОГЛЪЩАНЕ: Незабавно се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES EN CASO DE INGESTIÓN: Llamar inmediatamente a un CENTRO DE TOXICOLOGĺA/médico/… CS PŘI POŽITÍ: Okamžitě volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/…. DA I TILFÆLDE AF INDTAGELSE: Ring omgående til en GIFTINFORMATION/læge/… DE BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET ALLANEELAMISE KORRAL: võtta viivitamata ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΚΑΤΑΠΟΣΗΣ: καλέστε αμέσως το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/… EN IF SWALLOWED: Immediately call a POISON CENTER/doctor/… FR EN CAS D’INGESTION: Appeler immédiatement un CENTRE ANTIPOISON/un médecin/… GA MÁ SHLOGTAR: Cuir glao láithreach ar IONAD NIMHE/ar dhoctúir/… HR AKO SE PROGUTA: odmah nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT IN CASO DI INGESTIONE: contattare immediatamente un CENTRO ANTIVELENI/un medico/… LV NORĪŠANAS GADĪJUMĀ: Nekavējoties sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/… LT PRARIJUS: nedelsiant skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/… HU LENYELÉS ESETÉN: Azonnal forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT JEKK JINBELA’: Sejjaħ minnufih ĊENTRU TAL-AVVELENAMENT/tabib/… NL NA INSLIKKEN: onmiddellijk een ANTIGIFCENTRUM/arts/… raadplegen. PL W PRZYPADKU POŁKNIĘCIA: Natychmiast skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT EM CASO DE INGESTÃO: contacte imediatamente um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO ÎN CAZ DE ÎNGHIȚIRE: sunați imediat la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/… SK PO POŽITÍ: Okamžite volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL PRI ZAUŽITJU: Takoj pokličite CENTER ZA ZASTRUPITVE/zdravnika/… FI JOS KEMIKAALIA ON NIELTY: Ota välittömästi yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/… SV VID FÖRTÄRING: Kontakta genast GIFTINFORMATIONSCENTRALEN/läkare/… P301 + P312 Language BG ПРИ ПОГЛЪЩАНЕ: При неразположение се обадете в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES EN CASO DE INGESTIÓN: Llamar a un CENTRO DE TOXICOLOGĺA/médico/…/si la persona se encuentra mal. CS PŘI POŽITÍ: Necítíte-li se dobře, volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/… DA I TILFÆLDE AF INDTAGELSE: I tilfælde af ubehag, ring til en GIFTINFORMATION/læge/…/ DE BEI VERSCHLUCKEN: Bei Unwohlsein GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET ALLANEELAMISE KORRAL: halva enesetunde korral võtta ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΚΑΤΑΠΟΣΗΣ: Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/…/εάν αισθανθείτε αδιαθεσία. EN IF SWALLOWED: Call a POISON CENTER/doctor/…/if you feel unwell. FR EN CAS D’INGESTION: Appeler un CENTRE ANTIPOISON/un médecin/…/en cas de malaise. GA MÁ SHLOGTAR: Cuir glao ar IONAD NIMHE/ar dhoctúir/… mura mbraitheann tú go maith. HR AKO SE PROGUTA: u slučaju zdravstvenih tegoba nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT IN CASO DI INGESTIONE: contattare un CENTRO ANTIVELENI/un medico/…/in caso di malessere. LV NORĪŠANAS GADĪJUMĀ: Sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/.., ja jums ir slikta pašsajūta. LT PRARIJUS: pasijutus blogai, skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/… HU LENYELÉS ESETÉN: Rosszullét esetén forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT JEKK JINBELA’: Sejjaħ ĊENTRU TAL-AVVELENAMENT/tabib/…/jekk ma tħossokx f’sikktek. NL NA INSLIKKEN: bij onwel voelen een ANTIGIFCENTRUM/arts/… raadplegen. PL W PRZYPADKU POŁKNIĘCIA: W przypadku złego samopoczucia skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT EM CASO DE INGESTÃO: caso sinta indisposição, contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO ÎN CAZ DE ÎNGHIȚIRE: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/…/dacă nu vă simțiți bine. SK PO POŽITÍ: Pri zdravotných problémoch volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL PRI ZAUŽITJU: Ob slabem počutju pokličite CENTER ZA ZASTRUPITVE/zdravnika/…/. FI JOS KEMIKAALIA ON NIELTY: Ota yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/…/jos ilmenee pahoinvointia. SV VID FÖRTÄRING: Vid obehag, kontakta GIFTINFORMATIONSCENTRALEN/läkare/… P301 + P330 + P331 Language BG ПРИ ПОГЛЪЩАНЕ: изплакнете устата. НЕ предизвиквайте повръщане. ES EN CASO DE INGESTIÓN: Enjuagarse la boca. NO provocar el vómito. CS PŘI POŽITÍ: Vypláchněte ústa. NEVYVOLÁVEJTE zvracení. … 66 unchanged lines … SL PRI STIKU S KOŽO: nežno umiti z veliko mila in vode. FI JOS KEMIKAALIA JOUTUU IHOLLE: Pese varovasti runsaalla vedellä ja saippualla. SV VID HUDKONTAKT: Tvätta försiktigt med mycket tvål och vatten. P302 + P352 Language BG ПРИ КОНТАКТ С КОЖАТА: Измийте обилно със сапун и вода. ES EN CASO DE CONTACTO CON LA PIEL: Lavar con agua y jabón abundantes. CS PŘI STYKU S KŮŽÍ: Omyjte velkým množstvím vody a mýdla. DA VED KONTAKT MED HUDEN: Vask med rigeligt sæbe og vand. DE BEI KONTAKT MIT DER HAUT: Mit viel Wasser und Seife waschen. ET NAHALE SATTUMISE KORRAL: pesta rohke vee ja seebiga. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΠΑΦΗΣ ΜΕ ΤΟ ΔΕΡΜΑ: Πλύνετε με άφθονο νερό και σαπούνι. EN IF ON SKIN: Wash with plenty of soap and water. FR EN CAS DE CONTACT AVEC LA PEAU: laver abondamment à l’eau et au savon. GA I gCÁS TEAGMHÁLA LEIS AN gCRAICEANN: Nigh le neart gallúnaí agus uisce. HR U SLUČAJU DODIRA S KOŽOM: oprati velikom količinom sapuna i vode. IT IN CASO DI CONTATTO CON LA PELLE: lavare abbondantemente con acqua e sapone. LV SASKARĒ AR ĀDU: nomazgāt ar lielu ziepju un ūdens daudzumu. LT PATEKUS ANT ODOS: Nuplauti dideliu kiekiu muilo ir vandens. HU HA BŐRRE KERÜL: Lemosás bő szappanos vízzel. MT JEKK FUQ IL-ĠILDA: Aħsel b’ħafna sapun u ilma. NL BIJ CONTACT MET DE HUID: met veel water en zeep wassen. PL W PRZYPADKU KONTAKTU ZE SKÓRĄ: Umyć dużą ilością wody z mydłem. PT SE ENTRAR EM CONTACTO COM A PELE: lavar com sabonete e água abundantes. RO ÎN CAZ DE CONTACT CU PIELEA: spălați cu multă apă și săpun. SK PRI KONTAKTE S POKOŽKOU: Umyte veľkým množstvom vody a mydla. SL PRI STIKU S KOŽO: umiti z veliko mila in vode. FI JOS KEMIKAALIA JOUTUU IHOLLE: Pese runsaalla vedellä ja saippualla. SV VID HUDKONTAKT: Tvätta med mycket tvål och vatten. P303 + P361 + P353 Language BG ПРИ КОНТАКТ С КОЖАТА (или косата): Незабавно свалете цялото замърсено облекло. Облейте кожата с вода/вземете душ ES EN CASO DE CONTACTO CON LA PIEL (o el pelo): Quitarse inmediatamente las prendas contaminadas. Aclararse la piel con agua o ducharse. P302 + P352 Language BG ПРИ КОНТАКТ С КОЖАТА: Измийте обилно с вода/… ES EN CASO DE CONTACTO CON LA PIEL: Lavar con abundante agua/… CS PŘI STYKU S KŮŽÍ: Omyjte velkým množstvím vody/… DA VED KONTAKT MED HUDEN: Vask med rigeligt vand/… DE BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/…/waschen. ET NAHALE SATTUMISE KORRAL: pesta rohke veega/… EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΠΑΦΗΣ ΜΕ ΤΟ ΔΕΡΜΑ: Πλύντε με άφθονο νερό/… EN IF ON SKIN: Wash with plenty of water/… FR EN CAS DE CONTACT AVEC LA PEAU: Laver abondamment à l’eau/… GA I gCÁS TEAGMHÁLA LEIS AN gCRAICEANN: Nigh le neart gallúnaí agus uisce é. HR U SLUČAJU DODIRA S KOŽOM: oprati velikom količinom vode/… IT IN CASO DI CONTATTO CON LA PELLE: lavare abbondantemente con acqua/… LV SASKARĒ AR ĀDU: nomazgāt ar lielu ūdens/.. daudzumu. LT PATEKUS ANT ODOS: plauti dideliu vandens kiekiu/… HU HA BŐRRE KERÜL: Lemosás bő vízzel/…. MT JEKK JIĠI FUQ IL-ĠILDA: Baħbaħ b’ħafna ilma/… NL BIJ CONTACT MET DE HUID: met veel water/… wassen. PL W PRZYPADKU KONTAKTU ZE SKÓRĄ: Umyć dużą ilością wody/… PT SE ENTRAR EM CONTACTO COM A PELE: lavar abundantemente com água/… RO ÎN CAZ DE CONTACT CU PIELEA: spălați cu multă apă/… SK PRI KONTAKTE S POKOŽKOU: Umyte veľkým množstvom vody/… SL PRI STIKU S KOŽO: Umiti z veliko vode/… FI JOS KEMIKAALIA JOUTUU IHOLLE: Pese runsaalla vedellä/… SV VID HUDKONTAKT: Tvätta med mycket vatten/… P303 + P361 + P353 Language BG ПРИ КОНТАКТ С КОЖАТА (или косата): Незабавно свалете цялото замърсено облекло. Облейте кожата с вода/вземете душ. ES EN CASO DE CONTACTO CON LA PIEL (o el pelo): Quitar inmediatamente todas las prendas contaminadas. Aclararse la piel con agua/ducharse. CS PŘI STYKU S KŮŽÍ (nebo s vlasy): Veškeré kontaminované části oděvu okamžitě svlékněte. Opláchněte kůži vodou/osprchujte. DA VED KONTAKT MED HUDEN (eller håret): Tilsmudset tøj tages straks af/fjernes. Skyl/brus huden med vand. DE BEI KONTAKT MIT DER HAUT (oder dem Haar): Alle beschmutzten, getränkten Kleidungsstücke sofort ausziehen. Haut mit Wasser abwaschen/duschen. DA VED KONTAKT MED HUDEN (eller håret): Alt tilsmudset tøj tages straks af. Skyl/brus huden med vand. DE BEI BERÜHRUNG MIT DER HAUT (oder dem Haar): Alle kontaminierten Kleidungsstücke sofort ausziehen. Haut mit Wasser abwaschen/duschen. ET NAHALE (või juustele) SATTUMISE KORRAL: võtta viivitamata kõik saastunud rõivad seljast. Loputada nahka veega/loputada duši all. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΠΑΦΗΣ ΜΕ ΤΟ ΔΕΡΜΑ (ή με τα μαλλιά): Αφαιρέστε αμέσως όλα τα μολυσμένα ενδύματα. Ξεπλύνετε το δέρμα με νερό/στο ντους. EN IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. FR EN CAS DE CONTACT AVEC LA PEAU (ou les cheveux): enlever immédiatement les vêtements contaminés. Rincer la peau à l’eau/se doucher. GA I gCÁS TEAGMHÁLA LEIS AN gCRAICEANN(nó le gruaig): Bain díot láithreach na héadaí éillithe go léir. Sruthlaítear an craiceann le huisce/glac cithfholcadh. HR U SLUČAJU DODIRA S KOŽOM (ili kosom): odmah ukloniti/skinuti svu zagađenu odjeću. Isprati kožu vodom/tuširanjem. IT IN CASO DI CONTATTO CON LA PELLE (o con i capelli): togliersi di dosso immediatamente tutti gli indumenti contaminati. Sciacquare la pelle/fare una doccia. LV SASKARĒ AR ĀDU (vai matiem): noģērbt visu piesārņoto apģērbu. Noskalot ādu ar ūdeni/dušā. LT PATEKUS ANT ODOS (arba plaukų): Nedelsiant nuvilkti/pašalinti visus užterštus drabužius. Odą nuplauti vandeniu/čiurkšle. HU HA BŐRRE (vagy hajra) KERÜL: Az összes szennyezett ruhadarabot azonnal el kell távolítani/le kell vetni. A bőrt le kell öblíteni vízzel/zuhanyozás. MT JEKK FUQ IL-ĠILDA (jew xagħar): Neħħi/inża’ minnufih l-ilbies kontaminat. Laħlaħ il-ġilda bl-ilma/bix-xawer. NL BIJ CONTACT MET DE HUID (of het haar): verontreinigde kleding onmiddellijk uittrekken — huid met water afspoelen/afdouchen. PL W PRZYPADKU KONTATKU ZE SKÓRĄ (lub z włosami): Natychmiast usunąć/zdjąć całą zanieczyszczoną odzież. Spłukać skórę pod strumieniem wody/prysznicem. PT SE ENTRAR EM CONTACTO COM A PELE (ou o cabelo): despir/retirar imediatamente toda a roupa contaminada. Enxaguar a pele com água/tomar um duche. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΠΑΦΗΣ ΜΕ ΤΟ ΔΕΡΜΑ (ή με τα μαλλιά): Βγάλτε αμέσως όλα τα μολυσμένα ρούχα. Ξεπλύντε την επιδερμίδα με νερό/στο ντους. EN IF ON SKIN (or hair): Take off immediately all contaminated clothing. Rinse skin with water/shower. FR EN CAS DE CONTACT AVEC LA PEAU (ou les cheveux): Enlever immédiatement tous les vêtements contaminés. Rincer la peau à l’eau/Se doucher. GA I gCÁS TEAGMHÁLA LEIS AN gCRAICEANN (nó le gruaig): Bain díot láithreach na héadaí éillithe go léir. Sruthlaigh an craiceann le huisce/glac cithfholcadh. HR U SLUČAJU DODIRA S KOŽOM (ili kosom): odmah skinuti svu zagađenu odjeću. Isprati kožu vodom/tuširanjem. IT IN CASO DI CONTATTO CON LA PELLE (o con i capelli): togliere immediatamente tutti gli indumenti contaminati. Sciacquare la pelle/fare una doccia. LV SASKARĒ AR ĀDU (vai matiem): nekavējoties novilkt visu piesārņoto apģērbu. Noskalot ādu ar ūdeni/dušā. LT PATEKUS ANT ODOS (arba plaukų): nusivilkite visus užterštus drabužius. Nuplaukite odą vandeniu arba po dušu. HU HA BŐRRE (vagy hajra) KERÜL: Az összes szennyezett ruhadarabot azonnal le kell vetni. A bőrt le kell öblíteni vízzel/zuhanyozás. MT JEKK JIĠI FUQ IL-ĠILDA (jew fuq ix-xagħar) Neħħi minnufih il-ħwejjeg kontaminati kollha. Baħbaħ il-ġilda bl-ilma/taħt ix-xawer. NL BIJ CONTACT MET DE HUID (of het haar): verontreinigde kleding onmiddellijk uittrekken. Huid met water afspoelen/afdouchen. PL W PRZYPADKU KONTATKU ZE SKÓRĄ (lub z włosami): Natychmiast zdjąć całą zanieczyszczoną odzież. Spłukać skórę pod strumieniem wody/prysznicem. PT SE ENTRAR EM CONTACTO COM A PELE (ou o cabelo): retirar imediatamente toda a roupa contaminada. Enxaguar a pele com água/tomar um duche. RO ÎN CAZ DE CONTACT CU PIELEA (sau părul): scoateți imediat toată îmbrăcămintea contaminată. Clătiți pielea cu apă/faceți duș. SK PRI KONTAKTE S POKOŽKOU (alebo vlasmi): Odstráňte/vyzlečte všetky kontaminované časti odevu. Pokožku ihneď opláchnite vodou/sprchou. SL PRI STIKU S KOŽO (ali lasmi): takoj odstraniti/sleči vsa kontaminirana oblačila. Izprati kožo z vodo/prho. SK PRI KONTAKTE S POKOŽKOU (alebo vlasmi): Všetky kontaminované časti odevu okamžite vyzlečte. Pokožku opláchnite vodou/sprchou. SL PRI STIKU S KOŽO (ali lasmi): Takoj sleči vsa kontaminirana oblačila. Izprati kožo z vodo/prho. FI JOS KEMIKAALIA JOUTUU IHOLLE (tai hiuksiin): Riisu saastunut vaatetus välittömästi. Huuhdo/suihkuta iho vedellä. SV VID HUDKONTAKT (även håret): Ta omedelbart av alla nedstänkta kläder. Skölj huden med vatten/duscha. P304 + P340 Language BG ПРИ ВДИШВАНЕ: Изведете пострадалия на чист въздух и го поставете в позиция, улесняваща дишането. ES EN CASO DE INHALACIÓN: Transportar a la víctima al exterior y mantenerla en reposo en una posición confortable para respirar. CS PŘI VDECHNUTÍ: Přeneste postiženého na čerstvý vzduch a ponechte jej v klidu v poloze usnadňující dýchání. DA VED INDÅNDING: Flyt personen til et sted med frisk luft og sørg for, at vedkommende hviler i en stilling, som letter vejrtrækningen. DE BEI EINATMEN: An die frische Luft bringen und in einer Position ruhigstellen, die das Atmen erleichtert. ET SISSEHINGAMISE KORRAL: toimetada kannatanu värske õhu kätte ja asetada mugavasse puhkeasendisse, mis võimaldab kergesti hingata. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΙΣΠΝΟΗΣ: Μεταφέρετε τον παθόντα στον καθαρό αέρα και αφήστε τον να ξεκουραστεί σε στάση που διευκολύνει την αναπνοή. EN IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing. FR EN CAS D’INHALATION: transporter la victime à l’extérieur et la maintenir au repos dans une position où elle peut confortablement respirer. GA MÁ IONÁLAÍTEAR, tabhair amach faoin aer an duine agus coimeád socair é, i riocht ina bhféadfaidh sé anáil a tharraingt go réidh. HR AKO SE UDIŠE: premjestiti unesrećenog na svježi zrak, umiriti ga i postaviti u položaj koji olakšava disanje. IT IN CASO DI INALAZIONE: trasportare l'infortunato all’aria aperta e mantenerlo a riposo in posizione che favorisca la respirazione. LV IEELPOŠANAS GADĪJUMĀ: izvest cietušo svaigā gaisā un turēt miera stāvoklī, lai būtu ērti elpot. LT ĮKVĖPUS: Išnešti nukentėjusįjį į gryną orą; jam būtina ramybė ir padėtis, leidžianti laisvai kvėpuoti. HU BELÉLEGZÉS ESETÉN: Az érintett személyt friss levegőre kell vinni és olyan nyugalmi testhelyzetbe kell helyezni, hogy könnyen tudjon lélegezni. MT JEKK JITTIEĦED FIN-NIFS: Esponi lill-vittma għall-arja friska u żommha mistrieħa f’pożizzjoni komda biex tkun tista’ tieħu n-nifs. NL NA INADEMING: het slachtoffer in de frisse lucht brengen en laten rusten in een houding die het ademen vergemakkelijkt. PL W PRZYPADKU DOSTANIA SIĘ DO DRÓG ODDECHOWYCH: wyprowadzić lub wynieść poszkodowanego na świeże powietrze i zapewnić warunki do odpoczynku w pozycji umożliwiającej swobodne oddychanie. PT EM CASO DE INALAÇÃO: retirar a vítima para uma zona ao ar livre e mantê-la em repouso numa posição que não dificulte a respiração. RO ÎN CAZ DE INHALARE: transportați victima la aer liber și mențineți-o în stare de repaus, într-o poziție confortabilă pentru respirație. SK PO VDÝCHNUTÍ: Presuňte postihnutého na čerstvý vzduch a nechajte ho oddychovať v polohe, ktorá mu umožní pohodlné dýchanie. SL PRI VDIHAVANJU: prenesti žrtev na svež zrak in jo pustiti počivati v položaju, ki olajša dihanje. FI JOS KEMIKAALIA ON HENGITETTY: Siirrä henkilö raittiiseen ilmaan ja pidä lepoasennossa, jossa on helppo hengittää. SV VID INANDNING: Flytta personen till frisk luft och se till att han eller hon vilar i en ställning som underlättar andningen. P304 + P340 Language BG ПРИ ВДИШВАНЕ: Изведете лицето на чист въздух и го поставете в позиция, улесняваща дишането. ES EN CASO DE INHALACIÓN: Transportar a la persona al aire libre y mantenerla en una posición que le facilite la respiración. CS PŘI VDECHNUTÍ: Přeneste osobu na čerstvý vzduch a ponechte ji v poloze usnadňující dýchání. DA VED INDÅNDING: Flyt personen til et sted med frisk luft og sørg for, at vejrtrækningen lettes. DE BEI EINATMEN: Die Person an die frische Luft bringen und für ungehinderte Atmung sorgen. ET SISSEHINGAMISE KORRAL: toimetada isik värske õhu kätte ja hoida asendis, mis võimaldab kergesti hingata. EL ΣΕ ΠΕΡΙΠΤΩΣΗ ΕΙΣΠΝΟΗΣ: Μεταφέρατε τον παθόντα στον καθαρό αέρα και αφήστε τον να ξεκουραστεί σε στάση που διευκολύνει την αναπνοή. EN IF INHALED: Remove person to fresh air and keep comfortable for breathing. FR EN CAS D’INHALATION: transporter la personne à l’extérieur et la maintenir dans une position où elle peut confortablement respirer. GA MÁ IONANÁILTEAR: Tabhair an duine amach faoin aer úr agus coinnigh é compordach. HR AKO SE UDIŠE: premjestiti osobu na svježi zrak i postaviti ju u položaj koji olakšava disanje. IT IN CASO DI INALAZIONE: trasportare l’infortunato all’aria aperta e mantenerlo a riposo in posizione che favorisca la respirazione. LV IEELPOŠANAS GADĪJUMĀ: nogādāt cietušo svaigā gaisā un nodrošināt netraucētu elpošanu. LT ĮKVĖPUS: išnešti nukentėjusįjį į gryną orą; jam būtina patogi padėtis, leidžianti laisvai kvėpuoti. HU BELÉLEGZÉS ESETÉN: Az érintett személyt friss levegőre kell vinni, és olyan nyugalmi testhelyzetbe kell helyezni, hogy könnyen tudjon lélegezni. MT JEKK JINĠIBED MAN-NIFS: Qiegħed lill-persuna għall-arja friska f’pożizzjoni komda biex tieħu n-nifs. NL NA INADEMING: de persoon in de frisse lucht brengen en ervoor zorgen dat deze gemakkelijk kan ademen. PL W PRZYPADKU DOSTANIA SIĘ DO DRÓG ODDECHOWYCH: wyprowadzić lub wynieść poszkodowanego na świeże powietrze i zapewnić mu warunki do swobodnego oddychania. PT EM CASO DE INALAÇÃO: retirar a pessoa para uma zona ao ar livre e mantê-la numa posição que não dificulte a respiração. RO ÎN CAZ DE INHALARE: transportați persoana la aer liber și mențineți-o într-o poziție confortabilă pentru respirație. SK PO VDÝCHNUTÍ: Presuňte osobu na čerstvý vzduch a umožnite jej pohodlne dýchať. SL PRI VDIHAVANJU: Prenesti osebo na svež zrak in jo pustiti v udobnem položaju, ki olajša dihanje. FI JOS KEMIKAALIA ON HENGITETTY: Siirrä henkilö raittiiseen ilmaan ja varmista vaivaton hengitys. SV VID INANDNING: Flytta personen till frisk luft och se till att andningen underlättas. P304 + P341 Language BG ПРИ ВДИШВАНЕ: При затруднено дишане изведете пострадалия на чист въздух и го поставете в позиция, улесняваща дишането. ES EN CASO DE INHALACIÓN: Si respira con dificultad, transportar a la víctima al exterior y mantenerla en reposo en una posición confortable para respirar. CS PŘI VDECHNUTÍ: Při obtížném dýchání přeneste postiženého na čerstvý vzduch a ponechte jej v klidu v poloze usnadňující dýchání. … 66 unchanged lines … SL PRI STIKU Z OBLAČILI: takoj izprati kontaminirana oblačila in kožo z veliko vode pred odstranitvijo oblačil. FI JOS KEMIKAALIA JOUTUU VAATTEISIIN: Huuhdo saastunut vaatetus ja iho välittömästi runsaalla vedellä ennen vaatetuksen riisumista. SV VID KONTAKT MED KLÄDERNA: Skölj omedelbart nedstänkta kläder och hud med mycket vatten innan du tar av dig kläderna. P307 + P311 Language BG ПРИ експозиция: Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES EN CASO DE exposición: Llamar a un CENTRO DE INFORMACIÓN TOXICOLÓGICA o a un médico. CS PŘI expozici: Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA VED eksponering: Ring til en GIFTINFORMATION eller en læge. DE BEI Exposition: GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET Kokkupuute korral: võtta ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL ΣΕ ΠΕΡΙΠΤΩΣΗ έκθεσης: Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό. EN IF exposed: Call a POISON CENTER or doctor/physician. FR EN CAS d’exposition: appeler un CENTRE ANTIPOISON ou un médecin. GA I gCÁS nochta: Cuir glao ar IONAD NIMHE nó ar dhoctúir/lia. HR U SLUČAJU izloženosti: nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT IN CASO di esposizione, contattare un CENTRO ANTIVELENI o un medico. LV Ja ir saskarē: Sazināties ar SAINDĒŠANĀS CENTRU vai ārstu. LT Esant sąlyčiui: Skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU Expozíció esetén: forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT Jekk espost: Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib. NL NA blootstelling: een ANTIGIFCENTRUM of een arts raadplegen. PL W przypadku narażenia: Skontaktować się z OŚRODKIEM ZATRUĆ lub z lekarzem. PT EM CASO DE exposição: contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO ÎN CAZ DE expunere: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic. SK Po expozícii: volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL PRI izpostavljenosti: pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI Altistumisen tapahduttua: Ota yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin. SV Om du exponerats: Kontakta GIFTINFORMATIONSCENTRAL eller läkare. P308 + P311 Language BG ПРИ явна или предполагаема експозиция: Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES EN CASO DE exposición manifiesta o presunta: Llamar a un CENTRO DE TOXICOLOGĺA/médico/… CS PŘI expozici nebo podezření na ni: Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/…. DA VED eksponering eller mistanke om eksponering: Ring til en GIFTINFORMATION/læge/… DE BEI Exposition oder falls betroffen: GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET Kokkupuute korral: võtta ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL ΣΕ ΠΕΡΙΠΤΩΣΗ έκθεσης ή πιθανής έκθεσης: Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/… EN IF exposed or concerned: Call a POISON CENTER/doctor/… FR EN CAS d’exposition prouvée ou suspectée: Appeler un CENTRE ANTIPOISON/un médecin/… GA I gCÁS nochta nó má mheastar a bheith nochtaithe: Cuir glao ar IONAD NIMHE/ar dhoctúir/… HR U SLUČAJU izloženosti ili sumnje na izloženost: nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT In caso di esposizione o di possibile esposizione: contattare un CENTRO ANTIVELENI/un medico/… LV JA saskaras vai saistīts ar: sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/… LT Esant poveikiui arba jeigu numanomas poveikis: skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/… HU Expozíció vagy annak gyanúja esetén: Forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT JEKK espost jew konċernat: Sejjaħ ĊENTRU TAL-AVVELENAMENT/tabib/… NL NA (mogelijke) blootstelling: Een ANTIGIFCENTRUM/arts/… raadplegen. PL W przypadku narażenia lub styczności: Skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT EM CASO DE exposição ou suspeita de exposição: contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO ÎN CAZ de expunere sau de posibilă expunere: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/… SK PO expozícii alebo podozrení z nej: Volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL Pri izpostavljenosti ali sumu izpostavljenosti: Pokličite CENTER ZA ZASTRUPITVE/zdravnika/… FI Altistumisen tapahduttua tai jos epäillään altistumista: Ota yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/… SV Vid exponering eller misstanke om exponering: Kontakta GIFTINFORMATIONSCENTRALEN/läkare/… P308 + P313 Language BG ПРИ явна или предполагаема експозиция: Потърсете медицински съвет/помощ. ES EN CASO DE exposición manifiesta o presunta: Consultar a un médico. CS PŘI expozici nebo podezření na ni: Vyhledejte lékařskou pomoc/ošetření. … 138 unchanged lines … SL Če draženje oči ne preneha: poiščite zdravniško pomoč/oskrbo. FI Jos silmä-ärsytys jatkuu: Hakeudu lääkäriin. SV Vid bestående ögonirritation: Sök läkarhjälp. P342 + P311 Language BG При симптоми на затруднено дишане: Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ или на лекар. ES En caso de síntomas respiratorios: Llamar a un CENTRO DE INFORMACIÓN TOXICOLÓGICA o a un médico. CS Při dýchacích potížích: Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO nebo lékaře. DA Ved luftvejssymptomer: Ring til en GIFTINFORMATION eller en læge. DE Bei Symptomen der Atemwege: GIFTINFORMATIONSZENTRUM oder Arzt anrufen. ET Hingamisteede probleemide ilmnemise korral: võtta ühendust MÜRGISTUSTEABEKESKUSE või arstiga. EL Εάν παρουσιάζονται αναπνευστικά συμπτώματα: Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ ή ένα γιατρό. EN If experiencing respiratory symptoms: Call a POISON CENTER or doctor/physician. FR En cas de symptômes respiratoires: appeler un CENTRE ANTIPOISON ou un médecin. GA I gcás siomptóm riospráide: Cuir glao ar IONAD NIMHE nó ar dhoctúir/lia. HR Pri otežanom disanju: nazvati CENTAR ZA KONTROLU OTROVANJA ili liječnika. IT In caso di sintomi respiratori: contattare un CENTRO ANTIVELENI o un medico. LV Ja rodas elpas trūkuma simptomi: sazinieties ar SAINDĒŠANĀS CENTRU vai ārstu. LT Jeigu pasireiškia respiraciniai simptomai: skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ arba kreiptis į gydytoją. HU Légzési problémák esetén: forduljon TOXIKOLÓGIAI KÖZPONTHOZ vagy orvoshoz. MT Jekk ikollok sintomi respiratorji: Ikkuntattja ĊENTRU TA' L-AVVELENAMENT jew tabib. NL Bij ademhalingssymptomen: een ANTIGIFCENTRUM of een arts raadplegen. PL W przypadku wystąpienia objawów ze strony układu oddechowego: Skontaktować się z OŚRODKIEM ZATRUĆ lub z lekarzem. PT Em caso de sintomas respiratórios: contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS ou um médico. RO În caz de simptome respiratorii: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ sau un medic. SK Pri ťažkostiach s dýchaním: volajte NÁRODNÉ TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM alebo lekára. SL Pri respiratornih simptomih: pokličite CENTER ZA ZASTRUPITVE ali zdravnika. FI Jos ilmenee hengitysoireita: Ota yhteys MYRKYTYSTIETOKESKUKSEEN tai lääkäriin. SV Vid besvär i luftvägarna: Kontakta GIFTINFORMATIONSCENTRAL eller läkare. P342 + P311 Language BG При симптоми на затруднено дишане: Обадете се в ЦЕНТЪР ПО ТОКСИКОЛОГИЯ/на лекар/… ES En caso de síntomas respiratorios: Llamar a un CENTRO DE TOXICOLOGĺA/médico/… CS Při dýchacích potížích: Volejte TOXIKOLOGICKÉ INFORMAČNÍ STŘEDISKO/lékaře/… DA Ved luftvejssymptomer: Ring til en GIFTINFORMATION/læge/… DE Bei Symptomen der Atemwege: GIFTINFORMATIONSZENTRUM/Arzt/…/anrufen. ET Hingamisteede probleemide ilmnemise korral: võtta ühendust MÜRGISTUSTEABEKESKUSE/arstiga… EL Εάν παρουσιάζονται αναπνευστικά συμπτώματα: Καλέστε το ΚΕΝΤΡΟ ΔΗΛΗΤΗΡΙΑΣΕΩΝ/γιατρό/… EN If experiencing respiratory symptoms: Call a POISON CENTER/doctor/… FR En cas de symptômes respiratoires: Appeler un CENTRE ANTIPOISON/un médecin/… GA I gCÁS siomtóm riospráide: Cuir glao ar IONAD NIMHE/ar dhoctúir/… HR Pri otežanom disanju: nazvati CENTAR ZA KONTROLU OTROVANJA/liječnika/… IT In caso di sintomi respiratori: contattare un CENTRO ANTIVELENI/un medico/… LV Ja rodas elpas trūkuma simptomi: sazinieties ar SAINDĒŠANĀS INFORMĀCIJAS CENTRU/ārstu/… LT Jeigu pasireiškia respiraciniai simptomai: skambinti į APSINUODIJIMŲ KONTROLĖS IR INFORMACIJOS BIURĄ/kreiptis į gydytoją/… HU Légzési problémák esetén: Forduljon TOXIKOLÓGIAI KÖZPONTHOZ/orvoshoz/…. MT Jekk ikollok sintomi respiratorji: Sejjaħ ĊENTRU TAL-AVVELENAMENT/tabib/… NL Bij ademhalingssymptomen: Een ANTIGIFCENTRUM/arts/… raadplegen. PL W przypadku wystąpienia objawów ze strony układu oddechowego: Skontaktować się z OŚRODKIEM ZATRUĆ/lekarzem/… PT Em caso de sintomas respiratórios: contacte um CENTRO DE INFORMAÇÃO ANTIVENENOS/médico/… RO În caz de simptome respiratorii: sunați la un CENTRU DE INFORMARE TOXICOLOGICĂ/un medic/… SK Pri sťaženom dýchaní: Volajte TOXIKOLOGICKÉ INFORMAČNÉ CENTRUM/lekára/… SL Pri respiratornih simptomih: Pokličite CENTER ZA ZASTRUPITVE/zdravnika/… FI Jos ilmenee hengitysoireita: Ota yhteys MYRKYTYSTIETOKESKUKSEEN/lääkäriin/… SV Vid besvär i luftvägarna: Kontakta GIFTINFORMATIONSCENTRALEN/läkare/… P361 + P364 Language BG Незабавно свалете цялото замърсено облекло и го изперете преди повторна употреба. ES Quitar inmediatamente todas las prendas contaminadas y lavarlas antes de volver a usarlas. CS Veškeré kontaminované části oděvu okamžitě svlékněte a před opětovným použitím vyperte. DA Alt tilsmudset tøj tages straks af og vaskes inden genanvendelse. DE Alle kontaminierten Kleidungsstücke sofort ausziehen und vor erneutem Tragen waschen. ET Võtta viivitamata seljast kõik saastunud rõivad ja pesta enne korduskasutust. EL Βγάλτε αμέσως όλα τα μολυσμένα ρούχα και πλύντε τα πριν τα ξαναχρησιμοποιήσετε. EN Take off immediately all contaminated clothing and wash it before reuse. FR Enlever immédiatement tous les vêtements contaminés et les laver avant réutilisation. GA Bain díot láithreach na héadaí éillithe go léir agus nigh iad roimh iad a athúsáid. HR Odmah skinuti svu zagađenu odjeću i oprati je prije ponovne uporabe. IT Togliere immediatamente tutti gli indumenti contaminati e lavarli prima di indossarli nuovamente. LV Nekavējoties novilkt visu piesārņoto apģērbu un pirms atkārtotas lietošanas izmazgāt. LT Nedelsiant nusivilkti visus užterštus drabužius ir išskalbti prieš vėl apsivelkant. HU Az összes szennyezett ruhadarabot azonnal le kell vetni és újbóli használat előtt ki kell mosni. MT Neħħi minnufih il-ħwejjeġ kontaminati kollha u aħsilhom qabel terġa’ tilbishom. NL Verontreinigde kleding onmiddellijk uittrekken en wassen alvorens deze opnieuw te gebruiken. PL Natychmiast zdjąć całą zanieczyszczoną odzież i wyprać przed ponownym użyciem. PT Retirar imediatamente a roupa contaminada e lavá-la antes de a voltar a usar. RO Scoateți imediat toată îmbrăcămintea contaminată și spalați-o înainte de reutilizare. SK Všetky kontaminované časti odevu okamžite vyzlečte a pred ďalším použitím vyperte. SL Takoj sleči vsa kontaminirana oblačila in jih oprati pred ponovno uporabo. FI Riisu saastunut vaatetus välittömästi ja pese ennen uudelleenkäyttöä. SV Ta omedelbart av alla nedstänkta kläder och tvätta dem innan de används igen. P362 + P364 Language BG Свалете замърсеното облекло и го изперете преди повторна употреба. ES Quitar las prendas contaminadas y lavarlas antes de volver a usarlas. CS Kontaminovaný oděv svlékněte a před opětovným použitím vyperte. DA Alt tilsmudset tøj tages af og vaskes inden genanvendelse. DE Kontaminierte Kleidung ausziehen und vor erneutem Tragen waschen. ET Võtta seljast saastunud rõivad ja pesta enne korduskasutust. EL Βγάλτε τα μολυσμένα ρούχα και πλύντε τα πριν τα ξαναχρησιμοποιήσετε. EN Take off contaminated clothing and wash it before reuse. FR Enlever les vêtements contaminés et les laver avant réutilisation. GA Bain díot aon éadaí éillithe agus nigh iad roimh iad a athúsáid. HR Skinuti zagađenu odjeću i oprati je prije ponovne uporabe. IT Togliere tutti gli indumenti contaminati e lavarli prima di indossarli nuovamente. LV Novilkt piesārņoto apģērbu un pirms atkārtotas lietošanas izmazgāt. LT Nusivilkti užterštus drabužius ir išskalbti prieš vėl apsivelkant. HU A szennyezett ruhadarabot le kell vetni és újbóli használat előtt ki kell mosni. MT Neħħi l-ħwejjeġ kontaminati kollha u aħsilhom qabel terġa’ tilbishom. NL Verontreinigde kleding uittrekken en wassen alvorens deze opnieuw te gebruiken. PL Zanieczyszczoną odzież zdjąć i wyprać przed ponownym użyciem. PT Retirar a roupa contaminada e lavá-la antes de a voltar a usar. RO Scoateți îmbrăcămintea contaminată și spalați-o înainte de reutilizare. SK Kontaminovaný odev vyzlečte a pred ďalším použitím vyperte. SL Sleči kontaminirana oblačila in jih oprati pred ponovno uporabo. FI Riisu saastunut vaatetus ja pese ennen uudelleenkäyttöä. SV Ta av nedstänkta kläder och tvätta dem innan de används igen. P370 + P376 Language BG При пожар: Спрете теча, ако е безопасно. ES En caso de incendio: Detener la fuga, si no hay peligro en hacerlo. CS V případě požáru: Zastavte únik, můžete-li tak učinit bez rizika. … 18 unchanged lines … SL Ob požaru: zaustaviti puščanje, če je varno. FI Tulipalon sattuessa: Sulje vuoto, jos sen voi tehdä turvallisesti. SV Vid brand: Stoppa läckan om det kan göras på ett säkert sätt. P370 + P378 Language BG При пожар: Използвайте … за гасене. ES En caso de incendio: Utilizar … para apagarlo. CS V případě požáru: K hašení použijte … DA Ved brand: Anvend … til brandslukning. P370 + P378 Language BG При пожар: Използвайте…, за да загасите. ES En caso de incendio: Utilizar… para la extinción. CS V případě požáru: K uhašení použijte… DA Ved brand: Anvend… til brandslukning. DE Bei Brand: … zum Löschen verwenden. ET Tulekahju korral: kasutada kustutamiseks … EL Σε περίπτωση πυρκαγιάς: Χρησιμοποιήστε … για την κατάσβεση. EN In case of fire: Use … for extinction. FR En cas d’incendie: utiliser … pour l’extinction. ET Tulekahju korral: kasutada kustutamiseks… EL Σε περίπτωση πυρκαγιάς: Χρησιμοποιήστε… για να κατασβήσετε. EN In case of fire: Use… to extinguish. FR En cas d’incendie: Utiliser… pour l’extinction. GA I gcás dóiteáin: Úsáid … le haghaidh múchta. HR U slučaju požara: za gašenje rabiti … IT In caso di incendio: estinguere con… IT In caso d’incendio: utilizzare…per estinguere. LV Ugunsgrēka gadījumā: dzēšanai izmantojiet … LT Gaisro atveju: gesinimui naudoti … HU Tűz esetén: az oltáshoz …használandó. MT F’każ ta' nar: Uża’ … għat-tifi. HU Tűz esetén: oltásra …használandó. MT F’każ ta’ nar: Uża… biex titfi. NL In geval van brand: blussen met … PL W przypadku pożaru: Użyć … do gaszenia. PT Em caso de incêndio: para a extinção utilizar … RO În caz de incendiu: utilizați… pentru stingere. SK V prípade požiaru: na hasenie použite … SL Ob požaru: za gašenje uporabiti … FI Tulipalon sattuessa: Käytä palon sammuttamiseen … SV Vid brand: Släck branden med … PL W przypadku pożaru: Użyć… do gaszenia. PT Em caso de incêndio: para extinguir utilizar…. RO În caz de incendiu: a se utiliza… pentru a stinge. SK V prípade požiaru: Na hasenie použite… SL Ob požaru: Za gašenje se uporabi … FI Tulipalon sattuessa: Käytä palon sammuttamiseen… SV Vid brand: Släck med… P370 + P380 Language BG При пожар: Евакуирайте зоната. ES En caso de incendio: Evacuar la zona. CS V případě požáru: Vykliďte prostor. … 82 unchanged lines … IT Conservare… LV Glabāt… LT Laikyti… HU Tárolás: … . HU Tárolás: …. MT Aħżen … NL … bewaren. PL Przechowywać … … 205 unchanged lines … EN Do not expose to temperatures exceeding 50 oC/122oF. FR Ne pas exposer à une température supérieure à 50 oC/122 oF. GA Ná nocht do theocht níos airde ná 50 oC/122oF. HR Ne izlagati temperaturi višoj od 50 oC/122 oF. HR Ne izlagati temperaturi višoj od 50 oC/122 oF. IT Non esporre a temperature superiori a 50 oC/122oF. LV Nepakļaut temperatūrai, kas pārsniedz 50 oC/122oF. LT Nelaikyti aukštesnėje kaip 50 oC/122oF temperatūroje. … 185 unchanged lines … EN Protect from sunlight. Do no expose to temperatures exceeding 50 oC/122oF. FR Protéger du rayonnement solaire. Ne pas exposer à une température supérieure à 50 oC/122 oF. GA Cosain ó sholas na gréine. Ná nocht do theocht níos airde ná 50 oC/122oF. HR Zaštititi od sunčevog svjetla. Ne izlagati temperaturi višoj od 50 oC/122 oF. HR Zaštititi od sunčevog svjetla. Ne izlagati temperaturi višoj od 50 oC/122 oF. IT Proteggere dai raggi solari. Non esporre a temperature superiori a 50 oC/122oF. LV Aizsargāt no saules gaismas. Nepakļaut temperatūrai, kas pārsniedz 50 oC/122oF. LT Saugoti nuo saulės šviesos. Nelaikyti aukštesnėje kaip 50 oC/122oF temperatūroje. … 81 unchanged lines … SL Za podatke glede obnovitve/reciklaže se obrnite na proizvajalca/dobavitelja FI Hanki valmistajalta/toimittajalta tietoja uudelleenkäytöstä/kierrätyksestä SV Rådfråga tillverkare/leverantör om återvinning/återanvändning

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ANNEX V HAZARD PICTOGRAMS INTRODUCTION The hazard pictograms for each hazard class, differentiation of a hazard class and hazard category shall satisfy the provisions of this Annex and Annex I, section 1.2 and conform in terms of symbols and general format, to the specimens shown. 1. PART 1: PHYSICAL HAZARDS 1.1. Symbol: exploding bomb Pictogram (1) Hazard class and hazard category (2) GHS01 Section 2.1 Unstable explosives Explosives of Divisions 1.1, 1.2, 1.3, 1.4 Section 2.8 Self reactive substances and mixtures, Types A, B Section 2.15 Organic peroxides, Types A, B 1.2. Symbol: flame Pictogram (1) Hazard class and hazard category (2) GHS02 Section 2.2 Flammable gases, hazard category 1 Section 2.3 Flammable aerosols, Aerosols, hazard categories 1, 2 Section 2.6 Flammable liquids, hazard categories 1, 2, 3 Section 2.7 Flammable solids, hazard categories 1, 2 Section 2.8 Self-reactive substances and mixtures, Types B, C, D, E, F Section 2.9 Pyrophoric liquids, hazard category 1 Section 2.10 Pyrophoric solids, hazard category 1 Section 2.11 Self-heating substances and mixtures, hazard categories 1, 2 Section 2.12 Substances and mixtures, which in contact with water, emit flammable gases, hazard categories 1, 2, 3 Section 2.15 Organic peroxides, Types B, C, D, E, F 1.3. Symbol: flame over circle Pictogram (1) Hazard class and hazard category (2) GHS03 Section 2.4 Oxidising gases, hazard category 1 Section 2.13 Oxidising liquids, hazard categories 1, 2, 3 Section 2.14 Oxidising solids, hazard categories 1, 2, 3 1.4. Symbol: gas cylinder Pictogram (1) Hazard class and hazard category (2) GHS04 Section 2.5 Gases under pressure: Compressed gases; Liquefied gases; Refrigerated liquefied gases; Dissolved gases 1.5. Symbol: corrosion Pictogram (1) Hazard class and hazard category (2) GHS05 Section 2.16 Corrosive to metals, hazard category 1 1.6. A pictogram is not required for the following physical hazard classes and hazard categories: Section 2.1: Explosives of Division 1.5 Section 2.1: Explosives of Division 1.6 Section 2.2: Flammable gases, hazard Category 2 Section 2.3: Aerosols, hazard Category 3 Section 2.8: Self-reactive substances and mixtures, Type G Section 2.15: Organic peroxides, Type G 2. PART 2: HEALTH HAZARDS 2.1. Symbol: skull and crossbones Pictogram (1) Hazard class and hazard category (2) GHS06 Section 3.1 Acute toxicity (oral, dermal, inhalation), hazard categories 1, 2, 3 2.2. Symbol: corrosion Pictogram (1) Hazard class and hazard category (2) GHS05 Section 3.2 Skin corrosion, hazard categories 1A, 1B, 1C Section 3.3 Serious eye damage, hazard category 1 2.3. Symbol: exclamation mark Pictogram (1) Hazard class and hazard category (2) GHS07 Section 3.1 Acute toxicity (oral, dermal, inhalation), hazard category 4 Section 3.2 Skin irritation, hazard category 2 Section 3.3 Eye irritation, hazard category 2 Section 3.4 Skin sensitisation, hazard categories 1, 1A, 1B Section 3.8 Specific Target Organ Toxicity — Single exposure, hazard category 3 Respiratory tract irritation Narcotic effects 2.4. Symbol: health hazard Pictogram (1) Hazard class and hazard category (2) GHS08 Section 3.4 Respiratory sensitisation, hazard categories 1, 1A, 1B Section 3.5 Germ cell mutagenicity, hazard categories 1A, 1B, 2 Section 3.6 Carcinogenicity, hazard categories 1A, 1B, 2 Section 3.7 Reproductive toxicity, hazard categories 1A, 1B, 2 Section 3.8 Specific Target Organ Toxicity — Single exposure, hazard categories 1, 2 Section 3.9 Specific Target Organ Toxicity — Repeated exposure, hazard categories 1, 2 Section 3.10 Aspiration hazard, hazard category 1 2.5. A pictogram is not required for the following health hazard categories: Section 3.7: Reproductive toxicity, Effects on or via lactation, additional hazard category 3. PART 3: ENVIRONMENTAL HAZARDS 3.1. Symbol: environment Pictogram (1) Hazard class and hazard category (2) GHS09 Section 4.1 Hazardous to the aquatic environment Acute hazard category category: Acute 1 Long-term hazard categories: Chronic hazard categories 1, Chronic 2 A pictogram is not required for the following environmental hazard classes and hazard categories: Section 4.1: Hazardous to the aquatic environment — Long-term hazard categories: Chronic hazard categories 3, 4 Chronic 4. 4. PART 4: ADDITIONAL HAZARDS 4.1. Symbol: exclamation mark Pictogram Hazard class and hazard category (1) (2) GHS07 Section 5.1 Hazardous to the ozone layer, hazard category 1

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ANNEX VI Harmonised classification and labelling for certain hazardous substances Part 1 of this Annex provides an introduction to the list of harmonised classification and labelling, including information listed for each entry and related classifications and hazard statements in Table 3.1, subject to certain considerations arising from translating the classifications listed in Annex I to Directive 67/548/EEC. … 38 unchanged lines … Expl. 1.6 Flammable gas Flam. Gas 1 Flam. Gas 2 Flammable aerosol Flam. Aerosol 1 Flam. Aerosol 2 Chem. Unst. Gas A Chem. Unst. Gas B Aerosol Aerosol 1 Aerosol 2 Aerosol 3 Oxidising gas Ox. Gas 1 Gases under pressure Press. Gas Flammable liquid Flam. Liq. 1 … 60 unchanged lines … Aquatic Chronic 4 Hazardous for the ozone layer Ozone 1 1.1.2.1.2. Hazard statement codes The hazard statements assigned in accordance with Article 13(b), are indicated in accordance with Annex III. In addition, for certain hazard statements letters are added to the 3-digit code. The following additional codes are used: The hazard statements assigned in accordance with Article 13(b) are indicated in accordance with Annex III. In addition, for certain hazard statements, letters are added to the 3-digit hazard statement code for further differentiations. The following additional codes are used: H350i May cause cancer by inhalation. H360F May damage fertility. H360D May damage the unborn child. H361f Suspected of damaging fertility. H361d Suspected of damaging the unborn child. H360FD May damage fertility. May damage the unborn child. H361fd Suspected of damaging fertility. Suspected of damaging the unborn child. H360Fd May damage fertility. Suspected of damaging the unborn child. H360Df May damage the unborn child. Suspected of damaging fertility. 1.1.2.2. Labelling codes In the labelling column, the following elements are listed: (i) the hazard pictogram codes as specified in Annex V, in accordance with the precedence rules in Article 26; (ii) the signal word code Dgr for Dangeror Wng for Warning, in accordance with the precedence rule in Article 20(3); (iii) the hazard statement codes as specified in Annex III, in accordance with the classification; (iv) the codes for the supplemental statements assigned in accordance with Article 25(1) and the rules specified in Annex II, part 1. 1.1.2.3. Specific concentration limits and M-factors Specific concentration limits, where different from the generic concentration limits given in Annex I for a certain category, are given in a separate column together with the classification concerned using the same codes as under 1.1.2.1.1. Where no specific concentration limits are given in this Annex for a certain category, the generic concentration limits given in Annex I must be applied for the classification of substances containing impurities, additives or individual constituents or for mixtures. An asterisk (*) in this column indicates that the entry has specific concentration limits for acute toxicity under Directive 67/548/EEC (Table 3.2): see also section 1.2.1. Unless otherwise shown, the concentration limits are a percentage by weight of the substance calculated with reference to the total weight of the mixture. In case an M-factor has been harmonised for substances classified as hazardous to the aquatic environment in the categories Aquatic Acute 1 or Aquatic Chronic 1, this M-factor is given in Table 3.1 in the same column as the specific concentration limits. In case an M-factor for Aquatic Acute 1 and an M-factor for Aquatic Chronic 1 have been harmonised, each M-factor shall be listed in the same line as its corresponding differentiation. Where a single M-factor is given in Table 3.1 and the substance is classified as Aquatic Acute 1 and Aquatic Chronic 1, this M-factor shall be used by the manufacturer, importer or downstream user for the classification of a mixture containing this substance for acute and long-term aquatic hazards using the summation method. Where no M-factor is given in Table 3.1, M-factor(s) based on available data for the substance shall be set by the manufacturer, importer or downstream user. For the setting and use of M-factors, see section 4.1.3.5.5.5 of Annex I. In case an M-factor has been harmonised for substances classified as hazardous to the aquatic environment in the categories Aquatic Acute 1 or Aquatic Chronic 1, this M-factor is given in Table 3.1 in the same column as the specific concentration limits. In case an M-factor for Aquatic Acute 1 and an M-factor for Aquatic Chronic 1 have been harmonised, each M-factor shall be listed in the same line as its corresponding differentiation. Where a single M-factor is given in Table 3.1 and the substance is classified as Aquatic Acute 1 and Aquatic Chronic 1, this M-factor shall be used by the manufacturer, importer or downstream user for the classification of a mixture containing this substance for acute and long-term aquatic hazards using the summation method. Where no M-factor is given in Table 3.1, M-factor(s) based on available data for the substance shall be set by the manufacturer, importer or downstream user. For the setting and use of M-factors, see section 4.1.3.5.5.5 of Annex I. 1.1.3. Notes assigned to an entry The note(s) assigned to an entry are listed in the column entitled Notes. The meaning of the notes is as follows: 1.1.3.1. Notes relating to the identification, classification and labelling of substances … 94 unchanged lines … Where no concentration limits are given, the concentration limits to be used when applying the conventional method of assessing health hazards are those in Annex II, and when applying the conventional method of assessing environmental hazards are those in Annex III to Directive 1999/45/EC. 1.1.4.4. Non-conformity with Table 3.1 for physical hazards It is recommended to update the physical hazards of some entries in Table 3.2 in a forthcoming adaptation to technical progress. Until these entries are updated, the physical hazards of the corresponding entries in both tables will not be in conformity. These entries are indicated with reference in Table 3.2. Until these entries are updated, the physical hazards of the corresponding entries in both tables will not be in conformity. These entries are indicated with reference in Table 3.2. 1.2. Classifications and hazard statements in table 3.1 arising from translation of classifications listed in Annex i to directive 67/548/EEC 1.2.1. Minimum classification For certain hazard classes, including acute toxicity and STOT repeated exposure, the classification according to the criteria in Directive 67/548/EEC does not correspond directly to the classification in a hazard class and category under this Regulation. In these cases the classification in this Annex shall be considered as a minimum classification. This classification shall be applied if none of the following conditions are fulfilled: the manufacturer or importer has access to data or other information as specified in Part 1 of Annex I that lead to classification in a more severe category compared to the minimum classification. Classification in the more severe category must then be applied; the minimum classification can be further refined based on the translation table in Annex VII when the physical state of the substance used in the acute inhalation toxicity test is known to the manufacturer or importer. The classification as obtained from Annex VII shall then substitute the minimum classification indicated in this Annex if it differs from it. Minimum classification for a category is indicated by the reference * in the column Classification in Table 3.1. The reference * can also be found in the column Specific concentration Limits and M-factors where it indicates that the entry concerned has specific concentration limits under Directive 67/548/EEC (Table 3.2) for acute toxicity. These concentration limits cannot be translated into concentration limits under this Regulation, especially when a minimum classification is given. However, when the reference * is shown, the classification for acute toxicity for this entry may be of special concern. 1.2.2. Route of exposure cannot be excluded For certain hazard classes, e.g. STOT, the route of exposure should be indicated in the hazard statement only if it is conclusively proven that no other route of exposure can cause the hazard in accordance to the criteria in Annex I. Under Directive 67/548/EEC the route of exposure is indicated for classifications with R48 when there was data justifying the classification for this route of exposure. The classification under 67/548/EEC indicating the route of exposure has been translated into the corresponding class and category according to this Regulation, but with a general hazard statement not specifying the route of exposure as the necessary information is not available. These hazard statements are indicated by the reference ** in Table 3.1. 1.2.3. Hazard statements for reproductive toxicity Hazard statements H360 and H361 indicate a general concern for effects on both fertility and development: May damage/Suspected of damaging fertility or the unborn child. According to the criteria, the general hazard statement can be replaced by the hazard statement indicating only the property of concern, where either fertility or developmental effects are proven to be not relevant. Hazard statements H360 and H361 indicate a general concern for effects on fertility and/or development: May damage/Suspected of damaging fertility or the unborn child. According to the criteria, the general hazard statement can be replaced by the hazard statement indicating the specific effect of concern in accordance with section 1.1.2.1.2. When the other differentiation is not mentioned, this is due to evidence proving no such effect, inconclusive data or no data and the obligations in Article 4(3) shall apply for that differentiation. In order not to lose information from the harmonised classifications for fertility and developmental effects under Directive 67/548/EEC, the classifications have been translated only for those effects classified under that Directive. These hazard statements are indicated by the reference *** in Table 3.1. 1.2.4. Correct classification for physical hazards could not be established For some entries the correct classification for physical hazards could not be established because sufficient data are not available for the application of the classification criteria in this Regulation. The entry might be assigned to a different (also higher) category or even another hazard class than indicated. The correct classification shall be confirmed by testing. The entries with physical hazards that need to be confirmed by testing are indicated by the reference **** in Table 3.1. 2. PART 2: DOSSIERS FOR HARMONISED CLASSIFICATION AND LABELLING This Part lays down general principles for preparing dossiers to propose and justify harmonised classification and labelling. The relevant parts of sections 1, 2 and 3 of Annex I to Regulation (EC) No 1907/2006 shall be used for the methodology and format of any dossier. For all dossiers any relevant information from registration dossiers shall be considered and other available information may be used. For hazard information which has not been previously submitted to the Agency, a robust study summary shall be included in the dossier. A dossier for harmonised classification and labelling shall contain the following: Proposal The proposal shall include the identity of the substance or substances concerned and the harmonised classification and labelling proposed. Justification for the proposed harmonised classification and labelling A comparison of the available information with the criteria contained in Parts 2 to 5, taking into account the general principles in Part 1, of Annex I to this Regulation shall be completed and documented in the format set out in Part B of the Chemical Safety Report in Annex I to Regulation (EC) No 1907/2006. Justification for other effects at Community level For other effects than carcinogenity, mutagenicity, reprotoxicity and respiratory sensitisation a justification shall be provided that there is a need for action demonstrated at Community level. This does not apply for an active substance in the meaning of Directive 91/414/EEC or Directive 98/8/EC. 3. PART 3: HARMONISED CLASSIFICATION AND LABELLING TABLES Table 3.1: List of harmonised classification and labelling of hazardous substances. Table 3.2: The list of harmonised classification and labelling of hazardous substances from Annex I to Directive 67/548/EEC. Table 3.2: The list of harmonised classification and labelling of hazardous substances from Annex I to Directive 67/548/EEC. Table 3.1 List of harmonised classification and labelling of hazardous substances Index No International Chemical Identification EC No CAS No Classification Labelling Specific Conc. Limits, M-factors Notes … 189 unchanged lines … boric acid; [2] 233-139-2 [1] 234-343-4 [2] 10043-35-3 [1] 11113-50-1 [2] Repr. 1B H360FD GHS08 Dgr H360FD Repr. 1B; H360FD: C ≥ 5,5 % 005-008-00-8 diboron trioxide; Dgr H360FD Repr. 1B; H360FD: C ≥ 5,5 % 005-008-00-8 diboron trioxide; boric oxide 215-125-8 1303-86-2 Repr. 1B H360FD GHS08 Dgr H360FD Repr. 1B; H360FD: C ≥ 3,1 % 005-009-00-3 tetrabutylammonium butyltriphenylborate 418-080-4 120307-06-4 Skin Sens. 1 Dgr H360FD Repr. 1B; H360FD: C ≥ 3,1 % 005-009-00-3 tetrabutylammonium butyltriphenylborate 418-080-4 120307-06-4 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H317 H400 … 20 unchanged lines … 237-560-2 [3] 1330-43-4 [1] 12267-73-1 [2] 13840-56-7 [3] Repr. 1B H360FD GHS08 Dgr H360FD Repr. 1B; H360FD: C ≥ 4,5 % 005-011-01-1 disodium tetraborate decahydrate; Dgr H360FD Repr. 1B; H360FD: C ≥ 4,5 % 005-011-01-1 disodium tetraborate decahydrate; borax decahydrate 215-540-4 1303-96-4 Repr. 1B H360FD GHS08 Dgr H360FD Repr. 1B; H360FD: C ≥ 8,5 % 005-011-02-9 disodium tetraborate pentahydrate; Dgr H360FD Repr. 1B; H360FD: C ≥ 8,5 % 005-011-02-9 disodium tetraborate pentahydrate; borax pentahydrate 215-540-4 12179-04-3 Repr. 1B H360FD GHS08 Dgr H360FD Repr. 1B; H360FD: C ≥ 6,5 % 005-012-00-X diethyl{4-[1,5,5-tris(4-diethylaminophenyl)penta-2,4-dienylidene]cyclohexa-2,5-dienylidene}ammonium butyltriphenylborate 418-070-1 141714-54-7 Skin Sens. 1 Dgr H360FD Repr. 1B; H360FD: C ≥ 6,5 % 005-012-00-X diethyl{4-[1,5,5-tris(4-diethylaminophenyl)penta-2,4-dienylidene]cyclohexa-2,5-dienylidene}ammonium butyltriphenylborate 418-070-1 141714-54-7 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H317 H400 … 40 unchanged lines … H412 005-016-00-1 tetrabutylammonium butyl tris-(4-tert-butylphenyl)borate 431-370-5 — Aquatic Chronic 4 H413 — H413 005-017-00-7 sodium perborate; [1] sodium peroxometaborate; [2] sodium peroxoborate; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 231-556-4 [2] 15120-21-5 [1] 7632-04-4 [2] Ox. Sol. 2 Repr. 1B Acute Tox. 4 * STOT SE 3 Eye Dam. 1 H272 H360Df H302 H335 H318 GHS03 GHS05 GHS08 GHS07 Dgr H272 H360Df H302 H335 H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-017-01-4 sodium perborate; [1] H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-017-01-4 sodium perborate; [1] sodium peroxometaborate; [2] sodium peroxoborate; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 231-556-4 [2] 15120-21-5 [1] 7632-04-4 [2] Ox. Sol. 2 Repr. 1B Acute Tox. 3 * Acute Tox. 4 * STOT SE 3 Eye Dam. 1 H272 H360Df H331 H302 H335 H318 GHS03 GHS06 GHS05 GHS08 Dgr H272 H360Df H331 H302 H335 H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-018-00-2 perboric acid (H3BO2(O2)), monosodium salt trihydrate; [1] H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-018-00-2 perboric acid (H3BO2(O2)), monosodium salt trihydrate; [1] perboric acid, sodium salt, tetrahydrate; [2] perboric acid (HBO(O2)), sodium salt, tetrahydrate [3] sodium peroxoborate hexahydrate; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 231-556-4 [3] 13517-20-9 [1] 37244-98-7 [2] 10486-00-7 [3] Repr. 1B STOT SE 3 Eye Dam. 1 H360Df H335 H318 GHS05 GHS08 GHS07 Dgr H360Df H335 H318 Repr. 1B; H360Df: C ≥ 14 % Repr. 1B; H360D: 10 % ≤ C < 14 % Eye Dam. 1; H318: C ≥ 36 % Eye Irrit. 2; H319: 22 % ≤ C < 36 % 005-018-01-X perboric acid (H3BO2(O2)), monosodium salt, trihydrate; [1] H318 Repr. 1B; H360Df: C ≥ 14 % Repr. 1B; H360D: 10 % ≤ C < 14 % Eye Dam. 1; H318: C ≥ 36 % Eye Irrit. 2; H319: 22 % ≤ C < 36 % 005-018-01-X perboric acid (H3BO2(O2)), monosodium salt, trihydrate; [1] perboric acid, sodium salt, tetrahydrate; [2] perboric acid (HBO(O2)), sodium salt, tetrahydrate; [3] sodium peroxoborate hexahydrate; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 231-556-4 [3] 13517-20-9 [1] 37244-98-7 [2] 10486-00-7 [3] Repr. 1B Acute Tox. 4 * STOT SE 3 Eye Dam. 1 H360Df H332 H335 H318 GHS05 GHS08 GHS07 Dgr H360Df H332 H335 H318 Repr. 1B; H360 Df: C ≥ 14 % Repr. 1B; H360D: 10 % ≤ C < 14 % Eye Dam. 1; H318: C ≥ 36 % Eye Irrit. 2; H319: 22 % ≤ C < 36 % 005-019-00-8 perboric acid, sodium salt; [1] H318 Repr. 1B; H360 Df: C ≥ 14 % Repr. 1B; H360D: 10 % ≤ C < 14 % Eye Dam. 1; H318: C ≥ 36 % Eye Irrit. 2; H319: 22 % ≤ C < 36 % 005-019-00-8 perboric acid, sodium salt; [1] perboric acid, sodium salt, monohydrate; [2] perboric acid (HBO(O2)), sodium salt, monohydrate; [3] sodium peroxoborate; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 234-390-0 [1] [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 234-390-0 [1] 234-390-0 [2] 231-556-4 [3] 11138-47-9 [1] 12040-72-1 [2] 10332-33-9 [3] Ox. Sol. 3 Repr. 1B Acute Tox. 4 * STOT SE 3 Eye Dam. 1 H272 H360Df H302 H335 H318 GHS03 GHS05 GHS08 GHS07 Dgr H272 H360Df H302 H335 H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-019-01-5 perboric acid, sodium salt; [1] H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 005-019-01-5 perboric acid, sodium salt; [1] perboric acid, sodium salt, monohydrate; [2] perboric acid (HBO(O2)), sodium salt, monohydrate [3] sodium peroxoborate; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 234-390-0 [1] [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 234-390-0 [1] 234-390-0 [2] 231-556-4 [3] 11138-47-9 [1] 12040-72-1 [2] … 16 unchanged lines … H331 H302 H335 H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 006-001-00-2 carbon monoxide 211-128-3 630-08-0 Flam. Gas 1 H318 Repr. 1B; H360Df: C ≥ 9 % Repr. 1B; H360D: 6,5 % ≤ C < 9 % Eye Dam. 1; H318: C ≥ 22 % Eye Irrit. 2; H319: 14 % ≤ C < 22 % 006-001-00-2 carbon monoxide 211-128-3 630-08-0 Flam. Gas 1 Press. Gas Repr. 1A Acute Tox. 3 * … 32 unchanged lines … H361fd H372 ** H319 H315 Repr. 2; H361fd: C ≥ 1 % STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤C < 1 % 006-004-00-9 calcium carbide 200-848-3 75-20-7 Water-react. 1 H260 GHS02 H315 Repr. 2; H361fd: C ≥ 1 % STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤C < 1 % 006-004-00-9 calcium carbide 200-848-3 75-20-7 Water-react. 1 H260 GHS02 Dgr H260 T 006-005-00-4 thiram (ISO); tetramethylthiuram disulphide 205-286-2 137-26-8 Acute Tox. 4 * … 31 unchanged lines … GHS09 Dgr H224 H330 H410 006-006-01-7 hydrogen cyanide … %; hydrocyanic acid … % 200-821-6 74-90-8 Acute Tox. 2 * H410 006-006-01-7 hydrogen cyanide … %; hydrocyanic acid … % 200-821-6 74-90-8 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * Aquatic Acute 1 … 115 unchanged lines … Wng H351 H302 H373** H410 M = 10 006-016-00-4 propoxur (ISO); H410 M = 10 006-016-00-4 propoxur (ISO); 2-isopropyloxyphenyl N-methylcarbamate; 2-isopropoxyphenyl methylcarbamate 204-043-8 114-26-1 Acute Tox. 3 * Aquatic Acute 1 … 248 unchanged lines … H302 H319 H335 H315 Carc. 1B; H350: C ≥ 0,001 % 006-042-00-6 monuron (ISO); H315 Carc. 1B; H350: C ≥ 0,001 % 006-042-00-6 monuron (ISO); 3-(4-chlorophenyl)-1,1-dimethylurea 205-766-1 150-68-5 Carc. 2 Acute Tox. 4 * Aquatic Acute 1 … 401 unchanged lines … H410 GHS07 GHS09 Wng H302 H410 006-086-00-6 ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate; fenoxycarb 276-696-7 72490-01-8 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 006-087-00-1 furathiocarb (ISO); H410 006-086-00-6 fenoxycarb (ISO); ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate 276-696-7 72490-01-8 Carc. 2 Aquatic Acute 1 Aquatic Chronic 1 H351 H400 H410 GHS08 GHS09 Wng H351 H410 M = 1 M = 10000 006-087-00-1 furathiocarb (ISO); 2,3-dihydro-2,2-dimethyl-7-benzofuryl 2,4-dimethyl-6-oxa-5-oxo-3-thia-2,4-diazadecanoate 265-974-3 65907-30-4 Acute Tox. 2 * Acute Tox. 3 * STOT RE 2 * … 17 unchanged lines … H319 H315 H317 H410 M = 100 006-088-00-7 benfuracarb (ISO); H410 M = 100 006-088-00-7 benfuracarb (ISO); ethyl N-[2,3-dihydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio]-N-isopropyl- β-alaninate — 82560-54-1 Repr. 2 Acute Tox. 3 * Acute Tox. 4 * … 24 unchanged lines … H330 H314 H400 EUH006 M = 1000 U 006-089-01-X chlorine dioxide . . . % 233-162-8 10049-04-4 Acute Tox. 3 * 006-089-01-X chlorine dioxide . . . % 233-162-8 10049-04-4 Acute Tox. 3 * Skin Corr. 1B Aquatic Acute 1 H301 H314 H400 GHS06 GHS05 GHS09 Dgr H301 H314 H400 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 0,3 % ≤ C < 10 % STOT SE 3; H335: C ≥ 3 % H400 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 0,3 % ≤ C < 10 % STOT SE 3; H335: C ≥ 3 % M = 10 B 006-090-00-8 2-(3-iodoprop-2-yn-1-yloxy)ethyl phenylcarbamate 408-010-0 88558-41-2 Acute Tox. 4 * Eye Dam. 1 … 134 unchanged lines … H400 GHS05 GHS09 Dgr H314 H400 STOT SE 3; H335: C ≥ 5 % B H400 STOT SE 3; H335: C ≥ 5 % B 007-002-00-0 nitrogen dioxide; [1] dinitrogen tetraoxide [2] 233-272-6 [1] 234-126-4 [2] 10102-44-0 [1] 10544-72-6 [2] Press. Gas Ox. Gas 1 Acute Tox. 2 * Skin Corr. 1B H270 H330 H314 GHS04 GHS03 GHS06 GHS05 Dgr H270 H330 H314 * STOT SE 3; H335: C ≥ 0,5 % 5 STOT SE 3; H335: C ≥ 0,5 % 5 007-003-00-6 chlormequat chloride (ISO); 2-chloroethyltrimethylammonium chloride 213-666-4 999-81-5 Acute Tox. 4 * Acute Tox. 4 * H312 H302 GHS07 Wng H312 H302 007-004-00-1 nitric acid … % 231-714-2 7697-37-2 Ox. Liq. 3 H302 007-004-00-1 nitric acid … % 231-714-2 7697-37-2 Ox. Liq. 3 Skin Corr. 1A H272 H314 GHS03 GHS05 Dgr H272 H314 Skin Corr. 1A; H314: C ≥ 20 % Skin Corr. 1B; H314: 5 % ≤ C < 20 % Ox. Liq. 3; H272: C ≥ 65 % B H314 Skin Corr. 1A; H314: C ≥ 20 % Skin Corr. 1B; H314: 5 % ≤ C < 20 % Ox. Liq. 3; H272: C ≥ 65 % B 007-006-00-2 ethyl nitrite 203-722-6 109-95-5 Flam. Gas 1 Press. Gas Acute Tox. 4 * … 37 unchanged lines … H301 H314 H317 H410 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 3 % ≤ C < 10 % 007-009-00-9 dicyclohexylammonium nitrite 221-515-9 3129-91-7 Acute Tox. 4 * H410 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 3 % ≤ C < 10 % 007-009-00-9 dicyclohexylammonium nitrite 221-515-9 3129-91-7 Acute Tox. 4 * Acute Tox. 4 * H332 H302 GHS07 Wng H332 … 50 unchanged lines … H331 H311 H301 H411 Carc. 1B; H350: C ≥ 0,01 % 007-014-00-6 salts of hydrazine — — Carc. 1B H411 Carc. 1B; H350: C ≥ 0,01 % 007-014-00-6 salts of hydrazine — — Carc. 1B Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * … 229 unchanged lines … Dgr H271 H332 H302 H314 Ox. Liq. 1; H271: C ≥ 70 %**** Ox. Liq. 2; H272: 50 % ≤ C < 70 % **** H314 Ox. Liq. 1; H271: C ≥ 70 %**** Ox. Liq. 2; H272: 50 % ≤ C < 70 % **** * Skin Corr. 1A; H314: C ≥ 70 % Skin Corr. 1B; H314: 50 % ≤ C < 70 % Skin Irrit. 2; H315: 35 % ≤ C < 50 % Eye Dam. 1; H318: 8 % ≤ C < 50 % Eye Irrit. 2; H319: 5 % ≤ C < 8 % STOT SE 3; H335; C ≥ 35 % B Skin Corr. 1A; H314: C ≥ 70 % Skin Corr. 1B; H314: 50 % ≤ C < 70 % Skin Irrit. 2; H315: 35 % ≤ C < 50 % Eye Dam. 1; H318: 8 % ≤ C < 50 % Eye Irrit. 2; H319: 5 % ≤ C < 8 % STOT SE 3; H335; C ≥ 35 % B 009-001-00-0 fluorine 231-954-8 7782-41-4 Press. Gas Ox. Gas 1 Acute Tox. 2 * … 16 unchanged lines … Dgr H330 H310 H300 H314 009-003-00-1 hydrofluoric acid … % 231-634-8 7664-39-3 Acute Tox. 2 * H314 009-003-00-1 hydrofluoric acid … % 231-634-8 7664-39-3 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * Skin Corr. 1A H330 H310 H300 H314 GHS06 GHS05 Dgr H330 H310 H300 H314 Skin Corr. 1A; H314: C ≥ 7 % Skin Corr. 1B; H314: 1 % ≤ C < 7 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % B H314 Skin Corr. 1A; H314: C ≥ 7 % Skin Corr. 1B; H314: 1 % ≤ C < 7 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % B 009-004-00-7 sodium fluoride 231-667-8 7681-49-4 Acute Tox. 3 * Eye Irrit. 2 Skin Irrit. 2 H301 … 22 unchanged lines … GHS05 Dgr H301 H314 * Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-008-00-9 potassium bifluoride; Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-008-00-9 potassium bifluoride; potassium hydrogen difluoride 232-156-2 7789-29-9 Acute Tox. 3 * Skin Corr. 1B H301 H314 GHS06 GHS05 Dgr H301 H314 * Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-009-00-4 ammonium bifluoride; Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-009-00-4 ammonium bifluoride; ammonium hydrogen difluoride 215-676-4 1341-49-7 Acute Tox. 3 * Skin Corr. 1B H301 H314 GHS06 GHS05 Dgr H301 H314 * Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-010-00-X fluoroboric acid ... % 240-898-3 16872-11-0 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B 009-011-00-5 fluorosilicic acid ... % 241-034-8 16961-83-4 Skin Corr. 1B H314 GHS05 Skin Corr. 1B; H314: C ≥ 1 % Skin Irrit. 2; H315: 0,1 % ≤ C < 1 % Eye Irrit. 2; H319: 0,1 % ≤ C < 1 % 009-010-00-X fluoroboric acid ... % 240-898-3 16872-11-0 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B 009-011-00-5 fluorosilicic acid ... % 241-034-8 16961-83-4 Skin Corr. 1B H314 GHS05 Dgr H314 B 009-012-00-0 alkali fluorosilicates(Na); [1] alkali fluorosilicates(K); [2] … 41 unchanged lines … Dgr H331 H373 ** H400 U 009-016-00-2 trisodium hexafluoroaluminate [1] 237-410-6 [1] 13775-53-6 [1] STOT RE 1 009-016-00-2 trisodium hexafluoroaluminate [1] 237-410-6 [1] 13775-53-6 [1] STOT RE 1 Acute Tox. 4 Aquatic Chronic 2 H372 H332 H411 GHS07 GHS08 GHS09 Dgr H372 H332 H411 trisodium hexafluoroaluminate (cryolite) [2] 239-148-8 [2] 15096-52-3 [2] H411 trisodium hexafluoroaluminate (cryolite) [2] 239-148-8 [2] 15096-52-3 [2] 009-017-00-8 potassium mu-fluoro-bis(triethylaluminium) 400-040-2 12091-08-6 Flam. Sol. 1 Water-react. 1 Skin Corr. 1A … 15 unchanged lines … Dgr H260 H314 EUH014 011-002-00-6 sodium hydroxide; caustic soda 215-185-5 1310-73-2 Skin Corr. 1A H314 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 5 % Skin Corr. 1B; H314: 2 % ≤ C < 5 % Skin Irrit. 2; H315: 0,5 % ≤ C < 2 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % 011-003-00-1 sodium peroxide 215-209-4 1313-60-6 Ox. Sol. 1 Dgr H314 Skin Corr. 1A; H314: C ≥ 5 % Skin Corr. 1B; H314: 2 % ≤ C < 5 % Skin Irrit. 2; H315: 0,5 % ≤ C < 2 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % 011-003-00-1 sodium peroxide 215-209-4 1313-60-6 Ox. Sol. 1 Skin Corr. 1A H271 H314 GHS03 GHS05 … 117 unchanged lines … H302 H314 EUH014 EUH029 * STOT SE 3; H335: C ≥ 1 % T STOT SE 3; H335: C ≥ 1 % T 014-002-00-4 silicon tetrachloride 233-054-0 10026-04-7 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 … 24 unchanged lines … Dgr H225 H319 H335 H315 EUH014 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 014-005-00-0 tetraethyl silicate; H315 EUH014 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 014-005-00-0 tetraethyl silicate; ethyl silicate 201-083-8 78-10-4 Flam. Liq. 3 Acute Tox. 4 * Eye Irrit. 2 … 199 unchanged lines … H317 GHS07 Wng H302 H317 014-042-00-2 reaction mass of: O,O',O'',O'''-silanetetrayl tetrakis(4-methyl-2-pentanone oxime) (3 stereoisomers) 423-010-0 — Eye Dam. 1 H318 GHS05 Dgr H318 014-043-00-8 reaction product of amorphous silica (50-85 %), butyl (1-methylpropyl) magnesium (3-15 %), tetraethyl orthosilicate (5-15 %) and titanium tetrachloride (5-20 %) 432-200-2 — STOT SE 3 Dgr H318 014-043-00-8 reaction product of amorphous silica (50-85 %), butyl (1-methylpropyl) magnesium (3-15 %), tetraethyl orthosilicate (5-15 %) and titanium tetrachloride (5-20 %) 432-200-2 — STOT SE 3 Skin Irrit. 2 Eye Dam. 1 Aquatic Chronic 3 H335 … 90 unchanged lines … H302 H314 EUH014 EUH029 015-010-00-0 phosphorus pentoxide 215-236-1 1314-56-3 Skin Corr. 1A H314 GHS05 Dgr H314 015-011-00-6 phosphoric acid ... %, orthophosphoric acid ... % 231-633-2 7664-38-2 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B Dgr H314 015-011-00-6 phosphoric acid ... %, orthophosphoric acid ... % 231-633-2 7664-38-2 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B 015-012-00-1 tetraphosphorus trisulphide; phosphorus sesquisulphid 215-245-0 1314-85-8 Flam. Sol. 2 Water-react. 1 … 23 unchanged lines … H411 GHS08 GHS09 Dgr H370 ** H411 STOT SE 1; H370: C ≥ 1 % STOT SE 2; H371: 0,2 % ≤ C < 1 % C H411 STOT SE 1; H370: C ≥ 1 % STOT SE 2; H371: 0,2 % ≤ C < 1 % C 015-016-00-3 tricresyl phosphate (m-m-m-, m-m-p-, m-p-p-, p-p-p-); tritolyl phosphate (m-m-m-, m-m-p-, m-p-p-, p-p-p-); 201-105-6 78-32-0 Acute Tox. 4 * Acute Tox. 4 * … 243 unchanged lines … H400 H410 015-041-00-X malathion (ISO); 1,2-bis(ethoxycarbonyl)ethyl O,O-dimethyl phosphorodithioate; [containing ≤ 0,03 % isomalathion] 204-497-7 121-75-5 Acute Tox. 4 * [containing ≤ 0,03 % isomalathion] 204-497-7 121-75-5 Acute Tox. 4 * Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H302 … 636 unchanged lines … GHS09 Wng H319 H315 H410 Skin Irrit. 2; H315: C ≥ 5 % Eye Irrit. 2; H319: C ≥ 5 % 015-106-00-2 hexamethylphosphoric triamide; H410 Skin Irrit. 2; H315: C ≥ 5 % Eye Irrit. 2; H319: C ≥ 5 % 015-106-00-2 hexamethylphosphoric triamide; hexamethylphosphoramide 211-653-8 680-31-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 Carc. 1B; H350: C ≥ 0,01 % 015-107-00-8 ethoprophos (ISO); H340 Carc. 1B; H350: C ≥ 0,01 % 015-107-00-8 ethoprophos (ISO); ethyl-S,S-dipropyl phosphorodithioate 236-152-1 13194-48-4 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 3 * … 74 unchanged lines … GHS09 Dgr H310 H300 H410 M = 10 015-115-00-1 chlorthiophos (ISO); H410 M = 10 015-115-00-1 chlorthiophos (ISO); [isomeric reaction mass in which O-2,5-dichlorophenyl-4-methylthiophenyl O,O-diethyl phosphorothioate predominates] 244-663-6 21923-23-9 Acute Tox. 2 * Acute Tox. 3 * Aquatic Acute 1 Aquatic Chronic 1 H300 H311 H400 H410 GHS06 GHS09 Dgr H300 H311 H410 M = 1000 015-116-00-7 demephion-O (ISO); H410 M = 1000 015-116-00-7 demephion-O (ISO); O,O-dimethyl O-2-methylthioethyl phosphorothioate 211-666-9 682-80-4 Acute Tox. 2 * Acute Tox. 3 * H300 H311 GHS06 … 309 unchanged lines … H301 H373 ** H317 H410 015-154-00-4 2-chloroethylphosphonic acid; ethephon 240-718-3 16672-87-0 Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1B Aquatic Chronic 3 H332 H312 H410 015-154-00-4 ethephon; 2-chloroethylphosphonic acid 240-718-3 16672-87-0 Acute Tox. 3 Acute Tox. 4 Acute Tox. 4 Skin Corr. 1C Aquatic Chronic 2 H311 H332 H302 H314 H412 GHS05 GHS07 Dgr H332 H312 H411 GHS06 GHS05 GHS09 Dgr H311 H332 H302 H314 H412 STOT SE 3; H335: C ≥ 5 % 015-155-00-X glufosinate ammonium (ISO); H411 EUH071 015-155-00-X glufosinate ammonium (ISO); ammonium 2-amino-4-(hydroxymethylphosphinyl)butyrate 278-636-5 77182-82-2 Repr. 1B Acute Tox. 4 * Acute Tox. 4 * … 275 unchanged lines … Aquatic Chronic 3 H315 H412 GHS07 Wng H315 H412 015-192-00-1 tetrakis(2,6-dimethylphenyl)-m-phenylene biphosphate 432-770-2 139189-30-3 Skin Sens. 1 Aquatic Chronic 4 H317 H413 GHS07 Wng H317 H413 015-193-00-7 triphenyl(phenylmethyl)phosphonium 1,1,2,2,3,3,4,4,4-nonafluoro-N-methyl-1-butanesulfonamide (1:1) 442-960-7 332350-93-3 Acute Tox. 3 * H412 015-192-00-1 tetrakis(2,6-dimethylphenyl)-m-phenylene biphosphate 432-770-2 139189-30-3 Skin Sens. 1 H317 GHS07 Wng H317 015-193-00-7 triphenyl(phenylmethyl)phosphonium 1,1,2,2,3,3,4,4,4-nonafluoro-N-methyl-1-butanesulfonamide (1:1) 442-960-7 332350-93-3 Acute Tox. 3 * Eye Dam. 1 Aquatic Acute 1 Aquatic Chronic 1 H301 … 57 unchanged lines … Dgr H350 H361f H372 (lungs) STOT RE 1; H372: C ≥0,1 % H372: C ≥0,1 % Carc 1B; H350: C ≥0,01 % H350: C ≥0,01 % STOT RE 2; H373: 0,01 % ≤ C < 0,1 % 015-201-00-9 trixylyl phosphate 246-677-8 25155-23-1 Repr. 1B H360F GHS08 H373: 0,01 % ≤ C < 0,1 % 015-201-00-9 trixylyl phosphate 246-677-8 25155-23-1 Repr. 1B H360F GHS08 Dgr H360F 015-202-00-4 tris(nonylphenyl) phosphite 247-759-6 26523-78-4 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H317 … 71 unchanged lines … H400 GHS05 GHS09 Dgr H314 H400 EUH031 EUH031: C ≥ 1 % 016-009-00-8 disodium sulfide; H400 EUH031 EUH031: C ≥ 1 % 016-009-00-8 disodium sulfide; sodium sulfide 215-211-5 1313-82-2 Acute Tox. 3 * Acute Tox. 4 * Skin Corr. 1B … 37 unchanged lines … H332 H314 H400 EUH014 EUH029 STOT SE 3; H335: C ≥ 1 % 016-013-00-X sulphur dichloride 234-129-0 10545-99-0 Skin Corr. 1B EUH029 STOT SE 3; H335: C ≥ 1 % 016-013-00-X sulphur dichloride 234-129-0 10545-99-0 Skin Corr. 1B STOT SE 3 Aquatic Acute 1 H314 H335 H400 GHS05 GHS07 GHS09 Dgr H314 H335 H400 EUH014 STOT SE 3; H335: C ≥ 5 % 016-014-00-5 sulphur tetrachloride — 13451-08-6 Skin Corr. 1B H400 EUH014 STOT SE 3; H335: C ≥ 5 % 016-014-00-5 sulphur tetrachloride — 13451-08-6 Skin Corr. 1B Aquatic Acute 1 H314 H400 GHS05 GHS09 Dgr H314 H400 EUH014 STOT SE 3; H335: C ≥ 5 % 016-015-00-0 thionyl dichloride; H400 EUH014 STOT SE 3; H335: C ≥ 5 % 016-015-00-0 thionyl dichloride; thionyl chloride 231-748-8 7719-09-7 Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1A H332 H302 H314 GHS05 GHS07 Dgr H332 H302 H314 EUH014 EUH029 STOT SE 3; H335: C ≥ 1 % 016-016-00-6 sulphuryl chloride 232-245-6 7791-25-5 Skin Corr. 1B EUH029 STOT SE 3; H335: C ≥ 1 % 016-016-00-6 sulphuryl chloride 232-245-6 7791-25-5 Skin Corr. 1B STOT SE 3 H314 H335 GHS05 GHS07 Dgr H314 H335 EUH014 016-017-00-1 chlorosulphonic acid 232-234-6 7790-94-5 Skin Corr. 1A STOT SE 3 H314 H335 GHS05 GHS07 Dgr H314 H335 EUH014 016-018-00-7 fluorosulphonic acid 232-149-4 7789-21-1 Acute Tox. 4 * Skin Corr. 1A H332 H314 GHS05 GHS07 Dgr H332 H314 016-019-00-2 oleum ... % SO3 — — Skin Corr. 1A H314 016-019-00-2 oleum ... % SO3 — — Skin Corr. 1A STOT SE 3 H314 H335 GHS05 GHS07 Dgr H314 H335 EUH014 B 016-020-00-8 sulphuric acid ... % 231-639-5 7664-93-9 Skin Corr. 1A H314 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 15 % Skin Irrit. 2; H315: 5 % ≤ C < 15 % Eye Irrit. 2; H319: 5 % ≤ C < 15 % B 016-020-00-8 sulphuric acid ... % 231-639-5 7664-93-9 Skin Corr. 1A H314 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 15 % Skin Irrit. 2; H315: 5 % ≤ C < 15 % Eye Irrit. 2; H319: 5 % ≤ C < 15 % B 016-021-00-3 methanethiol; methyl mercaptan 200-822-1 74-93-1 Flam. Gas. 1 Press. Gas … 39 unchanged lines … H330 H301 H314 H317 Carc. 1B; H350: C ≥ 0,01 % Muta. 2; H341: C ≥ 0,01 % STOT SE 3; H335: C ≥ 5 % 016-024-00-X dimexano(ISO); H317 Carc. 1B; H350: C ≥ 0,01 % Muta. 2; H341: C ≥ 0,01 % STOT SE 3; H335: C ≥ 5 % 016-024-00-X dimexano(ISO); bis(methoxythiocarbonyl) disulphide 215-993-8 1468-37-7 Acute Tox. 4 * Aquatic Acute 1 Aquatic Chronic 1 H302 … 44 unchanged lines … H302 GHS02 GHS07 Dgr H251 H302 EUH031 016-029-00-7 p-toluenesulphonic acid, containing more than 5 % H2SO4 — — Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % 016-030-00-2 p-toluenesulphonic acid (containing a maximum of 5 % H2SO4) 203-180-0 104-15-4 Eye Irrit. 2 H302 EUH031 016-029-00-7 p-toluenesulphonic acid, containing more than 5 % H2SO4 — — Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % 016-030-00-2 p-toluenesulphonic acid (containing a maximum of 5 % H2SO4) 203-180-0 104-15-4 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 H335 H315 GHS07 Wng H319 H335 H315 STOT SE 3; H335: C ≥ 20 % 016-031-00-8 tetrahydrothiophene-1,1-dioxide; H315 STOT SE 3; H335: C ≥ 20 % 016-031-00-8 tetrahydrothiophene-1,1-dioxide; sulpholane 204-783-1 126-33-0 Acute Tox. 4 * H302 GHS07 Wng H302 016-032-00-3 1,3-propanesultone; 1,2-oxathiolane 2,2-dioxide 214-317-9 1120-71-4 Carc. 1B Acute Tox. 4 * Acute Tox. 4 * H350 H312 H302 GHS08 GHS07 Dgr H350 H312 H302 Carc. 1B; H350: C ≥ 0,01 % 016-033-00-9 dimethylsulfamoylchloride 236-412-4 13360-57-1 Carc. 1B H302 Carc. 1B; H350: C ≥ 0,01 % 016-033-00-9 dimethylsulfamoylchloride 236-412-4 13360-57-1 Carc. 1B Acute Tox. 2 * Acute Tox. 4 * Acute Tox. 4 * … 81 unchanged lines … H302 H319 H335 H317 016-055-00-9 tetrasodium 4-amino-3,6-bis(5-(6-chloro-4-(2-hydroxyethylamino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxynaphthalene-2,7-sulfonate (containing > 35 % sodium chloride and sodium acetate) 400-510-7 — Eye Dam. 1 H317 016-055-00-9 tetrasodium 4-amino-3,6-bis(5-(6-chloro-4-(2-hydroxyethylamino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxynaphthalene-2,7-sulfonate (containing > 35 % sodium chloride and sodium acetate) 400-510-7 — Eye Dam. 1 Skin Sens. 1 H318 H317 GHS05 GHS07 … 88 unchanged lines … H318 GHS05 GHS07 Dgr H302 H318 EUH031 016-064-00-8 sodium hydrogensulphite . . . %; sodium bisulphite . . . % 231-548-0 7631-90-5 Acute Tox. 4 * H302 GHS07 H318 EUH031 016-064-00-8 sodium hydrogensulphite . . . %; sodium bisulphite . . . % 231-548-0 7631-90-5 Acute Tox. 4 * H302 GHS07 Wng H302 EUH031 B 016-065-00-3 sodium 1-amino-4-[2-methyl-5-(4-methylphenylsulfonylamino)phenylamino]anthraquinone-2-sulfonate 400-100-8 84057-97-6 Aquatic Chronic 2 H411 GHS09 H411 016-066-00-9 tetrasodium [5-((4-amino-6-chloro-1,3,5-triazin-2-yl)amino)-2-((2-hydroxy-3,5-disulfonatophenylazo)-2- sulfonatobenzylidenehydrazino)benzoate]copper(II) 404-070-7 116912-62-0 Aquatic Chronic 3 H412 — H412 016-067-00-4 (4-methylphenyl)mesitylene sulfonate 407-530-5 67811-06-7 Aquatic Chronic 4 H413 — H413 016-068-00-X sodium 3,5-bis(tetradecyloxycarbonyl)benzenesulfinate 407-720-8 155160-86-4 Skin Sens. 1 Aquatic Chronic 2 H317 … 203 unchanged lines … H319 H335 H315 H400 M = 100 U H400 M = 100 U 017-002-00-2 hydrogen chloride 231-595-7 7647-01-0 Press. Gas Acute Tox. 3 * Skin Corr. 1A H331 H314 GHS04 GHS06 GHS05 Dgr H331 H314 U5 017-002-01-X hydrochloric acid ... % 231-595-7 — Skin Corr. 1B 017-002-01-X hydrochloric acid ... % 231-595-7 — Skin Corr. 1B STOT SE 3 H314 H335 GHS05 GHS07 Dgr H314 H335 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % STOT SE 3; H335: C ≥ 10 % B H335 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % STOT SE 3; H335: C ≥ 10 % B 017-003-00-8 barium chlorate 236-760-7 13477-00-4 Ox. Sol. 1 Acute Tox. 4 * Acute Tox. 4 * … 27 unchanged lines … GHS09 Dgr H271 H302 H411 017-006-00-4 perchloric acid ... % 231-512-4 7601-90-3 Ox. Liq. 1 H411 017-006-00-4 perchloric acid ... % 231-512-4 7601-90-3 Ox. Liq. 1 Skin Corr. 1A H271 H314 GHS03 GHS05 Dgr H271 H314 Skin Corr. 1A; H314: C ≥ 50 % Skin Corr. 1B; H314: 10 % ≤ C < 50 % Skin Irrit. 2; H315: 1 % ≤ C < 10 % Eye Irrit. 2; H319: 1 % ≤ C < 10 % Ox. Liq. 1; H271: C > 50 %: Ox. Liq. 2; H272: C ≤ 50 %: B H314 Skin Corr. 1A; H314: C ≥ 50 % Skin Corr. 1B; H314: 10 % ≤ C < 50 % Skin Irrit. 2; H315: 1 % ≤ C < 10 % Eye Irrit. 2; H319: 1 % ≤ C < 10 % Ox. Liq. 1; H271: C > 50 %: Ox. Liq. 2; H272: C ≤ 50 %: B 017-007-00-X barium perchlorate 236-710-4 13465-95-7 Ox. Sol. 1 Acute Tox. 4 * Acute Tox. 4 * H271 … 17 unchanged lines … H302 GHS03 GHS07 Dgr H271 H302 017-011-00-1 sodium hypochlorite, solution ... % Cl active 231-668-3 7681-52-9 Skin Corr. 1B H302 017-011-00-1 sodium hypochlorite, solution ... % Cl active 231-668-3 7681-52-9 Skin Corr. 1B Aquatic Acute 1 H314 H400 GHS05 GHS09 Dgr H314 H400 EUH031 EUH031: C ≥ 5 % B H400 EUH031 EUH031: C ≥ 5 % B 017-012-00-7 calcium hypochlorite 231-908-7 7778-54-3 Ox. Sol. 2 Acute Tox. 4 * Skin Corr. 1B Aquatic Acute 1 H272 H302 H314 H400 GHS03 GHS05 GHS07 GHS09 Dgr H272 H302 H314 H400 EUH031 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 1 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 3 % M = 10 T H400 EUH031 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 1 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 3 % M = 10 T 017-013-00-2 calcium chloride 233-140-8 10043-52-4 Eye Irrit. 2 H319 GHS07 Wng H319 017-014-00-8 ammonium chloride 235-186-4 12125-02-9 Acute Tox. 4 * Eye Irrit. 2 H302 … 71 unchanged lines … Dgr H270 H330 H314 H400 M = 10 5 H400 M = 10 5 017-026-01-0 chlorine dioxide … % 233-162-8 10049-04-4 Acute Tox. 3 * Skin Corr. 1B Aquatic Acute 1 H301 H314 H400 GHS06 GHS05 GHS09 Dgr H301 H314 H400 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 1 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,3 % ≤ C < 3 % STOT SE 3; H335: C ≥ 3 % M = 10 B H400 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 1 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,3 % ≤ C < 3 % STOT SE 3; H335: C ≥ 3 % M = 10 B 019-001-00-2 potassium 231-119-8 7440-09-7 Water-react. 1 Skin Corr. 1B H260 H314 GHS02 GHS05 Dgr H260 H314 EUH014 019-002-00-8 potassium hydroxide; caustic potash 215-181-3 1310-58-3 Acute Tox. 4 * Skin Corr. 1A H302 H314 GHS05 GHS07 Dgr H302 H314 Skin Corr. 1A; H314: C ≥ 5 % Skin Corr. 1B; H314: 2 % ≤ C < 5 % Skin Irrit. 2; H315: 0,5 % ≤ C < 2 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % 020-001-00-X calcium 231-179-5 7440-70-2 Water-react. 2 H261 GHS02 H314 Skin Corr. 1A; H314: C ≥ 5 % Skin Corr. 1B; H314: 2 % ≤ C < 5 % Skin Irrit. 2; H315: 0,5 % ≤ C < 2 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % 020-001-00-X calcium 231-179-5 7440-70-2 Water-react. 2 H261 GHS02 Dgr H261 020-002-00-5 calcium cyanide 209-740-0 592-01-8 Acute Tox. 2 * Aquatic Acute 1 Aquatic Chronic 1 H300 … 100 unchanged lines … H314 H334 H317 H410 STOT SE 3; H335: C ≥ 1 % 024-002-00-6 potassium dichromate 231-906-6 7778-50-9 Ox. Sol. 2 H410 STOT SE 3; H335: C ≥ 1 % 024-002-00-6 potassium dichromate 231-906-6 7778-50-9 Ox. Sol. 2 Carc. 1B Muta. 1B Repr. 1B … 33 unchanged lines … H314 H334 H317 H410 STOT SE 3; H335: C ≥ 5 % 3 H410 STOT SE 3; H335: C ≥ 5 % 3 024-003-00-1 ammonium dichromate 232-143-1 7789-09-5 Ox. Sol. 2 **** Carc. 1B Muta. 1B … 34 unchanged lines … H314 H334 H317 H410 STOT SE 3; H335: C ≥ 5 % Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % G3 H410 STOT SE 3; H335: C ≥ 5 % Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % G3 024-004-00-7 sodium dichromate 234-190-3 10588-01-9 Ox. Sol. 2 Carc. 1B Muta. 1B … 34 unchanged lines … H314 H334 H317 H410 Resp. Sens. 1; H334: C ≥ 0,2 % Skin Sens. 1; H317: C ≥ 0,2 % STOT SE 3; H335: C ≥ 5 % 3 H410 Resp. Sens. 1; H334: C ≥ 0,2 % Skin Sens. 1; H317: C ≥ 0,2 % STOT SE 3; H335: C ≥ 5 % 3 024-004-01-4 sodium dichromate, dihydrate 234-190-3 7789-12-0 Ox. Sol. 2 Carc. 1B Muta. 1B … 34 unchanged lines … H314 H334 H317 H410 STOT SE 3; H335: C ≥ 5 % Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % 3 H410 STOT SE 3; H335: C ≥ 5 % Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % 3 024-005-00-2 chromyl dichloride; chromic oxychloride 239-056-8 14977-61-8 Ox. Liq. 1 Carc. 1B … 17 unchanged lines … H340 H314 H317 H410 Skin Corr. 1A; H314: C ≥ 10 % Skin Corr. 1B; H314: 5 % ≤ C < 10 % Skin Irrit. 2; H315: 0,5 % ≤ C < 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 5 % STOT SE 3; H335: 0,5 % ≤ C < 5 % Skin Sens. 1; H317: C ≥ 0,5 % T3 H410 Skin Corr. 1A; H314: C ≥ 10 % Skin Corr. 1B; H314: 5 % ≤ C < 10 % Skin Irrit. 2; H315: 0,5 % ≤ C < 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 5 % STOT SE 3; H335: 0,5 % ≤ C < 5 % Skin Sens. 1; H317: C ≥ 0,5 % T3 024-006-00-8 potassium chromate 232-140-5 7789-00-6 Carc. 1B Muta. 1B Eye Irrit. 2 … 17 unchanged lines … H335 H315 H317 H410 Skin Sens. 1; H317: C ≥ 0,5 % 3 H410 Skin Sens. 1; H317: C ≥ 0,5 % 3 024-007-00-3 zinc chromates including zinc potassium chromate — — Carc. 1A Acute Tox. 4 * Skin Sens. 1 … 132 unchanged lines … H314 H334 H317 H410 Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % 3 H410 Resp. Sens.; H334: C ≥ 0,2 % Skin Sens.; H317: C ≥ 0,2 % 3 024-019-00-9 Main component: acetoacetic acid anilide/3-amino-1-hydroxybenzene (ATAN-MAP): trisodium {6-[(2 or 3 or 4)-amino-(4 or 5 or 6)-hydroxyphenylazo]-5'-(phenylsulfamoyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato}-{6''-[1-(phenylcarbamoyl)ethylazo]-5'''-(phenylsulfamoyl)-3''-sulfonatonaphthalene-2''-azobenzene-1'',2'''-diolato}chromate (III); by-product 1: acetoacetic acid anilide/acetoacetic acid anilide (ATAN-ATAN): trisodium bis{6-[1-(phenylcarbamoyl)ethylazo]-5'-(phenylsulfonyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato}chromate (III); by-product 2: 3-amino-1-hydroxybenzene/3-amino-1-hydroxybenzene (MAP-MAP): trisodium bis{6-[(2 or 3 or 4)-amino-(4 or 5 or 6)-hydroxyphenylazo]-5'-(phenylsulfamoyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato} chromate (III) 419-230-1 — Skin Sens. 1 … 58 unchanged lines … H315 GHS07 Wng H302 H319 H315 Skin Irrit. 2; H315: C ≥ 25 % 026-004-00-2 potassium ferrite 430-010-4 12160-44-0 Skin Corr. 1B H315 Skin Irrit. 2; H315: C ≥ 25 % 026-004-00-2 potassium ferrite 430-010-4 12160-44-0 Skin Corr. 1B Skin Sens. 1 H314 H317 GHS05 GHS07 … 45 unchanged lines … H302 H334 H317 H410 Carc. 1B; H350i: C ≥ 0,01 % H410 Carc. 1B; H350i: C ≥ 0,01 % M=10 1 027-005-00-0 cobalt sulfate 233-334-2 10124-43-3 Carc. 1B Muta. 2 … 18 unchanged lines … H302 H334 H317 H410 Carc. 1B; H350i: C ≥ 0,01 % H410 Carc. 1B; H350i: C ≥ 0,01 % M=10 1 027-006-00-6 cobalt di(acetate) 200-755-8 71-48-7 Carc. 1B Muta. 2 Repr. 1B Resp. Sens. 1 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H350i H341 H360F*** H334 H317 H400 H410 GHS08 GHS09 Dgr H350i H341 H360F*** H334 H317 H410 Carc. 1B; H350i: C ≥ 0,01 % M = 10 1 H410 Carc. 1B; H350i: C ≥ 0,01 % M = 10 1 027-007-00-1 zinc hexacyanocobaltate(III), tertiary butyl alcohol/polypropylene glycol complex 425-240-7 — Eye Dam. 1 Aquatic Chronic 2 H318 H411 GHS05 … 19 unchanged lines … H360F*** H334 H317 H410 Carc. 1B; H350i: C ≥ 0,01 % M = 10 1 H410 Carc. 1B; H350i: C ≥ 0,01 % M = 10 1 027-010-00-8 cobalt carbonate 208-169-4 513-79-1 Carc. 1B Muta. 2 Repr. 1B Resp. Sens. 1 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H350i H341 H360F*** H334 H317 H400 H410 GHS08 GHS09 Dgr H350i H341 H360F*** H334 H317 H410 Carc. 1B; H350i: C ≥ 0,01 % H410 Carc. 1B; H350i: C ≥ 0,01 % M=10 1 028-001-00-1 tetracarbonylnickel; nickel tetracarbonyl 236-669-2 13463-39-3 Flam. Liq. 2 … 24 unchanged lines … H372** H317 S7 028-002-01-4 nickel powder; [particle diameter < 1 mm] 231-111-4 7440-02-0 Carc. 2 [particle diameter < 1 mm] 231-111-4 7440-02-0 Carc. 2 STOT RE 1 Skin Sens. 1 Aquatic Chronic 3 H351 … 154 unchanged lines … H315 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-010-00-0 nickel carbonate; H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-010-00-0 nickel carbonate; basic nickel carbonate; carbonic acid, nickel (2+) salt; [1] carbonic acid, nickel salt; [2] … 68 unchanged lines … H315 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % < C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-012-00-1 nickel dinitrate; [1] H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % < C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-012-00-1 nickel dinitrate; [1] nitric acid, nickel salt [2] 236-068-5 [1] 238-076-4 [2] 13138-45-9 [1] 14216-75-2 [2] Ox. Sol. 2 … 36 unchanged lines … H318 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % < C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-013-00-7 nickel matte 273-749-6 69012-50-6 Carc. 1A H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % < C < 1 % Skin Irrit. 2; H315: C ≥ 20 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-013-00-7 nickel matte 273-749-6 69012-50-6 Carc. 1A STOT RE 1 Skin Sens. 1 Aquatic Acute 1 … 40 unchanged lines … H315 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 028-015-00-8 slimes and sludges, copper electrolyte refining, decopperised 305-433-1 94551-87-8 Carc. 1A Muta. 2 Repr. 1A … 44 unchanged lines … H314 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-017-00-9 nickel dipotassium bis(sulfate); [1] diammonium nickel bis(sulfate) [2] 237-563-9 [1] … 27 unchanged lines … H302 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-018-00-4 nickel bis(sulfamidate); nickel sulfamate 237-396-1 13770-89-3 Carc. 1A … 18 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-019-00-X nickel bis(tetrafluoroborate) 238-753-4 14708-14-6 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-021-00-0 nickel diformate; [1] formic acid, nickel salt; [2] … 23 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-022-00-6 nickel di(acetate); [1] nickel acetate [2] 206-761-7 [1] … 27 unchanged lines … H302 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-024-00-7 nickel dibenzoate 209-046-8 553-71-9 Carc. 1A H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M = 1 028-024-00-7 nickel dibenzoate 209-046-8 553-71-9 Carc. 1A Muta. 2 Repr. 1B STOT RE 1 … 15 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-025-00-2 nickel bis(4-cyclohexylbutyrate) 223-463-2 3906-55-6 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 028-026-00-8 nickel(II) stearate; nickel(II) octadecanoate 218-744-1 2223-95-2 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-027-00-3 nickel dilactate — 16039-61-5 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-028-00-9 nickel(II) octanoate 225-656-7 4995-91-9 Carc. 1A Muta. 2 … 21 unchanged lines … H314 H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-029-00-4 nickel difluoride; [1] nickel dibromide; [2] … 26 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-030-00-X nickel hexafluorosilicate 247-430-7 26043-11-8 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-031-00-5 nickel selenate 239-125-2 15060-62-5 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-032-00-0 nickel hydrogen phosphate; [1] nickel bis(dihydrogen phosphate); [2] … 263 unchanged lines … H372** H334 H317 H410 EUH032 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 EUH032 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-047-00-2 nickel dichromate 239-646-5 15586-38-6 Carc. 1A Muta. 2 … 17 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-048-00-8 nickel(II) selenite 233-263-7 10101-96-9 Carc. 1A STOT RE 1 … 101 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 %1 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 %1 M=1 H 028-054-00-0 nickel(II) trifluoroacetate; [1] nickel(II) propionate; [2] … 24 unchanged lines … (isodecanoato-O)(isononanoato-O)nickel; [27] (isononanoato-O)(neodecanoato-O)nickel; [28] fatty acids, C6-19-branched, nickel salts; [29] fatty acids, C8-18 and C18-unsaturated, nickel salts; [30] fatty acids, C8-18 and C18-unsaturated, nickel salts; [30] 2,7-naphthalenedisulfonic acid, nickel(II) salt; [31] 240-235-8 [1] 222-102-6 [2] 254-642-3 [3] … 76 unchanged lines … H372** H334 H317 H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % H410 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,1 % ≤ C < 1 % Skin Sens. 1; H317: C ≥ 0,01 % M=1 H 028-055-00-6 nickel(II) sulfite; [1] nickel tellurium trioxide; [2] … 210 unchanged lines … GHS09 Dgr H302 H314 H410 STOT SE 3; H335: C ≥ 5 % 030-004-00-8 dimethylzinc; [1] H410 STOT SE 3; H335: C ≥ 5 % 030-004-00-8 dimethylzinc; [1] diethylzinc [2] 208-884-1 [1] 209-161-3 [2] 544-97-8 [1] 557-20-0 [2] Pyr. Liq. 1 … 214 unchanged lines … GHS07 Dgr H314 H335 U 035-002-01-8 hydrobromic acid ... % — — Skin Corr. 1B 035-002-01-8 hydrobromic acid ... % — — Skin Corr. 1B STOT SE 3 H314 H335 GHS05 GHS07 Dgr H314 H335 Skin Corr. 1B; H314: C ≥ 40 % Skin Irrit. 2; H315: 10 % ≤ C < 40 % Eye Irrit. 2; H319: 10 % ≤ C < 40 % STOT SE 3; H335: C ≥ 10 % B H335 Skin Corr. 1B; H314: C ≥ 40 % Skin Irrit. 2; H315: 10 % ≤ C < 40 % Eye Irrit. 2; H319: 10 % ≤ C < 40 % STOT SE 3; H335: C ≥ 10 % B 035-003-00-6 potassium bromate 231-829-8 7758-01-2 Ox. Sol. 1 Carc. 1B Acute Tox. 3 * H271 … 26 unchanged lines … H250 T 040-002-00-9 zirconium powder, dry (non pyrophoric) — — Self-heat. 1 H251 GHS02 Dgr H251 T 040-003-00-4 reaction product of 3,5-di-tert-butylsalicylic acid and zirconium oxychloride, dehydrated, basic Zr: DTBS= 1,0: 1,0 to 1,0: 1,5 430-610-6 226996-19-6 Aquatic Acute 1 040-003-00-4 reaction product of 3,5-di-tert-butylsalicylic acid and zirconium oxychloride, dehydrated, basic Zr: DTBS= 1,0: 1,0 to 1,0: 1,5 430-610-6 226996-19-6 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 042-001-00-9 molybdenum trioxide 215-204-7 1313-27-5 Carc. 2 … 125 unchanged lines … H351 H373 ** H410 * STOT RE 2; H373: C ≥ 0,25 % 048-004-00-1 cadmium cyanide 208-829-1 542-83-6 Acute Tox. 2 * STOT RE 2; H373: C ≥ 0,25 % 048-004-00-1 cadmium cyanide 208-829-1 542-83-6 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * Carc. 2 STOT RE 2 * Aquatic Acute 1 Aquatic Chronic 1 H330 H310 H300 H351 H373 ** H400 H410 GHS06 GHS08 GHS09 Dgr H330 H310 H300 H351 H373 ** H410 EUH032 STOT RE 2; H373: C ≥ 0,1 % EUH032: C ≥ 1 % 048-005-00-7 cadmiumhexafluorosilicate(2-); H410 EUH032 STOT RE 2; H373: C ≥ 0,1 % EUH032: C ≥ 1 % 048-005-00-7 cadmiumhexafluorosilicate(2-); cadmium fluorosilica 241-084-0 17010-21-8 Acute Tox. 3 * Acute Tox. 3 * Carc. 2 STOT RE 2 * Aquatic Acute 1 Aquatic Chronic 1 H331 H301 H351 H373 ** H400 H410 GHS06 GHS08 GHS09 Dgr H331 H301 H351 H373 ** H410 * STOT RE 2; H373: C ≥ 0,1 % 048-006-00-2 cadmium fluoride 232-222-0 7790-79-6 Carc. 1B STOT RE 2; H373: C ≥ 0,1 % 048-006-00-2 cadmium fluoride 232-222-0 7790-79-6 Carc. 1B Muta. 1B Repr. 1B Acute Tox. 2 * … 16 unchanged lines … H330 H301 H372 ** H410 Carc. 1B; H350: C ≥ 0,01 % H410 Carc. 1B; H350: C ≥ 0,01 % * oral STOT RE 1; H372: C ≥ 7 % STOT RE 2: 0,1 % ≤ C < 7 % 048-007-00-8 cadmium iodide 232-223-6 7790-80-9 Acute Tox. 3 * STOT RE 1; H372: C ≥ 7 % STOT RE 2: 0,1 % ≤ C < 7 % 048-007-00-8 cadmium iodide 232-223-6 7790-80-9 Acute Tox. 3 * Acute Tox. 3 * Carc. 2 STOT RE 2 * Aquatic Acute 1 Aquatic Chronic 1 H331 H301 H351 H373 ** H400 H410 GHS06 GHS08 GHS09 Dgr H331 H301 H351 H373 ** H410 * STOT RE 2; H373: C ≥ 0,1 % 048-008-00-3 cadmium chloride 233-296-7 10108-64-2 Carc. 1B STOT RE 2; H373: C ≥ 0,1 % 048-008-00-3 cadmium chloride 233-296-7 10108-64-2 Carc. 1B Muta. 1B Repr. 1B Acute Tox. 2 * … 16 unchanged lines … H330 H301 H372 ** H410 Carc. 1B; H350: C ≥ 0,01 % H410 Carc. 1B; H350: C ≥ 0,01 % * oral STOT RE 1; H372: C ≥ 7 % STOT RE 2; H373: 0,1 % ≤ C < 7 % 048-009-00-9 cadmium sulphate 233-331-6 10124-36-4 Carc. 1B STOT RE 1; H372: C ≥ 7 % STOT RE 2; H373: 0,1 % ≤ C < 7 % 048-009-00-9 cadmium sulphate 233-331-6 10124-36-4 Carc. 1B Muta. 1B Repr. 1B Acute Tox. 2 * … 16 unchanged lines … H330 H301 H372 ** H410 Carc. 1B; H350: C ≥ 0,01 % H410 Carc. 1B; H350: C ≥ 0,01 % * oral STOT RE 1; H372: C ≥ 7 % STOT RE 2; H373: 0,1 % ≤ C < 7 % 048-010-00-4 cadmium sulphide 215-147-8 1306-23-6 Carc. 1B STOT RE 1; H372: C ≥ 7 % STOT RE 2; H373: 0,1 % ≤ C < 7 % 048-010-00-4 cadmium sulphide 215-147-8 1306-23-6 Carc. 1B Muta. 2 Repr. 2 STOT RE 1 Acute Tox. 4 * Aquatic Chronic 4 H350 H341 H361fd H372 ** H302 H413 GHS08 GHS07 Dgr H350 H341 H361fd H372 ** H302 H413 * STOT RE 1; H372: C ≥ 10 % STOT RE 2; H373: 0,1 % ≤ C < 10 % 1 STOT RE 1; H372: C ≥ 10 % STOT RE 2; H373: 0,1 % ≤ C < 10 % 1 048-011-00-X cadmium (pyrophoric) 231-152-8 7440-43-9 Pyr. Sol. 1 Carc. 1B Muta. 2 … 23 unchanged lines … Aquatic Chronic 3 H314 H412 GHS05 Dgr H314 H412 STOT SE 3; H335: C ≥ 5 % 050-002-00-0 cyhexatin (ISO); H412 STOT SE 3; H335: C ≥ 5 % 050-002-00-0 cyhexatin (ISO); hydroxytricyclohexylstannane; tri(cyclohexyl)tin hydroxide 236-049-1 13121-70-5 Acute Tox. 4 * Acute Tox. 4 * … 139 unchanged lines … H319 H315 H410 * STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,25 % ≤ C < 1 % Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % M = 10 A STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,25 % ≤ C < 1 % Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % M = 10 A 1 050-009-00-9 fluorotripentylstannane; [1] hexapentyldistannoxane [2] 243-546-7 [1] … 71 unchanged lines … Wng H319 H335 H315 H413 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % A1 H413 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % A1 050-017-00-2 fenbutatin oxide (ISO); bis(tris(2-methyl-2-phenylpropyl)tin)oxide 236-407-7 13356-08-6 Acute Tox. 2 * Eye Irrit. 2 … 85 unchanged lines … H312 H372** H314 H410 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 0,01 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,01 % ≤ C < 3 % H410 Skin Corr. 1B; H314: C ≥ 5 % Skin Irrit. 2; H315: 0,01 % ≤ C < 5 % Eye Dam. 1; H318: 3 % ≤ C < 5 % Eye Irrit. 2; H319: 0,01 % ≤ C < 3 % M=10 050-023-00-5 reaction mass of: bis[(2-ethyl-1-oxohexyl)oxy]dioctyl stannane; bis[((2-ethyl-1-oxohexyl)oxy)dioctylstannyl]oxide; bis(1-phenyl-1,3-decanedionyl)dioctyl stannane; … 29 unchanged lines … H410 050-025-00-6 trichloromethylstannane 213-608-8 993-16-8 Repr. 2 H361d GHS08 Wng H361d 050-026-00-1 2-ethylhexyl 10-ethyl-4-[[2-[(2-ethylhexyl)oxy]-2-oxoethyl]thio]-4-methyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 260-828-5 57583-34-3 Repr. 2 H361d GHS08 Wng H361d 050-027-00-7 2-ethylhexyl 10-ethyl-4,4-dioctyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 239-622-4 15571-58-1 Repr. 1B H360D GHS08 Dgr H360D 051-001-00-8 antimony trichloride 233-047-2 10025-91-9 Skin Corr. 1B Dgr H360D 050-028-00-2 2-ethylhexyl 10-ethyl-4,4-dimethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 260-829-0 57583-35-4 Repr. 2 Acute Tox. 4 STOT RE 1 Skin Sens. 1A H361d H302 H372 (nervous system, immune system) H317 GHS08 GHS07 Dgr H361d H302 H372 (nervous system, immune system) H317 050-029-00-8 dimethyltin dichloride 212-039-2 753-73-1 Repr. 2 Acute Tox. 2 Acute Tox. 3 Acute Tox. 3 STOT RE 1 Skin Corr. 1B H361d H330 H301 H311 H372 (nervous system, immune system) H314 GHS08 GHS06 GHS05 Dgr H361d H330 H301 H311 H372 (nervous system, immune system) H314 EUH071 051-001-00-8 antimony trichloride 233-047-2 10025-91-9 Skin Corr. 1B Aquatic Chronic 2 H314 H411 GHS05 GHS09 Dgr H314 H411 STOT SE 3; H335: C ≥ 5 % 051-002-00-3 antimony pentachloride 231-601-8 7647-18-9 Skin Corr. 1B H411 STOT SE 3; H335: C ≥ 5 % 051-002-00-3 antimony pentachloride 231-601-8 7647-18-9 Skin Corr. 1B Aquatic Chronic 2 H314 H411 GHS05 GHS09 Dgr H314 H411 STOT SE 3; H335: C ≥ 5 % 051-003-00-9 antimony compounds, with the exception of the tetroxide (Sb2O4), pentoxide (Sb2O5), trisulphide (Sb2S3), pentasulphide (Sb2S5) and those specified elsewhere in this Annex — — Acute Tox. 4 * H411 STOT SE 3; H335: C ≥ 5 % 051-003-00-9 antimony compounds, with the exception of the tetroxide (Sb2O4), pentoxide (Sb2O5), trisulphide (Sb2S3), pentasulphide (Sb2S5) and those specified elsewhere in this Annex — — Acute Tox. 4 * Acute Tox. 4 * Aquatic Chronic 2 H332 H302 … 36 unchanged lines … H400 053-002-00-9 hydrogen iodide 233-109-9 10034-85-2 Press. Gas Skin Corr. 1A H314 GHS04 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 10 % Skin Corr. 1B; H314: 0,2 % ≤ C < 10 % Skin Irrit. 2; H315: 0,02 % ≤ C < 0,2 % Eye Irrit. 2; H319: 0,02 % ≤ C < 0,2 % STOT SE 3; H335: C ≥ 0,02 % U5 053-002-01-6 hydriodic acid ... % — — Skin Corr. 1B H314 GHS05 Dgr Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B Dgr H314 Skin Corr. 1A; H314: C ≥ 10 % Skin Corr. 1B; H314: 0,2 % ≤ C < 10 % Skin Irrit. 2; H315: 0,02 % ≤ C < 0,2 % Eye Irrit. 2; H319: 0,02 % ≤ C < 0,2 % STOT SE 3; H335: C ≥ 0,02 % U5 053-002-01-6 hydriodic acid ... % — — Skin Corr. 1B H314 GHS05 Dgr Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B 053-003-00-4 iodoxybenzene — 696-33-3 Expl. **** **** **** **** 053-004-00-X calcium iodoxybenzoate — — Expl. **** **** **** **** C 053-005-00-5 (4-(1-methylethyl)phenyl)-(4-methylphenyl)iodonium tetrakis(pentafluorophenyl)borate (1-) 422-960-3 178233-72-2 Acute Tox. 4 * Acute Tox. 4 * … 254 unchanged lines … H300 H373 ** H410 * STOT RE 2; H373: C ≥ 0,1 % A1 STOT RE 2; H373: C ≥ 0,1 % A1 080-003-00-1 dimercury dichloride; mercurous chloride; calomel 233-307-5 10112-91-1 Acute Tox. 4 * … 30 unchanged lines … H300 H373 ** H410 * STOT RE 2; H373: C ≥ 0,1 % A1 STOT RE 2; H373: C ≥ 0,1 % A1 080-005-00-2 mercury difulminate; mercuric fulminate; fulminate of mercury 211-057-8 628-86-4 Unst. Expl. … 20 unchanged lines … H400 H410 080-005-01-X mercury difulminate; mercuric fulminate; fulminate of mercury [≥ 20 % phlegmatiser] 211-057-8 628-86-4 Expl. 1.1 fulminate of mercury [≥ 20 % phlegmatiser] 211-057-8 628-86-4 Expl. 1.1 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * … 58 unchanged lines … H300 H373 ** H410 * STOT RE 2; H373: C ≥ 0,05 % 1 STOT RE 2; H373: C ≥ 0,05 % 1 080-008-00-9 phenylmercury nitrate; [1] phenylmercury hydroxide; [2] basic phenylmercury nitrate [3] 200-242-9 [1] … 121 unchanged lines … H332 H302 H373 ** H410 Repr. 2; H361f: C ≥ 2,5 % H410 Repr. 2; H361f: C ≥ 2,5 % * STOT RE 2; H373: C ≥ 0,5 % A1 STOT RE 2; H373: C ≥ 0,5 % A1 082-002-00-1 lead alkyls — — Repr. 1A Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * STOT RE 2 * Aquatic Acute 1 Aquatic Chronic 1 H360Df H330 H310 H300 H373 ** H400 H410 GHS06 GHS08 GHS09 Dgr H360Df H330 H310 H300 H373 ** H410 Repr. 1A; H360D: C ≥ 0,1 % H410 Repr. 1A; H360D: C ≥ 0,1 % * STOT RE 2; H373: C ≥ 0,05 % A1 STOT RE 2; H373: C ≥ 0,05 % A1 082-003-00-7 lead diazide; lead azide 236-542-1 13424-46-9 Unst. Expl. Repr. 1A … 18 unchanged lines … H373 ** H410 1 082-003-01-4 lead diazide; lead azide [≥ 20 % phlegmatiser] 236-542-1 13424-46-9 Expl. 1.1 lead azide [≥ 20 % phlegmatiser] 236-542-1 13424-46-9 Expl. 1.1 Repr. 1A Acute Tox. 4 * Acute Tox. 4 * … 189 unchanged lines … Press. Gas H220 GHS02 GHS04 Dgr H220 C U 601-004-01-8 butane (containing ≥ 0,1 % butadiene (203-450-8)); [1] isobutane (containing ≥ 0,1 % butadiene (203-450-8)) [2] 203-448-7 [1] 601-004-01-8 butane (containing ≥ 0,1 % butadiene (203-450-8)); [1] isobutane (containing ≥ 0,1 % butadiene (203-450-8)) [2] 203-448-7 [1] 200-857-2 [2] 106-97-8 [1] 75-28-5 [2] Flam. Gas 1 Press. Gas … 29 unchanged lines … H304 H336 H411 EUH066 C 601-007-00-7 hexane (containing < 5 % n-hexane (203-777-6)); 601-007-00-7 hexane (containing < 5 % n-hexane (203-777-6)); 2-methylpentane; [1] 3-methylpentane; [2] 2,2-dimethylbutane; [3] … 316 unchanged lines … H312 H315 * C 601-023-00-4 ethylbenzene 202-849-4 100-41-4 Flam. Liq. 2 Acute Tox. 4 * H225 H332 GHS02 Acute Tox. 4* STOT RE 2 Asp. Tox. 1 H225 H332 H373 (hearing organs) H304 GHS02 GHS07 GHS08 Dgr H225 H332 601-024-00-X cumene; [1] H332 H373 (hearing organs) H304 601-024-00-X cumene; [1] propylbenzene [2] 202-704-5 [1] 203-132-9 [2] 98-82-8 [1] 103-65-1 [2] Flam. Liq. 3 … 20 unchanged lines … GHS09 Wng H226 H335 H411 STOT SE 3; H335: C ≥ 25 % 601-026-00-0 styrene 202-851-5 100-42-5 Flam. Liq. 3 Acute Tox. 4 * Eye Irrit. 2 Skin Irrit. 2 H226 H411 STOT SE 3; H335: C ≥ 25 % 601-026-00-0 styrene 202-851-5 100-42-5 Flam. Liq. 3 Repr. 2 Acute Tox. 4* STOT RE 1 Skin Irrit. 2 Eye Irrit. 2 H226 H361d H332 H319 H315 GHS02 H372 (hearing organs) H315 H319 GHS02 GHS08 GHS07 Wng H226 Dgr H226 H361d H332 H319 H315 * D H372 (hearing organs) H315 H319 * D 601-027-00-6 2-phenylpropene; α-methylstyrene 202-705-0 98-83-9 Flam. Liq. 3 Eye Irrit. 2 STOT SE 3 Aquatic Chronic 2 H226 H319 H335 H411 GHS02 GHS07 GHS09 Wng H226 H319 H335 H411 STOT SE 3; H335: C ≥ 25 % 601-028-00-1 2-methylstyrene; H411 STOT SE 3; H335: C ≥ 25 % 601-028-00-1 2-methylstyrene; 2-vinyltoluene 210-256-7 611-15-4 Acute Tox. 4 * Aquatic Chronic 2 H332 H411 GHS07 … 56 unchanged lines … H340 H360FD H317 H410 Carc. 1B; H350: C ≥ 0,01 % 601-033-00-9 benz[a]anthracene 200-280-6 56-55-3 Carc. 1B H410 Carc. 1B; H350: C ≥ 0,01 % 601-033-00-9 benz[a]anthracene 200-280-6 56-55-3 Carc. 1B Aquatic Acute 1 Aquatic Chronic 1 H350 H400 … 43 unchanged lines … H373 ** H315 H336 H411 STOT RE 2; H373: C ≥ 5 % 601-041-00-2 dibenz[a,h]anthracene 200-181-8 53-70-3 Carc. 1B H411 STOT RE 2; H373: C ≥ 5 % 601-041-00-2 dibenz[a,h]anthracene 200-181-8 53-70-3 Carc. 1B Aquatic Acute 1 Aquatic Chronic 1 H350 H400 H410 GHS08 GHS09 Dgr H350 H410 Carc. 1B; H350: C ≥ 0,01 % H410 Carc. 1B; H350: C ≥ 0,01 % M=100 601-042-00-8 biphenyl; diphenyl 202-163-5 92-52-4 Eye Irrit. 2 STOT SE 3 … 354 unchanged lines … Asp. Tox. 1 H304 GHS07 H304 STOT SE 3 H336 GHS08 Dgr H336 602-001-00-7 chloromethane; 601-088-00-9 4-vinylcyclohexene 202-848-9 100-40-3 Carc. 2 H351 GHS08 Wng H351 601-089-00-4 muscalure; cis-tricos-9-ene 248-505-7 27519-02-4 Skin Sens. 1B H317 GHS07 Wng H317 602-001-00-7 chloromethane; methyl chloride 200-817-4 74-87-3 Flam. Gas 1 Press. Gas Carc. 2 … 108 unchanged lines … H412 H420 * STOT RE 1; H372: C ≥ 1 % H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % 602-009-00-0 chloroethane 200-830-5 75-00-3 Flam. Gas 1 H373: 0,2 % ≤ C < 1 % 602-009-00-0 chloroethane 200-830-5 75-00-3 Flam. Gas 1 Press. Gas Carc. 2 Aquatic Chronic 3 H220 … 101 unchanged lines … GHS09 Dgr H351 H372 ** H411 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % 602-018-00-X 1-chloropropane; [1] H411 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % 602-018-00-X 1-chloropropane; [1] 2-chloropropane [2] 208-749-7 [1] 200-858-8 [2] 540-54-5 [1] 75-29-6 [2] Flam. Liq. 2 … 350 unchanged lines … H410 GHS08 GHS09 Wng H373 ** H410 STOT RE 2; H373: C ≥ 0,005 % C H410 STOT RE 2; H373: C ≥ 0,005 % C 602-040-00-X 2-chlorotoluene; [1] 3-chlorotoluene; [2] 4-chlorotoluene; [3] … 409 unchanged lines … H311 H301 H314 H410 Carc. 1B; H350: C ≥ 0,01 % STOT SE 3; H335: C ≥ 5 % 602-074-00-5 pentachlorobenzene 210-172-0 608-93-5 Flam. Sol. 1 H410 Carc. 1B; H350: C ≥ 0,01 % STOT SE 3; H335: C ≥ 5 % 602-074-00-5 pentachlorobenzene 210-172-0 608-93-5 Flam. Sol. 1 Acute Tox. 4 * Aquatic Acute 1 Aquatic Chronic 1 H228 … 36 unchanged lines … H319 H335 H315 H410 Carc. 2; H351: C ≥ 0,1 % 602-077-00-1 dodecachloropentacyclo[5.2.1.02,6.03,9.05,8]decane; H410 Carc. 2; H351: C ≥ 0,1 % 602-077-00-1 dodecachloropentacyclo[5.2.1.02,6.03,9.05,8]decane; mirex 219-196-6 2385-85-5 Carc. 2 Repr. 2 Lact. … 312 unchanged lines … H311 H301 H370 ** * STOT SE 1; H370: C ≥ 10 % STOT SE 2; H371: 3 % ≤ C < 10 % 603-002-00-5 ethanol; STOT SE 1; H370: C ≥ 10 % STOT SE 2; H371: 3 % ≤ C < 10 % 603-002-00-5 ethanol; ethyl alcohol 200-578-6 64-17-5 Flam. Liq. 2 H225 GHS02 Dgr H225 603-003-00-0 propan-1-ol; n-propanol 200-746-9 71-23-8 Flam. Liq. 2 … 63 unchanged lines … H335 GHS02 GHS07 Wng H226 H335 STOT SE 3; H335: C ≥ 25 % 603-009-00-3 cyclohexanol 203-630-6 108-93-0 Acute Tox. 4 * H335 STOT SE 3; H335: C ≥ 25 % 603-009-00-3 cyclohexanol 203-630-6 108-93-0 Acute Tox. 4 * Acute Tox. 4 * STOT SE 3 Skin Irrit. 2 H332 … 89 unchanged lines … H315 H400 603-016-00-1 4-hydroxy-4-methylpentan-2-one; diacetone alcohol 204-626-7 123-42-2 Eye Irrit. 2 H319 GHS07 Wng H319 Eye Irrit. 2; H319: C ≥ 10 % 603-018-00-2 furfuryl alcohol 202-626-1 98-00-0 Carc. 2 Wng H319 Eye Irrit. 2; H319: C ≥ 10 % 603-018-00-2 furfuryl alcohol 202-626-1 98-00-0 Carc. 2 Acute Tox. 3 * Acute Tox. 4 * Acute Tox. 4 * … 87 unchanged lines … H351 H319 H335 EUH019 STOT SE 3; H335: C ≥ 25 % H335: C ≥ 25 % Eye Irrit.2; H319: C ≥ 25 % 603-026-00-6 1-chloro-2,3-epoxypropane; H319: C ≥ 25 % 603-026-00-6 1-chloro-2,3-epoxypropane; epichlorhydrin 203-439-8 106-89-8 Flam. Liq. 3 Carc. 1B Acute Tox. 3 * … 49 unchanged lines … Dgr H332 H312 H302 H314 STOT SE 3; H335: C ≥ 5 % 603-031-00-3 1,2-dimethoxyethane; H314 STOT SE 3; H335: C ≥ 5 % 603-031-00-3 1,2-dimethoxyethane; ethylene glycol dimethyl ether; EGDME 203-794-9 110-71-4 Flam. Liq. 2 Repr. 1B … 43 unchanged lines … H412 603-033-01-1 oxydiethylene dinitrate; diethylene glycol dinitrate; digol dinitrate; [>25 % phlegmatiser] 211-745-8 693-21-0 Expl. 1.1 [>25 % phlegmatiser] 211-745-8 693-21-0 Expl. 1.1 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * … 33 unchanged lines … H373 ** H411 603-034-01-7 glycerol trinitrate; nitroglycerine; [>40 % phlegmatiser] 200-240-8 55-63-0 Expl. 1.1 [>40 % phlegmatiser] 200-240-8 55-63-0 Expl. 1.1 Acute Tox. 2 * Acute Tox. 1 Acute Tox. 2 * … 16 unchanged lines … P.E.T.N. 201-084-3 78-11-5 Unst. Expl. H200 GHS01 Dgr H200 603-035-01-2 pentaerythritol tetranitrate; pentaerythrite tetranitrate; P.E.T.N.; [>20 % phlegmatiser] 201-084-3 78-11-5 Expl. 1.1 H201 GHS01 [>20 % phlegmatiser] 201-084-3 78-11-5 Expl. 1.1 H201 GHS01 Dgr H201 T 603-036-00-0 mannitol hexanitrate; nitromannite 239-924-6 15825-70-4 Unst. Expl. H200 GHS01 Dgr H200 603-036-01-8 mannitol hexanitrate; nitromannite; [>40 % phlegmatiser] 239-924-6 15825-70-4 Expl. 1.1 H201 GHS01 [>40 % phlegmatiser] 239-924-6 15825-70-4 Expl. 1.1 H201 GHS01 Dgr H201 603-037-00-6 cellulose nitrate; nitrocellulose — — Expl. 1.1 H201 GHS01 Dgr H201 T … 131 unchanged lines … H350 H330 H311 H302 Carc. 1A; H350: C ≥ 0,001 % 603-047-00-0 2-dimethylaminoethanol; H302 Carc. 1A; H350: C ≥ 0,001 % 603-047-00-0 2-dimethylaminoethanol; N,N-dimethylethanolamine 203-542-8 108-01-0 Flam. Liq. 3 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1B H226 H332 H312 H302 H314 GHS02 GHS05 GHS07 Dgr H226 H332 H312 H302 H314 STOT SE 3; H335: C ≥ 5 % 603-048-00-6 2-diethylaminoethanol; H314 STOT SE 3; H335: C ≥ 5 % 603-048-00-6 2-diethylaminoethanol; N,N-diethylethanolamine 202-845-2 100-37-8 Flam. Liq. 3 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1B H226 H332 H312 H302 H314 GHS02 GHS05 GHS07 GHS09 Dgr H226 H332 H312 H302 H314 STOT SE 3; H335: C ≥ 5 % 603-049-00-1 chlorfenethol (ISO); H314 STOT SE 3; H335: C ≥ 5 % 603-049-00-1 chlorfenethol (ISO); 1,1-bis (4-chlorophenyl) ethanol 201-246-3 80-06-8 Acute Tox. 4 * Aquatic Chronic 2 H302 H411 GHS07 … 31 unchanged lines … H319 H335 H315 H412 STOT SE 3; H335: C ≥ 10 % 603-055-00-4 propylene oxide; H412 STOT SE 3; H335: C ≥ 10 % 603-055-00-4 propylene oxide; 1,2-epoxypropane; methyloxirane 200-879-2 75-56-9 Flam. Liq. 1 Carc. 1B … 81 unchanged lines … H311 H301 H314 603-061-00-7 tetrahydro-2-furylmethanol; tetrahydrofurfuryl alcohol 202-625-6 97-99-4 Eye Irrit. 2 H319 GHS07 Wng H319 603-062-00-2 tetrahydrofuran-2,5-diyldimethanol 203-239-0 104-80-3 Eye Irrit. 2 tetrahydrofurfuryl alcohol 202-625-6 97-99-4 Repr. 1B Eye Irrit. 2 H360Df H319 GHS08 GHS07 Dgr H360Df H319 603-062-00-2 tetrahydrofuran-2,5-diyldimethanol 203-239-0 104-80-3 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 H335 H315 GHS07 Wng H319 H335 H315 STOT SE 3; H335: C ≥ 10 % 603-063-00-8 2,3-epoxypropan-1-ol; H315 STOT SE 3; H335: C ≥ 10 % 603-063-00-8 2,3-epoxypropan-1-ol; glycidol; oxiranemethanol 209-128-3 556-52-5 Carc. 1B Muta. 2 … 141 unchanged lines … H317 GHS07 Wng H319 H315 H317 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 603-074-00-8 reaction product: bisphenol-A-(epichlorhydrin); H317 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 603-074-00-8 reaction product: bisphenol-A-(epichlorhydrin); epoxy resin (number average molecular weight ≤ 700) 500-033-5 25068-38-6 Eye Irrit. 2 Skin Irrit. 2 Skin Sens. 1 Aquatic Chronic 2 H319 H315 H317 H411 GHS07 GHS09 Wng H319 H315 H317 H411 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 603-075-00-3 chlormethyl methyl ether; H411 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 603-075-00-3 chlormethyl methyl ether; chlorodimethyl ether 203-480-1 107-30-2 Flam. Liq. 2 Carc. 1A Acute Tox. 4 * … 28 unchanged lines … H301 H312 H373 ** H317 Skin Corr. 1B; H314: C ≥ 50 % Skin Irrit. 2; H315: 25 % ≤ C < 50 % Eye Irrit. 2; H319: 25 % ≤ C < 50 % D H317 Skin Corr. 1B; H314: C ≥ 50 % Skin Irrit. 2; H315: 25 % ≤ C < 50 % Eye Irrit. 2; H319: 25 % ≤ C < 50 % D 603-077-00-4 1-dimethylaminopropan-2-ol; dimepranol (INN) 203-556-4 108-16-7 Flam. Liq. 3 Acute Tox. 4 * … 37 unchanged lines … H314 GHS05 GHS07 Dgr H312 H302 H314 STOT SE 3; H335: C ≥ 5 % 603-081-00-6 2,2'-thiodiethanol; H314 STOT SE 3; H335: C ≥ 5 % 603-081-00-6 2,2'-thiodiethanol; thiodiglycol 203-874-3 111-48-8 Eye Irrit. 