EU-ACTIVE_INTELLIGENT_FCM-ART_5_2_c_i

EU-ACTIVE_INTELLIGENT_FCM-ART_5_2_c_i

Active and Intelligent Materials - CMR Substances not allowed for use

EU. Carcinogens, Mutagens and Reproductive substances Not Allowed for Use in Components of Active and Intelligent Materials and Articles (Article 5(2)(c)(i)), Regulation 450/2009/EC, 30 May 2009

This list contains a non-exhaustive list of Carcinogens, Mutagens and Reproductive substances (CMRs) that are not allowed for use in components of active and intelligent materials and articles per Art. 5(2)(c)(i) of Regulation 450/2009/EC. The list is derived from a subset of substances on Table 3 of Annex VI to the CLP Regulation (1272/2008/EC).

Last updated 26 aprile 2024. Database contains 1679 unique substances/entries.

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Mostrati 1.251 - 1.300 su 1.679 risultati.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
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 °C to greater than 400 °C (392 °F to greater than 752 °F).] 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°C to greater than 400°C (392°F to greater than 752°F).	309-855-7	101316-49-8	648-049-00-2	Carc. 1B	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 °C to greater than 400 °C (392 °F to greater than 752 °F).
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 °C to 410 °C (7160 to 770 °F). Composed primarily of tri-and polynuclear aromatic hydrocarbons and heterocyclic compounds.] The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380°C to 410°C (716°F to 770°F). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.	295-313-4	91995-52-7	648-051-00-3	Carc. 1B	The redistillate obtained from the fractional distillation of pitch distillate and boiling in the range of approximately 380 °C to 410 °C (7160 to 770 °F). Composed primarily of tri- and polynuclear aromatic hydrocarbons and heterocyclic compounds.
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 °C to 470 °C (572 °F to 878 °F). The product may also contain heteroatoms.] 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°C to 470°C (572°F to 878°F). The product may also contain heteroatoms.	295-312-9	91995-51-6	648-048-00-7	Carc. 1B	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 °C to 470 °C (572 °F to 878 °F). The product may also contain heteroatoms.
Distillates (coal tar), heavy oils; Heavy Anthracene Oil [Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240°C to 400°C (464°F to 752 °F). Composed primarily of tri-and polynuclear hydrocarbons and heterocyclic compounds.] Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240°C to 400°C (464°F to 752°F). Composed primarily of tri- and polynuclear hydrocarbons and heterocyclic compounds.	292-607-4	90640-86-1	648-044-00-5	Carc. 1B	Distillate from the fractional distillation of coal tar of bituminous coal, with boiling range of 240 °C to 400 °C (464 °F to 752 °F). Composed primarily of tri-and polynuclear hydrocarbons and heterocyclic compounds.
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 °C to 400 °C (662 °F to 752 °F). Consists predominantly of tri-and polynuclear aromatics and heterocyclic hydrocarbons.] The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350°C to 400°C (662°F to 752°F). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.	295-304-5	91995-42-5	648-050-00-8	Carc. 1B	The redistillate obtained from the fractional distillation of pitch distillate boiling in the range of approximately 350 °C to 400 °C (662 °F to 752 °F). Consists predominantly of tri- and polynuclear aromatics and heterocyclic hydrocarbons.
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°C to 160 °C (175°F to 320°F).] 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°C to 160°C (175°F to 320°F).	283-482-7	84650-02-2	648-001-00-0	Carc. 1B	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 °C to 160 °C (175 °F to 320 °F).
disodium {5-[(4'-((2,6-hydroxy3-((2-hydroxy-5-sulphophenyl)azo)phenyl)azo)(1,1'-biphenyl)-4-yl)azo]salicylato (4-)}cuprate(2-); CI Direct Brown 95	240-221-1	16071-86-6	611-005-00-8	Carc. 1B