2 H319 GHS07 Wng H319 603-082-00-1 1-aminopropan-2-ol; isopropanolamine 201-162-7 78-96-6 Skin Corr. 1B H314 GHS05 … 638 unchanged lines … H315 GHS02 GHS07 Dgr H225 H315 603-182-00-5 reaction product of: saturated, monounsaturated and multiple unsaturated long-chained partly estrified alcohols of vegetable origin (Brassica napus L., Brassica rapa L., Helianthus annuus L., Glycine hispida, Gossypium hirsutum L., Cocos nucifera L., Elaeis guineensis) with O,O-diisobutyldithiophosphate and 2-ethylhexylamine and hydrogen peroxide 428-630-5 — Skin Sens. 1 H317 GHS07 H315 603-182-00-5 reaction product of: saturated, monounsaturated and multiple unsaturated long-chained partly estrified alcohols of vegetable origin (Brassica napus L., Brassica rapa L., Helianthus annuus L., Glycine hispida, Gossypium hirsutum L., Cocos nucifera L., Elaeis guineensis) with O,O-diisobutyldithiophosphate and 2-ethylhexylamine and hydrogen peroxide 428-630-5 — Skin Sens. 1 H317 GHS07 Wng H317 603-183-00-0 2-[2-(2-butoxyethoxy)ethoxy]ethanol; TEGBE; triethylene glycol monobutyl ether; butoxytriethylene glycol 205-592-6 143-22-6 Eye Dam. 1 H318 GHS05 Dgr H318 Eye Dam. 1; H318: C ≥ 30 % Eye Irrit. 2; H319: 20 % ≤ C < 30 % 603-184-00-6 2-(hydroxymethyl)-2-[[2-hydroxy-3-(isooctadecyloxy)propoxy]methyl]-1,3-propanediol 416-380-1 146925-83-9 Aquatic Acute 1 Dgr H318 Eye Dam. 1; H318: C ≥ 30 % Eye Irrit. 2; H319: 20 % ≤ C < 30 % 603-184-00-6 2-(hydroxymethyl)-2-[[2-hydroxy-3-(isooctadecyloxy)propoxy]methyl]-1,3-propanediol 416-380-1 146925-83-9 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 603-185-00-1 2,4-dichloro-3-ethyl-6-nitrophenol 420-740-1 99817-36-4 Acute Tox. 3 * … 47 unchanged lines … GHS07 Dgr H360Df H314 H317 STOT SE 3; H335: C ≥ 5 % 603-195-00-6 2-[4-(4-methoxyphenyl)-6-phenyl-1,3,5-triazin-2-yl]-phenol 430-810-3 154825-62-4 Aquatic Chronic 3 H412 — H412 603-196-00-1 2-(7-ethyl-1H-indol-3-yl)ethanol 431-020-1 41340-36-7 Acute Tox. 4 * H317 STOT SE 3; H335: C ≥ 5 % 603-195-00-6 2-[4-(4-methoxyphenyl)-6-phenyl-1,3,5-triazin-2-yl]-phenol 430-810-3 154825-62-4 Aquatic Chronic 3 H412 — H412 603-196-00-1 2-(7-ethyl-1H-indol-3-yl)ethanol 431-020-1 41340-36-7 Acute Tox. 4 * STOT RE 2 * Aquatic Chronic 2 H302 H373 ** … 81 unchanged lines … GHS07 Dgr H225 H360Df H319 EUH019 603-209-00-0 spinosad (ISO) (reaction mass of spinosyn A and spinosyn D in ratios between 95:5 to 50:50); reaction mass of 50-95 % of (2R, 3aS, 5aR, 5bS, 9S, 13S, 14R, 16aS, 16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione and 50-5 % (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione; [1] H319 EUH019 603-209-00-0 spinosad (ISO) (reaction mass of spinosyn A and spinosyn D in ratios between 95:5 to 50:50); reaction mass of 50-95 % of (2R, 3aS, 5aR, 5bS, 9S, 13S, 14R, 16aS, 16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione and 50-5 % (2S, 3aR, 5aS, 5bS, 9S, 13S, 14R, 16aS, 16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione; [1] spinosyn A; [2] spinosyn D [3] - [1] - [2] … 82 unchanged lines … H413 GHS07 Wng H317 H413 603-220-00-0 1-{]benzyl[}2-(2-methoxyphenoxy)ethyl{]amino[}-3-(9H-carbazol-4-yloxy)propan-2-ol 432-890-5 72955-94-3 Aquatic Chronic 4 H413 — H413 603-221-00-6 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-1,1-ethanediol, hydrochloride; [containing < 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Acute Tox. 4 * [containing < 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Acute Tox. 4 * Skin Corr. 1B Aquatic Chronic 2 H302 H314 H411 GHS05 GHS07 GHS09 Dgr H302 H314 H411 603-221-01-3 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-1,1-ethanediol, hydrochloride; [containing ≥ 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Carc. 1B [containing ≥ 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Carc. 1B Acute Tox. 4 * Skin Corr. 1B Aquatic Chronic 2 H350 … 82 unchanged lines … H301 H373 ** H314 * Skin Corr. 1B; H314: C ≥ 3 % Skin Irrit. 2; H315: 1 % ≤ C < 3 % Eye Irrit. 2; H319: 1 % ≤ C < 3 % 604-002-00-8 pentachlorophenol 201-778-6 87-86-5 Carc. 2 Skin Corr. 1B; H314: C ≥ 3 % Skin Irrit. 2; H315: 1 % ≤ C < 3 % Eye Irrit. 2; H319: 1 % ≤ C < 3 % 604-002-00-8 pentachlorophenol 201-778-6 87-86-5 Carc. 2 Acute Tox. 2 * Acute Tox. 3 * Acute Tox. 3 * … 195 unchanged lines … GHS09 Dgr H331 H314 H400 STOT SE 3; H335: C ≥ 1 % 604-013-00-8 2,3,4,6-tetrachlorophenol 200-402-8 58-90-2 Acute Tox. 3 * H400 STOT SE 3; H335: C ≥ 1 % 604-013-00-8 2,3,4,6-tetrachlorophenol 200-402-8 58-90-2 Acute Tox. 3 * Eye Irrit. 2 Skin Irrit. 2 Aquatic Acute 1 Aquatic Chronic 1 H301 H319 H315 H400 H410 GHS06 GHS09 Dgr H301 H319 H315 H410 * Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 604-014-00-3 chlorocresol; Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 604-014-00-3 chlorocresol; 4-chloro-m-cresol; 4-chloro-3-methylphenol 200-431-6 59-50-7 Acute Tox. 4 * Acute Tox. 4 * … 46 unchanged lines … H319 H315 H410 * Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 604-018-00-5 2,4,6-trichlorophenol 201-795-9 88-06-2 Carc. 2 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 604-018-00-5 2,4,6-trichlorophenol 201-795-9 88-06-2 Carc. 2 Acute Tox. 4 * Eye Irrit. 2 Skin Irrit. 2 … 416 unchanged lines … H361f*** GHS08 Dgr H350 H341 H361f*** Carc. 1B; H350: C ≥ 1 % 604-077-00-7 2-benzotriazol-2-yl-4-methyl-6-(2-methylallyl)phenol 419-750-9 98809-58-6 Aquatic Chronic 4 H413 — H413 604-079-00-8 4,4'-(1,3-phenylene-bis(1-methylethylidene))bis-phenol 428-970-4 13595-25-0 Repr. 2 H361f*** Carc. 1B; H350: C ≥ 1 % 604-077-00-7 2-benzotriazol-2-yl-4-methyl-6-(2-methylallyl)phenol 419-750-9 98809-58-6 Aquatic Chronic 4 H413 — H413 604-079-00-8 4,4'-(1,3-phenylene-bis(1-methylethylidene))bis-phenol 428-970-4 13595-25-0 Repr. 2 Skin Sens. 1 Aquatic Chronic 2 H361f*** H317 … 76 unchanged lines … H315 H317 H336 H410 605-001-00-5 formaldehyde ...% 200-001-8 50-00-0 Carc. 2 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * H410 604-090-00-8 4-tert-butylphenol 202-679-0 98-54-4 Repr. 2 Skin Irrit. 2 Eye Dam. 1 H361f H315 H318 GHS08 GHS05 Dgr H361f H315 H318 604-091-00-3 etofenprox (ISO); 2-(4-ethoxyphenyl)-2-methylpropyl 3-phenoxybenzyl ether 407-980-2 80844-07-1 Lact. Aquatic Acute 1 Aquatic Chronic 1 H362 H400 H410 GHS09 Wng H362 H410 M = 100 M = 1000 605-001-00-5 formaldehyde …% 200-001-8 50-00-0 Carc. 1B Muta. 2 Acute Tox. 3* Acute Tox. 3* Acute Tox. 3* Skin Corr. 1B Skin Sens. 1 H351 Skin Sens. 1 H350 H341 H301 H311 H331 H314 H317 GHS08 GHS06 GHS05 Dgr H350 H341 H301 H311 H301 H314 H317 GHS06 GHS08 GHS05 Dgr H351 H331 H311 H301 H314 H317 * Skin Corr. 1B; H314: C ≥25 % Skin Irrit. 2; H315: 5 % ≤ C < 25 % Eye Irrit. 2; H319: 5 % ≤ C < 25 % STOT SE 3; H335: C ≥ 5 % Skin Sens. 1; H317: C ≥ 0,2 % B D Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 5 % ≤ C < 25 % Eye Irrit. 2; H319: 5 % ≤ C < 25 % STOT SE 3; H335: C ≥ 5 % Skin Sens. 1; H317: C ≥ 0,2 % B, D 605-002-00-0 1,3,5-trioxan; trioxymethylene 203-812-5 110-88-3 Flam. Sol. 1 Repr. 2 … 31 unchanged lines … dimethyl acetal 208-589-8 534-15-6 Flam. Liq. 2 H225 GHS02 Dgr H225 605-008-00-3 acrolein; prop-2-enal; acrylaldehyde 203-453-4 107-02-8 Flam. Liq. 2 H225 GHS02 H225 EUH071 Skin Corr. 1; H314: C ≥ 0,1 % D Acute Tox. 1 H330 GHS06 H330 Acute Tox. 2 H300 GHS05 H300 Acute Tox. 3 H311 GHS09 H311 Skin Corr. 1 H314 Dgr H314 Aquatic Acute 1 H400 M = 100 Aquatic Chronic 1 H410 H410 M = 1 acrylaldehyde 203-453-4 107-02-8 Flam. Liq. 2 Acute Tox. 1 Acute Tox. 2 Acute Tox. 3 Skin Corr. 1B Aquatic Acute 1 Aquatic Chronic 1 H225 H330 H300 H311 H314 H400 H410 GHS02 GHS06 GHS05 GHS09 Dgr H225 H330 H300 H311 H314 H410 EUH071 Skin Corr. 1B; H314: C ≥ 0,1 % M = 100 M = 1 D 605-009-00-9 crotonaldehyde; 2-butenal; [1] (E)-2-butenal; … 143 unchanged lines … H334 H317 H400 * Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 0,5 % ≤ C < 10 % Eye Dam. ; H318: 2 % ≤ C < 10 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % STOT SE; H335: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 605-023-00-5 5-chloro-2-(4-chlorophenoxy)phenol 429-290-0 3380-30-1 Eye Dam. 1 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 0,5 % ≤ C < 10 % Eye Dam.; H318: 2 % ≤ C < 10 % Eye Irrit. 2; H319: 0,5 % ≤ C < 2 % STOT SE; H335: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 605-023-00-5 5-chloro-2-(4-chlorophenoxy)phenol 429-290-0 3380-30-1 Eye Dam. 1 Aquatic Acute 1 Aquatic Chronic 1 H318 H400 … 24 unchanged lines … H311 H301 H314 H400 STOT SE 3; H335: C ≥ 5 % 605-026-00-1 2,5,7,7-tetramethyloctanal 405-690-0 114119-97-0 Skin Irrit. 2 H400 STOT SE 3; H335: C ≥ 5 % 605-026-00-1 2,5,7,7-tetramethyloctanal 405-690-0 114119-97-0 Skin Irrit. 2 Skin Sens. 1 Aquatic Chronic 2 H315 H317 H411 GHS07 GHS09 Wng H315 H317 H411 605-027-00-7 reaction mass of: 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indene-6-carboxaldehyde; 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indene-5-carboxaldehyde 410-480-7 — Skin Sens. 1 Aquatic Chronic 2 H317 H411 GHS07 GHS09 Wng H317 H411 605-028-00-2 β-methyl-3-(1-methylethyl)-benzenepropanal 412-050-4 125109-85-5 Aquatic Chronic 2 H411 GHS09 H411 605-029-00-8 2-cyclohexylpropanal 412-270-0 2109-22-0 Skin Sens. 1 Aquatic Chronic 2 H317 H411 GHS07 GHS09 Wng H317 H411 605-030-00-3 1-(p-methoxyphenyl)acetaldehyde oxime 411-510-1 3353-51-3 Skin Sens. 1 H317 GHS07 Wng H317 605-031-00-9 reaction mass of: 2,2-dimethoxyethanal [this component is considered to be anhydrous in terms of identity, structure and composition. However, 2,2-dimethoxyethanal will exist in a hydrated form. 60 % anhydrous is equivalent to 70,4 % hydrate; Wng H317 605-031-00-9 reaction mass of: 2,2-dimethoxyethanal [this component is considered to be anhydrous in terms of identity, structure and composition. However, 2,2-dimethoxyethanal will exist in a hydrated form. 60 % anhydrous is equivalent to 70,4 % hydrate; water(Including free water and water in hydrated 2,2-dimethoxyethanal)] 421-890-0 — Skin Sens. 1 H317 GHS07 Wng H317 605-032-00-4 3-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-(E)-2-propenal 425-370-4 93957-50-7 Skin Sens. 1 Aquatic Acute 1 … 95 unchanged lines … H335 GHS02 GHS07 Wng H226 H335 STOT SE 3; H335: C ≥ 10 % 606-006-00-5 pentan-3-one; H335 STOT SE 3; H335: C ≥ 10 % 606-006-00-5 pentan-3-one; diethyl ketone 202-490-3 96-22-0 Flam. Liq. 2 STOT SE 3 STOT SE 3 H225 … 41 unchanged lines … H312 H302 H319 H335 STOT SE 3; H335: C ≥ 10 % 606-013-00-3 p-benzoquinone; H335 STOT SE 3; H335: C ≥ 10 % 606-013-00-3 p-benzoquinone; quinone 203-405-2 106-51-4 Acute Tox. 3 * Acute Tox. 3 * Eye Irrit. 2 … 86 unchanged lines … GHS07 Wng H226 H319 H335 STOT SE 3; H335: C ≥ 10 % 606-021-00-7 N-methyl-2-pyrrolidone; H335 STOT SE 3; H335: C ≥ 10 % 606-021-00-7 N-methyl-2-pyrrolidone; 1-methyl-2-pyrrolidone 212-828-1 872-50-4 Repr. 1B Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H360D*** H319 H335 H315 GHS08 GHS07 Dgr H360D*** H319 H335 H315 Repr. 1B; H360D: C ≥ 5 % STOT SE 3; H335: C ≥ 10 % 606-022-00-2 1-phenyl-3-pyrazolidone 202-155-1 92-43-3 Acute Tox. 4 * H315 Repr. 1B; H360D: C ≥ 5 % STOT SE 3; H335: C ≥ 10 % 606-022-00-2 1-phenyl-3-pyrazolidone 202-155-1 92-43-3 Acute Tox. 4 * Aquatic Chronic 2 H302 H411 GHS07 GHS09 … 633 unchanged lines … GHS09 Wng H373** H410 606-141-00-X sodium 3-(methoxycarbonyl)-4-oxo-3,4,5,6-tetrahydro-2-pyridinolate 418-410-7 — Eye Irrit. 2 H319 GHS07 Wng H319 606-142-00-5 reaction mass of: (1RS, 2SR, 7SR, 8SR, E) 9 and 10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; Wng H319 606-142-00-5 reaction mass of: (1RS, 2SR, 7SR, 8SR, E) 9 and 10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; (1RS, 2SR, 7SR, 8SR, Z)-10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; (1RS, 2SR, 7SR, 8SR, Z)-9-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one 434-290-9 — Acute Tox. 4 * Aquatic Chronic 2 H302 … 18 unchanged lines … H330 H372 (nervous system) H410 STOT RE 1; H372: C ≥ 5 % H372: C ≥ 5 % STOT RE 2; H373: 0,5 % ≤C<5 % M = 10000 avermectin B1a (purity ≥80 %); [2] 265-610-3 [2] 65195-55-3 [2] H373: 0,5 % ≤C<5 % M = 10000 avermectin B1a (purity ≥80 %); [2] 265-610-3 [2] 65195-55-3 [2] 606-144-00-6 acequinocyl (ISO); 3-dodecyl-1,4-dioxo-1,4-dihydronaphthalen-2-yl acetate — 57960-19-7 Skin Sens. 1 STOT SE 1 … 16 unchanged lines … M = 10 STOT RE 2 H373 (kidneys) GHS07 H373 (kidneys) Skin Sens. 1A H317 GHS09 H317 Aquatic Acute 1 H400 Wng Aquatic Chronic 1 H410 H410 607-001-00-0 formic acid ... % 200-579-1 64-18-6 Skin Corr. 1A H314 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 90 % Skin Corr. 1B; H314: 10 % ≤ C < 90 % Skin Irrit. 2; H315: 2 % ≤ C < 10 % Eye Irrit. 2; H319: 2 % ≤ C < 10 % B 607-002-00-6 acetic acid ... % 200-580-7 64-19-7 Flam. Liq. 3 606-146-00-7 tralkoxydim (ISO); 2-(N-ethoxypropanimidoyl)-3-hydroxy-5-mesitylcyclohex-2-en-1-one - 87820-88-0 Carc. 2 Acute Tox. 4 Aquatic Chronic 2 H351 H302 H411 GHS08 GHS07 GHS09 Wng H351 H302 H411 606-147-00-2 cycloxydim (ISO); 2-(N-ethoxybutanimidoyl)-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)cyclohex-2-en-1-one 405-230-9 101205-02-1 Repr. 2 H361d GHS08 Wng H361d 607-001-00-0 formic acid ... % 200-579-1 64-18-6 Skin Corr. 1A H314 GHS05 Dgr H314 Skin Corr. 1A; H314: C ≥ 90 % Skin Corr. 1B; H314: 10 % ≤ C < 90 % Skin Irrit. 2; H315: 2 % ≤ C < 10 % Eye Irrit. 2; H319: 2 % ≤ C < 10 % B 607-002-00-6 acetic acid ... % 200-580-7 64-19-7 Flam. Liq. 3 Skin Corr. 1A H226 H314 GHS02 GHS05 Dgr H226 H314 Skin Corr. 1A; H314: C ≥ 90 % Skin Corr. 1B; H314: 25 % ≤ C < 90 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B H314 Skin Corr. 1A; H314: C ≥ 90 % Skin Corr. 1B; H314: 25 % ≤ C < 90 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % B 607-003-00-1 chloroacetic acid 201-178-4 79-11-8 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * Skin Corr. 1B Aquatic Acute 1 H331 H311 H301 H314 H400 GHS06 GHS05 GHS09 Dgr H331 H311 H301 H314 H400 STOT SE 3; H335: C ≥ 5 % 607-004-00-7 TCA (ISO); H400 STOT SE 3; H335: C ≥ 5 % 607-004-00-7 TCA (ISO); trichloroacetic acid 200-927-2 76-03-9 Skin Corr. 1A Aquatic Acute 1 Aquatic Chronic 1 H314 H400 H410 GHS05 GHS09 Dgr H314 H410 STOT SE 3; H335: C ≥ 1 % 607-005-00-2 TCA-sodium (ISO); H410 STOT SE 3; H335: C ≥ 1 % 607-005-00-2 TCA-sodium (ISO); sodium trichloroacetate 211-479-2 650-51-1 STOT SE 3 Aquatic Acute 1 Aquatic Chronic 1 H335 … 22 unchanged lines … Dgr H226 H332 H302 H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 5 % ≤ C < 25 % Eye Dam. 1; H318: 5 % ≤ C < 25 % Eye Irrit. 2; H319: 1 % ≤ C < 5 % STOT SE 3; H335: C ≥ 5 % 607-009-00-4 phthalic anhydride 201-607-5 85-44-9 Acute Tox. 4 * H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 5 % ≤ C < 25 % Eye Dam. 1; H318: 5 % ≤ C < 25 % Eye Irrit. 2; H319: 1 % ≤ C < 5 % STOT SE 3; H335: C ≥ 5 % 607-009-00-4 phthalic anhydride 201-607-5 85-44-9 Acute Tox. 4 * STOT SE 3 Skin Irrit. 2 Eye Dam. 1 Resp. Sens. 1 Skin Sens. 1 H302 H335 H315 H318 H334 H317 GHS08 GHS05 GHS07 Dgr H302 H335 H315 H318 H334 H317 607-010-00-X propionic anhydride 204-638-2 123-62-6 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % 607-011-00-5 acetyl chloride 200-865-6 75-36-5 Flam. Liq. 2 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H315: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % 607-011-00-5 acetyl chloride 200-865-6 75-36-5 Flam. Liq. 2 Skin Corr. 1B H225 H314 GHS02 GHS05 … 196 unchanged lines … H319 H335 H315 H317 Skin Irrit. 2; H315: C ≥ 5 % Eye Irrit. 2; H319: C ≥ 5 % STOT SE 3; H335: C ≥ 5 % D H317 Skin Irrit. 2; H315: C ≥ 5 % Eye Irrit. 2; H319: C ≥ 5 % STOT SE 3; H335: C ≥ 5 % D 607-033-00-5 n-butyl methacrylate 202-615-1 97-88-1 Flam. Liq. 3 Eye Irrit. 2 STOT SE 3 … 361 unchanged lines … H312 H302 H314 H400 STOT SE 3; H335: C ≥ 1 % D H400 STOT SE 3; H335: C ≥ 1 % D 607-062-00-3 n-butyl acrylate 205-480-7 141-32-2 Flam. Liq. 3 Eye Irrit. 2 STOT SE 3 … 20 unchanged lines … H410 GHS05 GHS09 Dgr H314 H410 STOT SE 3; H335: C ≥ 5 % 607-065-00-X bromoacetic acid 201-175-8 79-08-3 Acute Tox. 3 * H410 STOT SE 3; H335: C ≥ 5 % 607-065-00-X bromoacetic acid 201-175-8 79-08-3 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * Skin Corr. 1A … 72 unchanged lines … H314 H317 H400 * Skin Sens. 1; H317: C ≥ 0,2 % D Skin Sens. 1; H317: C ≥ 0,2 % D 607-073-00-3 4-CPA (ISO); 4-chlorophenoxyacetic acid 204-581-3 122-88-3 Acute Tox. 4 * H302 GHS07 Wng H302 607-074-00-9 chlorfenac(ISO); … 116 unchanged lines … GHS07 Dgr H312 H302 H314 STOT SE 3; H335: C ≥ 1 % D 607-089-00-0 propionic acid ... % 201-176-3 79-09-4 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H319: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % STOT SE 3; H335: C ≥ 10 % B H314 STOT SE 3; H335: C ≥ 1 % D 607-089-00-0 propionic acid ... % 201-176-3 79-09-4 Skin Corr. 1B H314 GHS05 Dgr H314 Skin Corr. 1B; H314: C ≥ 25 % Skin Irrit. 2; H319: 10 % ≤ C < 25 % Eye Irrit. 2; H319: 10 % ≤ C < 25 % STOT SE 3; H335: C ≥ 10 % B 607-090-00-6 thioglycolic acid 200-677-4 68-11-1 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * Skin Corr. 1B H331 H311 H301 H314 GHS06 GHS05 Dgr H331 H311 H301 H314 * 607-091-00-1 trifluoroacetic acid . . . % 200-929-3 76-05-1 Acute Tox. 4 * H332 GHS05 H332 * B H314 * 607-091-00-1 trifluoroacetic acid . . . % 200-929-3 76-05-1 Acute Tox. 4 * H332 GHS05 H332 * B Skin Corr. 1A Aquatic Chronic 3 H314 H412 GHS07 … 22 unchanged lines … GHS05 Dgr H225 H314 EUH014 B D 607-094-00-8 peracetic acid . . . % 201-186-8 79-21-0 Flam. Liq. 3 607-094-00-8 peracetic acid . . . % 201-186-8 79-21-0 Flam. Liq. 3 Org. Perox. D **** Acute Tox. 4 * Acute Tox. 4 * … 16 unchanged lines … H302 H314 H400 * STOT SE 3; H335: C ≥ 1 % B D STOT SE 3; H335: C ≥ 1 % B D 607-095-00-3 maleic acid 203-742-5 110-16-7 Acute Tox. 4 * Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Skin Sens. 1 H302 H319 H335 H315 H317 GHS07 Wng H302 H319 H335 H315 H317 Skin Sens. 1; H317: C ≥ 0,1 % 607-096-00-9 maleic anhydride 203-571-6 108-31-6 Acute Tox. 4 * H317 Skin Sens. 1; H317: C ≥ 0,1 % 607-096-00-9 maleic anhydride 203-571-6 108-31-6 Acute Tox. 4 * Skin Corr. 1B Resp. Sens. 1 Skin Sens. 1 H302 … 54 unchanged lines … STOT SE 3 H319 H335 GHS07 Wng H319 H335 Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-101-00-4 1,4,5,6,7,7-hexachlorobicyclo [2,2,1]hept-5-ene-2,3-dicarboxylic anhydride chlorendic anhydride 204-077-3 115-27-5 Eye Irrit. 2 H335 Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-101-00-4 1,4,5,6,7,7-hexachlorobicyclo [2,2,1]hept-5-ene-2,3-dicarboxylic anhydride chlorendic anhydride 204-077-3 115-27-5 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 H335 H315 GHS07 Wng H319 H335 H315 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-102-00-X cyclohexane-1,2-dicarboxylic anhydride; [1] H315 Skin Irrit. 2; H315: C ≥ 1 % Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-102-00-X cyclohexane-1,2-dicarboxylic anhydride; [1] cis-cyclohexane-1,2-dicarboxylic anhydride; [2] trans-cyclohexane-1,2-dicarboxylic anhydride [3] 201-604-9 [1] 236-086-3 [2] … 16 unchanged lines … Wng H302 H319 H335 * Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-104-00-0 cyclopentane-1,2,3,4-tetracarboxylic dianhydride 227-964-7 6053-68-5 Eye Irrit. 2 Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-104-00-0 cyclopentane-1,2,3,4-tetracarboxylic dianhydride 227-964-7 6053-68-5 Eye Irrit. 2 STOT SE 3 H319 H335 GHS07 Wng H319 H335 Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-105-00-6 8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride; [1] H335 Eye Irrit. 2; H319: C ≥ 1 % STOT SE 3; H335: C ≥ 1 % 607-105-00-6 8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride; [1] 1,2,3,6-tetrahydro-3,6-methanophthalic anhydride; [2] (1α,2α,3β,6β)-1,2,3,6-tetrahydro-3,6-methanophthalic anhydride [3] 204-957-7 [1] 212-557-9 [2] … 22 unchanged lines … H319 H335 H315 H334 STOT SE 3; H335: C ≥ 10 % C H334 STOT SE 3; H335: C ≥ 10 % C 607-107-00-7 2-ethylhexyl acrylate 203-080-7 103-11-7 STOT SE 3 Skin Irrit. 2 Skin Sens. 1 H335 … 23 unchanged lines … H301 H314 H317 * Skin Sens. 1; H317: C ≥ 0,2 % C D Skin Sens. 1; H317: C ≥ 0,2 % C D 607-109-00-8 hexamethylene diacrylate; hexane-1,6-diol diacrylate 235-921-9 13048-33-4 Eye Irrit. 2 Skin Irrit. 2 … 55 unchanged lines … Skin Sens. 1 H335 H317 GHS07 Wng H335 H317 STOT SE 3; H335: C ≥ 10 % D H317 STOT SE 3; H335: C ≥ 10 % D 607-115-00-0 isobutyl acrylate 203-417-8 106-63-8 Flam. Liq. 3 Acute Tox. 4 * Acute Tox. 4 * … 17 unchanged lines … GHS09 Wng H335 H315 H411 STOT SE 3; H335: C ≥ 10 % D H411 STOT SE 3; H335: C ≥ 10 % D 607-117-00-1 2,3-epoxypropyl acrylate; glycidyl acrylate 203-440-3 106-90-1 Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * Skin Corr. 1B Skin Sens. 1 H331 H311 H301 H314 H317 GHS06 GHS05 Dgr H331 H311 H301 H314 H317 * Skin Sens. 1; H317: C ≥ 0,2 % D Skin Sens. 1; H317: C ≥ 0,2 % D 607-118-00-7 1-methyltrimethylene diacrylate; 1,3-butylene glycol diacrylate 243-105-9 19485-03-1 Acute Tox. 4 * Skin Corr. 1B … 26 unchanged lines … H319 H315 H317 * Skin Sens. 1; H317: C ≥ 0,2 % D Skin Sens. 1; H317: C ≥ 0,2 % D 607-121-00-3 8,9,10-trinorborn-2-yl acrylate — 10027-06-2 Acute Tox. 4 * Skin Irrit. 2 Skin Sens. 1 H312 … 135 unchanged lines … Wng H319 H335 H315 H411 STOT SE 3; H335: C ≥ 10 % A H411 STOT SE 3; H335: C ≥ 10 % A 607-134-00-4 monoalkyl or monoaryl or monoalkyaryl esters of methacrylic acid with the exception of those specified elsewhere in this Annex — — Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 H335 H315 GHS07 Wng H319 H335 H315 STOT SE 3; H335: C ≥ 10 % A H315 STOT SE 3; H335: C ≥ 10 % A 607-135-00-X butyric acid 203-532-3 107-92-6 Skin Corr. 1B H314 GHS05 Dgr H314 607-136-00-5 butyryl chloride 205-498-5 141-75-3 Flam. Liq. 2 Skin Corr. 1B H225 … 279 unchanged lines … H410 GHS07 GHS09 Wng H317 H410 M = 100 607-178-00-4 methyl α-((4,6-dimethoxypyrimidin-2-yl)ureidosulphonyl)-o-toluate 401-340-6 83055-99-6 Skin Sens. 1 H410 M = 100 607-178-00-4 methyl α-((4,6-dimethoxypyrimidin-2-yl)ureidosulphonyl)-o-toluate 401-340-6 83055-99-6 Skin Sens. 1 Aquatic Chronic 2 H317 H411 GHS07 GHS09 … 57 unchanged lines … H318 GHS05 GHS07 Dgr H302 H318 607-190-00-X methyl acrylamidomethoxyacetate (containing ≥ 0,1 % acrylamid) 401-890-7 77402-03-0 Carc. 1B H318 607-190-00-X methyl acrylamidomethoxyacetate (containing ≥ 0,1 % acrylamid) 401-890-7 77402-03-0 Carc. 1B Muta. 1B Acute Tox. 4 * Eye Irrit. 2 H350 … 110 unchanged lines … GHS09 Wng H302 H317 H410 607-210-00-7 methyl acrylamidoglycolate (containing ≥ 0,1 % acrylamide) 403-230-3 77402-05-2 Carc. 1B H410 607-210-00-7 methyl acrylamidoglycolate (containing ≥ 0,1 % acrylamide) 403-230-3 77402-05-2 Carc. 1B Muta. 1B Skin Corr. 1B Skin Sens. 1 H350 H340 H314 H317 GHS08 GHS05 GHS07 Dgr H350 H340 H314 H317 607-211-00-2 methyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate 403-270-1 6386-39-6 Acute Tox. 4 * Aquatic Chronic 2 H302 H411 GHS07 GHS09 Wng H302 H411 607-212-00-8 poly(oxypropylenecarbonyl-co-oxy(ethylethylene)carbonyl), containing 27 % hydroxyvalerate 403-300-3 — Skin Sens. 1 H317 GHS07 H411 607-212-00-8 poly(oxypropylenecarbonyl-co-oxy(ethylethylene)carbonyl), containing 27 % hydroxyvalerate 403-300-3 — Skin Sens. 1 H317 GHS07 Wng H317 607-213-00-3 ethyl 3,3-bis(tert-pentylperoxy)butyrate 403-320-2 67567-23-1 Org. Perox. D**** Flam. Liq. 3 Aquatic Chronic 2 H242 … 161 unchanged lines … H315 GHS07 Wng H319 H335 H315 STOT SE 3; H335: C ≥ 10 % 607-236-00-9 ethyl 2-cyanoacrylate 230-391-5 7085-85-0 Eye Irrit. 2 H315 STOT SE 3; H335: C ≥ 10 % 607-236-00-9 ethyl 2-cyanoacrylate 230-391-5 7085-85-0 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 H319 H335 H315 GHS07 Wng H319 H335 H315 STOT SE 3; H335: C ≥ 10 % 607-237-00-4 benzyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate; H315 STOT SE 3; H335: C ≥ 10 % 607-237-00-4 benzyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate; flurazole 276-942-3 72850-64-7 Aquatic Chronic 2 H411 GHS09 H411 607-238-00-X tau-fluvalinate (ISO); cyano-(3-phenoxyphenyl)methyl N-[2-chloro-4-(trifluoromethyl)phenyl]-D-valinate — 102851-06-9 Acute Tox. 4 * Skin Irrit. 2 … 97 unchanged lines … Wng H319 H335 H315 H410 STOT SE 3; H335: C ≥ 10 % 607-245-00-8 tert-butyl acrylate 216-768-7 1663-39-4 Flam. Liq. 2 H410 STOT SE 3; H335: C ≥ 10 % 607-245-00-8 tert-butyl acrylate 216-768-7 1663-39-4 Flam. Liq. 2 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * … 47 unchanged lines … Wng H319 H335 H315 H410 STOT SE 3; H335: C ≥ 10 % 607-248-00-4 naptalam-sodium (ISO); H410 STOT SE 3; H335: C ≥ 10 % 607-248-00-4 naptalam-sodium (ISO); sodium N-naphth-1-ylphthalamate 205-073-4 132-67-2 Acute Tox. 4 * H302 GHS07 Wng H302 607-249-00-X (1-methyl-1,2-ethanediyl)bis[oxy(methyl-2,1-ethanediyl)] diacrylate 256-032-2 42978-66-5 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Skin Sens. 1 Aquatic Chronic 2 H319 H335 H315 H317 H411 GHS07 GHS09 Wng H319 H335 H315 H317 H411 STOT SE 3; H335: C ≥ 10 % 607-250-00-5 4H-3,1-benzoxazine-2,4(1H)-dione 204-255-0 118-48-9 Eye Irrit. 2 H411 STOT SE 3; H335: C ≥ 10 % 607-250-00-5 4H-3,1-benzoxazine-2,4(1H)-dione 204-255-0 118-48-9 Eye Irrit. 2 Skin Sens. 1 H319 H317 GHS07 Wng H319 … 349 unchanged lines … GHS07 Dgr H360FD H302 H314 STOT SE 3; H335: C ≥ 5 % 607-313-00-7 neodecanoyl chloride 254-875-0 40292-82-8 Acute Tox. 2 * H314 STOT SE 3; H335: C ≥ 5 % 607-313-00-7 neodecanoyl chloride 254-875-0 40292-82-8 Acute Tox. 2 * Acute Tox. 4 * Skin Corr. 1B H330 H302 H314 GHS06 GHS06 Dgr H330 H302 H314 STOT SE 3; H335: C ≥ 5 % 607-314-00-2 ethofumesate (ISO); H314 STOT SE 3; H335: C ≥ 5 % 607-314-00-2 ethofumesate (ISO); (±)-2-ethoxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulfonate 247-525-3 26225-79-6 Aquatic Chronic 2 H411 GHS09 H411 607-315-00-8 glyphosate (ISO); N-(phosphonomethyl)glycine 213-997-4 1071-83-6 Eye Dam. 1 Aquatic Chronic 2 H318 … 407 unchanged lines … H317 H410 607-384-00-4 reaction mass of: esters of C14-C15 branched alcohols with 3,5-di-t-butyl-4-hydroxyphenyl propionic acid; C15 branched and linear alkyl 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoate; C13 branched and linear alkyl 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoate 413-750-2 171090-93-0 Aquatic Chronic 4 H413 — H413 607-385-00-X Copolymer of vinyl-alcohol and vinyl acetate partially acetilized with 4-(2-(4-formylphenyl)ethenyl)-1-methylpyridinium methylsulfate 414-590-6 125229-74-5 Aquatic Chronic 2 H411 GHS09 H411 607-386-00-5 reaction mass of: tetradecanoic acid (42,5- 47,5 %); poly(1-7)lactate esters of tetradecanoic acid (52,5- 57,5 %) 412-580-6 174591-51-6 Skin Irrit. 2 C13 branched and linear alkyl 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoate 413-750-2 171090-93-0 Aquatic Chronic 4 H413 — H413 607-385-00-X Copolymer of vinyl-alcohol and vinyl acetate partially acetilized with 4-(2-(4-formylphenyl)ethenyl)-1-methylpyridinium methylsulfate 414-590-6 125229-74-5 Aquatic Chronic 2 H411 GHS09 H411 607-386-00-5 reaction mass of: tetradecanoic acid (42,5- 47,5 %); poly(1-7)lactate esters of tetradecanoic acid (52,5- 57,5 %) 412-580-6 174591-51-6 Skin Irrit. 2 Eye Dam. 1 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H315 H318 H317 H400 H410 GHS05 GHS07 GHS09 Dgr H315 H318 H317 H410 607-387-00-0 reaction mass of: dodecanoic acid (35-40 %); poly(1-7)lactate esters of dodecanoic acid (60-65 %) 412-590-0 58856-63-6 Skin Irrit. 2 H410 607-387-00-0 reaction mass of: dodecanoic acid (35-40 %); poly(1-7)lactate esters of dodecanoic acid (60-65 %) 412-590-0 58856-63-6 Skin Irrit. 2 Eye Dam. 1 Skin Sens. 1 Aquatic Acute 1 … 35 unchanged lines … H411 607-396-00-X bis(1,2,2,6,6-pentamethyl-4-piperidinyl) 2-(4-methoxybenzylidene)malonate 414-840-4 147783-69-5 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 607-397-00-5 reaction mass of: Ca salicylates (branched C10-14 and C18-30 alkylated); Ca phenates (branched C10-14 and C18-30 alkylated); Ca sulfurised phenates (branched C10-14 and C18-30 alkylated) 415-930-6 — Repr. 2 Wng H410 607-397-00-5 reaction mass of: Ca salicylates (branched C10-14 and C18-30 alkylated); Ca phenates (branched C10-14 and C18-30 alkylated); Ca sulfurised phenates (branched C10-14 and C18-30 alkylated) 415-930-6 — Repr. 2 Skin Sens. 1 H361f*** H317 GHS08 GHS07 … 262 unchanged lines … Dgr H331 H302 H410 607-432-00-4 S-metolachlor; reaction mass of (S)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (80-100 %); [1] (R)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (0-20 %) [2] - [1] reaction mass of (S)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (80-100 %); [1] (R)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (0-20 %) [2] - [1] - [2] 87392-12-9 [1] 178961-20-1 [2] Skin Sens. 1 Aquatic Acute 1 … 210 unchanged lines … H317 GHS05 GHS07 Dgr H318 H317 607-491-00-6 reaction mass of: diester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:2); triester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:3) 427-140-9 — Carc. 2 H351 GHS08 H317 607-491-00-6 reaction mass of: diester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:2); triester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:3) 427-140-9 — Carc. 2 H351 GHS08 Wng H351 607-492-00-1 2-(1-(3',3'-dimethyl-1'-cyclohexyl)ethoxy)-2-methyl propyl propanoate 415-490-5 141773-73-1 Aquatic Chronic 2 H411 GHS09 H411 607-493-00-7 methyl (3aR,4R,7aR)-2-methyl-4-(1S,2R,3-triacetoxypropyl)-3a,7a-dihydro-4H-pyrano[3,4-d]oxazole-6-carboxylate 415-670-3 78850-37-0 Eye Dam. 1 H318 GHS05 Dgr H318 607-494-00-2 bis(2-ethylhexyl)octylphosphonate 417-170-0 52894-02-7 Aquatic Acute 1 Aquatic Chronic 1 H400 … 121 unchanged lines … Aquatic Chronic 3 H317 H412 GHS07 Wng H317 H412 607-522-00-3 sodium salt of the polymer of: sodium 2-methyl-buta-1,3-diene-1-sulfonate with acrylic acid and 2-hydroxyethyl-2-methylacrylate 429-720-7 184246-86-4 Aquatic Chronic 3 H412 — H412 607-523-00-9 reaction mass of mono to tetra(lithium and/or sodium)3-amino-10-[4-(4-amino-3-sulfonatoanilino)-6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to tetra(lithium and/or sodium)3-amino-10-[4,6-bis(4-amino-3-sulfonatoanilino)-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to penta(lithium and/or sodium)10,10'-diamino-6,6', 13,13'-tetrachloro-3,3'-[6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10-amino-6,6', 13,13'-tetrachloro-10'[4-(4-amino-3-sulfonatoanilino)-[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10,10'-diamino-6,6', 3,3'[(2-sulfonato)-1,4-phenylenediiminobis[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate 430-200-7 — Eye Dam. 1 H412 607-522-00-3 sodium salt of the polymer of: sodium 2-methyl-buta-1,3-diene-1-sulfonate with acrylic acid and 2-hydroxyethyl-2-methylacrylate 429-720-7 184246-86-4 Aquatic Chronic 3 H412 — H412 607-523-00-9 reaction mass of mono to tetra(lithium and/or sodium)3-amino-10-[4-(4-amino-3-sulfonatoanilino)-6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to tetra(lithium and/or sodium)3-amino-10-[4,6-bis(4-amino-3-sulfonatoanilino)-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to penta(lithium and/or sodium)10,10'-diamino-6,6', 13,13'-tetrachloro-3,3'-[6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10-amino-6,6', 13,13'-tetrachloro-10'[4-(4-amino-3-sulfonatoanilino)-[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10,10'-diamino-6,6', 3,3'[(2-sulfonato)-1,4-phenylenediiminobis[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate 430-200-7 — Eye Dam. 1 Aquatic Chronic 3 H318 H412 GHS05 Dgr H318 … 159 unchanged lines … H315 H318 H317 H411 607-552-00-7 hexadecyl 3-amino-4-isopropoxybenzoate 424-830-1 — Aquatic Chronic 4 H413 — H413 607-553-00-2 7-amino-4-hydroxy-2-naphthalenesulfonic acid, coupled with 5 (or 8) -amino-8 (or 5)-[[4-[[4-[[4-amino-6(or 7)-sulfo-1-naphthyl]azo]phenyl]amino]-3-sulfophenyl]azo]-2-naphthalenesulfonic acid and 4-hydroxy-7-(phenylamino)-2-naphthalenesulfonic acid, sodium salt 424-850-0 — Eye Dam. 1 H318 GHS05 H411 607-552-00-7 hexadecyl 3-amino-4-isopropoxybenzoate 424-830-1 — Aquatic Chronic 4 H413 — H413 607-553-00-2 7-amino-4-hydroxy-2-naphthalenesulfonic acid, coupled with 5 (or 8) -amino-8 (or 5)-[[4-[[4-[[4-amino-6(or 7)-sulfo-1-naphthyl]azo]phenyl]amino]-3-sulfophenyl]azo]-2-naphthalenesulfonic acid and 4-hydroxy-7-(phenylamino)-2-naphthalenesulfonic acid, sodium salt 424-850-0 — Eye Dam. 1 H318 GHS05 Dgr H318 607-554-00-8 2,4-diamino-5-[4-[(2-sulfoxyl ethyl)sulfonyl]phenylazo]benzenesulfonic acid 424-870-1 27624-67-5 Expl. 1.1 Eye Dam. 1 Aquatic Chronic 3 H201 … 358 unchanged lines … GHS07 Wng H351 H302 H319 Carc. 2; H351: C ≥ 5 % 607-621-00-1 milbemectin (ISO); [reaction mass of milbemycin A3 (CAS No 51596-10-2) and milbemycin A4 (CAS No 51596-11-3) (30:70)] — — Acute Tox. 4 * H319 Carc. 2; H351: C ≥ 5 % 607-621-00-1 milbemectin (ISO); [reaction mass of milbemycin A3 (CAS No 51596-10-2) and milbemycin A4 (CAS No 51596-11-3) (30:70)] — — Acute Tox. 4 * Acute Tox. 4 * Aquatic Acute 1 Aquatic Chronic 1 H332 H302 H400 H410 GHS07 GHS09 Wng H332 H302 H410 M=100 607-622-00-7 2-ethylhexyl-2-ethylhexanoate 231-057-1 7425-14-1 Repr. 2 H361d*** GHS08 Wng H361d*** 607-623-00-2 diisobutyl phthalate 201-553-2 84-69-5 Repr. 1B H360Df GHS08 Dgr H360Df Repr. 1B; H360Df: C ≥ 25 % Repr. 2; H361f: 5 % ≤ C < 25 % 607-624-00-8 perfluorooctane sulfonic acid; Dgr H360Df Repr. 1B; H360Df: C ≥ 25 % Repr. 2; H361f: 5 % ≤ C < 25 % 607-624-00-8 perfluorooctane sulfonic acid; heptadecafluorooctane-1-sulfonic acid; [1] potassium perfluorooctanesulfonate; potassium heptadecafluorooctane-1-sulfonate; [2] … 44 unchanged lines … Wng H302 H373** H317 H410 Skin Sens. 1; H317: C ≥ 0,001 % H410 Skin Sens. 1; H317: C ≥ 0,001 % M=1 607-626-00-9 ethyl 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylate 401-290-5 103112-35-2 Carc. 1B Aquatic Acute 1 Aquatic Chronic 1 H350 … 229 unchanged lines … H351 GHS02 GHS08 Dgr H242 H351 607-687-00-1 reaction mass of: 2-{]3,6-bis-[}(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,3-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,5-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %) 442-800-6 — Skin Irrit. 2 H351 607-687-00-1 reaction mass of: 2-{]3,6-bis-[}(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,3-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,5-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %) 442-800-6 — Skin Irrit. 2 Aquatic Chronic 2 H315 H411 GHS07 GHS09 Wng H315 H411 607-688-00-7 (R)-1-cyclohexa-1,4-dienyl-1-methoxycarbonyl-methylammoniumchloride 444-320-2 — Acute Tox. 4 * H302 GHS07 Wng H302 607-689-00-2 reaction mass of: methyl 1,4-dimethylcyclohexanecarboxylate (para-isomer including cis- and trans- isomers); methyl 1,3-dimethylcyclohexanecarboxylate (meta-isomer including cis- and trans-isomers) 444-920-4 — Aquatic Chronic 3 H412 — H412 607-690-00-8 dimethyl[2S, 2S']-6,6,6'6'-tetramethoxy-2,2'-[N,N'-bis(trifluoracetyl)-S, S'-bi(L-homocysteinyl) diimino]dihexanoate 432-860-1 255387-46-3 Skin Sens. 1 H317 GHS07 Wng H317 607-691-00-3 magnesium salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 448-690-6 — Aquatic Chronic 4 H413 — H413 607-692-00-9 zinc salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 446-470-4 — Aquatic Chronic 4 H413 — H413 607-693-00-4 hexyl 2-(1-(diethylaminohydroxyphenyl)methanoyl)benzoate 443-860-6 302776-68-7 Aquatic Chronic 4 H413 — H413 607-694-00-X ethyl 5,5-diphenyl-2-isoxazoline-3-carboxylate 443-870-0 163520-33-0 Acute Tox. 4 * Wng H317 607-691-00-3 magnesium salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 448-690-6 — Aquatic Chronic 4 H413 — H413 607-692-00-9 zinc salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 446-470-4 — Aquatic Chronic 4 H413 — H413 607-693-00-4 hexyl 2-(1-(diethylaminohydroxyphenyl)methanoyl)benzoate 443-860-6 302776-68-7 Aquatic Chronic 4 H413 — H413 607-694-00-X ethyl 5,5-diphenyl-2-isoxazoline-3-carboxylate 443-870-0 163520-33-0 Acute Tox. 4 * Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H302 … 49 unchanged lines … Acute Tox. 4 H302 H302 STOT RE 1 H372 (liver) H372 (liver) Eye Dam. 1 H318 H318 608-001-00-3 acetonitrile; 607-705-00-8 benzoic acid 200-618-2 65-85-0 STOT RE 1 Skin Irrit. 2 Eye Dam. 1 H372 (lungs) (inhalation) H315 H318 GHS08 GHS05 Dgr H372 (lungs) (inhalation) H315 H318 607-706-00-3 methyl 2,5-dichlorobenzoate 220-815-7 2905-69-3 Acute Tox. 4 STOT SE 3 Aquatic Chronic 2 H302 H336 H411 GHS07 GHS09 Wng H302 H336 H411 608-001-00-3 acetonitrile; cyanomethane 200-835-2 75-05-8 Flam. Liq. 2 Acute Tox. 4 * Acute Tox. 4 * … 161 unchanged lines … H311 H301 H317 * Skin Sens. 1; H317: C ≥ 0,2 % D Skin Sens. 1; H317: C ≥ 0,2 % D 608-011-00-8 oxalonitrile; cyanogen 207-306-5 460-19-5 Press. Gas Flam. Gas 1 … 328 unchanged lines … Dgr H331 H301 H317 H410 M = 10000 608-059-00-X 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile 421-240-6 120068-79-3 Aquatic Chronic 2 H411 GHS09 H411 608-060-00-5 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile 421-300-1 138564-59-7 Aquatic Acute 1 H410 M = 10000 608-059-00-X 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile 421-240-6 120068-79-3 Aquatic Chronic 2 H411 GHS09 H411 608-060-00-5 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile 421-300-1 138564-59-7 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 608-062-00-6 2-fluoro-4-hydroxybenzonitrile 422-810-7 82380-18-5 Acute Tox. 4 * … 336 unchanged lines … H410 1 609-019-01-1 lead 2,4,6-trinitro-m-phenylene dioxide; lead 2,4,6-trinitroresorcinoxide; lead styphnate (≥ 20 % phlegmatiser) 239-290-0 15245-44-0 Expl. 1.1 lead styphnate (≥ 20 % phlegmatiser) 239-290-0 15245-44-0 Expl. 1.1 Repr. 1A Acute Tox. 4 * Acute Tox. 4 * … 85 unchanged lines … H300 H373 ** H410 609-023-00-6 dinocap (ISO); (RS)-2,6-dinitro-4-octylphenyl crotonates and (RS)-2,4-dinitro-6-octylphenyl crotonates in which octyl is a reaction mass of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl groups 254-408-0 39300-45-3 Repr. 1B (RS)-2,6-dinitro-4-octylphenyl crotonates and (RS)-2,4-dinitro-6-octylphenyl crotonates in which octyl is a reaction mass of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl groups 254-408-0 39300-45-3 Repr. 1B Acute Tox. 4 * Acute Tox. 4 * STOT RE 2 * … 472 unchanged lines … H314 H317 H410 * STOT SE 3; H335: C ≥ 1 % T STOT SE 3; H335: C ≥ 1 % T 609-057-00-1 3-chloro-2,4-difluoronitrobenzene 411-980-8 3847-58-3 Acute Tox. 4 * Skin Corr. 1B Skin Sens. 1 … 930 unchanged lines … H317 GHS05 GHS07 Dgr H318 H317 611-142-00-3 product-by-process definition polyazodyestuff obtained by coupling 4-[4-(1-amino-8-hydroxy-3,6-disulfo-2-naphthylazo)phenylsulfonylamino]benzenediazonium with reaction mass of 4-carboxybenzenediazonium and diphenylamine-3-sulfo-4,4'-bisdiazonium, and further coupling of the obtained compounds with reaction mass of naphth-2-ol and 3-aminophenol, sodium salts; H317 611-142-00-3 product-by-process definition polyazodyestuff obtained by coupling 4-[4-(1-amino-8-hydroxy-3,6-disulfo-2-naphthylazo)phenylsulfonylamino]benzenediazonium with reaction mass of 4-carboxybenzenediazonium and diphenylamine-3-sulfo-4,4'-bisdiazonium, and further coupling of the obtained compounds with reaction mass of naphth-2-ol and 3-aminophenol, sodium salts; sodium chloride 425-740-5 — Eye Dam. 1 Aquatic Chronic 3 H318 H412 GHS05 … 122 unchanged lines … Aquatic Chronic 3 H319 H412 GHS07 Wng H319 H412 611-158-00-0 reaction product of: 2,3,4,2', 3', 4'-hexahydroxy-5,5'-diacethyl-diphenylmethane and 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonylchloride and 3-diazo-3,4-dihydro-6-methoxy-4-oxo-1-naphthalenesulfonylchloride 421-520-8 — **** H412 611-158-00-0 reaction product of: 2,3,4,2', 3', 4'-hexahydroxy-5,5'-diacethyl-diphenylmethane and 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonylchloride and 3-diazo-3,4-dihydro-6-methoxy-4-oxo-1-naphthalenesulfonylchloride 421-520-8 — **** Aquatic Chronic 4 **** H413 **** **** H413 611-159-00-6 disodium 4-amino-6-((4-((4-(2,4-diaminophenyl)azo)phenylsulfamoyl)phenyl)azo)-5-hydroxy-3-((4-nitrophenyl)azo)naphthalene-2,7-disulfonate 421-880-6 — Eye Dam. 1 Aquatic Chronic 3 H318 H412 GHS05 Dgr H318 H412 611-160-00-1 reaction mass of: 1,1,1-tris(phenyl-4'-(3''-diazo-3'', 4''-dihydro-4''-oxo-naphthalene-1''-sulfonato)ethane; 1,1,1-tris(phenyl-4'-(6''-diazo-5'', 6''-dihydro-5''-oxo-naphthalene-1''-sulfonato)ethane; reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (2:1); reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (1:2) 422-760-6 — **** reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (2:1); reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (1:2) 422-760-6 — **** Aquatic Chronic 4 **** H413 **** **** H413 611-161-00-7 trisodium [1,2'-(2-(8-amino-3,5-disulfonatonaphthalene)azo)-(4'-nitrobenzene)diolato-O,O,N][(Z)-2,2-((phenylcarbamoylprop-1'-enyl)azo)-5-sulfamoylbenzene)diolato-O,O,N]chromate(III) 423-100-1 — Eye Dam. 1 H318 GHS05 … 132 unchanged lines … H335 H315 H318 * Skin Irrit. 2; H315: C ≥ 5 % Eye Dam. 1; H318: C ≥ 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 5 % STOT SE 3; H335: C ≥ 5 % U5 612-001-01-6 mono-methylamine ... %; [1] di-methylamine ... %; [2] tri-methylamine ... % [3] 200-820-0 [1] Skin Irrit. 2; H315: C ≥ 5 % Eye Dam. 1; H318: C ≥ 5 % Eye Irrit. 2; H319: 0,5 % ≤ C < 5 % STOT SE 3; H335: C ≥ 5 % U5 612-001-01-6 mono-methylamine ... %; [1] di-methylamine ... %; [2] tri-methylamine ... % [3] 200-820-0 [1] 204-697-4 [2] 200-875-0 [3] 74-89-5 [1] 124-40-3 [2] 75-50-3 [3] Flam. Liq. 1 Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1B H224 H332 H302 H314 GHS02 GHS05 GHS07 Dgr H224 H332 H302 H314 * STOT SE 3; H335: C ≥ 5 % B STOT SE 3; H335: C ≥ 5 % B 612-002-00-4 ethylamine 200-834-7 75-04-7 Flam. Gas 1 Press. Gas Eye Irrit. 2 … 20 unchanged lines … H332 H312 H302 H314 STOT SE 3; H335: C ≥ 1 % 612-004-00-5 triethylamine 204-469-4 121-44-8 Flam. Liq. 2 H314 STOT SE 3; H335: C ≥ 1 % 612-004-00-5 triethylamine 204-469-4 121-44-8 Flam. Liq. 2 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1A H225 H332 H312 H302 H314 GHS02 GHS05 GHS07 Dgr H225 H332 H312 H302 H314 STOT SE 3; H335: C ≥ 1 % 612-005-00-0 butylamine 203-699-2 109-73-9 Flam. Liq. 2 H314 STOT SE 3; H335: C ≥ 1 % 612-005-00-0 butylamine 203-699-2 109-73-9 Flam. Liq. 2 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * Skin Corr. 1A H225 H332 H312 H302 H314 GHS02 GHS05 GHS07 Dgr H225 H332 H312 H302 H314 STOT SE 3; H335: C ≥ 1 % 612-006-00-6 ethylenediamine; H314 STOT SE 3; H335: C ≥ 1 % 612-006-00-6 ethylenediamine; 1,2-diaminoethane 203-468-6 107-15-3 Flam. Liq. 3 Acute Tox. 4 * Acute Tox. 4 * … 54 unchanged lines … H318 H317 H400 * STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % 612-009-00-2 salts of aniline — — Carc. 2 STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % 612-009-00-2 salts of aniline — — Carc. 2 Muta. 2 Acute Tox. 3 * Acute Tox. 3 * … 22 unchanged lines … H318 H317 H400 * STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % A STOT RE 1; H372: C ≥ 1 % STOT RE 2; H373: 0,2 % ≤ C < 1 % A 612-010-00-8 chloroanilines (with exception of those specified elsewhere in this Annex) — — Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * … 157 unchanged lines … GHS09 Dgr H350 H302 H411 Carc. 1A; H350: C ≥ 0,01 % 612-023-00-9 phenylhydrazine; [1] H411 Carc. 1A; H350: C ≥ 0,01 % 612-023-00-9 phenylhydrazine; [1] phenylhydrazinium chloride; [2] phenylhydrazine hydrochloride; [3] phenylhydrazinium sulphate (2:1) [4] 202-873-5 [1] … 197 unchanged lines … H302 H412 612-034-01-6 2-amino-4,6-dinitrophenol; picramic acid; [≥ 20 % water] 202-544-6 96-91-3 Acute Tox. 4 * [≥ 20 % water] 202-544-6 96-91-3 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * Aquatic Chronic 3 H332 … 97 unchanged lines … GHS09 Dgr H350 H302 H410 Carc. 1A; H350: C ≥ 0,01 % 612-043-00-8 N,N'-dimethylbenzidine — 2810-74-4 Acute Tox. 4 * H410 Carc. 1A; H350: C ≥ 0,01 % 612-043-00-8 N,N'-dimethylbenzidine — 2810-74-4 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * H332 H312 … 52 unchanged lines … H332 H312 H302 H314 STOT SE 3; H335: C ≥ 1 % 612-049-00-0 di-n-butylamine; [1] H314 STOT SE 3; H335: C ≥ 1 % 612-049-00-0 di-n-butylamine; [1] di-sec-butylamine [2] 203-921-8 [1] 210-937-9 [2] 111-92-2 [1] 626-23-3 [2] Flam. Liq. 3 … 433 unchanged lines … H330 H301 H372 ** H411 Carc. 1B; H350: C ≥ 0,001 % 612-078-00-9 2,2'-dichloro-4,4'-methylenedianiline; H411 Carc. 1B; H350: C ≥ 0,001 % 612-078-00-9 2,2'-dichloro-4,4'-methylenedianiline; 4,4'-methylene bis(2-chloroaniline) 202-918-9 101-14-4 Carc. 1B Acute Tox. 4 * Aquatic Acute 1 … 68 unchanged lines … H332 H319 H315 H411 Carc. 1B; H350: C ≥ 0,01 % 612-084-00-1 dapsone; H411 Carc. 1B; H350: C ≥ 0,01 % 612-084-00-1 dapsone; 4,4'-diamino diphenyl sulfone 201-248-4 80-08-0 Acute Tox. 4 * H302 GHS07 Wng H302 612-085-00-7 4,4'-methylenedi-o-toluidine 212-658-8 838-88-0 Carc. 1B Acute Tox. 4 * … 156 unchanged lines … GHS09 Dgr H350 H302 H411 Carc. 1B; H350: C ≥ 0,001 % 612-099-00-3 4-methyl-m-phenylenediamine; H411 Carc. 1B; H350: C ≥ 0,001 % 612-099-00-3 4-methyl-m-phenylenediamine; 2,4-toluenediamine 202-453-1 95-80-7 Carc. 1B Muta. 2 Repr. 2 … 238 unchanged lines … H302 H314 H317 H410 612-122-00-7 hydroxylamine … % [> 55 % in aqueous solution] 232-259-2 7803-49-8 Unst. Expl. H410 612-122-00-7 hydroxylamine … % [> 55 % in aqueous solution] 232-259-2 7803-49-8 Unst. Expl. Met. Corr. 1 Carc. 2 Acute Tox. 4 * … 29 unchanged lines … H318 H317 H400 B 612-122-01-4 hydroxylamine …% [≤ 55 % in aqueous solution] 232-259-2 7803-49-8 Met. Corr. 1 612-122-01-4 hydroxylamine …% [≤ 55 % in aqueous solution] 232-259-2 7803-49-8 Met. Corr. 1 Carc. 2 Acute Tox. 4 * Acute Tox. 4 * … 130 unchanged lines … Dgr H225 H332 H302 H314 STOT SE 3; H335: C ≥ 5 % 612-130-00-0 2,6-diamino-3,5-diethyltoluene; H314 STOT SE 3; H335: C ≥ 5 % 612-130-00-0 2,6-diamino-3,5-diethyltoluene; 4,6-diethyl-2-methyl-1,3-benzenediamine; [1] 2,4-diamino-3,5-diethyltoluene; 2,4-diethyl-6-methyl-1,3-benzenediamine; [2] … 81 unchanged lines … GHS09 Wng H302 H317 H410 Skin Sens. 1; H317: C ≥ 0,1 % 612-137-00-9 4-chloroaniline 203-401-0 106-47-8 Carc. 1B H410 Skin Sens. 1; H317: C ≥ 0,1 % 612-137-00-9 4-chloroaniline 203-401-0 106-47-8 Carc. 1B Acute Tox. 3 * Acute Tox. 3 * Acute Tox. 3 * … 217 unchanged lines … H317 H410 612-151-00-5 methyl-phenylene diamine; diaminotoluene; [technical product – reaction mass of 4-methyl-m-phenylene diamine (EC No 202-453-1) and 2-methyl-m-phenylene diamine (EC No 212-513-9)] — — Carc. 1B [technical product – reaction mass of 4-methyl-m-phenylene diamine (EC No 202-453-1) and 2-methyl-m-phenylene diamine (EC No 212-513-9)] — — Carc. 1B Muta. 2 Repr. 2 Acute Tox. 3 * … 547 unchanged lines … H301 H318 H317 H410 612-203-00-7 C8-10 alkyl dimethyl hydroxyethyl ammoniumchloride (chain < C8: <3 %, chain= C8: 15 %-70 %, chain= C10: 30 %-85 %, chain > C10: <3 %) 417-360-3 — Acute Tox. 4 * H410 612-203-00-7 C8-10 alkyl dimethyl hydroxyethyl ammoniumchloride (chain < C8: <3 %, chain= C8: 15 %-70 %, chain= C10: 30 %-85 %, chain > C10: <3 %) 417-360-3 — Acute Tox. 4 * Acute Tox. 4 * Skin Irrit. 2 H312 H302 … 16 unchanged lines … Dgr H351 H302 H318 H410 612-205-00-8 C.I. Basic Violet 3 with ≥ 0,1 % of Michler's ketone (EC no. 202-027-5) 208-953-6 548-62-9 Carc. 1B H410 612-205-00-8 C.I. Basic Violet 3 with ≥ 0,1 % of Michler's ketone (EC no. 202-027-5) 208-953-6 548-62-9 Carc. 1B Acute Tox. 4 * Eye Dam. 1 Aquatic Acute 1 … 469 unchanged lines … GHS09 Wng H302 H410 612-253-00-X 7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one; [containing < 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Aquatic Chronic 3 H412 — H412 612-253-01-7 7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one; [containing ≥ 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Repr. 1B [containing < 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Aquatic Chronic 3 H412 — H412 612-253-01-7 7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one; [containing ≥ 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Repr. 1B Aquatic Chronic 3 H360D*** H412 GHS08 Dgr H360D*** … 173 unchanged lines … STOT RE 2 H373 (gastro-intestinal tract, liver, immune system) GHS08 H373 (gastro-intestinal tract, liver, immune system) Skin Corr. 1B H314 GHS09 H314 Aquatic Acute 1 H400 Dgr Aquatic Chronic 1 H410 H410 613-001-00-1 ethyleneimine; 612-287-00-5 fluazinam (ISO); 3-chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-(trifluoromethyl)pyridin-2-amine - 79622-59-6 Repr. 2 Acute Tox. 4 Eye Dam. 1 Skin Sens. 1A Aquatic Acute 1 Aquatic Chronic 1 H361d H332 H318 H317 H400 H410 GHS08 GHS07 GHS05 GHS09 Dgr H361d H332 H318 H317 H410 M = 10 M = 10 613-001-00-1 ethyleneimine; aziridine 205-793-9 151-56-4 Flam. Liq. 2 Carc. 1B Muta. 1B … 79 unchanged lines … Dgr H330 H302 H314 H317 EUH014 STOT SE 3; H335: C ≥ 5 % 613-010-00-0 ametryn (ISO); H317 EUH014 STOT SE 3; H335: C ≥ 5 % 613-010-00-0 ametryn (ISO); N-ethyl-N'-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine 212-634-7 834-12-8 Acute Tox. 4 * Aquatic Acute 1 Aquatic Chronic 1 H302 H400 H410 GHS07 GHS09 Wng H302 H410 M = 100 613-011-00-6 amitrole (ISO); H410 M = 100 613-011-00-6 amitrole (ISO); 1,2,4-triazol-3-ylamine 200-521-5 61-82-5 Repr. 2 STOT RE 2 * Aquatic Chronic 2 H361d *** … 220 unchanged lines … H319 H335 H410 EUH031 * STOT SE 3; H335: C ≥ 10 % EUH031: C ≥ 10 % G STOT SE 3; H335: C ≥ 10 % EUH031: C ≥ 10 % G 613-030-01-7 troclosene sodium, dihydrate 220-767-7 51580-86-0 Acute Tox. 4 * Eye Irrit. 2 STOT SE 3 … 61 unchanged lines … H310 H300 H318 H411 Carc. 1B; H350: C ≥ 0,01 % 613-034-00-1 1,2-dimethylimidazole 217-101-2 1739-84-0 Acute Tox. 4 * H411 Carc. 1B; H350: C ≥ 0,01 % 613-034-00-1 1,2-dimethylimidazole 217-101-2 1739-84-0 Acute Tox. 4 * Skin Irrit. 2 Eye Dam. 1 H302 H315 … 117 unchanged lines … Wng H302 H314 H317 H410 Skin Corr. 1B; H314: C ≥ 50 % Skin Irrit. 2; H315: 30 % ≤ C < 50 % Eye Dam. 1; H318: 15 % ≤ C < 50 % Eye Irrit. 2; H319: 5 % ≤ C < 15 % 613-044-00-6 captan (ISO); H410 Skin Corr. 1B; H314: C ≥ 50 % Skin Irrit. 2; H315: 30 % ≤ C < 50 % Eye Dam. 1; H318: 15 % ≤ C < 50 % Eye Irrit. 2; H319: 5 % ≤ C < 15 % 613-044-00-6 captan (ISO); 1,2,3,6-tetrahydro-N-(trichloromethylthio)phthalimide 205-087-0 133-06-2 Carc. 2 Acute Tox. 3 * Eye Dam. 1 … 453 unchanged lines … H315 H318 H317 H400 Skin Sens. 1; H317: C ≥ 0,05 % 613-089-00-1 diquat dibromide; [1] H400 Skin Sens. 1; H317: C ≥ 0,05 % 613-089-00-1 diquat dibromide; [1] diquat dichloride; [2] 6,7-dihydrodipyrido[1,2-α:2',1'-c]pyrazinediylium dihydroxide [3] 201-579-4 [1] 223-714-6 [2] … 207 unchanged lines … H302 H314 H317 H410 Skin Sens. 1; H317: C ≥ 0,05 % 613-113-00-0 2-(morpholinothio)benzothiazole 203-052-4 102-77-2 Eye Irrit. 2 H410 Skin Sens. 1; H317: C ≥ 0,05 % 613-113-00-0 2-(morpholinothio)benzothiazole 203-052-4 102-77-2 Eye Irrit. 2 Skin Irrit. 2 Skin Sens. 1 Aquatic Chronic 2 H319 H315 H317 H411 GHS07 GHS09 Wng H319 H315 H317 H411 613-114-00-6 2,2',2"-(hexahydro-1,3,5-triazine-1,3,5-triyl)triethanol; 1,3,5-tris(2-hydroxyethyl)hexahydro-1,3,5-triazine 225-208-0 4719-04-4 Acute Tox. 4 * Skin Sens. 1 H302 H317 GHS07 Wng H302 H317 Skin Sens. 1; H317: C ≥ 0,1 % 613-115-00-1 hymexazol (ISO); H317 Skin Sens. 1; H317: C ≥ 0,1 % 613-115-00-1 hymexazol (ISO); 3-hydroxy-5-methylisoxazole 233-000-6 10004-44-1 Acute Tox. 4 * Eye Dam. 1 Aquatic Chronic 3 H302 H318 H412 GHS05 GHS07 Dgr H302 H318 H412 613-116-00-7 tolylfluanid (ISO); dichloro-N-[(dimethylamino)sulphonyl]fluoro-N-(p-tolyl)methanesulphenamide; [containing ≥ 0.1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Acute Tox. 2 * [containing ≥ 0.1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Acute Tox. 2 * STOT RE 1 Eye Irrit. 2 STOT SE 3 … 16 unchanged lines … H317 H400 M=10 613-116-01-4 tolylfluanid (ISO); dichloro-N-[(dimethylamino)sulphonyl]fluoro-N-(p-tolyl)methanesulphenamide; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Eye Irrit. 2 [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Skin Sens. 1 … 48 unchanged lines … (5-benzyl-3-furyl)methyl (1R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate 249-014-0 28434-01-7 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 M = 1000 613-121-00-4 chlorsulfuron (ISO); Wng H410 M = 1000 613-121-00-4 chlorsulfuron (ISO); 2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzenesulphonamide 265-268-5 64902-72-3 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 … 130 unchanged lines … methyl 2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate — 74223-64-6 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 M = 1000 613-140-00-8 cycloheximide (ISO); Wng H410 M = 1000 613-140-00-8 cycloheximide (ISO); 4-{(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl}piperidine-2,6-dione 200-636-0 66-81-9 Muta. 2 Repr. 1B Acute Tox. 2 * … 164 unchanged lines … H301 H314 H317 H410 Skin Corr. 1B; H314: C ≥ 0,6 % Skin Irrit. 2; H315: 0,06 % ≤ C < 0,6 % Eye Irrit. 2; H319: 0,06 % ≤ C < 0,6 % Skin Sens. 1; H317: C ≥ 0,0015 % 613-168-00-0 1-vinyl-2-pyrrolidone 201-800-4 88-12-0 Carc. 2 H410 Skin Corr. 1B; H314: C ≥ 0,6 % Skin Irrit. 2; H315: 0,06 % ≤ C < 0,6 % Eye Irrit. 2; H319: 0,06 % ≤ C < 0,6 % Skin Sens. 1; H317: C ≥ 0,0015 % 613-168-00-0 1-vinyl-2-pyrrolidone 201-800-4 88-12-0 Carc. 2 Acute Tox. 4 * Acute Tox. 4 * Acute Tox. 4 * … 132 unchanged lines … H317 GHS05 GHS07 Dgr H314 H317 STOT SE 3; H335: C ≥ 5 % 613-179-00-0 lithium 3-oxo-1,2(2H)-benzisothiazol-2-ide 411-690-1 111337-53-2 Acute Tox. 4 * H317 STOT SE 3; H335: C ≥ 5 % 613-179-00-0 lithium 3-oxo-1,2(2H)-benzisothiazol-2-ide 411-690-1 111337-53-2 Acute Tox. 4 * Skin Corr. 1B Skin Sens. 1 Aquatic Chronic 2 H302 … 190 unchanged lines … GHS09 Wng H361d*** H373** H410 M = 1000 613-205-00-0 propiconazole(ISO); H410 M = 1000 613-205-00-0 propiconazole(ISO); (±) 1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H—1,2,4-triazole 262-104-4 60207-90-1 Acute Tox. 4 * Skin Sens. 1 Aquatic Acute 1 … 220 unchanged lines … H412 GHS05 Dgr H318 H412 613-241-00-7 3-(2H-tetrazol-5-yl)pyridine 426-810-8 3250-74-6 Eye Dam. 1 H318 GHS05 Dgr H318 613-242-00-2 reaction products of 3,10-bis((2-aminopropyl)amino)-6,13-dichloro-4,11-triphenodioxazinedisulfonic acid with 2-amino-1,4-benzenedisulfonic acid, 2-((4-aminophenyl)sulfonyl)ethyl hydrogen sulfate and 2,4,6-trifluoro-1,3,5-triazine, sodium salts 426-860-0 191877-09-5 Eye Dam. 1 H318 GHS05 Dgr H318 613-242-00-2 reaction products of 3,10-bis((2-aminopropyl)amino)-6,13-dichloro-4,11-triphenodioxazinedisulfonic acid with 2-amino-1,4-benzenedisulfonic acid, 2-((4-aminophenyl)sulfonyl)ethyl hydrogen sulfate and 2,4,6-trifluoro-1,3,5-triazine, sodium salts 426-860-0 191877-09-5 Eye Dam. 1 H318 GHS05 Dgr H318 613-243-00-8 4,4'-(1,6-hexamethylenebis(formylimino))bis(2,2,6,6-tetramethyl-1-oxylpiperidine) 427-350-0 182235-14-9 Aquatic Chronic 2 H411 GHS09 H411 613-244-00-3 5,7-dichloro-4-hydroxyquinoline 427-420-0 21873-52-9 Aquatic Chronic 2 H411 GHS09 H411 613-245-00-9 2-fluoro-6-trifluoromethylpyridine 428-100-3 94239-04-0 Flam. Liq. 3 Acute Tox. 4 * Acute Tox. 4 * … 45 unchanged lines … H373** H318 H317 613-253-00-2 2,2-dialkyl-4-hydroxymethyl-1,3-dioxolane; reaction products with ethylene oxide (alkyl is C1-12 and the sum to C13, average degree of ethoxylation is 3,5) 430-580-4 — Skin Irrit. 2 reaction products with ethylene oxide (alkyl is C1-12 and the sum to C13, average degree of ethoxylation is 3,5) 430-580-4 — Skin Irrit. 2 Aquatic Chronic 2 H315 H411 GHS07 GHS09 … 94 unchanged lines … GHS07 Wng H302 H373** H412 613-270-00-5 5-amino-N-(2,6-dichloro-3-methylphenyl)-1H-1,2,4-triazole-3-sulfonamide 428-150-6 113171-13-4 Aquatic Chronic 3 H412 — H412 613-271-00-0 tritosulfuron (ISO) (containing ≤ 0,02 % AMTT); 1-[4-methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-yl]-3-[2-(trifluoromethyl)benzenesulfonyl]urea (containing ≤ 0,02 % AMTT) — 142469-14-5 Skin Sens. 1 H412 613-270-00-5 5-amino-N-(2,6-dichloro-3-methylphenyl)-1H-1,2,4-triazole-3-sulfonamide 428-150-6 113171-13-4 Aquatic Chronic 3 H412 — H412 613-271-00-0 tritosulfuron (ISO) (containing ≤ 0,02 % AMTT); 1-[4-methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-yl]-3-[2-(trifluoromethyl)benzenesulfonyl]urea (containing ≤ 0,02 % AMTT) — 142469-14-5 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H317 H400 … 128 unchanged lines … 219-989-7 [2] 2592-95-2 [1] 123333-53-9 [2] Expl. 1.3 H203 GHS01 Dgr H203 613-286-00-2 potassium 1-methyl-3-morpholinocarbonyl-4-[3-(1-methyl-3-morpholinocarbonyl-5-oxo-2-pyrazolin-4-ylidene)-1-propenyl]pyrazole-5-olate; [containing < 0,5 % N,N-dimethylformamide (EC no 200-679-5)] 418-260-2 183196-57-8 Skin Sens. 1 H317 GHS07 [containing < 0,5 % N,N-dimethylformamide (EC no 200-679-5)] 418-260-2 183196-57-8 Skin Sens. 1 H317 GHS07 Wng H317 613-286-01-X potassium 1-methyl-3-morpholinocarbonyl-4-[3-(1-methyl-3-morpholinocarbonyl-5-oxo-2-pyrazolin-4-ylidene)-1-propenyl]pyrazole-5-olate; [containing ≥ 0,5 % N,N-dimethylformamide (EC No 200-679-5)] 418-260-2 183196-57-8 Repr. 1B [containing ≥ 0,5 % N,N-dimethylformamide (EC No 200-679-5)] 418-260-2 183196-57-8 Repr. 1B Skin Sens. 1 H360D*** H317 GHS08 GHS07 … 177 unchanged lines … Dgr H341 H318 H317 H 614-001-00-4 nicotine (ISO); 613-317-00-X penconazole (ISO); 1-[2-(2,4-dichlorophenyl)pentyl]-1H-1,2,4-triazole 266-275-6 66246-88-6 Repr. 2 Acute Tox. 4 Aquatic Acute 1 Aquatic Chronic 1 H361d H302 H400 H410 GHS08 GHS07 GHS09 Wng H361d H302 H410 M = 1 M = 1 613-318-00-5 fenpyrazamine (ISO); S-allyl 5-amino-2-isopropyl-4-(2-methylphenyl)-3-oxo-2,3-dihydro-1H-pyrazole-1-carbothioate - 473798-59-3 Aquatic Chronic 2 H411 GHS09 H411 614-001-00-4 nicotine (ISO); 3-(N-methyl-2-pyrrolidinyl)pyridine 200-193-3 54-11-5 Acute Tox. 1 Acute Tox. 3 * Aquatic Chronic 2 H310 … 267 unchanged lines … H335 H315 H334 H317 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % Resp. Sens. 1; H334: C ≥ 0,1 % STOT SE 3; H335: C ≥ 5 % C2 H317 Eye Irrit. 2; H319: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % Resp. Sens. 1; H334: C ≥ 0,1 % STOT SE 3; H335: C ≥ 5 % C2 615-006-00-4 2-methyl-m-phenylene diisocyanate; toluene-2,4-di-isocyanate; [1] 4-methyl-m-phenylene diisocyanate; … 26 unchanged lines … H315 H334 H317 H412 Resp. Sens. 1; H334: C ≥ 0,1 % C H412 Resp. Sens. 1; H334: C ≥ 0,1 % C 615-007-00-X 1,5-naphthylene diisocyanate 221-641-4 3173-72-6 Acute Tox. 4 * Eye Irrit. 2 STOT SE 3 … 34 unchanged lines … H334 H317 H411 * Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens.1; H317: C ≥ 0,5 % 2 Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens.1; H317: C ≥ 0,5 % 2 615-009-00-0 4,4'-methylenedi(cyclohexyl isocyanate); dicyclohexylmethane-4,4'-di-isocyanate 225-863-2 5124-30-1 Acute Tox. 3 * Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Resp. Sens. 1 Skin Sens. 1 H331 H319 H335 H315 H334 H317 GHS06 GHS08 Dgr H331 H319 H335 H315 H334 H317 * Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 2 Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 2 615-010-00-6 2,2,4-trimethylhexamethylene-1,6-di-isocyanate; [1] 2,4,4-trimethylhexamethylene-1,6-di-isocyanate [2] 241-001-8 [1] 239-714-4 [2] 16938-22-0 [1] 15646-96-5 [2] Acute Tox. 3 * Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Resp. Sens. 1 H331 H319 H335 H315 H334 GHS06 GHS08 Dgr H331 H319 H335 H315 H334 * Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % C2 Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % C2 615-011-00-1 hexamethylene-di-isocyanate 212-485-8 822-06-0 Acute Tox. 3 * Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Resp. Sens. 1 Skin Sens. 1 H331 H319 H335 H315 H334 H317 GHS06 GHS08 Dgr H331 H319 H335 H315 H334 H317 * Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 2 Resp. Sens. 1; H334: C ≥ 0,5 % Skin Sens. 1; H317: C ≥ 0,5 % 2 615-012-00-7 4-isocyanatosulphonyltoluene; tosyl isocyanate 223-810-8 4083-64-1 Eye Irrit. 2 STOT SE 3 Skin Irrit. 2 Resp. Sens. 1 H319 H335 H315 H334 GHS08 GHS07 Dgr H319 H335 H315 H334 EUH014 Eye Irrit.; H319: C ≥ 5 % STOT SE 3; H335: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 615-013-00-2 cyanamide; H334 EUH014 Eye Irrit.; H319: C ≥ 5 % STOT SE 3; H335: C ≥ 5 % Skin Irrit. 2; H315: C ≥ 5 % 615-013-00-2 cyanamide; carbanonitril 206-992-3 420-04-2 Acute Tox. 3 * Acute Tox. 4 * Eye Irrit. 2 … 222 unchanged lines … H312 H302 H410 A 615-033-00-1 reaction product of diphenylmethanediisocyanate, octylamine, oleylamine and cyclohexylamine (1:1.58:0.32:0097) 430-980-9 — Aquatic Chronic 4 H413 — H413 615-034-00-7 reaction product of diphenylmethanediisocyanate, octylamine, 4-ethoxyaniline and ethylenediamine (1:0,37:1,53:0,05) 430-750-8 — Aquatic Chronic 4 H413 — H413 615-035-00-2 reaction product of diphenylmethanediisocyanate, octylamine and oleylamine (molar ratio 1:1.86:0.14) 430-930-6 122886-55-9 Aquatic Chronic 4 H413 — H413 615-036-00-8 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 4:1:7:1:2) 430-940-0 — Aquatic Chronic 4 H413 — H413 615-037-00-3 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine and oleylamine (molar ratio 4:1:9:1) 430-950-5 — Aquatic Chronic 4 H413 — H413 615-038-00-9 reaction product of toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate) and aniline (molarratio 1:2) 430-960-1 — Aquatic Chronic 4 H413 — H413 615-039-00-4 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 3.88:1:6.38:0.47:2.91) 430-970-4 — Aquatic Chronic 4 H413 — H413 615-044-00-1 4-chlorophenylisocyanate 203-176-9 104-12-1 Acute Tox. 2 * 615-033-00-1 reaction product of diphenylmethanediisocyanate, octylamine, oleylamine and cyclohexylamine (1:1.58:0.32:0097) 430-980-9 — Aquatic Chronic 4 H413 — H413 615-034-00-7 reaction product of diphenylmethanediisocyanate, octylamine, 4-ethoxyaniline and ethylenediamine (1:0,37:1,53:0,05) 430-750-8 — Aquatic Chronic 4 H413 — H413 615-035-00-2 reaction product of diphenylmethanediisocyanate, octylamine and oleylamine (molar ratio 1:1.86:0.14) 430-930-6 122886-55-9 Aquatic Chronic 4 H413 — H413 615-036-00-8 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 4:1:7:1:2) 430-940-0 — Aquatic Chronic 4 H413 — H413 615-037-00-3 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine and oleylamine (molar ratio 4:1:9:1) 430-950-5 — Aquatic Chronic 4 H413 — H413 615-038-00-9 reaction product of toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate) and aniline (molarratio 1:2) 430-960-1 — Aquatic Chronic 4 H413 — H413 615-039-00-4 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 3.88:1:6.38:0.47:2.91) 430-970-4 — Aquatic Chronic 4 H413 — H413 615-044-00-1 4-chlorophenylisocyanate 203-176-9 104-12-1 Acute Tox. 2 * Acute Tox. 4 * STOT SE 3 Skin Irrit. 2 … 143 unchanged lines … GHS07 Dgr H360D *** H332 H312 Repr. 1B; H360D: C ≥ 5 % 616-012-00-X N-(dichlorofluoromethylthio)phthalimide; H312 Repr. 1B; H360D: C ≥ 5 % 616-012-00-X N-(dichlorofluoromethylthio)phthalimide; N-(fluorodichloromethylthio)phthalimide 211-952-3 719-96-0 Skin Irrit. 2 H315 GHS07 Wng H315 616-013-00-5 butyraldehyde oxime 203-792-8 110-69-0 Acute Tox. 3 * Acute Tox. 4 * … 143 unchanged lines … H312 H410 616-034-00-X pyracarbolid; (ISO); 3,4-dihydro-6-methyl-2H-pyran-5-carboxanilide 246-419-4 24691-76-7 Aquatic Chronic 3 H412 — H412 616-035-00-5 cymoxanil (ISO); 2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino)acetamide 261-043-0 57966-95-7 Acute Tox. 4 * 2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino)acetamide 261-043-0 57966-95-7 Repr. 2 Acute Tox. 4 STOT RE 2 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H302 Aquatic Chronic 1 H361fd H302 H373 (blood, thymus) H317 H400 H410 GHS07 H410 GHS08 GHS07 GHS09 Wng H302 Wng H361fd H302 H373 (blood, thymus) H317 H410 616-036-00-0 2-chloracetamide 201-174-2 79-07-2 Repr. 2 H410 M = 1 M = 1 616-036-00-0 2-chloracetamide 201-174-2 79-07-2 Repr. 2 Acute Tox. 3 * Skin Sens. 1 H361f *** H301 H317 GHS06 GHS08 Dgr H361f *** H301 H317 Skin Sens. 1; H317: C ≥ 0,1 % 616-037-00-6 acetochlor (ISO); H317 Skin Sens. 1; H317: C ≥ 0,1 % 616-037-00-6 acetochlor (ISO); 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide 251-899-3 34256-82-1 Acute Tox. 4 * STOT SE 3 Skin Irrit. 2 … 689 unchanged lines … GHS09 Wng H317 H351 H410 M = 100 M = 100 616-206-00-4 flufenoxuron (ISO); H410 M = 100 M = 100 616-206-00-4 flufenoxuron (ISO); 1-(4-(2-cloro-α,α,α-p-trifluorotolyloxy)-2-fluorophenyl)-3-(2,6-difluorobenzolyl)urea 417-680-3 101463-69-8 Lact. H362 GHS09 H362 M = 10000 M = 10000 Aquatic Acute 1 H400 Wng Aquatic Chronic 1 H410 H410 616-207-00-X polyhexamethylene biguanide hydrochloride 27083-27-8 or 32289-58-0 Carc. 2 H351 GHS05 H351 M = 10 … 16 unchanged lines … 616-211-00-1 proquinazid (ISO); 6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one 189278-12-4 Carc. 2 H351 GHS08 H351 M = 1 M = 10 Aquatic Acute 1 H400 GHS09 Aquatic Chronic 1 H410 Wng H410 617-001-00-2 di-tert-butyl peroxide 203-733-6 110-05-4 Org. Perox. E 616-212-00-7 3-iodo-2-propynyl butylcarbamate; 3-iodoprop-2-yn-1-yl butylcarbamate 259-627-5 55406-53-6 Acute Tox. 3 Acute Tox. 4 STOT RE 1 Eye Dam. 1 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H331 H302 H372 (larynx) H318 H317 H400 H410 GHS06 GHS08 GHS05 GHS09 Dgr H331 H302 H372 (larynx) H318 H317 H410 M = 10 M = 1 617-001-00-2 di-tert-butyl peroxide 203-733-6 110-05-4 Org. Perox. E Flam. Liq. 2 Muta. 2 H242 H225 … 25 unchanged lines … H302 H373 ** H314 H411 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Dam. 1; H318: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 1 % ≤ C < 3 % STOT SE 3; H335: C < 10 % 617-003-00-3 dilauroyl peroxide 203-326-3 105-74-8 Org. Perox. D H242 GHS02 H411 Skin Corr. 1B; H314: C ≥ 10 % Skin Irrit. 2; H315: 3 % ≤ C < 10 % Eye Dam. 1; H318: 3 % ≤ C < 10 % Eye Irrit. 2; H319: 1 % ≤ C < 3 % STOT SE 3; H335: C < 10 % 617-003-00-3 dilauroyl peroxide 203-326-3 105-74-8 Org. Perox. D H242 GHS02 Dgr H242 617-004-00-9 1,2,3,4-tetrahydro-1-naphthyl hydroperoxide 212-230-0 771-29-9 Org. Perox. D Acute Tox. 4 * Skin Corr. 1B Aquatic Acute 1 Aquatic Chronic 1 H242 H302 H314 H400 H410 GHS02 GHS05 GHS07 GHS09 Dgr H242 H302 H314 H410 STOT SE 3; H335: C ≥ 5 % 617-006-00-X bis(α, α-dimethylbenzyl) peroxide 201-279-3 80-43-3 Org. Perox. F H410 STOT SE 3; H335: C ≥ 5 % 617-006-00-X bis(α, α-dimethylbenzyl) peroxide 201-279-3 80-43-3 Org. Perox. F Eye Irrit. 2 Skin Irrit. 2 Aquatic Chronic 2 H242 … 41 unchanged lines … GHS07 Dgr H240 H314 H302 STOT SE 3; H335: C ≥ 5 % C H302 STOT SE 3; H335: C ≥ 5 % C 617-010-01-9 1-hydroperoxycyclohexyl 1-hydroxycyclohexyl peroxide; [1] 1,1'-dioxybiscyclohexan-1-ol; [2] cyclohexylidene hydroperoxide; [3] cyclohexanone, peroxide [4] [≤ 91 % solution] 201-091-1 [1] [≤ 91 % solution] 201-091-1 [1] 219-306-2 [2] 220-279-4 [3] 235-527-7 [4] 78-18-2 [1] 2407-94-5 [2] 2699-11-8 [3] 12262-58-7 [4] Org. Perox. C Acute Tox. 4 * Skin Corr. 1B H242 H302 H314 GHS02 GHS05 GHS07 Dgr H242 H302 H314 STOT SE 3; H335: C ≥ 5 % C T H314 STOT SE 3; H335: C ≥ 5 % C T 617-012-00-2 8-p-menthyl hydroperoxide; p-menthane hydroperoxide 201-281-4 80-47-7 Org. Perox. D Skin Corr. 1B Acute Tox. 4 * H242 H314 H332 GHS02 GHS05 GHS07 Dgr H242 H314 H332 STOT SE 3; H335: C ≥ 5 % 617-013-00-8 O,O-tert-butyl O-docosyl monoperoxyoxalate 404-300-6 116753-76-5 Org. Perox. C **** H332 STOT SE 3; H335: C ≥ 5 % 617-013-00-8 O,O-tert-butyl O-docosyl monoperoxyoxalate 404-300-6 116753-76-5 Org. Perox. C **** Aquatic Acute 1 Aquatic Chronic 1 H242 H400 … 41 unchanged lines … H413 GHS02 Dgr H242 H413 T 617-018-00-5 reaction mass of: 1-methyl-1-(3-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 63 % by weight; 1-methyl-1-(4-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 31 % by weight 410-840-3 71566-50-2 Org. Perox. C **** 617-018-00-5 reaction mass of: 1-methyl-1-(3-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 63 % by weight; 1-methyl-1-(4-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 31 % by weight 410-840-3 71566-50-2 Org. Perox. C **** Aquatic Chronic 2 H242 H411 GHS02 GHS09 … 167 unchanged lines … Dgr H334 647-017-00-5 laccase 420-150-4 80498-15-3 Resp. Sens. 1 H334 GHS08 Dgr H334 648-001-00-0 Distillates (coal tar), benzole fraction; Light Oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists of hydrocarbons having carbon numbers primarily in the range of C4 to C10 and distilling in the approximate range of 80 oC to 160 oC (175 oF to 320 oF).] 283-482-7 84650-02-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists of hydrocarbons having carbon numbers primarily in the range of C4 to C10 and distilling in the approximate range of 80 oC to 160 oC (175 oF to 320 oF).] 283-482-7 84650-02-2 Carc. 1B H350 GHS08 Dgr H350 H 648-002-00-6 Tar oils, brown-coal; Light Oil; [The distillate from lignite tar boiling in the range of approximately 80 °C to 250 °C (176 °F to 482 °F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.] 302-674-4 94114-40-6 Carc. 1B [The distillate from lignite tar boiling in the range of approximately 80 °C to 250 °C (176 °F to 482 °F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.] 302-674-4 94114-40-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-003-00-1 Benzol forerunnings (coal); Light Oil Redistillate, low boiling; [The distillate from coke oven light oil having an approximate distillation range below 100 °C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.] 266-023-5 65996-88-5 Carc. 1B [The distillate from coke oven light oil having an approximate distillation range below 100 °C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.] 266-023-5 65996-88-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-004-00-7 Distillates (coal tar), benzole fraction, BTX-rich; Light Oil Redistillate, low boiling; [A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).] 309-984-9 101896-26-8 Carc. 1B [A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).] 309-984-9 101896-26-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 37 unchanged lines … H340 H J 648-012-00-0 Aromatic hydrocarbons, C8-9, hydrocarbon resin polymn. by-product; Light Oil Redistillate, high boiling; [A complex combination of hydrocarbons obtained from the evaporation of solvent under vacuum from polymerized hydrocarbon resin. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C9 and boiling in the range of approximately 120 °C to 215 °C (248 °F to 419 °F).] 295-281-1 91995-20-9 Carc. 1B [A complex combination of hydrocarbons obtained from the evaporation of solvent under vacuum from polymerized hydrocarbon resin. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C9 and boiling in the range of approximately 120 °C to 215 °C (248 °F to 419 °F).] 295-281-1 91995-20-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-013-00-6 Aromatic hydrocarbons, C9-12, benzene distn.; Light Oil Redistillate, high boiling 295-551-9 92062-36-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-014-00-1 Extract residues (coal), benzole fraction alk., acid ext.; Light Oil Extract Residues, low boiling; [The redistillate from the distillate, freed of tar acids and tar bases, from bituminous coal high temperature tar boiling in the approximate range of 90 °C to 160 °C (194 °F to 320 °F). It consists predominantly of benzene, toluene and xylenes.] 295-323-9 91995-61-8 Carc. 1B [The redistillate from the distillate, freed of tar acids and tar bases, from bituminous coal high temperature tar boiling in the approximate range of 90 °C to 160 °C (194 °F to 320 °F). It consists predominantly of benzene, toluene and xylenes.] 295-323-9 91995-61-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-015-00-7 Extract residues (coal tar), benzole fraction alk., acid ext.; Light Oil Extract Residues, low boiling; [A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195 °C (185 °F to 383 °F).] 309-868-8 101316-63-6 Carc. 1B [A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195 °C (185 °F to 383 °F).] 309-868-8 101316-63-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-016-00-2 Extract residues (coal), benzole fraction acid; Light Oil Extract Residues, low boiling; [An acid sludge by-product of the sulfuric acid refining of crude high temperature coal. Composed primarily of sulfuric acid and organic compounds.] 298-725-2 93821-38-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-017-00-8 Extract residues (coal), light oil alk., distn. overheads; Light Oil Extract Residues, low boiling; [The first fraction from the distillation of aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oil boiling substantially below 145 °C (293 °F). Composed primarily of C7 and C8 aliphatic and aromatic hydrocarbons.] 292-625-2 90641-02-4 Carc. 1B [The first fraction from the distillation of aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oil boiling substantially below 145 °C (293 °F). Composed primarily of C7 and C8 aliphatic and aromatic hydrocarbons.] 292-625-2 90641-02-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-018-00-3 Extract residues (coal), light oil alk., acid ext., indene fraction; Light Oil Extract Residues, intermediate boiling 309-867-2 101316-62-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-019-00-9 Extract residues (coal), light oil alk., indene naphtha fraction; Light Oil Extract Residues, high boiling; [The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155 °C to 180 °C (311 °F to 356 °F). Composed primarily of indene, indan and trimethylbenzenes.] 292-626-8 90641-03-5 Carc. 1B [The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155 °C to 180 °C (311 °F to 356 °F). Composed primarily of indene, indan and trimethylbenzenes.] 292-626-8 90641-03-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-020-00-4 Solvent naphtha (coal); Light Oil Extract Residues, high boiling; [The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130 °C to 210 °C (266 °F to 410 °F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.] 266-013-0 65996-79-4 Carc. 1B [The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130 °C to 210 °C (266 °F to 410 °F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.] 266-013-0 65996-79-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-021-00-X Distillates (coal tar), light oils, neutral fraction; Light Oil Extract Residues, high boiling; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F). May also include unsaturated hydrocarbons such as indene and coumarone.] 309-971-8 101794-90-5 Carc. 1B [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F). May also include unsaturated hydrocarbons such as indene and coumarone.] 309-971-8 101794-90-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-022-00-5 Distillates (coal tar), light oils, acid exts.; Light Oil Extract Residues, high boiling; [This oil is a complex reaction mass of aromatic hydrocarbons, primarily indene, naphthalene, coumarone, phenol, and o-, m- and p-cresol and boiling in the range of 140 °C to 215 °C (284 °F to 419 °F).] 292-609-5 90640-87-2 Carc. 1B [This oil is a complex reaction mass of aromatic hydrocarbons, primarily indene, naphthalene, coumarone, phenol, and o-, m- and p-cresol and boiling in the range of 140 °C to 215 °C (284 °F to 419 °F).] 292-609-5 90640-87-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-023-00-0 Distillates (coal tar), light oils; Carbolic Oil; [A complex combination of hydrocarbons obtained by distillation of coal tar. It consists of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills at the approximate range of 150 °C to 210 °C (302 °F to 410 °F).] 283-483-2 84650-03-3 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of coal tar. It consists of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills at the approximate range of 150 °C to 210 °C (302 °F to 410 °F).] 283-483-2 84650-03-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-024-00-6 Tar oils, coal; Carbolic Oil; [The distillate from high temperature coal tar having an approximate distillation range of 130 °C to 250 °C (266 °F to 410 °F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.] 266-016-7 65996-82-9 Carc. 1B [The distillate from high temperature coal tar having an approximate distillation range of 130 °C to 250 °C (266 °F to 410 °F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.] 266-016-7 65996-82-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 21 unchanged lines … H340 H J 648-029-00-3 Pyridine, alkyl derivs.; Crude Tar Bases; [The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150 °C (302 °F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.] 269-929-9 68391-11-7 Carc. 1B [The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150 °C (302 °F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.] 269-929-9 68391-11-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-030-00-9 Tar bases, coal, picoline fraction; Distillate Bases; [Pyridine bases boiling in the range of approximately 125 °C to 160 °C (257 °F 320 °F) obtained by distillation of neutralized acid extract of the base-containing tar fraction obtained by the distillation of bituminous coal tars. Composed chiefly of lutidines and picolines.] 295-548-2 92062-33-4 Carc. 1B [Pyridine bases boiling in the range of approximately 125 °C to 160 °C (257 °F 320 °F) obtained by distillation of neutralized acid extract of the base-containing tar fraction obtained by the distillation of bituminous coal tars. Composed chiefly of lutidines and picolines.] 295-548-2 92062-33-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-031-00-4 Tar bases, coal, lutidine fraction; Distillate Bases 293-766-2 91082-52-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-032-00-X Extract oils (coal), tar base, collidine fraction; Distillate Bases; [The extract produced by the acidic extraction of bases from crude coal tar aromatic oils, neutralization, and distillation of the bases. Composed primarily of collidines, aniline, toluidines, lutidines, xylidines.] 273-077-3 68937-63-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-033-00-5 Tar bases, coal, collidine fraction; Distillate Bases; [The distillation fraction boiling in the range of approximately 181 °C to 186 °C (356 °F to 367 °F) from the crude bases obtained from the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of bituminous coal tar. It contains chiefly aniline and collidines.] 295-543-5 92062-28-7 Carc. 1B [The distillation fraction boiling in the range of approximately 181 °C to 186 °C (356 °F to 367 °F) from the crude bases obtained from the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of bituminous coal tar. It contains chiefly aniline and collidines.] 295-543-5 92062-28-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-034-00-0 Tar bases, coal, aniline fraction; Distillate Bases; [The distillation fraction boiling in the range of approximately 180 °C to 200 °C (356 °F to 392 °F) from the crude bases obtained by dephenolating and debasing the carbolated oil from the distillation of coal tar. It contains chiefly aniline, collidines, lutidines and toluidines.] 295-541-4 92062-27-6 Carc. 1B [The distillation fraction boiling in the range of approximately 180 °C to 200 °C (356 °F to 392 °F) from the crude bases obtained by dephenolating and debasing the carbolated oil from the distillation of coal tar. It contains chiefly aniline, collidines, lutidines and toluidines.] 295-541-4 92062-27-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-035-00-6 Tar bases, coal, toluidine fraction; Distillate Bases 293-767-8 91082-53-0 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-036-00-1 Distillates (petroleum), alkene-alkyne manuf. pyrolysis oil, mixed with high-temp. coal tar, indene fraction; Redistillates; [A complex combination of hydrocarbons obtained as a redistillate from the fractional distillation of bituminous coal high temperature tar and residual oils that are obtained by the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of indene and boils in a range of approximately 160 °C to 190 °C (320 °F to 374 °F).] 295-292-1 91995-31-2 Carc. 1B [A complex combination of hydrocarbons obtained as a redistillate from the fractional distillation of bituminous coal high temperature tar and residual oils that are obtained by the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of indene and boils in a range of approximately 160 °C to 190 °C (320 °F to 374 °F).] 295-292-1 91995-31-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-037-00-7 Distillates (coal), coal tar-residual pyrolysis oils, naphthalene oils; Redistillates; [The redistillate obtained from the fractional distillation of bituminous coal high temperature tar and pyrolysis residual oils and boiling in the range of approximately 190 °C to 270 °C (374 °F to 518 °F). Composed primarily of substituted dinuclear aromatics.] 295-295-8 91995-35-6 Carc. 1B [The redistillate obtained from the fractional distillation of bituminous coal high temperature tar and pyrolysis residual oils and boiling in the range of approximately 190 °C to 270 °C (374 °F to 518 °F). Composed primarily of substituted dinuclear aromatics.] 295-295-8 91995-35-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-038-00-2 Extract oils (coal), coal tar-residual pyrolysis oils, naphthalene oil, redistillate; Redistillates; [The redistillate from the fractional distillation of dephenolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220 °C to 230 °C (428 °F to 446 °F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.] 295-329-1 91995-66-3 Carc. 1B [The redistillate from the fractional distillation of dephenolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220 °C to 230 °C (428 °F to 446 °F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.] 295-329-1 91995-66-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-039-00-8 Extract oils (coal), coal tar-residual pyrolysis oils, naphthalene oils; Redistillates; [A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225 °C to 255 °C (437 °F to 491 °F). Composed primarily of substituted dinuclear aromatic hydrocarbons.] 310-170-0 122070-79-5 Carc. 1B [A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225 °C to 255 °C (437 °F to 491 °F). Composed primarily of substituted dinuclear aromatic hydrocarbons.] 310-170-0 122070-79-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-040-00-3 Extract oils (coal), coal tar residual pyrolysis oils, naphthalene oil, distn. residues; Redistillates; [Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 °C to 260 °C (464 °F to 500 °F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.] 310-171-6 122070-80-8 Carc. 1B [Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 °C to 260 °C (464 °F to 500 °F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.] 310-171-6 122070-80-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-041-00-9 Absorption oils, bicyclo arom. and heterocyclic hydrocarbon fraction; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260 oC to 290 oC (500 oF to 554 oF).] 309-851-5 101316-45-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260 oC to 290 oC (500 oF to 554 oF).] 309-851-5 101316-45-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-042-00-4 Distillates (coal tar), upper, fluorene-rich; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists af aromatic and polycyclic hydrocarbons primarily fluorene and some acenaphthene.] 284-900-0 84989-11-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-043-00-X Creosote oil, acenaphthene fraction, acenaphthene-free; Wash Oil Redistillate; [The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.] 292-606-9 90640-85-0 Carc. 1B H350 GHS08 Dgr H350 H M 648-044-00-5 Distillates (coal tar), heavy oils; Heavy Anthracene Oil; [Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240 oC to 400 oC (464 oF to 752 oF). Composed primarily of tri- and polynuclear hydrocarbons and heterocyclic compounds.] 292-607-4 90640-86-1 Carc. 1B H350 GHS08 [Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240 oC to 400 oC (464 oF to 752 oF). Composed primarily of tri- and polynuclear hydrocarbons and heterocyclic compounds.] 292-607-4 90640-86-1 Carc. 1B H350 GHS08 Dgr H350 H 648-045-00-0 Distillates (coal tar), upper; Heavy Anthracene Oil; [The distillate from coal tar having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.] 266-026-1 65996-91-0 Carc. 1B H350 GHS08 [The distillate from coal tar having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.] 266-026-1 65996-91-0 Carc. 1B H350 GHS08 Dgr H350 H M 648-046-00-6 Anthracene oil, acid ext.; Anthracene Oil Extract Residue; [A complex combination of hydrocarbons from the base-freed fraction obtained from the distillation of coal tar and boiling in the range of approximately 325 oC to 365 oC (617 oF to 689 oF). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.] 295-274-3 91995-14-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the base-freed fraction obtained from the distillation of coal tar and boiling in the range of approximately 325 oC to 365 oC (617 oF to 689 oF). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.] 295-274-3 91995-14-1 Carc. 1B H350 GHS08 Dgr H350 H M 648-047-00-1 Distillates (coal tar); Heavy Anthracene Oil; [The distillate from coal tar having an approximate distillation range of 100 oC to 450 oC (212 oF to 842 oF). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.] 266-027-7 65996-92-1 Carc. 1B H350 GHS08 [The distillate from coal tar having an approximate distillation range of 100 oC to 450 oC (212 oF to 842 oF). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.] 266-027-7 65996-92-1 Carc. 1B H350 GHS08 Dgr H350 H M 648-048-00-7 Distillates (coal tar), pitch, heavy oils; Heavy Anthracene Oil; [The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300 oC to 470 oC (572 oF to 878 oF). The product may also contain heteroatoms.] 295-312-9 91995-51-6 Carc. 1B H350 GHS08 [The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300 oC to 470 oC (572 oF to 878 oF). The product may also contain heteroatoms.] 295-312-9 91995-51-6 Carc. 1B H350 GHS08 Dgr H350 H M 648-049-00-2 Distillates (coal tar), pitch; Heavy Anthracene Oil; [The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200 oC to greater than 400 oC (392 oF to greater than 752 oF).] 309-855-7 101316-49-8 Carc. 1B H350 GHS08 [The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200 oC to greater than 400 oC (392 oF to greater than 752 oF).] 309-855-7 101316-49-8 Carc. 1B H350 GHS08 Dgr H350 H M 648-050-00-8 Distillates (coal tar), heavy oils, pyrene fraction; Heavy Anthracene Oil Redistillate; [The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350 oC to 400 oC (662 oF to 752 oF). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.] 295-304-5 91995-42-5 Carc. 1B H350 GHS08 [The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350 oC to 400 oC (662 oF to 752 oF). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.] 295-304-5 91995-42-5 Carc. 1B H350 GHS08 Dgr H350 H M 648-051-00-3 Distillates (coal tar), pitch, pyrene fraction; Heavy Anthracene Oil Redistillate; [The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380 oC to 410 oC (7160 to 770 oF). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.] 295-313-4 91995-52-7 Carc. 1B H350 GHS08 [The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380 oC to 410 oC (7160 to 770 oF). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.] 295-313-4 91995-52-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-052-00-9 Paraffin waxes (coal), brown-coal high-temp. tar, carbon-treated; Coal Tar Extract; [A complet combination of hydrocarbons obtained by the treatment of lignite carbonization tar with activated carbon for removal of trace constituents and impurities. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-296-6 97926-76-6 Carc. 1B H350 GHS08 Dgr H350 H M 648-053-00-4 Paraffin waxes (coal), brown-coal high-temp tar, clay-treated; Coal Tar Extract; [A complex combination of hydrocarbons obtained by the treatment of lignite carbonization tar with bentonite for removal of trace constituents and impurities. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-297-1 97926-77-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-054-00-X Pitch; Pitch 263-072-4 61789-60-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-055-00-5 Pitch, coal tar, high-temp.; Pitch; [The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 266-028-2 65996-93-2 Carc. 1B H350 GHS08 [The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 266-028-2 65996-93-2 Carc. 1B H350 GHS08 Dgr H350 H 648-056-00-0 Pitch, coal tar, high-temp., heat-treated; Pitch; [The heat treated residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 80 oC to 180 oC (176 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 310-162-7 121575-60-8 Carc. 1B H350 GHS08 [The heat treated residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 80 oC to 180 oC (176 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 310-162-7 121575-60-8 Carc. 1B H350 GHS08 Dgr H350 H M 648-057-00-6 Pitch, coal tar, high-temp., secondary; Pitch Redistillate; [The residue obtained during the distillation of high boiling fractions from bituminous coal high temperature tar and/or pitch coke oil, with a softening point of 140 oC to 170 oC (284 oF to 392 oF) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.] 302-650-3 94114-13-3 Carc. 1B H350 GHS08 [The residue obtained during the distillation of high boiling fractions from bituminous coal high temperature tar and/or pitch coke oil, with a softening point of 140 oC to 170 oC (284 oF to 392 oF) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.] 302-650-3 94114-13-3 Carc. 1B H350 GHS08 Dgr H350 H M 648-058-00-1 Residues (coal tar), pitch distn.; Pitch Redistillate; [Residue from the fractional distillation of pitch distillate boiling in the range of approximately 400 oC to 470 oC (752 oF to 846 oF). Composed primarily of polynuclear aromatic hydrocarbons, and heterocyclic compounds.] 295-507-9 92061-94-4 Carc. 1B H350 GHS08 [Residue from the fractional distillation of pitch distillate boiling in the range of approximately 400 oC to 470 oC (752 oF to 846 oF). Composed primarily of polynuclear aromatic hydrocarbons, and heterocyclic compounds.] 295-507-9 92061-94-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-059-00-7 Tar, coal, high-temp., distn. and storage residues; Coal Tar Solids Residue; [Coke- and ash-containing solid residues that separate on distillation and thermal treatment of bituminous coal high temperature tar in distillation installations and storage vessels. Consists predominantly of carbon and contains a small quantity of hetero compounds as well as ash components.] 295-535-1 92062-20-9 Carc. 1B H350 GHS08 Dgr H350 H M 648-060-00-2 Tar, coal, storage residues; Coal Tar Solids Residue; [The deposit removed from crude coal tar storages. Composed primarily of coal tar and carbonaceous particulate matter.] 293-764-1 91082-50-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-061-00-8 Tar, coal, high-temp., residues; Coal Tar Solids Residue; [Solids formed during the coking of bituminous coal to produce crude bituminous coal high temperature tar. Composed primarily of coke and coal particles, highly aromatized compounds and mineral substances.] 309-726-5 100684-51-3 Carc. 1B H350 GHS08 Dgr H350 H M 648-062-00-3 Tar, coal, high-temp., high-solids; Coal Tar Solids Residue; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal-type materials.] 273-615-7 68990-61-4 Carc. 1B H350 GHS08 [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal-type materials.] 273-615-7 68990-61-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-063-00-9 Waste solids, coal-tar pitch coking; Coal Tar Solids Residue; … 17 unchanged lines … Dgr H350 H M 648-068-00-6 Tar, coal, low-temp., distn. residues; Tar Oil, intermediate boiling; [Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300 oC (572 oF). Composed primarily of aromatic compounds.] 309-887-1 101316-85-2 Carc. 1B H350 GHS08 [Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300 oC (572 oF). Composed primarily of aromatic compounds.] 309-887-1 101316-85-2 Carc. 1B H350 GHS08 Dgr H350 H M 648-069-00-1 Pitch, coal tar, low-temp; Pitch Residue; [A complex black solid or semi-solid obtained from the distillation of a low temperature coal tar. It has a softening point within the approximate range of 40 oC to 180 oC (104 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-651-4 90669-57-1 Carc. 1B H350 GHS08 [A complex black solid or semi-solid obtained from the distillation of a low temperature coal tar. It has a softening point within the approximate range of 40 oC to 180 oC (104 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-651-4 90669-57-1 Carc. 1B H350 GHS08 Dgr H350 H M 648-070-00-7 Pitch, coal tar, low-temp., oxidized; Pitch Residue, oxidised; [The product obtained by air-blowing, at elevated temperature, low-temperature coal tar pitch. It has a softening-point within the approximate range of 70 oC to 180 oC (158 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-654-0 90669-59-3 Carc. 1B H350 GHS08 [The product obtained by air-blowing, at elevated temperature, low-temperature coal tar pitch. It has a softening-point within the approximate range of 70 oC to 180 oC (158 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-654-0 90669-59-3 Carc. 1B H350 GHS08 Dgr H350 H M 648-071-00-2 Pitch, coal tar, low-temp., heat-treated; Pitch Residue, oxidised; Pitch Residue, heat-treated; [A complex black solid obtained by the heat treatment of low temperature coal tar pitch. It has a softening point within the approximate range of 50 oC to 140 oC (122 oF to 284 oF). Composed primarily of a complex mixture of aromatic compounds.] 292-653-5 90669-58-2 Carc. 1B H350 GHS08 [A complex black solid obtained by the heat treatment of low temperature coal tar pitch. It has a softening point within the approximate range of 50 oC to 140 oC (122 oF to 284 oF). Composed primarily of a complex mixture of aromatic compounds.] 292-653-5 90669-58-2 Carc. 1B H350 GHS08 Dgr H350 H M 648-072-00-8 Distillates (coal-petroleum), condensed-ring arom; Distillates; [The distillate from a mixture of coal and tar and aromatic petroleum streams having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.] 269-159-3 68188-48-7 Carc. 1B H350 GHS08 [The distillate from a mixture of coal and tar and aromatic petroleum streams having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.] 269-159-3 68188-48-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-073-00-3 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polyethylene-polypropylene pyrolysis-derived; Pyrolysis Products; [A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-956-6 101794-74-5 Carc. 1B H350 GHS08 [A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-956-6 101794-74-5 Carc. 1B H350 GHS08 Dgr H350 H M 648-074-00-9 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polyethylene pyrolysis-derived; Pyrolysis Products; [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-957-1 101794-75-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-957-1 101794-75-6 Carc. 1B H350 GHS08 Dgr H350 H M 648-075-00-4 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polystyrene pyrolysis-derived; Pyrolysis Products; [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-958-7 101794-76-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-958-7 101794-76-7 Carc. 1B H350 GHS08 Dgr H350 H M 648-076-00-X Pitch, coal tar-petroleum; Pitch Residues; [The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40 oC to 180 oC (140 oF to 356 oF). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.] 269-109-0 68187-57-5 Carc. 1B H350 GHS08 [The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40 oC to 180 oC (140 oF to 356 oF). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.] 269-109-0 68187-57-5 Carc. 1B H350 GHS08 Dgr H350 H M 648-077-00-5 Phenanthrene, distn. residues; Heavy Anthracene Oil Redistillate; [Residue from the distillation of crude phenanthrene boiling in the approximate range of 340 oC to 420 oC (644 oF to 788 oF). It consists predominantly of phenanthrene, anthracene and carbazole.] 310-169-5 122070-78-4 Carc. 1B H350 GHS08 [Residue from the distillation of crude phenanthrene boiling in the approximate range of 340 oC to 420 oC (644 oF to 788 oF). It consists predominantly of phenanthrene, anthracene and carbazole.] 310-169-5 122070-78-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-078-00-0 Distillates (coal tar), upper, fluorene-free; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists of aromatic polycyclic hydrocarbons, primarily diphenyl, dibenzofuran and acenaphthene.] 284-899-7 84989-10-6 Carc. 1B H350 GHS08 Dgr H350 H M 648-079-00-6 Anthracene oil; Anthracene oil; [A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 oC ot 400 oC (572 oF to 752 oF). Composed primarily of phenanthrene, anthracene and carbazole.] 292-602-7 90640-80-5 Carc. 1B H350 GHS08 [A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 oC ot 400 oC (572 oF to 752 oF). Composed primarily of phenanthrene, anthracene and carbazole.] 292-602-7 90640-80-5 Carc. 1B H350 GHS08 Dgr H350 H M 648-080-00-1 Residues (coal tar), creosote oil distn.; Wash Oil Redistillate; [The residue from the fractional distillation of wash oil boiling in the approximate range of 270 °C to 330 °C (518 °F to 626 °F). It consists predominantly of dinuclear aromatic and heterocyclic hydrocarbons.] 295-506-3 92061-93-3 Carc. 1B H350 GHS08 [The residue from the fractional distillation of wash oil boiling in the approximate range of 270 °C to 330 °C (518 °F to 626 °F). It consists predominantly of dinuclear aromatic and heterocyclic hydrocarbons.] 295-506-3 92061-93-3 Carc. 1B H350 GHS08 Dgr H350 H M 648-081-00-7 Tar, coal; Coal tar; [The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydro-carbons, phenolic compounds, nitrogen bases and thiophene.] 232-361-7 8007-45-2 Carc. 1A H350 GHS08 Dgr H350 H 648-082-00-2 Tar, coal, high-temp.; Coal tar; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.] 266-024-0 65996-89-6 Carc. 1A H350 GHS08 [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water.Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.] 266-024-0 65996-89-6 Carc. 1A H350 GHS08 Dgr H350 H 648-083-00-8 Tar, coal, low-temp.; Coal oil; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.] 266-025-6 65996-90-9 Carc. 1A H350 GHS08 [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.] 266-025-6 65996-90-9 Carc. 1A H350 GHS08 Dgr H350 H 648-084-00-3 Distillates (coal), coke-oven light oil, naphthalene cut; Naphthalene Oil; [The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148 °C (298 °F).] 285-076-5 85029-51-2 Carc. 1B [The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148 °C (298 °F).] 285-076-5 85029-51-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-085-00-9 Distillates (coal tar), naphthalene oils; Naphthalene Oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).] 283-484-8 84650-04-4 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).] 283-484-8 84650-04-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-086-00-4 Distillates (coal tar), naphthalene oils, naphthalene-low; Naphthalene Oil Redistillate; [A complex combination of hydrocarbons obtained by crystallization of naphthalene oil. Composed primarily of naphthalene, alkyl naphthalenes and phenolic compounds.] 284-898-1 84989-09-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-087-00-X Distillates (coal tar), naphthalene oil crystn. mother liquor; Naphthalene Oil Redistillate; [A complex combination of organic compounds obtained as a filtrate from the crystallization of the naphthalene fraction from coal tar and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Contains chiefly naphthalene, thionaphthene and alkylnaphthalenes.] 295-310-8 91995-49-2 Carc. 1B [A complex combination of organic compounds obtained as a filtrate from the crystallization of the naphthalene fraction from coal tar and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Contains chiefly naphthalene, thionaphthene and alkylnaphthalenes.] 295-310-8 91995-49-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 21 unchanged lines … H340 HJM 648-091-00-1 Extract residues (coal), naphthalene oil alk., distn. overheads; Naphthalene Oil Extract Residue; [The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180 °C to 220 °C (356 °F to 428 °F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.] 292-627-3 90641-04-6 Carc. 1B [The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180 °C to 220 °C (356 °F to 428 °F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.] 292-627-3 90641-04-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-092-00-7 Distillates (coal tar), naphthalene oils, methylnaphthalene fraction; Methylnaphthalene Oil; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437 °F to 491 °F).] 309-985-4 101896-27-9 Carc. 1B [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437 °F to 491 °F).] 309-985-4 101896-27-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-093-00-2 Distillates (coal tar), naphthalene oils, indole-methylnaphthalene fraction; Methylnaphthalene Oil; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).] 309-972-3 101794-91-6 Carc. 1B [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).] 309-972-3 101794-91-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-094-00-8 Distillates (coal tar), naphthalene oils, acid exts.; Methylnaphthalene Oil Extract Residue; [A complex combination of hydrocarbons obtained by debasing the methylnaphthalene fraction obtained by the distillation of coal tar and boiling in the range of approximately 230 °C to 255 °C (446 °F to 491 °F). Contains chiefly 1(2)-methylnaphthalene, naphthalene, dimethylnaphthalene and biphenyl.] 295-309-2 91995-48-1 Carc. 1B [A complex combination of hydrocarbons obtained by debasing the methylnaphthalene fraction obtained by the distillation of coal tar and boiling in the range of approximately 230 °C to 255 °C (446 °F to 491 °F). Contains chiefly 1(2)-methylnaphthalene, naphthalene, dimethylnaphthalene and biphenyl.] 295-309-2 91995-48-1 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-095-00-3 Extract residues (coal), naphthalene oil alk., distn. residues; Methylnaphthalene Oil Extract Residue; [The residue from the distillation of alkali-washed naphthalene oil having an approximate distillation range of 220 °C to 300 °C (428 °F to 572 °F). Composed primarily of naphthalene, alkylnaphthalenes and aromatic nitrogen bases.] 292-628-9 90641-05-7 Carc. 1B [The residue from the distillation of alkali-washed naphthalene oil having an approximate distillation range of 220 °C to 300 °C (428 °F to 572 °F). Composed primarily of naphthalene, alkylnaphthalenes and aromatic nitrogen bases.] 292-628-9 90641-05-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-096-00-9 Extract oils (coal), acidic, tar-base free; Methylnaphthalene Oil Extract Residue; [The extract oil boiling in the range of approximately 220 °C to 265 °C (428 °F to 509 °F) from coal tar alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove tar bases. Composed primarily of alkylnaphthalenes.] 284-901-6 84989-12-8 Carc. 1B [The extract oil boiling in the range of approximately 220 °C to 265 °C (428 °F to 509 °F) from coal tar alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove tar bases. Composed primarily of alkylnaphthalenes.] 284-901-6 84989-12-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-097-00-4 Distillates (coal tar), benzole fraction, distn. residues; Wash Oil; [A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150 °C to 300 °C (302 °F to 572 °F) or a semi-solid or solid with a melting point up to 70 °C (158 °F). It is composed primarily of naphthalene and alkyl naphthalenes.] 310-165-3 121620-46-0 Carc. 1B [A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150 °C to 300 °C (302 °F to 572 °F) or a semi-solid or solid with a melting point up to 70 °C (158 °F). It is composed primarily of naphthalene and alkyl naphthalenes.] 310-165-3 121620-46-0 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-098-00-X Creosote oil, acenaphthene fraction; Wash Oil; [A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464 °F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] 292-605-3 90640-84-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464 °F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] 292-605-3 90640-84-9 Carc. 1B H350 GHS08 Dgr H350 H M 648-099-00-5 Creosote oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).] 263-047-8 61789-28-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).] 263-047-8 61789-28-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-100-00-9 Creosote oil, high-boiling distillate; Wash Oil; [The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41 °F).] 274-565-9 70321-79-8 Carc. 1B H350 GHS08 [The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41 °F).] 274-565-9 70321-79-8 Carc. 1B H350 GHS08 Dgr H350 H M 648-101-00-4 Creosote; [The distillate of coal tar produced by the high temperature carbonization of bituminous coal. It consists primarily of aromatic hydrocarbons, tar acids and tar bases.] 232-287-5 8001-58-9 Carc. 1B H350 GHS08 Dgr H350 H 648-102-00-X Extract residues (coal), creosote oil acid; Wash Oil Extract Residue; [A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482 °F to 536 °F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.] 310-189-4 122384-77-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482 °F to 536 °F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.] 310-189-4 122384-77-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-103-00-5 Anthracene oil, anthracene paste; Anthracene Oil Fraction; [The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.] 292-603-2 90640-81-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-104-00-0 Anthracene oil, anthracene-low; Anthracene Oil Fraction; [The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.] 292-604-8 90640-82-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-105-00-6 Residues (coal tar), anthracene oil distn.; Anthracene Oil Fraction; [The residue from the fraction distillation of crude anthracene boiling in the approximate range of 340 °C to 400 °C (644 °F to 752 °F). It consists predominantly of tri- and polynuclear aromatic and heterocyclic hydrocarbons.] 295-505-8 92061-92-2 Carc. 1B [The residue from the fraction distillation of crude anthracene boiling in the approximate range of 340 °C to 400 °C (644 °F to 752 °F). It consists predominantly of tri- and polynuclear aromatic and heterocyclic hydrocarbons.] 295-505-8 92061-92-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-106-00-1 Anthracene oil, anthracene paste, anthracene fraction; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-275-9 91995-15-2 Carc. 1B [A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-275-9 91995-15-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-107-00-7 Anthracene oil, anthracene paste, carbazole fraction; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-276-4 91995-16-3 Carc. 1B [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-276-4 91995-16-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-108-00-2 Anthracene oil, anthracene paste, distn. lights; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.] 295-278-5 91995-17-4 Carc. 1B [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.] 295-278-5 91995-17-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-109-00-8 Tar oils, coal, low-temp.; Tar Oil, high boiling; [A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160 °C to 340 °C (320 °F to 644 °F).] 309-889-2 101316-87-4 Carc. 1B [A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160 °C to 340 °C (320 °F to 644 °F).] 309-889-2 101316-87-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-110-00-3 Extract residues (coal), low temp. coal atar alk.; [The residue from low temperature coal tar oils after an alkaline wash, such as aqueous sodium hydroxide, to remove crude coal tar acids. Composed primarily of hydrocarbons and aromatic nitrogen bases.] 310-191-5 122384-78-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-111-00-9 Phenols, ammonia liquor ext.; Alkaline Extract; [The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. It consists predominantly of a reaction mass of monohydric and dihydric phenols.] 284-881-9 84988-93-2 Carc. 1B [The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. It consists predominantly of a reaction mass of monohydric and dihydric phenols.] 284-881-9 84988-93-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 49 unchanged lines … H340 HJM 648-119-00-2 Tar acids, distn. residues; Distillate Phenols; [A residue from the distillation of crude phenol from coal. It consists predominantly of phenols having carbon numbers in the range of C8 through C10 with a softening point of 60 °C to 80 °C (140 °F to 176 °F).] 306-251-5 96690-55-0 Carc. 1B [A residue from the distillation of crude phenol from coal. It consists predominantly of phenols having carbon numbers in the range of C8 through C10 with a softening point of 60 °C to 80 °C (140 °F to 176 °F).] 306-251-5 96690-55-0 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-120-00-8 Tar acids, methylphenol fraction; Distillate Phenols; [The fraction of tar acid rich in 3- and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-892-9 84989-04-8 Carc. 1B [The fraction of tar acid rich in 3- and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-892-9 84989-04-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-121-00-3 Tar acids, polyalkylphenol fraction; Distillate Phenols; [The fraction of tar acids, recovered by distillation of low-temperature coal tar crude tar acids, having an approximate boiling range of 225 °C to 320 °C (437 °F to 608 °F). Composed primarily of polyalkylphenols.] 284-893-4 84989-05-9 Carc. 1B [The fraction of tar acids, recovered by distillation of low-temperature coal tar crude tar acids, having an approximate boiling range of 225 °C to 320 °C (437 °F to 608 °F). Composed primarily of polyalkylphenols.] 284-893-4 84989-05-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-122-00-9 Tar acids, xylenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-895-5 84989-06-0 Carc. 1B [The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-895-5 84989-06-0 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-123-00-4 Tar acids, ethylphenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 3- and 4-ethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-891-3 84989-03-7 Carc. 1B [The fraction of tar acids, rich in 3- and 4-ethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-891-3 84989-03-7 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-124-00-X Tar acids, 3,5-xylenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 3,5-dimethylphenol, recovered by distillation of low-temperature coal tar acids.] 284-896-0 84989-07-1 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-125-00-5 Tar acids, residues, distillates, first-cut; Distillate Phenols; [The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.] 270-713-1 68477-23-6 Carc. 1B [The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.] 270-713-1 68477-23-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-126-00-0 Tar acids, cresylic, residues; Distillate Phenols; [The residue from crude coal tar acids after removal of phenol, cresols, xylenols and any higher boiling phenols. A black solid with a melting point approximately 80 °C (176 °F). Composed primarily of polyalkylphenols, resin gums, and inorganic salts.] 271-418-0 68555-24-8 Carc. 1B [The residue from crude coal tar acids after removal of phenol, cresols, xylenols and any higher boiling phenols. A black solid with a melting point approximately 80 °C (176 °F). Composed primarily of polyalkylphenols, resin gums, and inorganic salts.] 271-418-0 68555-24-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-127-00-6 Phenols, C9-11; Distillate Phenols 293-435-2 91079-47-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-128-00-1 Tar acids, cresylic; Distillate Phenols; [A complex combination of organic compounds obtained from brown coal and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). It contains chiefly phenols and pyridine bases.] 295-540-9 92062-26-5 Carc. 1B [A complex combination of organic compounds obtained from brown coal and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). It contains chiefly phenols and pyridine bases.] 295-540-9 92062-26-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-129-00-7 Tar acids, brown-coal, C2-alkylphenol fraction; Distillate Phenols; [The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.] 302-662-9 94114-29-1 Carc. 1B [The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.] 302-662-9 94114-29-1 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 26 unchanged lines … H340 HJM 648-134-00-4 Hydrocarbon oils, arom., mixed with polyethylene and polypropylene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of a polyethylene/polypropylene reaction mass with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).] 309-745-9 100801-63-6 Carc. 1B [The oil obtained from the heat treatment of a polyethylene/polypropylene reaction mass with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).] 309-745-9 100801-63-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-135-00-X Hydrocarbon oils, arom., mixed with polyethylene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158 °F to 248 °F).] 309-748-5 100801-65-8 Carc. 1B [The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158 °F to 248 °F).] 309-748-5 100801-65-8 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-136-00-5 Hydrocarbon oils, arom., mixed with polystyrene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410 °F).] 309-749-0 100801-66-9 Carc. 1B [The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410 °F).] 309-749-0 100801-66-9 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-137-00-0 Extract residues (coal), tar oil alk., naphthalene distn. residues; Naphthalene Oil Extract Residue; [The residue obtained from chemical oil extracted after the removal of naphthalene by distillation composed primarily of two to four membered condensed ring aromatic hydrocarbons and aromatic nitrogen bases.] 277-567-8 73665-18-6 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 HJM 648-138-00-6 Creosote oil, low-boiling distillate; Wash Oil; [The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).] 274-566-4 70321-80-1 Carc. 1B H350 GHS08 [The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).] 274-566-4 70321-80-1 Carc. 1B H350 GHS08 Dgr H350 H M 648-139-00-1 Tar acids, cresylic, sodium salts, caustic solns.; Alkaline Extract 272-361-4 68815-21-4 Carc. 1B … 25 unchanged lines … [The substantially solvent-free product obtained by the distillation of the solvent from filtered coal extract solution produced by digesting coal in a liquid solvent. A black semi-solid, composed primarily of a complex combination of condensed-ring aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic compounds and other aromatic oxygen compounds, and their alkyl derivatives.] 302-683-3 94114-48-4 Carc. 1B H350 GHS08 Dgr H350 H M 648-145-00-4 Tar brown-coal; [An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivates, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150 oC to 360 oC (302 oF to 680 oF).] 309-885-0 101316-83-0 Carc. 1A H350 GHS08 [An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivates, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150 oC to 360 oC (302 oF to 680 oF).] 309-885-0 101316-83-0 Carc. 1A H350 GHS08 Dgr H350 H 648-146-00-X Tar, brown-coal, low-temp.; [A tar obtained from low temperature carbonization and low temperature gasification of brown coal. Composed primarily of aliphatic, naphthenic and cyclic aromatic hydrocarbons, heteroaromatic hydrocarbons and cyclic phenols.] 309-886-6 101316-84-1 Carc. 1A H350 GHS08 Dgr H350 H 648-147-00-5 Light oil (coal), coke-oven; Crude benzole; [The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.] 266-012-5 65996-78-3 Carc. 1B [The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.] 266-012-5 65996-78-3 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-148-00-0 Distillates (coal), liq. solvent extn., primary; [The liquid product of condensation of vapors emitted during the digestion of coal in a liquid solvent and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of partly hydrogenated condensed-ring aromatic hydrocarbons, aromatic compounds containing nitrogen, oxygen and sulfur, and their alkyl derivatives having carbon numbers predominantly in the range of C4 through C14.] 302-688-0 94114-52-0 Carc. 1B [The liquid product of condensation of vapors emitted during the digestion of coal in a liquid solvent and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of partly hydrogenated condensed-ring aromatic hydrocarbons, aromatic compounds containing nitrogen, oxygen and sulfur, and their alkyl derivatives having carbon numbers predominantly in the range of C4 through C14.] 302-688-0 94114-52-0 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-149-00-6 Distillates (coal), solvent extn., hydrocracked; [Distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 through C14. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-689-6 94114-53-1 Carc. 1B [Distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 through C14. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-689-6 94114-53-1 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-150-00-1 Naphtha (coal), solvent extn., hydrocracked; [Fraction of the distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 to C9. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-690-1 94114-54-2 Carc. 1B [Fraction of the distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 to C9. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-690-1 94114-54-2 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-151-00-7 Gasoline, coal solvent extn., hydrocracked naphtha; [Motor fuel produced by the reforming of the refined naphtha fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of aromatic and naphthenic hydrocarbons, their alkyl derivatives and alkyl hydrocarbons having carbon numbers in the range of C4 through C9.] 302-691-7 94114-55-3 Carc. 1B H350 GHS08 [Motor fuel produced by the reforming of the refined naphtha fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boilingin the range of approximately 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of aromatic and naphthenic hydrocarbons, their alkyl derivatives and alkyl hydrocarbons having carbon numbers in the range of C4 through C9.] 302-691-7 94114-55-3 Carc. 1B H350 GHS08 Dgr H350 H 648-152-00-2 Distillates (coal), solvent extn., hydrocracked middle; [Distillate obtained from the hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 300 °C (356 °F to 572 °F. Composed primarily of two-ring aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes having carbon numbers predominantly in the range of C9 through C14. Nitrogen, sulfur and oxygen-containing compounds are also present.] 302-692-2 94114-56-4 Carc. 1B [Distillate obtained from the hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 300 °C (356 °F to 572 °F. Composed primarily of two-ring aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes having carbon numbers predominantly in the range of C9 through C14. Nitrogen, sulfur and oxygen-containing compounds are also present.] 302-692-2 94114-56-4 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-153-00-8 Distillates (coal), solvent extn., hydrocracked hydrogenated middle; [Distillate from the hydrogenation of hydrocracked middle distillate from coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 280 °C (356 °F to 536 °F). Composed primarily of hydrogenated two- ring carbon compounds and their alkyl derivatives having carbon numbers predominantly in the range of C9 through C14.] 302-693-8 94114-57-5 Carc. 1B [Distillate from the hydrogenation of hydrocracked middle distillate from coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 280 °C (356 °F to 536 °F). Composed primarily of hydrogenated two- ring carbon compounds and their alkyl derivatives having carbon numbers predominantly in the range of C9 through C14.] 302-693-8 94114-57-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 H340 H J 648-154-00-3 Fuels, jet aircraft, coal solvent extn., hydrocracked hydrogenated; [Jet engine fuel produced by hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 oC to 225 oC (356 oF to 473 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C10 through C12.] 302-694-3 94114-58-6 Carc. 2 H351 GHS08 [Jet engine fuel produced by hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 oC to 225 oC (356 oF to 473 oF). Composed primarilyof hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C10 through C12.] 302-694-3 94114-58-6 Carc. 2 H351 GHS08 Wng H350 H 648-155-00-9 Fuels, diesel, coal solvent extn., hydrocracked hydrogenated; [Diesel engine fuel produced by the hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 200 oC to 280 oC (392 oF to 536 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C11 through C14.] 302-695-9 94114-59-7 Carc. 2 H351 GHS08 [Diesel engine fuel produced by the hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 200 oC to 280 oC (392 oF to 536 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C11 through C14.] 302-695-9 94114-59-7 Carc. 2 H351 GHS08 Wng H350 H 648-156-00-4 Light oil (coal), semi-coking process; Fresh oil; [The volatile organic liquid condensed from the gas evolved in the low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.] 292-635-7 90641-11-5 Carc. 1B [The volatile organic liquid condensed from the gas evolved in the low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.] 292-635-7 90641-11-5 Carc. 1B Muta. 1B H350 H340 GHS08 Dgr H350 … 17 unchanged lines … Wng H315 H411 649-008-00-1 Residues (petroleum), atm. tower; Heavy Fuel oil; [A complex residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-045-2 64741-45-3 Carc. 1B H350 GHS08 [A complex residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-045-2 64741-45-3 Carc. 1B H350 GHS08 Dgr H350 H 649-009-00-7 Gas oils (petroleum), heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 265-058-3 64741-57-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 265-058-3 64741-57-7 Carc. 1B H350 GHS08 Dgr H350 H 649-010-00-2 Distillates (petroleum), heavy catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-063-0 64741-61-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-063-0 64741-61-3 Carc. 1B H350 GHS08 Dgr H350 H 649-011-00-8 Clarified oils (petroleum), catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-064-6 64741-62-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-064-6 64741-62-4 Carc. 1B H350 GHS08 Dgr H350 H 649-012-00-3 Residues (petroleum), hydrocracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products of a hydrocracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF).] 265-076-1 64741-75-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products of a hydrocracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF).] 265-076-1 64741-75-9 Carc. 1B H350 GHS08 Dgr H350 H 649-013-00-9 Residues (petroleum), thermal cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-081-9 64741-80-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-081-9 64741-80-6 Carc. 1B H350 GHS08 Dgr H350 H 649-014-00-4 Distillates (petroleum), heavy thermal cracked; Heavy Fuel oil; [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C15 through C36 and boiling in the range of approximately 260 oC to 480 oC (500 oF to 896 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-082-4 64741-81-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C15 through C36 and boiling in the range of approximately 260 oC to 480 oC (500 oF to 896 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-082-4 64741-81-7 Carc. 1B H350 GHS08 Dgr H350 H 649-015-00-X Gas oils (petroleum), hydrotreated vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C50 and boiling in the range of approximately 230 oC to 600 oC (446 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-162-9 64742-59-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C50 and boiling in the range of approximately 230 oC to 600 oC (446 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-162-9 64742-59-2 Carc. 1B H350 GHS08 Dgr H350 H 649-016-00-5 Residues (petroleum), hydrodesulfurized atmospheric tower; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating an atmospheric tower residuum with hydrogen in the presence of a catalyst under conditions primarily to remove organic sulfur compounds. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-181-2 64742-78-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating an atmospheric tower residuum with hydrogen in the presence of a catalyst under conditions primarily to remove organic sulfur compounds. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-181-2 64742-78-5 Carc. 1B H350 GHS08 Dgr H350 H 649-017-00-0 Gas oils (petroleum), hydrodesulfurized heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oC). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-189-6 64742-86-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oC). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-189-6 64742-86-5 Carc. 1B H350 GHS08 Dgr H350 H 649-018-00-6 Residues (petroleum), steam-cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained as the residual fraction from the distillation of the products of a steam cracking process (including steam cracking to produce ethylene). It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C14 and boiling above approximately 260 oC (500 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-193-8 64742-90-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the residual fraction from the distillation of the products of a steam cracking process (including steam cracking to produce ethylene). It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C14 and boiling above approximately 260 oC (500 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-193-8 64742-90-1 Carc. 1B H350 GHS08 Dgr H350 H 649-019-00-1 Residues (petroleum), atmospheric; Heavy Fuel oil; [A complex residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-777-3 68333-22-2 Carc. 1B H350 GHS08 [A complex residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-777-3 68333-22-2 Carc. 1B H350 GHS08 Dgr H350 H 649-020-00-7 Clarified oils (petroleum), hydrodesulfurized catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-782-0 68333-26-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-782-0 68333-26-6 Carc. 1B H350 GHS08 Dgr H350 H 649-021-00-2 Distillates (petroleum), hydrodesulfurized intermediate catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating intermediate catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 269-783-6 68333-27-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating intermediate catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 269-783-6 68333-27-7 Carc. 1B H350 GHS08 Dgr H350 H 649-022-00-8 Distillates (petroleum), hydrodesulfurized heavy catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treatment of heavy catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 269-784-1 68333-28-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treatment of heavy catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 andboiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 269-784-1 68333-28-8 Carc. 1B H350 GHS08 Dgr H350 H 649-023-00-3 Fuel oil, residues-straight-run gas oils, high-sulfur; Heavy Fuel oil 270-674-0 68476-32-4 Carc. 1B H350 GHS08 Dgr H350 H 649-024-00-9 Fuel oil, residual; Heavy Fuel oil; [The liquid product from various refinery streams, usually residues. The composition is complex and varies with the source of the crude oil.] 270-675-6 68476-33-5 Carc. 1B H350 GHS08 Dgr H350 H 649-025-00-4 Residues (petroleum), catalytic reformer fractionator residue distn.; Heavy Fuel oil; [A complex residuum from the distillation of catalytic reformer fractionator residue. It boils approximately above 399 oC (750 oF).] 270-792-2 68478-13-7 Carc. 1B H350 GHS08 [A complex residuum from the distillation of catalytic reformer fractionator residue. It boils approximately above 399 oC (750 oF).] 270-792-2 68478-13-7 Carc. 1B H350 GHS08 Dgr H350 H 649-026-00-X Residues (petroleum), heavy coker gas oil and vacuum gas oil; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and vacuum gas oil. It predominantly consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-796-4 68478-17-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and vacuum gas oil. It predominantly consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-796-4 68478-17-1 Carc. 1B H350 GHS08 Dgr H350 H 649-027-00-5 Residues (petroleum), heavy coker and light vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and light vacuum gas oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-983-0 68512-61-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and light vacuum gas oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-983-0 68512-61-8 Carc. 1B H350 GHS08 Dgr H350 H 649-028-00-0 Residues (petroleum), light vacuum; Heavy Fuel oil; [A complex residuum from the vacuum distillation of the residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-984-6 68512-62-9 Carc. 1B H350 GHS08 [A complex residuum from the vacuum distillation of the residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-984-6 68512-62-9 Carc. 1B H350 GHS08 Dgr H350 H 649-029-00-6 Residues (petroleum), steam-cracked light; Heavy Fuel oil; [A complex residuum from the distillation of the products from a steam-cracking process. It consists predominantly of aromatic and unsaturated hydrocarbons having carbon numbers greater than C7 and boiling in the range of approximately 101 oC to 555 oC (214 oF to 1030 oF).] 271-013-9 68513-69-9 Carc. 1B H350 GHS08 [A complex residuum from the distillation of the products from a steam-cracking process. It consists predominantly of aromatic and unsaturated hydrocarbons having carbon numbers greater than C7 and boiling in the range of approximately 101 oC to 555 oC (214 oF to 1030 oF).] 271-013-9 68513-69-9 Carc. 1B H350 GHS08 Dgr H350 H 649-030-00-1 Fuel oil, No 6; Heavy Fuel oil; [A distillate oil having a minimum viscosity of 900 SUS at 37.7 oC (100 oF) to a maximum of 9000 SUS at 37.7 oC (100 oF).] 271-384-7 68553-00-4 Carc. 1B H350 GHS08 [A distillate oil having a minimum viscosity of 900 SUS at 37.7 oC (100 oF) to a maximum of 9000 SUS at 37.7 oC (100 oF).] 271-384-7 68553-00-4 Carc. 1B H350 GHS08 Dgr H350 H 649-031-00-7 Residues (petroleum), topping plant, low-sulfur; Heavy Fuel oil; [A low-sulfur complex combination of hydrocarbons produced as the residual fraction from the topping plant distillation of crude oil. It is the residuum after the straight-run gasoline cut, kerosene cut and gas oil cut have been removed.] 271-763-7 68607-30-7 Carc. 1B H350 GHS08 Dgr H350 H 649-032-00-2 Gas oils (petroleum), heavy atmospheric; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C35 and boiling in the range of approximately 121 oC to 510 oC (250 oF to 950 oF).] 272-184-2 68783-08-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C35 and boiling in the range of approximately 121 oC to 510 oC (250 oF to 950 oF).] 272-184-2 68783-08-4 Carc. 1B H350 GHS08 Dgr H350 H 649-033-00-8 Residues (petroleum), coker scrubber, Condensed-ring-arom.-contg.; Heavy Fuel oil; [A very complex combination of hydrocarbons produced as the residual fraction from the distillation of vaccum residuum and the products from a thermal cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed rind aromatic hydrocarbons.] 272-187-9 68783-13-1 Carc. 1B H350 GHS08 [A very complex combination of hydrocarbons produced as the residual fraction from the distillation of vaccum residuum and the products from a thermal cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed rind aromatic hydrocarbons.] 272-187-9 68783-13-1 Carc. 1B H350 GHS08 Dgr H350 H 649-034-00-3 Distillates (petroleum), petroleum residues vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from the atmospheric distillation of crude oil.] 273-263-4 68955-27-1 Carc. 1B H350 GHS08 Dgr H350 H 649-035-00-9 Residues (petroleum), steam-cracked, resinous; Heavy Fuel oil; [A complex residuum from the distillation of steam-cracked petroleum residues.] 273-272-3 68955-36-2 Carc. 1B H350 GHS08 Dgr H350 H 649-036-00-4 Distillates (petroleum), intermediate vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum, distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C14 through C42 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-683-0 70592-76-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the vacuum, distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C14 through C42 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-683-0 70592-76-6 Carc. 1B H350 GHS08 Dgr H350 H 649-037-00-X Distillates (petroleum), light vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C35 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF).] 274-684-6 70592-77-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C35 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF).] 274-684-6 70592-77-7 Carc. 1B H350 GHS08 Dgr H350 H 649-038-00-5 Distillates (petroleum), vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having numbers predominantly in the range of C15 through C50 and boiling in the range of approximately 270 oC to 600 oC (518 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-685-1 70592-78-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having numbers predominantly in the range of C15 through C50 and boiling in the range of approximately 270 oC to 600 oC (518 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-685-1 70592-78-8 Carc. 1B H350 GHS08 Dgr H350 H 649-039-00-0 Gas oils (petroleum), hydrodesulfurized coker heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by hydrodesulfurization of heavy coker distillate stocks, It consists predominantly of hydrocarbons having carbon numbers predominantly in the range C18 to C44 and boiling in the range of approximately 304 oC to 548 oC (579 oF to 1018 oF). Likely to contain 5 % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 285-555-9 85117-03-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by hydrodesulfurization of heavy coker distillate stocks, It consists predominantly of hydrocarbons having carbon numbers predominantly in the range C18 to C44 and boiling in the range of approximately 304 oC to 548 oC (579 oF to 1018 oF). Likely to contain 5 % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 285-555-9 85117-03-9 Carc. 1B H350 GHS08 Dgr H350 H 649-040-00-6 Residues (petroleum), steam-cracked, distillates; Heavy Fuel oil; [A complex combination of hydrocarbons obtained during the production of refined petroleum tar by the distillation of steam cracked tar. It consists predominantly of aromatic and other hydrocarbons and organic sulfur compounds.] 292-657-7 90669-75-3 Carc. 1B H350 GHS08 Dgr H350 H 649-041-00-1 Residues (petroleum), vacuum, light; Heavy Fuel oil; [A complex residuum from the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C24 and boiling above approximately 390 oC (734 oF).] 292-658-2 90669-76-4 Carc. 1B H350 GHS08 [A complex residuum from the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C24 and boiling above approximately 390 oC (734 oF).] 292-658-2 90669-76-4 Carc. 1B H350 GHS08 Dgr H350 H 649-042-00-7 Fuel oil, heavy, high-sulfur; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the distillation of crude petroleum. It consists predominantly of aliphatic, aromatic and cycloaliphatic hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 295-396-7 92045-14-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the distillation of crude petroleum. It consists predominantly of aliphatic, aromatic and cycloaliphatic hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 295-396-7 92045-14-2 Carc. 1B H350 GHS08 Dgr H350 H 649-043-00-2 Residues (petroleum), catalytic cracking; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of the products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF).] 295-511-0 92061-97-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from the distillation of the products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF).] 295-511-0 92061-97-7 Carc. 1B H350 GHS08 Dgr H350 H 649-044-00-8 Distillates (petroleum), intermediate catalytic cracked, thermally degraded; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 220 oC to 450 oC (428 oF to 842 oF). This stream is likely to contain organic sulfur compounds.] 295-990-6 92201-59-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 220 oC to 450 oC (428 oF to 842 oF). This stream is likely to contain organic sulfur compounds.] 295-990-6 92201-59-7 Carc. 1B H350 GHS08 Dgr H350 H 649-045-00-3 Residual oils (petroleum); Heavy Fuel oil; [A complex combination of hydrocarbons, sulfur compounds and metal-containing organic compounds obtained as the residue from refinery fractionation cracking processes. It produces a finished oil with a viscosity above 2cSt. at 100 oC.] 298-754-0 93821-66-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons, sulfur compounds and metal-containing organic compounds obtained as the residue from refinery fractionation cracking processes. It produces a finished oil with a viscosity above 2cSt. at 100 oC.] 298-754-0 93821-66-0 Carc. 1B H350 GHS08 Dgr H350 H 649-046-00-9 Residues, steam cracked, thermally treated; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the treatment and distillation of raw steam-cracked naphtha. It consists predominantly of unsaturated hydrocarbons boiling in the range above approximately 180 oC (356 oF).] 308-733-0 98219-64-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the treatment and distillation of raw steam-cracked naphtha. It consists predominantly of unsaturated hydrocarbons boiling in the range above approximately 180 oC (356 oF).] 308-733-0 98219-64-8 Carc. 1B H350 GHS08 Dgr H350 H 649-047-00-4 Distillates (petroleum), hydrodesulfurized full-range middle; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF).] 309-863-0 101316-57-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF).] 309-863-0 101316-57-8 Carc. 1B H350 GHS08 Dgr H350 H 649-048-00-X Residues (petroleum), catalytic reformer fractionator; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C25 and boiling in the range of approximately 160 oC to 400 oC (320 oF to 725 oF). This stream is likely to contain 5 wt. % or more of 4- or 6-membered condensed ring aromatic hydrocarbons.] 265-069-3 64741-67-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C25 and boiling in the range of approximately 160 oC to 400 oC (320 oF to 725 oF). This stream is likely to contain 5 wt. % or more of 4- or 6-membered condensed ring aromatic hydrocarbons.] 265-069-3 64741-67-9 Carc. 1B H350 GHS08 Dgr H350 H 649-049-00-5 Petroleum; Crude oil; [A complex combination of hydrocarbons, It consists predominantly of aliphatic, alicyclic and aromatic hydrocarbons. It may also contain small amounts of nitrogen, oxygen and sulfur compounds. This category encompasses light, medium, and heavy petroleums, as well as the oils extended from tar sands. Hydrocarbonaceous materials requiring major chemical changes for their recovery or conversion to petroleum refinery feedstocks such as crude shale oils; upgraded shale oils and liquid coal fuels are not included in this definition.] 232-298-5 8002-05-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons, It consists predominantly of aliphatic, alicyclic and aromatic hydrocarbons. It may also contain small amounts of nitrogen, oxygen and sulfur compounds. This category encompasses light, medium, and heavy petroleums, as well as the oils extended from tar sands. Hydrocarbonaceous materials requiring major chemical changes for theirrecovery or conversion to petroleum refinery feedstocks such as crude shale oils; upgraded shale oils and liquid coal fuels are not included in this definition.] 232-298-5 8002-05-9 Carc. 1B H350 GHS08 Dgr H350 H 649-050-00-0 Distillates (petroleum), light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons normally present in this distillation range of crude oil.] 265-051-5 64741-50-0 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons normally present in this distillation range of crude oil.] 265-051-5 64741-50-0 Carc. 1A H350 GHS08 Dgr H350 H 649-051-00-6 Distillates (petroleum), heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons.] 265-052-0 64741-51-1 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons.] 265-052-0 64741-51-1 Carc. 1A H350 GHS08 Dgr H350 H 649-052-00-1 Distillates (petroleum), light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-053-6 64741-52-2 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-053-6 64741-52-2 Carc. 1A H350 GHS08 Dgr H350 H 649-053-00-7 Distillates (petroleum), heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-054-1 64741-53-3 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-054-1 64741-53-3 Carc. 1A H350 GHS08 Dgr H350 H 649-054-00-2 Distillates (petroleum), acid-treated heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-117-3 64742-18-3 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-117-3 64742-18-3 Carc. 1A H350 GHS08 Dgr H350 H 649-055-00-8 Distillates (petroleum), acid-treated light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-118-9 64742-19-4 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-118-9 64742-19-4 Carc. 1A H350 GHS08 Dgr H350 H 649-056-00-3 Distillates (petroleum), acid-treated heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of a least 100 SUS at 100 oF (19cSt at 40 oC).] 265-119-4 64742-20-7 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of a least 100 SUS at 100 oF (19cSt at 40 oC).] 265-119-4 64742-20-7 Carc. 1A H350 GHS08 Dgr H350 H 649-057-00-9 Distillates (petroleum), acid-treated light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-121-5 64742-21-8 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-121-5 64742-21-8 Carc. 1A H350 GHS08 Dgr H350 H 649-058-00-4 Distillates (petroleum), chemically neutralized heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained from a treating process to remove acidic materials. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of aliphatic hydrocarbons.] 265-127-8 64742-27-4 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons obtained from a treating process to remove acidic materials. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of aliphatic hydrocarbons.] 265-127-8 64742-27-4 Carc. 1A H350 GHS08 Dgr H350 H 649-059-00-X Distillates (petroleum), chemically neutralized light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-128-3 64742-28-5 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-128-3 64742-28-5 Carc. 1A H350 GHS08 Dgr H350 H 649-060-00-5 Distillates (petroleum), chemically neutralized heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-135-1 64742-34-3 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-135-1 64742-34-3 Carc. 1A H350 GHS08 Dgr H350 H 649-061-00-0 Distillates (petroleum), chemically neutralized light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS a 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-136-7 64742-35-4 Carc. 1A H350 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS a 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-136-7 64742-35-4 Carc. 1A H350 GHS08 Dgr H350 H 649-062-00-6 Gases (petroleum), catalytic cracked naphtha depropanizer overhead, C3-rich acid-free; Petroleum gas; … 321 unchanged lines … H340 K U 649-087-00-2 Residues (petroleum), alkylation splitter, C4-rich; Petroleum gas; [A complex residuum from the distillation of streams various refinery operations. It consists of hydrocarbons having carbon numbers in the range of C4 through C5, predominantly butane and boiling in the range of approximately – 11.7 °C to 27.8 °C (11 °F to 82 °F).] 271-010-2 68513-66-6 Press. Gas [A complex residuum from the distillation of streams various refinery operations. It consists of hydrocarbons having carbon numbers in the range of C4 through C5, predominantly butane and boiling in the range of approximately – 11.7 °C to 27.8 °C (11 °F to 82 °F).] 271-010-2 68513-66-6 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 H350 H340 GHS04 GHS02 GHS08 Dgr H220 H350 H340 K U 649-088-00-8 Hydrocarbons, C1-4; Petroleum gas; [A complex combination of hydrocarbons provided by thermal cracking and absorber operations and by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately minus 164 °C to minus 0.5 °C (– 263 °F to 31 °F).] 271-032-2 68514-31-8 Press. Gas [A complex combination of hydrocarbons provided by thermal cracking and absorber operations and by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately minus 164 °C to minus 0.5 °C (– 263 °F to 31 °F).] 271-032-2 68514-31-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 H350 H340 GHS04 GHS02 GHS08 Dgr H220 H350 H340 K U 649-089-00-3 Hydrocarbons, C1-4, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting hydrocarbon gases to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 164 °C to – 0.5 °C (– 263 °F to 31 °F).] 271-038-5 68514-36-3 Press. Gas [A complex combination of hydrocarbons obtained by subjecting hydrocarbon gases to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 164 °C to – 0.5 °C (– 263 °F to 31 °F).] 271-038-5 68514-36-3 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 H350 H340 GHS04 GHS02 GHS08 Dgr H220 H350 H340 K U 649-090-00-9 Hydrocarbons, C1-3; Petroleum gas; [A complex combination of hydrocarbons having carbon numbers predominantly in the range of C1 through C3 and boiling in the range of approximately minus 164 °C to minus 42 °C (– 263 °F to – 44 °F).] 271-259-7 68527-16-2 Press. Gas [A complex combination of hydrocarbons having carbon numbers predominantly in the range of C1 through C3 and boiling in the range of approximately minus 164 °C to minus 42 °C (– 263 °F to – 44 °F).] 271-259-7 68527-16-2 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 107 unchanged lines … H340 K U 649-099-00-8 Gases (petroleum), C2-4, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C2 through C4 and boiling in the range of approximately – 51 °C to – 34 °C (– 60 °F to – 30 °F).] 272-205-5 68783-65-3 Press. Gas [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C2 through C4 and boiling in the range of approximately – 51 °C to – 34 °C (– 60 °F to – 30 °F).] 272-205-5 68783-65-3 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-101-00-7 Gases (petroleum), dehexanizer off; Petroleum gas; [A complex combination of hydrocarbons obtained by the fractionation of combined naphtha streams. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 272-872-2 68919-00-6 Press. Gas [A complex combination of hydrocarbons obtained by the fractionation of combined naphtha streams. It consists ofsaturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 272-872-2 68919-00-6 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 97 unchanged lines … H340 K U 649-109-00-0 Tail gas (petroleum), thermal-cracked distillate, gas oil and naphtha absorber; petroleum gas; [A complex combination of hydrocarbons obtained from the separation of thermal-cracked distillates, naphtha and gas oil. It consists pedrominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 273-175-6 68952-81-8 Press. Gas [A complex combination of hydrocarbons obtained from the separation of thermal-cracked distillates, naphtha and gas oil.It consists pedrominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 273-175-6 68952-81-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 69 unchanged lines … H340 K U 649-115-00-3 Gases (petroleum), steam-cracker C3-rich; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of products from a steam cracking process. It consists predominantly of propylene with some propane and boils in the range of approximately – 70 °C to 0 °C (– 94 °F to 32 °F).] 295-404-9 92045-22-2 Press. Gas [A complex combination of hydrocarbons produced by the distillation of products from a steam cracking process. It consists predominantly of propylene with some propane and boils in the range of approximately – 70 °C to 0 °C (– 94 °F to 32 °F).] 295-404-9 92045-22-2 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 H350 H340 GHS04 GHS02 GHS08 Dgr H220 H350 H340 K U 649-116-00-9 Hydrocarbons, C4, steam-cracker distillate; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of the products of a steam cracking process. It consists predominantly of hydrocarbons having a carbon number of C4, predominantly 1-butene and 2-butene, containing also butane and isobutene and boiling in the range of approximately minus 12 °C to 5 °C (10.4 °F to 41 °F).] 295-405-4 92045-23-3 Press. Gas [A complex combination of hydrocarbons produced by the distillation of the products of a steam cracking process. It consists predominantly of hydrocarbons having a carbon number of C4, predominantly 1-butene and 2-butene, containing also butane and isobutene and boiling in the range of approximately minus 12 °C to 5 °C (10.4 °F to 41 °F).] 295-405-4 92045-23-3 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 69 unchanged lines … H340 K U 649-122-00-1 Gases (petroleum), benzene unit recycle, hydrogen-rich; Refinery gas; [A complex combination of hydrocarbons obtained by recycling the gases of the benzene unit. It consists primarily of hydrogen with various small amounts of carbon monoxide and hydrocarbons having carbon numbers in the range of C1 through C6.] 270-748-2 68477-67-8 Press. Gas [A complex combination of hydrocarbons obtained by recycling the gases of thebenzene unit. It consists primarily of hydrogen with various small amounts of carbon monoxide and hydrocarbons having carbon numbers in the range of C1 through C6.] 270-748-2 68477-67-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 96 unchanged lines … H340 K U 649-130-00-5 Gases (petroleum), gas concn. reabsorber distn.; Refinery gas; [A complex combination of hydrocarbons produced by distillation of products from combined gas streams in a gas concentration reabsorber. It consists predominantly of hydrogen, carbon monoxide, carbon dioxide, nitrogen, hydrogen sulfide and hydrocarbons having carbon numbers in the range of C1 through C3.] 270-776-5 68477-93-0 Press. Gas [A complex combination of hydrocarbons produced by distillation of products from combined gas streams in a gas concentration reabsorber. Itconsists predominantly of hydrogen, carbon monoxide, carbon dioxide, nitrogen, hydrogen sulfide and hydrocarbons having carbon numbers in the range of C1 through C3.] 270-776-5 68477-93-0 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 58 unchanged lines … H340 K U 649-135-00-2 Gases (petroleum), reformer make-up, hydrogen-rich; Refinery gas; [A complex combination obtained from the reformers. It consists primarily of hydrogen with various small amounts of carbon monoxide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 270-784-9 68478-01-3 Press. Gas [A complex combination obtained from the reformers. It consists primarily of hydrogen with various small amounts ofcarbon monoxide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 270-784-9 68478-01-3 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 58 unchanged lines … H340 K U 649-140-00-X Tail gas (petroleum), catalytic cracker refractionation absorber; Refinery gas; [A complex combination of hydrocarbons obtained from refractionation of products from a catalytic cracking process. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.] 270-805-1 68478-25-1 Press. Gas [A complex combination of hydrocarbons obtained from refractionation of products from a catalytic cracking process. Itconsists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.] 270-805-1 68478-25-1 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 32 unchanged lines … H340 K U 649-143-00-6 Tail gas (petroleum), cracked distillate hydrotreater separator; Refinery gas; [A complex combination of hydrocarbons obtained by treating cracked distillates with hydrogen in the presence of a catalyst. It consists of hydrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 270-809-3 68478-29-5 Press. Gas [A complex combination of hydrocarbons obtained by treating cracked distillates with hydrogen in the presence of acatalyst. It consists of hydrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 270-809-3 68478-29-5 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 32 unchanged lines … H340 K U 649-146-00-2 Gases (petroleum), reformer effluent high-pressure flash drum off; Refinery gas; [A complex combination produced by the high-pressure flashing of the effluent from the reforming reactor. It consists primarily of hydrogen with various small amounts of methane, ethane, and propane.] 271-003-4 68513-18-8 Press. Gas [A complex combination produced by the high-pressureflashing of the effluent from the reforming reactor. It consists primarily of hydrogen with various small amounts of methane, ethane, and propane.] 271-003-4 68513-18-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 123 unchanged lines … H340 K U 649-156-00-7 Gases (petroleum), hydrotreated sour kerosine flash drum; Refinery gas; [A complex combination obtained from the flash drum of the unit treating sour kerosine with hydrogen in the presence of a catalyst. It consists primarily of hydrogen and methane with various small amounts of nitrogen, carbon monoxide, and hydrocarbons having carbon numbers predominantly in the range of C2 through C5.] 272-776-0 68911-59-1 Press. Gas [A complex combination obtained from the flash drum of the unit treating sour kerosine with hydrogen in the presence of a catalyst. It consists primarily of hydrogenand methane with various small amounts of nitrogen, carbon monoxide, and hydrocarbons having carbon numbers predominantly in the range of C2 through C5.] 272-776-0 68911-59-1 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 110 unchanged lines … H340 K U 649-165-00-6 Tail gas (petroleum), catalytic hydrodesulfurized naphtha separator; Refinery gas; [A complex combination of hydrocarbons obtained from the hydrodesulfurization of naphtha. It consists of hydrogen, methane, ethane, and propane.] 273-173-5 68952-79-4 Press. Gas [A complex combination of hydrocarbons obtained from thehydrodesulfurization of naphtha. It consists of hydrogen, methane, ethane, and propane.] 273-173-5 68952-79-4 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 32 unchanged lines … H340 K U 649-168-00-2 Gases (petroleum), crude distn. and catalytic cracking; Refinery gas; [A complex combination produced by crude distillation and catalytic cracking processes. It consists of hydrogen, hydrogen sulfide, nitrogen, carbon monoxide and paraffinic and olefinic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 273-563-5 68989-88-8 Press. Gas [A complex combination produced by crude distillation and catalytic cracking processes. It consists of hydrogen, hydrogen sulfide, nitrogen,carbon monoxide and paraffinic and olefinic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 273-563-5 68989-88-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-170-00-3 Gases (petroleum), gas oil hydrodesulfurization effluent; Refinery gas; [A complex combination obtained by separation of the liquid phase from the effluent from the hydrogenation reaction. It consists predominantly of hydrogen, hydrogen sulfide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C3.] 295-398-8 92045-16-4 Press. Gas [A complex combination obtained by separation of the liquid phase from the effluent from the hydrogenation reaction. It consists predominantly of hydrogen, hydrogensulfide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C3.] 295-398-8 92045-16-4 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 82 unchanged lines … H340 H K U 649-177-00-1 Gases (petroleum), C3-4; Petroleum gas; [A complex combination of hydrocarbons produced by distillation of products from the cracking of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C4, predominantly of propane and propylene, and boiling in the range of approximately – 51 °C to – 1 °C (– 60 °F to 30 °F.)] 268-629-5 68131-75-9 Press. Gas [A complex combination of hydrocarbons produced by distillation of products from the cracking of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C4, predominantly of propane and propylene, and boiling in the range of approximately – 51 °C to – 1 °C (– 60 °F to 30 °F.)] 268-629-5 68131-75-9 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-179-00-2 Tail gas (petroleum), catalytic polymn. naphtha fractionation stabilizer; Petroleum gas; [A complex combination of hydrocarbons from the fractionation stabilization products from polymerization of naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.] 269-618-8 68307-99-3 Press. Gas [A complex combination of hydrocarbons from the fractionation stabilization productsfrom polymerization of naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.] 269-618-8 68307-99-3 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-181-00-3 Tail gas (petroleum), cracked distillate hydrotreater stripper; Petroleum gas; [A complex combination of hydrocarbons obtained by treating thermal cracked distillates with hydrogen in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 269-620-9 68308-01-0 Press. Gas [A complex combination of hydrocarbons obtained by treating thermal crackeddistillates with hydrogen in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C1 through C6.] 269-620-9 68308-01-0 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 58 unchanged lines … H340 K U 649-186-00-0 Tail gas (petroleum), hydrodesulfurized distillate and hydrodesulfurized naphtha fractionator, acid-free; Petroleum gas; [A complex combination of hydrocarbons obtained from fractionation of hydrodesulfurized naphtha and distillate hydrocarbon streams and treated to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 269-626-1 68308-06-5 Press. Gas [A complex combination of hydrocarbons obtained from fractionation of hydrodesulfurized naphtha and distillatehydrocarbon streams and treated to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 269-626-1 68308-06-5 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-188-00-1 Tail gas (petroleum), light straight-run naphtha stabilizer, hydrogen sulfide-free; Petroleum gas; [A complex combination of hydrocarbons obtained from fractionation stabilization of light straight run naphtha and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 269-629-8 68308-09-8 Press. Gas [A complex combination of hydrocarbons obtained from fractionation stabilization of light straight run naphtha and from which hydrogen sulfide has been removed by aminetreatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 269-629-8 68308-09-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 32 unchanged lines … H340 K U 649-191-00-8 Gases (petroleum), catalytic cracked overheads; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of products from the catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C5 and boiling in the range of approximately – 48 °C to 32 °C (– 54 °F to 90 °F).] 270-071-2 68409-99-4 Press. Gas [A complex combination of hydrocarbons produced by the distillation of products from the catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C5 and boiling in the range of approximately – 48 °C to 32 °C (– 54 °F to 90 °F).] 270-071-2 68409-99-4 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 67 unchanged lines … H340 K U 649-198-00-6 Fuel gases, crude oil of distillates; Petroleum gas; [A complex combination of light gases produced by distillation of crude oil and by catalytic reforming of naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 217 °C to – 12 °C (– 423 °F to 10 °F).] 270-670-9 68476-29-9 Press. Gas [A complex combination of light gases produced by distillation of crude oil and by catalytic reforming of naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 217 °C to – 12 °C (– 423 °F to 10 °F).] 270-670-9 68476-29-9 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 42 unchanged lines … H340 K U 649-202-00-6 Petroleum gases, liquefied; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-704-2 68476-85-7 Press. Gas [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-704-2 68476-85-7 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 H350 H340 GHS04 GHS02 GHS08 Dgr H220 H350 H340 K S U 649-203-00-1 Petroleum gases, liquefied, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting liquefied petroleum gas mix to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-705-8 68476-86-8 Press. Gas [A complex combination of hydrocarbons obtained by subjecting liquefied petroleum gas mix to a sweetening process to convert mercaptans or to remove acidic impurities.It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-705-8 68476-86-8 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 19 unchanged lines … H340 K U 649-205-00-2 Distillates (petroleum), C3-6, piperylene-rich; Petroleum gas; [A complex combination of hydrocarbons from the distillation of saturated and unsaturated aliphatic hydrocarbons usually ranging in the carbon numbers C3 through C6. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C6, predominantly piperylenes.] 270-726-2 68477-35-0 Press. Gas [A complex combination of hydrocarbons from the distillation of saturated and unsaturated aliphatic hydrocarbons usually ranging in the carbon numbers C3 through C6.It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C6, predominantly piperylenes.] 270-726-2 68477-35-0 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 32 unchanged lines … H340 K U 649-208-00-9 Gases (petroleum), catalytic-cracked gas oil depropanizer bottoms, C4-rich acid-free; Petroleum gas; [A complex combination of hydrocarbons obtained from fractionation of catalytic cracked gas oil hydrocarbon stream and treated to remove hydrogen sulfide and other acidic components. It consists of hydrocarbons having carbon numbers in the range of C3 through C5, predominantly C4.] 270-752-4 68477-71-4 Press. Gas [A complex combination of hydrocarbons obtained from fractionation of catalytic cracked gas oil hydrocarbonstream and treated to remove hydrogen sulfide and other acidic components. It consists of hydrocarbons having carbon numbers in the range of C3 through C5, predominantly C4.] 270-752-4 68477-71-4 Press. Gas Flam. Gas 1 Carc. 1A Muta. 1B H220 … 36 unchanged lines … Dgr H350 H L 649-212-00-0 Distillates (petroleum), sweetened middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-088-7 64741-86-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-088-7 64741-86-2 Carc. 1B H350 GHS08 Dgr H350 H N 649-213-00-6 Gas oils (petroleum), solvent-refined; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-092-9 64741-90-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-092-9 64741-90-8 Carc. 1B H350 GHS08 Dgr H350 H N 649-214-00-1 Distillates (petroleum), solvent-refined middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-093-4 64741-91-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-093-4 64741-91-9 Carc. 1B H350 GHS08 Dgr H350 H N 649-215-00-7 Gas oils (petroleum), acid-treated; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-112-6 64742-12-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-112-6 64742-12-7 Carc. 1B H350 GHS08 Dgr H350 H N 649-216-00-2 Distillates (petroleum), acid-treated middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-113-1 64742-13-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-113-1 64742-13-8 Carc. 1B H350 GHS08 Dgr H350 H N 649-217-00-8 Distillates (petroleum), acid-treated light; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-114-7 64742-14-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-114-7 64742-14-9 Carc. 1B H350 GHS08 Dgr H350 H N 649-218-00-3 Gas oils (petroleum), chemically neutralized; Gasoil — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-129-9 64742-29-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-129-9 64742-29-6 Carc. 1B H350 GHS08 Dgr H350 H N 649-219-00-9 Distillates (petroleum), chemically neutralized middle; Gasoil — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-130-4 64742-30-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-130-4 64742-30-9 Carc. 1B H350 GHS08 Dgr H350 H N 649-220-00-4 Distillates (petroleum), clay-treated middle; Gasoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-139-3 64742-38-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-139-3 64742-38-7 Carc. 1B H350 GHS08 Dgr H350 H N 649-221-00-X Distillates (petroleum), hydrotreated middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-148-2 64742-46-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-148-2 64742-46-7 Carc. 1B H350 GHS08 Dgr H350 H N 649-222-00-5 Gas oils (petroleum), hydrodesulfurized; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-182-8 64742-79-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-182-8 64742-79-6 Carc. 1B H350 GHS08 Dgr H350 H N 649-223-00-0 Distillates (petroleum), hydrodesulfurized middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-183-3 64742-80-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-183-3 64742-80-9 Carc. 1B H350 GHS08 Dgr H350 H N 649-224-00-6 Fuels, diesel; Gasoil — unspecified; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 163 oC to 357 oC (325 oF to 675 oF).] 269-822-7 68334-30-5 Carc. 2 H351 GHS08 [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 163 oC to 357 oC (325 oF to 675 oF).] 269-822-7 68334-30-5 Carc. 2 H351 GHS08 Wng H351 H N 649-225-00-1 Fuel oil, No 2; 649-225-00-1 Fuel oil, No 2; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF) to a maximum of 37,9 SUS at 37,7 oC (100 oF).] 270-671-4 68476-30-2 Carc. 2 H351 GHS08 [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF) to a maximum of 37,9 SUS at 37,7 oC (100 oF).] 270-671-4 68476-30-2 Carc. 2 H351 GHS08 Wng H351 H 649-226-00-7 Fuel oil, No 4; 649-226-00-7 Fuel oil, No 4; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 45 SUS at 37,7 oC (100 oF) to a maximum of 125 SUS at 37,7 oC (100 oF).] 270-673-5 68476-31-3 Carc. 2 H351 GHS08 [A distillate oil having a minimum viscosity of 45 SUS at 37,7 oC (100 oF) to a maximum of 125 SUS at 37,7 oC (100 oF).] 270-673-5 68476-31-3 Carc. 2 H351 GHS08 Wng H351 H 649-227-00-2 Fuels, diesel, No 2; 649-227-00-2 Fuels, diesel, No 2; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF).] 270-676-1 68476-34-6 Carc. 2 H351 GHS08 [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF).] 270-676-1 68476-34-6 Carc. 2 H351 GHS08 Wng H351 H 649-228-00-8 Distillates (petroleum), catalytic reformer fractionator residue, high-boiling; Gasoil — unspecified; [A complex combination of hydrocarbons from the distillation of catalytic reformer fracftionator residue. It boils in the range of approximately 343 oC to 399 oC (650 oF to 750 oF).] 270-719-4 68477-29-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the distillation of catalytic reformer fracftionator residue. It boils in the range of approximately 343 oC to 399 oC (650 oF to 750 oF).] 270-719-4 68477-29-2 Carc. 1B H350 GHS08 Dgr H350 H N 649-229-00-3 Distillates (petroleum), catalytic reformer fractionator residue, intermediate-boiling; Gasoil — unspecified; [A complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils in the range of approximately 288 oC to 371 oC (550 oF to 700 oF).] 270-721-5 68477-30-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils in the range of approximately 288 oC to 371 oC (550 oF to 700 oF).] 270-721-5 68477-30-5 Carc. 1B H350 GHS08 Dgr H350 H N 649-230-00-9 Distillates (petroleum), catalytic reformer fractionator residue, low-boiling; Gasoil — unspecified; [The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288 oC (550 oF).] 270-722-0 68477-31-6 Carc. 1B H350 GHS08 [The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288 oC (550 oF).] 270-722-0 68477-31-6 Carc. 1B H350 GHS08 Dgr H350 H N 649-231-00-4 Distillates (petroleum), highly refined middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by the subjection of a petroleum fraction to several of the following steps: filtration, centrifugation, atmospheric distillation, vacuum distillation, acidification, neutralization and clay treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C20.] 292-615-8 90640-93-0 Carc. 1B H350 GHS08 Dgr H350 H N 649-232-00-X Distillates (petroleum) catalytic reformer, heavy arom. conc.; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from the distillation of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C16 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 295-294-2 91995-34-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from the distillation of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C16 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 295-294-2 91995-34-5 Carc. 1B H350 GHS08 Dgr H350 H N 649-233-00-5 Gas oils, paraffinic; Gasoil — unspecified; [A distillate obtained from the redistillation of a complex combination of hydrocarbons obtained by the distillation of the effluents from a severe catalytic hydrotreatment of paraffins. It boils in the range of approximately 190 oC to 330 oC (374 oF to 594 oF).] 300-227-8 93924-33-5 Carc. 1B H350 GHS08 [A distillate obtained from the redistillation of a complex combination of hydrocarbons obtained by the distillation of the effluents from a severe catalytic hydrotreatment of paraffins. It boils in the range of approximately 190 oC to 330 oC (374 oF to 594 oF).] 300-227-8 93924-33-5 Carc. 1B H350 GHS08 Dgr H350 H N 649-234-00-0 Naphtha (petroleum), solvent-refined hydrodesulfurized heavy; Gasoil — unspecified 307-035-3 97488-96-5 Carc. 1B H350 GHS08 Dgr H350 H N 649-235-00-6 Hydrocarbons, C16-20, hydrotreated middle distillate, distn. lights; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a middle distillate with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 290 oC to 350 oC (554 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-659-6 97675-85-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a middle distillate with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 290 oC to 350 oC (554 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-659-6 97675-85-9 Carc. 1B H350 GHS08 Dgr H350 H N 649-236-00-1 Hydrocarbons, C12-20, hydrotreated paraffinic, distn. lights; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of heavy paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 230 oC to 350 oC (446 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-660-1 97675-86-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of heavy paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 230 oC to 350 oC (446 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-660-1 97675-86-0 Carc. 1B H350 GHS08 Dgr H350 H N 649-237-00-7 Hydrocarbons, C11-17, solvent-extd. light naphthenic; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a visciosity of 2.2 cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 307-757-9 97722-08-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a visciosity of 2.2 cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 307-757-9 97722-08-2 Carc. 1B H350 GHS08 Dgr H350 H N 649-238-00-2 Gas oils, hydrotreated; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from the redistillation of the effluents from the treatment of paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C27 and boiling in the range of approximately 330 oC to 340 oC (626 oF to 644 oF).] 308-128-1 97862-78-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from the redistillation of the effluents from the treatment of paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C27 and boiling in the range of approximately 330 oC to 340 oC (626 oF to 644 oF).] 308-128-1 97862-78-7 Carc. 1B H350 GHS08 Dgr H350 H N 649-239-00-8 Distillates (petroleum), carbon-treated light paraffinic; Gasoil — unspecified; … 27 unchanged lines … Dgr H350 H N 649-247-00-1 Slack wax (petroleum), hydrotreated; Slack wax; [A complex combination of hydrocarbons obtained by treating slack wax with hydrogen in the presence of a catalyst. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C20.] 295-523-6 92062-09-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating slack wax with hydrogen in the presence of acatalyst. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C20.] 295-523-6 92062-09-4 Carc. 1B H350 GHS08 Dgr H350 H N 649-248-00-7 Slack wax (petroleum), low-melting; Slack wax; … 49 unchanged lines … Dgr H350 H N 649-261-00-8 Gasoline, natural; Low boiling point naphtha; [A complex combination of hydrocarbons separated from natural gas by processes such as refrigeration or absorption. It consists predominantly of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately minus 20 °C to 120 °C (– 4 °F to 248 °F).] 232-349-1 8006-61-9 Carc. 1B [A complex combination of hydrocarbons separated from natural gas by processes such as refrigeration or absorption. It consists predominantly of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately minus 20 °C to 120 °C (– 4 °F to 248 °F).] 232-349-1 8006-61-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-262-00-3 Naphtha; Low boiling point naphtha; [Refined, partly refined, or unrefined petroleum products produced by the distillation of natural gas. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 232-443-2 8030-30-6 Carc. 1B [Refined, partly refined, or unrefined petroleum products produced by the distillation of natural gas. It consists of hydrocarbons having carbon numberspredominantly in the range of C5 through C6 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 232-443-2 8030-30-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-263-00-9 Ligroine; Low boiling point naphtha; [A complex combination of hydrocarbons obtained by the fractional distillation of petroleum. This fraction boils in a range of approximately 20 °C to 135 °C (58 °F to 275 °F).] 232-453-7 8032-32-4 Carc. 1B [A complex combination of hydrocarbons obtained by the fractional distillation of petroleum. This fraction boils in a range of approximately 20 °C to 135 °C (58 °F to 275 °F).] 232-453-7 8032-32-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-264-00-4 Naphtha (petroleum), heavy straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-041-0 64741-41-9 Carc. 1B [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-041-0 64741-41-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-265-00-X Naphtha (petroleum), full-range straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 428 °F).] 265-042-6 64741-42-0 Carc. 1B [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 428 °F).] 265-042-6 64741-42-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-266-00-5 Naphtha (petroleum), light straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-046-8 64741-46-4 Carc. 1B [A complex combination of hydrocarbons produced by distillation of crude oil. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-046-8 64741-46-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-267-00-0 Solvent naphtha (petroleum), light aliph.; Low boiling point naphtha; [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 35 °C to 160 °C (95 °F to 320 °F).] 265-192-2 64742-89-8 Carc. 1B [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbonnumbers predominantly in the range of C5 through C10 and boiling in the range of approximately 35 °C to 160 °C (95 °F to 320 °F).] 265-192-2 64742-89-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-268-00-6 Distillates (petroleum), straight-run light; Low boiling point naphtha; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C7 and boiling in the range of approximately – 88 °C to 99 °C (– 127 °F to 210 °F).] 270-077-5 68410-05-9 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C7 and boiling in the range of approximately – 88 °C to 99 °C (– 127 °F to 210 °F).] 270-077-5 68410-05-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-269-00-1 Gasoline, vapor-recovery; Low boiling point naphtha; [A complex combination of hydrocarbons separated from the gases from vapor recovery systems by cooling. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 196 °C (– 4 °F to 384 °F).] 271-025-4 68514-15-8 Carc. 1B [A complex combination of hydrocarbons separated from the gases from vapor recovery systems by cooling. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 196 °C (– 4 °F to 384 °F).] 271-025-4 68514-15-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-270-00-7 Gasoline, straight-run, topping-plant; Low boiling point naphtha; [A complex combination of hydrocarbons produced from the topping plant by the distillation of crude oil. It boils in the range of approximately 36,1 °C to 193,3 °C (97 °F to 380 °F).] 271-727-0 68606-11-1 Carc. 1B [A complex combination of hydrocarbons produced from the topping plant by the distillation of crude oil. It boils in the range of approximately 36,1 °C to 193,3 °C (97 °F to 380 °F).] 271-727-0 68606-11-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-271-00-2 Naphtha (petroleum), unsweetened; Low boiling point naphtha; [A complex combination of hydrocarbons produced from the distillation of naphtha streams from various refinery processes. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 0 °C to 230 °C (25 °F to 446 °F).] 272-186-3 68783-12-0 Carc. 1B [A complex combination of hydrocarbons produced from the distillation of naphtha streams from various refinery processes. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 0 °C to 230 °C (25 °F to 446 °F).] 272-186-3 68783-12-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-272-00-8 Distillates (petroleum), light straight-run gasoline fractionation stabilizer overheads; Low boiling point naphtha; [A complex combination of hydrocarbons obtained by the fractionation of light straight-run gasoline. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6.] 272-931-2 68921-08-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-273-00-3 Naphtha (petroleum), heavy straight run, arom.-contg.; Low boiling point naphtha; [A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 309-945-6 101631-20-3 Carc. 1B [A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 309-945-6 101631-20-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-274-00-9 Naphtha (petroleum), full-range alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5 It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 220 °C (194 °F to 428 °F).] 265-066-7 64741-64-6 Carc. 1B [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5 It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 220 °C (194 °F to 428 °F).] 265-066-7 64741-64-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-275-00-4 Naphtha (petroleum), heavy alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 to C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 150 °C to 220 °C (302 °F to 428 °F).] 265-067-2 64741-65-7 Carc. 1B [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 to C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 150 °C to 220 °C (302 °F to 428 °F).] 265-067-2 64741-65-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-276-00-X Naphtha (petroleum), light alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 90 °C to 160 °C (194 °F to 320 °F).] 265-068-8 64741-66-8 Carc. 1B [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantlybranched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 90 °C to 160 °C (194 °F to 320 °F).] 265-068-8 64741-66-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-277-00-5 Naphtha (petroleum), isomerization; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained from catalytic isomerization of straight chain paraffinic C4 through C6 hydrocarbons. It consists predominantly of saturated hydrocarbons such as isobutane, isopentane, 2,2-dimethylbutane, 2-methylpentane, and 3-methylpentane.] 265-073-5 64741-70-4 Carc. 1B [A complex combination of hydrocarbons obtained from catalytic isomerization of straight chain paraffinic C4 through C6 hydrocarbons. It consists predominantly of saturated hydrocarbons such as isobutane, isopentane, 2,2-dimethylbutane, 2-methylpentane, and 3-methylpentane.] 265-073-5 64741-70-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-278-00-0 Naphtha (petroleum), solvent-refined light; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 265-086-6 64741-84-0 Carc. 1B [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbonnumbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 265-086-6 64741-84-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-279-00-6 Naphtha (petroleum), solvent-refined heavy; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-095-5 64741-92-0 Carc. 1B [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-095-5 64741-92-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 23 unchanged lines … H304 H P 649-282-00-2 Naphtha (petroleum), full-range alkylate, butane-contg.; Low boiling point modified naphta; [A complex combination of hydrocarbons produced by the distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 with some butanes and boiling in the range of approximately 35 °C to 200 °C (95 °F to 428 °F).] 271-267-0 68527-27-5 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 with some butanes and boiling in the range of approximately 35 °C to 200 °C (95 °F to 428 °F).] 271-267-0 68527-27-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-283-00-8 Distillates (petroleum), naphtha steam cracking-derived, solvent-refined light hydrotreated; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinates from a solvent extraction process of hydrotreated light distillate from steam-cracked naphtha.] 295-315-5 91995-53-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-284-00-3 Naphtha (petroleum), C4-12, butane-alkylate, isooctane-rich; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by alkylation of butanes. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12, rich in isooctane, and boiling in the range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-430-0 92045-49-3 Carc. 1B [A complex combination of hydrocarbons obtained by alkylation of butanes. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12, rich in isooctane, and boiling in the range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-430-0 92045-49-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-285-00-9 Hydrocarbons, hydrotreated light naphtha distillates, solvent-refined; Low boiling point modified naphtha; [A combination of hydrocarbons obtained from the distillation of hydrotreated naphtha followed by a solvent extraction and distillation process. It consists predominantly of saturated hydrocarbons boiling in the range of approximately 94 °C to 99 °C (201 °F to 210 °F).] 295-436-3 92045-55-1 Carc. 1B [A combination of hydrocarbons obtained from the distillation of hydrotreated naphtha followed by a solvent extraction and distillation process. It consists predominantly of saturated hydrocarbons boiling in the range of approximately 94 °C to 99 °C (201 °F to 210 °F).] 295-436-3 92045-55-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-286-00-4 Naphtha (petroleum), isomerization, C6-fraction; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by distillation of a gasoline which has been catalytically isomerized. It consists predominantly of hexane isomers boiling in the range of approximately 60 °C to 66 °C (140 °F to 151 °F).] 295-440-5 92045-58-4 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of a gasoline which has been catalytically isomerized. It consists predominantly of hexane isomers boiling in the range of approximately 60 °C to 66 °C (140 °F to 151 °F).] 295-440-5 92045-58-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-287-00-X Hydrocarbons, C6-7, naphtha-cracking, solvent-refined; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by the sorption of benzene from a catalytically fully hydrogenated benzene-rich hydrocarbon cut that was distillatively obtained from prehydrogenated cracked naphtha. It consists predominantly of paraffinic and naphthenic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 70 °C to 100 °C (158 °F to 212 °F).] 295-446-8 92045-64-2 Carc. 1B [A complex combination of hydrocarbons obtained by the sorption of benzene from a catalytically fully hydrogenated benzene-rich hydrocarbon cut that was distillatively obtained from prehydrogenated crackednaphtha. It consists predominantly of paraffinic and naphthenic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 70 °C to 100 °C (158 °F to 212 °F).] 295-446-8 92045-64-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-288-00-5 Hydrocarbons, C6-rich, hydrotreated light naphtha distillates, solvent-refined; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65 °C to 70 °C (149 °F to 158 °F).] 309-871-4 101316-67-0 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65 °C to 70 °C (149 °F to 158 °F).] 309-871-4 101316-67-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-289-00-0 Naphtha (petroleum), heavy catalytic cracked; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by a distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-055-7 64741-54-4 Carc. 1B [A complex combination of hydrocarbons produced by a distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling inthe range of approximately 65 °C to 230 °C (148 °F to 446 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-055-7 64741-54-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-290-00-6 Naphtha (petroleum), light catalytic cracked; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-056-2 64741-55-5 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-056-2 64741-55-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-291-00-1 Hydrocarbons, C3-11, catalytic cracker distillates; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillations of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C11 and boiling in a range approximately up to 204 °C (400 °F).] 270-686-6 68476-46-0 Carc. 1B [A complex combination of hydrocarbons produced by the distillations of products from a catalytic cracking process. It consists of hydrocarbonshaving carbon numbers predominantly in the range of C3 through C11 and boiling in a range approximately up to 204 °C (400 °F).] 270-686-6 68476-46-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 23 unchanged lines … H304 H P 649-294-00-8 Naphtha (petroleum), heavy catalytic cracked, sweetened; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting a catalytic cracked petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 60 °C to 200 °C (140 °F to 392 °F).] 295-431-6 92045-50-6 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a catalytic cracked petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 60 °C to 200 °C (140 °F to 392 °F).] 295-431-6 92045-50-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-295-00-3 Naphtha (petroleum), light catalytic cracked sweetened; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting naphtha from a catalytic cracking process to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons boiling in a range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-441-0 92045-59-5 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting naphtha from a catalytic cracking process to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons boiling in a range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-441-0 92045-59-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-296-00-9 Hydrocarbons, C8-12, catalytic-cracking, chem. neutralized; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of a cut from the catalytic cracking process, having undergone an alkaline washing. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 295-794-0 92128-94-4 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of a cut from the catalytic cracking process, having undergone an alkaline washing. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 295-794-0 92128-94-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-297-00-4 Hydrocarbons, C8-12, catalytic cracker distillates; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140 °C to 210 °C (284 °F to 410 °F).] 309-974-4 101794-97-2 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140 °C to 210 °C (284 °F to 410 °F).] 309-974-4 101794-97-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-298-00-X Hydrocarbons, C8-12, catalytic cracking, chem. neutralized, sweetened; Low boiling point cat-cracked naphtha 309-987-5 101896-28-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-299-00-5 Naphtha (petroleum), light catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 265-065-1 64741-63-5 Carc. 1B [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 265-065-1 64741-63-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-300-00-9 Naphtha (petroleum), heavy catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-070-9 64741-68-0 Carc. 1B [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-070-9 64741-68-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-301-00-4 Distillates (petroleum), catalytic reformed depentanizer; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons from the distillation of products from a catalytic reforming process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 63 °C (– 57 °F to 145 °F).] 270-660-4 68475-79-6 Carc. 1B [A complex combination of hydrocarbons from the distillation of products from a catalytic reforming process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 63 °C (– 57 °F to 145 °F).] 270-660-4 68475-79-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 22 unchanged lines … H304 H P 649-304-00-0 Naphtha (petroleum), light catalytic reformed, arom.-free; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained from distillation of products from a catalytic reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 35 °C to 120 °C (95 °F to 248 °F). It contains a relatively large proportion of branched chain hydrocarbons with the aromatic components removed.] 270-993-5 68513-03-1 Carc. 1B [A complex combination of hydrocarbons obtained from distillation of products from a catalytic reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 35 °C to 120 °C (95 °F to 248 °F). It contains a relatively large proportion of branched chain hydrocarbons with the aromatic components removed.] 270-993-5 68513-03-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-305-00-6 Distillates (petroleum), catalytic reformed straight-run naphtha overheads; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by the catalytic reforming of straight-run naphtha followed by the fractionation of the total effluent. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.] 271-008-1 68513-63-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-306-00-1 Petroleum products, hydrofiner-powerformer reformates; Low boiling point cat-reformed naphtha; [The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27 °C to 210 °C (80 °F to 410 °F).] 271-058-4 68514-79-4 Carc. 1B [The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27 °C to 210 °C (80 °F to 410 °F).] 271-058-4 68514-79-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-307-00-7 Naphtha (petroleum), full-range reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced by the distillation of the products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 272-895-8 68919-37-9 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of the products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 272-895-8 68919-37-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-308-00-2 Naphtha (petroleum), catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 220 °C (90 °F to 430 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 273-271-8 68955-35-1 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 220 °C (90 °F to 430 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 273-271-8 68955-35-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-309-00-8 Distillates (petroleum), catalytic reformed hydrotreated light, C8-12 arom. fraction; Low boiling point cat-reformed naphtha; [A complex combination of alkylbenzenes obtained by the catalytic reforming of petroleum naphtha. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 160 °C to 180 °C (320 °F to 356 °F).] 285-509-8 85116-58-1 Carc. 1B [A complex combination of alkylbenzenes obtained by the catalytic reforming of petroleum naphtha. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 160 °C to 180 °C (320 °F to 356 °F).] 285-509-8 85116-58-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-310-00-3 Aromatic hydrocarbons, C8, catalytic reforming-derived; Low boiling point cat-reformed naphtha 295-279-0 91995-18-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-311-00-9 Aromatic hydrocarbons, C7-12, C8-rich; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 (primarily C8) and can contain nonaromatic hydrocarbons, both boiling in the range of approximately 130 °C to 200 °C (266 °F to 392 °F).] 297-401-8 93571-75-6 Carc. 1B [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 (primarily C8) and can contain nonaromatic hydrocarbons, both boiling in the range of approximately 130 °C to 200 °C (266 °F to 392 °F).] 297-401-8 93571-75-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-312-00-4 Gasoline, C5-11, high-octane stabilised reformed; Low boiling point cat-reformed naphtha; [A complex high octane combination of hydrocarbons obtained by the catalytic dehydrogenation of a predominantly naphthenic naphtha. It consists predominantly of aromatics and non-aromatics having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 45 °C to 185 °C (113 °F to 365 °F).] 297-458-9 93572-29-3 Carc. 1B [A complex high octane combination of hydrocarbons obtained by the catalytic dehydrogenation of a predominantly naphthenic naphtha. It consists predominantly of aromatics and non-aromatics having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 45 °C to 185 °C (113 °F to 365 °F).] 297-458-9 93572-29-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-313-00-X Hydrocarbons, C7-12, C≥9-arom.-rich, reforming heavy fraction; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 120 °C to 210 °C (248 °F to 380 °F) and C9 and higher aromatic hydrocarbons.] 297-465-7 93572-35-1 Carc. 1B [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 120 °C to 210 °C (248 °F to 380 °F) and C9 and higher aromatic hydrocarbons.] 297-465-7 93572-35-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-314-00-5 Hydrocarbons, C5-11, nonaroms.-rich, reforming light fraction; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 125 °C (94 °F to 257 °F), benzene and toluene.] 297-466-2 93572-36-2 Carc. 1B [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 125 °C (94 °F to 257 °F), benzene and toluene.] 297-466-2 93572-36-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-315-00-0 Foots oil (petroleum), silicic acid-treated; Foots oil; [A complex combination of hydrocarbons obtained by the treatment of Foots oil with silicic acid for removal of trace constituents and impurities. It consists predominantly of straight chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-127-6 97862-77-6 Carc. 1B H350 H304 GHS08 Dgr H350 H304 H L 649-316-00-6 Naphtha (petroleum), light thermal cracked; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons from distillation of products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately – 10 °C to 130 °C (14 °F to 266 °F).] 265-075-6 64741-74-8 Carc. 1B [A complex combination of hydrocarbons from distillation of products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately – 10 °C to 130 °C (14 °F to 266 °F).] 265-075-6 64741-74-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-317-00-1 Naphtha (petroleum), heavy thermal cracked; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons from distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 220 °C (148 °F to 428 °F).] 265-085-0 64741-83-9 Carc. 1B [A complex combination of hydrocarbons from distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 220 °C (148 °F to 428 °F).] 265-085-0 64741-83-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 23 unchanged lines … H304 H P 649-320-00-8 Distillates (petroleum), naphtha-raffinate pyrolyzate-derived, gasoline-blending; Low boiling point thermally cracked naphtha; [The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204 °C (400 °F).] 270-344-6 68425-29-6 Carc. 1B [The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204 °C (400 °F).] 270-344-6 68425-29-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-321-00-3 Aromatic hydrocarbons, C6-8, naphtha-raffinate pyrolyzate-derived; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons obtained by the fractionation pyrolysis at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.] 270-658-3 68475-70-7 Carc. 1B [A complex combination of hydrocarbons obtained by the fractionation pyrolysis at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.] 270-658-3 68475-70-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-322-00-9 Distillates (petroleum), thermal cracked naphtha and gas oil; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by distillation of thermally cracked naphtha and/or gas oil. It consists predominantly of olefinic hydrocarbons having a carbon number of C5 and boiling in the range of approximately 33 °C to 60 °C (91 °F to 140 °F).] 271-631-9 68603-00-9 Carc. 1B [A complex combination of hydrocarbons produced by distillation of thermally cracked naphtha and/or gas oil. It consists predominantly of olefinic hydrocarbons having a carbon number of C5 and boiling in the range of approximately 33 °C to 60 °C (91 °F to 140 °F).] 271-631-9 68603-00-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-323-00-4 Distillates (petroleum), thermal cracked naphtha and gas oil, C5-dimer-contg.; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists predominantly of hydrocarbons having a carbon number of C5 with some dimerized C5 olefins and boiling in the range of approximately 33 °C to 184 °C (91 °F to 363 °F).] 271-632-4 68603-01-0 Carc. 1B [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists predominantly of hydrocarbons having a carbon number of C5 with some dimerized C5 olefins and boiling in the range of approximately 33 °C to 184 °C (91 °F to 363 °F).] 271-632-4 68603-01-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-324-00-X Distillates (petroleum), thermal cracked naphtha and gas oil, extractive; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists of paraffinic and olefinic hydrocarbons, predominantly isoamylenes such as 2-methyl-1-butene and 2-methyl-2-butene and boiling in the range of approximately 31 °C to 40 °C (88 °F to 104 °F).] 271-634-5 68603-03-2 Carc. 1B [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists of paraffinic and olefinic hydrocarbons, predominantly isoamylenes such as 2-methyl-1-butene and 2-methyl-2-butene and boiling in the range of approximately 31 °C to 40 °C (88 °F to 104 °F).] 271-634-5 68603-03-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-325-00-5 Distillates (petroleum), light thermal cracked, debutanized arom.; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a thermal cracking process. It consists predominantly of aromatic hydrocarbons, primarily benzene.] 273-266-0 68955-29-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-326-00-0 Naphtha (petroleum), light thermal cracked, sweetened; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate from the high temperature thermal cracking of heavy oil fractions to a sweetening process to convert mercaptans. It consists predominantly of aromatics, olefins and saturated hydrocarbons boiling in the range of approximately 20 °C to 100 °C (68 °F to 212 °F).] 295-447-3 92045-65-3 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate from the high temperature thermal cracking of heavy oil fractions to a sweetening process to convert mercaptans. It consists predominantly of aromatics, olefins and saturated hydrocarbons boiling in the range of approximately 20 °C to 100 °C (68 °F to 212 °F).] 295-447-3 92045-65-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-327-00-6 Naphtha (petroleum), hydrotreated heavy; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C13 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-150-3 64742-48-9 Carc. 1B [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C13 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-150-3 64742-48-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-328-00-1 Naphtha (petroleum), hydrotreated light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F).] 265-151-9 64742-49-0 Carc. 1B [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F).] 265-151-9 64742-49-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-329-00-7 Naphtha (petroleum), hydrodesulfurized light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-178-6 64742-73-0 Carc. 1B [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-178-6 64742-73-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-330-00-2 naphtha (petroleum), hydrodesulphurized heavy; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-185-4 64742-82-1 Carc. 1B H350 GHS08 H350 P [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-185-4 64742-82-1 Carc. 1B H350 GHS08 H350 P Muta. 1B H340 Dgr H340 STOT RE 1 H372 (central nervous system) H372 (central nervous system) Asp. Tox. 1 H304 H304 649-331-00-8 Distillates (petroleum), hydrotreated middle, intermediate boiling; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by the distillation of products from a middle distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 127 °C to 188 °C (262 °F to 370 °F).] 270-092-7 68410-96-8 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of products from a middle distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 127 °C to 188 °C (262 °F to 370 °F).] 270-092-7 68410-96-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-332-00-3 Distillates (petroleum), light distillate hydrotreating process, low-boiling; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by the distillation of products from the light distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C9 and boiling in the range of approximately 3 °C to 194 °C (37 °F to 382 °F).] 270-093-2 68410-97-9 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of products from the light distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C9 and boiling in the range of approximately 3 °C to 194 °C (37 °F to 382 °F).] 270-093-2 68410-97-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-333-00-9 Distillates (petroleum), hydrotreated heavy naphtha, deisohexanizer overheads; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by distillation of the products from a heavy naphtha hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 68 °C (– 57 °F to 155 °F).] 270-094-8 68410-98-0 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of the products from a heavy naphtha hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 68 °C (– 57 °F to 155 °F).] 270-094-8 68410-98-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-334-00-4 Solvent naphtha (petroleum), light arom., hydrotreated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 270-988-8 68512-78-7 Carc. 1B [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 270-988-8 68512-78-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-335-00-X Naphtha (petroleum), hydrodesulfurized thermal cracked light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by fractionation of hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 195 °C (73 °F to 383 °F).] 285-511-9 85116-60-5 Carc. 1B [A complex combination of hydrocarbons obtained by fractionation of hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 195 °C (73 °F to 383 °F).] 285-511-9 85116-60-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-336-00-5 Naphtha (petroleum), hydrotreated light, cycloalkane-contg.; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from the distillation of a petroleum fraction. It consists predominantly of alkanes and cycloalkanes boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 285-512-4 85116-61-6 Carc. 1B [A complex combination of hydrocarbons obtained from the distillation of a petroleum fraction. It consists predominantly of alkanes and cycloalkanes boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 285-512-4 85116-61-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-337-00-0 Naphtha (petroleum), heavy steam-cracked, hydrogenated; Low boiling point hydrogen treated naphtha 295-432-1 92045-51-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-338-00-6 Naphtha (petroleum), hydrodesulfurized full-range; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 250 °C (86 °F to 482 °F).] 295-433-7 92045-52-8 Carc. 1B [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 250 °C (86 °F to 482 °F).] 295-433-7 92045-52-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-339-00-1 Naphtha (petroleum), hydrotreated light steam-cracked; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction, derived from a pyrolysis process, with hydrogen in the presence of a catalyst. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 295-438-4 92045-57-3 Carc. 1B [A complex combination of hydrocarbons obtained by treating a petroleum fraction, derived from a pyrolysis process, with hydrogen in the presence of a catalyst. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 295-438-4 92045-57-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-340-00-7 Hydrocarbons, C4-12, naphtha-cracking, hydrotreated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by distillation from the product of a naphtha steam cracking process and subsequent catalytic selective hydrogenation of gum formers. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 230 °C (86 °F to 446 °F).] 295-443-1 92045-61-9 Carc. 1B [A complex combination of hydrocarbons obtained by distillation from the product of a naphtha steam cracking process and subsequent catalytic selective hydrogenation of gum formers. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 230 °C (86 °F to 446 °F).] 295-443-1 92045-61-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-341-00-2 Solvent naphtha (petroleum), hydrotreated light naphthenic; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of cycloparaffinic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 73 °C to 85 °C (163 °F to 185 °F).] 295-529-9 92062-15-2 Carc. 1B [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of cycloparaffinic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 73 °C to 85 °C (163 °F to 185 °F).] 295-529-9 92062-15-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-342-00-8 Naphtha (petroleum), light steam-cracked, hydrogenated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons produced from the separation and subsequent hydrogenation of the products of a steam-cracking process to produce ethylene. It consists predominantly of saturated and unsaturated paraffins, cyclic paraffins and cyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately 50 °C to 200 °C (122 °F to 392 °F). The proportion of benzene hydrocarbons may vary up to 30 wt. % and the stream may also contain small amounts of sulfur and oxygenated compounds.] 296-942-7 93165-55-0 Carc. 1B [A complex combination of hydrocarbons produced from the separation and subsequent hydrogenation of the products of a steam-cracking process to produce ethylene. It consists predominantly of saturated and unsaturated paraffins, cyclic paraffins and cyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately 50 °C to 200 °C (122 °F to 392 °F). The proportion of benzene hydrocarbons may vary up to 30 wt. % and the stream may also contain small amounts of sulfur and oxygenated compounds.] 296-942-7 93165-55-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 23 unchanged lines … H304 H P 649-345-00-4 stoddard solvent; Low boiling point naphtha — unspecified; [A colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).] 232-489-3 8052-41-3 Carc. 1B H350 GHS08 H350 P [A colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).] 232-489-3 8052-41-3 Carc. 1B H350 GHS08 H350 P Muta. 1B H340 Dgr H340 STOT RE 1 H372 (central nervous system) H372 (central nervous system) Asp. Tox. 1 H304 H304 649-346-00-X Natural gas condensates (petroleum); Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons separated as a liquid from natural gas in a surface separator by retrograde condensation. It consists mainly of hydrocarbons having carbon numbers predominantly in the range of C2 to C20. It is a liquid at atmospheric temperature and pressure.] 265-047-3 64741-47-5 Carc. 1B [A complex combination of hydrocarbons separated as a liquid from natural gas in a surface separator by retrograde condensation. It consists mainly of hydrocarbons having carbon numbers predominantly in the range of C2 to C20. It is a liquid at atmospheric temperature and pressure.] 265-047-3 64741-47-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-347-00-5 Natural gas (petroleum), raw liq. mix; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons separated as a liquid from natural gas in a gas recycling plant by processes such as refrigeration or absorption. It consists mainly of saturated aliphatic hydrocarbons having carbon numbers in the range of C2 through C8.] 265-048-9 64741-48-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-348-00-0 Naphtha (petroleum), light hydrocracked; Low boiling naphtha - unspecified; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C4 through C10, and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-071-4 64741-69-1 Carc. 1B [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C4 through C10, and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-071-4 64741-69-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-349-00-6 Naphtha (petroleum), heavy hydrocracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12, and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F).] 265-079-8 64741-78-2 Carc. 1B [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12, and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F).] 265-079-8 64741-78-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-350-00-1 Naphtha (petroleum), sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately – 10 °C to 230 °C (14 °F to 446 °F).] 265-089-2 64741-87-3 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately – 10 °C to 230 °C (14 °F to 446 °F).] 265-089-2 64741-87-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-351-00-7 Naphtha (petroleum), acid-treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-115-2 64742-15-0 Carc. 1B [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-115-2 64742-15-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-352-00-2 Naphtha (petroleum), chemically neutralized heavy; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-122-0 64742-22-9 Carc. 1B [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-122-0 64742-22-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-353-00-8 Naphtha (petroleum), chemically neutralized light; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-123-6 64742-23-0 Carc. 1B [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-123-6 64742-23-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-354-00-3 Naphtha (petroleum), catalytic dewaxed; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from the catalytic dewaxing of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 265-170-2 64742-66-1 Carc. 1B [A complex combination of hydrocarbons obtained from the catalytic dewaxing of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 265-170-2 64742-66-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-355-00-9 Naphtha (petroleum), light steam-cracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F). This stream is likely to contain 10 vol. % or more benzene.] 265-187-5 64742-83-2 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F). This stream is likely to contain 10 vol. % or more benzene.] 265-187-5 64742-83-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-356-00-4 Solvent naphtha (petroleum), light arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 265-199-0 64742-95-6 Carc. 1B [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 265-199-0 64742-95-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-357-00-X Aromatic hydrocarbons, C6-10, acid-treated, neutralized; Low boiling point naphtha - unspecified 268-618-5 68131-49-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-358-00-5 Distillates (petroleum), C3-5, 2-methyl-2-butene-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons from the distillation of hydrocarbons usually ranging in carbon numbers from C3 through C5, predominantly isopentane and 3-methyl-1-butene. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C5, predominantly 2-methyl-2-butene.] 270-725-7 68477-34-9 Carc. 1B [A complex combination of hydrocarbons from the distillation of hydrocarbons usually ranging in carbon numbers from C3 through C5, predominantly isopentane and 3-methyl-1-butene. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C5, predominantly 2-methyl-2-butene.] 270-725-7 68477-34-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 72 unchanged lines … H304 H P 649-366-00-9 Naphtha (petroleum), full-range coker; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C15 and boiling in the range of approximately 43 °C to 250 °C (110 °F-500 °F).] 270-991-4 68513-02-0 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C15 and boiling in the range of approximately 43 °C to 250 °C (110 °F-500 °F).] 270-991-4 68513-02-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-367-00-4 Naphtha (petroleum), steam-cracked middle arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by the distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 130 °C to 220 °C (266 °F to 428 °F).] 271-138-9 68516-20-1 Carc. 1B [A complex combination of hydrocarbons produced by the distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 130 °C to 220 °C (266 °F to 428 °F).] 271-138-9 68516-20-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-368-00-X Naphtha (petroleum), clay-treated full-range straight-run; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons resulting from treatment of full-range straight-run naphtha with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 429 °F).] 271-262-3 68527-21-9 Carc. 1B [A complex combination of hydrocarbons resulting from treatment of full-range straight-run naphtha with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 429 °F).] 271-262-3 68527-21-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-369-00-5 Naphtha (petroleum), clay-treated light straight-run; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons resulting from treatment of light straight-run naphtha with a natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 93 °C to 180 °C (200 °F to 356 °F).] 271-263-9 68527-22-0 Carc. 1B [A complex combination of hydrocarbons resulting from treatment of light straight-run naphtha with a natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numberspredominantly in the range of C7 through C10 and boiling in the range of approximately 93 °C to 180 °C (200 °F to 356 °F).] 271-263-9 68527-22-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-370-00-0 Naphtha (petroleum), light steam-cracked arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110 °C to 165 °C (230 °F to 329 °F).] 271-264-4 68527-23-1 Carc. 1B [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110 °C to 165 °C (230 °F to 329 °F).] 271-264-4 68527-23-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-371-00-6 Naphtha (petroleum), light steam-cracked, debenzenized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 80 °C to 218 °C (176 °F to 424 °F).] 271-266-5 68527-26-4 Carc. 1B [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 80 °C to 218 °C (176 °F to 424 °F).] 271-266-5 68527-26-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 22 unchanged lines … H304 H P 649-374-00-2 Naphtha (petroleum), light, sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 20 °C to 100 °C (– 4 °F to 212 °F).] 272-206-0 68783-66-4 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 20 °C to 100 °C (– 4 °F to 212 °F).] 272-206-0 68783-66-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 23 unchanged lines … H304 H P 649-377-00-9 Naphtha (petroleum), catalytic reformed light, arom.-free fraction; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons remaining after removal of aromatic compounds from catalytic reformed light naphtha in a selective absorption process. It consists predominantly of paraffinic and cyclic compounds having carbon numbers predominantly in the range of C5 to C8 and boiling in the range of approximately 66 °C to 121 °C (151 °F to 250 °F).] 285-510-3 85116-59-2 Carc. 1B [A complex combination of hydrocarbons remaining after removal of aromatic compounds from catalytic reformed light naphtha in a selective absorption process. It consists predominantly of paraffinic and cyclic compounds having carbon numbers predominantly in the range of C5 to C8 and boiling in the range of approximately 66 °C to 121 °C (151 °F to 250 °F).] 285-510-3 85116-59-2 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-378-00-4 Gasoline; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons consisting primarily of paraffins, cycloparaffins, aromatic and olefinic hydrocarbons having carbon numbers predominantly greater than C3 and boiling in the range of 30 °C to 260 °C (86 °F to 500 °F).] 289-220-8 86290-81-5 Carc. 1B [A complex combination of hydrocarbons consisting primarily of paraffins, cycloparaffins, aromatic and olefinic hydrocarbons having carbon numbers predominantly greater than C3 and boiling in the range of 30 °C to 260 °C (86 °F to 500 °F).] 289-220-8 86290-81-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-379-00-X Aromatic hydrocarbons, C7-8, dealkylation products, distn. residues; Low boiling point naphtha - unspecified 292-698-0 90989-42-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-380-00-5 Hydrocarbons, C4-6, depentanizer lights, arom. hydrotreater; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as first runnings from the depentanizer column before hydrotreatment of the aromatic charges. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C6, predominantly pentanes and pentenes, and boiling in the range of approximately 25 °C to 40 °C (77 °F to 104 °F).] 295-298-4 91995-38-9 Carc. 1B [A complex combination of hydrocarbons obtained as first runnings from the depentanizer column before hydrotreatment of the aromatic charges. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C6, predominantly pentanes and pentenes, and boiling in the range of approximately 25 °C to 40 °C (77 °F to 104 °F).] 295-298-4 91995-38-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-381-00-0 Distillates (petroleum), heat-soaked steam-cracked naphtha, C5-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of heat-soaked steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C4 through C6, predominantly C5.] 295-302-4 91995-41-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-382-00-6 Extracts (petroleum), catalytic reformed light naphtha solvent; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as the extract from the solvent extraction of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C8 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 295-331-2 91995-68-5 Carc. 1B [A complex combination of hydrocarbons obtained as the extract from the solvent extraction of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C8 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 295-331-2 91995-68-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-383-00-1 Naphtha (petroleum), hydrodesulfurized light, dearomatized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of hydrodesulfurized and dearomatized light petroleum fractions. It consists predominantly of C7 paraffins and cycloparaffins boiling in a range of approximately 90 °C to 100 °C (194 °F to 212 °F).] 295-434-2 92045-53-9 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of hydrodesulfurized and dearomatized light petroleum fractions. It consists predominantly of C7 paraffins and cycloparaffins boiling in a range of approximately 90 °C to 100 °C (194 °F to 212 °F).] 295-434-2 92045-53-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-384-00-7 Naphtha (petroleum), light, C5-rich, sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C5, predominantly C5, and boiling in the range of approximately minus 10 °C to 35 °C (14 °F to 95 °F).] 295-442-6 92045-60-8 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C5, predominantly C5, and boiling in the range of approximately minus 10 °C to 35 °C (14 °F to 95 °F).] 295-442-6 92045-60-8 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-385-00-2 Hydrocarbons, C8-11, naphtha-cracking, toluene cut; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation from prehydrogenated cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C11 and boiling in the range of approximately 130 °C to 205 °C (266 °F to 401 °F).] 295-444-7 92045-62-0 Carc. 1B [A complex combination of hydrocarbons obtained by distillation from prehydrogenated cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C11 and boiling in the range of approximately 130 °C to 205 °C (266 °F to 401 °F).] 295-444-7 92045-62-0 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-386-00-8 Hydrocarbons, C4-11, naphtha-cracking, arom.-free; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from prehydrogenated cracked naphtha after distillative separation of benzene- and toluene-containing hydrocarbon cuts and a higher boiling fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 205 °C (86 °F to 401 °F).] 295-445-2 92045-63-1 Carc. 1B [A complex combination of hydrocarbons obtained from prehydrogenated cracked naphtha after distillative separation of benzene- and toluene-containing hydrocarbon cuts and a higher boiling fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 205 °C (86 °F to 401 °F).] 295-445-2 92045-63-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-387-00-3 Naphtha (petroleum), light heat-soaked, steam-cracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the fractionation of steam cracked naphtha after recovery from a heat soaking process. It consists predominantly of hydrocarbons having a carbon number predominantly in the range of C4 through C6 and boiling in the range of approximately 0 °C to 80 °C (32 °F to 176 °F).] 296-028-8 92201-97-3 Carc. 1B [A complex combination of hydrocarbons obtained by the fractionation of steam cracked naphtha after recovery from a heat soaking process. It consists predominantly of hydrocarbons having a carbon number predominantly in the range of C4 through C6 and boiling in the range of approximately 0 °C to 80 °C (32 °F to 176 °F).] 296-028-8 92201-97-3 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-388-00-9 Distillates (petroleum), C6-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from the distillation of a petroleum feedstock. It consists predominantly of hydrocarbons having carbon numbers of C5 through C7, rich in C6, and boiling in the range of approximately 60 °C to 70 °C (140 °F to 158 °F).] 296-903-4 93165-19-6 Carc. 1B [A complex combination of hydrocarbons obtained from the distillation of a petroleum feedstock. It consists predominantly of hydrocarbons having carbon numbers of C5 through C7, rich in C6, and boiling in the range of approximately 60 °C to 70 °C (140 °F to 158 °F).] 296-903-4 93165-19-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-389-00-4 Gasoline, pyrolysis, hydrogenated; Low boiling point naphtha-unspecified; [A distillation fraction from the hydrogenation of pyrolysis gasoline boiling in the range of approximately 20 °C to 200 °C (68 °F to 392 °F).] 