dimethylsulfamoylchloride	236-412-4	13360-57-1	016-033-00-9	Carc. 1B
dimethylnitrosoamine; N-nitrosodimethylamine	200-549-8	62-75-9	612-077-00-3	Carc. 1B
dimethylcarbamoyl chloride	201-208-6	79-44-7	006-041-00-0	Carc. 1B
dichromium tris(chromate); chromium III chromate; chromic chromate	246-356-2	24613-89-6	024-010-00-X	Carc. 1B
dibenz[a,h]anthracene	200-181-8	53-70-3	601-041-00-2	Carc. 1B
diazomethane	206-382-7	334-88-3	006-068-00-8	Carc. 1B
cumene	202-704-5	98-82-8	601-024-00-X	Carc. 1B
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 o C (100 oF).] 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	648-138-00-6	Carc. 1B	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).
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).] 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	648-100-00-9	Carc. 1B	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).
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 o C to 280 o C (464°F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] 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	648-098-00-X	Carc. 1B	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.
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.] 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	648-043-00-X	Carc. 1B	The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.
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).] 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	648-099-00-5	Carc. 1B	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).
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.] 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	648-101-00-4	Carc. 1B	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.
Coal liquids, liq. solvent extn. soln. [The product obtained by filtration of coal mineral matter and undissolved coal from coal extract solution produced by digesting coal in a liquid solvent. A black, viscous, highly complex liquid combination composed primarily of aromatic and partly hydro-genated aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic and other aromatic oxygen compounds and their alkyl derivatives.] The product obtained by filtration of coal mineral matter and undissolved coal from coal extract solution produced by digesting coal in a liquid solvent. A black, viscous, highly complex liquid combination composed primarily of aromatic and partly hydrogenated aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic and other aromatic oxygen compounds and their alkyl derivatives.	302-682-8	94114-47-3	648-143-00-3	Carc. 1B	The product obtained by filtration of coal mineral matter and undissolved coal from coal extract solution produced by digesting coal in a liquid solvent. A black, viscous, highly complex liquid combination composed primarily of aromatic and partly hydro-genated aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic and other aromatic oxygen compounds and their alkyl derivatives.
Coal liquids, liq. solvent extn. [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.] 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	648-144-00-9	Carc. 1B	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.
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 °C (662 °F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 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°C (662°F). 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	649-020-00-7	Carc. 1B	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 °C (662 °F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.
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°C (662°F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 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°C (662°F). 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	649-011-00-8	Carc. 1B	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 °C (662 °F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.
chromium (VI) compounds, with the exception of barium chromate and of compounds specified elsewhere in this Annex	-	-	024-017-00-8	Carc. 1B