302-639-3 94114-03-1 Carc. 1B [A distillation fraction from the hydrogenation of pyrolysis gasoline boiling in the range of approximately 20 °C to 200 °C (68 °F to 392 °F).] 302-639-3 94114-03-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-390-00-X Distillates (petroleum), steam-cracked, C8-12 fraction, polymd., distn. lights; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of the polymerized C8 through C12 fraction from steam-cracked petroleum distillates. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C12.] 305-750-5 95009-23-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-391-00-5 Extracts (petroleum) heavy naphtha solvent, clay-treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment of heavy naphthic solvent petroleum extract with bleaching earth. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 80 °C to 180 °C (175 °F to 356 °F).] 308-261-5 97926-43-7 Carc. 1B [A complex combination of hydrocarbons obtained by the treatment of heavy naphthic solvent petroleum extract with bleaching earth. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 80 °C to 180 °C (175 °F to 356 °F).] 308-261-5 97926-43-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-392-00-0 Naphtha (petroleum), light steam-cracked, debenzenized, thermally treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment and distillation of debenzenized light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 95 °C to 200 °C (203 °F to 392 °F).] 308-713-1 98219-46-6 Carc. 1B [A complex combination of hydrocarbons obtained by the treatment and distillation of debenzenized light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 95 °C to 200 °C (203 °F to 392 °F).] 308-713-1 98219-46-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-393-00-6 Naphtha (petroleum), light steam-cracked, thermally treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment and distillation of light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 35 °C to 80 °C (95 °F to 176 °F).] 308-714-7 98219-47-7 Carc. 1B [A complex combination of hydrocarbons obtained by the treatment and distillation of light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 35 °C to 80 °C (95 °F to 176 °F).] 308-714-7 98219-47-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-394-00-1 Distillates (petroleum), C7-9, C8-rich, hydrodesulfurized dearomatized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 °C to 130 °C (248 °F to 266 °F).] 309-862-5 101316-56-7 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 °C to 130 °C (248 °F to 266 °F).] 309-862-5 101316-56-7 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-395-00-7 Hydrocarbons, C6-8, hydrogenated sorption-dearomatized, toluene raffination; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80 °C to 135 °C (176 °F to 275 °F).] 309-870-9 101316-66-9 Carc. 1B [A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80 °C to 135 °C (176 °F to 275 °F).] 309-870-9 101316-66-9 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-396-00-2 Naphtha (petroleum), hydrodesulfurised full-range coker; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 196 °C (73 °F to 385 °F).] 309-879-8 101316-76-1 Carc. 1B [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 196 °C (73 °F to 385 °F).] 309-879-8 101316-76-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-397-00-8 Naphtha (petroleum), sweetened light; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 °C to 130 °C (68 °F to 266 °F).] 309-976-5 101795-01-1 Carc. 1B [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 °C to 130 °C (68 °F to 266 °F).] 309-976-5 101795-01-1 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-398-00-3 Hydrocarbons, C3-6, C5-rich, steam-cracked naphtha; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly C5.] 310-012-0 102110-14-5 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-399-00-9 Hydrocarbons, C5-rich, dicyclopentadiene-contg.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30 °C to 170 °C (86 °F to 338 °F).] 310-013-6 102110-15-6 Carc. 1B [A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30 °C to 170 °C (86 °F to 338 °F).] 310-013-6 102110-15-6 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 H304 GHS08 Dgr H350 H340 H304 H P 649-400-00-2 Residues (petroleum), steam-cracked light, arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of the products of steam cracking or similar processes after taking off the very light products resulting in a residue starting with hydrocarbons having carbon numbers greater than C5. It consists predominantly of aromatic hydrocarbons having carbon numbers greater than C5 and boiling above approximately 40 °C (104 °F).] 310-057-6 102110-55-4 Carc. 1B [A complex combination of hydrocarbons obtained by the distillation of the products of steam cracking or similar processes after taking off the very light products resulting in a residue starting with hydrocarbons having carbon numbers greater than C5. It consists predominantly of aromatic hydrocarbons having carbon numbers greater than C5 and boiling above approximately 40 °C (104 °F).] 310-057-6 102110-55-4 Carc. 1B Muta. 1B Asp. Tox. 1 H350 H340 … 30 unchanged lines … H304 H P 649-404-00-4 Kerosine (petroleum); Straight run kerosine; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (320 oF to 554 oF).] 232-366-4 8008-20-6 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (320 oF to 554 oF).] 232-366-4 8008-20-6 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-405-00-X solvent naphtha (petroleum), medium aliph.; Straight run kerosine; [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).] 265-191-7 64742-88-7 STOT RE 1 H372 (central nervous system) GHS08 H372 (central nervous system) Asp. Tox. 1 H304 Dgr H304 [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).] 265-191-7 64742-88-7 STOT RE 1 H372 (central nervous system) GHS08 H372 (central nervous system) Asp. Tox. 1 H304 Dgr H304 649-406-00-5 Solvent naphtha (petroleum) heavy aliph.; Straight run kerosine; [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C11 through C16 and boiling in the range of approximately 190 oC to 290 oC (374 oF to 554 oF).] 265-200-4 64742-96-7 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C11 through C16 and boiling in the range of approximately 190 oC to 290 oC (374 oF to 554 oF).] 265-200-4 64742-96-7 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-407-00-0 Kerosine (petroleum), straight-run wide-cut; Straight run kerosine; [A complex combination of hydrocarbons obtained as a wide cut hydrocarbon fuel cut from atmospheric distillation and boiling in the range of approximately 70 oC to 220 oC (158 oF to 428 oF).] 295-418-5 92045-37-9 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained as a wide cut hydrocarbon fuel cut from atmospheric distillation and boiling in the range of approximately 70 oC to 220 oC (158 oF to 428 oF).] 295-418-5 92045-37-9 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-408-00-6 Distillates (petroleum), steam-cracked; Cracked kerosine; [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C7 through C16 and boiling in the range of approximately 90 oC to 290 oC (190 oF to 554 oF).] 265-194-3 64742-91-2 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C7 through C16 and boiling in the range of approximately 90 oC to 290 oC (190 oF to 554 oF).] 265-194-3 64742-91-2 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-409-00-1 Distillates (petroleum), cracked stripped steam-cracked petroleum distillates, C8-10 fraction; Cracked kerosine; [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists of hydro-carbons having carbon numbers in the range of C8 through C10 and boiling in the range of approximately 129 oC to 194 oC (264 oF to 382 oF).] 270-728-3 68477-39-4 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists of hydro-carbons having carbon numbers in the range of C8 through C10 and boiling in the range of approximately 129 oC to 194 oC (264 oF to 382 oF).] 270-728-3 68477-39-4 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-410-00-7 Distillates (petroleum), cracked stripped steam-cracked petroleum distillates, C10-12 fraction; Cracked kerosine; [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C10 through C12.] 270-729-9 68477-40-7 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-411-00-2 Distillates (petroleum), steam-cracked, C8-12 fraction; Cracked kerosine; [A complex combination of organic compounds obtained by the distillation of products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C8 through C12.] 270-737-2 68477-54-3 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-412-00-8 Kerosine (petroleum), hydrodesulfurized thermal cracked; Cracked kerosine; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons predominantly in the range of C8 to C16 and boiling in the range of approximately 120 oC to 283 oC (284 oF to 541 oF).] 285-507-7 85116-55-8 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons predominantly in the range of C8 to C16 and boiling in the range of approximately 120 oC to 283 oC (284 oF to 541 oF).] 285-507-7 85116-55-8 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-413-00-3 Aromtic hydrocarbons, C≥10, steam-cracking, hydrotreated; Cracked kerosine; [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly greater than C10 and boiling in the range of approximately 150 oC to 320 oC (302 oF to 608 oF).] 292-621-0 90640-98-5 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly greater than C10 and boiling in the range of approximately 150 oC to 320 oC (302 oF to 608 oF).] 292-621-0 90640-98-5 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-414-00-9 Naphtha (petroleum), steam-cracked, hydrotreated, C9-10-arom.-rich; Cracked kerosine; [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process thereafter treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C9 through C10 and boiling in the range of approximately 140 oC to 200 oC (284 oF to 392 oF).] 292-637-8 90641-13-7 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process thereafter treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C9 through C10 and boiling in the range of approximately 140 oC to 200 oC (284 oF to 392 oF).] 292-637-8 90641-13-7 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-415-00-4 Distillates (petroleum), thermal-cracked, alkylarom. hydrocarbon-rich; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF.] 309-866-7 101316-61-4 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF.] 309-866-7 101316-61-4 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-416-00-X Distillates (petroleum), catalytic cracked heavy tar light; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of catalytic cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-938-8 101631-13-4 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by distillation of catalytic cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-938-8 101631-13-4 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-417-00-5 Solvent naphtha (petroleum), hydrocracked heavy arom.; Cracked kerosine; [A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235 oC to 290 oC (455 oF to 554 oF).] 309-881-9 101316-80-7 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235 oC to 290 oC (455 oF to 554 oF).] 309-881-9 101316-80-7 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-418-00-0 Distillates (petroleum), steam-cracked heavy tar light; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-940-9 101631-15-6 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-940-9 101631-15-6 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-419-00-6 Distillates (petroleum), alkylate; Kerosine — unspecified; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydro-carbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 205 oC to 320 oC (401 oF to 608 oF).] 265-074-0 64741-73-7 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydro-carbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 205 oC to 320 oC (401 oF to 608 oF).] 265-074-0 64741-73-7 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-420-00-1 Extracts (petroleum), heavy naphtha solvent; Kerosine — unspecified; [A complex combination of hydrocarbons obtained as the extract from a solvent extraction process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 oC to 220 oC (194 oF to 428 oF).] 265-099-7 64741-98-6 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained as the extract from a solvent extraction process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 oC to 220 oC (194 oF to 428 oF).] 265-099-7 64741-98-6 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-421-00-7 Distillates (petroleum), chemically neutralized light; Kerosine — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-132-5 64742-31-0 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-132-5 64742-31-0 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-422-00-2 Distillates (petroleum), hydrotreated light; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-149-8 64742-47-8 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-149-8 64742-47-8 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-423-00-8 Kerosine (petroleum), hydrodesulfurized; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-184-9 64742-81-0 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-184-9 64742-81-0 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-424-00-3 Solvent naphtha (petroleum), heavy arom.; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 165 oC to 290 oC (330 oF to 554 oF).] 265-198-5 64742-94-5 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 165 oC to 290 oC (330 oF to 554 oF).] 265-198-5 64742-94-5 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-425-00-9 Naphtha (petroleum), heavy coker; Kerosine — unspecified; [A complex combination of hydrocarbons from the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C15 and boiling in the range of approximately 157 oC to 288 oC (315 oF to 550 oF).] 269-778-9 68333-23-3 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons from the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbonshaving carbon numbers predominantly in the range of C6 through C15 and boiling in the range of approximately 157 oC to 288 oC (315 oF to 550 oF).] 269-778-9 68333-23-3 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-426-00-4 Naphtha (petroleum), catalytic reformed hydrodesulfurized heavy, arom. fraction; Kerosine — unspecified; [A complex combination of hydrocarbons produced by fractionation from catalytically reformed hydrodesulfurized naphtha. It consists predominantly of aromatic hydrocarbons having carbon numbers predominently in the range of C7 to C 13 and boiling in the range of approximately 98 oC to 218 oC (208 oF to 424 oF).] 285-508-2 85116-57-0 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons produced by fractionation from catalytically reformed hydrodesulfurized naphtha. It consists predominantly of aromatic hydrocarbons having carbon numbers predominently in the range of C7 to C 13 and boiling in the range of approximately 98 oC to 218 oC (208 oF to 424 oF).] 285-508-2 85116-57-0 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-427-00-X Kerosine (petroleum), sweetened; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of 130 oC to 290 oC (266 oF to 554 oF).] 294-799-5 91770-15-9 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of 130 oC to 290 oC (266 oF to 554 oF).] 294-799-5 91770-15-9 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-428-00-5 Kerosine (petroleum), solvent-refined sweetened; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by solvent refining and sweetening and boiling in the range of approximately 150 oC to 260 oC (302 oF to 500 oF).] 295-416-4 92045-36-8 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained from a petroleum stock by solvent refining and sweetening and boiling in the range of approximately 150 oC to 260 oC (302 oF to 500 oF).] 295-416-4 92045-36-8 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-429-00-0 Hydrocarbons, C9-16, hydrotreated, dearomatized; Kerosine — unspecified; [A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.] 297-854-1 93763-35-0 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-430-00-6 Kerosine (petroleum), solvent-refined hydrodesulfurized; Kerosine — unspecified 307-033-2 97488-94-3 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-431-00-1 Distillates (petroleum), hydrodesulfurized full-range middle coker; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120 oC to 283 oC (248 oF to 541 oF).] 309-864-6 101316-58-9 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized coker distillate. It consists predominantly of hydrocarbons having carbonnumbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120 oC to 283 oC (248 oF to 541 oF).] 309-864-6 101316-58-9 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-432-00-7 Solvent naphtha (petroleum), hydrodesulfurized heavy arom.; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180 oC to 240 oC (356 oF to 464 oF).] 309-882-4 101316-81-8 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180 oC to 240 oC (356 oF to 464 oF).] 309-882-4 101316-81-8 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-433-00-2 Solvent naphtha (petroleum), hydrodesulfurized medium; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175 oC to 220 oC (347 oF to 428 oF).] 309-884-5 101316-82-9 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175 oC to 220 oC (347 oF to 428 oF).] 309-884-5 101316-82-9 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-434-00-8 Kerosine (petroleum), hydrotreated; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230 oC to 270 oC (446 oF to 518 oF).] 309-944-0 101631-19-0 Asp. Tox. 1 H304 GHS08 [A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230 oC to 270 oC (446 oF to 518 oF).] 309-944-0 101631-19-0 Asp. Tox. 1 H304 GHS08 Dgr H304 H 649-435-00-3 Distillates (petroleum), light catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 265-060-4 64741-59-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 265-060-4 64741-59-9 Carc. 1B H350 GHS08 Dgr H350 H 649-436-00-9 Distillates (petroleum), intermediate catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 265-062-5 64741-60-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 265-062-5 64741-60-2 Carc. 1B H350 GHS08 Dgr H350 H 649-437-00-4 Distillates (petroleum), light hydrocracked; Cracked gasoil; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C10 through C18 and boiling in the range of approximately 160 oC to 320 oC (320 oF to 608 oF).] 265-078-2 64741-77-1 Carc. 2 H351 GHS08 [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C10 through C18 and boiling in the range of approximately 160 oC to 320 oC (320 oF to 608 oF).] 265-078-2 64741-77-1 Carc. 2 H351 GHS08 Wng H351 H 649-438-00-X Distillates (petroleum), light thermal cracked; Cracked gasoil; [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C10 through C22 and boiling in the range of approximately 160 oC to 370 oC (320 oF to 698 oF).] 265-084-5 64741-82-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C10 through C22 and boiling in the range of approximately 160 oC to 370 oC (320 oF to 698 oF).] 265-084-5 64741-82-8 Carc. 1B H350 GHS08 Dgr H350 H 649-439-00-5 Distillates (petroleum), hydrodesulfurized light catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons obtained by treating light catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 269-781-5 68333-25-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating light catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 269-781-5 68333-25-5 Carc. 1B H350 GHS08 Dgr H350 H 649-440-00-0 Distillates (petroleum), light steam-cracked naphtha; Cracked gasoil; [A complex combination of hydrocarbons from the multiple distillation of products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C10 through C18.] 270-662-5 68475-80-9 Carc. 1B H350 GHS08 Dgr H350 H 649-441-00-6 Distillates (petroleum), cracked steam-cracked petroleum distillates; Cracked gasoil; [A complex combination of hydrocarbons produced by distilling cracked steam cracked distillate and/or its fractionation products. It consists of hydrocarbons having carbon numbers predominently in the range of C10 to low molecular weight polymers.] 270-727-8 68477-38-3 Carc. 1B H350 GHS08 Dgr H350 H 649-442-00-1 Gas oils (petroleum), steam-cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by distillation of the products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C9 and boiling in the range of from approximately 205 oC to 400 oC (400 oF to 752 oF).] 271-260-2 68527-18-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by distillation of the products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C9 and boiling in the range of from approximately 205 oC to 400 oC (400 oF to 752 oF).] 271-260-2 68527-18-4 Carc. 1B H350 GHS08 Dgr H350 H 649-443-00-7 Distillates (petroleum), hydrodesulfurized thermal cracked middle; Cracked gasoil; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized themal cracker distillate stocks. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 to C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 285-505-6 85116-53-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized themal cracker distillate stocks. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 to C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 285-505-6 85116-53-6 Carc. 1B H350 GHS08 Dgr H350 H 649-444-00-2 Gas oils (petroleum), thermal-cracked, hydrodesulfurized; Cracked gasoil 295-411-7 92045-29-9 Carc. 1B H350 GHS08 Dgr H350 H 649-445-00-8 Residues (petroleum), hydrogenated steam-cracked naphtha; Cracked gasoil; [A complex combination of hydrocarbons obtained as a residual fraction from the distillation of hydrotreated steam-cracked naphtha. It consists predominantly of hydrocarbons boiling in the range of approximately 200 oC to 350 oC (32 oF to 662 oF).] 295-514-7 92062-00-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a residual fraction from the distillation of hydrotreated steam-cracked naphtha. It consists predominantly of hydrocarbons boiling in the range of approximately 200 oC to 350 oC (32 oF to 662 oF).] 295-514-7 92062-00-5 Carc. 1B H350 GHS08 Dgr H350 H 649-446-00-3 Residues (petroleum), steam-cracked naphtha distn.; Cracked gasoil; [A complex combination of hydrocarbons obtained as a column bottom from the separation of effluents from steam cracking naphtha at a high temperature. It boils in the range of approximately 147 oC to 300 oC (297 oF to 572 oF) and produces a finished oil having a viscosity of 18cSt at 50 oC.] 295-517-3 92062-04-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as a column bottom from the separation of effluents from steam cracking naphtha at a high temperature. It boils in the range of approximately 147 oC to 300 oC (297 oF to 572 oF) and produces a finished oil having a viscosity of 18cSt at 50 oC.] 295-517-3 92062-04-9 Carc. 1B H350 GHS08 Dgr H350 H 649-447-00-9 Distillates (petroleum), light catalytic cracked, thermally degraded; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 190 oC to 340 oC (374 oF to 644 oF). This stream is likely to contain organic sulfur compounds.] 295-991-1 92201-60-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 190 oC to 340 oC (374 oF to 644 oF). This stream is likely to contain organic sulfur compounds.] 295-991-1 92201-60-0 Carc. 1B H350 GHS08 Dgr H350 H 649-448-00-4 Residues (petroleum), steam-cracked heat-soaked naphtha; Cracked gasoil; [A complex combination of hydrocarbons obtained as residue from the distillation of steam cracked heat soaked naphtha and boiling in the range of approximately 150 oC to 350 oC (302 oF to 662 oF).] 297-905-8 93763-85-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as residue from the distillation of steam cracked heat soaked naphtha and boiling in the range of approximately 150 oC to 350 oC (302 oF to 662 oF).] 297-905-8 93763-85-0 Carc. 1B H350 GHS08 Dgr H350 H 649-449-00-X Hydrocarbons, C16-20, solvent-dewaxed hydrocracked paraffinic distn. residue; Cracked gasoil; [A complex combination of hydrocarbons obtained by solvent dewaxing of a distillation residue from a hydrocracked paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 360 oC to 500 oC (680 oF to 932 oF). It produces a finished oil having a viscosity of 4,5 cSt at approximately 100 oC (212 oF).] 307-662-2 97675-88-2 Carc. 2 H351 GHS08 [A complex combination of hydrocarbons obtained by solvent dewaxing of a distillation residue from a hydrocracked paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 360 oC to 500 oC (680 oF to 932 oF). It produces a finished oil having a viscosity of 4,5 cSt at approximately 100 oC (212 oF).] 307-662-2 97675-88-2 Carc. 2 H351 GHS08 Wng H351 H 649-450-00-5 Gas oils (petroleum), light vacuum, thermal-cracked hydrodesulfurized; Cracked gasoil; [A complex combination of hydrocarbons obtained by catalytic dehydrosulfurization of thermal-cracked light vacuum petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C20 and boiling in the range of approximately 270 oC to 370 oC (518 oF to 698 oF).] 308-278-8 97926-59-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by catalytic dehydrosulfurization of thermal-cracked light vacuum petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C20 and boiling in the range of approximately 270 oC to 370 oC (518 oF to 698 oF).] 308-278-8 97926-59-5 Carc. 1B H350 GHS08 Dgr H350 H 649-451-00-0 Distillates (petroleum), hydrodesulfurized middle coker; Cracked gasoil; [A complex combination of hydrocarbons by fractionation from hydrodesulfurised coker distillate stocks. Is consists of hydro-carbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200 oC to 360 oC (392 oF to 680 oF).] 309-865-1 101316-59-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons by fractionation from hydrodesulfurised coker distillate stocks. Is consists of hydro-carbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200 oC to 360 oC (392 oF to 680 oF).] 309-865-1 101316-59-0 Carc. 1B H350 GHS08 Dgr H350 H 649-452-00-6 Distillates (petroleum), heavy steam-cracked; Cracked gasoil; [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250 oC to 400 oC (482 oF to 752 oF).] 309-939-3 101631-14-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250 oC to 400 oC (482 oF to 752 oF).] 309-939-3 101631-14-5 Carc. 1B H350 GHS08 Dgr H350 H 649-453-00-1 Distillates (petroleum), heavy hydrocracked; Baseoil — unspecified; [A complex combination of hydrocarbons from the distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers in the range of C15-C39 and boiling in the range of approximately 260 oC to 600 oC (500 oF to 1112 oF).] 265-077-7 64741-76-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons from the distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers in the range of C15-C39 and boiling in the range of approximately 260 oC to 600 oC (500 oF to 1112 oF).] 265-077-7 64741-76-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-454-00-7 Distillates (petroleum), solvent-refined heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-090-8 64741-88-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-090-8 64741-88-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-455-00-2 Distillates (petroleum), solvent-refined light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-091-3 64741-89-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-091-3 64741-89-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-456-00-8 Residual oils (petroleum), solvent deasphalted; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the solvent soluble fraction from C3-C4 solvent deasphalting of a residuum. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-096-0 64741-95-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the solvent soluble fraction from C3-C4 solvent deasphalting of a residuum. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-096-0 64741-95-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-457-00-3 Distillates (petroleum), solvent-refined heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt a 40 oC). It contains relatively few normal paraffins.] 265-097-6 64741-96-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt a 40 oC). It contains relatively few normal paraffins.] 265-097-6 64741-96-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-458-00-9 Distillates (petroleum), solvent-refined light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-098-1 64741-97-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-098-1 64741-97-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-459-00-4 Residual oils (petroleum,) solvent-refined; Baseoil — unspecified; [A complex combination by hydrocarbons obtained as the solvent insoluble fraction from solvent refining of a residuum using a polar organic solvent such as phenol or furfural. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-101-6 64742-01-4 Carc. 1B H350 GHS08 [A complex combination by hydrocarbons obtained as the solvent insoluble fraction from solvent refining of a residuum using a polar organic solvent such as phenol or furfural. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-101-6 64742-01-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-460-00-X Distillates (petroleum), clay-treated paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-137-2 64742-36-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-137-2 64742-36-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-461-00-5 Distillates (petroleum), clay-treated light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-138-8 64742-37-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-138-8 64742-37-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-462-00-0 Residual oils (petroleum), clay-treated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treatment of a residual oil with a natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydro-carbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-143-5 64742-41-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treatment of a residual oil with a natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydro-carbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-143-5 64742-41-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-463-00-6 Distillates (petroleum), clay-treated heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-146-1 64742-44-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-146-1 64742-44-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-464-00-1 Distillates (petroleum), clay-treated light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-147-7 64742-45-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and producesa finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-147-7 64742-45-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-465-00-7 Distillates (petroleum), hydrotreated heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-155-0 64742-52-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-155-0 64742-52-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-466-00-2 Distillates (petroleum), hydrotreated light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-156-6 64742-53-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-156-6 64742-53-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-467-00-8 Distillates (petroleum), hydrotreated heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-157-1 64742-54-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-157-1 64742-54-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-468-00-3 Distillates (petroleum), hydrotreated light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-158-7 64742-55-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-158-7 64742-55-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-469-00-9 Distillates (petroleum), solvent-dewaxed light paraffinic; Baseoil — unspecified; [A complex comination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-159-2 64742-56-9 Carc. 1B H350 GHS08 [A complex comination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-159-2 64742-56-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-470-00-4 Residual oils (petroleum), hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-160-8 64742-57-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-160-8 64742-57-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-471-00-X Residual oils (petroleum), solvent-dewaxed; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of long, branched chain hydrocarbons from a residual oil by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-166-0 64742-62-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by removal of long, branched chain hydrocarbons from a residual oil by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-166-0 64742-62-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-472-00-5 Distillates (petroleum), solvent-dewaxed heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 . through C50 and produces a finished oil of not less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-167-6 64742-63-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 . through C50 and produces a finished oil of not less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-167-6 64742-63-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-473-00-0 Distillates (petroleum), solvent-dewaxed light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-168-1 64742-64-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-168-1 64742-64-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-474-00-6 Distillates (petroleum), solvent-dewaxed heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity not less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-169-7 64742-65-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity not less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-169-7 64742-65-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-475-00-1 Naphthenic oils (petroleum), catalytic dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-172-3 64742-68-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-172-3 64742-68-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-476-00-7 Naphthenic oils (petroleum), catalytic dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-173-9 64742-69-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-173-9 64742-69-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-477-00-2 Paraffin oils (petroleum), catalytic dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-174-4 64742-70-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-174-4 64742-70-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-478-00-8 Paraffin oils (petroleum), catalytic dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-176-5 64742-71-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic dewxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-176-5 64742-71-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-479-00-3 Naphthenic oils (petroleum), complex dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removing straight chain paraffin hydrocarbons as a solid by treatment with an agent such as urea. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-179-1 64742-75-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by removing straight chainparaffin hydrocarbons as a solid by treatment with an agent such as urea. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-179-1 64742-75-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-480-00-9 Naphthenic oils (petroleum), complex dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-180-7 64742-76-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-180-7 64742-76-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-481-00-4 Lubricating oils (petroleum), C20-50, hydrotreated neutral oil-based, high-viscosity; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil, and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of approximately 112cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-736-3 72623-85-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil, andsolvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of approximately 112cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-736-3 72623-85-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-482-00-X Lubricating oils (petroleum), C15-30, hydrotreated neutral oil-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil and heavy vacuum gas oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of approximately 15cSt at 40 oC. It contains a relatively large proportion of saturated hydrocabons.] 276-737-9 72623-86-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating light vacuum gas oil and heavy vacuum gas oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of approximately 15cSt at 40 oC. It contains a relatively large proportion of saturated hydrocabons.] 276-737-9 72623-86-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-483-00-5 Lubricating oils (petroleum), C20-50, hydrotreated neutral oil-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of approximately 32cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-738-4 72623-87-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of approximately 32cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-738-4 72623-87-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-484-00-0 Lubricating oils; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from solvent extraction and dewaxing processes. It consists predominantly of saturated hydrocarbons having carbon numbers in the range C15 through C50.] 278-012-2 74869-22-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-485-00-6 Distillates (petroleum), complex dewaxed heavy paraffinci; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by dewaxing heavy paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of equal to or greater than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-613-7 90640-91-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by dewaxing heavy paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of equal to or greater than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-613-7 90640-91-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-486-00-1 Distillates (petroleum), complex dewaxed light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by dewaxing light paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-614-2 90640-92-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by dewaxing light paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-614-2 90640-92-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-487-00-7 Distillates (petroleum), solvent dewaxed heavy paraffinic, clay-treated; Baseoil — unspecified; … 19 unchanged lines … Dgr H350 H L 649-493-00-X Distillates (petroleum), dewaxed heavy paraffinic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C25 through C39 and produces a finished oil with a viscosity of approximately 44 cSt at 50 oC.] 295-300-3 91995-39-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C25 through C39 and produces a finished oil with a viscosity of approximately 44 cSt at 50 oC.] 295-300-3 91995-39-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-494-00-5 Distillates (petroleum), dewaxed light paraffinic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C21 through C29 and produces a finished oil with a viscosity of approximately 13 cSt at 50 oC.] 295-301-9 91995-40-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C21 through C29 and produces a finished oil with a viscosity of approximately 13 cSt at 50 oC.] 295-301-9 91995-40-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-495-00-0 Distillates (petroleum), hydrocracked solvent-refined, dewaxed; Baseoil — unspecified; [A complex combination of liquid hydrocarbons obtained by recrystallization of dewaxed hydrocracked solvent-refined petroleum distillates.] 295-306-6 91995-45-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-496-00-6 Distillates (petroleum), solvent-refined light naphthenic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst and removing the aromatic hydrocarbons by solvent extraction. It consists predominantly of naphthenic hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of between 13-15cSt at 40 oC.] 295-316-0 91995-54-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst and removing the aromatic hydrocarbons by solvent extraction. It consists predominantly of naphthenic hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of between 13-15cSt at 40 oC.] 295-316-0 91995-54-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-497-00-1 Lubricating oils (petroleum), C17-35, solvent-extd., dewaxed, hydrotreated; Baseoil — unspecified 295-423-2 92045-42-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-498-00-7 Lubricating oils (petroleum), hydrocracked nonarom. solvent-deparaffined; Baseoil — unspecified 295-424-8 92045-43-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-499-00-2 Residual oils (petroleum), hydrocracked acid-treated solvent-dewaxed; Baseoil — unspecified; [A complex combination of hydrocarbons produced by solvent removal of paraffins from the residue of the distillation of acid-treated, hydrocracked heavy paraffins and boiling approximately above 380 oC (716 oF).] 295-499-7 92061-86-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by solvent removal of paraffins from the residue of the distillation of acid-treated, hydrocracked heavy paraffins and boiling approximately above 380 oC (716 oF).] 295-499-7 92061-86-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-500-00-6 Paraffin oils (petroleum), solvent-refined dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from sulfur-containing paraffinic crude oil. It consists predominantly of a solvent refined deparaffinated lubricating oil with a viscosity of 65cSt at 50 oC.] 295-810-6 92129-09-4 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from sulfur-containing paraffinic crude oil. It consists predominantly of a solvent refined deparaffinated lubricating oil with a viscosity of 65cSt at 50 oC.] 295-810-6 92129-09-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-501-00-1 Lubricating oils (petroleum), base oils, paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by refining of crude oil. It consists predominantly of aromatics, naphthenics and paraffinics and produces a finished oil with a viscosity of 120 SUS at 100 oF (23cSt at 40 oC).] 297-474-6 93572-43-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by refining of crude oil. It consists predominantly of aromatics, naphthenics and paraffinics and produces a finished oil with a viscosity of 120 SUS at 100 oF (23cSt at 40 oC).] 297-474-6 93572-43-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-502-00-7 Hydrocarbons, hydrocracked paraffinic distn. residues, solvent-dewaxed; Baseoil — unspecified 297-857-8 93763-38-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-503-00-2 Hydrocarbons, C20-50, residual oil hydrogenation vacuum distillate; Baseoil — unspecified 300-257-1 93924-61-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-504-00-8 Distillates (petroleum), solvent-refined hydrotreated heavy; hydrogenated; Baseoil — unspecified 305-588-5 94733-08-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-505-00-3 Distillates (petroleum), solvent-refined hydrocracked light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent dearomatization of the residue of hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF).] 305-589-0 94733-09-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent dearomatization of the residue of hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF).] 305-589-0 94733-09-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-506-00-9 Lubricating oils (petroleum), C18-40, solvent-dewaxed hydrocracked distillate-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent deparaffination of the distillation residue from hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-594-8 94733-15-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent deparaffination of the distillation residue from hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-594-8 94733-15-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-507-00-4 Lubricating oils (petroleum), C18-40, solvent-dewaxed hydrogenated raffinate-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent deparaffination of the hydrogenated raffinate obtained by solvent extraction of a hydrotreated petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-595-3 94733-16-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent deparaffination of the hydrogenated raffinate obtained by solvent extraction of a hydrotreated petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-595-3 94733-16-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-508-00-X Hydrocarbons, C13-30, arom.-rich, solvent-extd. naphthenic distillate; Baseoil — unspecified 305-971-7 95371-04-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-509-00-5 Hydrocarbons, C16-32, arom. rich, solvent-extd. naphthenic distillate; Baseoil — unspecified 305-972-2 95371-05-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-510-00-0 Hydrocarbons, C37-68, dewaxed deasphalted hydrotreated vacuum distn. residues; Baseoil — unspecified 305-974-3 95371-07-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-511-00-6 Hydrocarbons, C37-65, hydrotreated deasphalted vacuum distn. residues; Baseoil — unspecified 305-975-9 95371-08-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-512-00-1 Distillates (petroleum), hydrocracked solvent-refined light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by the solvent treatment of a distillate from hydrocracked petroleum distillates. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF.] 307-010-7 97488-73-8 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by the solvent treatment of a distillate from hydrocracked petroleum distillates. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF.] 307-010-7 97488-73-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-513-00-7 Distillates (petroleum), solvent-refined hydrogenated heavy; Baseoil — unspecified; [A complex combination of hydrocarbons, obtained by the treatment of a hydrogenated petroleum distillate with a solvent. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390 oC to 550 oC (734 oF to 1022 oF).] 307-011-2 97488-74-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons, obtained by the treatment of a hydrogenated petroleum distillate with a solvent. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390 oC to 550 oC (734 oF to 1022 oF).] 307-011-2 97488-74-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-514-00-2 Lubricating oils (petroleum), C18-27, hydrocracked solvent-dewaxed; Baseoil — unspecified 307-034-8 97488-95-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-515-00-8 Hydrocarbons, C17-30, hydrotreated solvent-deasphalted atm. distn. residue, distn. lights; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a solvent deasphalted short residue with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C30 and boiling in the range of approximately 300 oC to 400 oC (572 oF to 752 oF). It produces a finished oil having a viscosity of 4cSt at approximately 100 oC (212 oF).] 307-661-7 97675-87-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a solvent deasphalted short residue with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C30 and boiling in the range of approximately 300 oC to 400 oC (572 oF to 752 oF). It produces a finished oil having a viscosity of 4cSt at approximately 100 oC (212 oF).] 307-661-7 97675-87-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-516-00-3 Hydrocarbons, C17-40, hydrotreated solvent-deasphalted distn. residue, vacuum distn. lights; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the catalytic hydrotreatment of a solvent deasphalted short residue having a viscosity of 8cSt at approximately 100 oC (212 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C40 and boiling in the range of approximately 300 oC to 500 oC (592 oF to 932 oF).] 307-755-8 97722-06-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the catalytic hydrotreatment of a solvent deasphalted short residue having a viscosity of 8cSt at approximately 100 oC (212 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C40 and boiling in the range of approximately 300 oC to 500 oC (592 oF to 932 oF).] 307-755-8 97722-06-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-517-00-9 Hydrocarbons, C13-27, solvent-extd. light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 9.5cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C27 and boiling in the range of approximately 240 oC to 400 oC (464 oF to 752 oF).] 307-758-4 97722-09-3 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 9.5cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C27 and boiling in the range of approximately 240 oC to 400 oC (464 oF to 752 oF).] 307-758-4 97722-09-3 Carc. 1B H350 GHS08 Dgr H350 H L 649-518-00-4 Hydrocarbons, C14-29, solvent-extd. light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 16cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C29 and boiling in the range of approximately 250 oC to 425 oC (482 oF to 797 oF).] 307-760-5 97722-10-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 16cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C29 and boiling in the range of approximately 250 oC to 425 oC (482 oF to 797 oF).] 307-760-5 97722-10-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-519-00-X Hydrocarbons, C27-42, dearomatized; Baseoil — unspecified 308-131-8 97862-81-2 Carc. 1B H350 GHS08 … 23 unchanged lines … Dgr H350 H L 649-527-00-3 Lubricating oils (petroleum), C>25, solvent-extd., deasphalted, dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100 oC (212 oF).] 309-874-0 101316-69-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100 oC (212 oF).] 309-874-0 101316-69-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-528-00-9 Lubricating oils (petroleum), C17-32, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produced a finished oil with a viscosity in the order of 17cSt to 23cSt at 40 oC (104 oF.] 309-875-6 101316-70-5 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produced a finished oil with a viscosity in the order of 17cSt to 23cSt at 40 oC (104 oF.] 309-875-6 101316-70-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-529-00-4 Lubricating oils (petroleum), C20-35, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40 oC (104 oF).] 309-876-1 101316-71-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40 oC (104 oF).] 309-876-1 101316-71-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-530-00-X Lubricating oils (petroleum), C24-50, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40 oC (104 oF).] 309-877-7 101316-72-7 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40 oC (104 oF).] 309-877-7 101316-72-7 Carc. 1B H350 GHS08 Dgr H350 H L 649-531-00-5 Extracts (petroleum), heavy naphthenic distillate solvent, arom. conc.; Distillate aromatic extract (treated); [An aromatic concentrate produced by adding water to heavy naphthenic distillate solvent extract and extraction solvent.] 272-175-3 68783-00-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-532-00-0 Extracts (petroleum), solvent-refined heavy paraffinic distillate solvent; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from the re-extraction of solvent-refined heavy paraffinic distillate. It consists of saturated and aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50.] 272-180-0 68783-04-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-533-00-6 Extracts (petroleum), heavy paraffinic distillates, solvent-deasphalted; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from a solvent extraction of heavy paraffinic distillate.] 272-342-0 68814-89-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-534-00-1 Extracts (petroleum), heavy naphthenic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by treating a heavy naphthenic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 19cSt at 40 oC (100 SUS at 100 oF).] 292-631-5 90641-07-9 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by treating a heavy naphthenic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 19cSt at 40 oC (100 SUS at 100 oF).] 292-631-5 90641-07-9 Carc. 1B H350 GHS08 Dgr H350 H L 649-535-00-7 Extracts (petroleum), heavy paraffinic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons produced by treating a heavy paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C21 through C33 and boiling in the range of approximately 350 oC to 480 oC (662 oF to 896 oF). 292-632-0 90641-08-0 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by treating a heavy paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C21 through C33 and boiling in the range of approximately 350 oC to 480 oC (662 oF to 896 oF). 292-632-0 90641-08-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-536-00-2 Extracts (petroleum), light paraffinic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons produced by treating a light paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C26 and boiling in the range of approximately 280 oC to 400 oC (536 oF to 752 oF).] 292-633-6 90641-09-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons produced by treating a light paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C26 and boiling in the range of approximately 280 oC to 400 oC (536 oF to 752 oF).] 292-633-6 90641-09-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-537-00-8 Extracts (petroleum), hydrotreated light paraffinic distillate solvent; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from solvent extraction of intermediate paraffinic top solvent distillate that is treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C36.] 295-335-4 91995-73-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-538-00-3 Extracts (petroleum), light naphthenic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by treating the extract, obtained from a solvent extraction process, with hydrogen in the presence of a catalyst under conditions primarily to remove sulfur compounds. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C15 through C30. This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 295-338-0 91995-75-4 Carc. 1B H350 GHS08 Dgr H350 H L 649-539-00-9 Extracts (petroleum), light paraffinic distillate solvent, acid-treated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as a fraction of the distillation of an extract from the solvent extraction of light paraffinic top petroleum distillates that is subjected to a sulfuric acid refining. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.] 295-339-6 91995-76-5 Carc. 1B H350 GHS08 Dgr H350 H L 649-540-00-4 Extracts (petroleum), light paraffinic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by solvent extraction of a light paraffin distillate and treated with hydrogen to convert the organic sulfur to hydrogen sulfide which is eliminated. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C40 and produces a finished oil with a viscosity of greater than 10cSt at 40 oC.] 295-340-1 91995-77-6 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained by solvent extraction of a light paraffin distillate and treated with hydrogen to convert the organic sulfur to hydrogen sulfide which is eliminated. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C40 and produces a finished oil with a viscosity of greater than 10cSt at 40 oC.] 295-340-1 91995-77-6 Carc. 1B H350 GHS08 Dgr H350 H L 649-541-00-X Extracts (petroleum), light vacuum gas oil solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons, obtained by solvent extraction from light vacuum petroleum gas oils and treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.] 295-342-2 91995-79-8 Carc. 1B H350 GHS08 Dgr H350 H L 649-542-00-5 Extracts (petroleum), heavy paraffinic distillate solvent, clay-treated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contact or percolation process to remove the trace amounts of polar compounds and impurities present. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50. This stream is likely to contain 5 wt.% or more 4-6 membered ring aromatic hydrocarbons.] 296-437-1 92704-08-0 Carc. 1B H350 GHS08 Dgr H350 H L 649-543-00-0 Extracts (petroleum), heavy naphthenic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-827-4 93763-10-1 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-827-4 93763-10-1 Carc. 1B H350 GHS08 Dgr H350 H L 649-544-00-6 Extracts (petroleum), solvent-dewaxed heavy paraffinic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained from a solvent dewaxed petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-829-5 93763-11-2 Carc. 1B H350 GHS08 [A complex combination of hydrocarbons obtained from a solvent dewaxed petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-829-5 93763-11-2 Carc. 1B H350 GHS08 Dgr H350 H L 649-545-00-1 Extracts (petroleum), light paraffinic distillate solvent, carbon-treated; Distillate aromatic extract (treated); … 145 unchanged lines … 8052-10-6 73138-82-6 Skin Sens. 1 H317 GHS07 Wng H317 650-016-00-2 Mineral wool, with the exception of those specified elsewhere in this Annex; [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+MgO+BaO) content greater than 18 % by weight] — — Carc. 2 H351 GHS08 [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+MgO+BaO) content greater than 18 % by weight] — — Carc. 2 H351 GHS08 Wng H351 AQR 650-017-00-8 Refractory Ceramic Fibres, Special Purpose Fibres, with the exception of those specified elsewhere in this Annex; [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+ MgO+BaO) content less or equal to 18 % by weight] — — Carc. 1B H350i GHS08 [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+ MgO+BaO) content less or equal to 18 % by weight] — — Carc. 1B H350i GHS08 Dgr H350i AR 650-018-00-3 Reaction product of: acetophenone, formaldehyde, cyclohexylamine, methanol and acetic acid 406-230-1 — Flam. Liq. 3 Carc. 2 … 140 unchanged lines … H312 H302 H314 H400 650-049-00-2 2-alkoyloxyethyl hydrogen maleate, where alkoyl represents (by weight) 70 to 85 % unsaturated octadecoyl, 0.5 to 10 % saturated octadecoyl, and 2 to 18 % saturated hexadecoyl 417-960-5 — Skin Irrit. 2 H400 650-049-00-2 2-alkoyloxyethyl hydrogen maleate, where alkoyl represents (by weight) 70 to 85 % unsaturated octadecoyl, 0.5 to 10 % saturated octadecoyl, and 2 to 18 % saturated hexadecoyl 417-960-5 — Skin Irrit. 2 Eye Dam. 1 Skin Sens. 1 Aquatic Acute 1 Aquatic Chronic 1 H315 H318 H317 H400 H410 GHS05 GHS07 GHS09 Dgr H315 H318 H317 H410 650-050-00-8 reaction mass of: 1-methyl-3-hydroxypropyl 3,5-[1,1-dimethylethyl]-4-hydroxydihydro-cinnamate and/or 3-hydroxybutyl 3,5-[1,1-dimethylethyl]-4-hydroxydihydrocinnamate; 1,3-butanediol bis[3-(3'-(1,1-dimethylethyl)4'-hydroxy-phenyl)propionate] isomers; 1,3-butanediol bis[3-(3',5'-(1,1-dimethylethyl)-4'-hydroxyphenyl)propionate] isomers 423-600-8 — Aquatic Chronic 2 H411 GHS09 H411 650-055-00-5 silver sodium zirconium hydrogenphosphate 422-570-3 155925-27-2 Aquatic Acute 1 Aquatic Chronic 1 H400 H410 GHS09 Wng H410 Table 3.2 The list of harmonised classification and labelling of hazardous substances from Annex I to Directive 67/548/EEC The list of harmonised classification and labelling of hazardous substances from Annex I to Directive 67/548/EEC Index No International Chemical Identification EC No CAS No Classification Labelling Concentration Limits Notes 001-001-00-9 hydrogen 215-605-7 1333-74-0 F+; R12 F+ R: 12 … 74 unchanged lines … 234-343-4 [2] 10043-35-3 [1] 11113-50-1 [2] Repr. Cat. 2; R60-61 T R: 60-61 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 5,5 % 005-008-00-8 diboron trioxide; S: 53-45 Repr. Cat. 2; R60-61: C ≥ 5,5 % 005-008-00-8 diboron trioxide; boric oxide 215-125-8 1303-86-2 Repr. Cat. 2; R60-61 T R: 60-61 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 3,1 % 005-009-00-3 tetrabutylammonium butyltriphenylborate 418-080-4 120307-06-4 R43 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 3,1 % 005-009-00-3 tetrabutylammonium butyltriphenylborate 418-080-4 120307-06-4 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-56-61 005-010-00-9 N,N-dimethylanilinium tetrakis(pentafluorophenyl)borate 422-050-6 118612-00-3 Carc. Cat. 3; R40 Xn; R22 Xi; R38-41 Xn R: 22-38-40-41 S: (2-)22-26-36/37/39 005-011-00-4 disodium tetraborate, anhydrous; boric acid, disodium salt; [1] tetraboron disodium heptaoxide, hydrate; [2] orthoboric acid, sodium salt [3] 215-540-4 [1] 235-541-3 [2] 237-560-2 [3] 1330-43-4 [1] 12267-73-1 [2] 13840-56-7 [3] Repr. Cat. 2; R60-61 T R: 60-61 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 4,5 % 005-011-01-1 disodium tetraborate decahydrate; S: 53-45 Repr. Cat. 2; R60-61: C ≥ 4,5 % 005-011-01-1 disodium tetraborate decahydrate; borax decahydrate 215-540-4 1303-96-4 Repr. Cat. 2; R60-61 T R: 60-61 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 8,5 % 005-011-02-9 disodium tetraborate pentahydrate; S: 53-45 Repr. Cat. 2; R60-61: C ≥ 8,5 % 005-011-02-9 disodium tetraborate pentahydrate; borax pentahydrate 215-540-4 12179-04-3 Repr. Cat. 2; R60-61 T R: 60-61 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 6,5 % 005-012-00-X diethyl{4-[1,5,5-tris(4-diethylaminophenyl)penta-2,4-dienylidene]cyclohexa-2,5-dienylidene}ammonium butyltriphenylborate 418-070-1 141714-54-7 R43 S: 53-45 Repr. Cat. 2; R60-61: C ≥ 6,5 % 005-012-00-X diethyl{4-[1,5,5-tris(4-diethylaminophenyl)penta-2,4-dienylidene]cyclohexa-2,5-dienylidene}ammonium butyltriphenylborate 418-070-1 141714-54-7 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 005-013-00-5 diethylmethoxyborane 425-380-9 7397-46-8 F; R17 … 16 unchanged lines … sodium peroxometaborate; [4] perboric acid (HBO(O2)), sodium salt, monohydrate; [5] sodium peroxoborate; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 234-390-0 [3] 231-556-4 [4] 231-556-4 [5] 15120-21-5 [1] 11138-47-9 [2] 12040-72-1 [3] 7632-04-4 [4] 10332-33-9 [5] O; R8 Repr. Cat. 2; R61 Repr. Cat. 3; R62 Xn; R22 Xi; R37-41 O; T R: 61-8-22-37-41-62 S: 53-45 Repr. Cat. 2; R61: C ≥ 6,5 % Repr. Cat. 3; R62: C ≥ 9 % Xi; R41: C ≥ 22 % Xi; R36: 14 % ≤ C < 22 % E S: 53-45 Repr. Cat. 2; R61: C ≥ 6,5 % Repr. Cat. 3; R62: C ≥ 9 % Xi; R41: C ≥ 22 % Xi; R36: 14 % ≤ C < 22 % E 005-017-01-4 sodium perborate; [1] perboric acid, sodium salt; [2] perboric acid, sodium salt, monohydrate; [3] sodium peroxometaborate; [4] perboric acid (HBO(O2)), sodium salt, monohydrate; [5] sodium peroxoborate; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 234-390-0 [3] 231-556-4 [4] 231-556-4 [5] 15120-21-5 [1] 11138-47-9 [2] 12040-72-1 [3] 7632-04-4 [4] 10332-33-9 [5] - O; R8 Repr. Cat. 2; R61 Repr. Cat. 3; R62 T; R23 Xn; R22 Xi; R37-41 O; T R: 61-8-22-23-37-41-62 S: 53-45 Repr. Cat. 2; R61: C ≥ 6,5 % Repr. Cat. 3; R62: C ≥ 9 % Xi; R41: C ≥ 22 % Xi; R36: 14 % ≤ C < 22 % E S: 53-45 Repr. Cat. 2; R61: C ≥ 6,5 % Repr. Cat. 3; R62: C ≥ 9 % Xi; R41: C ≥ 22 % Xi; R36: 14 % ≤ C < 22 % E 005-018-00-2 perboric acid (H3BO2(O2)), monosodium salt trihydrate; [1] perboric acid, sodium salt, tetrahydrate; [2] perboric acid (HBO(O2)), sodium salt, tetrahydrate; [3] sodium peroxoborate hexahydrate; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 231-556-4 [3] 13517-20-9 [1] 37244-98-7 [2] 10486-00-7 [3] - Repr. Cat. 2; R61 Repr. Cat. 3; R62 Xi; R37-41 T R: 61-37-41-62 S: 53-45-47 Repr. Cat. 2; R61: C ≥ 10 % Repr. Cat. 3; R62: C ≥ 14 % Xi; R41: C ≥ 36 % Xi; R36: 22 % ≤ C < 36 % 005-018-01-X perboric acid (H3BO2(O2)), monosodium salt, trihydrate; [1] S: 53-45-47 Repr. Cat. 2; R61: C ≥ 10 % Repr. Cat. 3; R62: C ≥ 14 % Xi; R41: C ≥ 36 % Xi; R36: 22 % ≤ C < 36 % 005-018-01-X perboric acid (H3BO2(O2)), monosodium salt, trihydrate; [1] perboric acid, sodium salt, tetrahydrate; [2] perboric acid (HBO(O2)), sodium salt, tetrahydrate; [3] sodium peroxoborate hexahydrate; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 239-172-9 [1] 234-390-0 [2] 231556-4 [3] 13517-20-9 [1] 37244-98-7 [2] 10486-00-7 [3] - Repr. Cat. 2; R61 Repr. Cat. 3; R62 Xn; R20 Xi; R37-41 T R: 61-20-37-41-62 S: 53-45-47 Repr. Cat. 2; R61: C ≥ 10 % Repr. Cat. 3; R62: C ≥ 14 % Xi; R41: C ≥ 36 % Xi; R36: 22 % ≤ C < 36 % E S: 53-45-47 Repr. Cat. 2; R61: C ≥ 10 % Repr. Cat. 3; R62: C ≥ 14 % Xi; R41: C ≥ 36 % Xi; R36: 22 % ≤ C < 36 % E 006-001-00-2 carbon monoxide 211-128-3 630-08-0 F+; R12 Repr. Cat. 1; R61 T; R23-48/23 F+; T R: 61-12-23-48/23 S: 53-45 E 006-002-00-8 phosgene; carbonyl chloride 200-870-3 75-44-5 T+; R26 C; R34 T+ R: 26-34 S: (1/2-)9-26-36/37/39-45 006-003-00-3 carbon disulphide 200-843-6 75-15-0 F; R11 Repr. Cat. 3; R62-63 T; R48/23 Xi; R36/38 F; T R: 11-36/38-48/23-62-63 S: (1/2-)16-33-36/37-45 Repr. Cat. 3; R62-63: C ≥ 1 % T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 006-004-00-9 calcium carbide 200-848-3 75-20-7 F; R15 F S: (1/2-)16-33-36/37-45 Repr. Cat. 3; R62-63: C ≥ 1 % T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 006-004-00-9 calcium carbide 200-848-3 75-20-7 F; R15 F R: 15 S: (2-)8-43 006-005-00-4 thiram (ISO); tetramethylthiuram disulphide 205-286-2 137-26-8 Xn; R20/22-48/22 Xi; R36/38 R43 N; R50-53 Xn; N R: 20/22-36/38-43-48/22-50/53 S: (2-)26-36/37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-006-00-X hydrogen cyanide; S: (2-)26-36/37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-006-00-X hydrogen cyanide; hydrocyanic acid 200-821-6 74-90-8 F+; R12 T+; R26 N; R50-53 F+; T+; N … 23 unchanged lines … Xn; R20/22 N; R50 Xn; N R: 20/22-40-50 S: (2-)36/37-46-61 N; R50: C ≥ 0,25 % 006-012-00-2 ziram (ISO); zinc bis dimethyldithiocarbamate 205-288-3 137-30-4 T+; R26 S: (2-)36/37-46-61 N; R50: C ≥ 0,25 % 006-012-00-2 ziram (ISO); zinc bis dimethyldithiocarbamate 205-288-3 137-30-4 T+; R26 Xn; R22-48/22 Xi; R37-41 R43 N; R50-53 T+; N R: 22-26-37-41-43-48/22-50/53 S: (1/2-)22-26-28-36/37/39-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-013-00-8 metam-sodium (ISO); S: (1/2-)22-26-28-36/37/39-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-013-00-8 metam-sodium (ISO); sodium methyldithiocarbamate 205-293-0 137-42-8 Xn; R22 R31 C; R34 R43 N; R50-53 C; N R: 22-31-34-43-50/53 S: (1/2-)26-36/37/39-45-60-61 006-014-00-3 nabam (ISO); disodium ethylenebis(N,N'-dithiocarbamate) 205-547-0 142-59-6 Xn; R22 Xi; R37 R43 N; R50-53 Xn; N R: 22-37-43-50/53 S: (2-)8-24/25-46-60-61 006-015-00-9 diuron (ISO); 3-(3,4-dichlorophenyl)-1,1-dimethylurea 206-354-4 330-54-1 Carc. Cat. 3; R40 Xn; R22-48/22 N; R50-53 Xn; N R: 22-40-48/22-50/53 S: (2-)13-36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-016-00-4 propoxur (ISO); S: (2-)13-36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-016-00-4 propoxur (ISO); 2-isopropyloxyphenyl N-methylcarbamate; 2-isopropoxyphenyl methylcarbamate 204-043-8 114-26-1 T; R25 N; R50-53 T; N … 114 unchanged lines … Xn; R22 Xi; R36/37/38 T R: 45-22-23-36/37/38 S: 53-45 Carc. Cat. 2; R45: C ≥ 0,001 % E S: 53-45 Carc. Cat. 2; R45: C ≥ 0,001 % E 006-042-00-6 monuron (ISO); 3-(4-chlorophenyl)-1,1-dimethylurea 205-766-1 150-68-5 Carc. Cat. 3; R40 Xn; R22 N; R50-53 Xn; N R: 22-40-50/53 S: (2-)36/37-60-61 006-043-00-1 3-(4-chlorophenyl)-1,1-dimethyluronium trichloroacetate; monuron-TCA — 140-41-0 Xi; R36/38 Carc. Cat. 3; R40 N; R50-53 Xn; N R: 36/38-40-50/53 S: (2-)36/37-60-61 006-044-00-7 isoproturon (ISO); 3-(4-isopropylphenyl)-1,1-dimethylurea 251-835-4 34123-59-6 Carc. Cat. 3; R40 N; R50-53 Xn; N R: 40-50/53 S: (2-)36/37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-045-00-2 methomyl (ISO); S: (2-)36/37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-045-00-2 methomyl (ISO); 1-(methylthio)ethylideneamino N-methylcarbamate 240-815-0 16752-77-5 T+; R28 N; R50-53 T+; N R: 28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-046-00-8 bendiocarb (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-046-00-8 bendiocarb (ISO); 2,2-dimethyl-1,3-benzodioxol-4-yl N-methylcarbamate 245-216-8 22781-23-3 T; R23/25 Xn; R21 N; R50-53 T; N … 117 unchanged lines … R43 N; R50 Xn; N R: 43-63-50 S: (2-)36/37-46-61 N; R50: C ≥ 2,5 % 006-077-00-7 maneb (ISO); S: (2-)36/37-46-61 N; R50: C ≥ 2,5 % 006-077-00-7 maneb (ISO); manganese ethylenebis(dithiocarbamate) (polymeric) 235-654-8 12427-38-2 Repr. Cat. 3; R63 Xn; R20 Xi; R36 R43 N; R50-53 Xn; N R: 20-36-43-63-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-078-00-2 zineb (ISO); S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 006-078-00-2 zineb (ISO); zinc ethylenebis(dithiocarbamate) (polymeric) 235-180-1 12122-67-7 Xi; R37 R43 Xi R: 37-43 … 31 unchanged lines … 2-butylphenyl methylcarbamate; 223-188-8 3766-81-2 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 006-086-00-6 ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate; fenoxycarb 276-696-7 72490-01-8 N; R50-53 N R: 50/53 S: 60-61 006-087-00-1 furathiocarb (ISO); S: (2-)60-61 006-086-00-6 fenoxycarb (ISO);ethyl [2-(4-phenoxyphenoxy)ethyl]carbamate 276-696-7 72490-01-8 Carc. Cat. 3; R40 N; R50-53 Xn; N R: 40-50/53 S: (2-)22-36/37-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 006-087-00-1 furathiocarb (ISO); 2,3-dihydro-2,2-dimethyl-7-benzofuryl 2,4-dimethyl-6-oxa-5-oxo-3-thia-2,4-diazadecanoate 265-974-3 65907-30-4 T+; R26 T; R25 Xn; R48/22 Xi; R36/38 R43 N; R50-53 T+; N R: 25-26-36/38-43-48/22-50/53 S: (1/2-)28-36/37-38-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-088-00-7 benfuracarb (ISO); S: (1/2-)28-36/37-38-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 006-088-00-7 benfuracarb (ISO); ethyl N-[2,3-dihydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio]-N-isopropyl- β-alaninate — 82560-54-1 Repr. Cat. 3; R62 T; R23 Xn; R22 N; R50-53 T; N R: 22-23-62-50/53 S: (1/2-)36/37-45-60-61 006-089-00-2 chlorine dioxide 233-162-8 10049-04-4 O; R8 R6 T+; R26 C; R34 N; R50 O; T+; N R: 6-8-26-34-50 S: (1/2-)23-26-28-36/37/39-38-45-61 N; R50: C ≥ 0,02 % 5 006-089-01-X chlorine dioxide … % 233-162-8 10049-04-4 T; R25 S: (1/2-)23-26-28-36/37/39-38-45-61 N; R50: C ≥ 0,02 % 5 006-089-01-X chlorine dioxide … % 233-162-8 10049-04-4 T; R25 C; R34 N; R50 T; N R: 25-34-50 S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 3 % ≤ C < 10 % Xi; R36: 0,3 % ≤ C < 3 % N; R50: C ≥ 3 % B S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 3 % ≤ C < 10 % Xi; R36: 0,3 % ≤ C < 3 % N; R50: C ≥ 3 % B 006-090-00-8 2-(3-iodoprop-2-yn-1-yloxy)ethyl phenylcarbamate 408-010-0 88558-41-2 Xn; R20 Xi; R41 R52-53 Xn … 49 unchanged lines … R42 N; R50-53 Xn; N R: 41-42-50/53 S: (2-)22-26-39-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 007-001-00-5 ammonia, anhydrous 231-635-3 7664-41-7 R10 S: (2-)22-26-39-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 007-001-00-5 ammonia, anhydrous 231-635-3 7664-41-7 R10 T; R23 C; R34 N; R50 T; N R: 10-23-34-50 S: (1/2-)9-16-26-36/37/39-45-61 007-001-01-2 ammonia ....% 215-647-6 1336-21-6 C; R34 N; R50 C; N R: 34-50 S: (1/2-)26-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % B S: (1/2-)26-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % B 007-002-00-0 nitrogen dioxide; [1] dinitrogen tetraoxide [2] 233-272-6 [1] 234-126-4 [2] 10102-44-0 [1] 10544-72-6 [2] O; R8 T+; R26 C; R34 O; T+ R: 8-26-34 S: (1/2-)9-26-28-36/37/39-45 T+; R26: C ≥ 10 % T; R23: 1 % ≤ C < 10 % Xn; R20: 0,1 % ≤ C < 1 % 5 S: (1/2-)9-26-28-36/37/39-45 T+; R26: C ≥ 10 % T; R23: 1 % ≤ C < 10 % Xn; R20: 0,1 % ≤ C < 1 % 5 007-003-00-6 chlormequat chloride (ISO); 2-chloroethyltrimethylammonium chloride 213-666-4 999-81-5 Xn; R21/22 Xn R: 21/22 S: (2-)36/37 007-004-00-1 nitric acid ... % 231-714-2 7697-37-2 O; R8 S: (2-)36/37 007-004-00-1 nitric acid ... % 231-714-2 7697-37-2 O; R8 C; R35 O; C R: 8-35 S: (1/2-)23-26-36-45 C; R35: C ≥ 20 % C; R34: 5 % ≤ C < 20 % S: (1/2-)23-26-36-45 C; R35: C ≥ 20 % C; R34: 5 % ≤ C < 20 % Footnote: O; R8: C ≥ 70 % B O; R8: C ≥ 70 % B 007-006-00-2 ethyl nitrite 203-722-6 109-95-5 E; R2 Xn; R20/21/22 E; Xn R: 2-20/21/22 S: (2-) 007-007-00-8 ethyl nitrate 210-903-3 625-58-1 E; R3 E R: 3 S: (2-)23-24/25 007-008-00-3 hydrazine 206-114-9 302-01-2 R10 Carc. Cat. 2; R45 T; R23/24/25 C; R34 R43 N; R50-53 T; N R: 45-10-23/24/25-34-43-50/53 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 3 % ≤ C < 10 % E S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 3 % ≤ C < 10 % E 007-009-00-9 dicyclohexylammonium nitrite 221-515-9 3129-91-7 Xn; R20/22 Xn R: 20/22 S: (2-)15-41 Xn; R20/22: C ≥ 10 % 007-010-00-4 sodium nitrite 231-555-9 7632-00-0 O; R8 S: (2-)15-41 Xn; R20/22: C ≥ 10 % 007-010-00-4 sodium nitrite 231-555-9 7632-00-0 O; R8 T; R25 N; R50 O; T; N R: 8-25-50 S: (1/2-)45-61 T; R25: C ≥ 5 % Xn; R22: 1 % ≤ C < 5 % 007-011-00-X potassium nitrite 231-832-4 7758-09-0 O; R8 S: (1/2-)45-61 T; R25: C ≥ 5 % Xn; R22: 1 % ≤ C < 5 % 007-011-00-X potassium nitrite 231-832-4 7758-09-0 O; R8 T; R25 N; R50 O; T; N R: 8-25-50 S: (1/2-)45-61 T; R25: C ≥ 5 % Xn; R22: 1 % ≤ C < 5 % 007-012-00-5 N,N-dimethylhydrazine 200-316-0 57-14-7 F; R11 S: (1/2-)45-61 T; R25: C ≥ 5 % Xn; R22: 1 % ≤ C < 5 % 007-012-00-5 N,N-dimethylhydrazine 200-316-0 57-14-7 F; R11 Carc. Cat. 2; R45 T; R23/25 C; R34 N; R51-53 F; T; N R: 45-11-23/25-34-51/53 S: 53-45-61 E 007-013-00-0 1,2-dimethylhydrazine — 540-73-8 Carc. Cat. 2; R45 T; R23/24/25 N; R51-53 T; N R: 45-23/24/25-51/53 S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E 007-014-00-6 salts of hydrazine — — Carc. Cat. 2; R45 T; R23/24/25 R43 … 73 unchanged lines … R: 21/22-35 S: (1/2-)26-36/37/39-45 008-001-00-8 oxygen 231-956-9 7782-44-7 O; R8 O R: 8 S: (2-)17 008-003-00-9 hydrogen peroxide solution ... % 231-765-0 7722-84-1 R5 S: (2-)17 008-003-00-9 hydrogen peroxide solution ... % 231-765-0 7722-84-1 R5 O; R8 C; R35 Xn; R20/22 O; C R: 5-8-20/22-35 S: (1/2-)17-26-28-36/37/39-45 Xn; R20: C ≥ 50 % Xn; R22: C ≥ 8 % C; R35: C ≥ 70 % C; R34: 50 % ≤ C < 70 % Xi; R37/38: 35 % ≤ C < 50 % Xi; R41: 8 % ≤ C < 50 % Xi; R36: 5 % ≤ C < 8 % S: (1/2-)17-26-28-36/37/39-45 Xn; R20: C ≥ 50 % Xn; R22: C ≥ 8 % C; R35: C ≥ 70 % C; R34: 50 % ≤ C < 70 % Xi; R37/38: 35 % ≤ C < 50 % Xi; R41: 8 % ≤ C < 50 % Xi; R36: 5 % ≤ C < 8 % Footnote: O; R8: C ≥ 50 % R5: C ≥ 70 % B O; R8: C ≥ 50 % R5: C ≥ 70 % B 009-001-00-0 fluorine 231-954-8 7782-41-4 O; R8 T+; R26 C; R35 O; T+; C R: 8-26-35 S: (1/2-)9-26-28-36/37/39-45 009-002-00-6 hydrogen fluoride 231-634-8 7664-39-3 T+; R26/27/28 C; R35 T+; C R: 26/27/28-35 S: (1/2-)7/9-26-36/37/39-45 009-003-00-1 hydrofluoric acid ... % 231-634-8 7664-39-3 T+; R26/27/28 S: (1/2-)7/9-26-36/37/39-45 009-003-00-1 hydrofluoric acid ... % 231-634-8 7664-39-3 T+; R26/27/28 C; R35 T+; C R: 26/27/28-35 S: (1/2-)7/9-26-36/37-45 C; R35: C ≥ 7 % C; R34: 1 % ≤ C < 7 % Xi; R36: 0,1 % ≤ C < 1 % B S: (1/2-)7/9-26-36/37-45 C; R35: C ≥ 7 % C; R34: 1 % ≤ C < 7 % Xi; R36: 0,1 % ≤ C < 1 % B 009-004-00-7 sodium fluoride 231-667-8 7681-49-4 T; R25 Xi; R36/38 R32 T R: 25-32-36/38 S: (1/2-)22-36-45 009-005-00-2 potassium fluoride 232-151-5 7789-23-3 T; R23/24/25 T R: 23/24/25 S: (1/2-)26-45 009-006-00-8 ammonium fluoride 235-185-9 12125-01-8 T; R23/24/25 T R: 23/24/25 S: (1/2-)26-45 009-007-00-3 sodium bifluoride; sodium hydrogen difluoride 215-608-3 1333-83-1 T; R25 C; R34 T; C R: 25-34 S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-008-00-9 potassium bifluoride; S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-008-00-9 potassium bifluoride; potassium hydrogen difluoride 232-156-2 7789-29-9 T; R25 C; R34 T; C R: 25-34 S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-009-00-4 ammonium bifluoride; S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-009-00-4 ammonium bifluoride; ammonium hydrogen difluoride 215-676-4 1341-49-7 T; R25 C; R34 T; C R: 25-34 S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-010-00-X fluoroboric acid ... % 240-898-3 16872-11-0 C; R34 C S: (1/2-)22-26-37-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % C; R34: C ≥ 1 % Xi; R36/38: 0,1 % ≤ C < 1 % 009-010-00-X fluoroboric acid ... % 240-898-3 16872-11-0 C; R34 C R: 34 S: (1/2-)26-27-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B 009-011-00-5 fluorosilicic acid ... % 241-034-8 16961-83-4 C; R34 C S: (1/2-)26-27-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B 009-011-00-5 fluorosilicic acid ... % 241-034-8 16961-83-4 C; R34 C R: 34 S: (1/2-)26-27-45 B 009-012-00-0 alkali fluorosilicates(Na); [1] alkali fluorosilicates(K); [2] alkali fluorosilicates(NH4) [3] 240-934-8 [1] 240-896-2 [2] 240-968-3 [3] 16893-85-9 [1] 16871-90-2 [2] 16919-19-0 [3] T; R23/24/25 T R: 23/24/25 S: (1/2-)26-45 T; R23/24/25: C ≥ 10 % Xn; R20/21/22: 1 % ≤ C < 10 % A S: (1/2-)26-45 T; R23/24/25: C ≥ 10 % Xn; R20/21/22: 1 % ≤ C < 10 % A 009-013-00-6 fluorosilicates, with the exception of those specified elsewhere in this annex — — Xn; R22 Xn R: 22 S: (2-)13-24/25 Xn; R22: C ≥ 10 % A S: (2-)13-24/25 Xn; R22: C ≥ 10 % A 009-014-00-1 lead hexafluorosilicate 247-278-1 25808-74-6 Repr. Cat. 1; R61 Repr. Cat. 3; R62 Xn; R20/22 … 16 unchanged lines … R: 11-14/15-20-35 S: (1/2-)16-30-36/39-43-45 009-018-00-3 magnesium hexafluorosilicate 241-022-2 16949-65-8 T; R25 T R: 25 S: (1/2-)24/25-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % 011-001-00-0 sodium 231-132-9 7440-23-5 F; 15 S: (1/2-)24/25-45 T; R25: C ≥ 10 % Xn; R22: 1 % ≤ C < 10 % 011-001-00-0 sodium 231-132-9 7440-23-5 F; 15 R14 C; R34 F; C R: 14/15-34 S: (1/2-)5-8-43-45 011-002-00-6 sodium hydroxide; caustic soda 215-185-5 1310-73-2 C; R35 C R: 35 S: (1/2-)26-37/39-45 C; R35: C ≥ 5 % C; R34: 2 % ≤ C < 5 % Xi; R36/38: 0,5 % ≤ C < 2 % 011-003-00-1 sodium peroxide 215-209-4 1313-60-6 O; R8 S: (1/2-)26-37/39-45 C; R35: C ≥ 5 % C; R34: 2 % ≤ C < 5 % Xi; R36/38: 0,5 % ≤ C < 2 % 011-003-00-1 sodium peroxide 215-209-4 1313-60-6 O; R8 C; R35 O; C R: 8-35 S: (1/2-)8-27-39-45 011-004-00-7 sodium azide 247-852-1 26628-22-8 T+; R28 R32 N; R50-53 T+; N R: 28-32-50/53 S: (1/2-)28-45-60-61 011-005-00-2 sodium carbonate 207-838-8 497-19-8 Xi; R36 Xi R: 36 S: (2-)22-26 011-006-00-8 sodium cyanate 213-030-6 917-61-3 Xn; R22 R52-53 Xn R: 22-52/53 S: (2-)24/25-61 011-007-00-3 propoxycarbazone-sodium — 181274-15-7 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 012-001-00-3 magnesium powder (pyrophoric) 231-104-6 7439-95-4 F; R15-17 F S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 012-001-00-3 magnesium powder (pyrophoric) 231-104-6 7439-95-4 F; R15-17 F R: 15-17 S: (2-)7/8-43 012-002-00-9 magnesium, powder or turnings 231-104-6 — F; R11-15 F R: 11-15 … 44 unchanged lines … R29 C; R35 F+; C R: 12-14-17-20/22-29-35 S: (2-)7/9-16-26-36/37/39-43-45 Xn; R20/22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 014-002-00-4 silicon tetrachloride 233-054-0 10026-04-7 R14 S: (2-)7/9-16-26-36/37/39-43-45 Xn; R20/22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 014-002-00-4 silicon tetrachloride 233-054-0 10026-04-7 R14 Xi; R36/37/38 Xi R: 14-36/37/38 S: (2-)7/8-26 014-003-00-X dimethyldichlorosilane 200-901-0 75-78-5 F; R11 Xi; R36/37/38 F; Xi R: 11-36/37/38 S: (2-) 014-004-00-5 trichloro(methyl)silane; methyltrichlorosilane 200-902-6 75-79-6 R14 F; R11 Xi; R36/37/38 F; Xi R: 11-14-36/37/38 S: (2-)26-39 Xi; R36/37/38: C ≥ 1 % 014-005-00-0 tetraethyl silicate; S: (2-)26-39 Xi; R36/37/38: C ≥ 1 % 014-005-00-0 tetraethyl silicate; ethyl silicate 201-083-8 78-10-4 R10 Xn; R20 Xi; R36/37 Xn … 96 unchanged lines … S: (2-)24-37-61 014-036-00-X (4-ethoxyphenyl)(3-(4-fluoro-3-phenoxyphenyl)propyl)dimethylsilane 405-020-7 105024-66-6 Repr. Cat.2; R60 N; R50-53 T; N R: 60-50/53 S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 014-037-00-5 2-butanone-O, O', O''-(phenylsilylidyne)trioxime 433-360-6 34036-80-1 Xn; R48/22 S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 014-037-00-5 2-butanone-O, O', O''-(phenylsilylidyne)trioxime 433-360-6 34036-80-1 Xn; R48/22 R43 R52-53 Xn R: 43-48/22-52/53 S: (2-)36/37-61 014-038-00-0 S-(3-(triethoxysilyl)propyl) octanethioate 436-690-9 220727-26-4 R43 Xi R: 43 S: (2-)24-37 014-039-00-6 (2,3-dimethylbut-2-yl)-trimethoxysilane 439-360-2 142877-45-0 Xi; R38-41 R52-53 Xi R: 38-41-52/53 S: (2-)26-37/39-61 014-041-00-7 N,N-bis(trimethylsilyl)aminopropylmethyldiethoxysilane 445-890-5 201290-01-9 Xn; R22 R43 Xn R: 22-43 S: (2-)24-37 014-042-00-2 reaction mass of: O,O',O'',O'''-silanetetrayl tetrakis(4-methyl-2-pentanone oxime) (3 stereoisomers) 423-010-0 - Xi; R41 Xi R: 41 S: (2-)26-39 014-043-00-8 reaction product of amorphous silica (50-85 %), butyl (1-methylpropyl) magnesium (3-15 %), tetraethyl orthosilicate (5-15 %) and titanium tetrachloride (5-20 %) 432-200-2 - F; R11 S: (2-)26-39 014-043-00-8 reaction product of amorphous silica (50-85 %), butyl (1-methylpropyl) magnesium (3-15 %), tetraethyl orthosilicate (5-15 %) and titanium tetrachloride (5-20 %) 432-200-2 - F; R11 Xi; R37/38-41 R52-53 F; Xi R: 11-37/38-41-52/53 … 16 unchanged lines … R29 N; R50 F; T+; N R: 15/29-28-50 S: (1/2-)22-28-36/37-43-45-61 N; R50: C ≥ 0,25 % 015-004-00-8 aluminium phosphide 244-088-0 20859-73-8 F; R15/29 S: (1/2-)22-28-36/37-43-45-61 N; R50: C ≥ 0,25 % 015-004-00-8 aluminium phosphide 244-088-0 20859-73-8 F; R15/29 T+; R26/28 Xn; R21 R32 N; R50 F; T+; N R: 15/29-21- 26/28-32-50 S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61 N; R50: C ≥ 0,25 % 015-005-00-3 magnesium phosphide; R: 15/29-21-26/28-32-50 S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61 N; R50: C ≥ 0,25 % 015-005-00-3 magnesium phosphide; trimagnesium diphosphide 235-023-7 12057-74-8 F; R15/29 T+; R26/28 Xn; R21 R32 N; R50 F; T+; N R: 15/29-21-26/28-32-50 S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61 N; R50: C ≥ 0,25 % 015-006-00-9 trizinc diphosphide; S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61 N; R50: C ≥ 0,25 % 015-006-00-9 trizinc diphosphide; zinc phosphide 215-244-5 1314-84-7 F; R15 T+; R28 R29 R32 N; R50-53 F; T+; N R: 15/29-28-32-50/53 S: (1/2-)28-30-36/37-43-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % T S: (1/2-)28-30-36/37-43-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % T 015-007-00-4 phosphorus trichloride 231-749-3 7719-12-2 R14 T+; R26/28 Xn; R48/20 … 15 unchanged lines … R: 14-22-26-35-48/23 S: (1/2-)7/8-26-36/37/39-45 015-010-00-0 phosphorus pentoxide 215-236-1 1314-56-3 C; R35 C R: 35 S: (1/2-)22-26-45 015-011-00-6 phosphoric acid ... %, orthophosphoric acid ... % 231-633-2 7664-38-2 C; R34 C S: (1/2-)22-26-45 015-011-00-6 phosphoric acid ... %, orthophosphoric acid ... % 231-633-2 7664-38-2 C; R34 C R: 34 S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B 015-012-00-1 tetraphosphorus trisulphide; phosphorus sesquisulphid 215-245-0 1314-85-8 F; R11 Xn; R22 N; R50 F; Xn; N R: 11-22-50 S: (2-)7-16-24/25-61 015-013-00-7 triethyl phosphate 201-114-5 78-40-0 Xn; R22 Xn R: 22 S: (2-)25 015-014-00-2 tributyl phosphate 204-800-2 126-73-8 Carc. Cat. 3; R40 Xn; R22 Xi; R38 Xn R: 22-38-40 S: (2-)36/37-46 015-015-00-8 tricresyl phosphate (o-o-o-, o-o-m-, o-o-p-, o-m-m-, o-m-p-, o-p-p-); tritolyl phosphate (o-o-o-, o-o-m-, o-o-p-, o-m-m-, o-m-p-, o-p-p-); 201-103-5 78-30-8 T; R39/23/24/25 N; R51-53 T; N R: 39/23/24/25-51/53 S: (1/2-)20/21-28-45-61 T; R39/23/24/25: C ≥ 1 % Xn; R68/20/21/22: 0,2 % ≤ C < 1 % C S: (1/2-)20/21-28-45-61 T; R39/23/24/25: C ≥ 1 % Xn; R68/20/21/22: 0,2 % ≤ C < 1 % C 015-016-00-3 tricresyl phosphate (m-m-m-, m-m-p-, m-p-p-, p-p-p-); tritolyl phosphate (m-m-m-, m-m-p-, m-p-p-, p-p-p-); 201-105-6 78-32-0 Xn; R21/22 N; R51-53 Xn; N R: 21/22-51/53 S: (2-)28-61 Xn; R21/22: C ≥ 5 % C S: (2-)28-61 Xn; R21/22: C ≥ 5 % C 015-019-00-X dichlorvos (ISO); 2,2-dichlorovinyl dimethyl phosphate 200-547-7 62-73-7 T+; R26 T; R24/25 R43 N; R50 T+; N R: 24/25-26-43-50 S: (1/2-)28-36/37-45-61 N; R50: C ≥ 0,025 % 015-020-00-5 mevinphos (ISO); S: (1/2-)28-36/37-45-61 N; R50: C ≥ 0,025 % 015-020-00-5 mevinphos (ISO); 2-methoxycarbonyl-1-methylvinyl dimethyl phosphate 232-095-1 7786-34-7 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 S: (1/2-)23-28-36/37-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-021-00-0 trichlorfon (ISO); S: (1/2-)23-28-36/37-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-021-00-0 trichlorfon (ISO); dimethyl 2,2,2-trichloro-1-hydroxyethylphosphonate 200-149-3 52-68-6 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-022-00-6 phosphamidon (ISO); S: (2-)24-37-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-022-00-6 phosphamidon (ISO); 2-chloro-2-diethylcarbamoyl-1-methylvinyl dimethyl phosphate 236-116-5 13171-21-6 T+; R28 T; R24 Muta. Cat. 3; R68 … 16 unchanged lines … O,O,O,O-tetraethyl dithiopyrophosphate 222-995-2 3689-24-5 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 S: (1/2-)23-28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-028-00-9 demeton-O (ISO); S: (1/2-)23-28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-028-00-9 demeton-O (ISO); O,O-diethyl-O-2-ethylthioethyl phosphorothioate 206-053-8 298-03-3 T+; R27/28 N; R50 T+; N R: 27/28-50 … 15 unchanged lines … O,O-diethyl ethylthiomethyl phosphorodithioate 206-052-2 298-02-2 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-034-00-1 parathion (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-034-00-1 parathion (ISO); O,O-diethyl O-4-nitrophenyl phosphorothioate 200-271-7 56-38-2 T+; R26/28 T; R24-48/25 N; R50-53 T+; N R: 24-26/28-48/25-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-035-00-7 parathion — methyl (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-035-00-7 parathion — methyl (ISO); O,O-dimethyl O-4-nitrophenyl phosphorothioate 206-050-1 298-00-0 R5 R10 T+; R26/28 T; R24 Xn; R48/22 N; R50-53 T+; N R: 5-10-24-26/28-48/22-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-036-00-2 O-ethyl O-4-nitrophenyl phenylphosphonothioate; S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-036-00-2 O-ethyl O-4-nitrophenyl phenylphosphonothioate; EPN 218-276-8 2104-64-5 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 … 18 unchanged lines … R: 22-50/53 S: (2-)24/25-60-61 015-041-00-X malathion (ISO); 1,2-bis(ethoxycarbonyl)ethyl O,O-dimethyl phosphorodithioate; [containing ≤ 0,03 % isomalathion] 204-497-7 121-75-5 Xn; R22 [containing ≤ 0,03 % isomalathion] 204-497-7 121-75-5 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-042-00-5 chlorthion S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-042-00-5 chlorthion O-(3-chloro-4-nitrophenyl) O,O-dimethyl phosphorothioate 207-902-5 500-28-7 Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)13-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-043-00-0 phosnichlor (ISO); S: (2-)13-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-043-00-0 phosnichlor (ISO); O-4-chloro-3-nitrophenyl O,O-dimethyl phosphorothioate — 5826-76-6 Xn; R20/21/22 Xn R: 20/21/22 S: (2-)13 015-044-00-6 carbophenothion (ISO); 4-chlorophenylthiomethyl O,O-diethyl phosphorodithioate 212-324-1 786-19-6 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)28-36/37-45-60-61 015-045-00-1 mecarbam (ISO); N-ethoxycarbonyl-N-methylcarbamoylmethyl O,O-diethyl phosphorodithioate 219-993-9 2595-54-2 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)36/37-45-60-61 015-046-00-7 oxydemeton-methyl; S-2-(ethylsulphinyl)ethyl O,O-dimethyl phosphorothioate 206-110-7 301-12-2 T; R24/25 N; R50 T; N R: 24/25-50 S: (1/2-)23-36/37-45-61 015-047-00-2 ethion (ISO); O,O,O',O'-tetraethyl S,S'-methylenedi (phosphorodithioate); diethion 209-242-3 563-12-2 T; R25 Xn; R21 N; R50-53 T; N R: 21-25-50/53 S: (1/2-)25-36/37-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-048-00-8 fenthion (ISO); S: (1/2-)25-36/37-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-048-00-8 fenthion (ISO); O,O-dimethyl-O-(4-methylthion-m-tolyl) phosphorothioate 200-231-9 55-38-9 Muta. Cat. 3; R68 T; R23-48/25 Xn; R21/22 N; R50-53 T; N R: 21/22-23-48/25-68-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-049-00-3 endothion (ISO); S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-049-00-3 endothion (ISO); S-5-methoxy-4-oxopyran-2-ylmethyl dimethyl phosphorothioate 220-472-3 2778-04-3 T; R24/25 T R: 24/25 S: (1/2-)36/37-45 015-050-00-9 thiometon (ISO); … 20 unchanged lines … Xi; R36/38 N; R50 Xn; N R: 21/22-36/38-50 S: (2-)36/37-61 N; R50: C ≥ 0,025 % 015-056-00-1 azinphos-ethyl (ISO); S: (2-)36/37-61 N; R50: C ≥ 0,025 % 015-056-00-1 azinphos-ethyl (ISO); O,O-diethyl 4-oxobenzotriazin-3-ylmethyl phosphorodithioate 220-147-6 2642-71-9 T+; R28 T; R24 N; R50-53 T+; N R: 24-28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-057-00-7 formothion (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-057-00-7 formothion (ISO); N-formyl-N-methylcarbamoylmethyl O,O-dimethyl phosphorodithioate 219-818-6 2540-82-1 Xn; R21/22 Xn R: 21/22 S: (2-)36/37 015-058-00-2 morphothion (ISO); … 20 unchanged lines … T; R24 N; R50-53 T+; N R: 24-26/28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-064-00-5 bromophos-ethyl (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-064-00-5 bromophos-ethyl (ISO); O-4-bromo-2,5-dichlorophenyl O,O-diethyl phosphorothioate 225-399-0 4824-78-6 T; R25 Xn; R21 N; R50-53 T; N R: 21-25-50/53 S: (1/2-)28-36/37-45-60-61 015-065-00-0 S-[2-(ethylsulphinyl)ethyl] O,O-dimethyl phosphorodithioate — 2703-37-9 T+; R26/27/28 N; R51-53 T+; N R: 26/27/28-51/53 S: (1/2-)13-28-45-61 015-066-00-6 omethoate (ISO); O,O-dimethyl S-methylcarbamoylmethyl phosphorothioate 214-197-8 1113-02-6 T; R25 Xn; R21 N; R50 T; N R: 21-25-50 S: (1/2-)23-36/37-45-61 015-067-00-1 phosalone (ISO); S-(6-chloro-2-oxobenzoxazolin-3-ylmethyl) O,O-diethyl phosphorodithioate 218-996-2 2310-17-0 T; R25 Xn; R20/21 R43 N; R50-53 T; N R: 20/21-25-43-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-068-00-7 dichlofenthion (ISO); S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-068-00-7 dichlofenthion (ISO); O-,4-dichlorophenyl O,O-diethyl phosphorothioate 202-564-5 97-17-6 Xn; R22 N; R50-53 Xn; N R: 22-50/53 … 32 unchanged lines … O,O-diethyl O-(4-methylcoumarin-7-yl) phosphorothioate — 299-45-6 T+; R26/27/28 N; R50-53 T+; N R: 26/27/28-50/53 S: (1/2-)13-28-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-077-00-6 2,2-dichlorovinyl 2-ethylsulphinylethyl methyl phosphate — 7076-53-1 T; R23/24/25 T S: (1/2-)13-28-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-077-00-6 2,2-dichlorovinyl 2-ethylsulphinylethyl methyl phosphate — 7076-53-1 T; R23/24/25 T R: 23/24/25 S: (1/2-)13-45 015-078-00-1 demeton-S-methylsulphon (ISO); S-2-ethylsulphonylethyl dimethyl phosphorothioate 241-109-5 17040-19-6 T; R25 … 20 unchanged lines … O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate 220-864-4 2921-88-2 T; R25 N; R50-53 T; N R: 25-50/53 S: (1/2-)45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-085-00-X chlorphonium chloride (ISO); S: (1/2-)45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-085-00-X chlorphonium chloride (ISO); tributyl (2,4-dichlorobenzyl) phosphonium chloride 204-105-4 115-78-6 T; R25 Xn; R21 Xi; R36/38 T … 44 unchanged lines … T; R24 N; R50-53 T+; N R: 24-28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-097-00-5 phenthoate (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-097-00-5 phenthoate (ISO); ethyl 2-(dimethoxyphosphinothioylthio)-2-phenylacetate 219-997-0 2597-03-7 Xn; R21/22 N; R50-53 Xn; N R: 21/22-50/53 S: (2-)22-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-098-00-0 trichloronate (ISO); S: (2-)22-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-098-00-0 trichloronate (ISO); O-ethyl O-2,4,5-trichlorophenyl ethylphosphonothioate 206-326-1 327-98-0 T+; R28 T; R24 N; R50-53 T+; N R: 24-28-50/53 S: (1/2-)23-28-36/37-45-60-61 015-099-00-6 pirimiphos-ethyl (ISO); O,O-diethyl O-2-diethylamino-6-methylpyrimidin-4-yl phosphorothioate 245-704-0 23505-41-1 T; R25 Xn; R21 N; R50-53 T; N R: 21-25-50/53 S: (1/2-)23-36/37-45-60-61 015-100-00-X phoxim (ISO); α-(diethoxyphosphinothioylimino) phenylacetonitrile 238-887-3 14816-18-3 Repr. Cat. 3; R62 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-62-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-101-00-5 phosmet (ISO); S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-101-00-5 phosmet (ISO); O,O-dimethyl phthalimidomethyl S-phosphorodithioate 211-987-4 732-11-6 Xn; R21/22 N; R50-53 Xn; N R: 21/22-50/53 S: (2-)22-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-102-00-0 tris(2-chloroethyl)phosphate 204-118-5 115-96-8 Carc. Cat. 3; R40 S: (2-)22-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-102-00-0 tris(2-chloroethyl)phosphate 204-118-5 115-96-8 Carc. Cat. 3; R40 Repr. Cat. 2; R60 Xn; R22 N; R51-53 T; N R: 60-22-40-51/53 S: 53-45-61 E 015-103-00-6 phosphorus tribromide 232-178-2 7789-60-8 R14 C; R34 Xi; R37 C R: 14-34-37 S: (1/2-)26-45 015-104-00-1 diphosphorus pentasulphide; phosphorus pentasulphide 215-242-4 1314-80-3 F; R11 R29 Xn; R20/22 N; R50 F; Xn; N R: 11-20/22-29-50 S: (2-)61 015-105-00-7 triphenyl phosphite 202-908-4 101-02-0 Xi; R36/38 N; R50-53 Xi; N R: 36/38-50/53 S: (2-)28-60-61 Xi; R36/38: C ≥ 5 % 015-106-00-2 hexamethylphosphoric triamide; S: (2-)28-60-61 Xi; R36/38: C ≥ 5 % 015-106-00-2 hexamethylphosphoric triamide; hexamethylphosphoramide 211-653-8 680-31-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 Carc. Cat. 2; R45: C ≥ 0,01 % 015-107-00-8 ethoprophos (ISO); S: 53-45 Carc. Cat. 2; R45: C ≥ 0,01 % 015-107-00-8 ethoprophos (ISO); ethyl-S,S-dipropyl phosphorodithioate 236-152-1 13194-48-4 T+; R26/27 T; R25 R43 N; R50-53 T+; N R: 25-26/27-43-50/53 S: (1/2-)27/28-36/37/39-45-60-61 015-108-00-3 bromophos (ISO); O-4-bromo-2,5-dichlorophenyl O,O-dimethyl phosphorothioate 218-277-3 2104-96-3 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-) 46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-109-00-9 crotoxyphos (ISO); S: (2-) 46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-109-00-9 crotoxyphos (ISO); 1-phenylethyl 3-(dimethoxyphosphinyloxy) isocrotonate 231-720-5 7700-17-6 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-110-00-4 cyanofenphos (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-110-00-4 cyanofenphos (ISO); O-4-cyanophenyl O-ethyl phenylphosphonothioate — 13067-93-1 T; R25-39/25 Xn; R21 Xi; R36 N; R51-53 T; N R: 21-25-36-39/25-51/53 S: (1/2-)36/37-45-61 015-111-00-X phosfolan (ISO); diethyl 1,3-dithiolan-2-ylidenephosphoramidate 213-423-2 947-02-4 T+; R27/28 T+ R: 27/28 S: (1/2-)28-36/37-45 015-112-00-5 thionazin (ISO); O,O-diethyl O-pyrazin-2-yl phosphorothioate; 206-049-6 297-97-2 T+; R27/28 T+ R: 27/28 S: (1/2-)36/37/39-38-45 015-113-00-0 tolclofos-methyl (ISO); O-(2,6-dichloro-p-tolyl)-O,O-dimethyl thiophosphate 260-515-3 57018-04-9 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 015-114-00-6 chlormephos (ISO); S-chloromethyl O,O-diethyl phosphorodithioate 246-538-1 24934-91-6 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 S: (1/2-)27-28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-115-00-1 chlorthiophos (ISO); S: (1/2-)27-28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-115-00-1 chlorthiophos (ISO); [isomeric reaction mass in which O-2,5-dichlorophenyl-4-methylthiophenyl O,O-diethyl phosphorothioate predominates] 244-663-6 21923-23-9 T+; R28 T; R24 N; R50-53 T+; N R: 24-28-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-116-00-7 demephion-O (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-116-00-7 demephion-O (ISO); O,O-dimethyl O-2-methylthioethyl phosphorothioate 211-666-9 682-80-4 T+; R28 T; R24 T+ R: 24-28 … 20 unchanged lines … O-6-ethoxy-2-ethylpyrimidin-4-yl O,O-dimethylphosphorothioate; 253-855-9 38260-54-7 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-123-00-5 fenamiphos (ISO); S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-123-00-5 fenamiphos (ISO); ethyl-4-methylthio-m-tolyl isopropyl phosphoramidate 244-848-1 22224-92-6 T+; R26/28 T; R24 Xi; R36 N; R50-53 T+; N R: 24-26/28-36-50/53 S: (1/2-)23-26-28-35-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-124-00-0 fosthietan (ISO); S: (1/2-)23-26-28-35-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-124-00-0 fosthietan (ISO); diethyl 1,3-dithietan-2-ylidenephosphoramidate; 244-437-7 21548-32-3 T+; R27/28 T+ R: 27/28 S: (1/2-)36/37-45 015-125-00-6 glyphosine (ISO); N,N-bis(phosphonomethyl)glycine 219-468-4 2439-99-8 Xi; R41 Xi R: 41 S: (2-)26 015-126-00-1 heptenophos (ISO); 7-chlorobicyclo(3.2.0)hepta-2,6-dien-6-yl dimethyl phosphate 245-737-0 23560-59-0 T; R25 N; R50-53 T; N R: 25-50/53 S: (1/2-)23-28-37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-127-00-7 iprobenfos (ISO); S: (1/2-)23-28-37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-127-00-7 iprobenfos (ISO); S-benzyl diisopropyl phosphorothioate 247-449-0 26087-47-8 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-)61 015-128-00-2 IPSP; S-ethylsulphinylmethyl O,O-diisopropylphosphorodithioate — 5827-05-4 T+; R27 T; R25 N; R50-53 T+; N R: 25-27-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-129-00-8 isofenphos (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-129-00-8 isofenphos (ISO); O-ethyl O-2-isopropoxycarbonylphenyl-isopropylphosphoramidothioate 246-814-1 25311-71-1 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-130-00-3 isothioate (ISO) S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-130-00-3 isothioate (ISO) S-2-isopropylthioethyl O,O-dimethyl phosphorodithioate; — 36614-38-7 T; R24/25 T R: 24/25 S: (1/2-)28-36/37-45 015-131-00-9 isoxathion (ISO); O,O-diethyl O-5-phenylisoxazol-3-ylphosphorothioate 242-624-8 18854-01-8 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)28-36/37-45-60-61 015-132-00-4 S-(chlorophenylthiomethyl) O,O-dimethylphosphorodithioate; methylcarbophenothione — 953-17-3 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-133-00-X piperophos (ISO); S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-133-00-X piperophos (ISO); S-2-methylpiperidinocarbonylmethyl-O,O-dipropyl phosphorodithioate — 24151-93-7 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-134-00-5 pirimiphos-methyl (ISO); S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 015-134-00-5 pirimiphos-methyl (ISO); O-(2-diethylamino-6-methylpyrimidin-4-yl) O,O-dimethyl phosphorothioate 249-528-5 29232-93-7 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 015-135-00-0 profenofos (ISO); O-(4-bromo-2-chlorophenyl) O-ethyl S-propyl phosphorothioate 255-255-2 41198-08-7 Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)36/37-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-136-00-6 trans-isopropyl-3-[[(ethylamino)methoxyfosfinothioyl]oxy]crotonate; S: (2-)36/37-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-136-00-6 trans-isopropyl-3-[[(ethylamino)methoxyfosfinothioyl]oxy]crotonate; isopropyl 3-[[(ethylamino)methoxyphosphinothioyl]oxy]isocrotonate; propetamphos (ISO) 250-517-2 31218-83-4 T; R25 N; R50-53 T; N R: 25-50/53 S: (1/2-)37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-137-00-1 pyrazophos (ISO); S: (1/2-)37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-137-00-1 pyrazophos (ISO); O,O-diethyl O-(6-ethoxycarbonyl-5-methylpyrazolo[2,3-a]pyrimidin-2-yl) phosphorothioate 236-656-1 13457-18-6 Xn; R20/22 N; R50-53 Xn; N R: 20/22-50/53 S: (2-)36/37-46-60-61 015-138-00-7 quinalphos (ISO); O,O-diethyl-O-quinoxalin-2-yl phosphorothioate 237-031-6 13593-03-8 T; R25 Xn; R21 N; R50-53 T; N R: 21-25-50/53 S: (1/2-)22-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-139-00-2 terbufos (ISO) S: (1/2-)22-36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-139-00-2 terbufos (ISO) S-tert-butylthiomethyl O,O-diethylphosphorodithioate; 235-963-8 13071-79-9 T+; R27/28 N; R50-53 T+; N R: 27/28-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-140-00-8 triazophos (ISO); S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 015-140-00-8 triazophos (ISO); O,O-diethyl-O-1-phenyl-1H-1,2,4-triazol-3-yl phosphorothioate 245-986-5 24017-47-8 T; R23/25 Xn; R21 N; R50-53 T; N R: 21-23/25-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-141-00-3 ethylenediammonium O,O-bis(octyl) phosphorodithioate, mixed isomers 400-520-1 — C; R34 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 015-141-00-3 ethylenediammonium O,O-bis(octyl) phosphorodithioate, mixed isomers 400-520-1 — C; R34 Xn; R22 N; R50-53 C; N R: 22-34-50/53 … 39 unchanged lines … R43 N; R50-53 T+; N R: 24/25-26-43-48/20-50/53 S: (1/2-)28-36/37-38-45-59-61 015-154-00-4 2-chloroethylphosphonic acid; ethephon 240-718-3 16672-87-0 Xn; R20/21 C; R34 R52-53 C R: 20/21-34-52/53 S: (1/2-)26-28-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 015-155-00-X glufosinate ammonium (ISO); S: (1/2-)28-36/37-38-45-59-61 015-154-00-4 ethephon; 2-chloroethylphosphonic acid 240-718-3 16672-87-0 C; R34 Xn; R20/21/22 N; R51-53 C; N R: 20/21/22-34-51/53 S: (1/2-)26-36/37/39-45-61 Xi; R37: 5 % ≤ C < 10 % 015-155-00-X glufosinate ammonium (ISO); ammonium 2-amino-4-(hydroxymethylphosphinyl)butyrate 278-636-5 77182-82-2 Repr. Cat. 2; R60 Repr. Cat. 3; R63 Xn; R20/21/22-48/20/22 T … 118 unchanged lines … O, O-dimethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate 227-011-5 5598-13-0 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)36/37-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-187-00-4 reaction mass of: tetrasodium(((2-hydroxyethyl)imino)bis(methylene))bisphosphonate, N-oxide; S: (2-)36/37-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 015-187-00-4 reaction mass of: tetrasodium(((2-hydroxyethyl)imino)bis(methylene))bisphosphonate, N-oxide; trisodium ((tetrahydro-2-hydroxy-4H-1,4,2-oxazaphosphorin-4-yl)-methyl)phosphonate, N-oxide, P-oxide 417-540-1 — Xi; R41 N; R51-53 Xi; N R: 41-51/53 S: (2-)26-39-61 015-188-00-X (1-methylethylidene)di-4,1-phenylenetetraphenyl diphosphate 425-220-8 5945-33-5 R53 R: 53 S: 61 015-189-00-5 phenyl bis(2,4,6-trimethylbenzoyl)-phosphine oxide 423-340-5 162881-26-7 R43 R53 Xi R: 43-53 S: (2-)22-24-37-61 015-190-00-0 bis(2,4-dicumylphenyl) neopentyl diphosphite; 3,9-bis[2,4-bis(1-methyl-1-phenylethyl)phenoxy]-2,4,8,10-tetraoxa-3,9-diphosphaspiro[5.5]undecane 421-920-2 154862-43-8 R53 R: 53 S: 61 015-191-00-6 dodecyldiphenyl phosphate 431-760-5 27460-02-2 Xi; R38 R52-53 Xi R: 38-52/53 S: (2-)37-61 015-192-00-1 tetrakis(2,6-dimethylphenyl)-m-phenylene biphosphate 432-770-2 139189-30-3 R43 R53 Xi R: 43-53 S: (2-)24-37-61 015-193-00-7 triphenyl(phenylmethyl)phosphonium 1,1,2,2,3,3,4,4,4-nonafluoro-N-methyl-1-butanesulfonamide (1:1) 442-960-7 332350-93-3 T; R25 S: (2-)37-61 015-192-00-1 tetrakis(2,6-dimethylphenyl)-m-phenylene biphosphate 432-770-2 139189-30-3 R43 Xi R: 43 S: (2-)24-37 015-193-00-7 triphenyl(phenylmethyl)phosphonium 1,1,2,2,3,3,4,4,4-nonafluoro-N-methyl-1-butanesulfonamide (1:1) 442-960-7 332350-93-3 T; R25 Xi; R41 N; R50-53 T; N R: 25-41-50/53 … 70 unchanged lines … C; R34 N; R50 C; N R: 31-34-50 S: (1/2-)26-45-61 C; R34: C ≥ 5 % Xi; R36/38: 1 % ≤ C < 5 % R31: C ≥ 1 % 016-009-00-8 disodium sulfide; S: (1/2-)26-45-61 C; R34: C ≥ 5 % Xi; R36/38: 1 % ≤ C < 5 % R31: C ≥ 1 % 016-009-00-8 disodium sulfide; sodium sulfide 215-211-5 1313-82-2 T; R24 Xn; R22 C; R34 R31 N; R50 T; C; N R: 22-24-31-34-50 S: (1/2-)26-36/37/39-45-61 016-010-00-3 sodium polysulphides 215-686-9 1344-08-7 T; R25 R31 C; R34 N; R50 T; N R: 25-31-34-50 S: (1/2-)26-36/37/39-45-61 016-011-00-9 sulphur dioxide 231-195-2 7446-09-5 T; R23 C; R34 T R: 23-34 S: (1/2-)9-26-36/37/39-45 T; R23: C ≥ 20 % Xn; R20: 5 % ≤ C < 20 % 5 S: (1/2-)9-26-36/37/39-45 T; R23: C ≥ 20 % Xn; R20: 5 % ≤ C < 20 % 5 016-012-00-4 disulphur dichloride; sulfur monochloride 233-036-2 10025-67-9 R14 T; R25 Xn; R20 R29 C; R35 N; R50 T; C; N R: 14-20-25-29-35-50 S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 016-013-00-X sulphur dichloride 234-129-0 10545-99-0 R14 S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 016-013-00-X sulphur dichloride 234-129-0 10545-99-0 R14 C; R34 Xi; R37 N; R50 C; N R: 14-34-37-50 S: (1/2-)26-45-61 016-014-00-5 sulphur tetrachloride — 13451-08-6 R14 C; R34 N; R50 C; N R: 14-34-50 S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 016-015-00-0 thionyl dichloride; S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 016-015-00-0 thionyl dichloride; thionyl chloride 231-748-8 7719-09-7 R14 Xn; R20/22 R29 C; R35 C R: 14-20/22-29-35 S: (1/2-)26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 016-016-00-6 sulphuryl chloride 232-245-6 7791-25-5 R14 S: (1/2-)26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 016-016-00-6 sulphuryl chloride 232-245-6 7791-25-5 R14 C; R34 Xi; R37 C R: 14-34-37 S: (1/2-)26-45 016-017-00-1 chlorosulphonic acid 232-234-6 7790-94-5 R14 C; R35 Xi; R37 C R: 14-35-37 S: (1/2-)26-45 016-018-00-7 fluorosulphonic acid 232-149-4 7789-21-1 Xn; R20 C; R35 C R: 20-35 S: (1/2-)26-45 016-019-00-2 oleum ... % SO3 — — R14 S: (1/2-)26-45 016-019-00-2 oleum ... % SO3 — — R14 C; R35 Xi; R37 C R: 14-35-37 S: (1/2-)26-30-45 B 016-020-00-8 sulphuric acid ... % 231-639-5 7664-93-9 C; R35 C 016-020-00-8 sulphuric acid ... % 231-639-5 7664-93-9 C; R35 C R: 35 S: (1/2-)26-30-45 C; R35: C ≥ 15 % Xi; R36/38: 5 % ≤ C < 15 % B S: (1/2-)26-30-45 C; R35: C ≥ 15 % Xi; R36/38: 5 % ≤ C < 15 % B 016-021-00-3 methanethiol; methyl mercaptan 200-822-1 74-93-1 F+; R12 T; R23 N; R50-53 F+; T; N R: 12-23-50/53 S: (2-)16-25-60-61 016-022-00-9 ethanethiol; ethyl mercaptan 200-837-3 75-08-1 F; R11 Xn; R20 N; R50-53 F; Xn; N R: 11-20-50/53 S: (2-)16-25-60-61 016-023-00-4 dimethyl sulphate 201-058-1 77-78-1 Carc. Cat. 2; R45 Muta. Cat. 3; R68 T+; R26 T; R25 C; R34 R43 T+ R: 45-25-26-34-43-68 S: 53-45 Car. Cat. 2; R45: C ≥ 0,01 % Muta. Cat. 3, R68: C ≥ 0,01 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E S: 53-45 Car. Cat. 2; R45: C ≥ 0,01 % Muta. Cat. 3, R68: C ≥ 0,01 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E 016-024-00-X dimexano (ISO); bis(methoxythiocarbonyl) disulphide 215-993-8 1468-37-7 Xn; R22 N; R50-53 Xn; N … 19 unchanged lines … R31 Xn; R22 Xn R: 7-22-31 S: (2-)7/8-26-28-43 016-029-00-7 p-toluenesulphonic acid, containing more than 5 % H2SO4 — — C; R34 C S: (2-)7/8-26-28-43 016-029-00-7 p-toluenesulphonic acid, containing more than 5 % H2SO4 — — C; R34 C R: 34 S: (1/2-)26-37/39-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % 016-030-00-2 p-toluenesulphonic acid (containing a maximum of 5 % H2SO4) 203-180-0 104-15-4 Xi; R36/37/38 Xi S: (1/2-)26-37/39-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % 016-030-00-2 p-toluenesulphonic acid (containing a maximum of 5 % H2SO4) 203-180-0 104-15-4 Xi; R36/37/38 Xi R: 36/37/38 S: (2-)26-37 016-031-00-8 tetrahydrothiophene-1,1-dioxide; sulpholane 204-783-1 126-33-0 Xn; R22 Xn R: 22 S: (2-)25 016-032-00-3 1,3-propanesultone; 1,2-oxathiolane 2,2-dioxide 214-317-9 1120-71-4 Carc. Cat. 2; R45 Xn; R21/22 T R: 45-21/22 S: 53-45 Carc. Cat. 2; R45: C ≥ 0,01 % E S: 53-45 Carc. Cat. 2; R45: C ≥ 0,01 % E 016-033-00-9 dimethylsulfamoylchloride 236-412-4 13360-57-1 Carc. Cat. 2; R45 T+; R26 Xn; R21/22 … 55 unchanged lines … Xi; R36/37 R43 T R: 22-23-36/37-43-48/23 S: (1/2-)22-24-36-45 016-055-00-9 tetrasodium 4-amino-3,6-bis(5-(6-chloro-4-(2-hydroxyethylamino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxynaphthalene-2,7-sulfonate (containing > 35 % sodium chloride and sodium acetate) 400-510-7 — Xi; R41 S: (1/2-)22-24-36-45 016-055-00-9 tetrasodium 4-amino-3,6-bis(5-(6-chloro-4-(2-hydroxyethylamino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxynaphthalene-2,7-sulfonate (containing > 35 % sodium chloride and sodium acetate) 400-510-7 — Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 016-056-00-4 potassium hydrogensulphate 231-594-1 7646-93-7 C; R34 … 31 unchanged lines … Xi; R41 R31 Xn R: 22-31-41 S: (2-)26-39-46 016-064-00-8 sodium hydrogensulphite … %; sodium bisulphite … % 231-548-0 7631-90-5 Xn; R22 S: (2-)26-39-46 016-064-00-8 sodium hydrogensulphite … %; sodium bisulphite … % 231-548-0 7631-90-5 Xn; R22 R31 Xn R: 22-31 S: (2-)25-46 B 016-065-00-3 sodium 1-amino-4-[2-methyl-5-(4-methylphenylsulfonylamino)phenylamino]anthraquinone-2-sulfonate 400-100-8 84057-97-6 N; R51-53 N R: 51/53 S: 61 016-066-00-9 tetrasodium [5-((4-amino-6-chloro-1,3,5-triazin-2-yl)amino)-2-((2-hydroxy-3,5-disulfonatophenylazo)-2- sulfonatobenzylidenehydrazino)benzoate]copper(II) 404-070-7 116912-62-0 R52-53 R: 52/53 S: 61 016-067-00-4 (4-methylphenyl)mesitylene sulfonate 407-530-5 67811-06-7 R53 R: 53 S: 61 016-068-00-X sodium 3,5-bis(tetradecyloxycarbonyl)benzenesulfinate 407-720-8 155160-86-4 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 016-069-00-5 3,5-bis-(tetradecyloxycarbonyl)benzenesulfinic acid 407-990-7 141915-64-2 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 016-070-00-0 4-benzyloxy-4'-(2,3-epoxy-2-methylprop-1-yloxy)diphenylsulfone 408-220-2 — R53 R: 53 S: 61 016-071-00-6 trisodium 3-amino-6,13-dichloro-10-((3-((4-chloro-6-(2-sulfophenylamino)-1,3,5-triazin-2-yl)amino)propyl) amino)-4,11-triphenoxydioxazinedisulfonate 410-130-3 136248-03-8 R43 Xi R: - 43 R: - 43 S: (2-)22-24-37 016-072-00-1 3-amino-4-hydroxy-N-(2-methoxyethyl)-benzenesulfonamide 411-520-6 112195-27-4 Xi; R41 R43 N; R51-53 Xi; N … 38 unchanged lines … 1-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenylsulfonyl]urea — 94125-34-5 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 016-085-00-2 flazasulfuron (ISO); S: (2-)60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 016-085-00-2 flazasulfuron (ISO); 1-(4,6-dimethoxypyrimidin-2-yl)-3-(3-trifluoromethyl-2-pyridylsulfonyl)urea — 104040-78-0 N; R50-53 N R: 50/53 S: 60-61 016-086-00-8 tetrasodium 10-amino-6,13-dichloro-3-(3-(4-(2,5-disulfonatoanilino)-6-fluoro-1,3,5-triazin-2-ylamino)prop-3-ylamino)-5,12-dioxa-7,14-diazapentacene-4,11-disulfonate 402-590-9 109125-56-6 Xi; R41 Xi … 45 unchanged lines … Xi; R36/37/38 N; R50 O; T; N R: 8-23-36/37/38-50 S: (1/2-)9-45-61 N; R50: C ≥ 0,25 % 017-002-00-2 hydrogen chloride 231-595-7 7647-01-0 T; R23 S: (1/2-)9-45-61 N; R50: C ≥ 0,25 % 017-002-00-2 hydrogen chloride 231-595-7 7647-01-0 T; R23 C; R35 T; C R: 23-35 S: (1/2-)9-26-36/37/39-45 5 017-002-01-X hydrochloric acid ... % 231-595-7 — C; R34 017-002-01-X hydrochloric acid ... % 231-595-7 — C; R34 Xi; R37 C R: 34-37 S: (1/2-)26-45 C; R34-37: C ≥ 25 % Xi; R36/37/38: 10 % ≤ C < 25 % B S: (1/2-)26-45 C; R34-37: C ≥ 25 % Xi; R36/37/38: 10 % ≤ C < 25 % B 017-003-00-8 barium chlorate 236-760-7 13477-00-4 O; R9 Xn; R20/22 N; R51-53 O; Xn; N R: 9-20/22-51/53 S: (2-)13-27-61 017-004-00-3 potassium chlorate 223-289-7 3811-04-9 O; R9 Xn; R20/22 N; R51-53 O; Xn; N R: 9-20/22-51/53 S: (2-)13-16-27-61 017-005-00-9 sodium chlorate 231-887-4 7775-09-9 O; R9 Xn; R22 N; R51-53 O; Xn; N R: 9-22-51/53 S: (2-)13-17-46-61 017-006-00-4 perchloric acid ... % 231-512-4 7601-90-3 R5 S: (2-)13-17-46-61 017-006-00-4 perchloric acid ... % 231-512-4 7601-90-3 R5 O; R8 C; R35 O; C R: 5-8-35 S: (1/2-)23-26-36-45 C; R35: C ≥ 50 % C; R34: 10 % ≤ C < 50 % Xi; R36/38: 1 % ≤ C < 10 % S: (1/2-)23-26-36-45 C; R35: C ≥ 50 % C; R34: 10 % ≤ C < 50 % Xi; R36/38: 1 % ≤ C < 10 % Footnote O; R5-8: C > 50 % B O; R5-8: C > 50 % B 017-007-00-X barium perchlorate 236-710-4 13465-95-7 O; R9 Xn; R20/22 O; Xn R: 9-20/22 S: (2-)27 017-008-00-5 potassium perchlorate 231-912-9 7778-74-7 O; R9 Xn; R22 O; Xn R: 9-22 S: (2-)13-22-27 017-009-00-0 ammonium perchlorate; [containing ≥ 80 % of 0-30 μm particles] 232-235-1 7790-98-9 E; R3 [containing ≥ 80 % of 0-30 μm particles] 232-235-1 7790-98-9 E; R3 O; R9 E R: 3-9 S: (2-)14-16-36/37 T 017-009-01-8 ammonium perchlorate; [containing < 80 % of 0-30 μm particles] 232-235-1 7790-98-9 E; R2 [containing < 80 % of 0-30 μm particles] 232-235-1 7790-98-9 E; R2 O; R9 E R: 2-9 S: (2-)14-16-36/37 T 017-010-00-6 sodium perchlorate 231-511-9 7601-89-0 O; R9 Xn; R22 O; Xn R: 9-22 S: (2-)13-22-27 017-011-00-1 sodium hypochlorite, solution ... % Cl active 231-668-3 7681-52-9 C; R34 S: (2-)13-22-27 017-011-00-1 sodium hypochlorite, solution ... % Cl active 231-668-3 7681-52-9 C; R34 R31 N; R50 C; N R: 31-34-50 S: (1/2-)28-45-50-61 R31: C ≥ 5 % B S: (1/2-)28-45-50-61 R31: C ≥ 5 % B 017-012-00-7 calcium hypochlorite 231-908-7 7778-54-3 O; R8 C; R34 Xn; R22 R31 N; R50 O; C; N R: 8-22-31-34-50 S: (1/2-)26-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R37/38-41: 3 % ≤ C < 10 % Xi; R36: 0,5 % ≤ C < 3 % N; R50: C ≥ 2,5 % 017-013-00-2 calcium chloride 233-140-8 10043-52-4 Xi; R36 Xi S: (1/2-)26-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R37/38-41: 3 % ≤ C < 10 % Xi; R36: 0,5 % ≤ C < 3 % N; R50: C ≥ 2,5 % 017-013-00-2 calcium chloride 233-140-8 10043-52-4 Xi; R36 Xi R: 36 S: (2-)22-24 017-014-00-8 ammonium chloride 235-186-4 12125-02-9 Xn; R22 Xi; R36 Xn … 31 unchanged lines … C; R34 N; R50 O; T+; N R: 6-8-26-34-50 S: (1/2-)23-26-28-36/37/39-38-45-61 N; R50: C ≥ 2,5 % 5 S: (1/2-)23-26-28-36/37/39-38-45-61 N; R50: C ≥ 2,5 % 5 017-026-01-0 chlorine dioxide … % 233-162-8 10049-04-4 T; R25 C; R34 N; R50 T; N R: 25-34-50 S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R37/38: 3 % ≤ C < 10 % Xi; R36: 0,3 % ≤ C < 10 % N; R50: C ≥ 2,5 % B S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 10 % Xi; R37/38: 3 % ≤ C < 10 % Xi; R36: 0,3 % ≤ C < 10 % N; R50: C ≥ 2,5 % B 019-001-00-2 potassium 231-119-8 7440-09-7 F; R15 R14 C; R34 F; C R: 14/15-34 S: (1/2-)5-8-45 019-002-00-8 potassium hydroxide; caustic potash 215-181-3 1310-58-3 Xn; R22 C; R35 C R: 22-35 S: (1/2-)26-36/37/39-45 C; R35: C ≥ 5 % C; R34: 2 % ≤ C < 5 % Xi; R36/38: 0.5 % ≤ C < 2 % 020-001-00-X calcium 231-179-5 7440-70-2 F; R15 F S: (1/2-)26-36/37/39-45 C; R35: C ≥ 5 % C; R34: 2 % ≤ C < 5 % Xi; R36/38: 0.5 % ≤ C < 2 % 020-001-00-X calcium 231-179-5 7440-70-2 F; R15 F R: 15 S: (2-)8-24/25-43 020-002-00-5 calcium cyanide 209-740-0 592-01-8 T+; R28 R32 … 39 unchanged lines … R42/43 N; R50-53 O; T+; N R: 45-46-9-24/25-26-35-42/43-48/23-62-50/53 S: 53-45-60-61 C: R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % E S: 53-45-60-61 C: R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % E 024-002-00-6 potassium dichromate 231-906-6 7778-50-9 O; R8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23 Xn; R21 C; R34 R42/43 N; R50-53 T+; N; O R: 45-46-60-61-8-21-25-26-34-42/43-48/23-50/53 S: 53-45-60-61 C; R34: C ≥ 10 %: Xi; R36/37/38: 5 % ≤ C < 10 % E3 S: 53-45-60-61 C; R34: C ≥ 10 %: Xi; R36/37/38: 5 % ≤ C < 10 % E3 024-003-00-1 ammonium dichromate 232-143-1 7789-09-5 E; R2 O; R8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23 Xn; R21 C; R34 R42/43 N; R50-53 E; T+; N R: 45-46-60-61-2-8-21-25-26-34-42/43-48/23-50/53 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E3 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E3 024-004-00-7 sodium dichromate 234-190-3 10588-01-9 O; R8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23 Xn; R21 C; R34 R42/43 N; R50-53 O; T+; N R: 45-46-60-61-8-21-25-26-34-42/43-48/23-50/53 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E 3 024-004-01-4 sodium dichromate, dihydrate 234-190-3 7789-12-0 O; R8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23 Xn; R21 C; R34 R42/43 N; R50-53 T+; N; O R: 45-46-60-61-8-21-25-26-34-42/43-48/23-50/53 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E3 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % R42/43: C ≥ 0,2 % E3 024-005-00-2 chromyl dichloride; chromic oxychloride 239-056-8 14977-61-8 O; R8 Carc. Cat. 2; R49 Muta. Cat. 2; R46 C; R35 R43 N; R50-53 O; T; C; N R: 49-46-8-35-43-50/53 S: 53-45-60-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 0,5 % ≤ C < 5 % R43: C ≥ 0,5 % 3 S: 53-45-60-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 0,5 % ≤ C < 5 % R43: C ≥ 0,5 % 3 024-006-00-8 potassium chromate 232-140-5 7789-00-6 Carc. Cat. 2; R49 Muta. Cat. 2; R46 Xi; R36/37/38 R43 N; R50-53 T; N R: 49-46-36/37/38-43-50/53 S: 53-45-60-61 R43: C ≥ 0,5 % 3 S: 53-45-60-61 R43: C ≥ 0,5 % 3 024-007-00-3 zinc chromates including zinc potassium chromate — — Carc. Cat. 1; R45 Xn; R22 R43 … 51 unchanged lines … R42/43 N; R50-53 T+; N R: 45-46-60-61-21-25-26-34-42/43-48/23-50/53 S: 53-45-60-61 R42/43: C ≥ 0,2 % E3 S: 53-45-60-61 R42/43: C ≥ 0,2 % E3 024-019-00-9 Main component: acetoacetic acid anilide/3-amino-1-hydroxybenzene (ATAN-MAP): trisodium {6-[(2 or 3 or 4)-amino-(4 or 5 or 6)-hydroxyphenylazo]-5'-(phenylsulfamoyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato}-{6''-[1-(phenylcarbamoyl)ethylazo]-5'''-(phenylsulfamoyl)-3''-sulfonatonaphthalene-2''-azobenzene-1'',2'''-diolato}chromate (III); by-product 1: acetoacetic acid anilide/acetoacetic acid anilide (ATAN-ATAN): trisodium bis{6-[1-(phenylcarbamoyl)ethylazo]-5'-(phenylsulfonyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato}chromate (III); by-product 2: 3-amino-1-hydroxybenzene/3-amino-1-hydroxybenzene (MAP-MAP): trisodium bis{6-[(2 or 3 or 4)-amino-(4 or 5 or 6)-hydroxyphenylazo]-5'-(phenylsulfamoyl)-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato} chromate (III) 419-230-1 — R43 … 34 unchanged lines … ferrous sulfate heptahydrate 231-753-5 7782-63-0 Xn; R22 Xi; R36/38 Xn R: 22-36/38 S: (2-)46 Xi; R38: C ≥ 25 % 026-004-00-2 potassium ferrite 430-010-4 12160-44-0 C; R34 S: (2-)46 Xi; R38: C ≥ 25 % 026-004-00-2 potassium ferrite 430-010-4 12160-44-0 C; R34 R43 C R: 34-43 S: (1/2-)22-26-36/37/39-40-45 027-001-00-9 cobalt 231-158-0 7440-48-4 R42/43 R53 Xn R: 42/43-53 S: (2-)22-24-37-61 027-002-00-4 cobalt oxide 215-154-6 1307-96-6 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 027-003-00-X cobalt sulfide 215-273-3 1317-42-6 R43 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 027-003-00-X cobalt sulfide 215-273-3 1317-42-6 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 027-004-00-5 cobalt dichloride 231-589-4 7646-79-9 Carc. Cat. 2; R49 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 027-004-00-5 cobalt dichloride 231-589-4 7646-79-9 Carc. Cat. 2; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R60 Xn; R22 R42/43 N; R50-53 T; N R: 49-60-22-42/43-68-50/53 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E1 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E1 027-005-00-0 cobalt sulfate 233-334-2 10124-43-3 Carc. Cat. 2; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R60 Xn; R22 R42/43 N; R50-53 T; N R: 49-60-22-42/43-68-50/53 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E1 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E1 027-006-00-6 cobalt di(acetate) 200-755-8 71-48-7 Carc. Cat. 2; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R60 R42/43 N; R50-53 T; N R: 49-60-42/43-68-50/53 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 027-007-00-1 zinc hexacyanocobaltate(III), tertiary butyl alcohol/polypropylene glycol complex 425-240-7 - Xi; R41 N; R51-53 Xi; N R: 41-51/53 S: (2-)22-26-39-61 027-008-00-7 complex of cobalt(III)-bis(N-phenyl-4-(5-ethylsulfonyl-2-hydroxyphenylazo)-3-hydroxynaphthylamide), hydrated (n H2O, 2<n<3) 427-390-9 - R43 Xi R: 43 S: (2-)24-37 027-009-00-2 cobalt dinitrate 233-402-1 10141-05-6 Carc. Cat. 2; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R60 R42/43 N; R50-53 T; N R: 49-60-42/43-68-50/53 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 027-010-00-8 cobalt carbonate 208-169-4 513-79-1 Carc. Cat. 2; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R60 R42/43 N; R50-53 T; N R: 49-60-42/43-68-50/53 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 S: 53-45-60-61 Carc. Cat. 2; R49: C ≥ 0,01 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 1 028-001-00-1 tetracarbonylnickel; nickel tetracarbonyl 236-669-2 13463-39-3 F; R11 Carc. Cat. 3; R40 Repr. Cat. 2; R61 T+; R26 N; R50-53 F; T+; N R: 61-11-26-40-50/53 S: 53-45-60-61 E 028-002-00-7 nickel 231-111-4 7440-02-0 Carc. Cat. 3; R40 T; R48/23 R43 T R: 40-43-48/23 S: (2-)36/37/39-45 S7 028-002-01-4 nickel powder; [particle diameter < 1 mm] 231-111-4 7440-02-0 Carc. Cat. 3; R40 [particle diameter < 1 mm] 231-111-4 7440-02-0 Carc. Cat. 3; R40 T; R48/23 R43 R52-53 T … 68 unchanged lines … R42/43 N; R50-53 T; N R: 49-61-20/22-38-42/43-48/23-68-50/53 S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E 028-010-00-0 nickel carbonate; basic nickel carbonate; carbonic acid, nickel (2+) salt; [1] … 23 unchanged lines … R42/43 N; R50-53 T; N R: 49-61-23/25-38-42/43-48/23-68-50/53 S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E 028-012-00-1 nickel dinitrate; [1] nitric acid, nickel salt [2] 236-068-5 [1] 238-076-4 [2] 13138-45-9 [1] 14216-75-2 [2] O; R8 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 Xn; R20/22 Xi; R38-41 R42/43 N; R50-53 O; T; N R: 49-61-8-20/22-38-41-42/43-48/23-68-50/53 S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E S: 53-45-60-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % Xi; R38: C ≥ 20 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E 028-013-00-7 nickel matte 273-749-6 69012-50-6 Carc. Cat. 1; R49 T; R48/23 R43 N; R50-53 T; N R: 49-43-48/23-50/53 S: 53-45-60-61 E H 028-014-00-2 slimes and sludges, copper electrolytic refining, decopperised, nickel sulfate 295-859-3 92129-57-2 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 Xn; R20/22 Xi; R38 R42/43 N; R50-53 T; N R: 49-61-20/22-38-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E S: 53-45-60-61 T R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E 028-015-00-8 slimes and sludges, copper electrolyte refining, decopperised 305-433-1 94551-87-8 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 1; R61 Repr. Cat. 3; R62 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-62-68-50/53 S: 53-45-60-61 E H 028-016-00-3 nickel diperchlorate; perchloric acid, nickel(II) salt 237-124-1 13637-71-3 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 C; R34 R42/43 N; R50-53 T; N R: 49-61-34-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % C; R34: C ≥ 5 %: Xi; R36/38: 1 % ≤ C < 5 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 % Xn; R48/20: 0,1 % ≤ C < 1 % C; R34: C ≥ 5 %: Xi; R36/38: 1 % ≤ C < 5 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-017-00-9 nickel dipotassium bis(sulfate); [1] diammonium nickel bis(sulfate) [2] 237-563-9 [1] 239-793-2 [2] 13842-46-1 [1] 15699-18-0 [2] Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 Xn; R20/22 R42/43 N; R50-53 T; N R: 49-61-20/22-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53:2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53:2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-018-00-4 nickel bis(sulfamidate); nickel sulfamate 237-396-1 13770-89-3 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-019-00-X nickel bis(tetrafluoroborate) 238-753-4 14708-14-6 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-021-00-0 nickel diformate; [1] formic acid, nickel salt; [2] formic acid, copper nickel salt [3] 222-101-0 [1] 239-946-6 [2] 268-755-0 [3] 3349-06-2 [1] 15843-02-4 [2] 68134-59-8 [3] Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-022-00-6 nickel di(acetate); [1] nickel acetate [2] 206-761-7 [1] 239-086-1 [2] 373-02-4 [1] 14998-37-9 [2] Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 Xn; R20/22 R42/43 N; R50-53 T; N R: 49-61-20/22-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-024-00-7 nickel dibenzoate 209-046-8 553-71-9 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-025-00-2 nickel bis(4-cyclohexylbutyrate) 223-463-2 3906-55-6 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 028-026-00-8 nickel(II) stearate; S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 028-026-00-8 nickel(II) stearate; nickel(II) octadecanoate 218-744-1 2223-95-2 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E U S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E U 028-027-00-3 nickel dilactate - 16039-61-5 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-028-00-9 nickel(II) octanoate 225-656-7 4995-91-9 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat 2; R61 T; R48/23 C; R35 R42/43 N; R50-53 T; C; N R: 49-61-35-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-029-00-4 nickel difluoride; [1] nickel dibromide; [2] nickel diiodide; [3] nickel potassium fluoride [4] 233-071-3 [1] 236-665-0 [2] 236-666-6 [3] - [4] 10028-18-9 [1] 13462-88-9 [2] 13462-90-3 [3] 11132-10-8 [4] Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-030-00-X nickel hexafluorosilicate 247-430-7 26043-11-8 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-031-00-5 nickel selenate 239-125-2 15060-62-5 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-032-00-0 nickel hydrogen phosphate; [1] nickel bis(dihydrogen phosphate); [2] trinickel bis(orthophosphate); [3] … 130 unchanged lines … R32 N; R50-53 T; N R: 49-61-32-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-047-00-2 nickel dichromate 239-646-5 15586-38-6 Carc. Cat. 1; R49 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T; R48/23 R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-048-00-8 nickel(II) selenite 233-263-7 10101-96-9 Carc. Cat. 1; R49 T; R48/23 R42/43 … 43 unchanged lines … R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-054-00-0 nickel(II) trifluoroacetate; [1] nickel(II) propionate; [2] nickel bis(benzenesulfonate); [3] … 23 unchanged lines … (isodecanoato-O)(isononanoato-O)nickel; [27] (isononanoato-O)(neodecanoato-O)nickel; [28] fatty acids, C6-19-branched, nickel salts; [29] fatty acids, C8-18 and C18-unsaturated, nickel salts; [30] fatty acids, C8-18 and C18-unsaturated, nickel salts; [30] 2,7-naphthalenedisulfonic acid, nickel(II) salt; [31] 240-235-8 [1] 222-102-6 [2] 254-642-3 [3] … 61 unchanged lines … R42/43 N; R50-53 T; N R: 49-61-42/43-48/23-68-50/53 S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H S: 53-45-60-61 T R48/23: C ≥ 1 %: Xn; R48/20: 0,1 % ≤ C < 1 % R43: C ≥ 0,01 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % E H 028-055-00-6 nickel(II) sulfite; [1] nickel tellurium trioxide; [2] nickel tellurium tetraoxide; [3] … 130 unchanged lines … Xn; R22 N; R50-53 C; N R: 22-34-50/53 S: (1/2-)26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 030-004-00-8 dimethylzinc; [1] S: (1/2-)26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 030-004-00-8 dimethylzinc; [1] diethylzinc [2] 208-884-1 [1] 209-161-3 [2] 544-97-8 [1] 557-20-0 [2] F; R17 … 42 unchanged lines … S: (1/2-)20/21-28-45-60-61 033-002-00-5 arsenic compounds, with the exception of those specified elsewhere in this Annex — — T; R23/25 N; R50-53 T; N R: 23/25-50/53 S: (1/2-)20/21-28-45-60-61 T; R23/25: C ≥ 0,2 % Xn; R20/22: 0,1 % ≤ C < 0,2 % A1 S: (1/2-)20/21-28-45-60-61 T; R23/25: C ≥ 0,2 % Xn; R20/22: 0,1 % ≤ C < 0,2 % A1 033-003-00-0 diarsenic trioxide; arsenic trioxide 215-481-4 1327-53-3 Carc. Cat. 1; R45 T+; R28 … 43 unchanged lines … S: (1/2-)7/9-26-45-61 035-002-00-0 hydrogen bromide 233-113-0 10035-10-6 C; R35 Xi; R37 C R: 35-37 S: (1/2-)7/9-26-45 035-002-01-8 hydrobromic acid ... % — — C; R34 S: (1/2-)7/9-26-45 035-002-01-8 hydrobromic acid ... % — — C; R34 Xi; R37 C R: 34-37 S: (1/2-)7/9-26-45 C; R34: C ≥ 40 % Xi; R36/38: 10 % ≤ C < 40 % Xi; R37: C ≥ 10 % B S: (1/2-)7/9-26-45 C; R34: C ≥ 40 % Xi; R36/38: 10 % ≤ C < 40 % Xi; R37: C ≥ 10 % B 035-003-00-6 potassium bromate 231-829-8 7758-01-2 O; R9 Carc. Cat. 2; R45 T; R25 T; O R: 45-9-25 S: 53-45 E 035-004-00-1 2-hydroxyethylammonium perbromide 407-440-6 — O; R8 Xn; R22 C; R35 R43 N; R50 O; C; N R: 8-22-35-43-50 S: (1/2-)3/7-14-26-36/37/39-45-60-61 040-001-00-3 zirconium powder (pyrophoric) 231-176-9 7440-67-7 F; R15-17 F R: 15-17 S: (2-)7/8-43 040-002-00-9 zirconium powder (non pyrophoric) — — F; R15 F R: 15 S: (2-)7/8-43 040-003-00-4 reaction product of 3,5-di-tert-butylsalicylic acid and zirconium oxychloride, dehydrated, basic Zr: DTBS = 1,0: 1,0 to 1,0: 1,5 430-610-6 226996-19-6 N; R50-53 N S: (2-)7/8-43 040-003-00-4 reaction product of 3,5-di-tert-butylsalicylic acid and zirconium oxychloride, dehydrated, basic Zr: DTBS = 1,0: 1,0 to 1,0: 1,5 430-610-6 226996-19-6 N; R50-53 N R: 50/53 S: 60-61 042-001-00-9 molybdenum trioxide 215-204-7 1313-27-5 Carc. Cat. 3; R40 Xi; R36/37 Xn … 28 unchanged lines … S: 60-61 048-001-00-5 cadmium compounds, with the exception of cadmium sulphoselenide (xCdS.yCdSe), reaction mass of cadmium sulphide with zinc sulphide (xCdS.yZnS), reaction mass of cadmium sulphide with mercury sulphide (xCdS.yHgS), and those specified elsewhere in this Annex — — Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)60-61 Xn; R20/21/22: C ≥ 0,1 % A1 S: (2-)60-61 Xn; R20/21/22: C ≥ 0,1 % A1 048-002-00-0 cadmium (non-pyrophoric); [1] cadmium oxide (non-pyrophoric) [2] 231-152-8 [1] 215-146-2 [2] 7440-43-9 [1] 1306-19-0 [2] Carc. Cat. 2; R45 Muta. Cat. 3; R68 Repr. Cat. 3; R62-63 T+; R26 T; R48/23/25 N; R50-53 T+; N R: 45-26-48/23/25-62-63-68-50/53 S: 53-45-60-61 E 048-003-00-6 cadmium diformate; cadmiumformate 224-729-0 4464-23-7 T; R23/25 R33 Xn; R68 N; R50-53 T; N R: 23/25-33-68-50/53 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,25 % ≤ C < 10 % R33: C ≥ 0,25 % 048-004-00-1 cadmium cyanide 208-829-1 542-83-6 T+; R26/27/28 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,25 % ≤ C < 10 % R33: C ≥ 0,25 % 048-004-00-1 cadmium cyanide 208-829-1 542-83-6 T+; R26/27/28 R32 R33 Xn; R68 N; R50-53 T+; N R: 26/27/28-32-33-68-50/53 S: (1/2-)7-28-29-45-60-61 R32: C ≥ 1 % R33: C ≥ 0,1 % 048-005-00-7 cadmiumhexafluorosilicate(2-); S: (1/2-)7-28-29-45-60-61 R32: C ≥ 1 % R33: C ≥ 0,1 % 048-005-00-7 cadmiumhexafluorosilicate(2-); cadmium fluorosilica 241-084-0 17010-21-8 T; R23/25 R33 Xn; R68 N; R50-53 T; N R: 23/25-33-68-50/53 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,1 % ≤ C < 10 % R33: C ≥ 0,1 % 048-006-00-2 cadmium fluoride 232-222-0 7790-79-6 Carc. Cat. 2; R45 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,1 % ≤ C < 10 % R33: C ≥ 0,1 % 048-006-00-2 cadmium fluoride 232-222-0 7790-79-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23/25 N; R50-53 T+; N R: 45-46-60-61-25-26-48/23/25-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E 048-007-00-8 cadmium iodide 232-223-6 7790-80-9 T; R23/25 R33 Xn; R68 N; R50-53 T; N R: 23/25-33-68-50/53 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,1 % ≤ C < 10 % R33: C ≥ 0,1 % 048-008-00-3 cadmium chloride 233-296-7 10108-64-2 Carc. Cat. 2; R45 S: (1/2-)22-45-60-61 T; R23/25: C ≥ 10 % Xn; R20/22: 0,1 % ≤ C < 10 % R33: C ≥ 0,1 % 048-008-00-3 cadmium chloride 233-296-7 10108-64-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23/25 N; R50-53 T+; N R: 45-46-60-61-25-26-48/23/25-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E 048-009-00-9 cadmium sulphate 233-331-6 10124-36-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Repr. Cat. 2; R60-61 T+; R26 T; R25-48/23/25 N; R50-53 T+; N R: 45-46-60-61-25-26-48/23/25-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % T; R25: C ≥ 10 % Xn; R22: 0,1 % ≤ C < 10 % T; R48/23/25: C ≥ 7 % Xn; R48/20/22: 0,1 % ≤ C < 7 % E 048-010-00-4 cadmium sulphide 215-147-8 1306-23-6 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Repr. Cat. 3; R62-63 T; R48/23/25 Xn; R22 R53 T; R: 45-22-48/23/25-62-63-68-53 S: 53-45-61 Xn; R22: C ≥ 10 % T; R48/23/25: C ≥ 10 % Xn; R48/20/22: 0,1 % ≤ C < 10 % E1 S: 53-45-61 Xn; R22: C ≥ 10 % T; R48/23/25: C ≥ 10 % Xn; R48/20/22: 0,1 % ≤ C < 10 % E1 048-011-00-X cadmium (pyrophoric) 231-152-8 7440-43-9 F; R17 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Repr. Cat. 3; R62-63 T+; R26 T; R48/23/25 N; R50-53 F; T+; N R: 45-17-26-48/23/25-62-63-68-50/53 S: 53-45-7/8-43-60-61 E 050-001-00-5 tin tetrachloride; stannic chloride 231-588-9 7646-78-8 C; R34 R52-53 C R: 34-52/53 S: (1/2-)7/8-26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 050-002-00-0 cyhexatin (ISO); S: (1/2-)7/8-26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 050-002-00-0 cyhexatin (ISO); hydroxytricyclohexylstannane; tri(cyclohexyl)tin hydroxide 236-049-1 13121-70-5 Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)13-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 050-003-00-6 fentin acetate (ISO); S: (2-)13-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 050-003-00-6 fentin acetate (ISO); triphenyltin acetate 212-984-0 900-95-8 Carc. Cat. 3; R40 Repr. Cat. 3; R63 T+; R26 T; R24/25-48/23 Xi; R37/38-41 N; R50-53 T+; N R: 24/25-26-37/38-40-41-48/23-63-50/53 S: (1/2-)26-28-36/37/39-45-60-61 Xi; R37: C ≥ 20 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-004-00-1 fentin hydroxide (ISO); S: (1/2-)26-28-36/37/39-45-60-61 Xi; R37: C ≥ 20 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-004-00-1 fentin hydroxide (ISO); triphenyltin hydroxide 200-990-6 76-87-9 Carc. Cat. 3; R40 Repr. Cat. 3; R63 T+; R26 T; R24/25-48/23 Xi; R37/38-41 N; R50-53 T+; N R: 24/25-26-37/38-40-41-48/23-63-50/53 S: (1/2-)26-28-36/37/39-45-60-61 Xi; R37: C ≥ 20 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-005-00-7 trimethyltin compounds, with the exception of those specified elsewhere in this Annex — — T+; R26/27/28 S: (1/2-)26-28-36/37/39-45-60-61 Xi; R37: C ≥ 20 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-005-00-7 trimethyltin compounds, with the exception of those specified elsewhere in this Annex — — T+; R26/27/28 N; R50-53 T+; N R: 26/27/28-50/53 S: (1/2-)26-27-28-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % A1 S: (1/2-)26-27-28-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % A1 050-006-00-2 triethyltin compounds, with the exception of those specified elsewhere in this Annex — — T+; R26/27/28 N; R50-53 T+; N R: 26/27/28-50/53 S: (1/2-)26-27-28-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % A1 S: (1/2-)26-27-28-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % A1 050-007-00-8 tripropyltin compounds, with the exception of those specified elsewhere in this Annex — — T; R23/24/25 N; R50-53 T; N R: 23/24/25-50/53 S: (1/2-)26-27-28-45-60-61 T; R23/24/25: C ≥ 0,5 % Xn; R20/21/22: 0,1 % ≤ C < 0,5 % A1 S: (1/2-)26-27-28-45-60-61 T; R23/24/25: C ≥ 0,5 % Xn; R20/21/22: 0,1 % ≤ C < 0,5 % A1 050-008-00-3 tributyltin compounds, with the exception of those specified elsewhere in this Annex — — T; R25-48/23/25 Xn; R21 Xi; R36/38 N; R50-53 T; N R: 21-25-36/38-48/23/25-50/53 S: (1/2-)36/37/39-45-60-61 T; R25: C ≥ 2,5 % Xn; R22: 0,25 % ≤ C < 2,5 % Xn: R21: C ≥ 1 % T; R48/23/25: C ≥ 1 % Xn; R48/20/22: 0,25 % ≤ C < 1 % Xi; R36/38: C ≥ 1 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A1 S: (1/2-)36/37/39-45-60-61 T; R25: C ≥ 2,5 % Xn; R22: 0,25 % ≤ C < 2,5 % Xn: R21: C ≥ 1 % T; R48/23/25: C ≥ 1 % Xn; R48/20/22: 0,25 % ≤ C < 1 % Xi; R36/38: C ≥ 1 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A1 050-009-00-9 fluorotripentylstannane; [1] hexapentyldistannoxane [2] 243-546-7 [1] 247-143-7 [2] 20153-49-5 [1] 25637-27-8 [2] Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % 1 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % 1 050-010-00-4 fluorotrihexylstannane 243-547-2 20153-50-8 Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % 1 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % 1 050-011-00-X triphenyltin compounds, with the exception of those specified elsewhere in this Annex — — T; R23/24/25 N; R50-53 T; N R: 23/24/25-50/53 S: (1/2-)26-27-28-45-60-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,25 % ≤ C < 1 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % A1 S: (1/2-)26-27-28-45-60-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,25 % ≤ C < 1 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % A1 050-012-00-5 tetracyclohexylstannane; [1] chlorotricyclohexylstannane; [2] butyltricyclohexylstannane [3] 215-910-5 [1] 221-437-5 [2] 230-358-5 [3] 1449-55-4 [1] 3091-32-5 [2] 7067-44-9 [3] Xn; R20/21/22 N; R50-53 Xn; N R: 20/21/22-50/53 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % A1 S: (2-)26-28-60-61 Xn; R20/21/22: C ≥ 1 % A1 050-013-00-0 trioctyltin compounds, with the exception of those specified elsewhere in this Annex — — Xi; R36/37/38 R53 Xi R: 36/37/38-53 S: (2-)61 Xi; R36/37/38: C ≥ 1 % A1 S: (2-)61 Xi; R36/37/38: C ≥ 1 % A1 050-017-00-2 fenbutatin oxide (ISO); bis(tris(2-methyl-2-phenylpropyl)tin)oxide 236-407-7 13356-08-6 T+; R26 Xi; R36/38 … 26 unchanged lines … Xn; R21 N; R50-53 T+; C; N R: 60-61-21-25-26-34-48/25-68-50/53 S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 0,01 % ≤ C < 10 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E S: 53-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 0,01 % ≤ C < 10 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % E 050-023-00-5 reaction mass of: bis[(2-ethyl-1-oxohexyl)oxy]dioctyl stannane; bis[((2-ethyl-1-oxohexyl)oxy)dioctylstannyl]oxide; bis(1-phenyl-1,3-decanedionyl)dioctyl stannane; ((2-ethyl-1-oxohexyl)oxy)-(1-phenyl-1,3-decanedionyl)dioctyl stannane 422-920-5 - Xn; R48/22 N; R50-53 Xn; N R: 48/22-50/53 S: (2-)23-36-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-024-00-0 reaction mass of: tri-p-tolyltin hydroxide; S: (2-)23-36-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 050-024-00-0 reaction mass of: tri-p-tolyltin hydroxide; hexa-p-tolyl-distannoxane 432-230-6 - T; R48/25 Xn; R22 Xi; R38-41 R43 N; R50-53 T; N R: 22-38-41-43-48/25-50/53 S: (1/2-)22-26-36/37/39-45-60-61 050-025-00-6 trichloromethylstannane 213-608-8 993-16-8 Repr. Cat. 3; R63 Xn R: 63 S: (2-)22-36/37 050-026-00-1 2-ethylhexyl 10-ethyl-4-[[2-[(2-ethylhexyl)oxy]-2-oxoethyl]thio]-4-methyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 260-828-5 57583-34-3 Repr. Cat. 3; R63 Xn R: 63 S: (2-)22-36/37 050-027-00-7 2-ethylhexyl 10-ethyl-4,4-dioctyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 239-622-4 15571-58-1 Repr. Cat. 2; R61 T R: 61 S: 45-53 051-001-00-8 antimony trichloride 233-047-2 10025-91-9 C; R34 S: 45-53 050-028-00-2 2-ethylhexyl 10-ethyl-4,4-dimethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate 260-829-0 57583-35-4 Repr. Cat. 3; R63 T; R48/25 Xn; R22 R43 T R: 22-43-48/25-63 S: (1/2-)36/37-45 050-029-00-8 dimethyltin dichloride 212-039-2 753-73-1 Repr. Cat. 3; R63 T+; R26 T; R24/25-48/25 C; R34 T+ R: 24/25-26-34-48/25-63 S: (1/2-)26-28-36/37/39-45-63 051-001-00-8 antimony trichloride 233-047-2 10025-91-9 C; R34 N; R51-53 C; N R: 34-51/53 S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 051-002-00-3 antimony pentachloride 231-601-8 7647-18-9 C; R34 S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 051-002-00-3 antimony pentachloride 231-601-8 7647-18-9 C; R34 N; R51-53 C; N R: 34-51/53 S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 051-003-00-9 antimony compounds, with the exception of the tetroxide (Sb2O4), pentoxide (Sb2O5), trisulphide (Sb2S3), pentasulphide (Sb2S5) and those specified elsewhere in this Annex — — Xn; R20/22 S: (1/2-)26-45-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 051-003-00-9 antimony compounds, with the exception of the tetroxide (Sb2O4), pentoxide (Sb2O5), trisulphide (Sb2S3), pentasulphide (Sb2S5) and those specified elsewhere in this Annex — — Xn; R20/22 N; R51-53 Xn; N R: 20/22-51/53 S: (2-)61 Xn; R20/22: C ≥ 0,25 % A1 S: (2-)61 Xn; R20/22: C ≥ 0,25 % A1 051-004-00-4 antimony trifluoride 232-009-2 7783-56-4 T; R23/24/25 N; R51-53 T; N R: 23/24/25-51/53 S: (1/2-)7-26-45-61 051-005-00-X antimony trioxide 215-175-0 1309-64-4 Carc. Cat. 3; R40 Xn R: 40 S: (2-)22-36/37 051-006-00-5 diphenyl(4-phenylthiophenyl)sulfonium hexafluoroantimonate 403-500-0 — R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 051-007-00-0 bis(4-dodecylphenyl)iodonium hexafluoroantimonate 404-420-9 71786-70-4 R43 R52-53 Xi R: 43-52/53 S: (2-)24-37-61 053-001-00-3 iodine 231-442-4 7553-56-2 Xn; R20/21 N; R50 Xn; N R: 20/21-50 S: (2-)23-25-61 053-002-00-9 hydrogen iodide 233-109-9 10034-85-2 C; R35 C R: 35 S: (1/2-)9-26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 0,2 % ≤ C < 10 % Xi; R36/37/38: 0,02 % ≤ C < 0,2 % 5 053-002-01-6 hydriodic acid ... % — — C; R34 C S: (1/2-)9-26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 0,2 % ≤ C < 10 % Xi; R36/37/38: 0,02 % ≤ C < 0,2 % 5 053-002-01-6 hydriodic acid ... % — — C; R34 C R: 34 S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % B 053-003-00-4 iodoxybenzene — 696-33-3 E; R2 E R: 2 S: (2-)35 053-004-00-X calcium iodoxybenzoate — — E; R2 E R: 2 S: (2-)35 C 053-005-00-5 (4-(1-methylethyl)phenyl)-(4-methylphenyl)iodonium tetrakis(pentafluorophenyl)borate (1-) 422-960-3 178233-72-2 Xn; R21/22-48/22 N; R50-53 Xn; N R: 21/22-48/22-50/53 S: (2-)22-36/37-60-61 056-001-00-1 barium peroxide 215-128-4 1304-29-6 O; R8 Xn; R20/22 O; Xn R: 8-20/22 S: (2-)13-27 056-002-00-7 barium salts, with the exception of barium sulphate, salts of 1-azo-2-hydroxynaphthalenyl aryl sulphonic acid, and of salts specified elsewhere in this Annex — — Xn; R20/22 Xn R: 20/22 S: (2-)28 Xn; R20/22: C ≥ 1 % A1 S: (2-)28 Xn; R20/22: C ≥ 1 % A1 056-003-00-2 barium carbonate 208-167-3 513-77-9 Xn; R22 Xn R: 22 S: (2-)24/25 056-004-00-8 barium chloride 233-788-1 10361-37-2 T; R25 … 78 unchanged lines … R33 N; R50-53 T+; N R: 26/27/28-33-50/53 S: (1/2-)13-28-45-60-61 T+; R26/27/28: C ≥ 2 % T; R23/24/25: 0,5 % ≤ C < 2 % Xn; R20/21/22: 0,1 % ≤ C < 0,5 % R33: C ≥ 0,1 % A1 S: (1/2-)13-28-45-60-61 T+; R26/27/28: C ≥ 2 % T; R23/24/25: 0,5 % ≤ C < 2 % Xn; R20/21/22: 0,1 % ≤ C < 0,5 % R33: C ≥ 0,1 % A1 080-003-00-1 dimercury dichloride; mercurous chloride; calomel 233-307-5 10112-91-1 Xn; R22 Xi; R36/37/38 N; R50-53 Xn; N R: 22-36/37/38-50/53 S: (2-)13-24/25-46-60-61 080-004-00-7 organic compounds of mercury with the exception of those specified elsewhere in this Annex — — T+; R26/27/28 R33 N; R50-53 T+; N R: 26/27/28-33-50/53 S: (1/2-)13-28-36-45-60-61 T+; R26/27/28: C ≥ 2 % T; R23/24/25: 0,5 % ≤ C < 2 % Xn; R20/21/22: 0,05 % ≤ C < 0,5 % R33: C ≥ 0,05 % A1 S: (1/2-)13-28-36-45-60-61 T+; R26/27/28: C ≥ 2 % T; R23/24/25: 0,5 % ≤ C < 2 % Xn; R20/21/22: 0,05 % ≤ C < 0,5 % R33: C ≥ 0,05 % A1 080-005-00-2 mercury difulminate; mercuric fulminate; fulminate of mercury 211-057-8 628-86-4 E; R3 T; R23/24/25 R33 N; R50-53 E; T; N R: 3-23/24/25-33-50/53 S: (1/2-)3-45-60-61 080-006-00-8 dimercury dicyanide oxide; mercuric oxycyanide 215-629-8 1335-31-5 E; R2 T; R23/24/25 R33 N; R50-53 E; T; N R: 2-23/24/25-33-50/53 S: (1/2-)28-36/37-45-60-61 080-007-00-3 dimethylmercury; [1] diethylmercury [2] 209-805-3 [1] 211-000-7 [2] 593-74-8 [1] 627-44-1 [2] T+; R26/27/28 R33 N; R50-53 T+; N R: 26/27/28-33-50/53 S: (1/2-)13-28-36-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % R33: C ≥ 0,05 % 1 S: (1/2-)13-28-36-45-60-61 T+; R26/27/28: C ≥ 0,5 % T; R23/24/25: 0,1 % ≤ C < 0,5 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % R33: C ≥ 0,05 % 1 080-008-00-9 phenylmercury nitrate; [1] phenylmercury hydroxide; [2] basic phenylmercury nitrate [3] 200-242-9 [1] … 41 unchanged lines … R33 N; R50-53 T; N R: 61-20/22-33-62-50/53 S: 53-45-60-61 Repr. Cat. 3; R62: C ≥ 2,5 % Xn; R20/22: C ≥ 1 % R33: C ≥ 0,5 % AE1 S: 53-45-60-61 Repr. Cat. 3; R62: C ≥ 2,5 % Xn; R20/22: C ≥ 1 % R33: C ≥ 0,5 % AE1 082-002-00-1 lead alkyls — — Repr. Cat. 1; R61 Repr. Cat. 3; R62 T+; R26/27/28 R33 N; R50-53 T+; N R: 61-26/27/28-33-62-50/53 S: 53-45-60-61 Repr. Cat. 1; R61: C ≥ 0,1 % T+; R26/27/28: C ≥ 0,25 % T; R23/24/25: 0,1 % ≤ C < 0,25 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % R33: C ≥ 0,05 % AE1 S: 53-45-60-61 Repr. Cat. 1; R61: C ≥ 0,1 % T+; R26/27/28: C ≥ 0,25 % T; R23/24/25: 0,1 % ≤ C < 0,25 % Xn; R20/21/22: 0,05 % ≤ C < 0,1 % R33: C ≥ 0,05 % AE1 082-003-00-7 lead diazide; lead azide 236-542-1 13424-46-9 E; R3 Repr. Cat. 1; R61 … 90 unchanged lines … 75-28-5 [2] F+; R12 F+ R: 12 S: (2-)9-16 C 601-004-01-8 butane (containing ≥ 0,1 % butadiene (203-450-8)); [1] isobutane (containing ≥ 0,1 % butadiene (203-450-8)) [2] 203-448-7 [1] 601-004-01-8 butane (containing ≥ 0,1 % butadiene (203-450-8)); [1] isobutane (containing ≥ 0,1 % butadiene (203-450-8)) [2] 203-448-7 [1] 200-857-2 [2] 106-97-8 [1] 75-28-5 [2] F+; R12 Carc. Cat. 1; R45 … 15 unchanged lines … N; R51-53 F+; Xn; N R: 12-51/53-65-66-67 S: (2-)9-16-29-33-61-62 C 601-007-00-7 hexane (containing < 5 % n-hexane (203-777-6)); 601-007-00-7 hexane (containing < 5 % n-hexane (203-777-6)); 2-methylpentane; [1] 3-methylpentane; [2] 2,2-dimethylbutane; [3] … 193 unchanged lines … Xn; R20/21 Xi; R38 Xn R: 10-20/21-38 S: (2-)25 Xn; R20/21: C ≥ 12,5 % C S: (2-)25 Xn; R20/21: C ≥ 12,5 % C 601-023-00-4 ethylbenzene 202-849-4 100-41-4 F; R11 Xn; R20 F; Xn R: 11-20 S: (2-)16-24/25-29 601-024-00-X cumene; [1] Xn; R20-48/20-65 F; Xn R: 11-20-48/20-65 S: (2-)16-24/25-29-62 601-024-00-X cumene; [1] propylbenzene [2] 202-704-5 [1] 203-132-9 [2] 98-82-8 [1] 103-65-1 [2] R10 Xn; R65 Xi; R37 N; R51-53 Xn; N R: 10-37-51/53-65 S: (2-)24-37-61-62 C 601-025-00-5 mesitylene; 1,3,5-trimethylbenzene 203-604-4 108-67-8 R10 Xi; R37 N; R51-53 Xi; N R: 10-37-51/53 S: (2-)61 Xi; R37: C ≥ 25 % 601-026-00-0 styrene 202-851-5 100-42-5 R10 Xn; R20 Xi; R36/38 Xn R: 10-20-36/38 S: (2-)23 Xn; R20: C ≥ 12,5 % Xi; R36/38: C ≥ 12,5 % D S: (2-)61 Xi; R37: C ≥ 25 % 601-026-00-0 styrene 202-851-5 100-42-5 Repr. Cat. 3; R63 Xn; R20-48/20 Xi; R36/38 R10 Xn R: 10-20-36/38-48/20-63 S: (2-)23-36/37-46 Xn; R20: C ≥ 12,5 % Xi; R36/38: C ≥ 12,5 % D 601-027-00-6 2-phenylpropene; α-methylstyrene 202-705-0 98-83-9 R10 Xi; R36/37 N; R51-53 Xi; N R: 10-36/37-51/53 S: (2-)61 Xi; R36/37: C ≥ 25 % 601-028-00-1 2-methylstyrene; S: (2-)61 Xi; R36/37: C ≥ 25 % 601-028-00-1 2-methylstyrene; 2-vinyltoluene 210-256-7 611-15-4 Xn; R20 N; R51-53 Xn; N R: 20-51/53 … 31 unchanged lines … R43 N; R50-53 T; N R: 45-46-60-61-43-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % 601-033-00-9 benz[a]anthracene 200-280-6 56-55-3 Carc. Cat. 2; R45 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % 601-033-00-9 benz[a]anthracene 200-280-6 56-55-3 Carc. Cat. 2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 601-034-00-4 benz[e]acephenanthrylene 205-911-9 205-99-2 Carc. Cat. 2; R45 S: 53-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 601-034-00-4 benz[e]acephenanthrylene 205-911-9 205-99-2 Carc. Cat. 2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 601-035-00-X benzo[j]fluoranthene 205-910-3 205-82-3 Carc. Cat. 2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 601-036-00-5 benzo[k]fluoranthene 205-916-6 207-08-9 Carc. Cat. 2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 601-037-00-0 n-hexane 203-777-6 110-54-3 F; R11 Repr. Cat. 3; R62 Xn; R65-48/20 Xi; R38 R67 N; R51-53 F; Xn; N R: 11-38-48/20-62-65-67-51/53 S: (2-)9-16-29-33-36/37-61-62 Xn; R48/20: C ≥ 5 % 601-041-00-2 dibenz[a,h]anthracene 200-181-8 53-70-3 Carc. Cat. 2; R45 S: (2-)9-16-29-33-36/37-61-62 Xn; R48/20: C ≥ 5 % 601-041-00-2 dibenz[a,h]anthracene 200-181-8 53-70-3 Carc. Cat. 2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 601-042-00-8 biphenyl; S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 601-042-00-8 biphenyl; diphenyl 202-163-5 92-52-4 Xi; R36/37/38 N; R50-53 Xi; N R: 36/37/38-50/53 … 163 unchanged lines … R67 F; Xn R: 11-65-67 S: 9-16-33-62 D 602-001-00-7 chloromethane; 601-088-00-9 4-vinylcyclohexene 202-848-9 100-40-3 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 601-089-00-4 muscalure; cis-tricos-9-ene 248-505-7 27519-02-4 R43 Xi R: 43 S: (2-)24-37 602-001-00-7 chloromethane; methyl chloride 200-817-4 74-87-3 F+; R12 Carc. Cat. 3; R40 Xn; R48/20 F+; Xn R: 12-40-48/20 S: (2-)9-16-33 602-002-00-2 bromomethane; methylbromide 200-813-2 74-83-9 Muta. Cat. 3; R68 T; R23/25 Xn; R48/20 Xi; R36/37/38 N; R50 N; R59 T; N R: 23/25-36/37/38-48/20-50-59-68 S: (1/2-)15-27-36/39-38-45-59-61 602-003-00-8 dibromomethane 200-824-2 74-95-3 Xn; R20 R52-53 Xn R: 20-52/53 S: (2-)24-61 Xn; R20: C ≥ 12,5 % 602-004-00-3 dichloromethane; S: (2-)24-61 Xn; R20: C ≥ 12,5 % 602-004-00-3 dichloromethane; methylene chloride 200-838-9 75-09-2 Carc. Cat. 3; R40 Xn R: 40 S: (2-)23-24/25-36/37 602-005-00-9 methyl iodide; … 20 unchanged lines … N; R59 R52-53 T; N R: 23/24/25-40-48/23-59-52/53 S: (1/2-)23-36/37-45-59-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 602-009-00-0 chloroethane 200-830-5 75-00-3 F+; R12 S: (1/2-)23-36/37-45-59-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 602-009-00-0 chloroethane 200-830-5 75-00-3 F+; R12 Carc. Cat. 3; R40 R52-53 F+; Xn R: 12-40-52/53 S: (2-)9-16-33-36/37-61 602-010-00-6 1,2-dibromoethane 203-444-5 106-93-4 Carc. Cat. 2; R45 T; R23/24/25 Xi; R36/37/38 N; R51-53 T; N R: 45-23/24/25-36/37/38-51/53 S: 53-45-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % E S: 53-45-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % E 602-011-00-1 1,1-dichloroethane 200-863-5 75-34-3 F; R11 Xn; R22 Xi; R36/37 R52-53 F; Xn R: 11-22-36/37-52/53 S: (2-)16-23-61 Xn; R22: C ≥ 12,5 % 602-012-00-7 1,2-dichloroethane; S: (2-)16-23-61 Xn; R22: C ≥ 12,5 % 602-012-00-7 1,2-dichloroethane; ethylene dichloride 203-458-1 107-06-2 F; R11 Carc. Cat. 2; R45 Xn; R22 Xi; R36/37/38 F; T R: 45-11-22-36/37/38 S: 53-45 E 602-013-00-2 1,1,1-trichloroethane; methyl chloroform 200-756-3 71-55-6 Xn; R20 N; R59 Xn; N R: 20-59 S: (2-)24/25-59-61 F 602-014-00-8 1,1,2-trichloroethane 201-166-9 79-00-5 Carc. Cat. 3; R40 Xn; R20/21/22 R66 Xn R: 20/21/22-40-66 S: (2-)9-36/37-46 Xn; R20/21/22: C ≥ 5 % 602-015-00-3 1,1,2,2-tetrachloroethane 201-197-8 79-34-5 T+; R26/27 S: (2-)9-36/37-46 Xn; R20/21/22: C ≥ 5 % 602-015-00-3 1,1,2,2-tetrachloroethane 201-197-8 79-34-5 T+; R26/27 N; R51-53 T+; N R: 26/27-51/53 S: (1/2-)38-45-61 602-016-00-9 1,1,2,2-tetrabromoethane 201-191-5 79-27-6 T+; R26 Xi; R36 R52-53 T+ R: 26-36-52/53 S: (1/2-)24-27-45-61 602-017-00-4 pentachloroethane 200-925-1 76-01-7 Carc. Cat. 3; R40 T; R48/23 N; R51-53 T; N R: 40-48/23-51/53 S: (1/2-)23-36/37-45-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 602-018-00-X 1-chloropropane; [1] S: (1/2-)23-36/37-45-61 T; R48/23: C ≥ 1 % Xn; R48/20: 0,2 % ≤ C < 1 % 602-018-00-X 1-chloropropane; [1] 2-chloropropane [2] 208-749-7 [1] 200-858-8 [2] 540-54-5 [1] 75-29-6 [2] F; R11 … 44 unchanged lines … Carc. Cat. 3; R40 Xn; R20 F+; Xn R: 12-20-40 S: (2-)7-16-29-36/37-46 Xn; R20: C ≥ 12,5 % D S: (2-)7-16-29-36/37-46 Xn; R20: C ≥ 12,5 % D 602-026-00-3 1,2-dichloroethylene; [1] cis-dichloroethylene; [2] trans-dichloroethylene [3] 208-750-2 [1] 205-859-7 [2] 205-860-2 [3] 540-59-0 [1] 156-59-2 [2] 156-60-5 [3] F; R11 Xn; R20 R52-53 F; Xn R: 11-20-52/53 S: (2-)7-16-29-61 Xn; R20: C ≥ 12,5 % C S: (2-)7-16-29-61 Xn; R20: C ≥ 12,5 % C 602-027-00-9 trichloroethylene; trichloroethene 201-167-4 79-01-6 Carc. Cat. 2; R45 Muta. Cat. 3; R68 … 38 unchanged lines … Xn; R20 N; R51-53 Xn; N R: 10-20-51/53 S: (2-)24/25-61 Xn; R20: C ≥ 5 % 602-034-00-7 1,2-dichlorobenzene; S: (2-)24/25-61 Xn; R20: C ≥ 5 % 602-034-00-7 1,2-dichlorobenzene; o-dichlorobenzene 202-425-9 95-50-1 Xn; R22 Xi; R36/37/38 N; R50-53 Xn; N R: 22-36/37/38-50/53 S: (2-)23-60-61 Xn; R22: C ≥ 5 % 602-035-00-2 1,4-dichlorobenzene; S: (2-)23-60-61 Xn; R22: C ≥ 5 % 602-035-00-2 1,4-dichlorobenzene; p-dichlorobenzene 203-400-5 106-46-7 Carc. Cat. 3; R40 Xi; R36 N; R50-53 Xn; N … 23 unchanged lines … PCB 215-648-1 1336-36-3 R33 N; R50-53 N R: 33-50/53 S: (2-)-60-61 R33: C ≥ 0,005 % C S: (2-)-60-61 R33: C ≥ 0,005 % C 602-040-00-X 2-chlorotoluene; [1] 3-chlorotoluene; [2] 4-chlorotoluene; [3] … 25 unchanged lines … R64 N; R50-53 T; N R: 20/21-25-48/22-64-50/53 S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 602-044-00-1 camphechlor (ISO) S: (1/2-)36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 602-044-00-1 camphechlor (ISO) toxaphene; 232-283-3 8001-35-2 Carc. Cat. 3; R40 T; R25 Xn; R21 … 32 unchanged lines … (1α,4α,4aβ, 5β,8β,8aβ)-1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-1,4:5,8-dimethanonaphthalene 207-366-2 465-73-6 T+; R26/27/28 N; R50-53 T+; N R: 26/27/28-50/53 S: (1/2-)13-28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 602-051-00-X endrin (ISO); S: (1/2-)13-28-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 602-051-00-X endrin (ISO); 1,2,3,4,10,10-hexachloro-6,7-epoxy-1,4,4a,5,6,7,8,8a-octahydro-1,4:5,8-dimethanonaphthalene 200-775-7 72-20-8 T+; R28 T; R24 N; R50-53 T+; N … 92 unchanged lines … C; R34 N; R50-53 T+; N R: 45-24/25-26-34-50/53 S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E S: 53-45-60-61 Carc. Cat. 2; R45: C ≥ 0,01 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E 602-074-00-5 pentachlorobenzene 210-172-0 608-93-5 F; R11 Xn; R22 N; R50-53 F; Xn; N R: 11-22-50/53 S: (2-)41-46-50-60-61 602-075-00-0 4,4,5,5-tetrachloro-1,3-dioxolan-2-one 404-060-2 22432-68-4 T+; R26 Xn; R22 C; R34 T+ R: 22-26-34 S: (1/2-)9-26-28-36/37/39-45 602-076-00-6 2,3,4-trichlorobut-1-ene 219-397-9 2431-50-7 Carc. Cat. 3; R40 T; R23 Xn; R22 Xi; R36/37/38 N; R50-53 T; N R: 22-23-36/37/38-40-50/53 S: (1/2-)36/37-45-60-61 Carc. Cat. 3; R40: C ≥ 0,1 % 602-077-00-1 dodecachloropentacyclo[5.2.1.02,6.03,9.05,8]decane; S: (1/2-)36/37-45-60-61 Carc. Cat. 3; R40: C ≥ 0,1 % 602-077-00-1 dodecachloropentacyclo[5.2.1.02,6.03,9.05,8]decane; mirex 219-196-6 2385-85-5 Carc. Cat. 3; R40 Repr. Cat. 3; R62-63 R64 … 137 unchanged lines … 603-001-00-X methanol 200-659-6 67-56-1 F; R11 T; R23/24/25-39/23/24/25 F; T R: 11-23/24/25-39/23/24/25 S: (1/2-)7-16-36/37-45 T; R23/24/25: C ≥ 20 % Xn; R20/21/22: 3 % ≤ C < 20 % T; R39/23/24/25: C ≥ 10 % Xn; R68/20/21/22: 3 % ≤ C < 10 % 603-002-00-5 ethanol; S: (1/2-)7-16-36/37-45 T; R23/24/25: C ≥ 20 % Xn; R20/21/22: 3 % ≤ C < 20 % T; R39/23/24/25: C ≥ 10 % Xn; R68/20/21/22: 3 % ≤ C < 10 % 603-002-00-5 ethanol; ethyl alcohol 200-578-6 64-17-5 F; R11 F R: 11 S: (2-)7-16 603-003-00-0 propan-1-ol; … 27 unchanged lines … methyl isobutyl carbinol 203-551-7 108-11-2 R10 Xi; R37 Xi R: 10-37 S: (2-)24/25 Xi; R37: C ≥ 25 % 603-009-00-3 cyclohexanol 203-630-6 108-93-0 Xn; R20/22 S: (2-)24/25 Xi; R37: C ≥ 25 % 603-009-00-3 cyclohexanol 203-630-6 108-93-0 Xn; R20/22 Xi; R37/38 Xn R: 20/22-37/38 S: (2-)24/25 603-010-00-9 2-methylcyclohexanol, mixed isomers; [1] … 34 unchanged lines … S: (1/2-)36/37/39-38-45-61 603-016-00-1 4-hydroxy-4-methylpentan-2-one; diacetone alcohol 204-626-7 123-42-2 Xi; R36 Xi R: 36 S: (2-)24/25 Xi; R36: C ≥ 10 % 603-018-00-2 furfuryl alcohol 202-626-1 98-00-0 Carc. Cat. 3; R40 S: (2-)24/25 Xi; R36: C ≥ 10 % 603-018-00-2 furfuryl alcohol 202-626-1 98-00-0 Carc. Cat. 3; R40 T; R23 Xn; R21/22-48/20 Xi; R36/37 T … 31 unchanged lines … Carc. Cat. 3; R40 Xi; R36/37 F; Xn; R: 11-19-40-36/37 S: (2-)(13-)16-29-33-36-37(-46) Xi; R36/37: C ≥ 25 % 603-026-00-6 1-chloro-2,3-epoxypropane; S: (2-)(13-)16-29-33-36-37(-46) Xi; R36/37: C ≥ 25 % 603-026-00-6 1-chloro-2,3-epoxypropane; epichlorhydrin 203-439-8 106-89-8 R10 Carc. Cat. 2; R45 T; R23/24/25 C; R34 R43 T R: 45-10-23/24/25-34-43 S: 53-45 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % E S: 53-45 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % E 603-027-00-1 ethanediol; ethylene glycol 203-473-3 107-21-1 Xn; R22 Xn R: 22 S: (2-) 603-028-00-7 2-chloroethanol; ethylene chlorohydrin 203-459-7 107-07-3 T+; R26/27/28 T+ R: 26/27/28 S: (1/2-)7/9-28-45 603-029-00-2 bis(2-chloroethyl) ether 203-870-1 111-44-4 Carc. Cat. 3; R40 T+; R26/27/28 T+ R: 26/27/28-40 S: (1/2-)7/9-27-28-36/37-45 603-030-00-8 2-aminoethanol; ethanolamine 205-483-3 141-43-5 Xn; R20/21/22 C; R34 C R: 20/21/22-34 S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-031-00-3 1,2-dimethoxyethane; S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-031-00-3 1,2-dimethoxyethane; ethylene glycol dimethyl ether; EGDME 203-794-9 110-71-4 F; R11 R19 … 31 unchanged lines … R: 3 S: (2-)35 T 603-037-01-3 cellulose nitrate; nitrocellulose, containing a maximum of 12,6 % nitrogen — — F; R11 $ F nitrocellulose, containing a maximum of 12,6 % nitrogen — — F; R11 $ F R: 11 S: (2-)16-33-37/39 603-038-00-1 allyl glycidyl ether; allyl 2,3-epoxypropyl ether; … 64 unchanged lines … T; R24 Xn; R22 F; T+ R: 45-11-22-24-26 S: 53-45 Carc. Cat. 1; R45: C ≥ 0,001 % E S: 53-45 Carc. Cat. 1; R45: C ≥ 0,001 % E 603-047-00-0 2-dimethylaminoethanol; N,N-dimethylethanolamine 203-542-8 108-01-0 R10 Xn; R20/21/22 C; R34 C R: 10-20/21/22-34 S: (1/2-)25-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-048-00-6 2-diethylaminoethanol; S: (1/2-)25-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-048-00-6 2-diethylaminoethanol; N,N-diethylethanolamine 202-845-2 100-37-8 R10 Xn; R20/21/22 C; R34 C R: 10-20/21/22-34 S: (1/2-)25-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-049-00-1 chlorfenethol (ISO); S: (1/2-)25-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-049-00-1 chlorfenethol (ISO); 1,1-bis (4-chlorophenyl) ethanol 201-246-3 80-06-8 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-)36-61 603-050-00-7 1-(2-Butoxypropoxy)propan-2-ol 246-011-6 24083-03-2 Xn; R21/22 Xn R: 21/22 S: (2-) 603-051-00-2 2-ethylbutan-1-ol 202-621-4 97-95-0 Xn; R21/22 Xn R: 21/22 S: (2-) 603-052-00-8 3-butoxypropan-2-ol; propylene glycol monobutyl ether 225-878-4 5131-66-8 Xi; R36/38 Xi R: 36/38 S: (2-) 603-053-00-3 2-methylpentane-2,4-diol 203-489-0 107-41-5 Xi; R36/38 Xi R: 36/38 S: (2-) Xi; R36/38: C ≥ 10 % 603-054-00-9 di-n-butyl ether; S: (2-) Xi; R36/38: C ≥ 10 % 603-054-00-9 di-n-butyl ether; dibutyl ether 205-575-3 142-96-1 R10 Xi; R36/37/38 R52-53 Xi R: 10-36/37/38-52/53 S: (2-)61 Xi; R36/37/38: C ≥ 10 % 603-055-00-4 propylene oxide; S: (2-)61 Xi; R36/37/38: C ≥ 10 % 603-055-00-4 propylene oxide; 1,2-epoxypropane; methyloxirane 200-879-2 75-56-9 F+; R12 Carc. Cat. 2; R45 … 34 unchanged lines … R: 45-46-24/25-26-34 S: 53-45 E 603-061-00-7 tetrahydro-2-furylmethanol; tetrahydrofurfuryl alcohol 202-625-6 97-99-4 Xi; R36 Xi R: 36 S: (2-)39 Xi; R36: C ≥ 10 % 603-062-00-2 tetrahydrofuran-2,5-diyldimethanol 203-239-0 104-80-3 Xi; R36/37/38 Xi tetrahydrofurfuryl alcohol 202-625-6 97-99-4 Repr. Cat. 2; R61 Repr. Cat. 3; R62 Xi; R36 T R: 36-61-62 S: 45-53 Xi; R36: C ≥ 10 % 603-062-00-2 tetrahydrofuran-2,5-diyldimethanol 203-239-0 104-80-3 Xi; R36/37/38 Xi R: 36/37/38 S: (2-)39 Xi; R36/37/38: C ≥ 10 % 603-063-00-8 2,3-epoxypropan-1-ol; S: (2-)39 Xi; R36/37/38: C ≥ 10 % 603-063-00-8 2,3-epoxypropan-1-ol; glycidol; oxiranemethanol 209-128-3 556-52-5 Carc. Cat. 2; R45 Muta. Cat. 3; R68 … 18 unchanged lines … 4-vinylcyclohexene diepoxide 203-437-7 106-87-6 Carc. Cat. 3; R40 T; R23/24/25 T R: 23/24/25-40 S: (1/2-)36/37-45-63 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % 603-067-00-X phenyl glycidyl ether; S: (1/2-)36/37-45-63 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,1 % ≤ C < 1 % 603-067-00-X phenyl glycidyl ether; 2,3-epoxypropyl phenyl ether; 1,2-epoxy-3-phenoxypropane 204-557-2 122-60-1 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Xn; R20 Xi; R37/38 R43 R52-53 T R: 45-20-37/38-43-68-52/53 S: 53-45-61 E 603-068-00-5 2,3-epoxypropyl-2-ethylcyclohexyl ether; ethylcyclohexylglycidyl ether — 130014-35-6 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)26-28-37/39 603-069-00-0 2,4,6-tris(dimethylaminomethyl)phenol 202-013-9 90-72-2 Xn; R22 Xi; R36/38 Xn R: 22-36/38 S: (2-)26-28 603-070-00-6 2-amino-2-methylpropanol 204-709-8 124-68-5 Xi; R36/38 R52-53 Xi R: 36/38-52/53 S: (2-)61 Xi; R36/38: C ≥ 10 % 603-071-00-1 2,2'-iminodiethanol; S: (2-)61 Xi; R36/38: C ≥ 10 % 603-071-00-1 2,2'-iminodiethanol; diethanolamine 203-868-0 111-42-2 Xn; R22-48/22 Xi; R38-41 Xn R: 22-38-41-48/22 S: (2-)26-36/37/39-46 603-072-00-7 1,4-bis(2,3 epoxypropoxy)butane; butanedioldiglycidyl ether 219-371-7 2425-79-8 Xn; R20/21 Xi; R36/38 R43 Xn R: 20/21-36/38-43 S: (2-)26-28-37/39 603-073-00-2 bis-[4-(2,3-epoxipropoxi)phenyl]propane 216-823-5 1675-54-3 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)28-37/39 Xi; R36/38: C ≥ 5 % 603-074-00-8 reaction product: bisphenol-A-(epichlorhydrin); S: (2-)28-37/39 Xi; R36/38: C ≥ 5 % 603-074-00-8 reaction product: bisphenol-A-(epichlorhydrin); epoxy resin (number average molecular weight ≤ 700) 500-033-5 25068-38-6 Xi; R36/38 R43 N; R51-53 Xi; N R: 36/38-43-51/53 S: (2-)28-37/39-61 Xi; R36/38: C ≥ 5 % 603-075-00-3 chlormethyl methyl ether; S: (2-)28-37/39-61 Xi; R36/38: C ≥ 5 % 603-075-00-3 chlormethyl methyl ether; chlorodimethyl ether 203-480-1 107-30-2 F; R11 Carc. Cat. 1; R45 Xn; R20/21/22 F; T R: 45-11-20/21/22 S: 53-45 E 603-076-00-9 but-2-yne-1,4-diol; 2-butyne-1,4-diol 203-788-6 110-65-6 C; R34 T; R23/25 Xn; R21-48/22 R43 C; T R: 21-23/25-34-43-48/22 S: (1/2-)25-26-36/37/39-45-46 C; R34: C ≥ 50 % Xi; R36/38: 25 % ≤ C < 50 % D S: (1/2-)25-26-36/37/39-45-46 C; R34: C ≥ 50 % Xi; R36/38: 25 % ≤ C < 50 % D 603-077-00-4 1-dimethylaminopropan-2-ol; dimepranol (INN) 203-556-4 108-16-7 R10 Xn; R22 … 15 unchanged lines … 2-(methylamino)ethanol 203-710-0 109-83-1 Xn; R21/22 C; R34 C R: 21/22-34 S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-081-00-6 2,2'-thiodiethanol; S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-081-00-6 2,2'-thiodiethanol; thiodiglycol 203-874-3 111-48-8 Xi; R36 Xi R: 36 S: (2-) 603-082-00-1 1-aminopropan-2-ol; isopropanolamine 201-162-7 78-96-6 C; R34 C R: 34 S: (1/2-)23-26-36-45 603-083-00-7 1,1'-iminodipropan-2-ol; di-isopropanolamine 203-820-9 110-97-4 Xi; R36 Xi R: 36 S: (2-)26 603-084-00-2 styrene oxide; (epoxyethyl)benzene; phenyloxirane 202-476-7 96-09-3 Carc. Cat. 2; R45 Xn; R21 Xi; R36 T R: 45-21-36 S: 53-45 E 603-085-00-8 bronopol (INN); 2-bromo-2-nitropropane-1,3-diol 200-143-0 52-51-7 Xn; R21/22 Xi; R37/38-41 N; R50 Xn; N R: 21/22-37/38-41-50 S: (2-)26-36/37/39-61 N; R50: C ≥ 2,5 % 603-086-00-3 ethirimol (ISO); S: (2-)26-36/37/39-61 N; R50: C ≥ 2,5 % 603-086-00-3 ethirimol (ISO); 5-butyl-2-ethylamino-6-methylpyrimidin-4-ol 245-949-3 23947-60-6 Xn; R21 Xn R: 21 S: (2-)36/37 603-087-00-9 2-ethylhexane-1,3-diol; … 345 unchanged lines … 2-methoxy-2-methylpropane 216-653-1 1634-04-4 F; R11 Xi; R38 F; Xi R: 11-38 S: (2-)9-16-24 603-182-00-5 reaction product of: saturated, monounsaturated and multiple unsaturated long-chained partly estrified alcohols of vegetable origin (Brassica napus L., Brassica rapa L., Helianthus annuus L., Glycine hispida, Gossypium hirsutum L., Cocos nucifera L., Elaeis guineensis) with O,O-diisobutyldithiophosphate and 2-ethylhexylamine and hydrogen peroxide 428-630-5 - R43 Xi S: (2-)9-16-24 603-182-00-5 reaction product of: saturated, monounsaturated and multiple unsaturated long-chained partly estrified alcohols of vegetable origin (Brassica napus L., Brassica rapa L., Helianthus annuus L., Glycine hispida, Gossypium hirsutum L., Cocos nucifera L., Elaeis guineensis) with O,O-diisobutyldithiophosphate and 2-ethylhexylamine and hydrogen peroxide 428-630-5 - R43 Xi R: 43 S: (2-)24-37 603-183-00-0 2-[2-(2-butoxyethoxy)ethoxy]ethanol; TEGBE; triethylene glycol monobutyl ether; butoxytriethylene glycol 205-592-6 143-22-6 Xi; R41 Xi R: 41 S: (2-)26-39-46 Xi; R41: C ≥ 30 % Xi; R36: 20 % ≤ C < 30 % 603-184-00-6 2-(hydroxymethyl)-2-[[2-hydroxy-3-(isooctadecyloxy)propoxy]methyl]-1,3-propanediol 416-380-1 146925-83-9 N; R50-53 N S: (2-)26-39-46 Xi; R41: C ≥ 30 % Xi; R36: 20 % ≤ C < 30 % 603-184-00-6 2-(hydroxymethyl)-2-[[2-hydroxy-3-(isooctadecyloxy)propoxy]methyl]-1,3-propanediol 416-380-1 146925-83-9 N; R50-53 N R: 50/53 S: 60-61 603-185-00-1 2,4-dichloro-3-ethyl-6-nitrophenol 420-740-1 99817-36-4 T; R25 Xi; R41 … 25 unchanged lines … C; R34 R43 T R: 61-34-43-62 S: 53-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-195-00-6 2-[4-(4-methoxyphenyl)-6-phenyl-1,3,5-triazin-2-yl]-phenol 430-810-3 154825-62-4 R52-53 R: 52/53 S: 53-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 603-195-00-6 2-[4-(4-methoxyphenyl)-6-phenyl-1,3,5-triazin-2-yl]-phenol 430-810-3 154825-62-4 R52-53 R: 52/53 S: 61 603-196-00-1 2-(7-ethyl-1H-indol-3-yl)ethanol 431-020-1 41340-36-7 Xn; 22-48/22 N; R51-53 Xn; N R: 22-48/22-51/53 S: (2-)36/37/39-61 603-197-00-7 tebuconazole (ISO); 1-(4-chlorophenyl)-4,4-dimethyl-3-(1,2,4-triazol-1-ylmethyl)pentan-3-ol 403-640-2 107534-96-3 Repr. Cat. 3; R63 Xn; R22 N; R51-53 Xn; N R: 22-51/53-63 S: (2-)22-36/37-61 603-199-00-8 etoxazol (ISO); (RS)-5-tert-butyl-2-[2-(2,6-difluorophenyl)-4,5-dihydro-1,3-oxazol-4-yl]phenetole — 153233-91-1 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 603-200-00-1 1-pentanol; [1] S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 603-200-00-1 1-pentanol; [1] 3-pentanol [2] 200-752-1 [1] 209-526-7 [2] 71-41-0 [1] 584-02-1 [2] R10 … 31 unchanged lines … Repr. Cat. 3; R62 Xi; R36 F; T R: 61-11-19-36-62 S: 53-45 603-209-00-0 spinosad (ISO) (reaction mass of spinosyn A and spinosyn D in ratios between 95:5 to 50:50); reaction mass of 50-95 % of (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione and 50-5 % (2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione; [1] S: 53-45 603-209-00-0 spinosad (ISO) (reaction mass of spinosyn A and spinosyn D in ratios between 95:5 to 50:50); reaction mass of 50-95 % of (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-14-methyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione and 50-5 % (2S,3aR,5aS,5bS,9S,13S,14R,16aS,16bS)-2-(6-deoxy-2,3,4-tri-O-methyl-α-l-mannopyranosyloxy)-13-(4-dimethylamino-2,3,4,6-tetradeoxy-β-d-erythropyranosyloxy)-9-ethyl-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-4,14-dimethyl-1H-8-oxacyclododeca[b]as-indacene-7,15-dione; [1] spinosyn A; [2] spinosyn D [3] - [1] - [2] - [3] - [1] 131929-60-7 [2] 131929-63-0 [3] N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 603-210-00-6 2,4-diethyl-1,5-pentanediol 429-310-8 57987-55-0 Xi; R41 Xi S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 603-210-00-6 2,4-diethyl-1,5-pentanediol 429-310-8 57987-55-0 Xi; R41 Xi R: 41 S: (2-)26-39 603-211-00-1 2,3-epoxypropyltrimethylammonium chloride …%; glycidyl trimethylammonium chloride …% 221-221-0 3033-77-0 Carc. Cat. 2; R45 … 31 unchanged lines … R: 43-53 S: (2-)24-37/39-61 603-220-00-0 1-{]benzyl[}2-(2-methoxyphenoxy)ethyl{]amino[}-3-(9H-carbazol-4-yloxy)propan-2-ol 432-890-5 72955-94-3 R53 R: 53 S: 61 603-221-00-6 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-1,1-ethanediol, hydrochloride; [containing < 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Xn; R22 [containing < 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Xn; R22 C; R34 N; R51-53 C; N R: 22-34-51/53 S: (1/2-)26-36/37/39-45-61 603-221-01-3 1-(2-amino-5-chlorophenyl)-2,2,2-trifluoro-1,1-ethanediol, hydrochloride; [containing ≥ 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Carc. Cat. 2; R45 [containing ≥ 0,1 % 4-chloroaniline (EC No 203-401-0)] 433-580-2 214353-17-0 Carc. Cat. 2; R45 Xn; R22 C; R34 N; R51-53 T; N … 45 unchanged lines … Xn; R48/20/21/22 C; R34 T; R: 23/24/25-34-48/20/21/22-68 S: (1/2-)24/25-26-28-36/37/39-45 T; R23/24/25: C ≥ 10 % Xn; R20/21/22: 3 % ≤ C < 10 % C; R34: C ≥ 3 % Xi; R36/38: 1 % ≤ C < 3 % 604-002-00-8 pentachlorophenol 201-778-6 87-86-5 Carc. Cat. 3; R40 S: (1/2-)24/25-26-28-36/37/39-45 T; R23/24/25: C ≥ 10 % Xn; R20/21/22: 3 % ≤ C < 10 % C; R34: C ≥ 3 % Xi; R36/38: 1 % ≤ C < 3 % 604-002-00-8 pentachlorophenol 201-778-6 87-86-5 Carc. Cat. 3; R40 T+; R26 T; R24/25 Xi; R36/37/38 … 20 unchanged lines … 1319-77-3 [4] T; R24/25 C; R34 T R: 24/25-34 S: (1/2-)36/37/39-45 T; R24/25: C ≥ 5 % Xn; R21/22: 1 % ≤ C < 5 % C; R34: C ≥ 5 % Xi; R36/38: 1 % ≤ C < 5 % C S: (1/2-)36/37/39-45 T; R24/25: C ≥ 5 % Xn; R21/22: 1 % ≤ C < 5 % C; R34: C ≥ 5 % Xi; R36/38: 1 % ≤ C < 5 % C 604-005-00-4 1,4-dihydroxybenzene; hydroquinone; quinol 204-617-8 123-31-9 Carc. Cat. 3; R40 Muta. Cat. 3; R68 Xn; R22 Xi; R41 R43 N; R50 Xn; N R: 22-40-41-43-68-50 S: (2-)26-36/37/39-61 N; R50: C ≥ 2,5 % 604-006-00-X 3,4-xylenol; [1] S: (2-)26-36/37/39-61 N; R50: C ≥ 2,5 % 604-006-00-X 3,4-xylenol; [1] 2,5-xylenol; [2] 2,4-xylenol; [3] 2,3-xylenol; [4] … 37 unchanged lines … Xn; R20/21/22 R52-53 Xn R: 20/21/22-68-52/53 S: (2-)36/37-61 Xn; R20/21/22: C ≥ 10 % 604-010-00-1 resorcinol; S: (2-)36/37-61 Xn; R20/21/22: C ≥ 10 % 604-010-00-1 resorcinol; 1,3-benzenediol 203-585-2 108-46-3 Xn; R22 Xi; R36/38 N; R50 Xn; N R: 22-36/38-50 S: (2-)26-61 Xn; R22: C ≥ 10 % 604-011-00-7 2,4-dichlorophenol 204-429-6 120-83-2 T; R24 S: (2-)26-61 Xn; R22: C ≥ 10 % 604-011-00-7 2,4-dichlorophenol 204-429-6 120-83-2 T; R24 Xn; R22 C; R34 N; R51-53 T; N R: 22-24-34-51/53 S: (1/2-)26-36/37/39-45-61 604-012-00-2 4-chloro-o-cresol; 4-chloro-2-methyl phenol 216-381-3 1570-64-5 T; R23 C; R35 N; R50 T; C; N R: 23-35-50 S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 604-013-00-8 2,3,4,6-tetrachlorophenol 200-402-8 58-90-2 T; R25 S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 604-013-00-8 2,3,4,6-tetrachlorophenol 200-402-8 58-90-2 T; R25 Xi; R36/38 N; R50-53 T; N R: 25-36/38-50/53 S: (1/2-)26-28-37-45-60-61 T; R25: C ≥ 5 % Xn; R22: 0,5 % ≤ C < 5 % Xi; R36/38: C ≥ 5 % 604-014-00-3 chlorocresol; S: (1/2-)26-28-37-45-60-61 T; R25: C ≥ 5 % Xn; R22: 0,5 % ≤ C < 5 % Xi; R36/38: C ≥ 5 % 604-014-00-3 chlorocresol; 4-chloro-m-cresol; 4-chloro-3-methylphenol 200-431-6 59-50-7 Xn; R21/22 Xi; R41 R43 N; R50 Xn; N R: 21/22-41-43-50 S: (2-)26-36/37/39-61 Xn; R21/22: C ≥ 10 % 604-015-00-9 2,2'-methylenebis-(3,4,6-trichlorophenol); S: (2-)26-36/37/39-61 Xn; R21/22: C ≥ 10 % 604-015-00-9 2,2'-methylenebis-(3,4,6-trichlorophenol); hexachlorophene 200-733-8 70-30-4 T; R24/25 N; R50-53 T; N R: 24/25-50/53 S: (1/2-)20-37-45-60-61 T; R24/25: C ≥ 2 % Xn; R21/22: 0,2 % ≤ C < 2 % 604-016-00-4 1,2-dihydroxybenzene; S: (1/2-)20-37-45-60-61 T; R24/25: C ≥ 2 % Xn; R21/22: 0,2 % ≤ C < 2 % 604-016-00-4 1,2-dihydroxybenzene; pyrocatechol 204-427-5 120-80-9 Xn; R21/22 Xi; R36/38 Xn R: 21/22-36/38 S: (2-)22-26-37 604-017-00-X 2,4,5-trichlorophenol 202-467-8 95-95-4 Xn; R22 Xi; R36/38 N; R50-53 Xn; N R: 22-36/38-50/53 S: (2-)26-28-60-61 Xn; R22: C ≥ 20 % Xi; R36/38: C ≥ 5 % 604-018-00-5 2,4,6-trichlorophenol 201-795-9 88-06-2 Carc. Cat. 3; R40 S: (2-)26-28-60-61 Xn; R22: C ≥ 20 % Xi; R36/38: C ≥ 5 % 604-018-00-5 2,4,6-trichlorophenol 201-795-9 88-06-2 Carc. Cat. 3; R40 Xn; R22 Xi; R36/38 N; R50-53 Xn; N … 189 unchanged lines … 5-chloro-2-(2,4-dichlorophenoxy)phenol 222-182-2 3380-34-5 Xi; R36/38 N; R50-53 Xi; N R: 36/38-50/53 S: 26-39-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 604-071-00-4 4,4'-(1-{]4-[}1-(4-hydroxyphenyl)-1-methylethyl{]phenyl[}ethylidene)diphenol 425-600-3 110726-28-8 R53 R: 53 S: 26-39-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 604-071-00-4 4,4'-(1-{]4-[}1-(4-hydroxyphenyl)-1-methylethyl{]phenyl[}ethylidene)diphenol 425-600-3 110726-28-8 R53 R: 53 S: 61 604-072-00-X 1,2-bis(phenoxymethyl)benzene 428-620-0 10403-74-4 N; R50-53 N R: 50/53 S: 22-60-61 604-073-00-5 (E)-3-[1-[4-[2-(dimethylamino)ethoxy]phenyl]-2-phenylbut-1-enyl]phenol 428-010-4 82413-20-5 Carc. Cat. 3; R40 Repr. Cat. 2; R60 R43 N; R50-53 T; N R: 60-40-43-50/53 S: 53-45-60-61 604-074-00-0 tetrabromobisphenol-A; 2,2', 6,6'-tetrabromo-4,4'-isopropylidenediphenol 201-236-9 79-94-7 N; R50-53 N R: 50/53 S: 60-61 604-075-00-6 4-(1,1,3,3-tetramethylbutyl)phenol; 4-tert-octylphenol 205-426-2 140-66-9 Xi; R38-41 N; R50-53 Xi; N R: 38-41-50/53 S: (2-)26-37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 604-076-00-1 phenolphthalein 201-004-7 77-09-8 Carc. Cat. 2; R45 S: (2-)26-37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 604-076-00-1 phenolphthalein 201-004-7 77-09-8 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Repr. Cat. 3; R62 T R: 45-62-68 S: 53-45 Carc. Cat. 2; R45: C ≥ 1 % 604-077-00-7 2-benzotriazol-2-yl-4-methyl-6-(2-methylallyl)phenol 419-750-9 98809-58-6 R53 R: 53 S: 53-45 Carc. Cat. 2; R45: C ≥ 1 % 604-077-00-7 2-benzotriazol-2-yl-4-methyl-6-(2-methylallyl)phenol 419-750-9 98809-58-6 R53 R: 53 S: 61 604-079-00-8 4,4'-(1,3-phenylene-bis(1-methylethylidene))bis-phenol 428-970-4 13595-25-0 Repr. Cat.3; R62 R43 N; R51-53 Xn; N … 31 unchanged lines … R67 N; R50-53 Xn; N R: 10-36/38-43-48/20/22-63-65-67-50/53 S: (2-)26-36/37-62-60-61 605-001-00-5 formaldehyde … % 200-001-8 50-00-0 Carc. Cat. 3; R40 S: (2-)26-36/37-62-60-61 604-090-00-8 4-tert-butylphenol 202-679-0 98-54-4 Repr. Cat. 3; R62 Xi; R38-41 Xn R: 38-41-62 S: (2-)26-36/37/39-46 604-091-00-3 etofenprox (ISO); 2-(4-ethoxyphenyl)-2-methylpropyl 3-phenoxybenzyl ether 407-980-2 80844-07-1 R64 N; R50-53 N R: 50/53-64 S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 605-001-00-5 formaldehyde …% 200-001-8 50-00-0 Carc. Cat. 2; R45 Muta. Cat. 3; R68 T; R23/24/25 C; R34 R43 T R: 23/24/25-34-40-43 S: (1/2-)26-36/37/39-45-51 T; R23/24/25: C ≥25 % Xn; R20/21/22: 5 % ≤ C < 25 % C; R34: C ≥25 % Xi; R36/37/38: 5 % ≤ C < 25 % R43: C ≥ 0,2 % B D R: 23/24/25-34-43-45-68 S: 45-53 T; R23/24/25: C ≥ 25 % Xn; R20/21/22: 5 % ≤ C < 25 % C; R34: C ≥ 25 % Xi; R36/37/38: 5 % ≤ C < 25 % R43: C ≥ 0,2 % B, D 605-002-00-0 1,3,5-trioxan; trioxymethylene 203-812-5 110-88-3 F; R11 Repr. Cat. 3; R63 … 23 unchanged lines … C; R34 N; R50 F; T+; N R: 11-24-26/28-34-50 S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 0,1 % N; R50: C ≥ 0,25 % D S: (1/2-)23-26-28-36/37/39-45-61 C; R34: C ≥ 0,1 % N; R50: C ≥ 0,25 % D 605-009-00-9 crotonaldehyde; 2-butenal; [1] (E)-2-butenal; … 30 unchanged lines … acetal 203-310-6 105-57-7 F; R11 Xi; R36/38 F; Xi R: 11-36/38 S: (2-)9-16-33 Xi; R36/38: C ≥ 10 % 605-016-00-7 glyoxal … %; S: (2-)9-16-33 Xi; R36/38: C ≥ 10 % 605-016-00-7 glyoxal … %; ethandial … % 203-474-9 107-22-2 Muta. Cat. 3; R68 Xn; R20 Xi; R36/38 R43 Xn R: 20-36/38-43-68 S: (2-)36/37 Xn; R20: C ≥ 10 % Xi; R36/38: C ≥ 10 % B S: (2-)36/37 Xn; R20: C ≥ 10 % Xi; R36/38: C ≥ 10 % B 605-017-00-2 1,3-dioxolane 211-463-5 646-06-0 F; R11 F R: 11 S: (2-)16 605-018-00-8 propanal; … 18 unchanged lines … R42/43 N; R50 T; N R: 23/25-34-42/43-50 S: (1/2-)26-36/37/39-45-61 T; R25: C ≥ 50 % Xn; R22: 2 % ≤ C < 50 % T; R23: C ≥ 25 % Xn; R20: 2 % ≤ C < 25 % C; R34: C ≥ 10 % Xi; R37/38-41: 2 % ≤ C < 10 % Xi; R36/37/38: 0,5 % ≤ C < 2 % R43: C ≥ 0,5 % 605-023-00-5 5-chloro-2-(4-chlorophenoxy)phenol 429-290-0 3380-30-1 Xi; R41 S: (1/2-)26-36/37/39-45-61 T; R25: C ≥ 50 % Xn; R22: 2 % ≤ C < 50 % T; R23: C ≥ 25 % Xn; R20: 2 % ≤ C < 25 % C; R34: C ≥ 10 % Xi; R37/38-41: 2 % ≤ C < 10 % Xi; R36/37/38: 0,5 % ≤ C < 2 % R43: C ≥ 0,5 % 605-023-00-5 5-chloro-2-(4-chlorophenoxy)phenol 429-290-0 3380-30-1 Xi; R41 N; R50-53 Xi; N R: 41-50/53 S: (2-)26-39-60-61 605-024-00-0 2-bromo-5-hydroxy-4-methoxybenzaldehyde 426-540-0 2973-59-3 R43 … 20 unchanged lines … R: 43-51/53 S: (2-)24-37-61 605-030-00-3 1-(p-methoxyphenyl)acetaldehyde oxime 411-510-1 3353-51-3 R43 Xi R: 43 S: (2-)24-37 605-031-00-9 reaction mass of: 2,2-dimethoxyethanal [(this component is considered to be anhydrous in terms of identity, structure and composition. However, 2,2-dimethoxyethanal will exist in a hydrated form. 60 % anhydrous is equivalent to 70.4 % hydrate; S: (2-)24-37 605-031-00-9 reaction mass of: 2,2-dimethoxyethanal [(this component is considered to be anhydrous in terms of identity, structure and composition. However, 2,2-dimethoxyethanal will exist in a hydrated form. 60 % anhydrous is equivalent to 70.4 % hydrate; water(Including free water and water in hydrated 2,2-dimethoxyethanal)] 421-890-0 — R43 Xi R: 43 S: (2-)24-37 605-032-00-4 3-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-(E)-2-propenal 425-370-4 93957-50-7 R43 … 54 unchanged lines … di-isobutyl ketone 203-620-1 108-83-8 R10 Xi; R37 Xi R: 10-37 S: (2-)24 Xi; R37: C ≥ 10 % 606-006-00-5 pentan-3-one; S: (2-)24 Xi; R37: C ≥ 10 % 606-006-00-5 pentan-3-one; diethyl ketone 202-490-3 96-22-0 F; R11 Xi; R37 R66 R67 F; Xi R: 11-37-66-67 S: (2-)9-16-25-33 606-007-00-0 3-methylbutan-2-one; methyl isopropyl ketone 209-264-3 563-80-4 F; R11 F R: 11 S: (2-)9-16-33 606-009-00-1 4-methylpent-3-en-2-one; mesityl oxide 205-502-5 141-79-7 R10 Xn; R20/21/22 Xn R: 10-20/21/22 S: (2-)25 Xn; R20/21/22: C ≥ 5 % 606-010-00-7 cyclohexanone 203-631-1 108-94-1 R10 S: (2-)25 Xn; R20/21/22: C ≥ 5 % 606-010-00-7 cyclohexanone 203-631-1 108-94-1 R10 Xn; R20 Xn R: 10-20 S: (2-)25 606-011-00-2 2-methylcyclohexanone 209-513-6 583-60-8 R10 Xn; R20 Xn R: 10-20 S: (2-)25 606-012-00-8 3,5,5-trimethylcyclohex-2-enone; isophorone 201-126-0 78-59-1 Carc. Cat. 3; R40 Xn; R21/22 Xi; R36/37 Xn R: 21/22-36/37-40 S: (2-)13-23-36/37/39-46 Xi; R36/37: C ≥ 10 % 606-013-00-3 p-benzoquinone; S: (2-)13-23-36/37/39-46 Xi; R36/37: C ≥ 10 % 606-013-00-3 p-benzoquinone; quinone 203-405-2 106-51-4 T; R23/25 Xi; R36/37/38 N; R50 T; N R: 23/25-36/37/38-50 S: (1/2-)26-28-45-61 N; R50: C ≥ 2,5 % 606-014-00-9 chlorophacinone (ISO); S: (1/2-)26-28-45-61 N; R50: C ≥ 2,5 % 606-014-00-9 chlorophacinone (ISO); 2-(2-(4-chlorophenyl)phenylacetyl)indan-1,3-dione 223-003-0 3691-35-8 T+; R27/28 T; R23-48/24/25 N; R50-53 T+; N … 21 unchanged lines … S: (1/2-)22-36/37-45-60-61 606-020-00-1 5-methylheptan-3-one 208-793-7 541-85-5 R10 Xi; R36/37 Xi R: 10-36/37 S: (2-)23 Xi; R36/37: C ≥ 10 % 606-021-00-7 N-methyl-2-pyrrolidone; S: (2-)23 Xi; R36/37: C ≥ 10 % 606-021-00-7 N-methyl-2-pyrrolidone; 1-methyl-2-pyrrolidone 212-828-1 872-50-4 Repr. Cat. 2; R61 Xi; R36/37/38 T R: 61-36/37/38 S: 53-45 Repr. Cat. 2; R61: C ≥ 5 % Xi; R36/37/38: C ≥ 10 % 606-022-00-2 1-phenyl-3-pyrazolidone 202-155-1 92-43-3 Xn; R22 S: 53-45 Repr. Cat. 2; R61: C ≥ 5 % Xi; R36/37/38: C ≥ 10 % 606-022-00-2 1-phenyl-3-pyrazolidone 202-155-1 92-43-3 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-)61 606-023-00-8 4-methoxy-4-methylpentan-2-one 203-512-4 107-70-0 R10 … 49 unchanged lines … 4-amino-4,5-dihydro-6-(1,1-dimethylethyl)-3-methylthio-1,2,4-triazin-5-one 244-209-7 21087-64-9 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 606-035-00-3 chloridazon (ISO); S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 606-035-00-3 chloridazon (ISO); 5-amino-4-chloro-2-phenylpyridazine-3-(2H)-one; pyrazon 216-920-2 1698-60-8 R43 N; R50-53 Xi; N … 305 unchanged lines … R43 N; R50-53 Xn; N R: 10-22-38-41-43-48/22-50/53 S: (2-)23-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 606-139-00-9 (S)-4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one 444-830-5 124379-29-9 R53 R: 53 S: (2-)23-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 606-139-00-9 (S)-4-(3,4-dichlorophenyl)-3,4-dihydro-2H-naphthalen-1-one 444-830-5 124379-29-9 R53 R: 53 S: 61 606-140-00-4 2-hydroxy-1-(4-(4-(2-hydroxy-2-methylpropionyl)benzyl)phenyl)-2-methylpropan-1-one 444-860-9 474510-57-1 Xn; R48/22 N; R50-53 Xn; N R: 48/22-50/53 S: (2-)22-36-60-61 606-141-00-X sodium 3-(methoxycarbonyl)-4-oxo-3,4,5,6-tetrahydro-2-pyridinolate 418-410-7 - Xi; R36 Xi R: 36 S: (2-)26 606-142-00-5 reaction mass of: (1RS, 2SR, 7SR, 8SR, E) 9 and 10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; S: (2-)26 606-142-00-5 reaction mass of: (1RS, 2SR, 7SR, 8SR, E) 9 and 10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; (1RS, 2SR, 7SR, 8SR, Z)-10-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one; (1RS, 2SR, 7SR, 8SR, Z)-9-ethylidene-3-oxatricyclo[6.2.1.0(2,7)]undecan-4-one 434-290-9 - Xn; R22 N; R51-53 Xn; N … 21 unchanged lines … R43 N; R50-53 Xn; N R: 43-48/22-63-50/53 S: (2-)22-36/37-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C< 2,5 % R43: C ≥ 0,1 % 607-001-00-0 formic acid … % 200-579-1 64-18-6 C; R35 C S: (2-)22-36/37-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C< 2,5 % R43: C ≥ 0,1 % 606-146-00-7 tralkoxydim (ISO); 2-(N-ethoxypropanimidoyl)-3-hydroxy-5-mesitylcyclohex-2-en-1-one – 87820-88-0 Carc. Cat. 3; R40 Xn; R22 N; R51-53 Xn; N R: 22-40-51/53 S: (2-)36/37-60-61 606-147-00-2 cycloxydim (ISO); 2-(N-ethoxybutanimidoyl)-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)cyclohex-2-en-1-one 405-230-9 101205-02-1 F; R11 Repr. Cat. 3; R63 F; Xn R: 11-63 S: (2-)16-36/37-46 607-001-00-0 formic acid … % 200-579-1 64-18-6 C; R35 C R: 35 S: (1/2-)23-26-45 C; R35: C ≥ 90 % C; R34: 10 % ≤ C < 90 % Xi; R36/38: 2 % ≤ C < 10 % B S: (1/2-)23-26-45 C; R35: C ≥ 90 % C; R34: 10 % ≤ C < 90 % Xi; R36/38: 2 % ≤ C < 10 % B 607-002-00-6 acetic acid … % 200-580-7 64-19-7 R10 C; R35 C R: 10-35 S: (1/2-)23-26-45 C; R35: C ≥ 90 % C; R34: 25 % ≤ C < 90 % Xi; R36/38: 10 % ≤ C < 25 % B S: (1/2-)23-26-45 C; R35: C ≥ 90 % C; R34: 25 % ≤ C < 90 % Xi; R36/38: 10 % ≤ C < 25 % B 607-003-00-1 chloroacetic acid 201-178-4 79-11-8 T; R23/24/25 C; R34 N; R50 T; N R: 23/24/25-34-50 S: (1/2-)26-36/37/39-45-61-63 C; R34: C ≥ 10 % Xn; R36/37/38: 5 % ≤ C < 10 % 607-004-00-7 TCA (ISO); S: (1/2-)26-36/37/39-45-61-63 C; R34: C ≥ 10 % Xn; R36/37/38: 5 % ≤ C < 10 % 607-004-00-7 TCA (ISO); trichloroacetic acid 200-927-2 76-03-9 C; R35 N; R50-53 C; N R: 35-50/53 S: (1/2-)26-36/37/39-45-60-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 607-005-00-2 TCA-sodium (ISO); S: (1/2-)26-36/37/39-45-60-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 607-005-00-2 TCA-sodium (ISO); sodium trichloroacetate 211-479-2 650-51-1 Xi; R37 N; R50-53 Xi; N R: 37-50/53 S: (2-)46-60-61 607-006-00-8 oxalic acid 205-634-3 144-62-7 Xn; R21/22 Xn R: 21/22 S: (2-)24/25 Xn; R21/22: C ≥ 5 % 607-007-00-3 salts of oxalic acid with the exception of those specified elsewhere in this Annex — — Xn; R21/22 Xn S: (2-)24/25 Xn; R21/22: C ≥ 5 % 607-007-00-3 salts of oxalic acid with the exception of those specified elsewhere in this Annex — — Xn; R21/22 Xn R: 21/22 S: (2-)24/25 Xn; R21/22: C ≥ 5 % A S: (2-)24/25 Xn; R21/22: C ≥ 5 % A 607-008-00-9 acetic anhydride 203-564-8 108-24-7 R10 Xn; R20/22 C; R34 C R: 10-20/22-34 S: (1/2-)26-36/37/39-45 C; R34: C ≥ 25 % Xi; R37/38-41: 5 % ≤ C < 25 % Xi; R36: 1 % ≤ C < 5 % 607-009-00-4 phthalic anhydride 201-607-5 85-44-9 Xn; R22 S: (1/2-)26-36/37/39-45 C; R34: C ≥ 25 % Xi; R37/38-41: 5 % ≤ C < 25 % Xi; R36: 1 % ≤ C < 5 % 607-009-00-4 phthalic anhydride 201-607-5 85-44-9 Xn; R22 Xi; R37/38-41 R42/43 Xn R: 22-37/38-41-42/43 S: (2-)23-24/25-26-37/39-46 607-010-00-X propionic anhydride 204-638-2 123-62-6 C; R34 C R: 34 S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % 607-011-00-5 acetyl chloride 200-865-6 75-36-5 F; R11 S: (1/2-)26-45 C; R34: C ≥ 25 % Xi; R36/38: 10 % ≤ C < 25 % 607-011-00-5 acetyl chloride 200-865-6 75-36-5 F; R11 R14 C; R34 F; C R: 11-14-34 … 113 unchanged lines … Xi; R36/37/38 R43 F; Xn R: 11-20/21/22-36/37/38-43 S: (2-)9-16-33-36/37 Xi; 36/37/38: C ≥ 5 % D S: (2-)9-16-33-36/37 Xi; 36/37/38: C ≥ 5 % D 607-033-00-5 n-butyl methacrylate 202-615-1 97-88-1 R10 Xi; R36/37/38 R43 Xi … 88 unchanged lines … Xi; R38-41 N; R50-53 Xn; N R: 22-38-41-50/53 S: (2-)13-26-37/39-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-050-00-8 salts of mecoprop — — Xn; R22 S: (2-)13-26-37/39-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-050-00-8 salts of mecoprop — — Xn; R22 Xi; R38-41 N; R50-53 Xn; N R: 22-38-41-50/53 S: (2-)13-26-37/39-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % A S: (2-)13-26-37/39-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % A 607-051-00-3 MCPA (ISO); 4-chloro-o-tolyloxyacetic acid 202-360-6 94-74-6 Xn; R22 Xi; R38-41 … 51 unchanged lines … C; R35 N; R50 C; N R: 10-20/21/22-35-50 S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % D S: (1/2-)26-36/37/39-45-61 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % D 607-062-00-3 n-butyl acrylate 205-480-7 141-32-2 R10 Xi; R36/37/38 R43 Xi R: 10-36/37/38-43 S: (2-)9 D 607-063-00-9 isobutyric acid 201-195-7 79-31-2 Xn; R21/22 Xn R: 21/22 S: (2-) 607-064-00-4 benzyl chloroformate 207-925-0 501-53-1 C; R34 N; R50-53 C; N R: 34-50/53 S: (1/2-)26-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 607-065-00-X bromoacetic acid 201-175-8 79-08-3 T; R23/24/25 S: (1/2-)26-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 607-065-00-X bromoacetic acid 201-175-8 79-08-3 T; R23/24/25 C; R35 R43 N; R50 T; C; N … 22 unchanged lines … R43 N; R50 T; N R: 24-34-43-50 S: (1/2-)26-36/39-45-61 T; R24: C ≥ 2 % Xn; R21: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D S: (1/2-)26-36/39-45-61 T; R24: C ≥ 2 % Xn; R21: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D 607-073-00-3 4-CPA (ISO); 4-chlorophenoxyacetic acid 204-581-3 122-88-3 Xn; R22 Xn R: 22 … 56 unchanged lines … 2-methylpropenoic acid 201-204-4 79-41-4 Xn; R21/22 C; R35 C R: 21/22-35 S: (1/2-)26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % D S: (1/2-)26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % D 607-089-00-0 propionic acid … % 201-176-3 79-09-4 C; R34 C R: 34 S: (1/2-)23-36-45 C; R34: C ≥ 25 % Xi; R36/37/38: 10 % ≤ C < 25 % B S: (1/2-)23-36-45 C; R34: C ≥ 25 % Xi; R36/37/38: 10 % ≤ C < 25 % B 607-090-00-6 thioglycolic acid 200-677-4 68-11-1 T; R23/24/25 C; R34 T R: 23/24/25-34 S: (1/2-)25-27-28-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % 607-091-00-1 trifluoroacetic acid . . . % 200-929-3 76-05-1 Xn; R20 S: (1/2-)25-27-28-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % 607-091-00-1 trifluoroacetic acid . . . % 200-929-3 76-05-1 Xn; R20 C; R35 R52-53 C R: 20-35-52/53 S: (1/2-)9-26-27-28-45-61 Xn; R20: C ≥ 10 % B S: (1/2-)9-26-27-28-45-61 Xn; R20: C ≥ 10 % B 607-092-00-7 methyl lactate; [1] methyl (±)-lactate; [2] methyl (R)-lactate; [3] methyl (S)-(-)-lactate [4] 208-930-0 [1] 218-449-8 [2] 241-420-6 [3] 248-704-9 [4] 547-64-8 [1] 2155-30-8 [2] 17392-83-5 [3] 27871-49-4 [4] R10 Xi; R36/37 Xi R: 10-36/37 S: (2-)24 C 607-093-00-2 propionyl chloride 201-170-0 79-03-8 F; R11 R14 C; R34 F; C R: 11-14-34 S: (1/2-)9-16-26-45 B D 607-094-00-8 peracetic acid . . . % 201-186-8 79-21-0 R10 607-094-00-8 peracetic acid . . . % 201-186-8 79-21-0 R10 O; R7 Xn; R20/21/22 C; R35 N; R50 O; C; N R: 7-10-20/21/22-35-50 S: (1/2-)3/7-14-36/37/39-45-61 Xn; R20/21/22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % B D S: (1/2-)3/7-14-36/37/39-45-61 Xn; R20/21/22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % B D 607-095-00-3 maleic acid 203-742-5 110-16-7 Xn; R22 Xi; R36/37/38 R43 Xn R: 22-36/37/38-43 S: (2-)24-26-28-37-46 R43: C ≥ 0,1 % 607-096-00-9 maleic anhydride 203-571-6 108-31-6 Xn; R22 S: (2-)24-26-28-37-46 R43: C ≥ 0,1 % 607-096-00-9 maleic anhydride 203-571-6 108-31-6 Xn; R22 C; R34 R42/43 C R: 22-34-42/43 … 23 unchanged lines … 607-100-00-9 benzophenone-3,3',4,4'-tetracarboxylic dianhydride; 4,4'-carbonyldi(phthalic anhydride) 219-348-1 2421-28-5 Xi; R36/37 Xi R: 36/37 S: (2-)25 Xi; R36/37: C ≥ 1 % 607-101-00-4 1,4,5,6,7,7-hexachlorobicyclo [2,2,1]hept-5-ene-2,3-dicarboxylic anhydride chlorendic anhydride 204-077-3 115-27-5 Xi; R36/37/38 Xi S: (2-)25 Xi; R36/37: C ≥ 1 % 607-101-00-4 1,4,5,6,7,7-hexachlorobicyclo [2,2,1]hept-5-ene-2,3-dicarboxylic anhydride chlorendic anhydride 204-077-3 115-27-5 Xi; R36/37/38 Xi R: 36/37/38 S: (2-)25 Xi; R36/37/38: C ≥ 1 % 607-102-00-X cyclohexane-1,2-dicarboxylic anhydride; [1] S: (2-)25 Xi; R36/37/38: C ≥ 1 % 607-102-00-X cyclohexane-1,2-dicarboxylic anhydride; [1] cis-cyclohexane-1,2-dicarboxylic anhydride; [2] trans-cyclohexane-1,2-dicarboxylic anhydride [3] 201-604-9 [1] 236-086-3 [2] 238-009-9 [3] 85-42-7 [1] 13149-00-3 [2] 14166-21-3 [3] Xi; R41 R42/43 Xn R: 41-42/43 S: (2-)23-24-26-37/39 C 607-103-00-5 succinic anhydride 203-570-0 108-30-5 Xn; R22 Xi; R36/37 Xn R: 22-36/37 S: (2-)25-46 Xn; R22: C ≥ 5 % Xi; R36/37: C ≥ 1 % 607-104-00-0 cyclopentane-1,2,3,4-tetracarboxylic dianhydride 227-964-7 6053-68-5 Xi; R36/37 Xi S: (2-)25-46 Xn; R22: C ≥ 5 % Xi; R36/37: C ≥ 1 % 607-104-00-0 cyclopentane-1,2,3,4-tetracarboxylic dianhydride 227-964-7 6053-68-5 Xi; R36/37 Xi R: 36/37 S: (2-)25 Xi; R36/37: C ≥ 1 % 607-105-00-6 8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride; [1] S: (2-)25 Xi; R36/37: C ≥ 1 % 607-105-00-6 8,9,10-trinorborn-5-ene-2,3-dicarboxylic anhydride; [1] 1,2,3,6-tetrahydro-3,6-methanophthalic anhydride; [2] (1α,2α,3β,6β)-1,2,3,6-tetrahydro-3,6-methanophthalic anhydride [3] 204-957-7 [1] 212-557-9 [2] 220-384-5 [3] 129-64-6 [1] 826-62-0 [2] 2746-19-2 [3] Xi; R41 R42/43 Xn R: 41-42/43 S: (2-)22-24-26-37/39 C 607-106-00-1 8,9-dinorborn-5-ene-2,3-dicarboxylic anhydride — 123748-85-6 Xn; R22 Xi; R36/37/38 R42 Xn R: 22-36/37/38-42 S: (2-)39 Xi; R36/37/38: C ≥ 10 % C S: (2-)39 Xi; R36/37/38: C ≥ 10 % C 607-107-00-7 2-ethylhexyl acrylate 203-080-7 103-11-7 Xi; R37/38 R43 Xi R: 37/38-43 S: (2-)36/37-46 D 607-108-00-2 2-hydroxy-1-methylethylacrylate; [1] 2-hydroxypropylacrylate; [2] acrylic acid, monoester with propane-1,2-diol [3] 220-852-9 [1] 213-663-8 [2] 247-118-0 [3] 2918-23-2 [1] 999-61-1 [2] 25584-83-2 [3] T; R23/24/25 C; R34 R43 T R: 23/24/25-34-43 S: (1/2-)26-36/37/39-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % C D S: (1/2-)26-36/37/39-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % C D 607-109-00-8 hexamethylene diacrylate; hexane-1,6-diol diacrylate 235-921-9 13048-33-4 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)39 D 607-110-00-3 pentaerythritol triacrylate 222-540-8 3524-68-3 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)39 D 607-111-00-9 2,2-bis(acryloyloxymethyl)butyl acrylate; trimethylolpropane triacrylate 239-701-3 15625-89-5 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)39 D 607-112-00-4 2,2-dimethyltrimethylene diacrylate; neopentyl glycol diacrylate 218-741-5 2223-82-7 T; R24 Xi; R36/38 R43 T R: 24-36/38-43 S: (1/2-)28-39-45 T; R24: C ≥ 5 % Xn; R21: 0,2 % ≤ C < 5 % D S: (1/2-)28-39-45 T; R24: C ≥ 5 % Xn; R21: 0,2 % ≤ C < 5 % D 607-113-00-X isobutyl methacrylate 202-613-0 97-86-9 R10 Xi; R36/37/38 R43 N; R50 Xi; N R: 10-36/37/38-43-50 S: (2-)24-37-61 D 607-114-00-5 ethylene dimethacrylate 202-617-2 97-90-5 Xi; R37 R43 Xi R: 37-43 S: (2-)24-37 Xi; R37: C ≥ 10 % D S: (2-)24-37 Xi; R37: C ≥ 10 % D 607-115-00-0 isobutyl acrylate 203-417-8 106-63-8 R10 Xn; R20/21 Xi; R38 R43 Xn R: 10-20/21-38-43 S: (2-)9-24-37 Xi; R38: C ≥ 10 % D S: (2-)9-24-37 Xi; R38: C ≥ 10 % D 607-116-00-6 cyclohexyl acrylate 221-319-3 3066-71-5 Xi; R37/38 N; R51-53 Xi; N R: 37/38-51/53 S: (2-)61 Xi; R37/38: C ≥ 10 % D S: (2-)61 Xi; R37/38: C ≥ 10 % D 607-117-00-1 2,3-epoxypropyl acrylate; glycidyl acrylate 203-440-3 106-90-1 T; R23/24/25 C; R34 R43 T R: 23/24/25-34-43 S: (1/2-)26-36/37/39-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D S: (1/2-)26-36/37/39-45 T; R23/24/25: C ≥ 2 % Xn; R20/21/22: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D 607-118-00-7 1-methyltrimethylene diacrylate; 1,3-butylene glycol diacrylate 243-105-9 19485-03-1 Xn; R21 C; R34 R43 C R: 21-34-43 S: (1/2-)26-36/37/39-45 D 607-119-00-2 tetramethylene diacrylate; 1,4-butyleneglycol diacrylate 213-979-6 1070-70-8 Xn; R21 C; R34 R43 C R: 21-34-43 S: (1/2-)26-36/37/39-45 D 607-120-00-8 2,2'-oxydiethyl diacrylate; diethylene glycol diacrylate 223-791-6 4074-88-8 T; R24 Xi; R36/38 R43 T R: 24-36/38-43 S: (1/2-)28-39-45 T; R24: C ≥ 2 % Xn; R21: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D S: (1/2-)28-39-45 T; R24: C ≥ 2 % Xn; R21: 0,2 % ≤ C < 2 % R43: C ≥ 0,2 % D 607-121-00-3 8,9,10-trinorborn-2-yl acrylate — 10027-06-2 Xn; R21 Xi; R38 R43 Xn R: 21-38-43 S: (2-)28 Xi; R38: C ≥ 10 % D S: (2-)28 Xi; R38: C ≥ 10 % D 607-122-00-9 pentaerythritol tetraacrylate 225-644-1 4986-89-4 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)26-39 D 607-123-00-4 2,3-epoxypropyl methacrylate; glycidyl methacrylate 203-441-9 106-91-2 Xn; R20/21/22 Xi; R36/38 R43 Xn R: 20/21/22-36/38-43 S: (2-)26-28 Xi; R36/38: C ≥ 10 % D S: (2-)26-28 Xi; R36/38: C ≥ 10 % D 607-124-00-X 2-hydroxyethyl methacrylate 212-782-2 868-77-9 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)26-28 D 607-125-00-5 2-hydroxypropyl methacrylate; [1] 3-hydroxypropyl methacrylate [2] 213-090-3 [1] 220-426-2 [2] 923-26-2 [1] 2761-09-3 [2] Xi; R36 R43 Xi R: 36-43 S: (2-)24/25-26-37/39 C D 607-126-00-0 2,2'-(ethylenedioxy)diethyl diacrylate; triethylene glycol diacrylate 216-853-9 1680-21-3 Xi; R36/38 R43 Xi R: 36/38-43 S: (2-)26-28 D 607-127-00-6 2-diethylaminoethyl methacrylate 203-275-7 105-16-8 Xn; R20 Xi; R36/38 R43 Xn R: 20-36/38-43 S: (2-)26 Xi; R36/38: C ≥ 10 % D S: (2-)26 Xi; R36/38: C ≥ 10 % D 607-128-00-1 2-tert-butylaminoethyl methacrylate 223-228-4 3775-90-4 Xi; R36/38 R43 Xi R: 36/38-43 … 35 unchanged lines … Xi; R36/38 R43 Xn R: 21/22-36/38-43 S: (2-)26-28 Xi; R36/38: C ≥ 10 % D S: (2-)26-28 Xi; R36/38: C ≥ 10 % D 607-133-00-9 monoalkyl or monoaryl or monoalkylaryl esters of acrylic acid with the exception of those specified elsewhere in this Annex — — Xi; R36/37/38 N; R51-53 Xi; N R: 36/37/38-51/53 S: (2-)26-28-61 Xi; R36/37/38: C ≥ 10 % A S: (2-)26-28-61 Xi; R36/37/38: C ≥ 10 % A 607-134-00-4 monoalkyl or monoaryl or monoalkyaryl esters of methacrylic acid with the exception of those specified elsewhere in this Annex — — Xi; R36/37/38 Xi R: 36/37/38 S: (2-)26-28 Xi; R36/37/38: C ≥ 10 % A S: (2-)26-28 Xi; R36/37/38: C ≥ 10 % A 607-135-00-X butyric acid 203-532-3 107-92-6 C; R34 C R: 34 S: (1/2-)26-36-45 607-136-00-5 butyryl chloride 205-498-5 141-75-3 F; R11 … 53 unchanged lines … Xi; R38-41 N; R50-53 T; N R: 23-38-40-41-50/53 S: (1/2-)26-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 607-152-00-2 2,3,6-TBA (ISO); S: (1/2-)26-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 607-152-00-2 2,3,6-TBA (ISO); 2,3,6-trichlorobenzoic acid 200-026-4 50-31-7 Xn; R22 N; R51-53 Xn; N R: 22-51/53 … 92 unchanged lines … methyl 2-[N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-N-methylcarbamoylsulfamoyl]benzoate 401-190-1 101200-48-0 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-178-00-4 methyl α-((4,6-dimethoxypyrimidin-2-yl)ureidosulphonyl)-o-toluate 401-340-6 83055-99-6 R43 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-178-00-4 methyl α-((4,6-dimethoxypyrimidin-2-yl)ureidosulphonyl)-o-toluate 401-340-6 83055-99-6 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 607-179-00-X (benzothiazol-2-ylthio)succinic acid 401-450-4 95154-01-1 R43 Xi … 31 unchanged lines … S: (2-)24-37-61 607-189-00-4 trimethylenediaminetetraacetic acid 400-400-9 1939-36-2 Xn; R22 Xi; R41 Xn R: 22-41 S: (2-)22-26-39 607-190-00-X methyl acrylamidomethoxyacetate (containing ≥ 0,1 % acrylamid) 401-890-7 77402-03-0 Carc. Cat. 2; R45 S: (2-)22-26-39 607-190-00-X methyl acrylamidomethoxyacetate (containing ≥ 0,1 % acrylamid) 401-890-7 77402-03-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R22 Xi; R36 T … 50 unchanged lines … R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)36/37-60-61 607-210-00-7 methyl acrylamidoglycolate (containing ≥ 0,1 % acrylamide) 403-230-3 77402-05-2 Carc. Cat. 2; R45 S: (2-)36/37-60-61 607-210-00-7 methyl acrylamidoglycolate (containing ≥ 0,1 % acrylamide) 403-230-3 77402-05-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 C; R34 R43 T R: 45-46-34-43 S: 53-45 607-211-00-2 methyl 3-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate 403-270-1 6386-39-6 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-)36-61 607-212-00-8 poly(oxypropylenecarbonyl-co-oxy(ethylethylene)carbonyl), containing 27 % hydroxyvalerate 403-300-3 — R43 Xi S: (2-)36-61 607-212-00-8 poly(oxypropylenecarbonyl-co-oxy(ethylethylene)carbonyl), containing 27 % hydroxyvalerate 403-300-3 — R43 Xi R: 43 S: (2-)24-37 607-213-00-3 ethyl 3,3-bis(tert-pentylperoxy)butyrate 403-320-2 67567-23-1 E; R3 O; R7 … 77 unchanged lines … S: 61 607-235-00-3 mecrilate; methyl 2-cyanoacrylate 205-275-2 137-05-3 Xi; R36/37/38 Xi R: 36/37/38 S: (2-)23-24/25-26 Xi; R36/37/38: C ≥ 10 % 607-236-00-9 ethyl 2-cyanoacrylate 230-391-5 7085-85-0 Xi; R36/37/38 Xi S: (2-)23-24/25-26 Xi; R36/37/38: C ≥ 10 % 607-236-00-9 ethyl 2-cyanoacrylate 230-391-5 7085-85-0 Xi; R36/37/38 Xi R: 36/37/38 S: (2-)23-24/25-26 Xi; R36/37/38: C ≥ 10 % 607-237-00-4 benzyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate; S: (2-)23-24/25-26 Xi; R36/37/38: C ≥ 10 % 607-237-00-4 benzyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate; flurazole 276-942-3 72850-64-7 N; R51-53 N R: 51/53 S: 61 607-238-00-X tau-fluvalinate (ISO); … 56 unchanged lines … S: 61 607-244-00-2 isooctyl acrylate 249-707-8 29590-42-9 Xi; R36/37/38 N; R50-53 Xi; N R: 36/37/38-50/53 S: (2-)26-28-60-61 Xi; R36/37/38: C ≥ 10 % 607-245-00-8 tert-butyl acrylate 216-768-7 1663-39-4 F; R11 S: (2-)26-28-60-61 Xi; R36/37/38: C ≥ 10 % 607-245-00-8 tert-butyl acrylate 216-768-7 1663-39-4 F; R11 Xn; R20/21/22 Xi; R37/38 R43 N; R51-53 F; Xn; N R: 11-20/21/22-37/38-43-51/53 S: (2-)16-25-37-61 D 607-246-00-3 allyl methacrylate; 2-methyl-2-propenoic acid 2-propenyl ester 202-473-0 96-05-9 R10 T; R23 Xn; R21/22 N; R50 T; N R: 10-21/22-23-50 S: (1/2-)36/37-45-61 607-247-00-9 dodecyl methacrylate 205-570-6 142-90-5 Xi; 36/37/38 N; R50-53 Xi; N R: 36/37/38-50/53 S: (2-)26-28-60-61 Xi; R36/37/38: C ≥ 10 % 607-248-00-4 naptalam-sodium (ISO); S: (2-)26-28-60-61 Xi; R36/37/38: C ≥ 10 % 607-248-00-4 naptalam-sodium (ISO); sodium N-naphth-1-ylphthalamate 205-073-4 132-67-2 Xn; R22 Xn R: 22 S: (2-) 607-249-00-X (1-methyl-1,2-ethanediyl)bis[oxy(methyl-2,1-ethanediyl)] diacrylate 256-032-2 42978-66-5 Xi; R36/37/38 R43 N; R51-53 Xi; N R: 36/37/38-43-51/53 S: (2-)24-37-61 Xi; R36/37/38: C ≥ 10 % 607-250-00-5 4H-3,1-benzoxazine-2,4(1H)-dione 204-255-0 118-48-9 Xi; R36 S: (2-)24-37-61 Xi; R36/37/38: C ≥ 10 % 607-250-00-5 4H-3,1-benzoxazine-2,4(1H)-dione 204-255-0 118-48-9 Xi; R36 R43 Xi R: 36-43 S: (2-)24-26-37 607-251-00-0 2-methoxypropyl acetate 274-724-2 70657-70-4 R10 Repr. Cat. 2; R61 Xi; R37 T R: 61-10-37 S: 53-45 607-252-00-6 lambda-cyhalothrin (ISO); reaction mass of (S)-α-cyano-3-phenoxybenzyl(Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate and (R)-α-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate (1:1) 415-130-7 91465-08-6 T+; R26 T; R25 Xn; R21 N; R50-53 T+; N R: 21-25-26-50/53 S: (1/2-)28-36/37/39-38-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 607-253-00-1 cyfluthrin (ISO); S: (1/2-)28-36/37/39-38-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 607-253-00-1 cyfluthrin (ISO); α-cyano-4-fluoro-3-phenoxybenzyl-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate 269-855-7 68359-37-5 T+; R28 T; R23 N; R50-53 T+; N R: 23-28-50/53 S: (1/2-)28-36/37/39-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 607-254-00-7 α-cyano-4-fluoro-3-phenoxybenzyl-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate; S: (1/2-)28-36/37/39-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 607-254-00-7 α-cyano-4-fluoro-3-phenoxybenzyl-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate; beta-cyfluthrin 269-855-7 68359-37-5 T+; R26/28 N; R50-53 T+; N R: 26/28-50/53 … 184 unchanged lines … Xn; R22 C; R34 T R: 60-61-22-34 S: 53-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E S: 53-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % E 607-313-00-7 neodecanoyl chloride 254-875-0 40292-82-8 T+; R26 Xn; R22 C; R34 T+ R: 22-26-34 S: (1/2-)26-28-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 607-314-00-2 ethofumesate (ISO); S: (1/2-)26-28-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 607-314-00-2 ethofumesate (ISO); (±)-2-ethoxy-2,3-dihydro-3,3-dimethylbenzofuran-5-yl methanesulfonate 247-525-3 26225-79-6 N; R51-53 N R: 51/53 S: 61 607-315-00-8 glyphosate (ISO); … 17 unchanged lines … (S)-α-cyano-3-phenoxybenzyl (1R, 3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate 258-256-6 52918-63-5 T; R23/25 N; R50-53 T; N R: 23/25-50/53 S: (1/2-)24-28-36/37/39-38-45-60-61 N; R50-53: C ≥ 0,000025 % N; R51-53: 0,0000025 % ≤ C < 0,000025 % R52-53: 0,00000025 % ≤ C < 0,0000025 % 607-320-00-5 bis[4-(ethenyloxy)butyl] 1,3-benzenedicarboxylate 413-930-0 130066-57-8 R43 S: (1/2-)24-28-36/37/39-38-45-60-61 N; R50-53: C ≥ 0,000025 % N; R51-53: 0,0000025 % ≤ C < 0,000025 % R52-53: 0,00000025 % ≤ C < 0,0000025 % 607-320-00-5 bis[4-(ethenyloxy)butyl] 1,3-benzenedicarboxylate 413-930-0 130066-57-8 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 607-321-00-0 (S)-methyl-2-chloropropionate 412-470-8 73246-45-4 R10 … 147 unchanged lines … S: (2-)22-24-26-37/39 607-370-00-8 2-[[2-(acetyloxy)-3-(1,1-dimethyl-ethyl)-5-methylphenyl]methyl]-6-(1,1-dimethylethyl)-4-methylphenol 412-210-3 41620-33-1 N; R50-53 N R: 50/53 S: 60-61 607-371-00-3 3-ethyl 5-methyl 4-(2-chlorophenyl)-1,4-dihydro-2-[2-(1,3-dihydro-1,3-dioxo-(2H)isoindol-2-yl)-ethoxymethyl]-6-methyl-3,5-pyridinedicarboxylate 413-410-3 88150-62-3 R53 R: 53 S: 61 607-372-00-9 ethoxylated bis phenol A di-(norbornene carboxylate) 412-410-0 — R52-53 R: 52/53 S: 61 607-372-00-9 ethoxylated bis phenol A di-(norbornene carboxylate) 412-410-0 — R52-53 R: 52/53 S: 61 607-373-00-4 (±) tetrahydrofurfuryl (R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenyloxy]propionate 414-200-4 119738-06-6 Muta. Cat. 3; R68 Repr. Cat. 2; R61 Repr. Cat. 3; R62 … 45 unchanged lines … C13 branched and linear alkyl 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoate 413-750-2 171090-93-0 R53 R: 53 S: 61 607-385-00-X Copolymer of vinyl-alcohol and vinyl acetate partially acetilized with 4-(2-(4-formylphenyl)ethenyl)-1-methylpyridinium methylsulfate 414-590-6 125229-74-5 N; R51-53 N R: 51/53 S: 61 607-386-00-5 reaction mass of: tetradecanoic acid (42.5-47.5 %); poly(1-7)lactate esters of tetradecanoic acid (52.5-57.5 %) 412-580-6 174591-51-6 Xi; R38-41 S: 61 607-386-00-5 reaction mass of: tetradecanoic acid (42.5-47.5 %); poly(1-7)lactate esters of tetradecanoic acid (52.5-57.5 %) 412-580-6 174591-51-6 Xi; R38-41 R43 N; R50-53 Xi; N R: 38-41-43-50/53 S: (2-)24-26-37/39-60-61 607-387-00-0 reaction mass of: dodecanoic acid (35-40 %); poly(1-7)lactate esters of dodecanoic acid (60-65 %) 412-590-0 58856-63-6 Xi; R38-41 S: (2-)24-26-37/39-60-61 607-387-00-0 reaction mass of: dodecanoic acid (35-40 %); poly(1-7)lactate esters of dodecanoic acid (60-65 %) 412-590-0 58856-63-6 Xi; R38-41 R43 N; R50-53 Xi; N R: 38-41-43-50/53 … 19 unchanged lines … R: 34-43-51/53 S: (1/2-)26-36/37/39-45-61 607-396-00-X bis(1,2,2,6,6-pentamethyl-4-piperidinyl) 2-(4-methoxybenzylidene)malonate 414-840-4 147783-69-5 N; R50-53 N R: 50/53 S: 22-60-61 607-397-00-5 reaction mass of: Ca salicylates (branched C10-14 and C18-30 alkylated); Ca phenates (branched C10-14 and C18-30 alkylated); Ca sulfurised phenates (branched C10-14 and C18-30 alkylated) 415-930-6 — Repr. Cat. 3; R62 S: 22-60-61 607-397-00-5 reaction mass of: Ca salicylates (branched C10-14 and C18-30 alkylated); Ca phenates (branched C10-14 and C18-30 alkylated); Ca sulfurised phenates (branched C10-14 and C18-30 alkylated) 415-930-6 — Repr. Cat. 3; R62 R43 Xn R: 43-62 S: (2-)23-36/37 607-398-00-0 ethyl N-(5-chloro-3-(4-(diethylamino)-2-methylphenylimino)-4-methyl-6-oxo-1,4-cyclohexadienyl)carbamate 414-820-5 125630-94-6 N; R50-53 N … 82 unchanged lines … Xi; R37 N; R50-53 T; N R: 25-37-48/22-50/53 S: (1/2-)36/37/39-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 607-423-00-5 esters of mecoprop and of mecoprop-P — — Xn; R22 S: (1/2-)36/37/39-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 607-423-00-5 esters of mecoprop and of mecoprop-P — — Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 … 43 unchanged lines … N; R50-53 T; N R: 22-23-50/53 S: (1/2-)45-60-61 607-432-00-4 S-metolachlor; reaction mass of (S)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (80-100 %); [1] (R)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (0-20 %) [2] - [1] reaction mass of (S)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (80-100 %); [1] (R)-2-chloro-N-(2-ethyl-6-methyl-phenyl)-N-(2-methoxy-1-methyl-ethyl)-acetamide (0-20 %) [2] - [1] - [2] 87392-12-9 [1] 178961-20-1 [2] R43 N; R50-53 Xi; N … 116 unchanged lines … S: (2-)22-24-37 607-476-00-4 trisodium N,N-bis(carboxymethyl)-β-alanine 414-070-9 129050-62-0 C; R34 R52-53 C R: 34-52/53 S: (1/2-)26-36/37/39-45-61 607-477-00-X (1α5α6α)-6-nitro-3-benzyl-3-azabicyclo[3.1.0]hexane methanesulfonate salt 426-740-8 - Xn; R22 S: (1/2-)26-36/37/39-45-61 607-477-00-X (1α5α6α)-6-nitro-3-benzyl-3-azabicyclo[3.1.0]hexane methanesulfonate salt 426-740-8 — Xn; R22 Xi; R41 N; R51-53 Xn; N R: 22-41-51/53 S: (2-)22-26-39-61 607-478-00-5 tetramethylammonium hydrogen phthalate 416-900-5 79723-02-7 T; R25 Xn; R48/22 N; R50 T; N R: 25-48/22-50 S: (1/2-)25-36-45-61 607-479-00-0 hexadecyl 4-chloro-3-[2-(5,5-dimethyl-2,4-dioxo-1,3-oxazolidin-3-yl)-4,4-dimethyl-3-oxopentamido]benzoate 418-550-9 168689-49-4 R53 R: 53 S: 61 607-480-00-6 1,2-benzenedicarboxylic acid; di-C7-11-branched and linear alkylesters 271-084-6 68515-42-4 Repr. Cat. 2; R61 Repr. Cat. 3; R62 T R: 61-62 S: 53-45 607-481-00-1 reaction mass of: trihexyl citrate; dihexyloctyl citrate; dioctylhexyl citrate; dihexyldecyl citrate 430-290-8 - R53 R: 53 dihexyldecyl citrate 430-290-8 — R53 R: 53 S: 61 607-482-00-7 N-[1-(S)-ethoxycarbonyl-3-phenylpropyl]-l-alanyl-N-carboxyanhydride 430-360-8 84793-24-8 Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 607-483-00-2 1,2-benzenedicarboxylic acid; di-C6-8-branched alkylesters, C7-rich 276-158-1 71888-89-6 Repr. Cat. 2; R61 T R: 61 S: 53-45 607-484-00-8 ethyl 2-{][}3-acetylamino-4-(6-bromo-2-methyl-1,3-dioxo-2,3-dihydro-1H-isoindol-5-ylazo)phenyl{]ethylamino[}propionate 430-480-0 221452-67-1 R53 R: 53 S: 61 607-485-00-3 (3S-trans)-phenyl-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)-1-piperidinecarboxylate 430-510-2 - R53 R: 53 S: 61 607-485-00-3 (3S-trans)-phenyl-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl)-1-piperidinecarboxylate 430-510-2 — R53 R: 53 S: 22-61 607-486-00-9 potassium sodium 5'-(6-chloro-4-(2-(2-vinylsulfonylethoxy)ethylamino)-1,3,5-triazin-2-ylamino)-4'-hydroxy-2,3'-azodinaphthalene-1,2', 5,7'-disulfonate 402-110-8 110081-40-8 R52-53 R: 52/53 S: 22-61 607-487-00-4 reaction mass of: disodium 4-(3-ethoxycarbonyl-4-(5-(3-ethoxycarbonyl-5-hydroxy-1-(4-sulfonatophenyl)pyrazol-4-yl)penta-2,4-dienylidene)-4,5-dihydro-5-oxopyrazol-1-yl)benzenesulfonate; trisodium 4-(3-ethoxycarbonyl-4-(5-(3-ethoxycarbonyl-5-oxido-1-(4-sulfonatophenyl)pyrazol-4-yl)penta-2,4-dienylidene)-4,5-dihydro-5-oxopyrazol-1-yl)benzenesulfonate 402-660-9 — Repr. Cat. 2; R61 R52-53 T R: 61-52/53 S: 53-45-61 607-488-00-X ethyl (2-acetylamino-5-fluoro-4-isothiocyanatophenoxy)acetate 414-210-9 147379-38-2 N; R50-53 N R: 50/53 S: 60-61 607-489-00-5 reaction mass of: 2-ethylhexyl linolenate, linoleate and oleate; 2-ethylhexyl epoxyoleate; 2-ethylhexyl diepoxylinoleate; 2-ethylhexyl triepoxylinolenate 414-890-7 71302-79-9 R43 Xi R: 43 S: (2-)24-37 607-490-00-0 N-[2-hydroxy-3-(C12-16-alkyloxy)propyl]-N-methyl glycinate 415-060-7 — Xi; R41 R43 Xi R: 41-43 S: (2-)24-26-37/39 607-491-00-6 reaction mass of: diester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:2); triester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:3) 427-140-9 - Carc. Cat. 3; R40 Xn S: (2-)24-26-37/39 607-491-00-6 reaction mass of: diester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:2); triester of 4,4'-methylenebis[2-(2-hydroxy-5-methylbenzyl)-3,6-dimethylphenol] and 6-diazo-5,6-dihydro-5-oxonaphthalene-1-sulfonic acid (1:3) 427-140-9 — Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 607-492-00-1 2-(1-(3',3'-dimethyl-1'-cyclohexyl)ethoxy)-2-methyl propyl propanoate 415-490-5 141773-73-1 N; R51-53 N R: 51/53 … 22 unchanged lines … R: 22-34-51/53 S: (1/2-)26-36/37/39-45-61 607-503-00-X 2,4,6-tri-n-propyl-2,4,6-trioxo-1,3,5,2,4,6-trioxatriphosphorinane 422-210-5 68957-94-8 C; R34 C R: 34 S: (1/2-)26-36/37/39-45 607-504-00-5 diammonium 1-hydroxy-2-(4-(4-carboxyphenylazo)-2,5-dimethoxyphenylazo)-7-amino-3-naphthalenesulfonate 422-670-7 - Repr. Cat. 3; R62 S: (1/2-)26-36/37/39-45 607-504-00-5 diammonium 1-hydroxy-2-(4-(4-carboxyphenylazo)-2,5-dimethoxyphenylazo)-7-amino-3-naphthalenesulfonate 422-670-7 — Repr. Cat. 3; R62 T; R25 Xn; R48/22 N; R50-53 T; N R: 25-48/22-62-50/53 S: (1/2-)36/37-45-60-61 607-505-00-0 pentasodium 7-(4-(4-(5-amino-4-sulfonato-2-(4-((2-(sulfonato-ethoxy)sulfonyl)phenylazo)phenylamino)-6-chloro-1,3,5-triazin-2-yl)amino-2-ureidophenylazo)naphtalene-1,3,6-trisulfonate 422-930-1 R52-53 R: 52/53 S: 22-61 607-506-00-6 reaction mass of: strontium (4-chloro-2-((4,5-dihydro-3-methyl-5-oxo-1-(3-sulfonatophenyl)-1H-pyrazol-4-yl)azo)-5-methyl)benzenesulfonate; disodium (4-chloro-2-((4,5-dihydro-3-methyl-5-oxo-1-(3-sulfonatophenyl)-1H-pyrazol-4-yl)azo)-5-methyl)benzenesulfonate 422-970-8 N; R51-53 N R: 51/53 S: 22-61 607-507-00-1 potassium,sodium 2,4-diamino-3-[4-(2-sulfonatoethoxysulfonyl)phenylazo]-5-[4-(2-sulfonatoethoxysulfonyl)-2-sulfonatophenylazo]-benzenesulfonate 422-980-2 187026-95-5 Xi; R41 Xi R: 41 S: (2-)22-26-39 607-508-00-7 disodium 3,3'-[iminobis[sulfonyl-4,1-phenylene-(5-hydroxy-3-methylpyrazole-1,4-diyl)azo-4,1-phenylenesulfonylimino-(4-amino-6-hydroxypyrimidine-2,5-diyl)azo-4,1-phenylenesulfonylimino(4-amino-6-hydroxypyrimidine-2,5-diyl)azo]bis(benzenesulfonate)] 423-110-4 — Xi; R41 Xi R: 41 S: (2-)22-26-39 607-509-00-2 2-phenoxyethyl 4-aminobenzoate 430-880-5 88938-23-2 N; R51-53 N R: 51/53 S: 61 607-510-00-8 (2S, 5R)-6,6-dibromo-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 4,4-dioxide 427-200-4 76646-91-8 Xn; R22 Xi; R38-41 R43 Xn R: 22-38-41-43 S: (2-)24-26-37/39 607-511-00-3 reaction mass of: 4-[(3-decyloxypropyl)(3-isobutoxy-1-isobutoxycarbonyl-3-oxopropyl)amino]-4-oxobutyric acid; 4-[(3-isobutoxy-1-isobutoxycarbonyl-3-oxopropyl)(3-octyloxypropyl)amino]-4-oxobutyric acid 423-750-4 - Xi; R36 4-[(3-isobutoxy-1-isobutoxycarbonyl-3-oxopropyl)(3-octyloxypropyl)amino]-4-oxobutyric acid 423-750-4 — Xi; R36 N; R51-53 Xi; N R: 36-51/53 S: (2-)26-61 607-512-00-9 trisodium 2,4-diamino-3,5-bis-[4-(2-sulfonatoethoxy)sulfonyl)phenylazo]benzenesulfonate 423-970-0 182926-43-8 R52-53 R: 52/53 … 23 unchanged lines … N; R50-53 Xi; N R: 37/38-41-50/53 S: (2-)26-37/39-60-61 607-520-00-2 reaction mass of: sodium 4,5-dihydro-2-[(propionato)(C6-18)alkyl]-3H-imidazolium-N-ethylphosphate; disodium 4,5-dihydro-2-[(dipropionato)(C6-18)alkyl]-3H-imidazolium-N-ethylphosphate 427-740-0 - Xi; R41 disodium 4,5-dihydro-2-[(dipropionato)(C6-18)alkyl]-3H-imidazolium-N-ethylphosphate 427-740-0 — Xi; R41 R43 Xi R: 41-43 S: (2-)24-26-37/39 607-521-00-8 tetraethyl N,N'-(methylenedicyclohexane-4,1-diyl)bis-dl-aspartate 429-270-1 136210-30-5 R43 R52-53 Xi R: 43-52/53 S: (2-)36/37-61 607-522-00-3 sodium salt of the polymer of: sodium 2-methyl-buta-1,3-diene-1-sulfonate with acrylic acid and 2-hydroxyethyl-2-methylacrylate 429-720-7 184246-86-4 R52-53 R: 52/53 S: 61 607-523-00-9 reaction mass of mono to tetra(lithium and/or sodium)3-amino-10-[4-(4-amino-3-sulfonatoanilino)-6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to tetra(lithium and/or sodium)3-amino-10-[4,6-bis(4-amino-3-sulfonatoanilino)-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to penta(lithium and/or sodium)10,10'-diamino-6,6', 13,13'-tetrachloro-3,3'-[6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10-amino-6,6', 13,13'-tetrachloro-10'[4-(4-amino-3-sulfonatoanilino)-[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10,10'-diamino-6,6', 3,3'[(2-sulfonato)-1,4-phenylenediiminobis[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate 430-200-7 - Xi; R41 S: (2-)36/37-61 607-522-00-3 sodium salt of the polymer of: sodium 2-methyl-buta-1,3-diene-1-sulfonate with acrylic acid and 2-hydroxyethyl-2-methylacrylate 429-720-7 184246-86-4 R52-53 R: 52/53 S: 61 607-523-00-9 reaction mass of mono to tetra(lithium and/or sodium)3-amino-10-[4-(4-amino-3-sulfonatoanilino)-6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to tetra(lithium and/or sodium)3-amino-10-[4,6-bis(4-amino-3-sulfonatoanilino)-1,3,5-triazin-2-ylamino]-6-13-dichlorobenzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to penta(lithium and/or sodium)10,10'-diamino-6,6', 13,13'-tetrachloro-3,3'-[6-[methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10-amino-6,6', 13,13'-tetrachloro-10'[4-(4-amino-3-sulfonatoanilino)-[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate; mono to hepta(lithium and/or sodium)10,10'-diamino-6,6', 3,3'[(2-sulfonato)-1,4-phenylenediiminobis[6-methyl-(2-sulfonatoethyl)amino]-1,3,5-triazin-2,4-diyldiimino]bis[benzo[1,2-B:4,5-B']di[1,4]benzoxazine-4,11-disulfonate 430-200-7 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 607-524-00-4 tall oil 2-[(tetrahydro-2H-pyran-2-yl) thio]ethyl esters 430-310-5 - R53 R: 53 S: (2-)26-39-61 607-524-00-4 tall oil 2-[(tetrahydro-2H-pyran-2-yl) thio]ethyl esters 430-310-5 — R53 R: 53 S: 61 607-525-00-X (Z)-2-methoxymino-2-[2-(tritylamino)thiazol-4-yl]acetic acid 431-520-1 64485-90-1 E; R2 Carc. Cat. 3; R40 R52-53 E; Xn … 16 unchanged lines … N; R51-53 Xn; N R: 48/22-51/53 S: (2-)22-36-61 607-532-00-8 (S)-1-[2-tert-butoxycarbonyl-3-(2-methoxyethoxy)propyl]-1-cyclopentanecarboxylic acid, cyclohexylamine salt 425-510-4 167944-94-7 R52-53 R: 52/53 S: 61 607-533-00-3 pentasodium monohydrogen 6-chloro-3,10-bis[2-[4-chloro-6-(2,4-disulfophenylamino)-1,3,5-triazin-2-yl-amino]ethylamino]-13-ethylbenzo[5.6][1.4]oxazino[2,3-b]phenoxazine-4,11-disulfonate 414-910-4 - Xi; R41 S: 61 607-533-00-3 pentasodium monohydrogen 6-chloro-3,10-bis[2-[4-chloro-6-(2,4-disulfophenylamino)-1,3,5-triazin-2-yl-amino]ethylamino]-13-ethylbenzo[5.6][1.4]oxazino[2,3-b]phenoxazine-4,11-disulfonate 414-910-4 — Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 607-534-00-9 ethyl 2-(3-benzoylphenyl)propanoate 414-920-9 60658-04-0 T; R25-48/25 R43 N; R51-53 T; N R: 25-43-48/25-51/53 S: (1/2-)36/37-45-61 607-535-00-4 potassium 4-iodo-2-sulfonato-benzoic acid 426-620-5 - Xi; R41 S: (1/2-)36/37-45-61 607-535-00-4 potassium 4-iodo-2-sulfonato-benzoic acid 426-620-5 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 607-536-00-X (2,6-xylyloxy) acetic acid 430-910-7 13335-71-2 Xn; R22 Xi; R41 R52-53 Xn R: 22-41-52/53 S: (2-)26-39-61 607-537-00-5 isopropylammonium 2-(3-benzoylphenyl)propionate 417-970-1 - T; R25-48/25 S: (2-)26-39-61 607-537-00-5 isopropylammonium 2-(3-benzoylphenyl)propionate 417-970-1 — T; R25-48/25 Xn; R21 Xi; R41 N; R50-53 T; N R: 21-25-41-48/25-50/53 S: (1/2-)22-26-36/37/39-45-60-61 607-539-00-6 propyl((4-(5-oxo-3-propylisoxazolidin-4-ylidenmethin)phenyl)propoxycarbonylmethyleneamino)acetate 431-000-2 198705-81-6 R53 R: 53 S: 61 607-540-00-1 1-(mercaptomethyl)cyclopropylacetic acid 420-240-3 162515-68-6 C; R34 Xn; R21/22 R43 N; R51-53 C; N R: 21/22-34-43-51/53 S: (1/2-)22-26-36/37/39-45-61 607-541-00-7 [(1-methyl-1,2-ethanediyl)bis[nitrilobis(methylene)]]tetrakis(phosphonic acid) 421-940-1 28698-31-9 Xi; R41 N; R50-53 Xi; N R: 41-50/53 S: (2-)26-39-60-61 607-542-00-2 methyl 2-(4-butanesulfonamidophenoxy)tetradecanoate 422-110-1 - N; R50-53 N S: (2-)26-39-60-61 607-542-00-2 methyl 2-(4-butanesulfonamidophenoxy)tetradecanoate 422-110-1 — N; R50-53 N R: 50/53 S: 60-61 607-543-00-8 poly-[((4-((4-(ethyl-ethylene)amino)phenyl)-(4-(ethyl-(2-oxyethylene)amino)phenyl)methinyl)-3-methylcyclohexa-2,5-dienylidene)-N-ethyl-N-(2-hydroxyethyl)ammonium acetate] 427-480-8 176429-22-4 Xi; R37/38-41 N; R50-53 Xi; N … 15 unchanged lines … R: 22-41-51/53 S: (2-)22-26-39-61 607-549-00-0 methyl (E)-2((3-(1,3-benzodioxol-5-yl)-2-methyl-1-propenyl)amino)benzoate 424-430-7 125778-19-0 N; R50-53 N R: 50/53 S: 60-61 607-550-00-6 2-amino-4-bromo-5-chlorobenzoic acid 424-700-4 - Xi; R41 S: 60-61 607-550-00-6 2-amino-4-bromo-5-chlorobenzoic acid 424-700-4 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 607-551-00-1 tetrabutylammonium 2-amino-6-iodopurinate 424-710-9 156126-48-6 Xn; R21/22-48/22 Xi; R38-41 R43 N; R51-53 Xn; N R: 21/22-38-41-43-48/22-51/53 S: (2-)26-36/37/39-61 607-552-00-7 hexadecyl 3-amino-4-isopropoxybenzoate 424-830-1 - R53 R: 53 S: 35-61 607-553-00-2 7-amino-4-hydroxy-2-naphthalenesulfonic acid, coupled with 5 (or 8) -amino-8 (or 5)-[[4-[[4-[[4-amino-6(or 7)-sulfo-1-naphthyl]azo]phenyl]amino]-3-sulfophenyl]azo]-2-naphthalenesulfonic acid and 4-hydroxy-7-(phenylamino)-2-naphthalenesulfonic acid, sodium salt 424-850-0 - Xi; R41 Xi S: (2-)26-36/37/39-61 607-552-00-7 hexadecyl 3-amino-4-isopropoxybenzoate 424-830-1 — R53 R: 53 S: 35-61 607-553-00-2 7-amino-4-hydroxy-2-naphthalenesulfonic acid, coupled with 5 (or 8) -amino-8 (or 5)-[[4-[[4-[[4-amino-6(or 7)-sulfo-1-naphthyl]azo]phenyl]amino]-3-sulfophenyl]azo]-2-naphthalenesulfonic acid and 4-hydroxy-7-(phenylamino)-2-naphthalenesulfonic acid, sodium salt 424-850-0 — Xi; R41 Xi R: 41 S: (2-)26-39 607-554-00-8 2,4-diamino-5-[4-[(2-sulfoxyl ethyl)sulfonyl]phenylazo]benzenesulfonic acid 424-870-1 27624-67-5 E; R3 Xi; R41 … 17 unchanged lines … S: 61 607-559-00-5 coconut oil, reaction products with glycerol esters of 3,5-bis(1,1-dimethylethyl)-4-hydroxybenzenepropanoic acid 425-400-6 179986-09-5 R53 R: 53 S: 61 607-560-00-0 (R,S)-2-butyloctanedioic acid 431-210-4 50905-10-7 Xi; R41 Xi R: 41 S: (2-)26-39 607-561-00-6 sodium 4-hydroxy-3-(N'-(2-(2-hydroxyethylenesulfonyl)ethylene)ureido)-5-nitrobenzenesulfonate 425-460-3 - R43 S: (2-)26-39 607-561-00-6 sodium 4-hydroxy-3-(N'-(2-(2-hydroxyethylenesulfonyl)ethylene)ureido)-5-nitrobenzenesulfonate 425-460-3 — R43 R52-53 Xi R: 43-52/53 S: (2-)24-37-61 607-562-00-1 reaction mass of: (2R, 3R)-3-(2-ethoxyphenoxy)-2-hydroxy-3-phenylpropylammonium methanesulfonate; (2S, 3S)-3-(2-ethoxyphenoxy)-2-hydroxy-3-phenylpropylammonium methanesulfonate 425-530-3 98769-75-6 Xn; R22 Xi; R41 N; R51-53 Xn; N R: 22-41-51/53 S: (2-)22-26-39-61 607-563-00-7 5,7-dichloro-4-hydroxyquinoline-3-carboxylic acid 431-250-2 171850-30-9 N; R51-53 N R: 51/53 S: 61 607-564-00-2 1,6-hexanediammonium, sodium 5-sulfato-1,3-benzenedicarboxylate 425-730-0 51178-75-7 R43 Xi R: 43 S: (2-)24-37 607-565-00-8 3-ethyl 5-methyl 2-(2-aminoethoxymethyl)-4-(2-chlorophenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate 425-820-1 88150-42-9 T; R25 Xn; R48/22 Xi; R41 N; R50-53 T; N R: 25-41-48/22-50/53 S: (1/2-)26-36/37/39-45-60-61 607-566-00-3 reaction mass of: dodecylphenyl dodecylhydroxybenzenecarboxylate; bis(dodecylphenyl)dodecyl hydroxybenzenedicarboxylate 426-140-6 - R53 R: 53 S: 61 607-567-00-9 potassium 3-iodo-6-methylbenzenesulfonate 426-300-5 - Xi; R41 Xi bis(dodecylphenyl)dodecyl hydroxybenzenedicarboxylate 426-140-6 — R53 R: 53 S: 61 607-567-00-9 potassium 3-iodo-6-methylbenzenesulfonate 426-300-5 — Xi; R41 Xi R: 41 S: (2-)26-39 607-568-00-4 potassium 2-chloro-3-(benzyloxy)propionate 426-350-8 138666-92-9 Xn; R22-48/22 Xi; R41 R43 Xn R: 22-41-43-48/22 S: (2-)26-36/37/39 607-569-00-X reaction mass of: sodium 2-amino-4-(2,6-difluoropyrimidin-4-ylamino)benzenesulfonate; sodium 2-amino-4-(4,6-difluoropyrimidin-4-ylamino)benzenesulfonate 426-470-0 - R43 Xi sodium 2-amino-4-(4,6-difluoropyrimidin-4-ylamino)benzenesulfonate 426-470-0 — R43 Xi R: 43 S: (2-)22-24-37 607-570-00-5 sodium (6R-trans)-7-amino-8-oxo-3-[[[1-(sulfomethyl)-1H-tetrazol-5-yl]thio]methyl]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate monohydrate 426-520-1 71420-85-4 R43 Xi R: 43 S: (2-)24-37 607-571-00-0 2-cyclopentene-1-acetic acid, 3-hydroxy-2-pentyl-, methyl ester acetate 431-400-7 57374-49-9 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 607-572-00-6 diethyl thiophosphoryl (Z)-(2-aminothiazol-4-yl)methoxyimino acetate 426-790-0 162208-27-7 Xn; R21/22-48/22 R43 N; R50-53 Xn; N R: 21/22-43-48/22-50/53 S: (2-)36/37-60-61 607-573-00-1 reaction mass of: disodium 7-(2,4-difluoropyrimidin-6-ylamino)-4-hydroxy-3-(4-methoxy-2-sulfonatophenylazo)naphthalene-2-sulfonate; disodium 7-(4,6-difluoropyrimidin-2-ylamino)-4-hydroxy-3-(4-methoxy-2-sulfonatophenylazo)naphthalene-2-sulfonate 426-840-1 - Xi; R41 Xi R: 41 S: (2-)22-26-39 607-574-00-7 [1R-(1-α, 2β,5α)]-mono[5-methyl-2-(1-methylethyl)cyclohexyl]butanedioate 426-890-4 77341-67-4 Xi; R41 Xi R: 41 S: (2-)26-39 607-575-00-2 4-(5-(5-[1-(4-carboxyphenyl)hexahydro-2,4,6-trioxopyrimidin-5-ylidene]penta-1,3-dienyl)-1,2,3,4-tetrahydro-6-hydroxy-2,4-dioxopyrimidin-1-yl)benzoic acid-triethylamine salt 426-900-7 - Xi; R37 S: (2-)26-39 607-575-00-2 4-(5-(5-[1-(4-carboxyphenyl)hexahydro-2,4,6-trioxopyrimidin-5-ylidene]penta-1,3-dienyl)-1,2,3,4-tetrahydro-6-hydroxy-2,4-dioxopyrimidin-1-yl)benzoic acid-triethylamine salt 426-900-7 — Xi; R37 R52-53 Xi R: 37-52/53 S: (2-)61 607-576-00-8 branched, octyl 3-[3,5-di(tert-butyl)-4-hydroxyphenyl]propanoate 427-030-0 - N; R50-53 N S: (2-)61 607-576-00-8 branched, octyl 3-[3,5-di(tert-butyl)-4-hydroxyphenyl]propanoate 427-030-0 — N; R50-53 N R: 50/53 S: 60-61 607-577-00-3 (2R*, 3S*)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (1R)-10-camphorsulfonate 427-100-0 - Xn; R22 S: 60-61 607-577-00-3 (2R*, 3S*)-2-(2,4-difluorophenyl)-3-(5-fluoro-4-pyrimidinyl)-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (1R)-10-camphorsulfonate 427-100-0 — Xn; R22 Xi; R41 R43 R52-53 Xn R: 22-41-43-52/53 S: (2-)22-24-26-37/39-61 607-578-00-9 ethyl 4-((4-diethylamino-2-methylphenyl)imino)-4,5-dihydro-1-isopropyl-5-oxo-1H-pyrazole-3-carboxylate 427-110-5 - Xn; R22-48/22 S: (2-)22-24-26-37/39-61 607-578-00-9 ethyl 4-((4-diethylamino-2-methylphenyl)imino)-4,5-dihydro-1-isopropyl-5-oxo-1H-pyrazole-3-carboxylate 427-110-5 — Xn; R22-48/22 R53 Xn R: 22-48/22-53 S: (2-)36-61 607-579-00-4 diethyl[(p-ethoxyanilino)methylene]malonate 431-430-0 103976-28-9 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-)61 607-580-00-X ethyl 7-chloro-1-(2,4-difluorophenyl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylate 422-360-1 100491-29-0 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)22-24-37-61 607-581-00-5 ethyl 2-ethoxy-4-carboxymethylbenzoate 427-630-2 99469-99-5 Xi; R41 Xi R: 41 S: (2-)26-39 607-582-00-0 reaction mass of: tetrasodium 7-(4-(4-fluoro-6-(4-(2-sulfonatoethylsulfonyl)phenylamino)-1,3,5-triazin-2-ylamino)-2-ureidophenylazo)naphthalene-1,3,6-trisulfonate; tetrasodium 7-(4-(4-hydroxy-6-(4-(2-sulfonatoethylsulfonyl)phenylamino)-1,3,5-triazin-2-ylamino)-2-ureidophenylazo)naphthalene-1,3,6-trisulfonate 427-650-1 - R52-53 R: 52/53 tetrasodium 7-(4-(4-hydroxy-6-(4-(2-sulfonatoethylsulfonyl)phenylamino)-1,3,5-triazin-2-ylamino)-2-ureidophenylazo)naphthalene-1,3,6-trisulfonate 427-650-1 — R52-53 R: 52/53 S: 22-61 607-583-00-6 4-amino-3-[[4-[[2-(sulfooxy)ethyl]sulfonyl]phenyl]azo]-1-naphthalene sulfonic acid 427-680-5 188907-52-0 Xi; R41 R43 R52-53 Xi R: 41-43-52/53 S: (2-)22-24-26-37/39-61 607-584-00-1 trisodium 3-[2-acetylamino-4-[4-chloro-6-[4-(2-sulfonatoxyethylsulfonyl)phenylamino]-1,3,5-triazine-2-ylamino]phenylazo]naphthalene-1,5-disulfonate 427-710-7 215612-56-9 Xi; R41 R43 R52-53 Xi R: 41-43-52/53 S: (2-)24-26-37/39-61 607-585-00-7 strontium 2-[(2-hydroxy-6-sulfonato-1-naphthyl)azo]naphthalene-1-sulfonate 427-930-3 - R43 Xi S: (2-)24-26-37/39-61 607-585-00-7 strontium 2-[(2-hydroxy-6-sulfonato-1-naphthyl)azo]naphthalene-1-sulfonate 427-930-3 — R43 Xi R: 43 S: (2-)22-24-37 607-586-00-2 dodecyl 3-amino-4-chlorobenzoate 428-020-9 6195-20-6 R43 R53 Xi R: 43-53 S: (2-)24-37-61 607-587-00-8 ethyl cis-4-[4-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazine-1-carboxylate 428-030-3 67914-69-6 Xn; R22-48/22 N; R50-53 Xn; N R: 22-48/22-50/53 S: (2-)36-60-61 607-588-00-3 reaction mass of: 2-ethylhexyl 2,3,4,5-tetrabromobenzoate; bis(2-ethylhexyl) 3,4,5,6-tetrabromophthalate 428-050-2 - R43 bis(2-ethylhexyl) 3,4,5,6-tetrabromophthalate 428-050-2 — R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)36/37-60-61 607-589-00-9 tetrakis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,2,3,4-butanetetracarboxylate 428-070-1 91788-83-9 T; R48/25 Xn; R22 N; R50-53 T; N R: 22-48/25-50/53 S: (1/2-)22-36-45-57-60-61 607-590-00-4 hexadecyl 3-[2-(5,5-dimethyl-2,4-dioxo-1,3-oxazolidin-3-yl)-4,4-dimethyl-3-oxovaleramido]-4-isopropoxybenzoate 428-140-1 210706-50-6 R53 R: 53 S: 61 607-591-00-X reaction mass of: trisodium 5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxy-3-(4-(2-sulfooxyethanesulfonyl)phenylazo)naphthalene-2,7-disulfonate; disodium 3-(4-ethenesulfonylphenylazo)-5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxynaphthalene-2,7-disulfonate 428-400-4 - Xi; R41 Xi disodium 3-(4-ethenesulfonylphenylazo)-5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxynaphthalene-2,7-disulfonate 428-400-4 — Xi; R41 Xi R: 41 S: (2-)22-26-39 607-592-00-5 di(C9-11-alkyl) cyclohexane-1,4-dicarboxylate 428-870-0 - R53 R: 53 S: (2-)22-26-39 607-592-00-5 di(C9-11-alkyl) cyclohexane-1,4-dicarboxylate 428-870-0 — R53 R: 53 S: 61 607-593-00-0 4-(2-methylacryloyloxy)phenyl 4-allyloxybenzoate 429-000-2 159235-16-2 R43 R52-53 Xi R: 43-52/53 S: (2-)24-37-61 607-594-00-6 ethyl (1S, 5R, 6S)-5-(1-ethylpropoxy)-7-oxabicyclo[4.1.0]hept-3-ene-3-carboxylate 429-020-1 204254-96-6 Xn; R48/22 R43 Xn R: 43-48/22 S: (2-)22-36/37 607-595-00-1 N-amidino-N-methylglycine-2-oxopropionate 429-120-5 208535-04-0 Xi; R41 Xi R: 41 S: (2-)26-39 607-596-00-7 ethyl 2-(4-phenoxyphenyl)lactate 429-220-9 132584-17-9 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)36/37-57-60-61 607-597-00-2 tetrasodium 4,4'-bis{]4-[}4-(2-hydroxyethylamino)-6-(4-sulfonatoanilino)-1,3,5-triazin-2-ylamino{]phenylazo[}stilbene-2,2'-disulfonate 429-230-3 - Xi; R41 Xi S: (2-)36/37-57-60-61 607-597-00-2 tetrasodium 4,4'-bis{]4-[}4-(2-hydroxyethylamino)-6-(4-sulfonatoanilino)-1,3,5-triazin-2-ylamino{]phenylazo[}stilbene-2,2'-disulfonate 429-230-3 — Xi; R41 Xi R: 41 S: (2-)22-26-39 607-598-00-8 trisodium 3-amino-4-[4-[4-(2-(2-ethenylsulfonylethoxy)ethylamino)-6-fluoro-1,3,5-triazine-2-ylamino]-2-sulfophenylazo]-5-hydroxynaphthalene-2,7-disulfonate 429-240-8 212652-59-0 Xi; R41 Xi R: 41 S: (2-)26-39 607-599-00-3 1,1-dimethylpropyl 3,5,5-trimethylperoxyhexanoate 431-610-9 68860-54-8 O; R7 R43 N; R50-53 O; Xi; N R: 7-43-50/53 S: (2-)3-14-36/37/39-60-61 607-600-00-7 (1S, 1'R)-[1-(3', 3'-dimethyl-1'-cyclohexyl)ethoxycarbonyl]methyl propanoate 431-700-8 - N; R51-53 N S: (2-)3-14-36/37/39-60-61 607-600-00-7 (1S, 1'R)-[1-(3', 3'-dimethyl-1'-cyclohexyl)ethoxycarbonyl]methyl propanoate 431-700-8 — N; R51-53 N R: 51/53 S: 61 607-601-00-2 1,4-dihydroxy-2,2,6,6-tetramethyl piperidinium-2-hydroxy-1,2,3-propanetricarboxylate 429-370-5 220410-74-2 Xn; R22 Xn R: 22 … 16 unchanged lines … calcium bis (C18-30-alkyl phenolate); calcium C10-14 branched alkylphenolato-C18-30-alkyl phenolate; C10-14 branched alkyl phenol; C18-30-alkyl phenol 430-180-1 - Xi; R38 C18-30-alkyl phenol 430-180-1 — Xi; R38 N; R51-53 Xi; N R: 38-51/53 S: (2-)24-37-61 607-608-00-0 pentapotassium 2-(4-{]5-[}1-(2,5-disulfophenyl)-4,5-dihydro-3-methylcarbamoyl-5-oxopyrazol-4-ylidene{]-3-(2-pyrrolidinone-1-yl)-1,3-pentadienyl[}-3-methylcarbamoyl-5-oxopyrazol-1-yl)benzene-1,4-disulfonate 430-210-1 - N; R50-53 N S: (2-)24-37-61 607-608-00-0 pentapotassium 2-(4-{]5-[}1-(2,5-disulfophenyl)-4,5-dihydro-3-methylcarbamoyl-5-oxopyrazol-4-ylidene{]-3-(2-pyrrolidinone-1-yl)-1,3-pentadienyl[}-3-methylcarbamoyl-5-oxopyrazol-1-yl)benzene-1,4-disulfonate 430-210-1 — N; R50-53 N R: 50/53 S: 60-61 607-609-00-6 ethyl (3R)-4-cyano-3-hydroxybutanoate 430-220-6 141942-85-0 Xi; R36 Xi R: 36 S: (2-)26 607-610-00-1 trisodium 4-hydroxy-6-(sulfonatomethylamino)-5-(2-(2-sulfatoethylsulfonyl)phenylazo)naphthalene-2-sulfonate 430-280-3 - R43 Xi S: (2-)26 607-610-00-1 trisodium 4-hydroxy-6-(sulfonatomethylamino)-5-(2-(2-sulfatoethylsulfonyl)phenylazo)naphthalene-2-sulfonate 430-280-3 — R43 Xi R: 43 S: (2-)22-24-37 607-611-00-7 methyl 3-amino-2,2,3-trimethylbutyrate 431-720-7 90886-53-6 C; R34 Xn; R22 … 30 unchanged lines … S: (1/2-)26-28-36/37/39-45 607-614-00-3 2-(10-oxo-10H-9-oxa-10-phosphaphenanthren-10-ylmethyl)succinic acid 426-480-5 63562-33-4 R43 R52-53 Xi R: 43-52/53 S: (2-)24-37-61 607-615-00-9 reaction product of thioglycerol and mercaptoacetic acid consisting mainly of 3-mercapto-1,2-bismercaptoacetoxypropane and oligomers of this substance 431-120-5 - T; R23 S: (2-)24-37-61 607-615-00-9 reaction product of thioglycerol and mercaptoacetic acid consisting mainly of 3-mercapto-1,2-bismercaptoacetoxypropane and oligomers of this substance 431-120-5 — T; R23 Xn; R22 Xi; R36 R43 T … 16 unchanged lines … Xn; R22 Xi; R36 Xn R: 22-36-40 S: (2-)26-36/37-46 Carc. Cat. 3; R40: C ≥ 5 % 607-621-00-1 milbemectin (ISO); [reaction mass of milbemycin A3 (CAS No 51596-10-2) and milbemycin A4 (CAS No 51596-11-3) (30:70)] - - Xn; R20/22 S: (2-)26-36/37-46 Carc. Cat. 3; R40: C ≥ 5 % 607-621-00-1 milbemectin (ISO); [reaction mass of milbemycin A3 (CAS No 51596-10-2) and milbemycin A4 (CAS No 51596-11-3) (30:70)] — — Xn; R20/22 N; R50-53 Xn; N R: 20/22-50/53 S: (2-)46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-622-00-7 2-ethylhexyl-2-ethylhexanoate 231-057-1 7425-14-1 Repr. Cat. 3; R63 Xn S: (2-)46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 607-622-00-7 2-ethylhexyl-2-ethylhexanoate 231-057-1 7425-14-1 Repr. Cat. 3; R63 Xn R: 63 S: (2-)36/37 607-623-00-2 diisobutyl phthalate 201-553-2 84-69-5 Repr. Cat. 2; R61 Repr. Cat. 3; R62 T R: 61-62 S: 53-45 Repr. Cat. 2; R61: C ≥ 25 % Repr. Cat. 3; R62: C ≥ 5 % 607-624-00-8 perfluorooctane sulfonic acid; S: 53-45 Repr. Cat. 2; R61: C ≥ 25 % Repr. Cat. 3; R62: C ≥ 5 % 607-624-00-8 perfluorooctane sulfonic acid; heptadecafluorooctane-1-sulfonic acid; [1] potassium perfluorooctanesulfonate; potassium heptadecafluorooctane-1-sulfonate; [2] … 17 unchanged lines … N; R51-53 T; N R: 61-20/22-40-48/25-64-51/53 S: 53-45-61 E 607-625-00-3 clodinafop-propargyl (ISO) - 105512-06-9 Xn; R22-48/22 607-625-00-3 clodinafop-propargyl (ISO) — 105512-06-9 Xn; R22-48/22 R43 N; R50-53. Xn; N R: 22-43-48/22-50/53 S: (2-)24-36/37-46-60-61 R43: C ≥ 0,001 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-626-00-9 ethyl 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylate 401-290-5 103112-35-2 Carc. Cat.2; R45 S: (2-)24-36/37-46-60-61 R43: C ≥ 0,001 % N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-626-00-9 ethyl 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylate 401-290-5 103112-35-2 Carc. Cat.2; R45 N; R50-53 T; N R: 45-50/53 S: 53-45-60-61 607-627-00-4 [(4S, 5S)-4-benzyl-2-oxo-5-oxazolidinyl]methyl 4-nitrobenzenesulfonate 416-360-0 162221-28-5 R43 Xi R: 43 S: (2-)22-24-37 607-628-00-X 4-oxo-4-(p-tolyl)butyric acid adduct with 4-ethylmorpholine 419-240-6 171054-89-0 Xi; R41 Xi R: 41 S: (2-)26-39 607-629-00-5 [[2-methyl-1-(1-oxopropoxy)propoxy](4-phenylbutyl)phosphinyl] acetic acid 419-270-1 123599-82-6 Xi; R36 Xi R: 36 S: (2-)26 607-630-00-0 acrylic acid, 3-(trimethoxysilyl)propyl ester 419-560-6 4369-14-6 Xn; R20 C; R34 R43 R52-53 C R: 20-34-43-52/53 S: (1/2-)26-36/37/39-45-61 607-631-00-6 reaction mass of: 2-(2-((oxo(phenyl)acetyl)oxy)ethoxy)ethyl oxo(phenyl)acetate; (2-(2-hydroxyethoxy)ethyl) oxo(phenyl)acetate 442-300-8 - R43 Xi (2-(2-hydroxyethoxy)ethyl) oxo(phenyl)acetate 442-300-8 — R43 Xi R: 43 S: (2-)24-37 607-632-00-1 N-[3-(2,4-di-(1,1-dimethyl-propyl)phenoxy)-propyl]-1-hydroxy-5-(2-methylpropyl-oxycarbonylamino)-naphthamide 420-210-1 111244-14-5 R53 R: 53 S: 61 607-633-00-7 trisodium 5-{][}4-chloro-6-(1-naphthylamino)-1,3,5-triazin-2-yl{]amino[}-4-hydroxy-3-[(E)-(4-methoxy-2-sulfonatophenyl)diazenyl]-2,7-naphthalenedisulfonate 440-480-2 341026-59-3 Xi; R41 … 94 unchanged lines … R43 N; R50-53 Xn; N R: 41-43-48/22-50/53 S: (2-)22-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 607-671-00-4 diethyl 1,4-cyclohexanedicarboxylate 417-310-0 72903-27-6 N; R51-53 N S: (2-)22-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 607-671-00-4 diethyl 1,4-cyclohexanedicarboxylate 417-310-0 72903-27-6 N; R51-53 N R: 51/53 S: 61 607-672-00-X reaction mass of: 2-hydroxy-3-(methacryloyloxy)propyl (2-benzoyl)benzoate; 1-hydroxymethyl-2-(methacryloyloxy)ethyl (2-benzoyl)benzoate; x-hydroxy-y-(methacryloyloxy)propyl(or -ethyl) (2-benzoyl)benzoate 419-000-0 - R43 x-hydroxy-y-(methacryloyloxy)propyl(or -ethyl) (2-benzoyl)benzoate 419-000-0 — R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 607-673-00-5 1-ethyl-5,6,7,8-tetrahydroquinolinium tosylate 419-570-0 - Xn; R22 S: (2-)24-37-61 607-673-00-5 1-ethyl-5,6,7,8-tetrahydroquinolinium tosylate 419-570-0 — Xn; R22 R52-53 Xn R: 22-52/53 S: (2-)61 607-675-00-6 reaction mass of: cis-9-octadecenedioic acid; cis-9-cis-12-octadecadienedioic acid; hexadecanedioic acid; octadecanedioic acid 422-260-8 - Xi; R41 octadecanedioic acid 422-260-8 — Xi; R41 N; R50-53 Xi; N R: 41-50/53 S: (2-)26-39-60-61 607-676-00-1 reaction mass of: 2-methylnonanedioic acid; 2,4-dimethyl-4-methoxycarbonylundecanedioic acid; 2,4,6-trimethyl-4,6-dimethoxycarbonyltridecanedioic acid; 8,9-dimethyl-8,9-dimethoxycarbonylhexadecanedioic acid 423-670-1 - Xi; R41 8,9-dimethyl-8,9-dimethoxycarbonylhexadecanedioic acid 423-670-1 — Xi; R41 R43 Xi R: 41-43 S: (2-)24-26-37/39 607-677-00-7 2,5-dioxopyrrolidin-1-yl N-{][}methyl[[2-(1-methylethyl)-4-thiazolyl{]methylaminocarbonyl[}-l-valinate 424-660-8 - Xn; R48/22 S: (2-)24-26-37/39 607-677-00-7 2,5-dioxopyrrolidin-1-yl N-{][}methyl[[2-(1-methylethyl)-4-thiazolyl{]methylaminocarbonyl[}-l-valinate 424-660-8 — Xn; R48/22 Xi; R41 R43 Xn R: 41-43-48/22 S: (2-)22-26-36/37/39 607-678-00-2 reaction mass of: ethyl (2R, 3R)-3-isopropylbicyclo[2.2.1]hept-5-ene-2-carboxylate; ethyl (2S, 3S)-3-isopropylbicyclo[2.2.1]hept-5-ene-2-carboxylate 427-090-8 - R43 ethyl (2S, 3S)-3-isopropylbicyclo[2.2.1]hept-5-ene-2-carboxylate 427-090-8 — R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)23-25-36/37-61 607-679-00-8 reaction mass of: 3-{]5-[}3-(4-{]1,6-dihydro-2-hydroxy-4-methyl-1-[}3-(methylammonio)propyl{]-6-oxo-3-pyridylazo[}benzamido)phenylazo{]-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl[}propyl(methyl)ammonium di(acetate); 3-{]5-[}4-(3-{]1,6-dihydro-2-hydroxy-4-methyl-1-[}3-(methylammonio)propyl{]-6-oxo-3-pyridylazo[}benzamido{]phenylazo-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl[}propyl(dimethyl)ammonium di(acetate); 3-{]5-[}3-(4-{]1-[}3-(dimethylammonio)propyl{]-1,6-dihydro-2-hydroxy-4-methyl-6-oxo-3-pyridylazo[}benzamido)phenylazo{]-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl[}propyl(dimethyl)ammonium di(acetate) 431-440-5 - Xi; R41 3-{]5-[}3-(4-{]1-[}3-(dimethylammonio)propyl{]-1,6-dihydro-2-hydroxy-4-methyl-6-oxo-3-pyridylazo[}benzamido)phenylazo{]-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl[}propyl(dimethyl)ammonium di(acetate) 431-440-5 — Xi; R41 N; R51-53 Xi; N R: 41-51/53 S: (2-)22-26-39-61 607-680-00-3 tert-butyl(6-{]2-[}4-(4-fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino{]pyrimidin-5-ylvinyl[}(4S, 6S)-2,2-dimethyl[1,3]dioxan-4-yl)acetate 432-810-9 - R53 R: 53 S: (2-)22-26-39-61 607-680-00-3 tert-butyl(6-{]2-[}4-(4-fluorophenyl)-6-isopropyl-2-[methyl(methylsulfonyl)amino{]pyrimidin-5-ylvinyl[}(4S, 6S)-2,2-dimethyl[1,3]dioxan-4-yl)acetate 432-810-9 — R53 R: 53 S: 61 607-681-00-9 reaction mass of: 9-nonyl-10-octyl-19-carbonyloxyhexadecylnonadecanoic acid; 9-nonyl-10-octyl-19-carbonyloxyoctadecylnonadecanoic acid; dihexadecyl 9-nonyl-10-octylnonadecandioate; 1-octadecyl, 19-hexadecyl 9-nonyl-10-octylnonadecandioate; dioctadecyl 9-nonyl-10-octylnonadecandioate 432-910-2 - R53 R: 53 dioctadecyl 9-nonyl-10-octylnonadecandioate 432-910-2 — R53 R: 53 S: 61 607-682-00-4 complex reaction mass of Chinese gum rosin post reacted with acrylic acid 434-230-1 144413-22-9 R53 R: 53 S: 61 607-683-00-X reaction mass of: methyl 3-((1E)-2-methylprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate; methyl 3-((1Z)-2-methylprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate (20:80) 435-450-0 - R43 methyl 3-((1Z)-2-methylprop-1-enyl)-2,2-dimethylcyclopropanecarboxylate (20:80) 435-450-0 — R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)24-37-61 607-684-00-5 alkenes, C12-14, hydroformylation products, distn. residues, C-(hydrogen sulfobutanedioates), disodium salts 435-660-2 243662-67-1 Xi; R38 R43 Xi R: 38-43 S: (2-)24-37 607-685-00-0 ammonium 2-cocoyloxyethanesulfonate 441-050-7 - Xi; R38-41 Xi S: (2-)24-37 607-685-00-0 ammonium 2-cocoyloxyethanesulfonate 441-050-7 — Xi; R38-41 Xi R: 38-41 S: (2-)26-37/39 607-686-00-6 6,6'-bis(diazo-5,5', 6,6'-tetrahydro-5,5'-dioxo)[methylene-bis(5-(6-diazo-5,6-dihydro-5-oxo-1-naphthylsulphonyloxy)-6-methyl-2-phenylene]di(naphthalene-1-sulfonate) 441-550-5 - E; R2 S: (2-)26-37/39 607-686-00-6 6,6'-bis(diazo-5,5', 6,6'-tetrahydro-5,5'-dioxo)[methylene-bis(5-(6-diazo-5,6-dihydro-5-oxo-1-naphthylsulphonyloxy)-6-methyl-2-phenylene]di(naphthalene-1-sulfonate) 441-550-5 — E; R2 F; R11 Carc. Cat. 3; R40 E; Xn R: 2-11-40 S: (2-)7-22-36/37 607-687-00-1 reaction mass of: 2-{]3,6-bis-[}(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,3-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,5-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %) 442-800-6 - Xi; R38 S: (2-)7-22-36/37 607-687-00-1 reaction mass of: 2-{]3,6-bis-[}(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,3-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3,6-bis-[}(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (2-10 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,5-dimethylphenyl)-methylamino]-6-[(2-ethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,4-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,3-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %); 2-{]3-[}(2,4-dimethylphenyl)-methylamino]-6-[(2,5-dimethylphenyl)-methylamino{]-xanthylium-9-yl[}-benzenesulfonate (7-20 %) 442-800-6 — Xi; R38 N; R51-53 Xi; N R: 38-51/53 S: (2-)37-61 607-688-00-7 (R)-1-cyclohexa-1,4-dienyl-1-methoxycarbonyl-methylammoniumchloride 444-320-2 - Xn; R22 Xn S: (2-)37-61 607-688-00-7 (R)-1-cyclohexa-1,4-dienyl-1-methoxycarbonyl-methylammoniumchloride 444-320-2 — Xn; R22 Xn R: 22 S: (2-) 607-689-00-2 reaction mass of: methyl 1,4-dimethylcyclohexanecarboxylate (para-isomer including cis- and trans- isomers); methyl 1,3-dimethylcyclohexanecarboxylate (meta-isomer including cis- and trans-isomers) 444-920-4 - R52-53 R: 52/53 methyl 1,3-dimethylcyclohexanecarboxylate (meta-isomer including cis- and trans-isomers) 444-920-4 — R52-53 R: 52/53 S: 61 607-690-00-8 dimethyl[2S, 2S']-6,6,6'6'-tetramethoxy-2,2'-[N,N'-bis(trifluoracetyl)-S, S'-bi(L-homocysteinyl) diimino]dihexanoate 432-860-1 255387-46-3 R43 Xi R: 43 S: (2-)24-37 607-691-00-3 magnesium salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 448-690-6 - R53 R: 53 S: 61 607-692-00-9 zinc salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 446-470-4 - R53 R: 53 S: (2-)24-37 607-691-00-3 magnesium salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 448-690-6 — R53 R: 53 S: 61 607-692-00-9 zinc salts, fatty acids, C16-18 and C18 unsaturated, branched and linear 446-470-4 — R53 R: 53 S: 61 607-693-00-4 hexyl 2-(1-(diethylaminohydroxyphenyl)methanoyl)benzoate 443-860-6 302776-68-7 R53 R: 53 S: 61 607-694-00-X ethyl 5,5-diphenyl-2-isoxazoline-3-carboxylate 443-870-0 163520-33-0 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)22-36/37-60-61 607-698-00-1 4-tert-butylbenzoic acid 202-696-3 98-73-7 Repr. Cat. 2; R60 T; R48/23/24/25 Xn; R22 T R: 60-22-48/23/24/25 S: 53-45 E 607-699-00-7 bifenthrin (ISO); (2-methylbiphenyl-3-yl)methyl rel-(1R,3R)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate 82657-04-3 Carc. Cat 3; R40 T; R23/25 Xn; R48/22 R43 N; R50-53 T; N R: 23/25-40-43-48/22-50/53 S: (1/2-)23-24-36/37-38- 45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C< 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 607-700-00-0 indoxacarb (ISO); S: (1/2-)23-24-36/37-38- 45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C< 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 607-700-00-0 indoxacarb (ISO); methyl (4aS)-7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate 173584-44-6 T; R25-48/25 Xn; R20 R43 N; R50-53 T; N R: 20-25-43-48/25-50/53 S: (1/2-)24-37-45-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-701-00-6 reaction mass of (S)- Indoxacarb and (R)- Indoxacarb 75:25; S: (1/2-)24-37-45-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-701-00-6 reaction mass of (S)- Indoxacarb and (R)- Indoxacarb 75:25; methyl 7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate 144171-61-9 T; R48/25 Xn; R20/22 R43 N; R50-53 T; N R: 20/22-43-48/25-50/53 S: (1/2-)24-37-45-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-702-00-1 dihexyl phthalate 201-559-5 84-75-3 Repr. Cat. 2; R60-61 T S: (1/2-)24-37-45-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 607-702-00-1 dihexyl phthalate 201-559-5 84-75-3 Repr. Cat. 2; R60-61 T R: 60-61 S: 45-53 607-703-00-7 ammoniumpentade- cafluorooctanoate 223-320-4 3825-26-1 Carc. Cat. 3; R40 Repr. Cat. 2; R61 R64 T; R48/23 Xn; R20/22-48/21/22 Xi; R41 T R: 61-20/22-40-41- 48/23-48/21/22-64 S: 45-53 607-704-00-2 perfluorooctanoic acid 206-397-9 335-67-1 Carc. Cat. 3; R40 Repr. Cat. 2; R61 R64 T; R48/23 Xn; R20/22-48/21/22 Xi; R41 T R: 61-20/22-40-41-48/23-48/21/22-64 S: 45-53 608-001-00-3 acetonitrile; S: 45-53 607-705-00-8 benzoic acid 200-618-2 65-85-0 T; R48/23 Xi; R38-41 T R: 38-41-48/23 S: (1/2-)26-39-45-63 607-706-00-3 methyl 2,5-dichlorobenzoate 220-815-7 2905-69-3 Xn; R22 N; R51-53 Xn; N R: 22-51/53 S: (2-) 46-61 608-001-00-3 acetonitrile; cyanomethane 200-835-2 75-05-8 F; R11 Xn; R20/21/22 Xi; R36 F; Xn R: 11-20/21/22-36 S: (2-)16-36/37 608-002-00-9 trichloroacetonitrile 208-885-7 545-06-2 T; R23/24/25 N; R51-53 T; N R: 23/24/25-51/53 S: (1/2-)45-61 608-003-00-4 acrylonitrile 203-466-5 107-13-1 F; R11 Carc. Cat. 2; R45 T; R23/24/25 Xi; R37/38-41 R43 N; R51-53 F; T; N R: 45-11-23/24/25-37/38-41-43-51/53 S: - 53-45-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % D E S: - 53-45-61 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % D E 608-004-00-X 2-hydroxy-2-methylpropionitrile; 2-cyanopropan-2-ol; acetone cyanohydrin 200-909-4 75-86-5 T+; R26/27/28 N; R50-53 T+; N R: 26/27/28-50/53 S: (1/2-)7/9-27-45-60-61 608-005-00-5 n-butyronitrile 203-700-6 109-74-0 F; R11 T; R23/24/25 F; T R: 11-23/24/25 S: (1/2-)16-36/37-45-63 608-006-00-0 bromoxynil (ISO) 3,5-dibromo-4-hydroxybenzonitrile; bromoxynil phenol 216-882-7 1689-84-5 Repr. Cat. 3; R63 T+; R26 T; R25 R43 N; R50-53 T+; N R: 25-26-43-63-50/53 S: (1/2-)27/28-36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-007-00-6 ioxynil (ISO) S: (1/2-)27/28-36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-007-00-6 ioxynil (ISO) 4-hydroxy-3,5-diiodobenzonitrile 216-881-1 1689-83-4 Repr. Cat. 3; R63 T; R23/25 Xn; R21-48/22 Xi; R36 N; R50-53 T; N R: 21-23/25-36-48/22-63-50/53 S: (1/2-)36/37-45-60-61-63 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-008-00-1 chloroacetonitrile 203-467-0 107-14-2 T; R23/24/25 S: (1/2-)36/37-45-60-61-63 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-008-00-1 chloroacetonitrile 203-467-0 107-14-2 T; R23/24/25 N; R51-53 T; N R: 23/24/25-51/53 S: (1/2-)45-61 608-009-00-7 malononitrile 203-703-2 109-77-3 T; R23/24/25 N; R50-53 T; N R: 23/24/25-50/53 S: (1/2-)23-27-45-60-61 608-010-00-2 methacrylonitrile; 2-methyl-2-propene nitrile 204-817-5 126-98-7 F; R11 T; R23/24/25 R43 F; T R: 11-23/24/25-43 S: (1/2-)9-16-18-29-45 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % R43: C ≥ 0,2 % D S: (1/2-)9-16-18-29-45 T; R23/24/25: C ≥ 1 % Xn; R20/21/22: 0,2 % ≤ C < 1 % R43: C ≥ 0,2 % D 608-011-00-8 oxalonitrile; cyanogen 207-306-5 460-19-5 F+; R12 T; R23 N; R50-53 F+; T; N R: 12-23-50/53 S: (1/2-)9-16-23-33-45-63-60-61 608-012-00-3 benzonitrile 202-855-7 100-47-0 Xn; R21/22 Xn R: 21/22 S: (2-)23 608-013-00-9 2-chlorobenzonitrile 212-836-5 873-32-5 Xn; R21/22 Xi; R36 Xn R: 21/22-36 S: (2-)23 608-014-00-4 chlorothalonil (ISO); tetrachloroisophthalonitrile 217-588-1 1897-45-6 Carc. Cat. 3; R40 T+; R26 Xi; R37-41 R43 N; R50-53 T+; N R: 26-37-40-41-43-50/53 S: (1/2-)28-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-015-00-X dichlobenil (ISO); S: (1/2-)28-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-015-00-X dichlobenil (ISO); 2,6-dichlorobenzonitrile 214-787-5 1194-65-6 Xn; R21 N; R51-53 Xn; N R: 21-51/53 S: (2-)36/37-61 608-016-00-5 1,4-Dicyano-2,3,5,6-tetra-chloro-benzene 401-550-8 1897-41-2 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 608-017-00-0 bromoxynil octanoate (ISO); 2,6-dibromo-4-cyanophenyl octanoate 216-885-3 1689-99-2 Repr. Cat. 3; R63 T; R23 Xn; R22 R43 N; R50-53 T; N R: 22-23-43-63-50/53 S: (1/2-)36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-018-00-6 ioxynil octanoate (ISO); S: (1/2-)36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-018-00-6 ioxynil octanoate (ISO); 4-cyano-2,6-diiodophenyl octanoate 223-375-4 3861-47-0 Repr. Cat. 3; R63 T; R25 Xi; R36 R43 N; R50-53 T; N R: 25-36-43-63-50/53 S: (1/2-)26-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-019-00-1 2,2'-dimethyl-2,2'-azodipropiononitrile; S: (1/2-)26-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-019-00-1 2,2'-dimethyl-2,2'-azodipropiononitrile; ADZN 201-132-3 78-67-1 E; R2 F; R11 Xn; R20/22 … 45 unchanged lines … Xn; R22 N; R50-53 T; N R: 22-23-50/53 S: (1/2-)13-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 608-035-00-9 (±)-α-[(2-acetyl-5-methylphenyl)-amino]-2,6-dichlorobenzene-aceto-nitrile 419-290-9 — R43 S: (1/2-)13-36/37-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 608-035-00-9 (±)-α-[(2-acetyl-5-methylphenyl)-amino]-2,6-dichlorobenzene-aceto-nitrile 419-290-9 — R43 R53 Xi R: 43-53 S: (2-)24-37-61 608-036-00-4 3-(2-{4-[2-(4-cyanophenyl)vinyl]phenyl}vinyl)benzonitrile 419-060-8 79026-02-1 R53 R: 53 … 34 unchanged lines … N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 608-050-00-0 reaction mass of: 5-(2-cyano-4-nitrophenylazo)-2-(2-(2-hydroxyethoxy)ethylamino)-4-methyl-6-phenylaminonicotinonitrile; 5-(2-cyano-4-nitrophenylazo)-6-(2-(2-hydroxyethoxy)ethylamino)-4-methyl-2-phenylaminonicotinonitrile 429-760-5 - R53 R: 53 5-(2-cyano-4-nitrophenylazo)-6-(2-(2-hydroxyethoxy)ethylamino)-4-methyl-2-phenylaminonicotinonitrile 429-760-5 — R53 R: 53 S: 61 608-051-00-6 (R)-4-(4-dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 430-760-2 219861-18-4 Xn; R22 R43 N; R51-53 Xn; N R: 22-43-51/53 S: (2-)36/37-61 608-052-00-1 (S)-4-(4-dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 430-770-7 128173-52-4 Xn; R22 R43 N; R51-53 Xn; N R: 22-43-51/53 S: (2-)36/37-61 608-053-00-7 (R,S)-4-(4-dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile 430-780-1 103146-25-4 Xn; R22 R43 N; R51-53 Xn; N R: 22-43-51/53 S: (2-)36/37-61 608-054-00-2 (R,S)-4-(4-dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile hemisulfate 430-790-6 - Xn; R22 S: (2-)36/37-61 608-054-00-2 (R,S)-4-(4-dimethylamino-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile hemisulfate 430-790-6 — Xn; R22 Xi; R41 R43 N; R51-53 Xn; N R: 22-41-43-51/53 S: (2-)22-26-36/37/39-61 608-055-00-8 fipronil (ISO); 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile - 120068-37-3 T; R23/24/25-48/25 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile — 120068-37-3 T; R23/24/25-48/25 N; R50-53 T; N R: 23/24/25-48/25-50/53 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-056-00-3 N-methyl-N-cyanomethylmorpholiniummethylsulfate 429-340-1 - Xn; R22 S: (1/2-)28-36/37-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 608-056-00-3 N-methyl-N-cyanomethylmorpholiniummethylsulfate 429-340-1 — Xn; R22 Xi; R41 Xn R: 22-41 S: (2-)22-26-39 608-057-00-9 4-(cyanomethyl)-4-methylmorpholin-4-ium hydrogen sulfate 431-200-1 208538-34-5 Xn; R22 Xi; R41 R43 Xn R: 22-41-43 S: (2-)22-24-26-37/39 608-058-00-4 esfenvalerate (ISO); (S)-α-cyano-3-phenoxybenzyl-(S)-2-(4-chlorophenyl)-3-methylbutyrate — 66230-04-4 T; R23/25 R43 N; R50-53 T; N R: 23/25-43-50/53 S: (1/2-)24-36/37/39-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 608-059-00-X 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile 421-240-6 120068-79-3 N; R51-53 N S: (1/2-)24-36/37/39-45-60-61 N; R50-53: C ≥ 0,0025 % N; R51-53: 0,00025 % ≤ C < 0,0025 % R52-53: 0,000025 % ≤ C < 0,00025 % 608-059-00-X 5-amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-pyrazole-3-carbonitrile 421-240-6 120068-79-3 N; R51-53 N R: 51/53 S: 22-61 608-060-00-5 5-methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile 421-300-1 138564-59-7 N; R50-53 N R: 50/53 S: 22-60-61 608-062-00-6 2-fluoro-4-hydroxybenzonitrile 422-810-7 82380-18-5 Xn; R22 Xi; R41 N; R51-53 Xn; N R: 22-41-51/53 S: (2-)22-26-39-61 608-063-00-1 (S)-α-hydroxy-3-phenoxy-benzeneacetonitrile 441-070-6 61826-76-4 T; R25 Xi; R41 R43 N; R50-53 T; N R: 25-41-43-50/53 S: (1/2-)9-26-36/37/39-45-60-61 608-064-00-7 cyanomethyltrimethylammoniummethylsulfate 433-720-2 - R52-53 R: 52/53 S: (1/2-)9-26-36/37/39-45-60-61 608-064-00-7 cyanomethyltrimethylammoniummethylsulfate 433-720-2 — R52-53 R: 52/53 S: 61 608-065-00-2 salts of bromoxynil with the exception of those specified elsewhere in this Annex — — Repr. Cat. 3; R63 T+; R26 T; R25 R43 N; R50-53 T+; N R: 25-26-43-50/53 S: (1/2-)27/28-36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A S: (1/2-)27/28-36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A 608-066-00-8 salts of ioxynil with the exception of those specified elsewhere in this Annex — — Repr. Cat. 3; R63 T; R23/25 Xn; R21-48/22 Xi; R36 N; R50-53 T; N R: 21-23/25-36-48/22-63-50/53 S: (1/2-)36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A S: (1/2-)36/37-45-63-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % A 609-001-00-6 1-nitropropane 203-544-9 108-03-2 R10 Xn; R20/21/22 Xn R: 10-20/21/22 S: (2-)9 Xn; R20/21/22: C ≥ 5 % 609-002-00-1 2-nitropropane 201-209-1 79-46-9 R10 S: (2-)9 Xn; R20/21/22: C ≥ 5 % 609-002-00-1 2-nitropropane 201-209-1 79-46-9 R10 Carc. Cat. 2; R45 Xn; R20/22 T R: 45-10-20/22 … 112 unchanged lines … N; R50-53 T+; N R: 26/27/28-33-50/53 S: (1/2-)13-28-45-60-61 609-023-00-6 dinocap (ISO); (RS)-2,6-dinitro-4-octylphenyl crotonates and (RS)-2,4-dinitro-6-octylphenyl crotonates in which octyl is a reaction mass of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl groups 254-408-0 39300-45-3 Repr. Cat. 2; R61 (RS)-2,6-dinitro-4-octylphenyl crotonates and (RS)-2,4-dinitro-6-octylphenyl crotonates in which octyl is a reaction mass of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl groups 254-408-0 39300-45-3 Repr. Cat. 2; R61 Xn; R20/22-48/22 Xi; R38 R43 N; R50-53 T; N R: 61-20/22-38-43-48/22-50/53 S: 53-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % E S: 53-45-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % E 609-024-00-1 binapacryl (ISO); 2-sec-butyl-4,6-dinitrophenyl-3-methylcrotonate 207-612-9 485-31-4 Repr. Cat. 2; R61 Xn; R21/22 … 58 unchanged lines … 609-035-00-1 nitroethane 201-188-9 79-24-3 R10 Xn; R20/22 Xn R: 10-20/22 S: (2-)9-25-41 Xn; R20/22: C ≥ 12,5 % 609-036-00-7 nitromethane 200-876-6 75-52-5 R5-10 S: (2-)9-25-41 Xn; R20/22: C ≥ 12,5 % 609-036-00-7 nitromethane 200-876-6 75-52-5 R5-10 Xn; R22 Xn R: 5-10-22 S: (2-)41 Xn; R22: C ≥ 12,5 % 609-037-00-2 5-nitroacenaphthene 210-025-0 602-87-9 Carc. Cat. 2; R45 T S: (2-)41 Xn; R22: C ≥ 12,5 % 609-037-00-2 5-nitroacenaphthene 210-025-0 602-87-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 609-038-00-8 2-nitronaphthalene 209-474-5 581-89-5 Carc. Cat. 2; R45 N; R51-53 T; N … 36 unchanged lines … R43 N; R50-53 Xn; N R: 40-43-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 609-047-00-7 2-nitroanisole 202-052-1 91-23-6 Carc. Cat. 2; R45 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 609-047-00-7 2-nitroanisole 202-052-1 91-23-6 Carc. Cat. 2; R45 Xn; R22 T R: 45-22 S: 53-45 E … 70 unchanged lines … R43 N; R50-53 E; C; N R: 2-22-35-40-43-48/22-50/53 S: (1/2-)23-26-36/37/39-45-60-61 Xn; R22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 609-057-00-1 3-chloro-2,4-difluoronitrobenzene 411-980-8 3847-58-3 Xn; R22 S: (1/2-)23-26-36/37/39-45-60-61 Xn; R22: C ≥ 10 % C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 609-057-00-1 3-chloro-2,4-difluoronitrobenzene 411-980-8 3847-58-3 Xn; R22 C; R34 R43 N; R50-53 C; N … 59 unchanged lines … R43 R52-53 Xn R: 22-43-62-52/53 S: (2-)22-36/37-61 609-073-00-9 lithium potassium sodium N,N''-bis{]6-[}7-[4-(4-chloro-1,3,5-triazin-2-yl)amino-4-(2-ureidophenylazo){]naphthalene-1,3,6-trisulfonato[}-N'-(2-aminoethyl)piperazine 427-850-9 - R43 Xi S: (2-)22-36/37-61 609-073-00-9 lithium potassium sodium N,N''-bis{]6-[}7-[4-(4-chloro-1,3,5-triazin-2-yl)amino-4-(2-ureidophenylazo){]naphthalene-1,3,6-trisulfonato[}-N'-(2-aminoethyl)piperazine 427-850-9 — R43 Xi R: 43 S: (2-)22-24-37 610-001-00-3 trichloronitromethane; chloropicrin 200-930-9 76-06-2 Xn; R22 … 24 unchanged lines … S: (1/2-)28-36/37-45-61 A C 610-007-00-6 1-chloro-1-nitropropane 209-990-0 600-25-9 Xn; R20/22 Xn R: 20/22 S: (2-) Xn; R20/22: C ≥ 5 % 610-008-00-1 2,6-dichloro-4-nitroanisole 403-350-6 17742-69-7 T; R25 S: (2-) Xn; R20/22: C ≥ 5 % 610-008-00-1 2,6-dichloro-4-nitroanisole 403-350-6 17742-69-7 T; R25 N; R51-53 T; N R: 25-51/53 S: (1/2-)36/37-45-61 610-009-00-7 2-chloro-4-nitroaniline 204-502-2 121-87-9 Xn; R22 … 170 unchanged lines … pentasodium 7-amino-8-[4-[4-[4-[4-(2-amino-5-hydroxy-7-sulfonato-naphthalen-1-ylazo)-7-sulfonatonaphthalen-1-ylazo]-phenylamino]-3-sulfonato-phenylazo]-6-sulfonato-naphthalen-1-ylazo]-4-hydroxy-naphthalene-2-sulfonate; pentasodium 7-amino-8-[4-[4-[4-[4-(6-amino-1-hydroxy-3-sulfonato-naphthalen-1-ylazo)-7-sulfonatonaphthalen-1-ylazo]-phenylamino]-3-sulfonato-phenylazo]-6-sulfonato-naphthalen-1-ylazo]-4-hydroxy-naphthalene-2-sulfonate; tetrasodium 7-amino-4-hydroxy-3-[4-[4-[4-(4-hydroxy-7-sulfonato-naphthalen-1-ylazo)-2-sulfonato-phenylamino]phenylazo]-6-sulfonato-naphthalen-1-ylazo]naphthalene-2-sulfonate; tetrasodium 7-amino-4-hydroxy-3-[4-[4-[4-(4-amino-7-sulfonato-naphthalen-1-ylazo)-2-sulfonato-phenylamino]phenylazo]-6-sulfonato-naphthalen-1-ylazo]naphthalene-2-sulfonate 415-350-3 - Xi; R41 tetrasodium 7-amino-4-hydroxy-3-[4-[4-[4-(4-amino-7-sulfonato-naphthalen-1-ylazo)-2-sulfonato-phenylamino]phenylazo]-6-sulfonato-naphthalen-1-ylazo]naphthalene-2-sulfonate 415-350-3 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)22-26-39-61 611-051-00-9 2-(4-(N-ethyl-N-(2-hydroxy)ethyl)amino-2-methylphenyl)azo-6-methoxy-3-methyl-benzothiazolium chloride 411-110-7 136213-74-6 N; R50-53 N … 265 unchanged lines … S: 61 611-138-00-1 2-(4-aminophenyl)-6-tert-butyl-1H-pyrazolo[1,5-b][1,2,4]triazole 415-910-7 152828-25-6 R43 N; R51-53 Xi; N R: 43-51/53 S: (2-)22-24-37-61 611-139-00-7 reaction product of: C.I. Leuco Sulfur Black 1 with (3-chloro-2-hydroxypropyl)trimethylammonium chloride 424-510-1 - Xi; R41 S: (2-)22-24-37-61 611-139-00-7 reaction product of: C.I. Leuco Sulfur Black 1 with (3-chloro-2-hydroxypropyl)trimethylammonium chloride 424-510-1 — Xi; R41 N; R51-53 Xi; N R: 41-51/53 S: (2-)26-39-61 611-140-00-2 azafenidin (ISO) 2-(2,4-dichloro-5-prop-2-ynyloxyphenyl)-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyridin-3(2H)-one — 68049-83-2 Repr. Cat. 2; R61 Repr. Cat. 3; R62 Xn; R48/22 N; R50-53 T; N R: 61-48/22-62-50/53 S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % E 611-141-00-8 5-(4-[4-[4-(3,5-dicarboxy-phenyl-azo)phenylamino]-6-morpholin-4-yl-1,3,5-triazin-2-ylamino]phenylazo)isophthalic acid, mixed monosodium and diammonium salt 414-410-6 - Xi; R41 S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % E 611-141-00-8 5-(4-[4-[4-(3,5-dicarboxy-phenyl-azo)phenylamino]-6-morpholin-4-yl-1,3,5-triazin-2-ylamino]phenylazo)isophthalic acid, mixed monosodium and diammonium salt 414-410-6 — Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 611-142-00-3 product-by-process definition polyazodyestuff obtained by coupling 4-[4-(1-amino-8-hydroxy-3,6-disulfo-2-naphthylazo)phenylsulfonylamino]benzenediazonium with reaction mass of 4-carboxybenzenediazonium and diphenylamine-3-sulfo-4,4'-bisdiazonium, and further coupling of the obtained compounds with reaction mass of naphth-2-ol and 3-aminophenol, sodium salts; sodium chloride 425-740-5 - Xi; R41 S: (2-)22-24-26-37/39 611-142-00-3 product-by-process definition polyazodyestuff obtained by coupling 4-[4-(1-amino-8-hydroxy-3,6-disulfo-2-naphthylazo)phenylsulfonylamino]benzenediazonium with reaction mass of 4-carboxybenzenediazonium and diphenylamine-3-sulfo-4,4'-bisdiazonium, and further coupling of the obtained compounds with reaction mass of naphth-2-ol and 3-aminophenol, sodium salts; sodium chloride 425-740-5 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 611-143-00-9 reaction mass of: trisodium 2-(2-[α-(2-carboxylato-κ-O-4-sulfonatophenylazo)benzylidene]hydrazino-κ-N')-6-(2,6-difluoropyrimidin-4-ylamino)-4-sulfonatophenolatocuprate (II); trisodium 2-(2-[α-(2-carboxylato-κ-O-4-sulfonatophenylazo)benzylidene]hydrazino-κ-N')-6-(4,6-difluoropyrimidin-2-ylamino)-4-sulfonatophenolatocuprate (II) 428-260-4 - Xi; R41 Xi trisodium 2-(2-[α-(2-carboxylato-κ-O-4-sulfonatophenylazo)benzylidene]hydrazino-κ-N')-6-(4,6-difluoropyrimidin-2-ylamino)-4-sulfonatophenolatocuprate (II) 428-260-4 — Xi; R41 Xi R: 41 S: (2-)22-26-39 611-144-00-4 reaction mass of: 7-amino-3,8-bis-[4-(2-sulfoxyethylsulfonyl)phenylazo]-4-hydroxynaphthalene-2-sulfonic acid, Na/K salt; 7-amino-3-[4-(2-sulfoxyethylsulfonyl)phenylazo]-4-hydroxy-8-[4-(2-sulfoxyethylsulfonyl)-2-sulfophenylazo]naphthalene-2-sulfonic acid, Na/K salt; 7-amino-8-[4-(2-sulfoxyethylsulfonyl)-phenylazo]-4-hydroxy-3-[4-(2-sulfoxyethylsulfonyl)-2-sulfophenylazo]naphthalene-2-sulfonic acid, Na/K salt; 7-amino-3,8-bis-[4-(2-sulfoxyethylsulfonyl)-2-sulfophenylazo]-4-hydroxynaphthalene-2-sulfonic acid, Na/K salt 429-070-4 214362-06-8 Xi; R41 Xi R: 41 S: (2-)22-26-39 611-145-00-X reaction mass of: tetrasodium 3-(1,5-disulfonatonaphthalene-2-ylazo)-4-hydroxy-7-{]4-chloro-6-[}4-(2-sulfoxyethylsulfonyl)phenylamino{]-1,3,5-triazine-2-ylamino[}naphthalene-2-sulfonate; 3-(2,5-disulfophenylazo)-4-hydroxy-7-{]4-chloro-6-[}4-(2-sulfoxyethylsulfonyl)phenylamino{]-1,3,5-triazine-2-ylamino[}naphthalene-2-sulfonic acid, sodium salt 429-440-5 - Xi; R41 Xi 3-(2,5-disulfophenylazo)-4-hydroxy-7-{]4-chloro-6-[}4-(2-sulfoxyethylsulfonyl)phenylamino{]-1,3,5-triazine-2-ylamino[}naphthalene-2-sulfonic acid, sodium salt 429-440-5 — Xi; R41 Xi R: 41 S: (2-)22-26-39 611-146-00-5 reaction mass of: pentasodium 3-(4-(4-(7-(2,4-diamino-5-sulfonato-3-(4-sulfonatophenylazo)phenylazo)-1-hydroxy-3-sulfonatonaphthalen-2-ylazo)-2-sulfonatophenylamino)phenylazo)-4-hydroxy-6-(2-oxo-1-phenylcarbamoylpropylazo)naphthalene-2-sulfonate; pentasodium 6-((2,4-diamino-5-sulfonatophenyl)azo)-3-((4-((4-((7-((2,4-diamino-5-sulfonatophenyl)azo)-1-hydroxy-3-sulfonatonaphthalen-2-yl)azo)phenyl)amino)-2-sulfonatophenyl)azo)-4-hydroxynaphthalene-2-sulfonate; pentasodium 6-((2,4-diamino-5-sulfonato-3-((4-sulfonatophenyl)azo)phenyl)azo)-3-((4-((4-((1,7-dihydroxy-3-sulfonatonaphthalen-2-yl)azo)-2-sulfonatophenyl)amino)phenyl)azo)-4-hydroxynaphthalene-2-sulfonate; hexasodium 6-((2,4-diamino-5-sulfonatophenyl)azo)-3-((4-((4-((7-((2,4-diamino-5-sulfonato-3-((4-sulfonatophenyl)azo)phenyl)azo)-1-hydroxy-3-sulfonatonaphthalen-2-yl)azo)-2-sulfonatophenyl)amino)phenyl)azo)-4-hydroxynaphthalene-2-sulfonate 430-070-1 - N; R51-53 N hexasodium 6-((2,4-diamino-5-sulfonatophenyl)azo)-3-((4-((4-((7-((2,4-diamino-5-sulfonato-3-((4-sulfonatophenyl)azo)phenyl)azo)-1-hydroxy-3-sulfonatonaphthalen-2-yl)azo)-2-sulfonatophenyl)amino)phenyl)azo)-4-hydroxynaphthalene-2-sulfonate 430-070-1 — N; R51-53 N R: 51/53 S: 61 611-147-00-0 sodium, potassium, lithium 5-amino-3,6-bis(5-(4-chloro-6-(methyl-(2-methylaminoacetyl)amino)-1,3,5-triazin-2-ylamino)-2-sulfonatophenylazo)-4-hydroxynaphthalene-2,7-disulfonate 430-090-0 205764-96-1 Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 611-148-00-6 reaction mass of: 2-(3-(2,6-dichloro-4-nitrophenylazo)carbazol-9-yl)ethanol; 2-(2-(3-(2,6-dichloro-4-nitro-phenylazo)-carbazol-9-yl)-ethoxy)ethanol; 3-(2,6-dichloro-4-nitrophenylazo)carbazol 429-590-1 - R43 3-(2,6-dichloro-4-nitrophenylazo)carbazol 429-590-1 — R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-60-61 611-149-00-1 2-(2-chloroacetoxy)ethyl 3-((4-(2,5-dichloro-4-fluorosulfonylphenylazo)-3-methylphenyl)ethylamino)propionate 427-570-7 193486-83-8 N; R51-53 N R: 51/53 S: 61 611-150-00-7 tetralithium 2-[6-[7-[2-(carboxylato)phenylazo]-8-hydroxy-3,6-disulfonato-1-naphthylamino]-4-hydroxy-1,3,5-triazine-2-ylamino]benzoate 440-460-3 - Xi; R36 S: 61 611-150-00-7 tetralithium 2-[6-[7-[2-(carboxylato)phenylazo]-8-hydroxy-3,6-disulfonato-1-naphthylamino]-4-hydroxy-1,3,5-triazine-2-ylamino]benzoate 440-460-3 — Xi; R36 R52-53 Xi R: 36-52/53 S: (2-)26-39-61 611-151-00-2 chrysoidine; … 51 unchanged lines … potassium sodium 3-[(E)-(6-{]3,4-dihydroxy-2-[}(Z)-(3-sulfonatophenyl)diazenyl{]benzyl[}-2,3-dihydroxyphenyl)diazenyl]benzenesulfonate 432-590-4 243869-48-9 Xi; R36 R52-53 Xi R: 36-52/53 S: (2-)26-61 611-158-00-0 reaction product of: 2,3,4,2', 3', 4'-hexahydroxy-5,5'-diacethyl-diphenylmethane and 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonylchloride and 3-diazo-3,4-dihydro-6-methoxy-4-oxo-1-naphthalenesulfonylchloride 421-520-8 - F; R11 S: (2-)26-61 611-158-00-0 reaction product of: 2,3,4,2', 3', 4'-hexahydroxy-5,5'-diacethyl-diphenylmethane and 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonylchloride and 3-diazo-3,4-dihydro-6-methoxy-4-oxo-1-naphthalenesulfonylchloride 421-520-8 — F; R11 R53 F R: 11-53 S: (2-)3-12-16-33-61 611-159-00-6 disodium 4-amino-6-((4-((4-(2,4-diaminophenyl)azo)phenylsulfamoyl)phenyl)azo)-5-hydroxy-3-((4-nitrophenyl)azo)naphthalene-2,7-disulfonate 421-880-6 - Xi; R41 S: (2-)3-12-16-33-61 611-159-00-6 disodium 4-amino-6-((4-((4-(2,4-diaminophenyl)azo)phenylsulfamoyl)phenyl)azo)-5-hydroxy-3-((4-nitrophenyl)azo)naphthalene-2,7-disulfonate 421-880-6 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 611-160-00-1 reaction mass of: 1,1,1-tris(phenyl-4'-(3''-diazo-3'', 4''-dihydro-4''-oxo-naphthalene-1''-sulfonato)ethane; 1,1,1-tris(phenyl-4'-(6''-diazo-5'', 6''-dihydro-5''-oxo-naphthalene-1''-sulfonato)ethane; reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (2:1); reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (1:2) 422-760-6 - F; R11 reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (2:1); reaction product of 1,1,1-tris(p-hydroxyphenyl)ethane with 6-diazo-5,6-dihydro-5-oxo-1-naphthylsulfonylchloride and 3-diazo-3,4-dihydro-4-oxo-1-naphthylsulfonylchloride (1:2) 422-760-6 — F; R11 R53 F R: 11-53 S: (2-)3-12-33-61 611-161-00-7 trisodium [1,2'-(2-(8-amino-3,5-disulfonatonaphthalene)azo)-(4'-nitrobenzene)diolato-O, O, N][(Z)-2,2-((phenylcarbamoylprop-1'-enyl)azo)-5-sulfamoylbenzene)diolato-O, O, N]chromate(III) 423-100-1 - Xi; R41 Xi S: (2-)3-12-33-61 611-161-00-7 trisodium [1,2'-(2-(8-amino-3,5-disulfonatonaphthalene)azo)-(4'-nitrobenzene)diolato-O, O, N][(Z)-2,2-((phenylcarbamoylprop-1'-enyl)azo)-5-sulfamoylbenzene)diolato-O, O, N]chromate(III) 423-100-1 — Xi; R41 Xi R: 41 S: (2-)26-39 611-162-00-2 2,4-bis(((2-(dimethylammonio)ethyloxy)carbonyl)phen-2-ylazo)benzene-1,3-diolbis(methanesulfonate) 429-600-4 - Xn; R22 S: (2-)26-39 611-162-00-2 2,4-bis(((2-(dimethylammonio)ethyloxy)carbonyl)phen-2-ylazo)benzene-1,3-diolbis(methanesulfonate) 429-600-4 — Xn; R22 Xi; R41 N; R51-53 Xn; N R: 22-41-51/53 S: (2-)22-26-39-61 611-163-00-8 2,4-bis(((2-(dimethylammonio)ethyloxy)carbonyl)phen-2-ylazo)benzene-1,3-diol sulfate 429-610-9 - Xn; R22 S: (2-)22-26-39-61 611-163-00-8 2,4-bis(((2-(dimethylammonio)ethyloxy)carbonyl)phen-2-ylazo)benzene-1,3-diol sulfate 429-610-9 — Xn; R22 Xi; R41 N; R51-53 Xn; N R: 22-41-51/53 S: (2-)22-26-39-61 611-164-00-3 reaction mass of: 2,2'-dimethyl-2,2'-azobutanenitrile; 2-methylpentanenitrile-2-azo-2'-(2'-methylpropanenitrile); 2,2'-dimethyl-2,2'-azoheptanenitrile; 2-methylheptanenitrile-2-azo-2'-(2'-methylpropanenitrile); 2-methylheptanenitrile-2-azo-2'-(2'-methylbutanenitrile) 429-710-2 - R10 2-methylheptanenitrile-2-azo-2'-(2'-methylbutanenitrile) 429-710-2 — R10 R32 R44 Xn; R22 N; R51-53 Xn; N R: 10-22-32-44-51/53 S: (2-)12-15-16-47-51-61 611-165-00-9 reaction mass of: tetrasodium 4-amino-6-(5-(2,6-difluoropyrimidin-4-ylamino)-2-sulfonatophenylazo)-5-hydroxy-3-(4-(sulfatoethylsulfonyl)phenylazo)naphthalene-2,7-disulfonate; tetrasodium 4-amino-6-(5-(4,6-difluoropyrimidin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxy-3-(4-(2-sulfatoethylsulfonyl)phenylazo)naphthalene-2,7-disulfonate 431-830-5 - R52-53 R: 52/53 tetrasodium 4-amino-6-(5-(4,6-difluoropyrimidin-2-ylamino)-2-sulfonatophenylazo)-5-hydroxy-3-(4-(2-sulfatoethylsulfonyl)phenylazo)naphthalene-2,7-disulfonate 431-830-5 — R52-53 R: 52/53 S: 61 611-166-00-4 reaction mass of: pentasodium 4-amino-5-hydroxy-3-{](E)-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-6-{](E)-2-sulfonato-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}naphthalene-2,7-disulfonate; tetrasodium 4-amino-5-hydroxy-3-{](E)-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-6-[(E)-2-sulfonato-4-(vinylsulfonyl)phenylazo{]naphthalene-2,7-disulfonate; tetrasodium 4-amino-5-hydroxy-6-(E)-2-sulfonato-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-3-[(E)-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate 432-100-9 - Xi; R41 tetrasodium 4-amino-5-hydroxy-6-(E)-2-sulfonato-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-3-[(E)-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate 432-100-9 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)26-39-61 611-167-00-X sodium bis[tris(2-hydroxyethyl)ammonium][6-anilino-4'-(4,8-disulfonato-2-naphthylazo)-5'-methyl-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato]cuprate(II) 435-240-9 - R52-53 R: 52/53 S: (2-)26-39-61 611-167-00-X sodium bis[tris(2-hydroxyethyl)ammonium][6-anilino-4'-(4,8-disulfonato-2-naphthylazo)-5'-methyl-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato]cuprate(II) 435-240-9 — R52-53 R: 52/53 S: 61 611-168-00-5 reaction mass of: 3-[[4-chloro-6-[[7-[(1,5-disulfo-2-naphthalenyl)azo]-8-hydroxy-3,6-disulfo-1-naphthalenyl]amino]-1,3,5-triazin-2-yl]amino]-5-[[4-chloro-6-[[8-hydroxy-3,6-disulfo-7-[(2-sulfophenyl)azo]-1-naphthalenyl]amino]-1,3,5-triazin-2-yl]amino]benzoic acid; 3,5-bis[[4-chloro-6-[[7-[(1,5-disulfo-2-naphthalenyl)azo]-8-hydroxy-3,6-disulfo-1-naphthalenyl]amino]-1,3,5-triazin-2-yl]amino]benzoic acid 435-440-6 - Xi; R41 Xi 3,5-bis[[4-chloro-6-[[7-[(1,5-disulfo-2-naphthalenyl)azo]-8-hydroxy-3,6-disulfo-1-naphthalenyl]amino]-1,3,5-triazin-2-yl]amino]benzoic acid 435-440-6 — Xi; R41 Xi R: 41 S: (2-)22-26-39 611-169-00-0 sodium 5-(2-carboxyphenylazo)-6-hydroxynaphthalene-2-sulfonate 435-800-2 - R52-53 R: 52/53 S: (2-)22-26-39 611-169-00-0 sodium 5-(2-carboxyphenylazo)-6-hydroxynaphthalene-2-sulfonate 435-800-2 — R52-53 R: 52/53 S: 61 611-170-00-6 reaction mass of: trisodium 2-((1-(2-hydroxy-κ-O-5-(2-sulfonatoethansulfonyl)phenylazo-κ-N2)-1-phenylmethyl)azo-κ-N1)-4-sulfonatobenzoate(5-)-κ-O)cuprate(II); disodium 2-((1-(5-ethenesulfonyl-2-hydroxy-κ-O-phenylazo-κ-N2)-1-phenylmethyl)azo-κ-N1)-4-sulfonatobenzoate-κ-O-(5-))cuprate(II) 435-880-9 - R52-53 R: 52/53 disodium 2-((1-(5-ethenesulfonyl-2-hydroxy-κ-O-phenylazo-κ-N2)-1-phenylmethyl)azo-κ-N1)-4-sulfonatobenzoate-κ-O-(5-))cuprate(II) 435-880-9 — R52-53 R: 52/53 S: 22-61 611-171-00-1 reaction mass of: trisodium 3-(5-(2,6-difluoropyrimidin-4-ylamino)-2-sulfonatophenylazo)-5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxy-2,7-naphthalenedisulfonate; trisodium 3-(5-(4,6-difluoropyrimidin-2-ylamino)-2-sulfonatophenylazo)-5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxy-2,7-naphthalenedisulfonate 436-890-6 - Xi; R41 trisodium 3-(5-(4,6-difluoropyrimidin-2-ylamino)-2-sulfonatophenylazo)-5-(4-fluoro-6-morpholin-4-yl-1,3,5-triazin-2-ylamino)-4-hydroxy-2,7-naphthalenedisulfonate 436-890-6 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)22-26-39-61 611-172-00-7 reaction mass of: triammonium 6-amino-3-((2,5-diethoxy-4-(3-phosphonophenyl)azo)phenyl)azo-4-hydroxy-2-naphthalenesulfonate; diammonium 3-((4-((7-amino-1-hydroxy-3-sulfo-naphthalen-2-yl)azo)-2,5-diethoxyphenyl)azo)benzoate 438-310-7 - E; R2 diammonium 3-((4-((7-amino-1-hydroxy-3-sulfo-naphthalen-2-yl)azo)-2,5-diethoxyphenyl)azo)benzoate 438-310-7 — E; R2 Repr. Cat. 3; R62 Xn; R22-48/22 R52-53 E; Xn R: 2-22-48/22-62-52/53 S: (2-)22-35-36/37-61 611-173-00-2 reaction mass of: 3-[3-carbamoyl-5-(5-{]4-chloro-6-[}4-(2-sulfonatooxyethylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-2-sulfonatophenylazo)-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl]propanoic acid, trisodium salt; 3-[3-carbamoyl-5-(5-{]4-chloro-6-[}4-(vinylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-2-sulfonatophenylazo)-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl]propanoic acid, disodium salt 440-510-4 - Xi; R41 3-[3-carbamoyl-5-(5-{]4-chloro-6-[}4-(vinylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-2-sulfonatophenylazo)-1,2-dihydro-6-hydroxy-4-methyl-2-oxo-1-pyridyl]propanoic acid, disodium salt 440-510-4 — Xi; R41 R43 Xi R: 41-43 S: (2-)22-26-36/37/39 611-174-00-8 reaction mass of: 3-[5-(4-ethenesulfonylbutyrylamino)-2-sulfophenylazo{]-5-4-chloro-[}6-(4-(3-amino-5-hydroxy-2,7-disulfonaphthalene-4-ylazo)-3-sulfophenylamino{]-1,3,5-triazin-2-ylamino[}-4-hydroxynaphthalene-2,7-disulfonic acid, sodium salt; 3-[5-(4-(2-chloroethanesulfonyl)butyrylamino)-2-sulfophenylazo{]-5-4-chloro-[}6-(4-(3-amino-5-hydroxy-2,7-disulfonaphthalene-4-ylazo)-3-sulfophenylamino{]-1,3,5-triazin-2-ylamino[}-4-hydroxynaphthalene-2,7-disulfonic acid, sodium salt 442-290-5 457624-86-1 Xi; R41 Xi R: 41 S: (2-)22-26-39 611-175-00-3 reaction mass of: trisodium 5-{]4-chloro-6-[}N-ethyl-(3-(2-sulfonatooxy)ethylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-4-hydroxy-3-[4-(vinylsulfonyl)phenylazo{]naphthalene-2,7-disulfonate; trisodium 5-4-chloro-6-[}N-ethyl-3-(vinylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-4-hydroxy-3-[4-(2-(sulfonatooxy)ethylsulfonyl)phenylazo{]naphthalene-2,7-disulfonate; disodium 5-4-chloro-6-[}N-ethyl-3-(vinylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-4-hydroxy-3-[(4-vinylsulfonyl)phenylazo{]naphthalene-2,7-disulfonate; tetrasodium 5-4-chloro-6-[}N-ethyl-3-(2-(sulfonatooxy)ethylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-3-[4-(2-(sulfonatooxy)ethylsulfonyl)phenylazo]-4-hydroxynaphthalene-2,7-disulfonate 444-050-5 - Xi; R41 tetrasodium 5-4-chloro-6-[}N-ethyl-3-(2-(sulfonatooxy)ethylsulfonyl)anilino{]-1,3,5-triazin-2-ylamino[}-3-[4-(2-(sulfonatooxy)ethylsulfonyl)phenylazo]-4-hydroxynaphthalene-2,7-disulfonate 444-050-5 — Xi; R41 R52-53 Xi R: 41-52/53 S: (2-)22-26-39-61 611-176-00-9 2,6-bis(2,3,4-trihydroxybenzyl)-p-cresol ester with 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonate 444-250-2 - E; R2 S: (2-)22-26-39-61 611-176-00-9 2,6-bis(2,3,4-trihydroxybenzyl)-p-cresol ester with 6-diazo-5,6-dihydro-5-oxo-1-naphthalenesulfonate 444-250-2 — E; R2 F; R11 N; R51-53 E; N R: 2-11-51/53 S: (2-)22-61 611-177-00-4 reaction mass of: pentasodium bis[6-anilino-3,5'-disulfonatonaphthalene-2-azobenzene-1,2'-diolato]cobaltate(III); tetrasodium [6-anilino-3,5'-disulfonatonaphthalene-2-azobenzene-1,2'-diolato][6-anilino-5'-sulfamoyl-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato]cobaltate(III); trisodium bis[6-anilino-5'-sulfamoyl-3-sulfonatonaphthalene-2-azobenzene-1,2'-diolato]cobaltate(III) 444-290-0 508202-43-5 Xi; R41 R43 R52-53 Xi R: 41-43-52/53 S: (2-)22-24-26-37/39-61 611-178-00-X reaction mass of: pentasodium 4-amino-5-hydroxy-3-{](E)-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-6-{](E)-2-sulfonato-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}naphthalene-2,7-disulfonate; tetrasodium 4-amino-5-hydroxy-3-{](E)-4-[}2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-6-[(E)-2-sulfonato-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate; tetrasodium 4-amino-5-hydroxy-6-[(E)-2-sulfonato-4-[2-(sulfonatooxy)ethylsulfonyl{]phenylazo[}-3-[(E)-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate; trisodium 4-amino-5-hydroxy-3-[(E)-4-(vinylsulfonyl)phenylazo]-6-[(E)-2-sulfonato-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate; trisodium 4-amino-5-hydroxy-3-[(2-hydroxyethylsulfonyl)-phenylazo]-6-[(E)-2-sulfonato-4-(vinylsulfonyl)phenylazo]naphthalene-2,7-disulfonate; trisodium 4-amino-5-hydroxy-3-[(E)-4-(vinylsulfonyl)phenylazo]-6-[-2-sulfonato-4-(2-hydroxyethylsulfonyl)phenylazo]naphthalene-2,7-disulfonate 445-280-9 - Xi; R41 trisodium 4-amino-5-hydroxy-3-[(E)-4-(vinylsulfonyl)phenylazo]-6-[-2-sulfonato-4-(2-hydroxyethylsulfonyl)phenylazo]naphthalene-2,7-disulfonate 445-280-9 — Xi; R41 R43 R52-53 Xi R: 41-43-52/53 S: (2-)24-26-37/39-61 611-179-00-5 reaction mass of: pentasodium 2-[[8-[[4-chloro-6-[[4-(2-sulfonato ethylsulfonyl)]phenyl]amino]-1,3,5-triazin-2-yl]amino-1- hydroxy-3,6-disulfonato-2-naphthalenyl]azo]naphthalene-1,5-disulfonate; 2-[[8-[[4-chloro-6-[[4-[[2-ethenyl]sulfonyl]phenyl]amino]-1,3,5-triazin-2-yl]amino]-1-hydroxy-3,6-disulfonato-2-naphthalenyl]azo]naphthalene-1,5-disulfonate 450-010-8 - Xi; R41 2-[[8-[[4-chloro-6-[[4-[[2-ethenyl]sulfonyl]phenyl]amino]-1,3,5-triazin-2-yl]amino]-1-hydroxy-3,6-disulfonato-2-naphthalenyl]azo]naphthalene-1,5-disulfonate 450-010-8 — Xi; R41 R43 Xi R: 41-43 S: (2-)22-24-26-37/39 611-180-00-0 iron, complexes with diazotised 4-aminobenzenesulfonamide, diazotised 3-aminobenzenesulfonic acid, diazotised 3-amino-4-hydroxybenzenesulfonamide, diazotised 3-amino-4-hydroxy-N-phenylbenzenesulfonamide, diazotised 5-amino-2-(phenylamino)benzenesulfonic acid and resorcinol, sodium salts 417-850-7 - N; R51-53 N S: (2-)22-24-26-37/39 611-180-00-0 iron, complexes with diazotised 4-aminobenzenesulfonamide, diazotised 3-aminobenzenesulfonic acid, diazotised 3-amino-4-hydroxybenzenesulfonamide, diazotised 3-amino-4-hydroxy-N-phenylbenzenesulfonamide, diazotised 5-amino-2-(phenylamino)benzenesulfonic acid and resorcinol, sodium salts 417-850-7 — N; R51-53 N R: 51/53 S: 22-61 612-001-00-9 mono-methylamine; [1] di-methylamine; [2] tri-methylamine [3] 200-820-0 [1] 204-697-4 [2] 200-875-0 [3] 74-89-5 [1] 124-40-3 [2] 75-50-3 [3] F+; R12 Xn; R20 Xi; R37/38-41 F+; Xn R: 12-20-37/38-41 S: (2-)16-26-39 Xn; R20: C ≥ 5 % Xi; R37/38-41: C ≥ 5 % Xi; R36: 0,5 % ≤ C < 5 % 5 612-001-01-6 mono-methylamine ... %; [1] di-methylamine ... %; [2] tri-methylamine ... % [3] 200-820-0 [1] S: (2-)16-26-39 Xn; R20: C ≥ 5 % Xi; R37/38-41: C ≥ 5 % Xi; R36: 0,5 % ≤ C < 5 % 5 612-001-01-6 mono-methylamine ... %; [1] di-methylamine ... %; [2] tri-methylamine ... % [3] 200-820-0 [1] 204-697-4 [2] 200-875-0 [3] 74-89-5 [1] 124-40-3 [2] 75-50-3 [3] F+; R12 Xn; R20/22 C; R34 F+; C R: 12-20/22-34 S: (1/2-)3-16-26-29-36/37/39-45 Xn; R20/22: C ≥ 15 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % B S: (1/2-)3-16-26-29-36/37/39-45 Xn; R20/22: C ≥ 15 % C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % B 612-002-00-4 ethylamine 200-834-7 75-04-7 F+; R12 Xi; R36/37 F+; Xi R: 12-36/37 S: (2-)16-26-29 612-003-00-X diethylamine 203-716-3 109-89-7 F; R11 Xn; R20/21/22 C; R35 F; C R: 11-20/21/22-35 S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-004-00-5 triethylamine 204-469-4 121-44-8 F; R11 S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-004-00-5 triethylamine 204-469-4 121-44-8 F; R11 Xn; R20/21/22 C; R35 F; C R: 11-20/21/22-35 S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-005-00-0 butylamine 203-699-2 109-73-9 F; R11 S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-005-00-0 butylamine 203-699-2 109-73-9 F; R11 Xn; R20/21/22 C; R35 F; C R: 11-20/21/22-35 S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-006-00-6 ethylenediamine; S: (1/2-)3-16-26-29-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-006-00-6 ethylenediamine; 1,2-diaminoethane 203-468-6 107-15-3 R10 Xn; R21/22 C; R34 R42/43 C R: 10-21/22-34-42/43 S: (1/2-)23-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-007-00-1 2-aminopropane; S: (1/2-)23-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-007-00-1 2-aminopropane; isopropylamine 200-860-9 75-31-0 F+; R12 Xi; R36/37/38 F+; Xi R: 12-36/37/38 S: (2-)16-26-29 612-008-00-7 aniline 200-539-3 62-53-3 Carc. Cat. 3; R40 Muta. Cat. 3; R68 T; R23/24/25-48/23/24/25 Xi; R41 R43 N; R50 T; N R: 23/24/25-40-41-43-48/23/24/25-68-50 S: (1/2-)26-27-36/37/39-45-46-61-63 T; R23/24/25: C ≥ 25 % Xn; R20/21/22: 1 % ≤ C < 25 % T; R48/23/24/25: C ≥ 1 % Xn; R48/20/21/22: 0,2 % ≤ C < 1 % 612-009-00-2 salts of aniline — — Carc. Cat. 3; R40 S: (1/2-)26-27-36/37/39-45-46-61-63 T; R23/24/25: C ≥ 25 % Xn; R20/21/22: 1 % ≤ C < 25 % T; R48/23/24/25: C ≥ 1 % Xn; R48/20/21/22: 0,2 % ≤ C < 1 % 612-009-00-2 salts of aniline — — Carc. Cat. 3; R40 Muta. Cat. 3; R68 T; R23/24/25-48/23/24/25 Xi; R41 R43 N; R50 T; N R: 23/24/25-40-41-43-48/23/24/25-68-50 S: (1/2-)26-27-36/37/39-45-61-63 T; R23/24/25: C ≥ 25 % Xn; R20/21/22: 1 % ≤ C < 25 % T; R48/23/24/25: C ≥ 1 % Xn; R48/20/21/22: 0,2 % ≤ C < 1 % A S: (1/2-)26-27-36/37/39-45-61-63 T; R23/24/25: C ≥ 25 % Xn; R20/21/22: 1 % ≤ C < 25 % T; R48/23/24/25: C ≥ 1 % Xn; R48/20/21/22: 0,2 % ≤ C < 1 % A 612-010-00-8 chloroanilines, with exception of those specified elsewhere in this Annex — — T; R23/24/25 R33 N; R50-53 T; N … 50 unchanged lines … Xn; R22 N; R51-53 T; N R: 45-22-51/53 S: 53-45-61 Carc. Cat. 1; R45: C ≥ 0,01 % E S: 53-45-61 Carc. Cat. 1; R45: C ≥ 0,01 % E 612-023-00-9 phenylhydrazine; [1] phenylhydrazinium chloride; [2] phenylhydrazine hydrochloride; [3] … 107 unchanged lines … Xn; R22 N; R50-53 T; N R: 45-22-50/53 S: 53-45-60-61 Carc. Cat. 1; R45: C ≥ 0,01 % E S: 53-45-60-61 Carc. Cat. 1; R45: C ≥ 0,01 % E 612-043-00-8 N,N'-dimethylbenzidine — 2810-74-4 Xn; R20/21/22 Xn R: 20/21/22 S: (2-)22-36 612-044-00-3 N,N'-diacetylbenzidine 210-338-2 613-35-4 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Xn; R20/21/22 T R: 45-20/21/22-68 S: 53-45 E 612-046-00-4 allylamine 203-463-9 107-11-9 F; R11 T; R23/24/25 N; R51-53 F; T; N R: 11-23/24/25-51/53 S: (1/2-)9-16-24/25-45-61 612-047-00-X benzylamine 202-854-1 100-46-9 Xn; R21/22 C; R34 C R: 21/22-34 S: (1/2-)26-36/37/39-45 612-048-00-5 dipropylamine 205-565-9 142-84-7 F; R11 Xn; R20/21/22 C; R35 F; C R: 11-20/21/22-35 S: (1/2-)16-26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-049-00-0 di-n-butylamine; [1] S: (1/2-)16-26-36/37/39-45 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % 612-049-00-0 di-n-butylamine; [1] di-sec-butylamine [2] 203-921-8 [1] 210-937-9 [2] 111-92-2 [1] 626-23-3 [2] R10 Xn; R20/21/22 Xn R: 10-20/21/22 S: (2-) 612-050-00-6 cyclohexylamine 203-629-0 108-91-8 R10 Repr. Cat. 3; R62 Xn; R21/22 C; R34 C R: 10-21/22-34-62 S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-051-00-1 4,4'-diaminodiphenylmethane; S: (1/2-)26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-051-00-1 4,4'-diaminodiphenylmethane; 4,4'-methylenedianiline 202-974-4 101-77-9 Carc. Cat. 2; R45 Muta. Cat. 3; R68 T; R39/23/24/25 … 24 unchanged lines … R33 N; R51-53 T; N R: 23/24/25-33-51/53 S: (1/2-)28-37-45-61 T; R23/24/25: C ≥ 5 % Xn; R20/21/22: 1 % ≤ C < 5 % 612-055-00-3 N-methyl-o-toluidine; [1] S: (1/2-)28-37-45-61 T; R23/24/25: C ≥ 5 % Xn; R20/21/22: 1 % ≤ C < 5 % 612-055-00-3 N-methyl-o-toluidine; [1] N-methyl-m-toluidine; [2] N-methyl-p-toluidine [3] 210-260-9 [1] 211-795-0 [2] 210-769-6 [3] 611-21-2 [1] 696-44-6 [2] 623-08-5 [3] T; R23/24/25 R33 R52-53 T R: 23/24/25-33-52/53 S: (1/2-)28-36/37-45-61 C 612-056-00-9 N,N-dimethyl-p-toluidine; [1] N,N-dimethyl-m-toluidine; [2] N,N-dimethyl-o-toluidine [3] 202-805-4 [1] 204-495-6 [2] 210-199-8 [3] 99-97-8 [1] 121-72-2 [2] 609-72-3 [3] T; R23/24/25 R33 R52-53 T R: 23/24/25-33-52/53 S: (1/2-)28-36/37-45-61 T; R23/24/25: C ≥ 5 % Xn; R20/21/22: 1 % ≤ C < 5 % C S: (1/2-)28-36/37-45-61 T; R23/24/25: C ≥ 5 % Xn; R20/21/22: 1 % ≤ C < 5 % C 612-057-00-4 piperazine; [solid] 203-808-3 110-85-0 Repr. Cat. 3; R62-63 C; R34 … 54 unchanged lines … C; R34 N; R50-53 C; N R: 22-34-50/53 S: (1/2-)26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-067-00-9 3-aminomethyl-3,5,5-trimethylcyclohexylamine 220-666-8 2855-13-2 Xn; R21/22 S: (1/2-)26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/38: 2 % ≤ C < 10 % 612-067-00-9 3-aminomethyl-3,5,5-trimethylcyclohexylamine 220-666-8 2855-13-2 Xn; R21/22 C; R34 R43 R52-53 C … 66 unchanged lines … T; R25-48/25 N; R51-53 T+; N R: 45-25-26-48/25-51/53 S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,001 % E S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,001 % E 612-078-00-9 2,2'-dichloro-4,4'-methylenedianiline; 4,4'-methylene bis(2-chloroaniline) 202-918-9 101-14-4 Carc. Cat. 2; R45 Xn; R22 … 32 unchanged lines … Xi; R36/38 N; R51-53 T; N R: 45-20-36/38-51/53 S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E 612-084-00-1 dapsone; 4,4'-diamino diphenyl sulfone 201-248-4 80-08-0 Xn; R22 Xn R: 22 S: (2-)22 612-085-00-7 4,4'-methylenedi-o-toluidine 212-658-8 838-88-0 Carc. Cat. 2; R45 Xn; R22 R43 N; R50-53 T; N R: 45-22-43-50/53 S: 53-45-60-61 E 612-086-00-2 amitraz (ISO); N,N-bis(2,4-xylyliminomethyl) methylamine 251-375-4 33089-61-1 Xn; R22-48/22 R43 N; R50-53 Xn; N R: 22-43-48/22-50/53 S: (2-)22-24-60-36/37-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-087-00-8 guazatine (ISO) 108173-90-6 T+; R26 S: (2-)22-24-60-36/37-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-087-00-8 guazatine (ISO) 108173-90-6 T+; R26 Xn; R21/22 Xi; R37/38-41 N; R50-53 T+; N … 45 unchanged lines … Xn; R22 N; R51-53 T; N R: 45-22-51/53 S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,001 % E S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,001 % E 612-099-00-3 4-methyl-m-phenylenediamine; 2,4-toluenediamine 202-453-1 95-80-7 Carc. Cat. 2; R45 Muta. Cat. 3; R68 … 91 unchanged lines … R43 N; R50-53 Xn; N R: 40-43-50/53 S: (2-)36/37-60-61 R43: C ≥ 0,1 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 612-121-00-1 amines, polyethylenepoly-; S: (2-)36/37-60-61 R43: C ≥ 0,1 % N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 612-121-00-1 amines, polyethylenepoly-; HEPA 268-626-9 68131-73-7 Xn; R21/22 C; R34 R43 N; R50-53 C; N R: 21/22-34-43-50/53 S: (1/2-)26-36/37/39-45-60-61 612-122-00-7 hydroxylamine....% [> 55 % in aqueous solution] 232-259-2 7803-49-8 E; R2 S: (1/2-)26-36/37/39-45-60-61 612-122-00-7 hydroxylamine....% [> 55 % in aqueous solution] 232-259-2 7803-49-8 E; R2 Carc. Cat. 3; R40 Xn; R21/22-48/22 Xi; R37/38-41 R43 N; R50 E; Xn; N R: 2-21/22-37/38-40-41-43-48/22-50 S: (2-)26-36/37/39-61 B 612-122-01-4 hydroxylamine …% [≤ 55 % in aqueous solution] 232-259-2 7803-49-8 R5 612-122-01-4 hydroxylamine …% [≤ 55 % in aqueous solution] 232-259-2 7803-49-8 R5 Carc. Cat. 3; R40 Xn; R21/22-48/22 Xi; R37/38-41 … 41 unchanged lines … Xn; R20/22 C; R34 F; C R: 11-20/22-34 S: (1/2-)16-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 612-130-00-0 2,6-diamino-3,5-diethyltoluene; S: (1/2-)16-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 612-130-00-0 2,6-diamino-3,5-diethyltoluene; 4,6-diethyl-2-methyl-1,3-benzenediamine; [1] 2,4-diamino-3,5-diethyltoluene; 2,4-diethyl-6-methyl-1,3-benzenediamine; [2] … 34 unchanged lines … R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-60-61 R43: C ≥ 0,1 % 612-137-00-9 4-chloroaniline 203-401-0 106-47-8 Carc. Cat. 2; R45 S: (2-)24-37-60-61 R43: C ≥ 0,1 % 612-137-00-9 4-chloroaniline 203-401-0 106-47-8 Carc. Cat. 2; R45 T; R23/24/25 R43 N; R50-53 T; N … 71 unchanged lines … R: 20/21/22-38-43-50/53 S: (2-)36/37/39-46-60-61 612-151-00-5 methyl-phenylene diamine; diaminotoluene; [technical product – reaction mass of 4-methyl-m-phenylene diamine (EC No 202-453-1) and 2-methyl-m-phenylene diamine (EC No 212-513-9)] — — Carc. Cat. 2; R45 [technical product – reaction mass of 4-methyl-m-phenylene diamine (EC No 202-453-1) and 2-methyl-m-phenylene diamine (EC No 212-513-9)] — — Carc. Cat. 2; R45 Muta. Cat. 3; R68 Repr. Cat. 3; R62 T; R25 … 222 unchanged lines … R43 N; R50-53 T; N R: 23/24/25-41-43-50/53 S: (1/2-)26-36/37/39-45-60-61 612-203-00-7 C8-10 alkyl dimethyl hydroxyethyl ammoniumchloride (chain < C8: <3 %, chain = C8: 15 %-70 %, chain = C10: 30 %-85 %, chain > C10: <3 %) 417-360-3 - Xn; R21/22 S: (1/2-)26-36/37/39-45-60-61 612-203-00-7 C8-10 alkyl dimethyl hydroxyethyl ammoniumchloride (chain < C8: <3 %, chain = C8: 15 %-70 %, chain = C10: 30 %-85 %, chain > C10: <3 %) 417-360-3 - Xn; R21/22 Xi; R38 Xn R: 21/22-38 S: (2-)25-36/37 612-204-00-2 C.I. Basic Violet 3; 4-[4,4'-bis(dimethylamino) benzhydrylidene]cyclohexa-2,5-dien-1-ylidene]dimethylammonium chloride 208-953-6 548-62-9 Carc. Cat. 3; R40 Xn; R22 Xi; R41 N; R50-53 Xn; N R: 22-40-41-50/53 S: (2-)26-36/37/39-46-60-61 612-205-00-8 C.I. Basic Violet 3 with ≥ 0.1 % of Michler's ketone (EC no. 202-027-5) 208-953-6 548-62-9 Carc. Cat. 2; R45 S: (2-)26-36/37/39-46-60-61 612-205-00-8 C.I. Basic Violet 3 with ≥ 0.1 % of Michler's ketone (EC no. 202-027-5) 208-953-6 548-62-9 Carc. Cat. 2; R45 Xn; R22 Xi; R41 N; R50-53 T; N … 48 unchanged lines … Xn; R22 R52-53 F; C R: 11-22-34-52/53 S: (1/2-)9-26-36/37/39-45-61 612-219-00-4 (2-hydroxy-3-(3,4-dimethyl-9-oxo-10-thiaanthracen-2-yloxy)propyl)trimethylammonium chloride 402-200-7 - R52-53 R: 52/53 S: (1/2-)9-26-36/37/39-45-61 612-219-00-4 (2-hydroxy-3-(3,4-dimethyl-9-oxo-10-thiaanthracen-2-yloxy)propyl)trimethylammonium chloride 402-200-7 — R52-53 R: 52/53 S: 61 612-220-00-X N-nitro-N-(3-methyl-3,6-dihydro-2H-1,3,5-oxadiazin-4-yl)amine 431-060-1 153719-38-1 Xn; R22 R43 R52-53 Xn … 30 unchanged lines … N-benzyl-N'-[3-(trimethoxysilyl)propyl]ethylenediamine; N,N'-bis-benzyl-N'-[3-(trimethoxysilyl)propyl]ethylenediamine; N,N,N'-tris-benzyl-N'-[3-(trimethoxysilyl)propyl]ethylenediamine; N,N-bis-benzyl-N'-[3-(trimethoxysilyl)propyl]ethylenediamine 414-340-6 - R10 N,N-bis-benzyl-N'-[3-(trimethoxysilyl)propyl]ethylenediamine 414-340-6 — R10 Xn; R20/21/22-68/20/21/22 Xi; R41 R43 R52-53 Xn R: 10-20/21/22-41-43-68/20/21/22-52/53 S: (2-)26-36/37/39-61 612-229-00-9 mepanipyrim; 4-methyl-N-phenyl-6-(1-propynyl)-2-pyrimidinamine - 110235-47-7 Carc. Cat. 3; R40 4-methyl-N-phenyl-6-(1-propynyl)-2-pyrimidinamine — 110235-47-7 Carc. Cat. 3; R40 N; R50-53 Xn; N R: 40-50/53 S: (2-)36/37-46-60-61 612-230-00-4 N,N-bis(cocoyl-2-oxypropyl)-N,N-dibutylammonium bromide 431-530-4 - C; R35 S: (2-)36/37-46-60-61 612-230-00-4 N,N-bis(cocoyl-2-oxypropyl)-N,N-dibutylammonium bromide 431-530-4 — C; R35 R43 N; R50-53 C; N R: 35-43-50/53 … 29 unchanged lines … Muta. Cat. 3; R68 T R: 45-68 S: 53-45 612-240-00-9 pyrimethanil (ISO); N-(4,6-dimethylpyrimidin-2-yl)aniline - 53112-28-0 N; R51-53 N N-(4,6-dimethylpyrimidin-2-yl)aniline — 53112-28-0 N; R51-53 N R: 51/53 S: 61 612-241-00-4 piperazine hydrochloride; [1] piperazine dihydrochloride; [2] piperazine phosphate [3] 228-042-7 [1] 205-551-2 [2] 217-775-8 [3] 6094-40-2 [1] 142-64-3 [2] 1951-97-9 [3] Repr. Cat. 3; R62-63 Xi; R36/38 R42/43 R52-53 Xn R: 36/38-42/43-62-63-52/53 S: (1/2-)22-36/37-45-63-61 612-242-00-X cyprodinil (ISO); 4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine - 121552-61-2 R43 4-cyclopropyl-6-methyl-N-phenylpyrimidin-2-amine — 121552-61-2 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-243-00-5 (1S-cis)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine 2-hydroxy-2-phenylacetate 420-560-3 79617-97-3 Xi; R41 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-243-00-5 (1S-cis)-4-(3,4-dichlorophenyl)-1,2,3,4-tetrahydro-N-methyl-1-naphthalenamine 2-hydroxy-2-phenylacetate 420-560-3 79617-97-3 Xi; R41 N; R50-53 Xi; N R: 41-50/53 S: (2-)26-39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-244-00-0 3-(piperazin-1-yl)-benzo[d]isothiazole hydrochloride 421-310-6 87691-88-1 Repr. Cat. 3; R62 S: (2-)26-39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-244-00-0 3-(piperazin-1-yl)-benzo[d]isothiazole hydrochloride 421-310-6 87691-88-1 Repr. Cat. 3; R62 Xn; R22 Xi; R36 R43 N; R50-53 Xn; N R: 22-36-43-62-50/53 S: (2-)22-26-36/37/39-60-61 612-245-00-6 2-ethylphenylhydrazine hydrochloride 421-460-2 19398-06-2 Carc. Cat. 3; R40 T; R48/25 Xn; R22 Xi; R41 R43 N; R50-53 T; N R: 22-40-41-43-48/25-50/53 S: (1/2-)22-26-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-246-00-1 (2-chloroethyl)(3-hydroxypropyl)ammonium chloride 429-740-6 40722-80-3 Carc. Cat. 2; R45 S: (1/2-)22-26-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-246-00-1 (2-chloroethyl)(3-hydroxypropyl)ammonium chloride 429-740-6 40722-80-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R48/22 R43 R52-53 T R: 45-46-43-48/22-52/53 S: 53-45-61 E 612-247-00-7 N-[3-(1,1-dimethylethyl)-1H-pyrazol-5-yl]-N'-hydroxy-4-nitrobenzenecarboximidamide 423-530-8 152828-23-4 T; R48/25 Xn; R22 R52-53 T R: 22-48/25-52/53 S: (1/2-)22-36-45-61 612-248-00-2 reaction product of diphenylamine, phenothiazine, and alkenes, branched (C8-10, C9-rich) 439-540-0 - Xi; R38 S: (1/2-)22-36-45-61 612-248-00-2 reaction product of diphenylamine, phenothiazine, and alkenes, branched (C8-10, C9-rich) 439-540-0 — Xi; R38 R43 R53 Xi R: 38-43-53 … 21 unchanged lines … N; R50-53 Xn; N R: 22-50/53 S: (2-)22-57-60-61 612-253-00-X 7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one; [containing < 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 R52-53 R: R52/53 [containing < 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 R52-53 R: R52/53 S: 61 612-253-01-7 7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one; [containing ≥ 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Repr. Cat. 2; R61 [containing ≥ 0,5 % formamide (EC No 200-842-0)] 429-400-7 199327-61-2 Repr. Cat. 2; R61 R52-53 T R: 61-52/53 S: 53-45-61 612-254-00-5 reaction products of diisopropanolamine with formaldehyde (1:4) 432-440-8 220444-73-5 Carc. Cat. 3; R40 … 17 unchanged lines … R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-265-00-5 bis(2-hydroxyethyl)-(2-hydroxypropyl)ammonium acetate 444-360-0 191617-13-7 R52-53 R: 52/53 S: (2-)24-37-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-265-00-5 bis(2-hydroxyethyl)-(2-hydroxypropyl)ammonium acetate 444-360-0 191617-13-7 R52-53 R: 52/53 S: 61 612-266-00-0 3-chloro-4-(3-fluorobenzyloxy)aniline 445-590-4 202197-26-0 Muta. Cat. 3; R68 Xn; R22-48/22 N; R50-53 Xn; N R: 22-48/22-68-50/53 S: (2-)22-36/37-60-61 612-267-00-6 bis(hydrogenated tallow C16-18-alkyl)hydroxylamine 418-370-0 - R43 S: (2-)22-36/37-60-61 612-267-00-6 bis(hydrogenated tallow C16-18-alkyl)hydroxylamine 418-370-0 — R43 R53 Xi R: 43-53 S: (2-)36/37-61 612-269-00-7 reaction mass of: 1-[di(4-octylphenyl)aminomethyl]-5-methyl-1H-benzotriazole; 1-[di(4-octylphenyl)aminomethyl]-4-methyl-1H-benzotriazole; reaction mass of: N-[(5-methyl-1H-benzotriazol-1-yl)methyl]-4-octyl-N-(4-octylphenyl)aniline; N-[(4-methyl-1H-benzotriazol-1-yl)methyl]-4-octyl-N-(4-octylphenyl)aniline 420-720-2 - R53 R: 53 S: 22-61 612-270-00-2 (S)-azetidine-2-carboxylic acid 4-cyanobenzylamide hydrochloride 433-010-2 - Xn; R22 N-[(4-methyl-1H-benzotriazol-1-yl)methyl]-4-octyl-N-(4-octylphenyl)aniline 420-720-2 — R53 R: 53 S: 22-61 612-270-00-2 (S)-azetidine-2-carboxylic acid 4-cyanobenzylamide hydrochloride 433-010-2 — Xn; R22 R43 R52-53 Xn R: 22-43-52/53 S: (2-)22-36/37-61 612-271-00-8 reaction mass of: ethyl 2-((4-(5,6-dichlorobenzothiazol-2-ylazo)phenyl)ethylamino)benzoate; ethyl 2-((4-(6,7-dichlorobenzothiazol-2-ylazo)phenyl)ethylamino)benzoate 434-970-5 160987-57-5 R53 R: 53 S: 61 612-272-00-3 ammonium (η-6-2-(2-(1,2-dicarboxylatoethylamino)ethylamino)butane-1,4-dioato(4-))iron(3+) monohydrate 435-210-5 - N; R51-53 N S: 61 612-272-00-3 ammonium (η-6-2-(2-(1,2-dicarboxylatoethylamino)ethylamino)butane-1,4-dioato(4-))iron(3+) monohydrate 435-210-5 — N; R51-53 N R: 51/53 S: 61 612-273-00-9 alkyl(rapeseed oil), bis(2-hydroxyethyl)ammonium fluoride 435-650-8 - Xn; R22 S: 61 612-273-00-9 alkyl(rapeseed oil), bis(2-hydroxyethyl)ammonium fluoride 435-650-8 — Xn; R22 C; R35 N; R50-53 C; N R: 22-35-50/53 S: (1/2-)26-36/37/39-45-60-61 612-274-00-4 (R, S)-1-[2-amino-1(4-methoxyphenyl)ethyl]cyclohexanol acetate 445-750-3 - Xn; R22 S: (1/2-)26-36/37/39-45-60-61 612-274-00-4 (R, S)-1-[2-amino-1(4-methoxyphenyl)ethyl]cyclohexanol acetate 445-750-3 — Xn; R22 Xi; R41 R43 R52-53 Xn R: 22-41-43-52/53 S: (2-)22-24-26-37/39-61 612-275-00-X fatty acids, C18-unsatd., dimers, reaction products with 1-piperazineethanamine and tall oil 447-880-6 206565-89-1 Xi; R38-41 R43 N; R50-53 Xi; N R: 38-41-43-50/53 S: (2-)23-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-276-00-5 1-amino-4-[(4-amino-2-sulfofenyl)amino]-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid, disodium salt, reaction products with 2-[[3-[(4,6-dichloro-1,3,5-triazin-2-yl)ethylamino]phenyl]sulfonyl]ethyl hydrogen sulfate, sodium salts 451-430-4 500717-36-2 Xi; R41 S: (2-)23-26-36/37/39-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-276-00-5 1-amino-4-[(4-amino-2-sulfofenyl)amino]-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid, disodium salt, reaction products with 2-[[3-[(4,6-dichloro-1,3,5-triazin-2-yl)ethylamino]phenyl]sulfonyl]ethyl hydrogen sulfate, sodium salts 451-430-4 500717-36-2 Xi; R41 R43 R52-53 Xi R: 41-43-52/53 … 22 unchanged lines … Xi; R38-41 N; R50-53 Xn; N R: 38-41-48/22-65-50/53 S: (2-)26-36/37/39-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-283-00-3 (Z)-octadec-9-enylamine 204-015-5 112-90-3 Xn; R22-48/22-65 S: (2-)26-36/37/39-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-283-00-3 (Z)-octadec-9-enylamine 204-015-5 112-90-3 Xn; R22-48/22-65 C; R34 N; R50-53 C; N R: 22-34-48/22-65-50/53 S: (1/2-)23-26-36/37/39-45-60-61-62 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-284-00-9 amines, hydrogenated tallow alkyl 262-976-6 61788-45-2 Xn; R48/22-65 S: (1/2-)23-26-36/37/39-45-60-61-62 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-284-00-9 amines, hydrogenated tallow alkyl 262-976-6 61788-45-2 Xn; R48/22-65 Xi; R38-41 N; R50-53 Xn; N R: 38-41-48/22-65-50/53 S: (2-)26-36/37/39-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-285-00-4 amines, coco alkyl 262-977-1 61788-46-3 Xn; R22-48/22-65 S: (2-)26-36/37/39-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-285-00-4 amines, coco alkyl 262-977-1 61788-46-3 Xn; R22-48/22-65 C; R35 N; R50-53 C; N R: 22-35-48/22-65-50/53 S: (1/2-)23-26-36/37/39-45-60-61-62 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-286-00-X amines, tallow alkyl 263-125-1 61790-33-8 Xn; R22-48/22-65 S: (1/2-)23-26-36/37/39-45-60-61-62 C; R35: C ≥ 10 % C; R34: 5 % ≤ C < 10 % Xi; R36/37/38: 1 % ≤ C < 5 % N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-286-00-X amines, tallow alkyl 263-125-1 61790-33-8 Xn; R22-48/22-65 C; R35 N; 50-53 C; N R: 22-35-48/22-65-50/53 S: (1/2-)26-36/37/39-45-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-001-00-1 ethyleneimine; S: (1/2-)26-36/37/39-45-60-61-62 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 612-287-00-5 fluazinam (ISO); 3-chloro-N-[3-chloro-2,6-dinitro-4-(trifluoromethyl)phenyl]-5-(trifluoromethyl)pyridin-2-amine — 79622-59-6 Repr. Cat. 3; R63 Xn; R20 Xi; R41 R43 N; R50-53 Xn; N R: 20-41-43-50/53-63 S: (2-)26-36/37/39-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-001-00-1 ethyleneimine; aziridine 205-793-9 151-56-4 F; R11 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T+; R26/27/28 C; R34 N; R51-53 F; T+; N R: 45-46-11-26/27/28-34-51/53 S: 53-45-61 D E 613-002-00-7 pyridine 203-809-9 110-86-1 F; R11 Xn; R20/21/22 F; Xn R: 11-20/21/22 S: (2-)26-28 Xn; R20/21/22: C ≥ 5 % 613-003-00-2 1,2,3,4-tetranitrocarbazole — 6202-15-9 E; R2 S: (2-)26-28 Xn; R20/21/22: C ≥ 5 % 613-003-00-2 1,2,3,4-tetranitrocarbazole — 6202-15-9 E; R2 Xn; R20/21/22 E; Xn R: 2-20/21/22 S: (2-)35-36/37 613-004-00-8 crimidine (ISO); … 15 unchanged lines … C; R34 R43 T+; R: 14-22-26-34-43 S: (1/2-)26-28-36/37/39-45-46-63 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 613-010-00-0 ametryn (ISO); S: (1/2-)26-28-36/37/39-45-46-63 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 613-010-00-0 ametryn (ISO); N-ethyl-N′-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine 212-634-7 834-12-8 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)36-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-011-00-6 amitrole (ISO); S: (2-)36-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-011-00-6 amitrole (ISO); 1,2,4-triazol-3-ylamine 200-521-5 61-82-5 Repr. Cat. 3; R63 Xn; R48/22 N; R51-53 Xn; N … 22 unchanged lines … Xi; R43 N; R50-53 Xn; N R: 40-48/22-22-43-50/53 S: (2)-22-36/37-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 613-017-00-9 bis (8-hydroxyquinolinium) sulphate 205-137-1 134-31-6 Xn; R22 Xn S: (2)-22-36/37-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 613-017-00-9 bis (8-hydroxyquinolinium) sulphate 205-137-1 134-31-6 Xn; R22 Xn R: 22 S: (2-)36 613-018-00-4 morfamquat (ISO); 1,1'-bis(3,5-dimethylmorpholinocarbonylmethyl)-4,4'-bipyridilium ion — 7411-47-4 Xn; R22 … 38 unchanged lines … T; R23/24 C; R34 F; T R: 11-23/24-34 S: (1/2-)16-26-27-45 T; R23/24: C ≥ 5 % Xn; R20/21: 1 % ≤ C < 5 % C; R34: C ≥ 5 % Xi: R36/38: 1 % ≤ C < 5 % 613-028-00-9 morpholine 203-815-1 110-91-8 R10 S: (1/2-)16-26-27-45 T; R23/24: C ≥ 5 % Xn; R20/21: 1 % ≤ C < 5 % C; R34: C ≥ 5 % Xi: R36/38: 1 % ≤ C < 5 % 613-028-00-9 morpholine 203-815-1 110-91-8 R10 Xn; R20/21/22 C; R34 C R: 10-20/21/22-34 S: (1/2-)23-36-45 C; R34: C ≥ 10 % Xi; R36/38: 1 % ≤ C < 10 % 613-029-00-4 dichloro-1,3,5-triazinetrione; S: (1/2-)23-36-45 C; R34: C ≥ 10 % Xi; R36/38: 1 % ≤ C < 10 % 613-029-00-4 dichloro-1,3,5-triazinetrione; dichloroisocyanuric acid 220-487-5 2782-57-2 O; R8 Xn; R22 R31 Xi; R36/37 N; R50-53 O; Xn; N R: 8-22-31-36/37-50/53 S: (2-)8-26-41-60-61 613-030-00-X troclosene potassium; [1] troclosene sodium [2] 218-828-8 [1] 220-767-7 [2] 2244-21-5 [1] 2893-78-9 [2] E; R2 O; R8 Xn; R22 Xi; R36/37 R31 N; R50-53 E; Xn; N R: 2-8-22-31-36/37-50/53 S: (2-)8-26-41-45-60-61 Xn; R22: C ≥ 10 % Xi; R36/37: C ≥ 10 % R31: C ≥ 10 % T S: (2-)8-26-41-45-60-61 Xn; R22: C ≥ 10 % Xi; R36/37: C ≥ 10 % R31: C ≥ 10 % T 613-030-01-7 troclosene sodium, dihydrate 220-767-7 51580-86-0 Xn; R22 R31 Xi; R36/37 … 19 unchanged lines … Xi; R41 N; R51-53 F; T+; N R: 45-11-26/27/28-41-51/53 S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E S: 53-45-61 Carc. Cat. 2; R45: C ≥ 0,01 % E 613-034-00-1 1,2-dimethylimidazole 217-101-2 1739-84-0 Xn; R22 Xi; R38-41 Xn R: 22-38-41 … 51 unchanged lines … R43 N; R50-53 C; N R: 22-34-43-50/53 S: (2-)26-36/37/39-45-60-61 C; R34: C ≥ 50 % Xi; R38: 30 % ≤ C < 50 % Xi; R41: 15 % ≤ C < 50 % Xi; R36: 5 % ≤ C < 15 % 613-044-00-6 captan (ISO); S: (2-)26-36/37/39-45-60-61 C; R34: C ≥ 50 % Xi; R38: 30 % ≤ C < 50 % Xi; R41: 15 % ≤ C < 50 % Xi; R36: 5 % ≤ C < 15 % 613-044-00-6 captan (ISO); 1,2,3,6-tetrahydro-N-(trichloromethylthio)phthalimide 205-087-0 133-06-2 Carc. Cat. 3; R40 T; R23 Xi; R41 R43 N; R50 T; N R: 23-40-41-43-50 S: (1/2-)26-29-36/37/39-45-61 N; R50: C ≥ 2,5 % 613-045-00-1 folpet (ISO); S: (1/2-)26-29-36/37/39-45-61 N; R50: C ≥ 2,5 % 613-045-00-1 folpet (ISO); N-(trichloromethylthio)phthalimide 205-088-6 133-07-3 Carc. Cat. 3; R40 Xn; R20 Xi; R36 R43 N; R50 Xn; N R: 20-36-40-43-50 S: (2-)36/37-46-61 N; R50: C ≥ 2,5 % 613-046-00-7 captafol (ISO); S: (2-)36/37-46-61 N; R50: C ≥ 2,5 % 613-046-00-7 captafol (ISO); 1,2,3,6-tetrahydro-N-(1,1,2,2-tetrachloroethylthio)phthalimide 219-363-3 2425-06-1 Carc. Cat. 2; R45 R43 N; R50-53 T; N … 15 unchanged lines … R43 N; R50-53 T; N R: 46-60-61-37/38-43-50/53 S: 53-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-050-00-9 carbadox (INN); S: 53-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-050-00-9 carbadox (INN); methyl 3-(quinoxalin-2-ylmethylene)carbazate 1,4-dioxide; 2-(methoxycarbonylhydrazonomethyl)quinoxaline 1,4-dioxide 229-879-0 6804-07-5 F; R11 Carc. Cat. 2; R45 Xn; R22 F; T R: 45-11-22 S: 53-45 E 613-051-00-4 molinate (ISO); S-ethyl 1-perhydroazepinecarbothioate; S-ethyl perhydroazepine-1-carbothioate 218-661-0 2212-67-1 Carc. Cat. 3; R40 Repr. Cat. 3; R62 Xn; R20/2248/22 R43 N; R50-53 Xn; N R: 20/22-40-43-48/22-62-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-052-00-X trifenmorph (ISO); S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-052-00-X trifenmorph (ISO); 4-tritylmorpholine 215-812-2 1420-06-0 Xn; R22 N; R50-53 Xn; N R: 22-50/53 … 17 unchanged lines … R43 N; R50-53 Xn; N R: 20/22-43-50/53 S: (2-)13-24-36/37/39-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-059-00-8 profluralin (ISO); S: (2-)13-24-36/37/39-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-059-00-8 profluralin (ISO); N-(cyclopropylmethyl)-α,α,α-trifluoro-2,6-dinitro-N-propyl-p-toluidine 247-656-6 26399-36-0 Xi; R36 N; R50-53 Xi; N R: 36-50/53 S: (2-)60-61 613-060-00-3 resmethrin (ISO); 5-benzyl-3-furylmethyl (±)-cis-trans-chrysanthemate 233-940-7 10453-86-8 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-061-00-9 6-(1α,5aβ,8aβ,9-pentahydroxy-7β-isopropyl-2β,5β,8β-trimethylperhydro-8bα,9-epoxy-5,8-ethanocyclopenta[1,2-b]indenyl) pyrrole-2-carboxylate; S: (2-)60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-061-00-9 6-(1α,5aβ,8aβ,9-pentahydroxy-7β-isopropyl-2β,5β,8β-trimethylperhydro-8bα,9-epoxy-5,8-ethanocyclopenta[1,2-b]indenyl) pyrrole-2-carboxylate; ryania 239-732-2 15662-33-6 Xn; R21/22 N; R50-53 Xn; N R: 21/22-50/53 … 104 unchanged lines … R43 N; R50 Xn; N R: 22-38-41-43-50 S: (2-)24-26-37/39-61 R43: C ≥ 0,05 % 613-089-00-1 diquat dibromide; [1] S: (2-)24-26-37/39-61 R43: C ≥ 0,05 % 613-089-00-1 diquat dibromide; [1] diquat dichloride; [2] 6,7-dihydrodipyrido[1,2-α:2',1'-c]pyrazinediylium dihydroxide [3] 201-579-4 [1] 223-714-6 [2] … 91 unchanged lines … R43 N; R50-53 T; N R: 22-23/24-34-43-50/53 S: (1/2-)26-36/37/39-45-60-61 R43: C ≥ 0,05 % 613-113-00-0 2-(morpholinothio)benzothiazole 203-052-4 102-77-2 Xi; R36/38 S: (1/2-)26-36/37/39-45-60-61 R43: C ≥ 0,05 % 613-113-00-0 2-(morpholinothio)benzothiazole 203-052-4 102-77-2 Xi; R36/38 R43 N; R51-53 Xi; N R: 36/38-43-51/53 S: (2-)24-26-37-61 613-114-00-6 2,2',2"-(hexahydro-1,3,5-triazine-1,3,5-triyl)triethanol; 1,3,5-tris(2-hydroxyethyl)hexahydro-1,3,5-triazine 225-208-0 4719-04-4 Xn; R22 R43 Xn R: 22-43 S: (2-)24-37 R43: C ≥ 0,1 % 613-115-00-1 hymexazol (ISO); S: (2-)24-37 R43: C ≥ 0,1 % 613-115-00-1 hymexazol (ISO); 3-hydroxy-5-methylisoxazole 233-000-6 10004-44-1 Xn; R22 Xi; R41 R52-53 Xn R: 22-41-52/53 S: (2-)26-39-61 613-116-00-7 tolylfluanid (ISO); dichloro-N-[(dimethylamino)sulphonyl]fluoro-N-(p-tolyl)methanesulphenamide; [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 T+; R26 [containing ≥ 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 T+; R26 T; R48/23 Xi; R36/37/38 R43 N; R50 T+; N R: 26-36/37/38-43-48/23-50 S: (1/2-)28-36/37/39-45-63-61 N; R50: C ≥ 2,5 % 613-116-01-4 tolylfluanid (ISO); S: (1/2-)28-36/37/39-45-63-61 N; R50: C ≥ 2,5 % 613-116-01-4 tolylfluanid (ISO); dichloro-N-[(dimethylamino)sulphonyl]fluoro-N-(p-tolyl)methanesulphenamide; [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Xi; R36/37/38 [containing < 0,1 % (w/w) of particles with an aerodynamic diameter of below 50 μm] 211-986-9 731-27-1 Xi; R36/37/38 R43 N; R50 Xi; N R: 36/37/38-43-50 S: (2-)25-36/37-46-61 N; R50: C ≥ 2,5 % 613-117-00-2 diniconazole (ISO); S: (2-)25-36/37-46-61 N; R50: C ≥ 2,5 % 613-117-00-2 diniconazole (ISO); (E)-β-[(2,4-dichlorophenyl)methylene]-α-(1,1-dimethylethyl)-1H-1,2,4-triazol-1-ethanol; (E)-(RS)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol — 76714-88-0 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 613-118-00-8 flubenzimine (ISO); N-[3-phenyl-4,5-bis[(trifluoromethyl)imino]thiazolidin-2-ylidene]aniline; 253-703-1 37893-02-0 Xi; R36 N; R50-53 Xi; N R: 36-50/53 S: (2-)26-60-61 613-119-00-3 (benzothiazol-2-ylthio)methyl thiocyanate; TCMTB 244-445-0 21564-17-0 T+; R26 Xn; R22 Xi; R36/38 R43 N; R50-53 T+; N R: 22-26-36/38-43-50/53 S: (1/2-)28-36/37-38-45-60-61 613-120-00-9 bioresmethrin (ISO); (5-benzyl-3-furyl)methyl (1R)-2,2-dimethyl-3-(2-methylprop-1-en-1-yl)cyclopropanecarboxylate 249-014-0 28434-01-7 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-121-00-4 chlorsulfuron (ISO); S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-121-00-4 chlorsulfuron (ISO); 2-chloro-N-[[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)amino]carbonyl]benzenesulphonamide; 265-268-5 64902-72-3 N; R50-53 N R: 50/53 S: 60-61 613-122-00-X diclobutrazole (ISO); … 68 unchanged lines … S: (2-)24-37-46-60-61 613-139-00-2 metsulfuron-methyl (ISO); methyl 2-{[(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamoyl]sulfamoyl}benzoate — 74223-64-6 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-140-00-8 cycloheximide (ISO); S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-140-00-8 cycloheximide (ISO); 4-{(2R)-2-[(1S,3S,5S)-3,5-dimethyl-2-oxocyclohexyl]-2-hydroxyethyl}piperidine-2,6-dione 200-636-0 66-81-9 Muta. Cat. 3; R68 Repr. Cat. 2; R61 T+; R28 … 64 unchanged lines … S: (2-)36/37-61 613-163-00-3 azimsulfuron (ISO); 1-(4,6-dimethoxypyrimidin-2-yl)-3-[1-methyl-4-(2-methyl-2H-tetrazol-5-yl)pyrazol-5-ylsulfonyl]urea — 120162-55-2 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-164-00-9 flufenacet (ISO); S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-164-00-9 flufenacet (ISO); N-(4-fluorophenyl)-N-isopropyl-2-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yloxy)acetamide — 142459-58-3 Xn; R22-48/22 R43 N; R50-53 Xn; N R: 22-43-48/22-50/53 S: (2-)13-24-37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-165-00-4 flupyrsulfuron-methyl-sodium (ISO); S: (2-)13-24-37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-165-00-4 flupyrsulfuron-methyl-sodium (ISO); methyl 2-[[(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-6-trifluoromethyl]nicotinate, monosodium salt — 144740-54-5 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-166-00-X flumioxazin (ISO); S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-166-00-X flumioxazin (ISO); N-(7-fluoro-3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide — 103361-09-7 Repr. Cat. 2; R61 N; R50-53 T; N R: 61-50/53 S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-167-00-5 reaction mass of: 5-chloro-2-methyl-4-isothiazolin-3-one [EC no. 247-500-7] S: 53-45-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-167-00-5 reaction mass of: 5-chloro-2-methyl-4-isothiazolin-3-one [EC no. 247-500-7] and 2-methyl-2H -isothiazol-3-one [EC no. 220-239-6] (3:1); reaction mass of: 5-chloro-2-methyl-4-isothiazolin-3-one [EC no. 247-500-7] and 2-methyl-4-isothiazolin-3-one [EC no. 220-239-6] (3:1) — 55965-84-9 T; R23/24/25 C; R34 R43 N; R50-53 T; N R: 23/24/25-34-43-50/53 S: (2-)26-28-36/37/39-45-60-61 C; R34: C ≥ 0,6 % Xi; R36/38: 0,06 % ≤ C < 0,6 % R43: C ≥ 0,0015 % 613-168-00-0 1-vinyl-2-pyrrolidone 201-800-4 88-12-0 Carc. Cat. 3; R40 S: (2-)26-28-36/37/39-45-60-61 C; R34: C ≥ 0,6 % Xi; R36/38: 0,06 % ≤ C < 0,6 % R43: C ≥ 0,0015 % 613-168-00-0 1-vinyl-2-pyrrolidone 201-800-4 88-12-0 Carc. Cat. 3; R40 Xn; R20/21/22-48/20 Xi; R37-41 Xn R: 20/21/22-37-40-41-48/20 S: (2-)26-36/37/39 D 613-169-00-6 9-vinylcarbazole 216-055-0 1484-13-5 Muta. Cat. 3; R68 Xn; R21/22 Xi; R38 R43 N; R50-53 Xn; N R: 21/22-38-43-68-50/53 S: (2-)22-23-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-170-00-1 2,2-ethylmethylthiazolidine 404-500-3 694-64-4 Xn; R22 S: (2-)22-23-36/37-60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-170-00-1 2,2-ethylmethylthiazolidine 404-500-3 694-64-4 Xn; R22 Xi; R41 R43 N; R51-53 Xn; N … 35 unchanged lines … S: (2-)36/37-61 613-178-00-5 4-ethyl-2-methyl-2-isopentyl-1,3-oxazolidine 410-470-2 137796-06-6 C; R34 R43 C R: 34-43 S: (1/2-)7/8-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 613-179-00-0 lithium 3-oxo-1,2(2H)-benzisothiazol-2-ide 411-690-1 111337-53-2 Xn; R22 S: (1/2-)7/8-26-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 613-179-00-0 lithium 3-oxo-1,2(2H)-benzisothiazol-2-ide 411-690-1 111337-53-2 Xn; R22 C; R34 R43 N; R51-53 C; N … 27 unchanged lines … R43 N; R51-53 Xi; N R: 36-43-51/53 S: (2-)24-26-37-61 613-187-00-4 5-(2-amino-5-cyano-6-[2-(2-hydroxyethoxy)ethylamino]-4-methylpyridin-3-ylazo)-3-methyl-2,4-dicarbonitrilethiophene 410-530-8 - R43 Xi S: (2-)24-26-37-61 613-187-00-4 5-(2-amino-5-cyano-6-[2-(2-hydroxyethoxy)ethylamino]-4-methylpyridin-3-ylazo)-3-methyl-2,4-dicarbonitrilethiophene 410-530-8 — R43 Xi R: 43 S: (2-)24-37 613-188-00-X 1-(3-(4-fluorophenoxy)propyl)-3-methoxy-4-piperidinone 411-500-7 116256-11-2 Xn; R22 Xi; R41 … 57 unchanged lines … - [2] 129630-19-9 [1] 129630-17-7 [2] N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-204-00-5 oxadiargyl (ISO); S: 60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-204-00-5 oxadiargyl (ISO); 3-[2,4-dichloro-5-(2-propynyloxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one; 254-637-6 39807-15-3 Repr. Cat. 3; R63 Xn; R48/22 N; R50-53 Xn; N R: 48/22-63-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-205-00-0 propiconazole (ISO); S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,025 % N; R51-53: 0,0025 % ≤ C < 0,025 % R52-53: 0,00025 % ≤ C < 0,0025 % 613-205-00-0 propiconazole (ISO); (±)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole 262-104-4 60207-90-1 Xn; R22 R43 N; R50-53 Xn; N … 102 unchanged lines … R: 41-52/53 S: (2-)26-39-61 613-241-00-7 3-(2H-tetrazol-5-yl)pyridine 426-810-8 3250-74-6 Xi; R41 Xi R: 41 S: (2-)22-26-39 613-242-00-2 reaction products of 3,10-bis((2-aminopropyl)amino)-6,13-dichloro-4,11-triphenodioxazinedisulfonic acid with 2-amino-1,4-benzenedisulfonic acid, 2-((4-aminophenyl)sulfonyl)ethyl hydrogen sulfate and 2,4,6-trifluoro-1,3,5-triazine, sodium salts 426-860-0 191877-09-5 Xi; R41 Xi S: (2-)22-26-39 613-242-00-2 reaction products of 3,10-bis((2-aminopropyl)amino)-6,13-dichloro-4,11-triphenodioxazinedisulfonic acid with 2-amino-1,4-benzenedisulfonic acid, 2-((4-aminophenyl)sulfonyl)ethyl hydrogen sulfate and 2,4,6-trifluoro-1,3,5-triazine, sodium salts 426-860-0 191877-09-5 Xi; R41 Xi R: 41 S: (2-)22-26-39 613-243-00-8 4,4'-(1,6-hexamethylenebis(formylimino))bis(2,2,6,6-tetramethyl-1-oxylpiperidine) 427-350-0 182235-14-9 N; R51-53 N R: 51/53 … 15 unchanged lines … R: 41-43-51/53 S: (2-)24-26-37/39-61 613-250-00-6 reaction mass of: carbonato-bis-N-ethyl-2-isopropyl-1,3-oxazolidine; methyl carbonato-N-ethyl-2-isopropyl-1,3-oxazolidine; 2-isopropyl-N-hydroxyethyl 1,3-oxazolidine 429-990-6 - Xi; R41 2-isopropyl-N-hydroxyethyl 1,3-oxazolidine 429-990-6 — Xi; R41 R43 R52-53 Xi R: 41-43-52/53 S: (2-)24-26-37/39-61 613-251-00-1 (R)-3-[(1-methylpyrrolidin-2-yl)methyl]-5-[2-(phenylsulfonyl)ethenyl]-1H-indole 430-560-5 180637-89-2 Xn; R22-48/22 Xi; R41 R43 Xn R: 22-41-43-48/22 S: (2-)26-36/37/39 613-253-00-2 2,2-dialkyl-4-hydroxymethyl-1,3-dioxolane; reaction products with ethylene oxide (alkyl is C1-12 and the sum to C13, average degree of ethoxylation is 3,5) 430-580-4 - R19 reaction products with ethylene oxide (alkyl is C1-12 and the sum to C13, average degree of ethoxylation is 3,5) 430-580-4 — R19 Xi; R38 N; R51-53 Xi; N R: 19-38-51/53 S: (2-)37-61 613-254-00-8 forchlorfenuron (ISO); 1-(2-chloro-4-pyridyl)-3-phenylurea - 68157-60-8 Carc. Cat. 3; R40 1-(2-chloro-4-pyridyl)-3-phenylurea — 68157-60-8 Carc. Cat. 3; R40 N; R51-53 Xn; N R: 40-51/53 S: (2-)36/37-46-61 613-255-00-3 reaction mass of isomers of: sodium [(2-hydroxyethylsulfamoyl){][}2-(2-piperazin-1-ylethylamino)ethylsulfamoyl][2-(4-aminoethylpiperazine-1-yl)ethylsulfamoyl{](sulfamoyl)[}(sulfonatophthalocyaninato)]copper(II) 424-270-8 - Xi; R41 Xi S: (2-)36/37-46-61 613-255-00-3 reaction mass of isomers of: sodium [(2-hydroxyethylsulfamoyl){][}2-(2-piperazin-1-ylethylamino)ethylsulfamoyl][2-(4-aminoethylpiperazine-1-yl)ethylsulfamoyl{](sulfamoyl)[}(sulfonatophthalocyaninato)]copper(II) 424-270-8 — Xi; R41 Xi R: 41 S: (2-)26-39 613-256-00-9 3'5'-anhydro thymidine 425-810-5 38313-48-3 R52-53 R: 52/53 S: 61 613-257-00-4 2-phthalimidoethyl N-[4-(2-cyano-4-nitrophenylazo)phenyl]-N-methyl-β-alaninate 426-400-9 170222-39-6 R43 R53 Xi R: 43-53 S: (2-)24-37-61 613-258-00-X reaction mass of: 4-chloro-7-methylbenzotriazole sodium salt; 4-chloro-5-methylbenzotriazole sodium salt; 5-chloro-4-methylbenzotriazole sodium salt 427-730-6 202420-04-0 C; R34 R52-53 C R: 34-52/53 S: (1/2-)26-28-36/37/39-45-61 613-259-00-5 reaction mass of: [2,4-dioxo-(2-propyn-1-yl)imidazolidin-3-yl]methyl(1R)-cis-chrysanthemate; [2,4-dioxo-(2-propyn-1-yl)imidazolidin-3-yl]methyl(1R)-trans-chrysanthemate 428-790-6 72963-72-5 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 613-260-00-0 (±)-4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-1-methyl-2(1H)-quinolin 430-730-9 - Xi; R41 S: (2-)60-61 613-260-00-0 (±)-4-(3-chlorophenyl)-6-[(4-chlorophenyl)hydroxy(1-methyl-1H-imidazol-5-yl)methyl]-1-methyl-2(1H)-quinolin 430-730-9 — Xi; R41 N; R50-53 Xi; N R: 41-50/53 S: (2-)22-26-39-60-61 613-261-00-6 pyrazole-1-carboxamidine monohydrochloride 429-520-1 4023-02-3 Xn; R22-48/22 Xi; R41 R43 R52-53 Xn R: 22-41-43-48/22-52/53 S: (2-)22-26-36/37/39-61 613-262-00-1 disodium (E)-1,2-bis-(4-(4-methylamino-6-(4-methylcarbamoylphenylamino)-1,3,5-triazin-2-ylamino)phenyl-2-sulfonato)ethene 427-310-2 180850-95-7 Xi; R41 Xi R: 41 S: (2-)26-39 613-263-00-7 monosodium 3-cyano-5-fluoro-6-hydroxypyridine-2-olate 429-570-2 - R43 Xi S: (2-)26-39 613-263-00-7 monosodium 3-cyano-5-fluoro-6-hydroxypyridine-2-olate 429-570-2 — R43 Xi R: 43 S: (2-)24-37 613-266-00-3 2-chloro-5-chloromethylthiazole 429-830-5 105827-91-6 T; R24 C; R34 Xn; R22 R43 N; R51-53 T; N R: 22-24-34-43-51/53 S: (1/2-)26-36/37/39-45-61 613-267-00-9 thiamethoxam (ISO); 3-(2-chloro-thiazol-5-ylmethyl)-5-methyl[1,3,5]oxadiazinan-4-ylidene-N-nitroamine 428-650-4 153719-23-4 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-268-00-4 (4aS-cis-)-6-benzyl-octahydropyrrolo[3.4-b]pyridine 425-930-8 151213-39-7 C; R34 S: (2-)60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-268-00-4 (4aS-cis-)-6-benzyl-octahydropyrrolo[3.4-b]pyridine 425-930-8 151213-39-7 C; R34 Xn; R20/22-48/22 N; R51-53 C; N R: 20/22-34-48/22-51/53 S: (1/2-)26-36/37/39-45-61 613-269-00-X 2-thiazolidinylidenecyanamide 427-720-1 26364-65-8 Xn; R22-48/22 R52-53 Xn R: 22-48/22-52/53 S: (2-)22-36-61 613-270-00-5 5-amino-N-(2,6-dichloro-3-methylphenyl)-1H-1,2,4-triazole-3-sulfonamide 428-150-6 113171-13-4 R52-53 R: 52/53 S: 61 613-271-00-0 tritosulfuron (ISO) (containing ≤ 0,02 % AMTT); 1-[4-methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-yl]-3-[2-(trifluoromethyl)benzenesulfonyl]urea (containing ≤ 0,02 % AMTT) - 142469-14-5 R43 S: 61 613-271-00-0 tritosulfuron (ISO) (containing ≤ 0,02 % AMTT); 1-[4-methoxy-6-(trifluoromethyl)-1,3,5-triazin-2-yl]-3-[2-(trifluoromethyl)benzenesulfonyl]urea (containing ≤ 0,02 % AMTT) — 142469-14-5 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-272-00-6 pyraclostrobin (ISO); methyl N-{]2-[}1-(4-chlorophenyl)-1H-pyrazol-3-yloxymethyl{]phenyl[}(N-methoxy)carbamate - - T; R23 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-272-00-6 pyraclostrobin (ISO); methyl N-{]2-[}1-(4-chlorophenyl)-1H-pyrazol-3-yloxymethyl{]phenyl[}(N-methoxy)carbamate — — T; R23 Xi; R38 N; R50-53 T; N R: 23-38-50/53 S: (1/2-)45-60-61-63 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-273-00-1 tetrahydro-3-methyl-5-((2-phenylthio)thiazol-5-ylmethyl)-[4H]-1,3,5-oxadiazinan-4-ylidene-N-nitroamine 427-600-9 192439-46-6 N; R51-53 N S: (1/2-)45-60-61-63 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 613-273-00-1 tetrahydro-3-methyl-5-((2-phenylthio)thiazol-5-ylmethyl)-[4H]-1,3,5-oxadiazinan-4-ylidene-N-nitroamine 427-600-9 192439-46-6 N; R51-53 N R: 51/53 S: 61 613-274-00-7 2,6-dichloro-1-fluoropyridiniumtetrafluoroborate 427-400-1 140623-89-8 C; R34 Xn; R22 R43 N; R50-53 C; N R: 22-34-43-50/53 S: (1/2-)26-36/37/39-45-60-61 613-275-00-2 3-(2-chloroethyl)-6,7,8,9-tetra-hydro-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one monohydrochloride 424-530-0 93076-03-0 T; R25 Xn; R68/21-48/22 Xi; R41 R43 N; R51-53 T; N R: 25-41-43-48/22-68/21-51/53 S: (1/2-)22-26-36/37/39-45-61 613-276-00-8 1-(2-chlorophenyl)-1,2-dihydro-5H-tetrazol-5-one 426-110-2 98377-35-6 R43 R52-53 Xi R: 43-52/53 S: (2-)24/25-37-61 613-277-00-3 (4-(6-diethylamino-2-methylpyridin-3-yl)imino-4,5-dihydro-3-methyl-1-(4-methylphenyl)-1H-pyrazol-5-one 427-070-9 - R53 R: 53 S: (2-)24/25-37-61 613-277-00-3 (4-(6-diethylamino-2-methylpyridin-3-yl)imino-4,5-dihydro-3-methyl-1-(4-methylphenyl)-1H-pyrazol-5-one 427-070-9 — R53 R: 53 S: 61 613-278-00-9 (3-aminophenyl)pyridin-3-ylmethanone 428-230-0 79568-06-2 Xn; R48/22 N; R50-53 Xn; N R: 48/22-50/53 S: (2-)22-36-60-61 613-279-00-4 2-ethyl-2,3-dihydro-2-methyl-1H-perimidine 424-380-6 43057-68-7 Xn; R22-48/22 N; R50-53 Xn; N R: 22-48/22-50/53 S: (2-)36/37-60-61 613-280-00-X tetrahydro-1,3-dimethyl-1H-pyrimidin-2-one; dimethyl propyleneurea 230-625-6 7226-23-5 Repr. Cat. 3; R62 Xn; R22 Xi; R41 Xn R: 22-41-62 S: 26-36/37/39 613-281-00-5 quinoline 202-051-6 91-22-5 Carc. Cat. 2; R45 Muta. Cat. 3; R68 Xn; R21/22 Xi; R36/38 N; R51-53 T; N R: 45-21/22-36/38-68-51/53 S: 53-45-61 E 613-282-00-0 triticonazole (ISO); (RS)-(E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-methyl)cyclopentanol - 131983-72-7 N; R51-53 N (RS)-(E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-methyl)cyclopentanol — 131983-72-7 N; R51-53 N R: 51/53 S: 61 613-283-00-6 ketoconazole; 1-[4-[4-[[(2SR, 4RS)-2-(2,4-dichlorophenyl)-2-(imidazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy]phenyl]piperazin-1-yl]ethanone 265-667-4 65277-42-1 Repr. Cat. 2; R60 T; R25 Xn; R48/22 N; R50-53 T; N R: 60-25-48/22-50/53 S: 53-45-60-61 E 613-284-00-1 metconazole (ISO); (1RS, 5RS;1RS, 5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol - 125116-23-6 Repr. Cat. 3; R63 Xn; R22 N; R51-53 Xn; N R: 22-63-51/53 S: (2-)36/37-46-61 613-285-00-7 1-hydroxybenzotriazole, anhydrous; [1] 1-hydroxybenzotriazole, monohydrated [2] 219-989-7 [1] 219-989-7 [2] 2592-95-2 [1] 123333-53-9 [2] E; R2 E R: 2 S: 16-35 613-286-00-2 potassium 1-methyl-3-morpholinocarbonyl-4-[3-(1-methyl-3-morpholinocarbonyl-5-oxo-2-pyrazolin-4-ylidene)-1-propenyl]pyrazole-5-olate; [containing < 0,5 % N,N-dimethylformamide (EC no 200-679-5)] 418-260-2 183196-57-8 R43 Xi [containing < 0,5 % N,N-dimethylformamide (EC no 200-679-5)] 418-260-2 183196-57-8 R43 Xi R: 43 S: (2-)24-37 613-286-01-X potassium 1-methyl-3-morpholinocarbonyl-4-[3-(1-methyl-3-morpholinocarbonyl-5-oxo-2-pyrazolin-4-ylidene)-1-propenyl]pyrazole-5-olate; [containing ≥ 0,5 % N,N-dimethylformamide (EC No 200-679-5)] 418-260-2 183196-57-8 Repr. Cat. 2; R61 [containing ≥ 0,5 % N,N-dimethylformamide (EC No 200-679-5)] 418-260-2 183196-57-8 Repr. Cat. 2; R61 R43 T R: 61-43 S: 53-45 613-287-00-8 1-(3-iodo-4-aminobenzyl)-1H-1,2,4-triazole 419-540-7 160194-26-3 Xn; R22 … 22 unchanged lines … Xi; R41 R52-53 Xn R: 22-41-52/53 S: (2-)22-26-39-61 613-296-00-7 pentapotassium 2-(4-(5-[1-(2,5-disulfonatophenyl)-4,5-dihydro-3-methylcarbamoyl-5-oxopyrazol-4-ylidene]-3-methyl-1,3-pentadienyl)-3-methylcarbamoyl-5-oxidopyrazol-1-yl)benzene-1,4-disulfonate 418-270-7 - R43 S: (2-)22-26-39-61 613-296-00-7 pentapotassium 2-(4-(5-[1-(2,5-disulfonatophenyl)-4,5-dihydro-3-methylcarbamoyl-5-oxopyrazol-4-ylidene]-3-methyl-1,3-pentadienyl)-3-methylcarbamoyl-5-oxidopyrazol-1-yl)benzene-1,4-disulfonate 418-270-7 — R43 R52-53 Xi R: 43-52/53 S: (2-)24-37-47-61 613-297-00-2 5-(2-bromophenyl)-2-tert-butyl-2H-tetrazole 420-820-6 - R10 Xn; R22 N; R51-53 Xn; N R: 10-22-51/53 S: (2-)16-61 613-298-00-8 bis-(6-hydroxy-4-methyl-5-(3-methylimidazolium-1-yl)-3-(4-phenylazo)-1H-pyridin-2-one)ethylene dilactate 421-560-6 - Xn; R48/22 S: (2-)16-61 613-298-00-8 bis-(6-hydroxy-4-methyl-5-(3-methylimidazolium-1-yl)-3-(4-phenylazo)-1H-pyridin-2-one)ethylene dilactate 421-560-6 — Xn; R48/22 Xi; R41 N; R51-53 Xn; N R: 41-48/22-51/53 S: (2-)22-26-36/39-61 613-299-00-3 main component 1 (isomer 1): 2-{]6-fluoro-4-[}3-(2,5-disulfo-phenylazo)-4-hydroxy-2-sulfonapht-7-ylamino{]-1,3,5-triazin-2-ylamino[}-3-{]6-fluoro-4-[}3-(1,5-disulfonaphth-2-ylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-propane sodium salt; main component 1 (isomer 2): 2-{]6-fluoro-4-[}3-(2,5-disulfo-phenylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-3-{]6-fluoro-4-[}3-(2,5-disulfo-phenylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-propane sodium salt; main component 2: 2,3-bis-{]6-fluoro-4-[}3-(2,5-disulfo-phenylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-propane sodium salt; main component 3: 2,3-bis-{]6-fluoro-4-[}3-(1,5-disulfonaphth-2-ylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-propane sodium salt 422-610-1 - Xi; R41 Xi main component 3: 2,3-bis-{]6-fluoro-4-[}3-(1,5-disulfonaphth-2-ylazo)-4-hydroxy-2-sulfonaphth-7-ylamino{]-1,3,5-triazin-2-ylamino[}-propane sodium salt 422-610-1 — Xi; R41 Xi R: 41 S: (2-)22-26-39 613-300-00-7 1-imidazol-1-yl-octadecan-2-ol 434-120-3 - R43 S: (2-)22-26-39 613-300-00-7 1-imidazol-1-yl-octadecan-2-ol 434-120-3 — R43 R53 Xi R: 43-53 S: (2-)24-37-61 613-301-00-2 dimethyl-1-{][}2-methoxy-5-(2-methyl-butoxycarbonyl)phenylcarbamoyl]-[2-octadecyl-1,1-dioxo-1,2,4-benzothiadiazin-3-yl{]methyl[} imidazole-4,5-dicarboxylate 443-910-7 - R53 R: 53 S: (2-)24-37-61 613-301-00-2 dimethyl-1-{][}2-methoxy-5-(2-methyl-butoxycarbonyl)phenylcarbamoyl]-[2-octadecyl-1,1-dioxo-1,2,4-benzothiadiazin-3-yl{]methyl[} imidazole-4,5-dicarboxylate 443-910-7 — R53 R: 53 S: 61 613-302-00-8 disodium 2-(5-carbamoyl-1-ethyl-2-hydroxy-4-methyl-6-oxo-1,6-dihydro-pyridine-3-ylazo)-4-(4-fluoro-6-(4-(2-sulfonyloxy-ethylsulfonyl)-phenylamino)-1,3,5-triazine-2-ylamino)benzene sulfonate 432-980-4 243858-60-8 Xi; R41 Xi R: 41 S: (2-)22-26-39 613-303-00-3 2-(1-methyl-2-(4-phenoxyphenoxy)ethoxy)pyridine 429-800-1 95737-68-1 N; R50-53 N R: 50/53 S: 60-61 613-304-00-9 5,6-dihydroxy-2,3-dihydro-1H-indolium bromide 421-170-6 138937-28-7 Xn; R22 Xi; R41 Xn R: 22-41 S: (2-)22-26-39 613-305-00-4 2-(2-hydroxy-4-octyloxyphenyl)-2H-benzotriazole 448-630-9 3147-77-1 R53 R: 53 S: 61 613-306-00-X (2,5-dioxopyrrolidin-1-yl)-9H-fluoren-9-ylmethyl carbonate 433-520-5 82911-69-1 Xn; R22 R43 N; R51-53 Xn; N R: 22-43-51/53 S: (2-)24-37-61 613-307-00-5 clothianidin (ISO); 3-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-methyl-1-nitroguanidine - 210880-92-5 Xn; R22 3-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-methyl-1-nitroguanidine — 210880-92-5 Xn; R22 N; R50-53 Xn; N R: 22-50/53 S: (2-)46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-308-00-0 2-amino-5-methylthiazole 423-800-5 7305-71-7 Xn; R22-48/22 S: (2-)46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 613-308-00-0 2-amino-5-methylthiazole 423-800-5 7305-71-7 Xn; R22-48/22 N; R50-53 Xn; N R: 22-48/22-50/53 S: (2-)22-36-60-61 613-309-00-6 1-methyl-3-phenyl-1-piperazine 431-180-2 5271-27-2 Xn; R21/22 Xi; R38-41 R52-53 Xn R: 21/22-38-41-52/53 S: (2-)26-36/37/39-61 613-310-00-1 (–)(3S, 4R)-4-(4-fluorophenyl)-3-(3,4-methylenedioxy-phenoxymethyl)-N-benzylpiperidine hydrochloride 432-360-3 105813-13-6 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)22-24-37-60-61 613-311-00-7 methyl-5-nitrophenyl-guanidine 435-500-1 152460-07-6 Xn; R22 Xi; R36 R43 R52-53 Xn R: 22-36-43-52/53 S: (2-)22-24-26-37-61 613-312-00-2 2-(4-methyl-2-phenyl-1-piperazinyl)benzenemethanol monohydrochloride 420-200-5 - Xn; R22 S: (2-)22-24-26-37-61 613-312-00-2 2-(4-methyl-2-phenyl-1-piperazinyl)benzenemethanol monohydrochloride 420-200-5 — Xn; R22 Xi; R41 R43 R52-53 Xn R: 22-41-43-52/53 S: (2-)22-26-36/37/39-61 613-313-00-8 2-(4-(4-(3-pyridinyl)-1H-imidazol-1-yl)butyl)-1H-isoindole-1,3(2H)-dione 442-780-9 173838-67-0 R52-53 R: 52/53 S: 61 613-314-00-3 4-decyloxazolidin-2-one; 4-decyl-1,3-oxazolidin-2-one 443-770-7 7693-82-5 N; R50-53 N R: 50/53 S: 22-24-60-61 613-315-00-9 tetrapotassium 4-[5-[3-carboxylato-4,5-dihydro-5-oxo-1-(4-sulfonatophenyl)pyrazol-4-ylidene]-3-(piperidinocarbonyl)penta-1,3-dienylidene]-5-hydroxy-1-(4-sulfonatophenyl)pyrazole-3-carboxylate 430-390-1 - Xn; R20 S: 22-24-60-61 613-315-00-9 tetrapotassium 4-[5-[3-carboxylato-4,5-dihydro-5-oxo-1-(4-sulfonatophenyl)pyrazol-4-ylidene]-3-(piperidinocarbonyl)penta-1,3-dienylidene]-5-hydroxy-1-(4-sulfonatophenyl)pyrazole-3-carboxylate 430-390-1 — Xn; R20 R52-53 Xn R: 20-52/53 S: (2-)25-61 613-316-00-4 trimethylopropane tri(3-aziridinylpropanoate); (TAZ) 257-765-0 52234-82-9 Muta. Cat. 3; R68 Xi; R41 R43 Xn R: 41-43-68 S: 26-36/37/39-42 H 614-001-00-4 nicotine (ISO); 613-317-00-X penconazole (ISO); 1-[2-(2,4-dichlorophenyl)pentyl]-1H-1,2,4-triazole 266-275-6 66246-88-6 Repr. Cat. 3; R63 Xn; R22 N; R50-53 Xn; N R: 22-50/53-63 S: (2-) 36/37-46-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 613-318-00-5 fenpyrazamine (ISO); S-allyl 5-amino-2-isopropyl-4-(2-methylphenyl)-3-oxo-2,3-dihydro-1H-pyrazole-1-carbothioate — 473798-59-3 N; R51-53 N R: 51/53 S: 60-61 614-001-00-4 nicotine (ISO); 3-(N-methyl-2-pyrrolidinyl)pyridine 200-193-3 54-11-5 T+; R27 T; R25 N; R51-53 T+; N … 128 unchanged lines … Xi; R36/37/38 R42/43 Xn R: 20-36/37/38-40-42/43-48/20 S: (1/2-)23-36/37-45 Xi; R36/37/38: C ≥ 5 % R42: C ≥ 0,1 % C2 S: (1/2-)23-36/37-45 Xi; R36/37/38: C ≥ 5 % R42: C ≥ 0,1 % C2 615-006-00-4 2-methyl-m-phenylene diisocyanate; toluene-2,4-di-isocyanate; [1] 4-methyl-m-phenylene diisocyanate; toluene-2,6-di-isocyanate; [2] m-tolylidene diisocyanate; toluene-diisocyanate [3] 202-039-0 [1] 209-544-5 [2] 247-722-4 [3] 91-08-7 [1] 584-84-9 [2] 26471-62-5 [3] Carc. Cat. 3; R40 T+; R26 Xi; R36/37/38 R42/43 R52-53 T+ R: 26-36/37/38-40-42/43-52/53 S: (1/2-)23-36/37-45-61 R42: C ≥ 0,1 % C2 S: (1/2-)23-36/37-45-61 R42: C ≥ 0,1 % C2 615-007-00-X 1,5-naphthylene diisocyanate 221-641-4 3173-72-6 Xn; R20 Xi; R36/37/38 R42 R52-53 Xn R: 20-36/37/38-42-52/53 S: (2-)26-28-38-45-61 615-008-00-5 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate; isophorone di-isocyanate 223-861-6 4098-71-9 T; R23 Xi; R36/37/38 R42/43 N; R51-53 T; N R: 23-36/37/38-42/43-51/53 S: (1/2-)26-28-38-45-61 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 S: (1/2-)26-28-38-45-61 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 615-009-00-0 4,4'-methylenedi(cyclohexyl isocyanate); dicyclohexylmethane-4,4'-di-isocyanate 225-863-2 5124-30-1 T; R23 Xi; R36/37/38 R42/43 T R: 23-36/37/38-42/43 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 615-010-00-6 2,2,4-trimethylhexamethylene-1,6-di-isocyanate; [1] 2,4,4-trimethylhexamethylene-1,6-di-isocyanate [2] 241-001-8 [1] 239-714-4 [2] 16938-22-0 [1] 15646-96-5 [2] T; R23 Xi; R36/37/38 R42 T R: 23-36/37/38-42 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42: C ≥ 0,5 % C2 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42: C ≥ 0,5 % C2 615-011-00-1 hexamethylene-di-isocyanate 212-485-8 822-06-0 T; R23 Xi; R36/37/38 R42/43 T R: 23-36/37/38-42/43 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 S: (1/2-)26-28-38-45 T; R23: C ≥ 2 % Xn; R20: 0,5 % ≤ C < 2 % R42/43: C ≥ 0,5 % 2 615-012-00-7 4-isocyanatosulphonyltoluene; tosyl isocyanate 223-810-8 4083-64-1 R14 Xi; R36/37/38 R42 Xn R: 14-36/37/38-42 S: (2-)26-28-30 Xi; R36/37/38: C ≥ 5 % 615-013-00-2 cyanamide; S: (2-)26-28-30 Xi; R36/37/38: C ≥ 5 % 615-013-00-2 cyanamide; carbanonitril 206-992-3 420-04-2 T; R25 Xn; R21 Xi; R36/38 … 85 unchanged lines … N; R50-53 Xn; N R: 20/21/22-32-50/53 S: (2-)13-36/37-46-60-61 A 615-033-00-1 reaction product of diphenylmethanediisocyanate, octylamine, oleylamine and cyclohexylamine (1:1.58:0.32:0097) 430-980-9 - R53 R: 53 615-033-00-1 reaction product of diphenylmethanediisocyanate, octylamine, oleylamine and cyclohexylamine (1:1.58:0.32:0097) 430-980-9 — R53 R: 53 S: 61 615-034-00-7 reaction product of diphenylmethanediisocyanate, octylamine, 4-ethoxyaniline and ethylenediamine (1:0,37:1,53:0,05) 430-750-8 - R53 R: 53 S: 61 615-035-00-2 reaction product of diphenylmethanediisocyanate, octylamine and oleylamine (molar ratio 1:1.86:0.14) 430-930-6 122886-55-9 R53 R: 53 S: 61 615-036-00-8 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 4:1:7:1:2) 430-940-0 - R53 R: 53 S: 61 615-037-00-3 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine and oleylamine (molar ratio 4:1:9:1) 430-950-5 - R53 R: 53 S: 61 615-038-00-9 reaction product of toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate) and aniline (molarratio 1:2) 430-960-1 - R53 R: 53 S: 61 615-039-00-4 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 3.88:1:6.38:0.47:2.91) 430-970-4 - R53 R: 53 S: 61 615-036-00-8 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 4:1:7:1:2) 430-940-0 - R53 R: 53 S: 61 615-037-00-3 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine and oleylamine (molar ratio 4:1:9:1) 430-950-5 — R53 R: 53 S: 61 615-038-00-9 reaction product of toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate) and aniline (molarratio 1:2) 430-960-1 — R53 R: 53 S: 61 615-039-00-4 reaction product of diphenylmethanediisocyanate, toluenediisocyanate (reaction mass of isomers: 65 % 2,4- and 35 % 2,6-diisocyanate), octylamine, oleylamine and 4-ethoxyaniline (molar ratio 3.88:1:6.38:0.47:2.91) 430-970-4 - R53 R: 53 S: 61 615-044-00-1 4-chlorophenylisocyanate 203-176-9 104-12-1 T+; R26 Xn; R22 Xi; R37/38-41 … 36 unchanged lines … R43 N; R50 Xn; N R: 20-36-43-50 S: (2-)24-37-61 N; R50: C ≥ 2,5 % 616-007-00-2 diphenamid (ISO); S: (2-)24-37-61 N; R50: C ≥ 2,5 % 616-007-00-2 diphenamid (ISO); N,N-dimethyl-2,2-diphenylacetamide 213-482-4 957-51-7 Xn; R22 R52-53 Xn R: 22-52/53 S: (2-)61 616-008-00-8 propachlor (ISO); 2-chloro-N-isopropylacetanilide; α-chloro-N-isopropylacetanilide 217-638-2 1918-16-7 Xn; R22 Xi; R36 R43 N; R50-53 Xn; N R: 22-36-43-50/53 S: (2-)24-37-60-61 616-009-00-3 propanil (ISO); 3', 4'-dichloropropionanilide 211-914-6 709-98-8 Xn; R22 N; R50 Xn; N R: 22-50 S: (2-)22-61 N; R50: C ≥ 2,5 % 616-010-00-9 tosylchloramide sodium 204-854-7 127-65-1 Xn; R22 S: (2-)22-61 N; R50: C ≥ 2,5 % 616-010-00-9 tosylchloramide sodium 204-854-7 127-65-1 Xn; R22 R31 C; R34 R42 C R: 22-31-34-42 S: (1/2-)7-22-26-36/37/39-45 616-011-00-4 N,N-dimethylacetamide 204-826-4 127-19-5 Repr. Cat. 2; R61 Xn; R20/21 T R: 61-20/21 S: 53-45 Repr. Cat. 2; R61: C ≥ 5 % E S: 53-45 Repr. Cat. 2; R61: C ≥ 5 % E 616-012-00-X N-(dichlorofluoromethylthio)phthalimide; N-(fluorodichloromethylthio)phthalimide 211-952-3 719-96-0 Xi; R38 Xi R: 38 S: (2-)28 616-013-00-5 butyraldehyde oxime 203-792-8 110-69-0 T; R24 Xn; R22 Xi; R36 T R: 22-24-36 S: (1/2-)23-36-45 616-014-00-0 2-butanone oxime; ethyl methyl ketoxime; ethyl methyl ketone oxime 202-496-6 96-29-7 Carc. Cat. 3; R40 Xn; R21 Xi; R41 R43 Xn R: 21-40-41-43 S: (2-)13-23-26-36/37/39 616-015-00-6 alachlor (ISO); 2-chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide 240-110-8 15972-60-8 Carc. Cat. 3; R40 Xn; R22 R43 N; R50-53 Xn; N R: 22-40-43-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,2,5 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-016-00-1 1-(3,4-dichlorophenylimino) thiosemicarbazide — 5836-73-7 T+; R28 T+ S: (2-)36/37-46-60-61 N; R50-53: C ≥ 0,2,5 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-016-00-1 1-(3,4-dichlorophenylimino) thiosemicarbazide — 5836-73-7 T+; R28 T+ R: 28 S: (1/2-)22-36/37-45 616-017-00-7 cartap hydrochloride 239-309-2 15263-52-2 Xn; R21/22 N; R50-53 Xn; N … 58 unchanged lines … S: (1/2-)36/37-60-61 616-034-00-X pyracarbolid (ISO); 3,4-dihydro-6-methyl-2H-pyran-5-carboxanilide 246-419-4 24691-76-7 R52-53 R: 52/53 S: 61 616-035-00-5 cymoxanil (ISO); 2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino)acetamide 261-043-0 57966-95-7 Xn; R22 2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino)acetamide 261-043-0 57966-95-7 Repr. Cat. 3; R62-63 Xn; R22-48/22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)36/37-60-61 616-036-00-0 2-chloracetamide 201-174-2 79-07-2 Repr. Cat. 3; R62 R: 22-43-48/22-62-63-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 25 % N; R51-53: 2,5 % ≤ C < 25 % R52-53: 0,25 % ≤ C < 2,5 % 616-036-00-0 2-chloracetamide 201-174-2 79-07-2 Repr. Cat. 3; R62 T; R25 R43 T R: 25-43-62 S: (1/2-)22-36/37-45 R43: C ≥ 0,1 % 616-037-00-6 acetochlor (ISO); S: (1/2-)22-36/37-45 R43: C ≥ 0,1 % 616-037-00-6 acetochlor (ISO); 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide 251-899-3 34256-82-1 Xn; R20 Xi; R37/38 R43 … 218 unchanged lines … S: (2-)46-60-61 616-113-00-9 desmedipham (ISO); ethyl 3-phenylcarbamoyloxyphenylcarbamate 237-198-5 13684-56-5 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-114-00-4 dodecanamide, N,N'-(9,9',10,10'-tetrahydro-9,9',10,10'-tetraoxo(1,1'-bianthracene)-4,4'-diyl)bis- 418-010-2 136897-58-0 R53 R: 53 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-114-00-4 dodecanamide, N,N'-(9,9',10,10'-tetrahydro-9,9',10,10'-tetraoxo(1,1'-bianthracene)-4,4'-diyl)bis- 418-010-2 136897-58-0 R53 R: 53 S: 22-61 616-115-00-X N-(3-acetyl-2-hydroxyphenyl)-4-(4-phenylbutoxy)benzamide 416-150-9 136450-06-1 R53 R: 53 S: 61 616-116-00-5 N-(4-dimethylaminopyridinium)-3-methoxy-4-(1-methyl-5-nitroindol-3-ylmethyl)-N-(o-tolylsulfonyl)benzamidate 416-790-9 143052-96-4 R53 R: 53 S: 61 616-117-00-0 N-[2-(3-acetyl-5-nitrothiophen-2-ylazo)-5-diethylaminophenyl]acetamide 416-860-9 777891-21-1 Repr. Cat. 3; R62 … 69 unchanged lines … (RS)-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)-p-toluamide - 156052-68-5 R43 N; R50-53 Xi; N R: 43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-142-00-7 1,3-Bis(vinylsulfonylacetamido)propane 428-350-3 93629-90-4 Muta. Cat. 3; R68 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-142-00-7 1,3-Bis(vinylsulfonylacetamido)propane 428-350-3 93629-90-4 Muta. Cat. 3; R68 Xi; R41 R43 R52-53 Xn R: 41-43-68-52/53 S: (2-)22-26-36/37/39-61 616-143-00-2 N,N'-dihexadecyl-N,N'-bis(2-hydroxyethyl)propanediamide 422-560-9 149591-38-8 Repr. Cat. 3; R62 Xi; R36 R53 Xn R: 36-62-53 S: (2-)26-36/37-61 616-144-00-8 3,4-dichloro-N-[5-chloro-4-[2-[4-dodecyloxyphenylsulfonyl]butyramido]-2-hydroxyphenyl]benzamide 431-130-1 - R53 R: 53 S: 61 616-145-00-3 pethoxamide (ISO); 2-chloro-N-(2-ethoxyethyl)-N-(2-methyl-1-phenylprop-1-enyl)acetamide - 106700-29-2 Xn; R22 R43 N; R50-53 Xn; N R: 22-43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0, 25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-146-00-9 N-(2-methoxy-5-octadecanoylaminophenyl)-2-(3-benzyl-2,5-dioxoimidazolidin-1-yl)-4,4-dimethyl-3-oxopentanoic acidamide 431-330-7 142776-95-2 R53 R: 53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 0, 25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-146-00-9 N-(2-methoxy-5-octadecanoylaminophenyl)-2-(3-benzyl-2,5-dioxoimidazolidin-1-yl)-4,4-dimethyl-3-oxopentanoic acidamide 431-330-7 142776-95-2 R53 R: 53 S: 22-61 616-147-00-4 1-methyl-4-(2-methyl-2H-tetrazol-5-yl)-1H-pyrazole-5-sulfonamide 424-160-1 139481-22-4 Xn; R22 R52-53 Xn R: 22-52/53 … 40 unchanged lines … Xn; R20 N; R50-53 Xn; N R: 20-40-63-50/53 S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-165-00-2 beflubutamid (ISO); S: (2-)36/37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-165-00-2 beflubutamid (ISO); (RS)-N-benzyl-2-(α, α, α, 4-tetrafluoro-m-tolyoxy)butyramide - 113614-08-7 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-166-00-8 cyazofamid (ISO); S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 % ≤ C < 0,025 % 616-166-00-8 cyazofamid (ISO); 4-chloro-2-cyano-N,N-dimethyl-5-p-tolylimidazole-1-sulfonamide - 120116-88-3 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-167-00-3 N,N-dibutyl-(2,5-dihydro-5-thioxo-1H-tetrazol-1-yl)acetamide 418-290-6 168612-06-4 Xi; R36 S: 60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-167-00-3 N,N-dibutyl-(2,5-dihydro-5-thioxo-1H-tetrazol-1-yl)acetamide 418-290-6 168612-06-4 Xi; R36 R43 Xi R: 36-43 S: (2-)24-26-37 616-168-00-9 1-dimethylcarbamoyl-4-(2-sulfonatoethyl)pyridinium 418-440-0 136997-71-2 R43 Xi … 82 unchanged lines … R33 N; R50-53 N R: 33-64-50/53 S: (2-)22-36/37-46-60-61 N; R50-53 C ≥ 0,0025 % N; R51-53 0,00025 % ≤ C < 0,0025 % R52-53 0,000025 % ≤ C < 0,00025 % 616-207-00-X polyhexamethylene biguanide hydrochloride 27083-27-8 or 32289-58-0 Carc. Cat 3; R40 S: (2-)22-36/37-46-60-61 N; R50-53 C ≥ 0,0025 % N; R51-53 0,00025 % ≤ C < 0,0025 % R52-53 0,000025 % ≤ C < 0,00025 % 616-207-00-X polyhexamethylene biguanide hydrochloride 27083-27-8 or 32289-58-0 Carc. Cat 3; R40 Xn; R22 T; R48/23 Xi; R41 R43 N; R50-53 T; N R: 22-40-41-43-48/23-50/53 S: (1/2-)22-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-208-00-5 N-ethyl-2-pyrrolidone; S: (1/2-)22-36/37/39-45-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-208-00-5 N-ethyl-2-pyrrolidone; 1-ethylpyrrolidin-2-one 220-250-6 2687-91-4 Repr. Cat. 2; R61 T R: 61 S: 45-53 616-209-00-0 amidosulfuron (ISO); 3-(4,6-dimethoxypyrimidin-2-yl)-1-((N-methyl-N-methylsulfonylamino)sulfonyl)urea 407-380-0 120923-37-7 N; R50-53 N R: 50/53 S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 %≤ C < 0,025 % 616-210-00-6 tebufenpyrad (ISO); S: 60-61 N; R50-53: C ≥ 0,25 % N; R51-53: 0,025 % ≤ C < 0,25 % R52-53: 0,0025 %≤ C < 0,025 % 616-210-00-6 tebufenpyrad (ISO); N-(4-tertbutylbenzyl)-4-chloro-3-ethyl-1-methyl-1Hpyrazole-5- carboxamide 119168-77-3 Xn; R20/22 R43 N; R50-53 Xn; N R: 20/22-43-50/53 S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-211-00-1 proquinazid (ISO); S: (2-)24-37-46-60-61 N; R50-53: C ≥ 2,5 % N; R51-53: 0,25 % ≤ C < 2,5 % R52-53: 0,025 % ≤ C < 0,25 % 616-211-00-1 proquinazid (ISO); 6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one 189278-12-4 Carc. Cat. 3; R40 N; R50-53 Xn; N R: 40-50/53 S: (2-)36/37-46-60-61 617-001-00-2 di-tert-butyl peroxide 203-733-6 110-05-4 O; R7 S: (2-)36/37-46-60-61 616-212-00-7 3-iodo-2-propynyl butylcarbamate; 3-iodoprop-2-yn-1-yl butylcarbamate 259-627-5 55406-53-6 T; R23-48/23 Xn; R22 Xi; R41 R43 N; R50 T; N R: 22-23-41-43-48/23-50 S: (1/2-)24-26-37/39-45-63 N; R50: C ≥ 2,5 % 617-001-00-2 di-tert-butyl peroxide 203-733-6 110-05-4 O; R7 F; R11 Muta. Cat. 3, R68 O; F; Xn R: 7-11-68 S: (2-)3/7-14-16-23-36/37/39 617-002-00-8 α,α-dimethylbenzyl hydroperoxide; cumene hydroperoxide 201-254-7 80-15-9 O; R7 T; R23 Xn; R21/22-48/20/22 C; R34 N; R51-53 O; T; N R: 7-21/22-23-34-48/20/22-51/53 S: (1/2-)3/7-14-36/37/39-45-50-61 C; R34: C ≥ 10 % Xi; R37/38-41: 3 % ≤ C < 10 % Xi; R36/37: 1 % ≤ C < 3 % 617-003-00-3 dilauroyl peroxide 203-326-3 105-74-8 O; R7 O S: (1/2-)3/7-14-36/37/39-45-50-61 C; R34: C ≥ 10 % Xi; R37/38-41: 3 % ≤ C < 10 % Xi; R36/37: 1 % ≤ C < 3 % 617-003-00-3 dilauroyl peroxide 203-326-3 105-74-8 O; R7 O R: 7 S: (2-)3/7-14-36/37/39 617-004-00-9 1,2,3,4-tetrahydro-1-naphthyl hydroperoxide 212-230-0 771-29-9 O; R7 Xn; R22 C; R34 N; R50-53 O; C; N R: 7-22-34-50/53 S: (1/2-)3/7-14-26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 617-006-00-X bis(α,α-dimethylbenzyl) peroxide 201-279-3 80-43-3 O; R7 S: (1/2-)3/7-14-26-36/37/39-45-60-61 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 617-006-00-X bis(α,α-dimethylbenzyl) peroxide 201-279-3 80-43-3 O; R7 Xi; R36/38 N; R51-53 O; Xi; N R: 7-36/38-51/53 … 21 unchanged lines … C; R34 Xn; R22 E; C R: 3-7-22-34 S: (1/2-)3/7-14-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % C S: (1/2-)3/7-14-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % C 617-012-00-2 8-p-menthyl hydroperoxide; p-menthane hydroperoxide 201-281-4 80-47-7 O; R7 C; R34 Xn; R20 O; C R: 7-20-34 S: (1/2-)3/7-14-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 617-013-00-8 O,O-tert-butyl O-docosyl monoperoxyoxalate 404-300-6 116753-76-5 O; R7 S: (1/2-)3/7-14-36/37/39-45 C; R34: C ≥ 10 % Xi; R36/37/38: 5 % ≤ C < 10 % 617-013-00-8 O,O-tert-butyl O-docosyl monoperoxyoxalate 404-300-6 116753-76-5 O; R7 N; R50-53 O; N R: 7-50/53 S: (2-)7-14-36/37/39-47-60-61 617-014-00-3 6-(nonylamino)-6-oxo-peroxyhexanoic acid 406-680-9 104788-63-8 O; R7 … 16 unchanged lines … R53 E R: 2-7-53 S: (2-)3/7-14-36/37/39-61 T 617-018-00-5 reaction mass of: 1-methyl-1-(3-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 63 % by weight; 1-methyl-1-(4-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 31 % by weight 410-840-3 71566-50-2 O; R7 617-018-00-5 reaction mass of: 1-methyl-1-(3-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 63 % by weight; 1-methyl-1-(4-(1-methylethyl)phenyl)ethyl-1-methyl-1-phenylethylperoxide, 31 % by weight 410-840-3 71566-50-2 O; R7 N; R51-53 O; N R: 7-51/53 S: (2-)3/7-14-36/37/39-61 617-019-00-0 6-(phthalimido)peroxyhexanoic acid 410-850-8 128275-31-0 O; R7 … 64 unchanged lines … R: 42 S: (2-)23-45 648-001-00-0 Distillates (coal tar), benzole fraction; Light Oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists of hydrocarbons having carbon numbers primarily in the range of C4 to C10 and distilling in the approximate range of 80 oC to 160 oC (175 oF to 320 oF).] 283-482-7 84650-02-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists of hydrocarbons having carbon numbers primarily in the range of C4 to C10 and distilling in the approximate range of 80 oC to 160 oC (175 oF to 320 oF).] 283-482-7 84650-02-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 648-002-00-6 Tar oils, brown-coal; Light Oil; [The distillate from lignite tar boiling in the range of approximately 80 °C to 250 °C (176 °F to 482 °F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.] 302-674-4 94114-40-6 Carc. Cat. 2; R45 [The distillate from lignite tar boiling in the range of approximately 80 °C to 250 °C (176 °F to 482 °F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.] 302-674-4 94114-40-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-003-00-1 Benzol forerunnings (coal); Light Oil Redistillate, low boiling; [The distillate from coke oven light oil having an approximate distillation range below 100 °C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.] 266-023-5 65996-88-5 Carc. Cat. 2; R45 [The distillate from coke oven light oil having an approximate distillation range below 100 °C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.] 266-023-5 65996-88-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-004-00-7 Distillates (coal tar), benzole fraction, BTX-rich; Light Oil Redistillate, low boiling; [A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).] 309-984-9 101896-26-8 Carc. Cat. 2; R45 [A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).] 309-984-9 101896-26-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J … 30 unchanged lines … S: 53-45 H J 648-012-00-0 Aromatic hydrocarbons, C8-9, hydrocarbon resin polymn. by-product; Light Oil Redistillate, high boiling; [A complex combination of hydrocarbons obtained from the evaporation of solvent under vacuum from polymerized hydrocarbon resin. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C9 and boiling in the range of approximately 120 °C to 215 °C (248 °F to 419 °F).] 295-281-1 91995-20-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the evaporation of solvent under vacuum from polymerized hydrocarbon resin. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C9 and boiling in the range of approximately 120 °C to 215 °C (248 °F to 419 °F).] 295-281-1 91995-20-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-013-00-6 Aromatic hydrocarbons, C9-12, benzene distn.; Light Oil Redistillate, high boiling 295-551-9 92062-36-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-014-00-1 Extract residues (coal), benzole fraction alk., acid ext.; Light Oil Extract Residues, low boiling; [The redistillate from the distillate, freed of tar acids and tar bases, from bituminous coal high temperature tar boiling in the approximate range of 90 °C to 160 °C (194 °F to 320 °F). It consists predominantly of benzene, toluene and xylenes.] 295-323-9 91995-61-8 Carc. Cat. 2; R45 [The redistillate from the distillate, freed of tar acids and tar bases, from bituminous coal high temperature tar boiling in the approximate range of 90 °C to 160 °C (194 °F to 320 °F). It consists predominantly of benzene, toluene and xylenes.] 295-323-9 91995-61-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-015-00-7 Extract residues (coal tar), benzole fraction alk., acid ext.; Light Oil Extract Residues, low boiling; [A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195 °C (185 °F to 383 °F).] 309-868-8 101316-63-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195 °C (185 °F to 383 °F).] 309-868-8 101316-63-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-016-00-2 Extract residues (coal), benzole fraction acid; Light Oil Extract Residues, low boiling; [An acid sludge by-product of the sulfuric acid refining of crude high temperature coal. Composed primarily of sulfuric acid and organic compounds.] 298-725-2 93821-38-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-017-00-8 Extract residues (coal), light oil alk., distn. overheads; Light Oil Extract Residues, low boiling; [The first fraction from the distillation of aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oil boiling substantially below 145 °C (293 °F). Composed primarily of C7 and C8 aliphatic and aromatic hydrocarbons.] 292-625-2 90641-02-4 Carc. Cat. 2; R45 [The first fraction from the distillation of aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oil boiling substantially below 145 °C (293 °F). Composed primarily of C7 and C8 aliphatic and aromatic hydrocarbons.] 292-625-2 90641-02-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-018-00-3 Extract residues (coal), light oil alk., acid ext., indene fraction; Light Oil Extract Residues, intermediate boiling 309-867-2 101316-62-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-019-00-9 Extract residues (coal), light oil alk., indene naphtha fraction; Light Oil Extract Residues, high boiling; [The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155 °C to 180 °C (311 °F to 356 °F). Composed primarily of indene, indan and trimethylbenzenes.] 292-626-8 90641-03-5 Carc. Cat. 2; R45 [The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155 °C to 180 °C (311 °F to 356 °F). Composed primarily of indene, indan and trimethylbenzenes.] 292-626-8 90641-03-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-020-00-4 Solvent naphtha (coal); Light Oil Extract Residues, high boiling; [The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130 °C to 210 °C (266 °F to 410 °F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.] 266-013-0 65996-79-4 Carc. Cat. 2; R45 [The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130 °C to 210 °C (266 °F to 410 °F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.] 266-013-0 65996-79-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-021-00-X Distillates (coal tar), light oils, neutral fraction; Light Oil Extract Residues, high boiling; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F). May also include unsaturated hydrocarbons such as indene and coumarone.] 309-971-8 101794-90-5 Carc. Cat. 2; R45 [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F). May also include unsaturated hydrocarbons such as indene and coumarone.] 309-971-8 101794-90-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-022-00-5 Distillates (coal tar), light oils, acid exts.; Light Oil Extract Residues, high boiling; [This oil is a complex reaction mass of aromatic hydrocarbons, primarily indene, naphthalene, coumarone, phenol, and o-, m- and p-cresol and boiling in the range of 140 °C to 215 °C (284 °F to 419 °F).] 292-609-5 90640-87-2 Carc. Cat. 2; R45 [This oil is a complex reaction mass of aromatic hydrocarbons, primarily indene, naphthalene, coumarone, phenol, and o-, m- and p-cresol and boiling in the range of 140 °C to 215 °C (284 °F to 419 °F).] 292-609-5 90640-87-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-023-00-0 Distillates (coal tar), light oils; Carbolic Oil; [A complex combination of hydrocarbons obtained by distillation of coal tar. It consists of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills at the approximate range of 150 °C to 210 °C (302 °F to 410 °F).] 283-483-2 84650-03-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of coal tar. It consists of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills at the approximate range of 150 °C to 210 °C (302 °F to 410 °F).] 283-483-2 84650-03-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-024-00-6 Tar oils, coal; Carbolic Oil; [The distillate from high temperature coal tar having an approximate distillation range of 130 °C to 250 °C (266 °F to 410 °F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.] 266-016-7 65996-82-9 Carc. Cat. 2; R45 [The distillate from high temperature coal tar having an approximate distillation range of 130 °C to 250 °C (266 °F to 410 °F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.] 266-016-7 65996-82-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J … 17 unchanged lines … S: 53-45 H J 648-029-00-3 Pyridine, alkyl derivs.; Crude Tar Bases; [The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150 °C (302 °F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.] 269-929-9 68391-11-7 Carc. Cat. 2; R45 [The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150 °C (302 °F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.] 269-929-9 68391-11-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-030-00-9 Tar bases, coal, picoline fraction; Distillate Bases; [Pyridine bases boiling in the range of approximately 125 °C to 160 °C (257 °F 320 °F) obtained by distillation of neutralized acid extract of the base-containing tar fraction obtained by the distillation of bituminous coal tars. Composed chiefly of lutidines and picolines.] 295-548-2 92062-33-4 Carc. Cat. 2; R45 [Pyridine bases boiling in the range of approximately 125 °C to 160 °C (257 °F 320 °F) obtained by distillation of neutralized acid extract of the base-containing tar fraction obtained by the distillation of bituminous coal tars. Composed chiefly of lutidines and picolines.] 295-548-2 92062-33-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-031-00-4 Tar bases, coal, lutidine fraction; Distillate Bases 293-766-2 91082-52-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-032-00-X Extract oils (coal), tar base, collidine fraction; Distillate Bases; [The extract produced by the acidic extraction of bases from crude coal tar aromatic oils, neutralization, and distillation of the bases. Composed primarily of collidines, aniline, toluidines, lutidines, xylidines.] 273-077-3 68937-63-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-033-00-5 Tar bases, coal, collidine fraction; Distillate Bases; [The distillation fraction boiling in the range of approximately 181 °C to 186 °C (356 °F to 367 °F) from the crude bases obtained from the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of bituminous coal tar. It contains chiefly aniline and collidines.] 295-543-5 92062-28-7 Carc. Cat. 2; R45 [The distillation fraction boiling in the range of approximately 181 °C to 186 °C (356 °F to 367 °F) from the crude bases obtained from the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of bituminous coal tar. It contains chiefly aniline and collidines.] 295-543-5 92062-28-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-034-00-0 Tar bases, coal, aniline fraction; Distillate Bases; [The distillation fraction boiling in the range of approximately 180 °C to 200 °C (356 °F to 392 °F) from the crude bases obtained by dephenolating and debasing the carbolated oil from the distillation of coal tar. It contains chiefly aniline, collidines, lutidines and toluidines.] 295-541-4 92062-27-6 Carc. Cat. 2; R45 [The distillation fraction boiling in the range of approximately 180 °C to 200 °C (356 °F to 392 °F) from the crude bases obtained by dephenolating and debasing the carbolated oil from the distillation of coal tar. It contains chiefly aniline, collidines, lutidines and toluidines.] 295-541-4 92062-27-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-035-00-6 Tar bases, coal, toluidine fraction; Distillate Bases 293-767-8 91082-53-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-036-00-1 Distillates (petroleum), alkene-alkyne manuf. pyrolysis oil, mixed with high-temp. coal tar, indene fraction; Redistillates; [A complex combination of hydrocarbons obtained as a redistillate from the fractional distillation of bituminous coal high temperature tar and residual oils that are obtained by the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of indene and boils in a range of approximately 160 °C to 190 °C (320 °F to 374 °F).] 295-292-1 91995-31-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as a redistillate from the fractional distillation of bituminous coal high temperature tar and residual oils that are obtained by the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of indene and boils in a range of approximately 160 °C to 190 °C (320 °F to 374 °F).] 295-292-1 91995-31-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-037-00-7 Distillates (coal), coal tar-residual pyrolysis oils, naphthalene oils; Redistillates; [The redistillate obtained from the fractional distillation of bituminous coal high temperature tar and pyrolysis residual oils and boiling in the range of approximately 190 °C to 270 °C (374 °F to 518 °F). Composed primarily of substituted dinuclear aromatics.] 295-295-8 91995-35-6 Carc. Cat. 2; R45 [The redistillate obtained from the fractional distillation of bituminous coal high temperature tar and pyrolysis residual oils and boiling in the range of approximately 190 °C to 270 °C (374 °F to 518 °F). Composed primarily of substituted dinuclear aromatics.] 295-295-8 91995-35-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-038-00-2 Extract oils (coal), coal tar-residual pyrolysis oils, naphthalene oil, redistillate; Redistillates; [The redistillate from the fractional distillation of dephenolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220 °C to 230 °C (428 °F to 446 °F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.] 295-329-1 91995-66-3 Carc. Cat. 2; R45 [The redistillate from the fractional distillation of dephenolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220 °C to 230 °C (428 °F to 446 °F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.] 295-329-1 91995-66-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-039-00-8 Extract oils (coal), coal tar-residual pyrolysis oils, naphthalene oils; Redistillates; [A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225 °C to 255 °C (437 °F to 491 °F). Composed primarily of substituted dinuclear aromatic hydrocarbons.] 310-170-0 122070-79-5 Carc. Cat. 2; R45 [A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225 °C to 255 °C (437 °F to 491 °F). Composed primarily of substituted dinuclear aromatic hydrocarbons.] 310-170-0 122070-79-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-040-00-3 Extract oils (coal), coal tar residual pyrolysis oils, naphthalene oil, distn. residues; Redistillates; [Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 °C to 260 °C (464 °F to 500 °F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.] 310-171-6 122070-80-8 Carc. Cat. 2; R45 [Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 °C to 260 °C (464 °F to 500 °F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.] 310-171-6 122070-80-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-041-00-9 Absorption oils, bicyclo arom. and heterocyclic hydrocarbon fraction; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260 oC to 290 oC (500 oF to 554 oF).] 309-851-5 101316-45-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a redistillate from the distillation of wash oil. It consists predominantly of 2-ringed aromatic and heterocyclic hydrocarbons boiling in the range of approximately 260 oC to 290 oC (500 oF to 554 oF).] 309-851-5 101316-45-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-042-00-4 Distillates (coal tar), upper, fluorene-rich; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists af aromatic and polycyclic hydrocarbons primarily fluorene and some acenaphthene.] 284-900-0 84989-11-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-043-00-X Creosote oil, acenaphthene fraction, acenaphthene-free; Wash Oil Redistillate; [The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.] 292-606-9 90640-85-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-044-00-5 Distillates (coal tar), heavy oils; Heavy Anthracene Oil; [Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240 oC to 400 oC (464 oF to 752 oF). Composed primarily of tri- and polynuclear hydrocarbons and heterocyclic compounds.] 292-607-4 90640-86-1 Carc. Cat. 2; R45 T [Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240 oC to 400 oC (464 oF to 752 oF). Composed primarily of tri- and polynuclear hydrocarbons and heterocyclic compounds.] 292-607-4 90640-86-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 648-045-00-0 Distillates (coal tar), upper; Heavy Anthracene Oil; [The distillate from coal tar having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.] 266-026-1 65996-91-0 Carc. Cat. 2; R45 T [The distillate from coal tar having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.] 266-026-1 65996-91-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-046-00-6 Anthracene oil, acid ext.; Anthracene Oil Extract Residue; [A complex combination of hydrocarbons from the base-freed fraction obtained from the distillation of coal tar and boiling in the range of approximately 325 oC to 365 oC (617 oF to 689 oF). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.] 295-274-3 91995-14-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the base-freed fraction obtained from the distillation of coal tar and boiling in the range of approximately 325 oC to 365 oC (617 oF to 689 oF). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.] 295-274-3 91995-14-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-047-00-1 Distillates (coal tar); Heavy Anthracene Oil; [The distillate from coal tar having an approximate distillation range of 100 oC to 450 oC (212 oF to 842 oF). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.] 266-027-7 65996-92-1 Carc. Cat. 2; R45 T [The distillate from coal tar having an approximate distillation range of 100 oC to 450 oC (212 oF to 842 oF). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.] 266-027-7 65996-92-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-048-00-7 Distillates (coal tar), pitch, heavy oils; Heavy Anthracene Oil; [The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300 oC to 470 oC (572 oF to 878 oF). The product may also contain heteroatoms.] 295-312-9 91995-51-6 Carc. Cat. 2; R45 T [The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300 oC to 470 oC (572 oF to 878 oF). The product may also contain heteroatoms.] 295-312-9 91995-51-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-049-00-2 Distillates (coal tar), pitch; Heavy Anthracene Oil; [The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200 oC to greater than 400 oC (392 oF to greater than 752 oF).] 309-855-7 101316-49-8 Carc. Cat. 2; R45 T [The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200 oC to greater than 400 oC (392 oF to greater than 752 oF).] 309-855-7 101316-49-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-050-00-8 Distillates (coal tar), heavy oils, pyrene fraction; Heavy Anthracene Oil Redistillate; [The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350 oC to 400 oC (662 oF to 752 oF). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.] 295-304-5 91995-42-5 Carc. Cat. 2; R45 T [The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350 oC to 400 oC (662 oF to 752 oF). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.] 295-304-5 91995-42-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-051-00-3 Distillates (coal tar), pitch, pyrene fraction; Heavy Anthracene Oil Redistillate; [The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380 oC to 410 oC (7160 to 770 oF). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.] 295-313-4 91995-52-7 Carc. Cat. 2; R45 T [The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380 oC to 410 oC (7160 to 770 oF). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.] 295-313-4 91995-52-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-052-00-9 Paraffin waxes (coal), brown-coal high-temp. tar, carbon-treated; Coal Tar Extract; [A complet combination of hydrocarbons obtained by the treatment of lignite carbonization tar with activated carbon for removal of trace constituents and impurities. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-296-6 97926-76-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-053-00-4 Paraffin waxes (coal), brown-coal high-temp tar, clay-treated; Coal Tar Extract; [A complex combination of hydrocarbons obtained by the treatment of lignite carbonization tar with bentonite for removal of trace constituents and impurities. It consists predominantly of saturated straight and branched chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-297-1 97926-77-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-054-00-X Pitch; Pitch 263-072-4 61789-60-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-055-00-5 Pitch, coal tar, high-temp.; Pitch; [The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 266-028-2 65996-93-2 Carc. Cat. 2; R45 T [The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 266-028-2 65996-93-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 648-056-00-0 Pitch, coal tar, high-temp., heat-treated; Pitch; [The heat treated residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 80 oC to 180 oC (176 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 310-162-7 121575-60-8 Carc. Cat. 2; R45 T [The heat treated residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 80 oC to 180 oC (176 oF to 356 oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] 310-162-7 121575-60-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-057-00-6 Pitch, coal tar, high-temp., secondary; Pitch Redistillate; [The residue obtained during the distillation of high boiling fractions from bituminous coal high temperature tar and/or pitch coke oil, with a softening point of 140 oC to 170 oC (284 oF to 392 oF) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.] 302-650-3 94114-13-3 Carc. Cat. 2; R45 T [The residue obtained during the distillation of high boiling fractions from bituminous coal high temperature tar and/or pitch coke oil, with a softening point of 140 oC to 170 oC (284 oF to 392 oF) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.] 302-650-3 94114-13-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-058-00-1 Residues (coal tar), pitch distn.; Pitch Redistillate; [Residue from the fractional distillation of pitch distillate boiling in the range of approximately 400 oC to 470 oC (752 oF to 846 oF). Composed primarily of polynuclear aromatic hydrocarbons, and heterocyclic compounds.] 295-507-9 92061-94-4 Carc. Cat. 2; R45 T [Residue from the fractional distillation of pitch distillate boiling in the range of approximately 400 oC to 470 oC (752 oF to 846 oF). Composed primarily of polynuclear aromatic hydrocarbons, and heterocyclic compounds.] 295-507-9 92061-94-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-059-00-7 Tar, coal, high-temp., distn. and storage residues; Coal Tar Solids Residue; [Coke- and ash-containing solid residues that separate on distillation and thermal treatment of bituminous coal high temperature tar in distillation installations and storage vessels. Consists predominantly of carbon and contains a small quantity of hetero compounds as well as ash components.] 295-535-1 92062-20-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-060-00-2 Tar, coal, storage residues; Coal Tar Solids Residue; [The deposit removed from crude coal tar storages. Composed primarily of coal tar and carbonaceous particulate matter.] 293-764-1 91082-50-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-061-00-8 Tar, coal, high-temp., residues; Coal Tar Solids Residue; [Solids formed during the coking of bituminous coal to produce crude bituminous coal high temperature tar. Composed primarily of coke and coal particles, highly aromatized compounds and mineral substances.] 309-726-5 100684-51-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-062-00-3 Tar, coal, high-temp., high-solids; Coal Tar Solids Residue; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal-type materials.] 273-615-7 68990-61-4 Carc. Cat. 2; R45 T [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal-type materials.] 273-615-7 68990-61-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-063-00-9 Waste solids, coal-tar pitch coking; … 23 unchanged lines … S: 53-45 H M 648-068-00-6 Tar, coal, low-temp., distn. residues; Tar Oil, intermediate boiling; [Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300 oC (572 oF). Composed primarily of aromatic compounds.] 309-887-1 101316-85-2 Carc. Cat. 2; R45 T [Residues from fractional distillation of low temperature coal tar to remove oils that boil in a range up to approximately 300 oC (572 oF). Composed primarily of aromatic compounds.] 309-887-1 101316-85-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-069-00-1 Pitch, coal tar, low-temp; Pitch Residue; [A complex black solid or semi-solid obtained from the distillation of a low temperature coal tar. It has a softening point within the approximate range of 40 oC to 180 oC (104 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-651-4 90669-57-1 Carc. Cat. 2; R45 T [A complex black solid or semi-solid obtained from the distillation of a low temperature coal tar. It has a softening point within the approximate range of 40 oC to 180 oC (104 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-651-4 90669-57-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-070-00-7 Pitch, coal tar, low-temp., oxidized; Pitch Residue, oxidised; [The product obtained by air-blowing, at elevated temperature, low-temperature coal tar pitch. It has a softening-point within the approximate range of 70 oC to 180 oC (158 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-654-0 90669-59-3 Carc. Cat. 2; R45 T [The product obtained by air-blowing, at elevated temperature, low-temperature coal tar pitch. It has a softening-point within the approximate range of 70 oC to 180 oC (158 oF to 356 oF). Composed primarily of a complex mixture of hydrocarbons.] 292-654-0 90669-59-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-071-00-2 Pitch, coal tar, low-temp., heat-treated; Pitch Residue, oxidised; Pitch Residue, heat-treated; [A complex black solid obtained by the heat treatment of low temperature coal tar pitch. It has a softening point within the approximate range of 50 oC to 140 oC (122 oF to 284 oF). Composed primarily of a complex mixture of aromatic compounds.] 292-653-5 90669-58-2 Carc. Cat. 2; R45 T [A complex black solid obtained by the heat treatment of low temperature coal tar pitch. It has a softening point within the approximate range of 50 oC to 140 oC (122 oF to 284 oF). Composed primarily of a complex mixture of aromatic compounds.] 292-653-5 90669-58-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-072-00-8 Distillates (coal-petroleum), condensed-ring arom; Distillates; [The distillate from a mixture of coal and tar and aromatic petroleum streams having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.] 269-159-3 68188-48-7 Carc. Cat. 2; R45 T [The distillate from a mixture of coal and tar and aromatic petroleum streams having an approximate distillation range of 220 oC to 450 oC (428 oF to 842 oF). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.] 269-159-3 68188-48-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-073-00-3 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polyethylene-polypropylene pyrolysis-derived; Pyrolysis Products; [A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-956-6 101794-74-5 Carc. Cat. 2; R45 T [A complex combination hydrocarbons obtained from mixed coal tar pitch-polyethylene-polypropylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-956-6 101794-74-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-074-00-9 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polyethylene pyrolysis-derived; Pyrolysis Products; [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-957-1 101794-75-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-957-1 101794-75-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-075-00-4 Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polystyrene pyrolysis-derived; Pyrolysis Products; [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-958-7 101794-76-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from mixed coal tar pitch-polystyrene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C28 and having a softening point of 100 oC to 220 oC (212 oF to 428 oF) according to DIN 52025.] 309-958-7 101794-76-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-076-00-X Pitch, coal tar-petroleum; Pitch Residues; [The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40 oC to 180 oC (140 oF to 356 oF). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.] 269-109-0 68187-57-5 Carc. Cat. 2; R45 T [The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40 oC to 180 oC (140 oF to 356 oF). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.] 269-109-0 68187-57-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-077-00-5 Phenanthrene, distn. residues; Heavy Anthracene Oil Redistillate; [Residue from the distillation of crude phenanthrene boiling in the approximate range of 340 oC to 420 oC (644 oF to 788 oF). It consists predominantly of phenanthrene, anthracene and carbazole.] 310-169-5 122070-78-4 Carc. Cat. 2; R45 T [Residue from the distillation of crude phenanthrene boiling in the approximate range of 340 oC to 420 oC (644 oF to 788 oF). It consists predominantly of phenanthrene, anthracene and carbazole.] 310-169-5 122070-78-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-078-00-0 Distillates (coal tar), upper, fluorene-free; Wash Oil Redistillate; [A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists of aromatic polycyclic hydrocarbons, primarily diphenyl, dibenzofuran and acenaphthene.] 284-899-7 84989-10-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-079-00-6 Anthracene oil; Anthracene oil; [A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 oC ot 400 oC (572 oF to 752 oF). Composed primarily of phenanthrene, anthracene and carbazole.] 292-602-7 90640-80-5 Carc. Cat. 2; R45 T [A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 oC ot 400 oC (572 oF to 752 oF). Composed primarily of phenanthrene, anthracene and carbazole.] 292-602-7 90640-80-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-080-00-1 Residues (coal tar), creosote oil distn.; Wash Oil Redistillate; [The residue from the fractional distillation of wash oil boiling in the approximate range of 270 °C to 330 °C (518 °F to 626 °F). It consists predominantly of dinuclear aromatic and heterocyclic hydrocarbons.] 295-506-3 92061-93-3 Carc. Cat. 2; R45 T [The residue from the fractional distillation of wash oil boiling in the approximate range of 270 °C to 330 °C (518 °F to 626 °F). It consists predominantly of dinuclear aromatic and heterocyclic hydrocarbons.] 295-506-3 92061-93-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-081-00-7 Tar, coal; Coal tar; [The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydro-carbons, phenolic compounds, nitrogen bases and thiophene.] 232-361-7 8007-45-2 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 648-082-00-2 Tar, coal, high-temp.; Coal tar; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.] 266-024-0 65996-89-6 Carc. Cat. 1; R45 T [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.] 266-024-0 65996-89-6 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 648-083-00-8 Tar, coal, low-temp.; Coal oil; [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.] 266-025-6 65996-90-9 Carc. Cat. 1; R45 T [The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700 oC (1292 oF)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.] 266-025-6 65996-90-9 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 648-084-00-3 Distillates (coal), coke-oven light oil, naphthalene cut; Naphthalene Oil; [The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148 °C (298 °F).] 285-076-5 85029-51-2 Carc. Cat. 2; R45 [The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148 °C (298 °F).] 285-076-5 85029-51-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-085-00-9 Distillates (coal tar), naphthalene oils; Naphthalene Oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).] 283-484-8 84650-04-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).] 283-484-8 84650-04-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-086-00-4 Distillates (coal tar), naphthalene oils, naphthalene-low; Naphthalene Oil Redistillate; [A complex combination of hydrocarbons obtained by crystallization of naphthalene oil. Composed primarily of naphthalene, alkyl naphthalenes and phenolic compounds.] 284-898-1 84989-09-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-087-00-X Distillates (coal tar), naphthalene oil crystn. mother liquor; Naphthalene Oil Redistillate; [A complex combination of organic compounds obtained as a filtrate from the crystallization of the naphthalene fraction from coal tar and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Contains chiefly naphthalene, thionaphthene and alkylnaphthalenes.] 295-310-8 91995-49-2 Carc. Cat. 2; R45 [A complex combination of organic compounds obtained as a filtrate from the crystallization of the naphthalene fraction from coal tar and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Contains chiefly naphthalene, thionaphthene and alkylnaphthalenes.] 295-310-8 91995-49-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM … 17 unchanged lines … S: 53-45 HJM 648-091-00-1 Extract residues (coal), naphthalene oil alk., distn. overheads; Naphthalene Oil Extract Residue; [The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180 °C to 220 °C (356 °F to 428 °F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.] 292-627-3 90641-04-6 Carc. Cat. 2; R45 [The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180 °C to 220 °C (356 °F to 428 °F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.] 292-627-3 90641-04-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-092-00-7 Distillates (coal tar), naphthalene oils, methylnaphthalene fraction; Methylnaphthalene Oil; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437 °F to 491 °F).] 309-985-4 101896-27-9 Carc. Cat. 2; R45 [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437 °F to 491 °F).] 309-985-4 101896-27-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-093-00-2 Distillates (coal tar), naphthalene oils, indole-methylnaphthalene fraction; Methylnaphthalene Oil; [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).] 309-972-3 101794-91-6 Carc. Cat. 2; R45 [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).] 309-972-3 101794-91-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-094-00-8 Distillates (coal tar), naphthalene oils, acid exts.; Methylnaphthalene Oil Extract Residue; [A complex combination of hydrocarbons obtained by debasing the methylnaphthalene fraction obtained by the distillation of coal tar and boiling in the range of approximately 230 °C to 255 °C (446 °F to 491 °F). Contains chiefly 1(2)-methylnaphthalene, naphthalene, dimethylnaphthalene and biphenyl.] 295-309-2 91995-48-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by debasing the methylnaphthalene fraction obtained by the distillation of coal tar and boiling in the range of approximately 230 °C to 255 °C (446 °F to 491 °F). Contains chiefly 1(2)-methylnaphthalene, naphthalene, dimethylnaphthalene and biphenyl.] 295-309-2 91995-48-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-095-00-3 Extract residues (coal), naphthalene oil alk., distn. residues; Methylnaphthalene Oil Extract Residue; [The residue from the distillation of alkali-washed naphthalene oil having an approximate distillation range of 220 °C to 300 °C (428 °F to 572 °F). Composed primarily of naphthalene, alkylnaphthalenes and aromatic nitrogen bases.] 292-628-9 90641-05-7 Carc. Cat. 2; R45 [The residue from the distillation of alkali-washed naphthalene oil having an approximate distillation range of 220 °C to 300 °C (428 °F to 572 °F). Composed primarily of naphthalene, alkylnaphthalenes and aromatic nitrogen bases.] 292-628-9 90641-05-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-096-00-9 Extract oils (coal), acidic, tar-base free; Methylnaphthalene Oil Extract Residue; [The extract oil boiling in the range of approximately 220 °C to 265 °C (428 °F to 509 °F) from coal tar alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove tar bases. Composed primarily of alkylnaphthalenes.] 284-901-6 84989-12-8 Carc. Cat. 2; R45 [The extract oil boiling in the range of approximately 220 °C to 265 °C (428 °F to 509 °F) from coal tar alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove tar bases. Composed primarily of alkylnaphthalenes.] 284-901-6 84989-12-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-097-00-4 Distillates (coal tar), benzole fraction, distn. residues; Wash Oil; [A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150 °C to 300 °C (302 °F to 572 °F) or a semi-solid or solid with a melting point up to 70 °C (158 °F). It is composed primarily of naphthalene and alkyl naphthalenes.] 310-165-3 121620-46-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150 °C to 300 °C (302 °F to 572 °F) or a semi-solid or solid with a melting point up to 70 °C (158 °F). It is composed primarily of naphthalene and alkyl naphthalenes.] 310-165-3 121620-46-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-098-00-X Creosote oil, acenaphthene fraction; Wash Oil; [A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464 °F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] 292-605-3 90640-84-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464 °F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] 292-605-3 90640-84-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-099-00-5 Creosote oil; [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).] 263-047-8 61789-28-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).] 263-047-8 61789-28-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-100-00-9 Creosote oil, high-boiling distillate; Wash Oil; [The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41 °F).] 274-565-9 70321-79-8 Carc. Cat. 2; R45 T [The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41 °F).] 274-565-9 70321-79-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-101-00-4 Creosote; [The distillate of coal tar produced by the high temperature carbonization of bituminous coal. It consists primarily of aromatic hydrocarbons, tar acids and tar bases.] 232-287-5 8001-58-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 648-102-00-X Extract residues (coal), creosote oil acid; Wash Oil Extract Residue; [A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482 °F to 536 °F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.] 310-189-4 122384-77-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482 °F to 536 °F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.] 310-189-4 122384-77-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-103-00-5 Anthracene oil, anthracene paste; Anthracene Oil Fraction; [The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.] 292-603-2 90640-81-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-104-00-0 Anthracene oil, anthracene-low; Anthracene Oil Fraction; [The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.] 292-604-8 90640-82-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-105-00-6 Residues (coal tar), anthracene oil distn.; Anthracene Oil Fraction; [The residue from the fraction distillation of crude anthracene boiling in the approximate range of 340 °C to 400 °C (644 °F to 752 °F). It consists predominantly of tri- and polynuclear aromatic and heterocyclic hydrocarbons.] 295-505-8 92061-92-2 Carc. Cat. 2; R45 [The residue from the fraction distillation of crude anthracene boiling in the approximate range of 340 °C to 400 °C (644 °F to 752 °F). It consists predominantly of tri- and polynuclear aromatic and heterocyclic hydrocarbons.] 295-505-8 92061-92-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-106-00-1 Anthracene oil, anthracene paste, anthracene fraction; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-275-9 91995-15-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-275-9 91995-15-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-107-00-7 Anthracene oil, anthracene paste, carbazole fraction; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-276-4 91995-16-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.] 295-276-4 91995-16-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-108-00-2 Anthracene oil, anthracene paste, distn. lights; Anthracene Oil Fraction; [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.] 295-278-5 91995-17-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.] 295-278-5 91995-17-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-109-00-8 Tar oils, coal, low-temp.; Tar Oil, high boiling; [A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160 °C to 340 °C (320 °F to 644 °F).] 309-889-2 101316-87-4 Carc. Cat. 2; R45 [A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160 °C to 340 °C (320 °F to 644 °F).] 309-889-2 101316-87-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-110-00-3 Extract residues (coal), low temp. coal atar alk.; [The residue from low temperature coal tar oils after an alkaline wash, such as aqueous sodium hydroxide, to remove crude coal tar acids. Composed primarily of hydrocarbons and aromatic nitrogen bases.] 310-191-5 122384-78-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-111-00-9 Phenols, ammonia liquor ext.; Alkaline Extract; [The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. It consists predominantly of a reaction mass of monohydric and dihydric phenols.] 284-881-9 84988-93-2 Carc. Cat. 2; R45 [The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. It consists predominantly of a reaction mass of monohydric and dihydric phenols.] 284-881-9 84988-93-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM … 41 unchanged lines … S: 53-45 HJM 648-119-00-2 Tar acids, distn. residues; Distillate Phenols; [A residue from the distillation of crude phenol from coal. It consists predominantly of phenols having carbon numbers in the range of C8 through C10 with a softening point of 60 °C to 80 °C (140 °F to 176 °F).] 306-251-5 96690-55-0 Carc. Cat. 2; R45 [A residue from the distillation of crude phenol from coal. It consists predominantly of phenols having carbon numbers in the range of C8 through C10 with a softening point of 60 °C to 80 °C (140 °F to 176 °F).] 306-251-5 96690-55-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-120-00-8 Tar acids, methylphenol fraction; Distillate Phenols; [The fraction of tar acid rich in 3- and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-892-9 84989-04-8 Carc. Cat. 2; R45 [The fraction of tar acid rich in 3- and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-892-9 84989-04-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-121-00-3 Tar acids, polyalkylphenol fraction; Distillate Phenols; [The fraction of tar acids, recovered by distillation of low-temperature coal tar crude tar acids, having an approximate boiling range of 225 °C to 320 °C (437 °F to 608 °F). Composed primarily of polyalkylphenols.] 284-893-4 84989-05-9 Carc. Cat. 2; R45 [The fraction of tar acids, recovered by distillation of low-temperature coal tar crude tar acids, having an approximate boiling range of 225 °C to 320 °C (437 °F to 608 °F). Composed primarily of polyalkylphenols.] 284-893-4 84989-05-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-122-00-9 Tar acids, xylenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-895-5 84989-06-0 Carc. Cat. 2; R45 [The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-895-5 84989-06-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-123-00-4 Tar acids, ethylphenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 3- and 4-ethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-891-3 84989-03-7 Carc. Cat. 2; R45 [The fraction of tar acids, rich in 3- and 4-ethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.] 284-891-3 84989-03-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-124-00-X Tar acids, 3,5-xylenol fraction; Distillate Phenols; [The fraction of tar acids, rich in 3,5-dimethylphenol, recovered by distillation of low-temperature coal tar acids.] 284-896-0 84989-07-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-125-00-5 Tar acids, residues, distillates, first-cut; Distillate Phenols; [The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.] 270-713-1 68477-23-6 Carc. Cat. 2; R45 [The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.] 270-713-1 68477-23-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-126-00-0 Tar acids, cresylic, residues; Distillate Phenols; [The residue from crude coal tar acids after removal of phenol, cresols, xylenols and any higher boiling phenols. A black solid with a melting point approximately 80 °C (176 °F). Composed primarily of polyalkylphenols, resin gums, and inorganic salts.] 271-418-0 68555-24-8 Carc. Cat. 2; R45 [The residue from crude coal tar acids after removal of phenol, cresols, xylenols and any higher boiling phenols. A black solid with a melting point approximately 80 °C (176 °F). Composed primarily of polyalkylphenols, resin gums, and inorganic salts.] 271-418-0 68555-24-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-127-00-6 Phenols, C9-11; Distillate Phenols 293-435-2 91079-47-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-128-00-1 Tar acids, cresylic; Distillate Phenols; [A complex combination of organic compounds obtained from brown coal and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). It contains chiefly phenols and pyridine bases.] 295-540-9 92062-26-5 Carc. Cat. 2; R45 [A complex combination of organic compounds obtained from brown coal and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). It contains chiefly phenols and pyridine bases.] 295-540-9 92062-26-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-129-00-7 Tar acids, brown-coal, C2-alkylphenol fraction; Distillate Phenols; [The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.] 302-662-9 94114-29-1 Carc. Cat. 2; R45 [The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.] 302-662-9 94114-29-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM … 21 unchanged lines … S: 53-45 HJM 648-134-00-4 Hydrocarbon oils, arom., mixed with polyethylene and polypropylene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of a polyethylene/polypropylene reaction mass with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).] 309-745-9 100801-63-6 Carc. Cat. 2; R45 [The oil obtained from the heat treatment of a polyethylene/polypropylene reaction mass with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).] 309-745-9 100801-63-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-135-00-X Hydrocarbon oils, arom., mixed with polyethylene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158 °F to 248 °F).] 309-748-5 100801-65-8 Carc. Cat. 2; R45 [The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158 °F to 248 °F).] 309-748-5 100801-65-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-136-00-5 Hydrocarbon oils, arom., mixed with polystyrene, pyrolyzed, light oil fraction; Heat Treatment Products; [The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410 °F).] 309-749-0 100801-66-9 Carc. Cat. 2; R45 [The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410 °F).] 309-749-0 100801-66-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-137-00-0 Extract residues (coal), tar oil alk., naphthalene distn. residues; Naphthalene Oil Extract Residue; [The residue obtained from chemical oil extracted after the removal of naphthalene by distillation composed primarily of two to four membered condensed ring aromatic hydrocarbons and aromatic nitrogen bases.] 277-567-8 73665-18-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 HJM 648-138-00-6 Creosote oil, low-boiling distillate; Wash Oil; [The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).] 274-566-4 70321-80-1 Carc. Cat. 2; R45 T [The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).] 274-566-4 70321-80-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H M 648-139-00-1 Tar acids, cresylic, sodium salts, caustic solns.; … 26 unchanged lines … R: 45 S: 53-45 H M 648-145-00-4 Tar brown-coal; [An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivates, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150 oC to 360 oC (302 oF to 680 oF).] 309-885-0 101316-83-0 Carc. Cat. 1; R45 T [An oil distilled from brown-coal tar. Composed primarily of aliphatic, naphthenic and one- to three-ring aromatic hydrocarbons, their alkyl derivates, heteroaromatics and one- and two-ring phenols boiling in the range of approximately 150 oC to 360 oC (302 oF to 680 oF).] 309-885-0 101316-83-0 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 648-146-00-X Tar, brown-coal, low-temp.; [A tar obtained from low temperature carbonization and low temperature gasification of brown coal. Composed primarily of aliphatic, naphthenic and cyclic aromatic hydrocarbons, heteroaromatic hydrocarbons and cyclic phenols.] 309-886-6 101316-84-1 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 648-147-00-5 Light oil (coal), coke-oven; Crude benzole; [The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.] 266-012-5 65996-78-3 Carc. Cat. 2; R45 [The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.] 266-012-5 65996-78-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-148-00-0 Distillates (coal), liq. solvent extn., primary; [The liquid product of condensation of vapors emitted during the digestion of coal in a liquid solvent and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of partly hydrogenated condensed-ring aromatic hydrocarbons, aromatic compounds containing nitrogen, oxygen and sulfur, and their alkyl derivatives having carbon numbers predominantly in the range of C4 through C14.] 302-688-0 94114-52-0 Carc. Cat. 2; R45 [The liquid product of condensation of vapors emitted during the digestion of coal in a liquid solvent and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of partly hydrogenated condensed-ring aromatic hydrocarbons, aromatic compounds containing nitrogen, oxygen and sulfur, and their alkyl derivatives having carbon numbers predominantly in the range of C4 through C14.] 302-688-0 94114-52-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-149-00-6 Distillates (coal), solvent extn., hydrocracked; [Distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 through C14. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-689-6 94114-53-1 Carc. Cat. 2; R45 [Distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 through C14. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-689-6 94114-53-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-150-00-1 Naphtha (coal), solvent extn., hydrocracked; [Fraction of the distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 to C9. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-690-1 94114-54-2 Carc. Cat. 2; R45 [Fraction of the distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 to C9. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.] 302-690-1 94114-54-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-151-00-7 Gasoline, coal solvent extn., hydrocracked naphtha; [Motor fuel produced by the reforming of the refined naphtha fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of aromatic and naphthenic hydrocarbons, their alkyl derivatives and alkyl hydrocarbons having carbon numbers in the range of C4 through C9.] 302-691-7 94114-55-3 Carc. Cat. 2; R45 T [Motor fuel produced by the reforming of the refined naphtha fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 oC to 180 oC (86 oF to 356 oF). Composed primarily of aromatic and naphthenic hydrocarbons, their alkyl derivatives and alkyl hydrocarbons having carbon numbers in the range of C4 through C9.] 302-691-7 94114-55-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 648-152-00-2 Distillates (coal), solvent extn., hydrocracked middle; [Distillate obtained from the hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 300 °C (356 °F to 572 °F. Composed primarily of two-ring aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes having carbon numbers predominantly in the range of C9 through C14. Nitrogen, sulfur and oxygen-containing compounds are also present.] 302-692-2 94114-56-4 Carc. Cat. 2; R45 [Distillate obtained from the hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 300 °C (356 °F to 572 °F. Composed primarily of two-ring aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes having carbon numbers predominantly in the range of C9 through C14. Nitrogen, sulfur and oxygen-containing compounds are also present.] 302-692-2 94114-56-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-153-00-8 Distillates (coal), solvent extn., hydrocracked hydrogenated middle; [Distillate from the hydrogenation of hydrocracked middle distillate from coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 280 °C (356 °F to 536 °F). Composed primarily of hydrogenated two- ring carbon compounds and their alkyl derivatives having carbon numbers predominantly in the range of C9 through C14.] 302-693-8 94114-57-5 Carc. Cat. 2; R45 [Distillate from the hydrogenation of hydrocracked middle distillate from coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 280 °C (356 °F to 536 °F). Composed primarily of hydrogenated two- ring carbon compounds and their alkyl derivatives having carbon numbers predominantly in the range of C9 through C14.] 302-693-8 94114-57-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J 648-154-00-3 Fuels, jet aircraft, coal solvent extn., hydrocracked hydrogenated; [Jet engine fuel produced by hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 oC to 225 oC (356 oF to 473 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C10 through C12.] 302-694-3 94114-58-6 Carc. Cat. 3; R40 Xn [Jet engine fuel produced by hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 oC to 225 oC (356 oF to 473 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C10 through C12.] 302-694-3 94114-58-6 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 648-155-00-9 Fuels, diesel, coal solvent extn., hydrocracked hydrogenated; [Diesel engine fuel produced by the hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 200 oC to 280 oC (392 oF to 536 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C11 through C14.] 302-695-9 94114-59-7 Carc. Cat. 3; R40 Xn [Diesel engine fuel produced by the hydrogenation of the middle distillate fraction of the products of hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 200 oC to 280 oC (392 oF to 536 oF). Composed primarily of hydrogenated two-ring hydrocarbons and their alkyl derivatives having carbon numbers predominantly in the range of C11 through C14.] 302-695-9 94114-59-7 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 648-156-00-4 Light oil (coal), semi-coking process; Fresh oil; [The volatile organic liquid condensed from the gas evolved in the low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.] 292-635-7 90641-11-5 Carc. Cat. 2; R45 [The volatile organic liquid condensed from the gas evolved in the low-temperature (less than 700 °C (1292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.] 292-635-7 90641-11-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 T R: 45-46 S: 53-45 H J … 20 unchanged lines … R: 38-51/53 S: (2-)28-37-61 649-008-00-1 Residues (petroleum), atm. tower; Heavy Fuel oil; [A complex residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-045-2 64741-45-3 Carc. Cat. 2; R45 T [A complex residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-045-2 64741-45-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-009-00-7 Gas oils (petroleum), heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 265-058-3 64741-57-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 265-058-3 64741-57-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-010-00-2 Distillates (petroleum), heavy catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-063-0 64741-61-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-063-0 64741-61-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-011-00-8 Clarified oils (petroleum), catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-064-6 64741-62-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-064-6 64741-62-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-012-00-3 Residues (petroleum), hydrocracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products of a hydrocracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF).] 265-076-1 64741-75-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from distillation of the products of a hydrocracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF).] 265-076-1 64741-75-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-013-00-9 Residues (petroleum), thermal cracked; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-081-9 64741-80-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-081-9 64741-80-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-014-00-4 Distillates (petroleum), heavy thermal cracked; Heavy Fuel oil; [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C15 through C36 and boiling in the range of approximately 260 oC to 480 oC (500 oF to 896 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-082-4 64741-81-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C15 through C36 and boiling in the range of approximately 260 oC to 480 oC (500 oF to 896 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-082-4 64741-81-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-015-00-X Gas oils (petroleum), hydrotreated vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C50 and boiling in the range of approximately 230 oC to 600 oC (446 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-162-9 64742-59-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C50 and boiling in the range of approximately 230 oC to 600 oC (446 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-162-9 64742-59-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-016-00-5 Residues (petroleum), hydrodesulfurized atmospheric tower; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating an atmospheric tower residuum with hydrogen in the presence of a catalyst under conditions primarily to remove organic sulfur compounds. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-181-2 64742-78-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating an atmospheric tower residuum with hydrogen in the presence of a catalyst under conditions primarily to remove organic sulfur compounds. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-181-2 64742-78-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-017-00-0 Gas oils (petroleum), hydrodesulfurized heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oC). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-189-6 64742-86-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and boiling in the range of approximately 350 oC to 600 oC (662 oF to 1112 oC). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-189-6 64742-86-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-018-00-6 Residues (petroleum), steam-cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained as the residual fraction from the distillation of the products of a steam cracking process (including steam cracking to produce ethylene). It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C14 and boiling above approximately 260 oC (500 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-193-8 64742-90-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the residual fraction from the distillation of the products of a steam cracking process (including steam cracking to produce ethylene). It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly greater than C14 and boiling above approximately 260 oC (500 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 265-193-8 64742-90-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-019-00-1 Residues (petroleum), atmospheric; Heavy Fuel oil; [A complex residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-777-3 68333-22-2 Carc. Cat. 2; R45 T [A complex residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-777-3 68333-22-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-020-00-7 Clarified oils (petroleum), hydrodesulfurized catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-782-0 68333-26-6 Carc. Cat. 2; R45 T Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 269-782-0 68333-26-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-021-00-2 Distillates (petroleum), hydrodesulfurized intermediate catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating intermediate catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 269-783-6 68333-27-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating intermediate catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 269-783-6 68333-27-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-022-00-8 Distillates (petroleum), hydrodesulfurized heavy catalytic cracked; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treatment of heavy catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 269-784-1 68333-28-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treatment of heavy catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C35 and boiling in the range of approximately 260 oC to 500 oC (500 oF to 932 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 269-784-1 68333-28-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-023-00-3 Fuel oil, residues-straight-run gas oils, high-sulfur; Heavy Fuel oil 270-674-0 68476-32-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-024-00-9 Fuel oil, residual; Heavy Fuel oil; [The liquid product from various refinery streams, usually residues. The composition is complex and varies with the source of the crude oil.] 270-675-6 68476-33-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-025-00-4 Residues (petroleum), catalytic reformer fractionator residue distn.; Heavy Fuel oil; [A complex residuum from the distillation of catalytic reformer fractionator residue. It boils approximately above 399 oC (750 oF).] 270-792-2 68478-13-7 Carc. Cat. 2; R45 T [A complex residuum from the distillation of catalytic reformer fractionator residue. It boils approximately above 399 oC (750 oF).] 270-792-2 68478-13-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-026-00-X Residues (petroleum), heavy coker gas oil and vacuum gas oil; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and vacuum gas oil. It predominantly consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-796-4 68478-17-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and vacuum gas oil. It predominantly consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-796-4 68478-17-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-027-00-5 Residues (petroleum), heavy coker and light vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and light vacuum gas oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-983-0 68512-61-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from the distillation of heavy coker gas oil and light vacuum gas oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-983-0 68512-61-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-028-00-0 Residues (petroleum), light vacuum; Heavy Fuel oil; [A complex residuum from the vacuum distillation of the residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-984-6 68512-62-9 Carc. Cat. 2; R45 T [A complex residuum from the vacuum distillation of the residuum from the atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly greater than C13 and boiling above approximately 230 oC (446 oF).] 270-984-6 68512-62-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-029-00-6 Residues (petroleum), steam-cracked light; Heavy Fuel oil; [A complex residuum from the distillation of the products from a steam-cracking process. It consists predominantly of aromatic and unsaturated hydrocarbons having carbon numbers greater than C7 and boiling in the range of approximately 101 oC to 555 oC (214 oF to 1030 oF).] 271-013-9 68513-69-9 Carc. Cat. 2; R45 T [A complex residuum from the distillation of the products from a steam-cracking process. It consists predominantly of aromatic and unsaturated hydrocarbons having carbon numbers greater than C7 and boiling in the range of approximately 101 oC to 555 oC (214 oF to 1030 oF).] 271-013-9 68513-69-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-030-00-1 Fuel oil, No 6; 649-030-00-1 Fuel oil, No 6; Heavy Fuel oil; [A distillate oil having a minimum viscosity of 900 SUS at 37.7 oC (100 oF) to a maximum of 9000 SUS at 37.7 oC (100 oF).] 271-384-7 68553-00-4 Carc. Cat. 2; R45 T [A distillate oil having a minimum viscosity of 900 SUS at 37.7 oC (100 oF) to a maximum of 9000 SUS at 37.7 oC (100 oF).] 271-384-7 68553-00-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-031-00-7 Residues (petroleum), topping plant, low-sulfur; Heavy Fuel oil; [A low-sulfur complex combination of hydrocarbons produced as the residual fraction from the topping plant distillation of crude oil. It is the residuum after the straight-run gasoline cut, kerosene cut and gas oil cut have been removed.] 271-763-7 68607-30-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-032-00-2 Gas oils (petroleum), heavy atmospheric; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C35 and boiling in the range of approximately 121 oC to 510 oC (250 oF to 950 oF).] 272-184-2 68783-08-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C35 and boiling in the range of approximately 121 oC to 510 oC (250 oF to 950 oF).] 272-184-2 68783-08-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-033-00-8 Residues (petroleum), coker scrubber, Condensed-ring-arom.-contg.; Heavy Fuel oil; [A very complex combination of hydrocarbons produced as the residual fraction from the distillation of vaccum residuum and the products from a thermal cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed rind aromatic hydrocarbons.] 272-187-9 68783-13-1 Carc. Cat. 2; R45 T [A very complex combination of hydrocarbons produced as the residual fraction from the distillation of vaccum residuum and the products from a thermal cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 oC (662 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed rind aromatic hydrocarbons.] 272-187-9 68783-13-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-034-00-3 Distillates (petroleum), petroleum residues vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from the atmospheric distillation of crude oil.] 273-263-4 68955-27-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-035-00-9 Residues (petroleum), steam-cracked, resinous; Heavy Fuel oil; [A complex residuum from the distillation of steam-cracked petroleum residues.] 273-272-3 68955-36-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-036-00-4 Distillates (petroleum), intermediate vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum, distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C14 through C42 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-683-0 70592-76-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the vacuum, distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C14 through C42 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-683-0 70592-76-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-037-00-X Distillates (petroleum), light vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C35 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF).] 274-684-6 70592-77-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C35 and boiling in the range of approximately 250 oC to 545 oC (482 oF to 1013 oF).] 274-684-6 70592-77-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-038-00-5 Distillates (petroleum), vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having numbers predominantly in the range of C15 through C50 and boiling in the range of approximately 270 oC to 600 oC (518 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-685-1 70592-78-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having numbers predominantly in the range of C15 through C50 and boiling in the range of approximately 270 oC to 600 oC (518 oF to 1112 oF). This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 274-685-1 70592-78-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-039-00-0 Gas oils (petroleum), hydrodesulfurized coker heavy vacuum; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by hydrodesulfurization of heavy coker distillate stocks, It consists predominantly of hydrocarbons having carbon numbers predominantly in the range C18 to C44 and boiling in the range of approximately 304 oC to 548 oC (579 oF to 1018 oF). Likely to contain 5 % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 285-555-9 85117-03-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by hydrodesulfurization of heavy coker distillate stocks, It consists predominantly of hydrocarbons having carbon numbers predominantly in the range C18 to C44 and boiling in the range of approximately 304 oC to 548 oC (579 oF to 1018 oF). Likely to contain 5 % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 285-555-9 85117-03-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-040-00-6 Residues (petroleum), steam-cracked, distillates; Heavy Fuel oil; [A complex combination of hydrocarbons obtained during the production of refined petroleum tar by the distillation of steam cracked tar. It consists predominantly of aromatic and other hydrocarbons and organic sulfur compounds.] 292-657-7 90669-75-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-041-00-1 Residues (petroleum), vacuum, light; Heavy Fuel oil; [A complex residuum from the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C24 and boiling above approximately 390 oC (734 oF).] 292-658-2 90669-76-4 Carc. Cat. 2; R45 T [A complex residuum from the vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C24 and boiling above approximately 390 oC (734 oF).] 292-658-2 90669-76-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-042-00-7 Fuel oil, heavy, high-sulfur; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the distillation of crude petroleum. It consists predominantly of aliphatic, aromatic and cycloaliphatic hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 295-396-7 92045-14-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the distillation of crude petroleum. It consists predominantly of aliphatic, aromatic and cycloaliphatic hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 295-396-7 92045-14-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-043-00-2 Residues (petroleum), catalytic cracking; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from the distillation of the products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF).] 295-511-0 92061-97-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from the distillation of the products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C11 and boiling above approximately 200 oC (392 oF).] 295-511-0 92061-97-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-044-00-8 Distillates (petroleum), intermediate catalytic cracked, thermally degraded; Heavy Fuel oil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 220 oC to 450 oC (428 oF to 842 oF). This stream is likely to contain organic sulfur compounds.] 295-990-6 92201-59-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 220 oC to 450 oC (428 oF to 842 oF). This stream is likely to contain organic sulfur compounds.] 295-990-6 92201-59-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-045-00-3 Residual oils (petroleum); Heavy Fuel oil; [A complex combination of hydrocarbons, sulfur compounds and metal-containing organic compounds obtained as the residue from refinery fractionation cracking processes. It produces a finished oil with a viscosity above 2cSt. at 100 oC.] 298-754-0 93821-66-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons, sulfur compounds and metal-containing organic compounds obtained as the residue from refinery fractionation cracking processes. It produces a finished oil with a viscosity above 2cSt. at 100 oC.] 298-754-0 93821-66-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-046-00-9 Residues, steam cracked, thermally treated; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by the treatment and distillation of raw steam-cracked naphtha. It consists predominantly of unsaturated hydrocarbons boiling in the range above approximately 180 oC (356 oF).] 308-733-0 98219-64-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the treatment and distillation of raw steam-cracked naphtha. It consists predominantly of unsaturated hydrocarbons boiling in the range above approximately 180 oC (356 oF).] 308-733-0 98219-64-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-047-00-4 Distillates (petroleum), hydrodesulfurized full-range middle; Heavy Fuel oil; [A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF).] 309-863-0 101316-57-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF).] 309-863-0 101316-57-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-048-00-X Residues (petroleum), catalytic reformer fractionator; Heavy Fuel oil; [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C25 and boiling in the range of approximately 160 oC to 400 oC (320 oF to 725 oF). This stream is likely to contain 5 wt. % or more of 4- or 6-membered condensed ring aromatic hydrocarbons.] 265-069-3 64741-67-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced as the residual fraction from distillation of the product from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C25 and boiling in the range of approximately 160 oC to 400 oC (320 oF to 725 oF). This stream is likely to contain 5 wt. % or more of 4- or 6-membered condensed ring aromatic hydrocarbons.] 265-069-3 64741-67-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-049-00-5 Petroleum; Crude oil; [A complex combination of hydrocarbons, It consists predominantly of aliphatic, alicyclic and aromatic hydrocarbons. It may also contain small amounts of nitrogen, oxygen and sulfur compounds. This category encompasses light, medium, and heavy petroleums, as well as the oils extended from tar sands. Hydrocarbonaceous materials requiring major chemical changes for their recovery or conversion to petroleum refinery feedstocks such as crude shale oils; upgraded shale oils and liquid coal fuels are not included in this definition.] 232-298-5 8002-05-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-050-00-0 Distillates (petroleum), light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons normally present in this distillation range of crude oil.] 265-051-5 64741-50-0 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons normally present in this distillation range of crude oil.] 265-051-5 64741-50-0 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-051-00-6 Distillates (petroleum), heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons.] 265-052-0 64741-51-1 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated aliphatic hydrocarbons.] 265-052-0 64741-51-1 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-052-00-1 Distillates (petroleum), light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-053-6 64741-52-2 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-053-6 64741-52-2 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-053-00-7 Distillates (petroleum), heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-054-1 64741-53-3 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by vacuum distillation of the residuum from atmospheric distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-054-1 64741-53-3 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-054-00-2 Distillates (petroleum), acid-treated heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-117-3 64742-18-3 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-117-3 64742-18-3 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-055-00-8 Distillates (petroleum), acid-treated light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-118-9 64742-19-4 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-118-9 64742-19-4 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-056-00-3 Distillates (petroleum), acid-treated heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of a least 100 SUS at 100 oF (19cSt at 40 oC).] 265-119-4 64742-20-7 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of a least 100 SUS at 100 oF (19cSt at 40 oC).] 265-119-4 64742-20-7 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-057-00-9 Distillates (petroleum), acid-treated light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-121-5 64742-21-8 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-121-5 64742-21-8 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-058-00-4 Distillates (petroleum), chemically neutralized heavy paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons obtained from a treating process to remove acidic materials. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of aliphatic hydrocarbons.] 265-127-8 64742-27-4 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons obtained from a treating process to remove acidic materials. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of aliphatic hydrocarbons.] 265-127-8 64742-27-4 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-059-00-X Distillates (petroleum), chemically neutralized light paraffinic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-128-3 64742-28-5 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-128-3 64742-28-5 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-060-00-5 Distillates (petroleum), chemically neutralized heavy naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-135-1 64742-34-3 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-135-1 64742-34-3 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-061-00-0 Distillates (petroleum), chemically neutralized light naphthenic; Unrefined or mildly refined baseoil; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS a 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-136-7 64742-35-4 Carc. Cat. 1; R45 T [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS a 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-136-7 64742-35-4 Carc. Cat. 1; R45 T R: 45 S: 53-45 H 649-062-00-6 Gases (petroleum), catalytic cracked naphtha depropanizer overhead, C3-rich acid-free; … 172 unchanged lines … S: 53-45 H K 649-087-00-2 Residues (petroleum), alkylation splitter, C4-rich; Petroleum gas; [A complex residuum from the distillation of streams various refinery operations. It consists of hydrocarbons having carbon numbers in the range of C4 through C5, predominantly butane and boiling in the range of approximately – 11,7 °C to 27.8 °C (11 °F to 82 °F).] 271-010-2 68513-66-6 F+; R12 [A complex residuum from the distillation of streams various refinery operations. It consists of hydrocarbons having carbon numbers in the range of C4 through C5, predominantly butane and boiling in the range of approximately – 11,7 °C to 27.8 °C (11 °F to 82 °F).] 271-010-2 68513-66-6 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-088-00-8 Hydrocarbons, C1-4; Petroleum gas; [A complex combination of hydrocarbons provided by thermal cracking and absorber operations and by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately minus 164 °C to minus 0,5 °C (– 263 °F to 31 °F).] 271-032-2 68514-31-8 F+; R12 [A complex combination of hydrocarbons provided by thermal cracking and absorber operations and by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately minus 164 °C to minus 0,5 °C (– 263 °F to 31 °F).] 271-032-2 68514-31-8 F+; R12 Carc. Cat 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-089-00-3 Hydrocarbons, C1-4, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting hydrocarbon gases to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 164 °C to – 0,5 °C (– 263 °F to 31 °F).] 271-038-5 68514-36-3 F+; R12 [A complex combination of hydrocarbons obtained by subjecting hydrocarbon gases to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 164 °C to – 0,5 °C (– 263 °F to 31 °F).] 271-038-5 68514-36-3 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-090-00-9 Hydrocarbons, C1-3; Petroleum gas; [A complex combination of hydrocarbons having carbon numbers predominantly in the range of C1 through C3 and boiling in the range of approximately minus 164 °C to minus 42 °C (– 263 °F to – 44 °F).] 271-259-7 68527-16-2 F+; R12 [A complex combination of hydrocarbons having carbon numbers predominantly in the range of C1 through C3 and boiling in the range of approximately minus 164 °C to minus 42 °C (– 263 °F to – 44 °F).] 271-259-7 68527-16-2 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 53 unchanged lines … S: 53-45 H K 649-099-00-8 Gases (petroleum), C2-4, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C2 through C4 and boiling in the range of approximately – 51 °C to – 34 °C (– 60 °F to – 30 °F).] 272-205-5 68783-65-3 F+; R12 [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C2 through C4 and boiling in the range of approximately – 51 °C to – 34 °C (– 60 °F to – 30 °F).] 272-205-5 68783-65-3 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 103 unchanged lines … S: 53-45 H K 649-115-00-3 Gases (petroleum), steam-cracker C3-rich; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of products from a steam cracking process. It consists predominantly of propylene with some propane and boils in the range of approximately – 70 °C to 0 °C (– 94 °F to 32 °F).] 295-404-9 92045-22-2 F+; R12 [A complex combination of hydrocarbons produced by the distillation of products from a steam cracking process. It consists predominantly of propylene with some propane and boils in the range of approximately – 70 °C to 0 °C (– 94 °F to 32 °F).] 295-404-9 92045-22-2 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-116-00-9 Hydrocarbons, C4, steam-cracker distillate; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of the products of a steam cracking process. It consists predominantly of hydrocarbons having a carbon number of C4, predominantly 1-butene and 2-butene, containing also butane and isobutene and boiling in the range of approximately minus 12 °C to 5 °C (10,4 °F to 41 °F).] 295-405-4 92045-23-3 F+; R12 [A complex combination of hydrocarbons produced by the distillation of the products of a steam cracking process. It consists predominantly of hydrocarbons having a carbon number of C4, predominantly 1-butene and 2-butene, containing also butane and isobutene and boiling in the range of approximately minus 12 °C to 5 °C (10,4 °F to 41 °F).] 295-405-4 92045-23-3 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-117-00-4 Petroleum gases, liquefied, sweetened, C4 fraction; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting a liquified petroleum gas mix to a sweetening process to oxidize mercaptans or to remove acidic impurities. It consists predominantly of C4 saturated and unsaturated hydrocarbons.] 295-463-0 92045-80-2 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 HKS 649-118-00-X Hydrocarbons, C4, 1,3-butadiene- and isobutene-free; Petroleum gas 306-004-1 95465-89-7 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-119-00-5 Raffinates (petroleum), steam-cracked C4 fraction cuprous ammonium acetate extn., C3-5 and C3-5 unsatd., butadiene-free; 649-119-00-5 Raffinates (petroleum), steam-cracked C4 fraction cuprous ammonium acetate extn., C3-5 and C3-5 unsatd., butadiene-free; Petroleum gas 307-769-4 97722-19-5 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T … 84 unchanged lines … S: 53-45 H K 649-132-00-6 Gases (petroleum), hydrogen-rich; Refinery gas; [A complex combination separated as a gas from hydrocarbon gases by chilling. It consists primarily of hydrogen with various small amounts of carbon monoxide, nitrogen, methane, and C2 hydrocarbons.] 270-780-7 68477-97-4 F+; R12 [A complex combination separated as a gas from hydrocarbon gases by chilling. It consists primarily of hydrogen with various small amounts of carbon monoxide, nitrogen, methane, and C2 hydrocarbons.] 270-780-7 68477-97-4 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 304 unchanged lines … S: 53-45 H L 649-177-00-1 Gases (petroleum), C3-4; Petroleum gas; [A complex combination of hydrocarbons produced by distillation of products from the cracking of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C4, predominantly of propane and propylene, and boiling in the range of approximately – 51 °C to – 1 °C (– 60 °F to 30 °F.)] 268-629-5 68131-75-9 F+; R12 [A complex combination of hydrocarbons produced by distillation of products from the cracking of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C4, predominantly of propane and propylene, and boiling in the range of approximately – 51 °C to – 1 °C (– 60 °F to 30 °F.)] 268-629-5 68131-75-9 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 91 unchanged lines … S: 53-45 H K 649-191-00-8 Gases (petroleum), catalytic cracked overheads; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of products from the catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C5 and boiling in the range of approximately – 48 °C to 32 °C (– 54 °F to 90 °F).] 270-071-2 68409-99-4 F+; R12 [A complex combination of hydrocarbons produced by the distillation of products from the catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C5 and boiling in the range of approximately – 48 °C to 32 °C (– 54 °F to 90 °F).] 270-071-2 68409-99-4 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 31 unchanged lines … S: 53-45 H K 649-198-00-6 Fuel gases, crude oil of distillates; Petroleum gas; [A complex combination of light gases produced by distillation of crude oil and by catalytic reforming of naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 217 °C to – 12 °C (– 423 °F to 10 °F).] 270-670-9 68476-29-9 F+; R12 [A complex combination of light gases produced by distillation of crude oil and by catalytic reforming of naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately – 217 °C to – 12 °C (– 423 °F to 10 °F).] 270-670-9 68476-29-9 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 18 unchanged lines … S: 53-45 H K 649-202-00-6 Petroleum gases, liquefied; Petroleum gas; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-704-2 68476-85-7 F+; R12 [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-704-2 68476-85-7 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 HKS 649-203-00-1 Petroleum gases, liquefied, sweetened; Petroleum gas; [A complex combination of hydrocarbons obtained by subjecting liquefied petroleum gas mix to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-705-8 68476-86-8 F+; R12 [A complex combination of hydrocarbons obtained by subjecting liquefied petroleum gas mix to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately – 40 °C to 80 °C (– 40 °F to 176 °F).] 270-705-8 68476-86-8 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 HKS 649-204-00-7 gases (petroleum), C3-4, isobutane-rich; Petroleum gas; [A complex combination of hydrocarbons from the distillation of saturated and unsaturated hydrocarbons usually ranging in carbon numbers from C3 through C6, predominantly butane and isobutane. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C4, predominantly isobutane.] 270-724-1 68477-33-8 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 S: 53-45 H K 649-205-00-2 Distillates (petroleum), C3-6, piperylene-rich; Petroleum gas; [A complex combination of hydrocarbons from the distillation of saturated and unsaturated aliphatic hydrocarbons usually ranging in the carbon numbers C3 through C6. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C6, predominantly piperylenes.] 270-726-2 68477-35-0 F+; R12 [A complex combination of hydrocarbons from the distillation of saturated and unsaturated aliphatic hydrocarbons usually ranging in the carbon numbers C3 through C6. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C6, predominantly piperylenes.] 270-726-2 68477-35-0 F+; R12 Carc. Cat. 1; R45 Muta. Cat. 2; R46 F+; T R: 45-46-12 … 40 unchanged lines … S: 53-45 H L 649-212-00-0 Distillates (petroleum), sweetened middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-088-7 64741-86-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-088-7 64741-86-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-213-00-6 Gas oils (petroleum), solvent-refined; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-092-9 64741-90-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-092-9 64741-90-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-214-00-1 Distillates (petroleum), solvent-refined middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-093-4 64741-91-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-093-4 64741-91-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-215-00-7 Gas oils (petroleum), acid-treated; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-112-6 64742-12-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-112-6 64742-12-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-216-00-2 Distillates (petroleum), acid-treated middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-113-1 64742-13-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-113-1 64742-13-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-217-00-8 Distillates (petroleum), acid-treated light; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-114-7 64742-14-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-114-7 64742-14-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-218-00-3 Gas oils (petroleum), chemically neutralized; Gasoil — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-129-9 64742-29-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-129-9 64742-29-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-219-00-9 Distillates (petroleum), chemically neutralized middle; Gasoil — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-130-4 64742-30-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C20 and boiling in the range of approximately 205 oC to 345 oC (401 oF to 653 oF).] 265-130-4 64742-30-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-220-00-4 Distillates (petroleum), clay-treated middle; Gasoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-139-3 64742-38-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 150 oC to 345 oC (302 oF to 653 oF).] 265-139-3 64742-38-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-221-00-X Distillates (petroleum), hydrotreated middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-148-2 64742-46-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-148-2 64742-46-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-222-00-5 Gas oils (petroleum), hydrodesulfurized; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-182-8 64742-79-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C25 and boiling in the range of approximately 230 oC to 400 oC (446 oF to 752 oF).] 265-182-8 64742-79-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-223-00-0 Distillates (petroleum), hydrodesulfurized middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-183-3 64742-80-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 265-183-3 64742-80-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-224-00-6 Fuels, diesel; Gasoil — unspecified; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 163 oC to 357 oC (325 oF to 675 oF).] 269-822-7 68334-30-5 Carc. Cat. 3; R40 Xn [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C20 and boiling in the range of approximately 163 oC to 357 oC (325 oF to 675 oF).] 269-822-7 68334-30-5 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H N 649-225-00-1 Fuel oil, No 2; 649-225-00-1 Fuel oil, No 2; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF) to a maximum of 37,9 SUS at 37,7 oC (100 oF).] 270-671-4 68476-30-2 Carc. Cat. 3; R40 Xn [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF) to a maximum of 37,9 SUS at 37,7 oC (100 oF).] 270-671-4 68476-30-2 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 649-226-00-7 Fuel oil, No 4; 649-226-00-7 Fuel oil, No 4; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 45 SUS at 37,7 oC (100 oF) to a maximum of 125 SUS at 37,7 oC (100 oF).] 270-673-5 68476-31-3 Carc. Cat. 3; R40 Xn [A distillate oil having a minimum viscosity of 45 SUS at 37,7 oC (100 oF) to a maximum of 125 SUS at 37,7 oC (100 oF).] 270-673-5 68476-31-3 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 649-227-00-2 Fuels, diesel, No 2; 649-227-00-2 Fuels, diesel, No 2; Gasoil — unspecified; [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF).] 270-676-1 68476-34-6 Carc. Cat. 3; R40 Xn [A distillate oil having a minimum viscosity of 32,6 SUS at 37,7 oC (100 oF).] 270-676-1 68476-34-6 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 649-228-00-8 Distillates (petroleum), catalytic reformer fractionator residue, high-boiling; Gasoil — unspecified; [A complex combination of hydrocarbons from the distillation of catalytic reformer fracftionator residue. It boils in the range of approximately 343 oC to 399 oC (650 oF to 750 oF).] 270-719-4 68477-29-2 Carc. Cat. 2; R45 T Gasoil — unspecified; [A complex combination of hydrocarbons from the distillation of catalytic reformer fracftionator residue. It boils in the range of approximately 343 oC to 399 oC (650 oF to 750 oF).] 270-719-4 68477-29-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-229-00-3 Distillates (petroleum), catalytic reformer fractionator residue, intermediate-boiling; Gasoil — unspecified; [A complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils in the range of approximately 288 oC to 371 oC (550 oF to 700 oF).] 270-721-5 68477-30-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils in the range of approximately 288 oC to 371 oC (550 oF to 700 oF).] 270-721-5 68477-30-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-230-00-9 Distillates (petroleum), catalytic reformer fractionator residue, low-boiling; Gasoil — unspecified; [The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288 oC (550 oF).] 270-722-0 68477-31-6 Carc. Cat. 2; R45 T [The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288 oC (550 oF).] 270-722-0 68477-31-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-231-00-4 Distillates (petroleum), highly refined middle; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by the subjection of a petroleum fraction to several of the following steps: filtration, centrifugation, atmospheric distillation, vacuum distillation, acidification, neutralization and clay treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C20.] 292-615-8 90640-93-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-232-00-X Distillates (petroleum) catalytic reformer, heavy arom. conc.; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from the distillation of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C16 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 295-294-2 91995-34-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from the distillation of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C10 through C16 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 295-294-2 91995-34-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-233-00-5 Gas oils, paraffinic; Gasoil — unspecified; [A distillate obtained from the redistillation of a complex combination of hydrocarbons obtained by the distillation of the effluents from a severe catalytic hydrotreatment of paraffins. It boils in the range of approximately 190 oC to 330 oC (374 oF to 594 oF).] 300-227-8 93924-33-5 Carc. Cat. 2; R45 T [A distillate obtained from the redistillation of a complex combination of hydrocarbons obtained by the distillation of the effluents from a severe catalytic hydrotreatment of paraffins. It boils in the range of approximately 190 oC to 330 oC (374 oF to 594 oF).] 300-227-8 93924-33-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-234-00-0 Naphtha (petroleum), solvent-refined hydrodesulfurized heavy; Gasoil — unspecified 307-035-3 97488-96-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-235-00-6 Hydrocarbons, C16-20, hydrotreated middle distillate, distn. lights; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a middle distillate with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 290 oC to 350 oC (554 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-659-6 97675-85-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a middle distillate with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 290 oC to 350 oC (554 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-659-6 97675-85-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-236-00-1 Hydrocarbons, C12-20, hydrotreated paraffinic, distn. lights; Gasoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of heavy paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 230 oC to 350 oC (446 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-660-1 97675-86-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of heavy paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 230 oC to 350 oC (446 oF to 662 oF). It produces a finished oil having a viscosity of 2cSt at 100 oC (212 oF).] 307-660-1 97675-86-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-237-00-7 Hydrocarbons, C11-17, solvent-extd. light naphthenic; Gasoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a visciosity of 2.2 cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 307-757-9 97722-08-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a visciosity of 2.2 cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 200 oC to 300 oC (392 oF to 572 oF).] 307-757-9 97722-08-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-238-00-2 Gas oils, hydrotreated; Gasoil — unspecified; [A complex combination of hydrocarbons obtained from the redistillation of the effluents from the treatment of paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C27 and boiling in the range of approximately 330 oC to 340 oC (626 oF to 644 oF).] 308-128-1 97862-78-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from the redistillation of the effluents from the treatment of paraffins with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C27 and boiling in the range of approximately 330 oC to 340 oC (626 oF to 644 oF).] 308-128-1 97862-78-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H N 649-239-00-8 Distillates (petroleum), carbon-treated light paraffinic; … 106 unchanged lines … S: 53-45 H N 649-261-00-8 Gasoline, natural; Low boiling point naphtha; [A complex combination of hydrocarbons separated from natural gas by processes such as refrigeration or absorption. It consists predominantly of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately minus 20 °C to 120 °C (– 4 °F to 248 °F).] 232-349-1 8006-61-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons separated from natural gas by processes such as refrigeration or absorption. It consists predominantly of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately minus 20 °C to 120 °C (– 4 °F to 248 °F).] 232-349-1 8006-61-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-262-00-3 Naphtha; Low boiling point naphtha; [Refined, partly refined, or unrefined petroleum products produced by the distillation of natural gas. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 232-443-2 8030-30-6 Carc. Cat. 2; R45 [Refined, partly refined, or unrefined petroleum products produced by the distillation of natural gas. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 232-443-2 8030-30-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-263-00-9 Ligroine; Low boiling point naphtha; [A complex combination of hydrocarbons obtained by the fractional distillation of petroleum. This fraction boils in a range of approximately 20 °C to 135 °C (58 °F to 275 °F).] 232-453-7 8032-32-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the fractional distillation of petroleum. This fraction boils in a range of approximately 20 °C to 135 °C (58 °F to 275 °F).] 232-453-7 8032-32-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-264-00-4 Naphtha (petroleum), heavy straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-041-0 64741-41-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-041-0 64741-41-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-265-00-X Naphtha (petroleum), full-range straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 428 °F).] 265-042-6 64741-42-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 428 °F).] 265-042-6 64741-42-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-266-00-5 Naphtha (petroleum), light straight-run; Low boiling point naphtha; [A complex combination of hydrocarbons produced by distillation of crude oil. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-046-8 64741-46-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of crude oil. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-046-8 64741-46-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-267-00-0 Solvent naphtha (petroleum), light aliph.; Low boiling point naphtha; [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 35 °C to 160 °C (95 °F to 320 °F).] 265-192-2 64742-89-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 35 °C to 160 °C (95 °F to 320 °F).] 265-192-2 64742-89-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-268-00-6 Distillates (petroleum), straight-run light; Low boiling point naphtha; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C7 and boiling in the range of approximately – 88 °C to 99 °C (– 127 °F to 210 °F).] 270-077-5 68410-05-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C7 and boiling in the range of approximately – 88 °C to 99 °C (– 127 °F to 210 °F).] 270-077-5 68410-05-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-269-00-1 Gasoline, vapor-recovery; Low boiling point naphtha; [A complex combination of hydrocarbons separated from the gases from vapor recovery systems by cooling. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 196 °C(-4 °F to 384 °F).] 271-025-4 68514-15-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons separated from the gases from vapor recovery systems by cooling. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 196 °C(-4 °F to 384 °F).] 271-025-4 68514-15-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-270-00-7 Gasoline, straight-run, topping-plant; Low boiling point naphtha; [A complex combination of hydrocarbons produced from the topping plant by the distillation of crude oil. It boils in the range of approximately 36,1 °C to 193,3 °C (97 °F to 380 °F).] 271-727-0 68606-11-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced from the topping plant by the distillation of crude oil. It boils in the range of approximately 36,1 °C to 193,3 °C (97 °F to 380 °F).] 271-727-0 68606-11-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-271-00-2 Naphtha (petroleum), unsweetened; Low boiling point naphtha; [A complex combination of hydrocarbons produced from the distillation of naphtha streams from various refinery processes. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 0 °C to 230 °C (25 °F to 446 °F).] 272-186-3 68783-12-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced from the distillation of naphtha streams from various refinery processes. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 0 °C to 230 °C (25 °F to 446 °F).] 272-186-3 68783-12-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-272-00-8 Distillates (petroleum), light straight-run gasoline fractionation stabilizer overheads; Low boiling point naphtha; [A complex combination of hydrocarbons obtained by the fractionation of light straight-run gasoline. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6.] 272-931-2 68921-08-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-273-00-3 Naphtha (petroleum), heavy straight run, arom.-contg.; Low boiling point naphtha; [A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 309-945-6 101631-20-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 309-945-6 101631-20-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-274-00-9 Naphtha (petroleum), full-range alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5 It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 220 °C (194 °F to 428 °F).] 265-066-7 64741-64-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5 It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 220 °C (194 °F to 428 °F).] 265-066-7 64741-64-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-275-00-4 Naphtha (petroleum), heavy alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 to C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 150 °C to 220 °C (302 °F to 428 °F).] 265-067-2 64741-65-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 to C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 150 °C to 220 °C (302 °F to 428 °F).] 265-067-2 64741-65-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-276-00-X Naphtha (petroleum), light alkylate; Low boiling point modified naphtha; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 90 °C to 160 °C (194 °F to 320 °F).] 265-068-8 64741-66-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 90 °C to 160 °C (194 °F to 320 °F).] 265-068-8 64741-66-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-277-00-5 Naphtha (petroleum), isomerization; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained from catalytic isomerization of straight chain paraffinic C4 through C6 hydrocarbons. It consists predominantly of saturated hydrocarbons such as isobutane, isopentane, 2,2-dimethylbutane, 2-methylpentane, and 3-methylpentane.] 265-073-5 64741-70-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from catalytic isomerization of straight chain paraffinic C4 through C6 hydrocarbons. It consists predominantly of saturated hydrocarbons such as isobutane, isopentane, 2,2-dimethylbutane, 2-methylpentane, and 3-methylpentane.] 265-073-5 64741-70-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-278-00-0 Naphtha (petroleum), solvent-refined light; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 265-086-6 64741-84-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 265-086-6 64741-84-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-279-00-6 Naphtha (petroleum), solvent-refined heavy; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-095-5 64741-92-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-095-5 64741-92-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-280-00-1 Raffinates (petroleum), catalytic reformer ethylene glycol-water countercurrent exts.; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinate from the UDEX extraction process on the catalytic reformer stream. It consists of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C9.] 270-088-5 68410-71-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-281-00-7 Raffinates (petroleum), reformer, Lurgi unit-sepd.; Low boiling point modified naphtha; [The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.] 270-349-3 68425-35-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-282-00-2 Naphtha (petroleum), full-range alkylate, butane-contg.; Low boiling point modified naphta; [A complex combination of hydrocarbons produced by the distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 with some butanes and boiling in the range of approximately 35 °C to 200 °C (95 °F to 428 °F).] 271-267-0 68527-27-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 with some butanes and boiling in the range of approximately 35 °C to 200 °C (95 °F to 428 °F).] 271-267-0 68527-27-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-283-00-8 Distillates (petroleum), naphtha steam cracking-derived, solvent-refined light hydrotreated; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained as the raffinates from a solvent extraction process of hydrotreated light distillate from steam-cracked naphtha.] 295-315-5 91995-53-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-284-00-3 Naphtha (petroleum), C4-12, butane-alkylate, isooctane-rich; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by alkylation of butanes. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12, rich in isooctane, and boiling in the range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-430-0 92045-49-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by alkylation of butanes. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12, rich in isooctane, and boiling in the range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-430-0 92045-49-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-285-00-9 Hydrocarbons, hydrotreated light naphtha distillates, solvent-refined; Low boiling point modified naphtha; [A combination of hydrocarbons obtained from the distillation of hydrotreated naphtha followed by a solvent extraction and distillation process. It consists predominantly of saturated hydrocarbons boiling in the range of approximately 94 °C to 99 °C (201 °F to 210 °F).] 295-436-3 92045-55-1 Carc. Cat. 2; R45 [A combination of hydrocarbons obtained from the distillation of hydrotreated naphtha followed by a solvent extraction and distillation process. It consists predominantly of saturated hydrocarbons boiling in the range of approximately 94 °C to 99 °C (201 °F to 210 °F).] 295-436-3 92045-55-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-286-00-4 Naphtha (petroleum), isomerization, C6-fraction; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by distillation of a gasoline which has been catalytically isomerized. It consists predominantly of hexane isomers boiling in the range of approximately 60 °C to 66 °C (140 °F to 151 °F).] 295-440-5 92045-58-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of a gasoline which has been catalytically isomerized. It consists predominantly of hexane isomers boiling in the range of approximately 60 °C to 66 °C (140 °F to 151 °F).] 295-440-5 92045-58-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-287-00-X Hydrocarbons, C6-7, naphtha-cracking, solvent-refined; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by the sorption of benzene from a catalytically fully hydrogenated benzene-rich hydrocarbon cut that was distillatively obtained from prehydrogenated cracked naphtha. It consists predominantly of paraffinic and naphthenic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 70 °C to 100 °C (158 °F to 212 °F).] 295-446-8 92045-64-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the sorption of benzene from a catalytically fully hydrogenated benzene-rich hydrocarbon cut that was distillatively obtained from prehydrogenated cracked naphtha. It consists predominantly of paraffinic and naphthenic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 70 °C to 100 °C (158 °F to 212 °F).] 295-446-8 92045-64-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-288-00-5 Hydrocarbons, C6-rich, hydrotreated light naphtha distillates, solvent-refined; Low boiling point modified naphtha; [A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65 °C to 70 °C (149 °F to 158 °F).] 309-871-4 101316-67-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65 °C to 70 °C (149 °F to 158 °F).] 309-871-4 101316-67-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-289-00-0 Naphtha (petroleum), heavy catalytic cracked; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by a distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-055-7 64741-54-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by a distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-055-7 64741-54-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-290-00-6 Naphtha (petroleum), light catalytic cracked; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-056-2 64741-55-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F). It contains a relatively large proportion of unsaturated hydrocarbons.] 265-056-2 64741-55-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-291-00-1 Hydrocarbons, C3-11, catalytic cracker distillates; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillations of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C11 and boiling in a range approximately up to 204 °C (400 °F).] 270-686-6 68476-46-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillations of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C11 and boiling in a range approximately up to 204 °C (400 °F).] 270-686-6 68476-46-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-292-00-7 Naphtha (petroleum), catalytic cracked light distd.; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.] 272-185-8 68783-09-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-293-00-2 Distillates (petroleum), naphtha steam cracking-derived, hydrotreated light arom.; Low boiling point cat-cracked naphtha.; [A complex combination of hydrocarbons obtained by treating a light distillate from steam-cracked naphtha. It consists predominantly of aromatic hydrocarbons.] 295-311-3 91995-50-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-294-00-8 Naphtha (petroleum), heavy catalytic cracked, sweetened; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting a catalytic cracked petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 60 °C to 200 °C (140 °F to 392 °F).] 295-431-6 92045-50-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a catalytic cracked petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 60 °C to 200 °C (140 °F to 392 °F).] 295-431-6 92045-50-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-295-00-3 Naphtha (petroleum), light catalytic cracked sweetened; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting naphtha from a catalytic cracking process to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons boiling in a range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-441-0 92045-59-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting naphtha from a catalytic cracking process to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons boiling in a range of approximately 35 °C to 210 °C (95 °F to 410 °F).] 295-441-0 92045-59-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-296-00-9 Hydrocarbons, C8-12, catalytic-cracking, chem. neutralized; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of a cut from the catalytic cracking process, having undergone an alkaline washing. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 295-794-0 92128-94-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of a cut from the catalytic cracking process, having undergone an alkaline washing. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).] 295-794-0 92128-94-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-297-00-4 Hydrocarbons, C8-12, catalytic cracker distillates; Low boiling point cat-cracked naphtha; [A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140 °C to 210 °C (284 °F to 410 °F).] 309-974-4 101794-97-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140 °C to 210 °C (284 °F to 410 °F).] 309-974-4 101794-97-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-298-00-X Hydrocarbons, C8-12, catalytic cracking, chem. neutralized, sweetened; Low boiling point cat-cracked naphtha 309-987-5 101896-28-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-299-00-5 Naphtha (petroleum), light catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 265-065-1 64741-63-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 265-065-1 64741-63-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-300-00-9 Naphtha (petroleum), heavy catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-070-9 64741-68-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-070-9 64741-68-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-301-00-4 Distillates (petroleum), catalytic reformed depentanizer; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons from the distillation of products from a catalytic reforming process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 63 °C (– 57 °F to 145 °F).] 270-660-4 68475-79-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from the distillation of products from a catalytic reforming process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 63 °C (– 57 °F to 145 °F).] 270-660-4 68475-79-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-302-00-X Hydrocarbons, C2-6, C6-8 catalytic reformer; Low boiling point cat-reformed naphtha 270-687-1 68476-47-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-303-00-5 Residues (petroleum), C6-8 catalytic reformer; Low boiling point cat-reformed naphtha; [A complex residuum from the catalytic reforming of C6-8 feed. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C6.] 270-794-3 68478-15-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-304-00-0 Naphtha (petroleum), light catalytic reformed, arom.-free; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained from distillation of products from a catalytic reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 35 °C to 120 °C (95 °F to 248 °F). It contains a relatively large proportion of branched chain hydrocarbons with the aromatic components removed.] 270-993-5 68513-03-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from distillation of products from a catalytic reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 35 °C to 120 °C (95 °F to 248 °F). It contains a relatively large proportion of branched chain hydrocarbons with the aromatic components removed.] 270-993-5 68513-03-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-305-00-6 Distillates (petroleum), catalytic reformed straight-run naphtha overheads; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by the catalytic reforming of straight-run naphtha followed by the fractionation of the total effluent. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.] 271-008-1 68513-63-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-306-00-1 Petroleum products, hydrofiner-powerformer reformates; Low boiling point cat-reformed naphtha; [The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27 °C to 210 °C (80 °F to 410 °F).] 271-058-4 68514-79-4 Carc. Cat. 2; R45 [The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27 °C to 210 °C (80 °F to 410 °F).] 271-058-4 68514-79-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-307-00-7 Naphtha (petroleum), full-range reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced by the distillation of the products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 272-895-8 68919-37-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of the products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 272-895-8 68919-37-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-308-00-2 Naphtha (petroleum), catalytic reformed; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 220 °C (90 °F to 430 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 273-271-8 68955-35-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 220 °C (90 °F to 430 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.] 273-271-8 68955-35-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-309-00-8 Distillates (petroleum), catalytic reformed hydrotreated light, C8-12 arom. fraction; Low boiling point cat-reformed naphtha; [A complex combination of alkylbenzenes obtained by the catalytic reforming of petroleum naphtha. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 160 °C to 180 °C (320 °F to 356 °F).] 285-509-8 85116-58-1 Carc. Cat. 2; R45 [A complex combination of alkylbenzenes obtained by the catalytic reforming of petroleum naphtha. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 160 °C to 180 °C (320 °F to 356 °F).] 285-509-8 85116-58-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-310-00-3 Aromatic hydrocarbons, C8, catalytic reforming-derived; Low boiling point cat-reformed naphtha 295-279-0 91995-18-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-311-00-9 Aromatic hydrocarbons, C7-12, C8-rich; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 (primarily C8) and can contain nonaromatic hydrocarbons, both boiling in the range of approximately 130 °C to 200 °C (266 °F to 392 °F).] 297-401-8 93571-75-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 (primarily C8) and can contain nonaromatic hydrocarbons, both boiling in the range of approximately 130 °C to 200 °C (266 °F to 392 °F).] 297-401-8 93571-75-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-312-00-4 Gasoline, C5-11, high-octane stabilised reformed; Low boiling point cat-reformed naphtha; [A complex high octane combination of hydrocarbons obtained by the catalytic dehydrogenation of a predominantly naphthenic naphtha. It consists predominantly of aromatics and non-aromatics having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 45 °C to 185 °C (113 °F to 365 °F).] 297-458-9 93572-29-3 Carc. Cat. 2; R45 [A complex high octane combination of hydrocarbons obtained by the catalytic dehydrogenation of a predominantly naphthenic naphtha. It consists predominantly of aromatics and non-aromatics having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 45 °C to 185 °C (113 °F to 365 °F).] 297-458-9 93572-29-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-313-00-X Hydrocarbons, C7-12, C≥9-arom.-rich, reforming heavy fraction; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 120 °C to 210 °C (248 °F to 380 °F) and C9 and higher aromatic hydrocarbons.] 297-465-7 93572-35-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 120 °C to 210 °C (248 °F to 380 °F) and C9 and higher aromatic hydrocarbons.] 297-465-7 93572-35-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-314-00-5 Hydrocarbons, C5-11, nonaroms.-rich, reforming light fraction; Low boiling point cat-reformed naphtha; [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 125 °C (94 °F to 257 °F), benzene and toluene.] 297-466-2 93572-36-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 125 °C (94 °F to 257 °F), benzene and toluene.] 297-466-2 93572-36-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-315-00-0 Foots oil (petroleum), silicic acid-treated; Foots oil; [A complex combination of hydrocarbons obtained by the treatment of Foots oil with silicic acid for removal of trace constituents and impurities. It consists predominantly of straight chain hydrocarbons having carbon numbers predominantly greater than C12.] 308-127-6 97862-77-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-316-00-6 Naphtha (petroleum), light thermal cracked; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons from distillation of products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately – 10 °C to 130 °C (14 °F to 266 °F).] 265-075-6 64741-74-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from distillation of products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately – 10 °C to 130 °C (14 °F to 266 °F).] 265-075-6 64741-74-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-317-00-1 Naphtha (petroleum), heavy thermal cracked; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons from distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 220 °C (148 °F to 428 °F).] 265-085-0 64741-83-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 220 °C (148 °F to 428 °F).] 265-085-0 64741-83-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-318-00-7 Distillates (petroleum), heavy arom.; Low boiling point thermally cracked naphtha; [The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5. This stream may contain benzene.] 267-563-4 67891-79-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-319-00-2 Distillates (petroleum), light arom.; Low boiling point thermally cracked naphtha; [The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5. This stream may contain benzene.] 267-565-5 67891-80-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-320-00-8 Distillates (petroleum), naphtha-raffinate pyrolyzate-derived, gasoline-blending; Low boiling point thermally cracked naphtha; [The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204 °C (400 °F).] 270-344-6 68425-29-6 Carc. Cat. 2; R45 [The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204 °C (400 °F).] 270-344-6 68425-29-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-321-00-3 Aromatic hydrocarbons, C6-8, naphtha-raffinate pyrolyzate-derived; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons obtained by the fractionation pyrolysis at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.] 270-658-3 68475-70-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the fractionation pyrolysis at 816 °C (1500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.] 270-658-3 68475-70-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-322-00-9 Distillates (petroleum), thermal cracked naphtha and gas oil; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by distillation of thermally cracked naphtha and/or gas oil. It consists predominantly of olefinic hydrocarbons having a carbon number of C5 and boiling in the range of approximately 33 °C to 60 °C (91 °F to 140 °F).] 271-631-9 68603-00-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of thermally cracked naphtha and/or gas oil. It consists predominantly of olefinic hydrocarbons having a carbon number of C5 and boiling in the range of approximately 33 °C to 60 °C (91 °F to 140 °F).] 271-631-9 68603-00-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-323-00-4 Distillates (petroleum), thermal cracked naphtha and gas oil, C5-dimer-contg.; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists predominantly of hydrocarbons having a carbon number of C5 with some dimerized C5 olefins and boiling in the range of approximately 33 °C to 184 °C (91 °F to 363 °F).] 271-632-4 68603-01-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists predominantly of hydrocarbons having a carbon number of C5 with some dimerized C5 olefins and boiling in the range of approximately 33 °C to 184 °C (91 °F to 363 °F).] 271-632-4 68603-01-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-324-00-X Distillates (petroleum), thermal cracked naphtha and gas oil, extractive; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists of paraffinic and olefinic hydrocarbons, predominantly isoamylenes such as 2-methyl-1-butene and 2-methyl-2-butene and boiling in the range of approximately 31 °C to 40 °C (88 °F to 104 °F).] 271-634-5 68603-03-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists of paraffinic and olefinic hydrocarbons, predominantly isoamylenes such as 2-methyl-1-butene and 2-methyl-2-butene and boiling in the range of approximately 31 °C to 40 °C (88 °F to 104 °F).] 271-634-5 68603-03-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-325-00-5 Distillates (petroleum), light thermal cracked, debutanized arom.; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons produced by the distillation of products from a thermal cracking process. It consists predominantly of aromatic hydrocarbons, primarily benzene.] 273-266-0 68955-29-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-326-00-0 Naphtha (petroleum), light thermal cracked, sweetened; Low boiling point thermally cracked naphtha; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate from the high temperature thermal cracking of heavy oil fractions to a sweetening process to convert mercaptans. It consists predominantly of aromatics, olefins and saturated hydrocarbons boiling in the range of approximately 20 °C to 100 °C (68 °F to 212 °F).] 295-447-3 92045-65-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate from the high temperature thermal cracking of heavy oil fractions to a sweetening process to convert mercaptans. It consists predominantly of aromatics, olefins and saturated hydrocarbons boiling in the range of approximately 20 °C to 100 °C (68 °F to 212 °F).] 295-447-3 92045-65-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-327-00-6 Naphtha (petroleum), hydrotreated heavy; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C13 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-150-3 64742-48-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C13 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-150-3 64742-48-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-328-00-1 Naphtha (petroleum), hydrotreated light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F).] 265-151-9 64742-49-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F).] 265-151-9 64742-49-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-329-00-7 Naphtha (petroleum), hydrodesulfurized light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-178-6 64742-73-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-178-6 64742-73-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-330-00-2 naphtha (petroleum), hydrodesulphurized heavy; Low boiling point hydrogen treated naphtha; [À complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-185-4 64742-82-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-185-4 64742-82-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R48/20-65 T R: 45-46-48/20-65 S: 45-53 P 649-331-00-8 Distillates (petroleum), hydrotreated middle, intermediate boiling; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by the distillation of products from a middle distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 127 °C to 188 °C (262 °F to 370 °F).] 270-092-7 68410-96-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of products from a middle distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 127 °C to 188 °C (262 °F to 370 °F).] 270-092-7 68410-96-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-332-00-3 Distillates (petroleum), light distillate hydrotreating process, low-boiling; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by the distillation of products from the light distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C9 and boiling in the range of approximately 3 °C to 194 °C (37 °F to 382 °F).] 270-093-2 68410-97-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of products from the light distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C9 and boiling in the range of approximately 3 °C to 194 °C (37 °F to 382 °F).] 270-093-2 68410-97-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-333-00-9 Distillates (petroleum), hydrotreated heavy naphtha, deisohexanizer overheads; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by distillation of the products from a heavy naphtha hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 68 °C (– 57 °F to 155 °F).] 270-094-8 68410-98-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of the products from a heavy naphtha hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 49 °C to 68 °C (– 57 °F to 155 °F).] 270-094-8 68410-98-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-334-00-4 Solvent naphtha (petroleum), light arom., hydrotreated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 270-988-8 68512-78-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 270-988-8 68512-78-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-335-00-X Naphtha (petroleum), hydrodesulfurized thermal cracked light; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by fractionation of hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 195 °C (73 °F to 383 °F).] 285-511-9 85116-60-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by fractionation of hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 195 °C (73 °F to 383 °F).] 285-511-9 85116-60-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-336-00-5 Naphtha (petroleum), hydrotreated light, cycloalkane-contg.; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from the distillation of a petroleum fraction. It consists predominantly of alkanes and cycloalkanes boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 285-512-4 85116-61-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the distillation of a petroleum fraction. It consists predominantly of alkanes and cycloalkanes boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 285-512-4 85116-61-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-337-00-0 Naphtha (petroleum), heavy steam-cracked, hydrogenated; Low boiling point hydrogen treated naphtha 295-432-1 92045-51-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-338-00-6 Naphtha (petroleum), hydrodesulfurized full-range; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 250 °C (86 °F to 482 °F).] 295-433-7 92045-52-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 250 °C (86 °F to 482 °F).] 295-433-7 92045-52-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-339-00-1 Naphtha (petroleum), hydrotreated light steam-cracked; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction, derived from a pyrolysis process, with hydrogen in the presence of a catalyst. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 295-438-4 92045-57-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by treating a petroleum fraction, derived from a pyrolysis process, with hydrogen in the presence of a catalyst. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).] 295-438-4 92045-57-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-340-00-7 Hydrocarbons, C4-12, naphtha-cracking, hydrotreated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by distillation from the product of a naphtha steam cracking process and subsequent catalytic selective hydrogenation of gum formers. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 230 °C (86 °F to 446 °F).] 295-443-1 92045-61-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation from the product of a naphtha steam cracking process and subsequent catalytic selective hydrogenation of gum formers. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 230 °C (86 °F to 446 °F).] 295-443-1 92045-61-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-341-00-2 Solvent naphtha (petroleum), hydrotreated light naphthenic; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of cycloparaffinic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 73 °C to 85 °C (163 °F to 185 °F).] 295-529-9 92062-15-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of cycloparaffinic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 73 °C to 85 °C (163 °F to 185 °F).] 295-529-9 92062-15-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-342-00-8 Naphtha (petroleum), light steam-cracked, hydrogenated; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons produced from the separation and subsequent hydrogenation of the products of a steam-cracking process to produce ethylene. It consists predominantly of saturated and unsaturated paraffins, cyclic paraffins and cyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately 50 °C to 200 °C (122 °F to 392 °F). The proportion of benzene hydrocarbons may vary up to 30 wt. % and the stream may also contain small amounts of sulfur and oxygenated compounds.] 296-942-7 93165-55-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced from the separation and subsequent hydrogenation of the products of a steam-cracking process to produce ethylene. It consists predominantly of saturated and unsaturated paraffins, cyclic paraffins and cyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately 50 °C to 200 °C (122 °F to 392 °F). The proportion of benzene hydrocarbons may vary up to 30 wt. % and the stream may also contain small amounts of sulfur and oxygenated compounds.] 296-942-7 93165-55-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-343-00-3 Hydrocarbons, C6-11, hydrotreated, dearomatized; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.] 297-852-0 93763-33-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-344-00-9 Hydrocarbons, C9-12, hydrotreated, dearomatized; Low boiling point hydrogen treated naphtha; [A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.] 297-853-6 93763-34-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-345-00-4 stoddard solvent; Low boiling point naphtha — unspecified; [À colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).] 232-489-3 8052-41-3 Carc. Cat. 2; R45 [A colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).] 232-489-3 8052-41-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R48/20-65 T R: 45-46-48/20-65 S: 45-53 P 649-346-00-X Natural gas condensates (petroleum); Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons separated as a liquid from natural gas in a surface separator by retrograde condensation. It consists mainly of hydrocarbons having carbon numbers predominantly in the range of C2 to C20. It is a liquid at atmospheric temperature and pressure.] 265-047-3 64741-47-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons separated as a liquid from natural gas in a surface separator by retrograde condensation. It consists mainly of hydrocarbons having carbon numbers predominantly in the range of C2 to C20. It is a liquid at atmospheric temperature and pressure.] 265-047-3 64741-47-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-347-00-5 Natural gas (petroleum), raw liq. mix; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons separated as a liquid from natural gas in a gas recycling plant by processes such as refrigeration or absorption. It consists mainly of saturated aliphatic hydrocarbons having carbon numbers in the range of C2 through C8.] 265-048-9 64741-48-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-348-00-0 Naphtha (petroleum), light hydrocracked; Low boiling naphtha - unspecified; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C4 through C10, and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-071-4 64741-69-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C4 through C10, and boiling in the range of approximately – 20 °C to 180 °C (– 4 °F to 356 °F).] 265-071-4 64741-69-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-349-00-6 Naphtha (petroleum), heavy hydrocracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12, and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F).] 265-079-8 64741-78-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12, and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F).] 265-079-8 64741-78-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-350-00-1 Naphtha (petroleum), sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately – 10 °C to 230 °C (14 °F to 446 °F).] 265-089-2 64741-87-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately – 10 °C to 230 °C (14 °F to 446 °F).] 265-089-2 64741-87-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-351-00-7 Naphtha (petroleum), acid-treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-115-2 64742-15-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).] 265-115-2 64742-15-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-352-00-2 Naphtha (petroleum), chemically neutralized heavy; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-122-0 64742-22-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).] 265-122-0 64742-22-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-353-00-8 Naphtha (petroleum), chemically neutralized light; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-123-6 64742-23-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 190 °C (– 4 °F to 374 °F).] 265-123-6 64742-23-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-354-00-3 Naphtha (petroleum), catalytic dewaxed; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from the catalytic dewaxing of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 265-170-2 64742-66-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the catalytic dewaxing of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).] 265-170-2 64742-66-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-355-00-9 Naphtha (petroleum), light steam-cracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F). This stream is likely to contain 10 vol. % or more benzene.] 265-187-5 64742-83-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (– 4 °F to 374 °F). This stream is likely to contain 10 vol. % or more benzene.] 265-187-5 64742-83-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-356-00-4 Solvent naphtha (petroleum), light arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 265-199-0 64742-95-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).] 265-199-0 64742-95-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-357-00-X Aromatic hydrocarbons, C6-10, acid-treated, neutralized; Low boiling point naphtha - unspecified 268-618-5 68131-49-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-358-00-5 Distillates (petroleum), C3-5, 2-methyl-2-butene-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons from the distillation of hydrocarbons usually ranging in carbon numbers from C3 through C5, predominantly isopentane and 3-methyl-1-butene. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C5, predominantly 2-methyl-2-butene.] 270-725-7 68477-34-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons from the distillation of hydrocarbons usually ranging in carbon numbers from C3 through C5, predominantly isopentane and 3-methyl-1-butene. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C5, predominantly 2-methyl-2-butene.] 270-725-7 68477-34-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 … 48 unchanged lines … S: 53-45 H P 649-366-00-9 Naphtha (petroleum), full-range coker; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C15 and boiling in the range of approximately 43 °C to 250 °C (110 °F-500 °F).] 270-991-4 68513-02-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C15 and boiling in the range of approximately 43 °C to 250 °C (110 °F-500 °F).] 270-991-4 68513-02-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-367-00-4 Naphtha (petroleum), steam-cracked middle arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by the distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 130 °C to 220 °C (266 °F to 428 °F).] 271-138-9 68516-20-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by the distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 130 °C to 220 °C (266 °F to 428 °F).] 271-138-9 68516-20-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-368-00-X Naphtha (petroleum), clay-treated full-range straight-run; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons resulting from treatment of full-range straight-run naphtha with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 429 °F).] 271-262-3 68527-21-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons resulting from treatment of full-range straight-run naphtha with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately – 20 °C to 220 °C (– 4 °F to 429 °F).] 271-262-3 68527-21-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-369-00-5 Naphtha (petroleum), clay-treated light straight-run; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons resulting from treatment of light straight-run naphtha with a natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 93 °C to 180 °C (200 °F to 356 °F).] 271-263-9 68527-22-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons resulting from treatment of light straight-run naphtha with a natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 93 °C to 180 °C (200 °F to 356 °F).] 271-263-9 68527-22-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-370-00-0 Naphtha (petroleum), light steam-cracked arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110 °C to 165 °C (230 °F to 329 °F).] 271-264-4 68527-23-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110 °C to 165 °C (230 °F to 329 °F).] 271-264-4 68527-23-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-371-00-6 Naphtha (petroleum), light steam-cracked, debenzenized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 80 °C to 218 °C (176 °F to 424 °F).] 271-266-5 68527-26-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 80 °C to 218 °C (176 °F to 424 °F).] 271-266-5 68527-26-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-372-00-1 Naphtha (petroleum), arom.-contg.; Low boiling point naphtha - unspecified 271-635-0 68603-08-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-373-00-7 Gasoline, pyrolysis, debutanizer bottoms; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from the fractionation of depropanizer bottoms. It consists of hydrocarbons having carbon numbers predominantly greater than C5.] 271-726-5 68606-10-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-374-00-2 Naphtha (petroleum), light, sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 20 °C to 100 °C (– 4 °F to 212 °F).] 272-206-0 68783-66-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately – 20 °C to 100 °C (– 4 °F to 212 °F).] 272-206-0 68783-66-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-375-00-8 Natural gas condensates; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons separated and/or condensed from natural gas during transportation and collected at the wellhead and/or from the production, gathering, transmission, and distribution pipelines in deeps, scrubbers, etc. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C2 through C8.] 272-896-3 68919-39-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-376-00-3 Distillates (petroleum), naphtha unifiner stripper; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons produced by stripping the products from the naphtha unifiner. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.] 272-932-8 68921-09-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-377-00-9 Naphtha (petroleum), catalytic reformed light, arom.-free fraction; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons remaining after removal of aromatic compounds from catalytic reformed light naphtha in a selective absorption process. It consists predominantly of paraffinic and cyclic compounds having carbon numbers predominantly in the range of C5 to C8 and boiling in the range of approximately 66 °C to 121 °C (151 °F to 250 °F).] 285-510-3 85116-59-2 Carc. Cat. 2; R45 [A complex combination of hydrocarbons remaining after removal of aromatic compounds from catalytic reformed light naphtha in a selective absorption process. It consists predominantly of paraffinic and cyclic compounds having carbon numbers predominantly in the range of C5 to C8 and boiling in the range of approximately 66 °C to 121 °C (151 °F to 250 °F).] 285-510-3 85116-59-2 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-378-00-4 Gasoline; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons consisting primarily of paraffins, cycloparaffins, aromatic and olefinic hydrocarbons having carbon numbers predominantly greater than C3 and boiling in the range of 30 °C to 260 °C (86 °F to 500 °F).] 289-220-8 86290-81-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons consisting primarily of paraffins, cycloparaffins, aromatic and olefinic hydrocarbons having carbon numbers predominantly greater than C3 and boiling in the range of 30 °C to 260 °C (86 °F to 500 °F).] 289-220-8 86290-81-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-379-00-X Aromatic hydrocarbons, C7-8, dealkylation products, distn. residues; Low boiling point naphtha - unspecified 292-698-0 90989-42-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-380-00-5 Hydrocarbons, C4-6, depentanizer lights, arom. hydrotreater; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as first runnings from the depentanizer column before hydrotreatment of the aromatic charges. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C6, predominantly pentanes and pentenes, and boiling in the range of approximately 25 °C to 40 °C (77 °F to 104 °F).] 295-298-4 91995-38-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as first runnings from the depentanizer column before hydrotreatment of the aromatic charges. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C6, predominantly pentanes and pentenes, and boiling in the range of approximately 25 °C to 40 °C (77 °F to 104 °F).] 295-298-4 91995-38-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-381-00-0 Distillates (petroleum), heat-soaked steam-cracked naphtha, C5-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of heat-soaked steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C4 through C6, predominantly C5.] 295-302-4 91995-41-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-382-00-6 Extracts (petroleum), catalytic reformed light naphtha solvent; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained as the extract from the solvent extraction of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C8 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 295-331-2 91995-68-5 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained as the extract from the solvent extraction of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C8 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).] 295-331-2 91995-68-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-383-00-1 Naphtha (petroleum), hydrodesulfurized light, dearomatized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of hydrodesulfurized and dearomatized light petroleum fractions. It consists predominantly of C7 paraffins and cycloparaffins boiling in a range of approximately 90 °C to 100 °C (194 °F to 212 °F).] 295-434-2 92045-53-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of hydrodesulfurized and dearomatized light petroleum fractions. It consists predominantly of C7 paraffins and cycloparaffins boiling in a range of approximately 90 °C to 100 °C (194 °F to 212 °F).] 295-434-2 92045-53-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-384-00-7 Naphtha (petroleum), light, C5-rich, sweetened; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C5, predominantly C5, and boiling in the range of approximately minus 10 °C to 35 °C (14 °F to 95 °F).] 295-442-6 92045-60-8 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C5, predominantly C5, and boiling in the range of approximately minus 10 °C to 35 °C (14 °F to 95 °F).] 295-442-6 92045-60-8 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-385-00-2 Hydrocarbons, C8-11, naphtha-cracking, toluene cut; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation from prehydrogenated cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C11 and boiling in the range of approximately 130 °C to 205 °C (266 °F to 401 °F).] 295-444-7 92045-62-0 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation from prehydrogenated cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C11 and boiling in the range of approximately 130 °C to 205 °C (266 °F to 401 °F).] 295-444-7 92045-62-0 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-386-00-8 Hydrocarbons, C4-11, naphtha-cracking, arom.-free; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from prehydrogenated cracked naphtha after distillative separation of benzene- and toluene-containing hydrocarbon cuts and a higher boiling fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 205 °C (86 °F to 401 °F).] 295-445-2 92045-63-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from prehydrogenated cracked naphtha after distillative separation of benzene- and toluene-containing hydrocarbon cuts and a higher boiling fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 205 °C (86 °F to 401 °F).] 295-445-2 92045-63-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-387-00-3 Naphtha (petroleum), light heat-soaked, steam-cracked; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the fractionation of steam cracked naphtha after recovery from a heat soaking process. It consists predominantly of hydrocarbons having a carbon number predominantly in the range of C4 through C6 and boiling in the range of approximately 0 °C to 80 °C (32 °F to 176 °F).] 296-028-8 92201-97-3 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the fractionation of steam cracked naphtha after recovery from a heat soaking process. It consists predominantly of hydrocarbons having a carbon number predominantly in the range of C4 through C6 and boiling in the range of approximately 0 °C to 80 °C (32 °F to 176 °F).] 296-028-8 92201-97-3 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-388-00-9 Distillates (petroleum), C6-rich; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained from the distillation of a petroleum feedstock. It consists predominantly of hydrocarbons having carbon numbers of C5 through C7, rich in C6, and boiling in the range of approximately 60 °C to 70 °C (140 °F to 158 °F).] 296-903-4 93165-19-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained from the distillation of a petroleum feedstock. It consists predominantly of hydrocarbons having carbon numbers of C5 through C7, rich in C6, and boiling in the range of approximately 60 °C to 70 °C (140 °F to 158 °F).] 296-903-4 93165-19-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-389-00-4 Gasoline, pyrolysis, hydrogenated; Low boiling point naphtha-unspecified; [A distillation fraction from the hydrogenation of pyrolysis gasoline boiling in the range of approximately 20 °C to 200 °C (68 °F to 392 °F).] 302-639-3 94114-03-1 Carc. Cat. 2; R45 [A distillation fraction from the hydrogenation of pyrolysis gasoline boiling in the range of approximately 20 °C to 200 °C (68 °F to 392 °F).] 302-639-3 94114-03-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-390-00-X Distillates (petroleum), steam-cracked, C8-12 fraction, polymd., distn. lights; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of the polymerized C8 through C12 fraction from steam-cracked petroleum distillates. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C12.] 305-750-5 95009-23-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-391-00-5 Extracts (petroleum) heavy naphtha solvent, clay-treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment of heavy naphthic solvent petroleum extract with bleaching earth. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 80 °C to 180 °C (175 °F to 356 °F).] 308-261-5 97926-43-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the treatment of heavy naphthic solvent petroleum extract with bleaching earth. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 80 °C to 180 °C (175 °F to 356 °F).] 308-261-5 97926-43-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-392-00-0 Naphtha (petroleum), light steam-cracked, debenzenized, thermally treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment and distillation of debenzenized light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 95 °C to 200 °C (203 °F to 392 °F).] 308-713-1 98219-46-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the treatment and distillation of debenzenized light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 95 °C to 200 °C (203 °F to 392 °F).] 308-713-1 98219-46-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-393-00-6 Naphtha (petroleum), light steam-cracked, thermally treated; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the treatment and distillation of light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 35 °C to 80 °C (95 °F to 176 °F).] 308-714-7 98219-47-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the treatment and distillation of light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 35 °C to 80 °C (95 °F to 176 °F).] 308-714-7 98219-47-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-394-00-1 Distillates (petroleum), C7-9, C8-rich, hydrodesulfurized dearomatized; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 °C to 130 °C (248 °F to 266 °F).] 309-862-5 101316-56-7 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 °C to 130 °C (248 °F to 266 °F).] 309-862-5 101316-56-7 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-395-00-7 Hydrocarbons, C6-8, hydrogenated sorption-dearomatized, toluene raffination; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80 °C to 135 °C (176 °F to 275 °F).] 309-870-9 101316-66-9 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80 °C to 135 °C (176 °F to 275 °F).] 309-870-9 101316-66-9 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-396-00-2 Naphtha (petroleum), hydrodesulfurised full-range coker; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 196 °C (73 °F to 385 °F).] 309-879-8 101316-76-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 196 °C (73 °F to 385 °F).] 309-879-8 101316-76-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-397-00-8 Naphtha (petroleum), sweetened light; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 °C to 130 °C (68 °F to 266 °F).] 309-976-5 101795-01-1 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 °C to 130 °C (68 °F to 266 °F).] 309-976-5 101795-01-1 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-398-00-3 Hydrocarbons, C3-6, C5-rich, steam-cracked naphtha; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly C5.] 310-012-0 102110-14-5 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-399-00-9 Hydrocarbons, C5-rich, dicyclopentadiene-contg.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30 °C to 170 °C (86 °F to 338 °F).] 310-013-6 102110-15-6 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30 °C to 170 °C (86 °F to 338 °F).] 310-013-6 102110-15-6 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 S: 53-45 H P 649-400-00-2 Residues (petroleum), steam-cracked light, arom.; Low boiling point naphtha - unspecified; [A complex combination of hydrocarbons obtained by the distillation of the products of steam cracking or similar processes after taking off the very light products resulting in a residue starting with hydrocarbons having carbon numbers greater than C5. It consists predominantly of aromatic hydrocarbons having carbon numbers greater than C5 and boiling above approximately 40 °C (104 °F).] 310-057-6 102110-55-4 Carc. Cat. 2; R45 [A complex combination of hydrocarbons obtained by the distillation of the products of steam cracking or similar processes after taking off the very light products resulting in a residue starting with hydrocarbons having carbon numbers greater than C5. It consists predominantly of aromatic hydrocarbons having carbon numbers greater than C5 and boiling above approximately 40 °C (104 °F).] 310-057-6 102110-55-4 Carc. Cat. 2; R45 Muta. Cat. 2; R46 Xn; R65 T R: 45-46-65 … 18 unchanged lines … S: 53-45 H P 649-404-00-4 Kerosine (petroleum); Straight run kerosine; [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (320 oF to 554 oF).] 232-366-4 8008-20-6 Xn; R65 Xn [A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (320 oF to 554 oF).] 232-366-4 8008-20-6 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-405-00-X solvent naphtha (petroleum), medium aliph.; Straight run kerosine; [À complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).] 265-191-7 64742-88-7 Xn; R48/20-65 Xn [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).] 265-191-7 64742-88-7 Xn; R48/20-65 Xn R: 48/20-65 S: (2-)23-24-62 649-406-00-5 Solvent naphtha (petroleum) heavy aliph.; Straight run kerosine; [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C11 through C16 and boiling in the range of approximately 190 oC to 290 oC (374 oF to 554 oF).] 265-200-4 64742-96-7 Xn; R65 Xn [A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C11 through C16 and boiling in the range of approximately 190 oC to 290 oC (374 oF to 554 oF).] 265-200-4 64742-96-7 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-407-00-0 Kerosine (petroleum), straight-run wide-cut; Straight run kerosine; [A complex combination of hydrocarbons obtained as a wide cut hydrocarbon fuel cut from atmospheric distillation and boiling in the range of approximately 70 oC to 220 oC (158 oF to 428 oF).] 295-418-5 92045-37-9 Xn; R65 Xn [A complex combination of hydrocarbons obtained as a wide cut hydrocarbon fuel cut from atmospheric distillation and boiling in the range of approximately 70 oC to 220 oC (158 oF to 428 oF).] 295-418-5 92045-37-9 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-408-00-6 Distillates (petroleum), steam-cracked; Cracked kerosine; [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C7 through C16 and boiling in the range of approximately 90 oC to 290 oC (190 oF to 554 oF).] 265-194-3 64742-91-2 Xn; R65 Xn [A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C7 through C16 and boiling in the range of approximately 90 oC to 290 oC (190 oF to 554 oF).] 265-194-3 64742-91-2 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-409-00-1 Distillates (petroleum), cracked stripped steam-cracked petroleum distillates, C8-10 fraction; Cracked kerosine; [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists of hydro-carbons having carbon numbers in the range of C8 through C10 and boiling in the range of approximately 129 oC to 194 oC (264 oF to 382 oF).] 270-728-3 68477-39-4 Xn; R65 Xn [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists of hydro-carbons having carbon numbers in the range of C8 through C10 and boiling in the range of approximately 129 oC to 194 oC (264 oF to 382 oF).] 270-728-3 68477-39-4 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-410-00-7 Distillates (petroleum), cracked stripped steam-cracked petroleum distillates, C10-12 fraction; Cracked kerosine; [A complex combination of hydrocarbons obtained by distilling cracked stripped steam-cracked distillates. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C10 through C12.] 270-729-9 68477-40-7 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-411-00-2 Distillates (petroleum), steam-cracked, C8-12 fraction; Cracked kerosine; [A complex combination of organic compounds obtained by the distillation of products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C8 through C12.] 270-737-2 68477-54-3 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-412-00-8 Kerosine (petroleum), hydrodesulfurized thermal cracked; Cracked kerosine; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons predominantly in the range of C8 to C16 and boiling in the range of approximately 120 oC to 283 oC (284 oF to 541 oF).] 285-507-7 85116-55-8 Xn; R65 Xn [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons predominantly in the range of C8 to C16 and boiling in the range of approximately 120 oC to 283 oC (284 oF to 541 oF).] 285-507-7 85116-55-8 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-413-00-3 Aromtic hydrocarbons, C≥10, steam-cracking, hydrotreated; Cracked kerosine; [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly greater than C10 and boiling in the range of approximately 150 oC to 320 oC (302 oF to 608 oF).] 292-621-0 90640-98-5 Xn; R65 Xn [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly greater than C10 and boiling in the range of approximately 150 oC to 320 oC (302 oF to 608 oF).] 292-621-0 90640-98-5 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-414-00-9 Naphtha (petroleum), steam-cracked, hydrotreated, C9-10-arom.-rich; Cracked kerosine; [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process thereafter treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C9 through C10 and boiling in the range of approximately 140 oC to 200 oC (284 oF to 392 oF).] 292-637-8 90641-13-7 Xn; R65 Xn [A complex combination of hydrocarbons produced by the distillation of the products from a steam cracking process thereafter treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers in the range of C9 through C10 and boiling in the range of approximately 140 oC to 200 oC (284 oF to 392 oF).] 292-637-8 90641-13-7 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-415-00-4 Distillates (petroleum), thermal-cracked, alkylarom. hydrocarbon-rich; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF.] 309-866-7 101316-61-4 Xn; R65 Xn [A complex combination of hydrocarbons obtained by distillation of thermal-cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF.] 309-866-7 101316-61-4 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-416-00-X Distillates (petroleum), catalytic cracked heavy tar light; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of catalytic cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-938-8 101631-13-4 Xn; R65 Xn [A complex combination of hydrocarbons obtained by distillation of catalytic cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-938-8 101631-13-4 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-417-00-5 Solvent naphtha (petroleum), hydrocracked heavy arom.; Cracked kerosine; [A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235 oC to 290 oC (455 oF to 554 oF).] 309-881-9 101316-80-7 Xn; R65 Xn [A complex combination of hydrocarbons obtained by the distillation of hydrocracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 235 oC to 290 oC (455 oF to 554 oF).] 309-881-9 101316-80-7 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-418-00-0 Distillates (petroleum), steam-cracked heavy tar light; Cracked kerosine; [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-940-9 101631-15-6 Xn; R65 Xn [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy tars. It consists predominantly of highly alkylated aromatic hydrocarbons boiling in the range of approximately 100 oC to 250 oC (212 oF to 482 oF).] 309-940-9 101631-15-6 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-419-00-6 Distillates (petroleum), alkylate; Kerosine — unspecified; [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydro-carbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 205 oC to 320 oC (401 oF to 608 oF).] 265-074-0 64741-73-7 Xn; R65 Xn [A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydro-carbons having carbon numbers predominantly in the range of C11 through C17 and boiling in the range of approximately 205 oC to 320 oC (401 oF to 608 oF).] 265-074-0 64741-73-7 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-420-00-1 Extracts (petroleum), heavy naphtha solvent; Kerosine — unspecified; [A complex combination of hydrocarbons obtained as the extract from a solvent extraction process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 oC to 220 oC (194 oF to 428 oF).] 265-099-7 64741-98-6 Xn; R65 Xn [A complex combination of hydrocarbons obtained as the extract from a solvent extraction process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 oC to 220 oC (194 oF to 428 oF).] 265-099-7 64741-98-6 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-421-00-7 Distillates (petroleum), chemically neutralized light; Kerosine — unspecified; [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-132-5 64742-31-0 Xn; R65 Xn [A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-132-5 64742-31-0 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-422-00-2 Distillates (petroleum), hydrotreated light; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-149-8 64742-47-8 Xn; R65 Xn [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-149-8 64742-47-8 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-423-00-8 Kerosine (petroleum), hydrodesulfurized; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-184-9 64742-81-0 Xn; R65 Xn [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 150 oC to 290 oC (302 oF to 554 oF).] 265-184-9 64742-81-0 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-424-00-3 Solvent naphtha (petroleum), heavy arom.; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 165 oC to 290 oC (330 oF to 554 oF).] 265-198-5 64742-94-5 Xn; R65 Xn [A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of approximately 165 oC to 290 oC (330 oF to 554 oF).] 265-198-5 64742-94-5 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-425-00-9 Naphtha (petroleum), heavy coker; Kerosine — unspecified; [A complex combination of hydrocarbons from the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C15 and boiling in the range of approximately 157 oC to 288 oC (315 oF to 550 oF).] 269-778-9 68333-23-3 Xn; R65 Xn [A complex combination of hydrocarbons from the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C15 and boiling in the range of approximately 157 oC to 288 oC (315 oF to 550 oF).] 269-778-9 68333-23-3 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-426-00-4 Naphtha (petroleum), catalytic reformed hydrodesulfurized heavy, arom. fraction; Kerosine — unspecified; [A complex combination of hydrocarbons produced by fractionation from catalytically reformed hydrodesulfurized naphtha. It consists predominantly of aromatic hydrocarbons having carbon numbers predominently in the range of C7 to C 13 and boiling in the range of approximately 98 oC to 218 oC (208 oF to 424 oF).] 285-508-2 85116-57-0 Xn; R65 Xn [A complex combination of hydrocarbons produced by fractionation from catalytically reformed hydrodesulfurized naphtha. It consists predominantly of aromatic hydrocarbons having carbon numbers predominently in the range of C7 to C 13 and boiling in the range of approximately 98 oC to 218 oC (208 oF to 424 oF).] 285-508-2 85116-57-0 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-427-00-X Kerosine (petroleum), sweetened; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of 130 oC to 290 oC (266 oF to 554 oF).] 294-799-5 91770-15-9 Xn; R65 Xn [A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C16 and boiling in the range of 130 oC to 290 oC (266 oF to 554 oF).] 294-799-5 91770-15-9 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-428-00-5 Kerosine (petroleum), solvent-refined sweetened; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from a petroleum stock by solvent refining and sweetening and boiling in the range of approximately 150 oC to 260 oC (302 oF to 500 oF).] 295-416-4 92045-36-8 Xn; R65 Xn [A complex combination of hydrocarbons obtained from a petroleum stock by solvent refining and sweetening and boiling in the range of approximately 150 oC to 260 oC (302 oF to 500 oF).] 295-416-4 92045-36-8 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-429-00-0 Hydrocarbons, C9-16, hydrotreated, dearomatized; Kerosine — unspecified; [A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.] 297-854-1 93763-35-0 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-430-00-6 Kerosine (petroleum), solvent-refined hydrodesulfurized; Kerosine — unspecified 307-033-2 97488-94-3 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-431-00-1 Distillates (petroleum), hydrodesulfurized full-range middle coker; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120 oC to 283 oC (248 oF to 541 oF).] 309-864-6 101316-58-9 Xn; R65 Xn [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C16 and boiling in the range of approximately 120 oC to 283 oC (248 oF to 541 oF).] 309-864-6 101316-58-9 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-432-00-7 Solvent naphtha (petroleum), hydrodesulfurized heavy arom.; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180 oC to 240 oC (356 oF to 464 oF).] 309-882-4 101316-81-8 Xn; R65 Xn [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 180 oC to 240 oC (356 oF to 464 oF).] 309-882-4 101316-81-8 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-433-00-2 Solvent naphtha (petroleum), hydrodesulfurized medium; Kerosine — unspecified; [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175 oC to 220 oC (347 oF to 428 oF).] 309-884-5 101316-82-9 Xn; R65 Xn [A complex combination of hydrocarbons obtained by the catalytic hydrodesulfurization of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C10 through C13 and boiling in the range of approximately 175 oC to 220 oC (347 oF to 428 oF).] 309-884-5 101316-82-9 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-434-00-8 Kerosine (petroleum), hydrotreated; Kerosine — unspecified; [A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230 oC to 270 oC (446 oF to 518 oF).] 309-944-0 101631-19-0 Xn; R65 Xn [A complex combination of hydrocarbons obtained from the distillation of petroleum and subsequent hydrotreatment. It consists predominantly of alkanes, cycloalkanes and alkylbenzenes having carbon numbers predominantly in the range of C12 through C16 and boiling in the range of approximately 230 oC to 270 oC (446 oF to 518 oF).] 309-944-0 101631-19-0 Xn; R65 Xn R: 65 S: (2-)23-24-62 H 649-435-00-3 Distillates (petroleum), light catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 265-060-4 64741-59-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 265-060-4 64741-59-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-436-00-9 Distillates (petroleum), intermediate catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 265-062-5 64741-60-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C11 through C30 and boiling in the range of approximately 205 oC to 450 oC (401 oF to 842 oF). It contains a relatively large proportion of tricyclic aromatic hydrocarbons.] 265-062-5 64741-60-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-437-00-4 Distillates (petroleum), light hydrocracked; Cracked gasoil; [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C10 through C18 and boiling in the range of approximately 160 oC to 320 oC (320 oF to 608 oF).] 265-078-2 64741-77-1 Carc. Cat. 3; R40 Xn [A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C10 through C18 and boiling in the range of approximately 160 oC to 320 oC (320 oF to 608 oF).] 265-078-2 64741-77-1 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 649-438-00-X Distillates (petroleum), light thermal cracked; Cracked gasoil; [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C10 through C22 and boiling in the range of approximately 160 oC to 370 oC (320 oF to 698 oF).] 265-084-5 64741-82-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C10 through C22 and boiling in the range of approximately 160 oC to 370 oC (320 oF to 698 oF).] 265-084-5 64741-82-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-439-00-5 Distillates (petroleum), hydrodesulfurized light catalytic cracked; Cracked gasoil; [A complex combination of hydrocarbons obtained by treating light catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 269-781-5 68333-25-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating light catalytic cracked distillates with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150 oC to 400 oC (302 oF to 752 oF). It contains a relatively large proportion of bicyclic aromatic hydrocarbons.] 269-781-5 68333-25-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-440-00-0 Distillates (petroleum), light steam-cracked naphtha; Cracked gasoil; [A complex combination of hydrocarbons from the multiple distillation of products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C10 through C18.] 270-662-5 68475-80-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-441-00-6 Distillates (petroleum), cracked steam-cracked petroleum distillates; Cracked gasoil; [A complex combination of hydrocarbons produced by distilling cracked steam cracked distillate and/or its fractionation products. It consists of hydrocarbons having carbon numbers predominently in the range of C10 to low molecular weight polymers.] 270-727-8 68477-38-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-442-00-1 Gas oils (petroleum), steam-cracked; Cracked gasoil; [A complex combination of hydrocarbons produced by distillation of the products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C9 and boiling in the range of from approximately 205 oC to 400 oC (400 oF to 752 oF).] 271-260-2 68527-18-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by distillation of the products from a steam cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C9 and boiling in the range of from approximately 205 oC to 400 oC (400 oF to 752 oF).] 271-260-2 68527-18-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-443-00-7 Distillates (petroleum), hydrodesulfurized thermal cracked middle; Cracked gasoil; [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized themal cracker distillate stocks. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 to C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 285-505-6 85116-53-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized themal cracker distillate stocks. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C11 to C25 and boiling in the range of approximately 205 oC to 400 oC (401 oF to 752 oF).] 285-505-6 85116-53-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-444-00-2 Gas oils (petroleum), thermal-cracked, hydrodesulfurized; Cracked gasoil 295-411-7 92045-29-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-445-00-8 Residues (petroleum), hydrogenated steam-cracked naphtha; Cracked gasoil; [A complex combination of hydrocarbons obtained as a residual fraction from the distillation of hydrotreated steam-cracked naphtha. It consists predominantly of hydrocarbons boiling in the range of approximately 200 oC to 350 oC (32 oF to 662 oF).] 295-514-7 92062-00-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a residual fraction from the distillation of hydrotreated steam-cracked naphtha. It consists predominantly of hydrocarbons boiling in the range of approximately 200 oC to 350 oC (32 oF to 662 oF).] 295-514-7 92062-00-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-446-00-3 Residues (petroleum), steam-cracked naphtha distn.; Cracked gasoil; [A complex combination of hydrocarbons obtained as a column bottom from the separation of effluents from steam cracking naphtha at a high temperature. It boils in the range of approximately 147 oC to 300 oC (297 oF to 572 oF) and produces a finished oil having a viscosity of 18cSt at 50 oC.] 295-517-3 92062-04-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as a column bottom from the separation of effluents from steam cracking naphtha at a high temperature. It boils in the range of approximately 147 oC to 300 oC (297 oF to 572 oF) and produces a finished oil having a viscosity of 18cSt at 50 oC.] 295-517-3 92062-04-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-447-00-9 Distillates (petroleum), light catalytic cracked, thermally degraded; Cracked gasoil; [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 190 oC to 340 oC (374 oF to 644 oF). This stream is likely to contain organic sulfur compounds.] 295-991-1 92201-60-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process which has been used as a heat transfer fluid. It consists predominantly of hydrocarbons boiling in the range of approximately 190 oC to 340 oC (374 oF to 644 oF). This stream is likely to contain organic sulfur compounds.] 295-991-1 92201-60-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-448-00-4 Residues (petroleum), steam-cracked heat-soaked naphtha; Cracked gasoil; [A complex combination of hydrocarbons obtained as residue from the distillation of steam cracked heat soaked naphtha and boiling in the range of approximately 150 oC to 350 oC (302 oF to 662 oF).] 297-905-8 93763-85-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as residue from the distillation of steam cracked heat soaked naphtha and boiling in the range of approximately 150 oC to 350 oC (302 oF to 662 oF).] 297-905-8 93763-85-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-449-00-X Hydrocarbons, C16-20, solvent-dewaxed hydrocracked paraffinic distn. residue; Cracked gasoil; [A complex combination of hydrocarbons obtained by solvent dewaxing of a distillation residue from a hydrocracked paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 360 oC to 500 oC (680 oF to 932 oF). It produces a finished oil having a viscosity of 4,5 cSt at approximately 100 oC (212 oF).] 307-662-2 97675-88-2 Carc. Cat. 3; R40 Xn [A complex combination of hydrocarbons obtained by solvent dewaxing of a distillation residue from a hydrocracked paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C20 and boiling in the range of approximately 360 oC to 500 oC (680 oF to 932 oF). It produces a finished oil having a viscosity of 4,5 cSt at approximately 100 oC (212 oF).] 307-662-2 97675-88-2 Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 H 649-450-00-5 Gas oils (petroleum), light vacuum, thermal-cracked hydrodesulfurized; Cracked gasoil; [A complex combination of hydrocarbons obtained by catalytic dehydrosulfurization of thermal-cracked light vacuum petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C20 and boiling in the range of approximately 270 oC to 370 oC (518 oF to 698 oF).] 308-278-8 97926-59-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by catalytic dehydrosulfurization of thermal-cracked light vacuum petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C20 and boiling in the range of approximately 270 oC to 370 oC (518 oF to 698 oF).] 308-278-8 97926-59-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-451-00-0 Distillates (petroleum), hydrodesulfurized middle coker; Cracked gasoil; [A complex combination of hydrocarbons by fractionation from hydrodesulfurised coker distillate stocks. Is consists of hydro-carbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200 oC to 360 oC (392 oF to 680 oF).] 309-865-1 101316-59-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons by fractionation from hydrodesulfurised coker distillate stocks. Is consists of hydro-carbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200 oC to 360 oC (392 oF to 680 oF).] 309-865-1 101316-59-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-452-00-6 Distillates (petroleum), heavy steam-cracked; Cracked gasoil; [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250 oC to 400 oC (482 oF to 752 oF).] 309-939-3 101631-14-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250 oC to 400 oC (482 oF to 752 oF).] 309-939-3 101631-14-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H 649-453-00-1 Distillates (petroleum), heavy hydrocracked; Baseoil — unspecified; [A complex combination of hydrocarbons from the distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers in the range of C15-C39 and boiling in the range of approximately 260 oC to 600 oC (500 oF to 1112 oF).] 265-077-7 64741-76-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons from the distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers in the range of C15-C39 and boiling in the range of approximately 260 oC to 600 oC (500 oF to 1112 oF).] 265-077-7 64741-76-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-454-00-7 Distillates (petroleum), solvent-refined heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-090-8 64741-88-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-090-8 64741-88-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-455-00-2 Distillates (petroleum), solvent-refined light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-091-3 64741-89-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-091-3 64741-89-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-456-00-8 Residual oils (petroleum), solvent deasphalted; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the solvent soluble fraction from C3-C4 solvent deasphalting of a residuum. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-096-0 64741-95-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the solvent soluble fraction from C3-C4 solvent deasphalting of a residuum. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-096-0 64741-95-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-457-00-3 Distillates (petroleum), solvent-refined heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt a 40 oC). It contains relatively few normal paraffins.] 265-097-6 64741-96-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt a 40 oC). It contains relatively few normal paraffins.] 265-097-6 64741-96-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-458-00-9 Distillates (petroleum), solvent-refined light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-098-1 64741-97-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-098-1 64741-97-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-459-00-4 Residual oils (petroleum,) solvent-refined; Baseoil — unspecified; [A complex combination by hydrocarbons obtained as the solvent insoluble fraction from solvent refining of a residuum using a polar organic solvent such as phenol or furfural. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-101-6 64742-01-4 Carc. Cat. 2; R45 T [A complex combination by hydrocarbons obtained as the solvent insoluble fraction from solvent refining of a residuum using a polar organic solvent such as phenol or furfural. It consists of hydrocarbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-101-6 64742-01-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-460-00-X Distillates (petroleum), clay-treated paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-137-2 64742-36-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-137-2 64742-36-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-461-00-5 Distillates (petroleum), clay-treated light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-138-8 64742-37-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-138-8 64742-37-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-462-00-0 Residual oils (petroleum), clay-treated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treatment of a residual oil with a natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydro-carbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-143-5 64742-41-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treatment of a residual oil with a natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydro-carbons having carbon numbers predominantly higher than C25 and boiling above approximately 400 oC (752 oF).] 265-143-5 64742-41-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-463-00-6 Distillates (petroleum), clay-treated heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-146-1 64742-44-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-146-1 64742-44-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-464-00-1 Distillates (petroleum), clay-treated light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-147-7 64742-45-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contacting or percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-147-7 64742-45-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-465-00-7 Distillates (petroleum), hydrotreated heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-155-0 64742-52-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-155-0 64742-52-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-466-00-2 Distillates (petroleum), hydrotreated light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-156-6 64742-53-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-156-6 64742-53-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-467-00-8 Distillates (petroleum), hydrotreated heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-157-1 64742-54-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-157-1 64742-54-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-468-00-3 Distillates (petroleum), hydrotreated light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-158-7 64742-55-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains a relatively large proportion of saturated hydrocarbons.] 265-158-7 64742-55-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-469-00-9 Distillates (petroleum), solvent-dewaxed light paraffinic; Baseoil — unspecified; [A complex comination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-159-2 64742-56-9 Carc. Cat. 2; R45 T [A complex comination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-159-2 64742-56-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-470-00-4 Residual oils (petroleum), hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-160-8 64742-57-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-160-8 64742-57-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-471-00-X Residual oils (petroleum), solvent-dewaxed; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of long, branched chain hydrocarbons from a residual oil by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-166-0 64742-62-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by removal of long, branched chain hydrocarbons from a residual oil by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly greater than C25 and boiling above approximately 400 oC (752 oF).] 265-166-0 64742-62-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-472-00-5 Distillates (petroleum), solvent-dewaxed heavy naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 . through C50 and produces a finished oil of not less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-167-6 64742-63-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 . through C50 and produces a finished oil of not less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-167-6 64742-63-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-473-00-0 Distillates (petroleum), solvent-dewaxed light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-168-1 64742-64-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists of hydrocarbons having carbon numbers predominantly in the range C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-168-1 64742-64-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-474-00-6 Distillates (petroleum), solvent-dewaxed heavy paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity not less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-169-7 64742-65-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by removal of normal paraffins from a petroleum fraction by solvent crystallization. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity not less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-169-7 64742-65-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-475-00-1 Naphthenic oils (petroleum), catalytic dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-172-3 64742-68-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-172-3 64742-68-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-476-00-7 Naphthenic oils (petroleum), catalytic dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-173-9 64742-69-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-173-9 64742-69-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-477-00-2 Paraffin oils (petroleum), catalytic dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-174-4 64742-70-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC).] 265-174-4 64742-70-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-478-00-8 Paraffin oils (petroleum), catalytic dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-176-5 64742-71-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic dewxing process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC).] 265-176-5 64742-71-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-479-00-3 Naphthenic oils (petroleum), complex dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by removing straight chain paraffin hydrocarbons as a solid by treatment with an agent such as urea. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-179-1 64742-75-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by removing straight chain paraffin hydrocarbons as a solid by treatment with an agent such as urea. It consists of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of at least 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-179-1 64742-75-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-480-00-9 Naphthenic oils (petroleum), complex dewaxed light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon' numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-180-7 64742-76-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a catalytic dewaxing process. It consists of hydrocarbons having carbon' numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 265-180-7 64742-76-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-481-00-4 Lubricating oils (petroleum), C20-50, hydrotreated neutral oil-based, high-viscosity; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil, and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of approximately 112cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-736-3 72623-85-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil, and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil having a viscosity of approximately 112cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-736-3 72623-85-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-482-00-X Lubricating oils (petroleum), C15-30, hydrotreated neutral oil-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil and heavy vacuum gas oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of approximately 15cSt at 40 oC. It contains a relatively large proportion of saturated hydrocabons.] 276-737-9 72623-86-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating light vacuum gas oil and heavy vacuum gas oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil having a viscosity of approximately 15cSt at 40 oC. It contains a relatively large proportion of saturated hydrocabons.] 276-737-9 72623-86-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-483-00-5 Lubricating oils (petroleum), C20-50, hydrotreated neutral oil-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of approximately 32cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-738-4 72623-87-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating light vacuum gas oil, heavy vacuum gas oil and solvent deasphalted residual oil with hydrogen in the presence of a catalyst in a two stage process with dewaxing being carried out between the two stages. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of approximately 32cSt at 40 oC. It contains a relatively large proportion of saturated hydrocarbons.] 276-738-4 72623-87-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-484-00-0 Lubricating oils; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from solvent extraction and dewaxing processes. It consists predominantly of saturated hydrocarbons having carbon numbers in the range C15 through C50.] 278-012-2 74869-22-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-485-00-6 Distillates (petroleum), complex dewaxed heavy paraffinci; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by dewaxing heavy paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of equal to or greater than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-613-7 90640-91-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by dewaxing heavy paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil with a viscosity of equal to or greater than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-613-7 90640-91-8 Carc. Cat. 2; R45 T R: 4 S: 53-45 H L 649-486-00-1 Distillates (petroleum), complex dewaxed light paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by dewaxing light paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-614-2 90640-92-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by dewaxing light paraffinic distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C30 and produces a finished oil with a viscosity of less than 100 SUS at 100 oF (19cSt at 40 oC). It contains relatively few normal paraffins.] 292-614-2 90640-92-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-487-00-7 Distillates (petroleum), solvent dewaxed heavy paraffinic, clay-treated; … 26 unchanged lines … S: 53-45 H L 649-493-00-X Distillates (petroleum), dewaxed heavy paraffinic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C25 through C39 and produces a finished oil with a viscosity of approximately 44 cSt at 50 oC.] 295-300-3 91995-39-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C25 through C39 and produces a finished oil with a viscosity of approximately 44 cSt at 50 oC.] 295-300-3 91995-39-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-494-00-5 Distillates (petroleum), dewaxed light paraffinic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C21 through C29 and produces a finished oil with a viscosity of approximately 13 cSt at 50 oC.] 295-301-9 91995-40-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from an intensive treatment of dewaxed distillate by hydrogenation in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C21 through C29 and produces a finished oil with a viscosity of approximately 13 cSt at 50 oC.] 295-301-9 91995-40-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-495-00-0 Distillates (petroleum), hydrocracked solvent-refined, dewaxed; Baseoil — unspecified; [A complex combination of liquid hydrocarbons obtained by recrystallization of dewaxed hydrocracked solvent-refined petroleum distillates.] 295-306-6 91995-45-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-496-00-6 Distillates (petroleum), solvent-refined light naphthenic, hydrotreated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst and removing the aromatic hydrocarbons by solvent extraction. It consists predominantly of naphthenic hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of between 13-15cSt at 40 oC.] 295-316-0 91995-54-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst and removing the aromatic hydrocarbons by solvent extraction. It consists predominantly of naphthenic hydrocarbons having carbon numbers predominantly in the range of C15 through C30 and produces a finished oil with a viscosity of between 13-15cSt at 40 oC.] 295-316-0 91995-54-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-497-00-1 Lubricating oils (petroleum), C17-35, solvent-extd., dewaxed, hydrotreated; Baseoil — unspecified 295-423-2 92045-42-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-498-00-7 Lubricating oils (petroleum), hydrocracked nonarom. solvent-deparaffined; Baseoil — unspecified 295-424-8 92045-43-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-499-00-2 Residual oils (petroleum), hydrocracked acid-treated solvent-dewaxed; Baseoil — unspecified; [A complex combination of hydrocarbons produced by solvent removal of paraffins from the residue of the distillation of acid-treated, hydrocracked heavy paraffins and boiling approximately above 380 oC (716 oF).] 295-499-7 92061-86-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by solvent removal of paraffins from the residue of the distillation of acid-treated, hydrocracked heavy paraffins and boiling approximately above 380 oC (716 oF).] 295-499-7 92061-86-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-500-00-6 Paraffin oils (petroleum), solvent-refined dewaxed heavy; Baseoil — unspecified; [A complex combination of hydrocarbons obtained from sulfur-containing paraffinic crude oil. It consists predominantly of a solvent refined deparaffinated lubricating oil with a viscosity of 65cSt at 50 oC.] 295-810-6 92129-09-4 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from sulfur-containing paraffinic crude oil. It consists predominantly of a solvent refined deparaffinated lubricating oil with a viscosity of 65cSt at 50 oC.] 295-810-6 92129-09-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-501-00-1 Lubricating oils (petroleum), base oils, paraffinic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by refining of crude oil. It consists predominantly of aromatics, naphthenics and paraffinics and produces a finished oil with a viscosity of 120 SUS at 100 oF (23cSt at 40 oC).] 297-474-6 93572-43-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by refining of crude oil. It consists predominantly of aromatics, naphthenics and paraffinics and produces a finished oil with a viscosity of 120 SUS at 100 oF (23cSt at 40 oC).] 297-474-6 93572-43-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-502-00-7 Hydrocarbons, hydrocracked paraffinic distn. residues, solvent-dewaxed; Baseoil — unspecified 297-857-8 93763-38-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-503-00-2 Hydrocarbons, C20-50, residual oil hydrogenation vacuum distillate; Baseoil — unspecified 300-257-1 93924-61-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-504-00-8 Distillates (petroleum), solvent-refined hydrotreated heavy, hydrogenated; Baseoil — unspecified 305-588-5 94733-08-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-505-00-3 Distillates (petroleum), solvent-refined hydrocracked light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent dearomatization of the residue of hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF).] 305-589-0 94733-09-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent dearomatization of the residue of hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF).] 305-589-0 94733-09-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-506-00-9 Lubricating oils (petroleum), C18-40, solvent-dewaxed hydrocracked distillate-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent deparaffination of the distillation residue from hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-594-8 94733-15-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent deparaffination of the distillation residue from hydrocracked petroleum. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-594-8 94733-15-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-507-00-4 Lubricating oils (petroleum), C18-40, solvent-dewaxed hydrogenated raffinate-based; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent deparaffination of the hydrogenated raffinate obtained by solvent extraction of a hydrotreated petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-595-3 94733-16-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent deparaffination of the hydrogenated raffinate obtained by solvent extraction of a hydrotreated petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C40 and boiling in the range of approximately 370 oC to 550 oC (698 oF to 1022 oF).] 305-595-3 94733-16-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-508-00-X Hydrocarbons, C13-30, arom.-rich, solvent-extd. naphthenic distillate; Baseoil — unspecified 305-971-7 95371-04-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-509-00-5 Hydrocarbons, C16-32, arom. rich, solvent-extd. naphthenic distillate; Baseoil — unspecified 305-972-2 95371-05-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-510-00-0 Hydrocarbons, C37-68, dewaxed deasphalted hydrotreated vacuum distn. residues; Baseoil — unspecified 305-974-3 95371-07-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-511-00-6 Hydrocarbons, C37-65, hydrotreated deasphalted vacuum distn. residues; Baseoil — unspecified 305-975-9 95371-08-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-512-00-1 Distillates (petroleum), hydrocracked solvent-refined light; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by the solvent treatment of a distillate from hydrocracked petroleum distillates. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF.] 307-010-7 97488-73-8 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by the solvent treatment of a distillate from hydrocracked petroleum distillates. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C18 through C27 and boiling in the range of approximately 370 oC to 450 oC (698 oF to 842 oF.] 307-010-7 97488-73-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-513-00-7 Distillates (petroleum), solvent-refined hydrogenated heavy; Baseoil — unspecified; [A complex combination of hydrocarbons, obtained by the treatment of a hydrogenated petroleum distillate with a solvent. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390 oC to 550 oC (734 oF to 1022 oF).] 307-011-2 97488-74-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons, obtained by the treatment of a hydrogenated petroleum distillate with a solvent. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C19 through C40 and boiling in the range of approximately 390 oC to 550 oC (734 oF to 1022 oF).] 307-011-2 97488-74-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-514-00-2 Lubricating oils (petroleum), C18-27, hydrocracked solvent-dewaxed; Baseoil — unspecified 307-034-8 97488-95-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-515-00-8 Hydrocarbons, C17-30, hydrotreated solvent-deasphalted atm. distn. residue, distn. lights; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a solvent deasphalted short residue with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C30 and boiling in the range of approximately 300 oC to 400 oC (572 oF to 752 oF). It produces a finished oil having a viscosity of 4cSt at approximately 100 oC (212 oF).] 307-661-7 97675-87-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the treatment of a solvent deasphalted short residue with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C30 and boiling in the range of approximately 300 oC to 400 oC (572 oF to 752 oF). It produces a finished oil having a viscosity of 4cSt at approximately 100 oC (212 oF).] 307-661-7 97675-87-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-516-00-3 Hydrocarbons, C17-40, hydrotreated solvent-deasphalted distn. residue, vacuum distn. lights; Baseoil — unspecified; [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the catalytic hydrotreatment of a solvent deasphalted short residue having a viscosity of 8cSt at approximately 100 oC (212 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C40 and boiling in the range of approximately 300 oC to 500 oC (592 oF to 932 oF).] 307-755-8 97722-06-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained as first runnings from the vacuum distillation of effluents from the catalytic hydrotreatment of a solvent deasphalted short residue having a viscosity of 8cSt at approximately 100 oC (212 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C40 and boiling in the range of approximately 300 oC to 500 oC (592 oF to 932 oF).] 307-755-8 97722-06-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-517-00-9 Hydrocarbons, C13-27, solvent-extd. light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 9.5cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C27 and boiling in the range of approximately 240 oC to 400 oC (464 oF to 752 oF.] 307-758-4 97722-09-3 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 9.5cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C13 through C27 and boiling in the range of approximately 240 oC to 400 oC (464 oF to 752 oF.] 307-758-4 97722-09-3 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-518-00-4 Hydrocarbons, C14-29, solvent-extd. light naphthenic; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 16cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C29 and boiling in the range of approximately 250 oC to 425 oC (482 oF to 797 oF).] 307-760-5 97722-10-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by extraction of the aromatics from a light naphthenic distillate having a viscosity of 16cSt at 40 oC (104 oF). It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C14 through C29 and boiling in the range of approximately 250 oC to 425 oC (482 oF to 797 oF).] 307-760-5 97722-10-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-519-00-X Hydrocarbons, C27-42, dearomatized; … 32 unchanged lines … S: 53-45 H L 649-527-00-3 Lubricating oils (petroleum), C >25, solvent-extd., deasphalted, dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100 oC (212 oF).] 309-874-0 101316-69-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of vacuum distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly greater than C25 and produces a finished oil with a viscosity in the order of 32cSt to 37cSt at 100 oC (212 oF).] 309-874-0 101316-69-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-528-00-9 Lubricating oils (petroleum), C17-32, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produced a finished oil with a viscosity in the order of 17cSt to 23cSt at 40 oC (104 oF.] 309-875-6 101316-70-5 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C32 and produced a finished oil with a viscosity in the order of 17cSt to 23cSt at 40 oC (104 oF.] 309-875-6 101316-70-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-529-00-4 Lubricating oils (petroleum), C20-35, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40 oC (104 oF).] 309-876-1 101316-71-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C20 through C35 and produces a finished oil with a viscosity in the order of 37cSt to 44cSt at 40 oC (104 oF).] 309-876-1 101316-71-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-530-00-X Lubricating oils (petroleum), C24-50, solvent-extd., dewaxed, hydrogenated; Baseoil — unspecified; [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40 oC (104 oF).] 309-877-7 101316-72-7 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent extraction and hydrogenation of atmospheric distillation residues. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C24 through C50 and produces a finished oil with a viscosity in the order of 16cSt to 75cSt at 40 oC (104 oF).] 309-877-7 101316-72-7 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-531-00-5 Extracts (petroleum), heavy naphthenic distillate solvent, arom. conc.; Distillate aromatic extract (treated); [An aromatic concentrate produced by adding water to heavy naphthenic distillate solvent extract and extraction solvent.] 272-175-3 68783-00-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-532-00-0 Extracts (petroleum), solvent-refined heavy paraffinic distillate solvent; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from the re-extraction of solvent-refined heavy paraffinic distillate. It consists of saturated and aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50.] 272-180-0 68783-04-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-533-00-6 Extracts (petroleum), heavy paraffinic distillates, solvent-deasphalted; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from a solvent extraction of heavy paraffinic distillate.] 272-342-0 68814-89-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-534-00-1 Extracts (petroleum), heavy naphthenic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by treating a heavy naphthenic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 19cSt at 40 oC (100 SUS at 100 oF).] 292-631-5 90641-07-9 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by treating a heavy naphthenic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50 and produces a finished oil of at least 19cSt at 40 oC (100 SUS at 100 oF).] 292-631-5 90641-07-9 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-535-00-7 Extracts (petroleum), heavy paraffinic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons produced by treating a heavy paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C21 through C33 and boiling in the range of approximately 350 oC to 480 oC (662 oF to 896 oF). 292-632-0 90641-08-0 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by treating a heavy paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C21 through C33 and boiling in the range of approximately 350 oC to 480 oC (662 oF to 896 oF). 292-632-0 90641-08-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-536-00-2 Extracts (petroleum), light paraffinic distillate solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons produced by treating a light paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C26 and boiling in the range of approximately 280 oC to 400 oC (536 oF to 752 oF).] 292-633-6 90641-09-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons produced by treating a light paraffinic distillate solvent extract with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C17 through C26 and boiling in the range of approximately 280 oC to 400 oC (536 oF to 752 oF).] 292-633-6 90641-09-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-537-00-8 Extracts (petroleum), hydrotreated light paraffinic distillate solvent; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as the extract from solvent extraction of intermediate paraffinic top solvent distillate that is treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C36.] 295-335-4 91995-73-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-538-00-3 Extracts (petroleum), light naphthenic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by treating the extract, obtained from a solvent extraction process, with hydrogen in the presence of a catalyst under conditions primarily to remove sulfur compounds. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C15 through C30. This stream is likely to contain 5 wt.% or more of 4- to 6-membered condensed ring aromatic hydrocarbons.] 295-338-0 91995-75-4 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-539-00-9 Extracts (petroleum), light paraffinic distillate solvent, acid-treated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained as a fraction of the distillation of an extract from the solvent extraction of light paraffinic top petroleum distillates that is subjected to a sulfuric acid refining. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.] 295-339-6 91995-76-5 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-540-00-4 Extracts (petroleum), light paraffinic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained by solvent extraction of a light paraffin distillate and treated with hydrogen to convert the organic sulfur to hydrogen sulfide which is eliminated. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C40 and produces a finished oil with a viscosity of greater than 10cSt at 40 oC.] 295-340-1 91995-77-6 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained by solvent extraction of a light paraffin distillate and treated with hydrogen to convert the organic sulfur to hydrogen sulfide which is eliminated. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C40 and produces a finished oil with a viscosity of greater than 10cSt at 40 oC.] 295-340-1 91995-77-6 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-541-00-X Extracts (petroleum), light vacuum gas oil solvent, hydrotreated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons, obtained by solvent extraction from light vacuum petroleum gas oils and treated with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.] 295-342-2 91995-79-8 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-542-00-5 Extracts (petroleum), heavy paraffinic distillate solvent, clay-treated; Distillate aromatic extract (treated); [A complex combination of hydrocarbons resulting from treatment of a petroleum fraction with natural or modified clay in either a contact or percolation process to remove the trace amounts of polar compounds and impurities present. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C20 through C50. This stream is likely to contain 5 wt.% or more 4-6 membered ring aromatic hydrocarbons.] 296-437-1 92704-08-0 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-543-00-0 Extracts (petroleum), heavy naphthenic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-827-4 93763-10-1 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-827-4 93763-10-1 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-544-00-6 Extracts (petroleum), solvent-dewaxed heavy paraffinic distillate solvent, hydrodesulfurized; Distillate aromatic extract (treated); [A complex combination of hydrocarbons obtained from a solvent dewaxed petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-829-5 93763-11-2 Carc. Cat. 2; R45 T [A complex combination of hydrocarbons obtained from a solvent dewaxed petroleum stock by treating with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C15 through C50 and produces a finished oil with a viscosity of greater than 19cSt at 40 oC.] 297-829-5 93763-11-2 Carc. Cat. 2; R45 T R: 45 S: 53-45 H L 649-545-00-1 Extracts (petroleum), light paraffinic distillate solvent, carbon-treated; … 91 unchanged lines … 73138-82-6 R43 Xi R: 43 S: (2-)24-37 650-016-00-2 Mineral wool, with the exception of those specified elsewhere in this Annex; [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+MgO+BaO) content greater than 18 % by weight] — — Carc. Cat. 3; R40 Xn [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+MgO+BaO) content greater than 18 % by weight] — — Carc. Cat. 3; R40 Xn R: 40 S: (2-)36/37 AQR 650-017-00-8 Refractory Ceramic Fibres, Special Purpose Fibres, with the exception of those specified elsewhere in this Annex; [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+ MgO+BaO) content less or equal to 18 % by weight] — — Carc. Cat. 2; R49 T [Man-made vitreous (silicate) fibres with random orientation with alkaline oxide and alkali earth oxide (Na2O+K2O+CaO+ MgO+BaO) content less or equal to 18 % by weight] — — Carc. Cat. 2; R49 T R: 49 S: 53-45 AR 650-018-00-3 reaction product of: acetophenone, formaldehyde, cyclohexylamine, methanol and acetic acid 406-230-1 — R10 … 48 unchanged lines … C; R35 N; R50 O; C; N R: 7-20/21/22-35-50 S: (1/2-)3/7-14-26-36/37/39-45-61 650-049-00-2 2-alkoyloxyethyl hydrogen maleate, where alkoyl represents (by weight) 70 to 85 % unsaturated octadecoyl, 0.5 to 10 % saturated octadecoyl, and 2 to 18 % saturated hexadecoyl 417-960-5 — Xi; R38-41 S: (1/2-)3/7-14-26-36/37/39-45-61 650-049-00-2 2-alkoyloxyethyl hydrogen maleate, where alkoyl represents (by weight) 70 to 85 % unsaturated octadecoyl, 0.5 to 10 % saturated octadecoyl, and 2 to 18 % saturated hexadecoyl 417-960-5 — Xi; R38-41 R43 N; R50-53 Xi; N R: 38-41-43-50/53 S: (2-)24-26-37/39-60-61 650-050-00-8 reaction mass of: 1-methyl-3-hydroxypropyl 3,5-[1,1-dimethylethyl]-4-hydroxydihydro-cinnamate and/or 3-hydroxybutyl 3,5-[1,1-dimethylethyl]-4-hydroxydihydrocinnamate; 1,3-butanediol bis[3-(3'-(1,1-dimethylethyl)4'-hydroxy-phenyl)propionate] isomers; 1,3-butanediol bis[3-(3',5'-(1,1-dimethylethyl)-4'-hydroxyphenyl)propionate] isomers 423-600-8 — N; R51-53 N R: 51/53 S: 61 650-055-00-5 silver sodium zirconium hydrogenphosphate 422-570-3 155925-27-2 N; R50-53 N R: 50/53 S: 60-61

02008R1272-20150101 → 02008R1272-20150601

ANNEX VII Translation table from classification under Directive 67/548/EEC to classification under this Regulation This Annex includes a table to assist translation of a classification made for a substance or a mixture under Directive 67/548/EEC or Directive 1999/45/EC, respectively, into the corresponding classification under this Regulation. Whenever data for the substance or mixture are available, an evaluation and classification shall be done in accordance with Articles 9 to13 of this Regulation. 1. Translation table The codes used are introduced in Table 1.1 and section 1.1.2.2 of Annex VI. Table 1.1 Translation between classification in accordance with Directive 67/548/EEC and this Regulation Note 1 For these classes it is possible to use the recommended minimum classification as defined in section 1.2.1.1 in Annex VI. Data or other information may be available to indicate that re-classification in a more severe category is appropriate. Note 2 It is recommended to classify in Category 1B even if it also could be possible that 1C could be applicable for certain cases. Going back to original data, may not result in a possibility to distinguish between Category 1B or 1C, since the exposure period has normally been up to 4 hours according to Regulation (EC) No 440/2008. However, for the future, when data are derived from tests following a sequential approach as foreseen in the Regulation (EC) No 440/2008, Category 1C should be considered. Note 3 The route of exposure could be added to the hazard statement if it is conclusively proven that no other routes of exposure cause the hazard. Note 4 Hazard statements H360 and H361 indicate a general concern for both the reproductive properties related to effects on fertility and developmental effects; and/or development: May damage/Suspected of damaging fertility or the unborn child. According to the classification criteria (Annex I, section 3.7) criteria, the general hazard statement can be replaced by the hazard statement indicating only the property specific effect of concern, concern in case either fertility accordance with section 1.1.2.1.2 of Annex VI. When the other differentiation is not mentioned, this is due to evidence proving no such effect, inconclusive data or developmental effects are proven to be not relevant. no data and the obligations in Article 4(3) shall apply for that differentiation. Classification under Directive 67/548/EEC Physical state of the substance when relevant Classification under this Regulation Note Hazard Class-and-Category Hazard statement E; R2 No direct translation possible. E; R3 No direct translation possible. O; R7 Org. Perox. CD H242 Org. Perox. EF H242 O; R8 … 620 unchanged words … H412 R53 Aquatic Chronic 4 H413 N; R59 Ozone H420 Table 1.2 Translation between risk phrases assigned under Directive 67/548/EEC and supplementary labelling requirements under this Regulation Directive 67/548/EEC This Regulation R1 EUH001 R6 EUH006 R14 EUH014 R18 EUH018 R19 EUH019 R44 EUH044 R29 EUH029 R31 EUH031 R32 EUH032 R66 EUH066 R39-41 EUH070