chloroprene (stabilised); 2-chlorobuta-1,3-diene (stabilised)	204-818-0	126-99-8	602-036-00-8	Carc. 1B
carbadox (INN);methyl 3-(quinoxalin-2-ylmethylene)carbazate 1,4-dioxide; 2-(methoxycarbonylhydrazonomethyl) quinoxaline 1,4-dioxide	229-879-0	6804-07-5	613-050-00-9	Carc. 1B
captafol (ISO);1,2,3,6-tetrahydro-N-(1,1,2,2- tetrachloroethylthio)phthalimide	219-363-3	2425-06-1	613-046-00-7	Carc. 1B
calcium chromate	237-366-8	13765-19-0	024-008-00-9	Carc. 1B
C.I. Basic Violet 3 with ≥ 0,1 % of Michler's ketone (EC no.202-027-5);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	612-205-00-8	Carc. 1B
butanone oxime; ethyl methyl ketoxime; ethyl methyl ketone oxime	202-496-6	96-29-7	616-014-00-0	Carc. 1B
bromoethylene	209-800-6	593-60-2	602-024-00-2	Carc. 1B
beryllium oxide	215-133-1	1304-56-9	004-003-00-8	Carc. 1B
beryllium compounds with the exception of aluminium beryllium silicates, and with those specified elsewhere in this Annex show/hide Beryllium acetylide EC / List no: 208-050-7 \| CAS no: 506-66-1 Beryllium nitrate trihydrate EC / List no: - \| CAS no: 7787-55-5 Beryllium selenide EC / List no: 235-450-9 \| CAS no: 12232-25-6 Beryllium hydroxide EC / List no: 236-368-6 \| CAS no: 13327-32-7 Beryllium diammonium tetrafluoride EC / List no: 238-948-4 \| CAS no: 14874-86-3 Beryllium diboride EC / List no: 235-443-0 \| CAS no: 12228-40-9 Beryllium sulfate tetrahydrate EC / List no: 629-461-1 \| CAS no: 7787-56-6 Octadecanoic acid, beryllium salt EC / List no: - \| CAS no: 16687-38-0 Phosphoric acid, beryllium salt EC / List no: 252-356-3 \| CAS no: 35089-00-0 Beryllium dibromide EC / List no: 232-115-9 \| CAS no: 7787-46-4 Beryllium hexaboride EC / List no: 235-657-4 \| CAS no: 12429-94-6 Beryllium sulphide EC / List no: 237-064-6 \| CAS no: 13598-22-6 Diethylberyllium EC / List no: 208-823-9 \| CAS no: 542-63-2 Beryllium carbonate EC / List no: 236-030-8 \| CAS no: 13106-47-3 Nitric acid, beryllium salt, tetrahydrate EC / List no: 690-699-4 \| CAS no: 13510-48-0 Beryllium nitrate EC / List no: 237-062-5 \| CAS no: 13597-99-4 Beryllium zinc silicate EC / List no: 247-151-0 \| CAS no: 25638-88-4 Beryllium orthosilicate EC / List no: 239-251-8 \| CAS no: 15191-85-2 Beryllium diiodide EC / List no: 232-119-0 \| CAS no: 7787-53-3 Copper alloy, Cu 96, Be 2.2-2.8, Ni 1.1 (CDA 827) EC / List no: - \| CAS no: 11108-64-8 Beryllium telluride EC / List no: 235-451-4 \| CAS no: 12232-27-8 Beryllium, bis(carbonato(2-))dihydroxytri- EC / List no: - \| CAS no: 66104-24-3 Beryllium chloride EC / List no: 232-116-4 \| CAS no: 7787-47-5 Zinc beryllium silicate EC / List no: - \| CAS no: 39413-47-3 Phosphoric acid, beryllium salt (2:3) EC / List no: - \| CAS no: 13598-26-0 Aluminium alloy, Al,Be EC / List no: 603-236-8 \| CAS no: 12770-50-2 Beryllium hydrogen phosphate (1:1) EC / List no: - \| CAS no: 13598-15-7 Beryllium phosphide (BeP2) EC / List no: - \| CAS no: 1268721-56-7 Beryllium sulphate EC / List no: 236-842-2 \| CAS no: 13510-49-1 Disodium tetrafluoroberyllate EC / List no: 237-630-2 \| CAS no: 13871-27-7 Tetraberyllium boride EC / List no: 235-695-1 \| CAS no: 12536-52-6 Beryllium fluoride EC / List no: 232-118-5 \| CAS no: 7787-49-7 Silicic acid, beryllium salt EC / List no: 261-293-0 \| CAS no: 58500-38-2 Beryllium di(acetate) EC / List no: 208-850-6 \| CAS no: 543-81-7 Beryllium diboride EC / List no: 235-694-6 \| CAS no: 12536-51-5 Steel manufacture, chemicals This category includes the chemical substances which are manufactured as part of steel and alloy steels. The following list identifies those elements which may exist in steel or which may comprise compounds present in steel or alloy steels. Aluminum, beryllium, boron, calcium, carbon, cerium, chromium, cobalt, copper, hafnium, iron, lanthanum, lead, magnesium, manganese, molybdenum, nickel, niobium, nitrogen, oxygen, phosphorus, selenium, silicon, sulfur, tantalum, tin, titanium, tungsten, vanadium, yttrium, zinc, zirconium. EC / List no: 266-048-1 \| CAS no: 65997-19-5 Beryllium phosphide EC / List no: 261-137-1 \| CAS no: 58127-61-0 Bis(pentane-2,4-dionato-O,O')beryllium EC / List no: 233-513-5 \| CAS no: 10210-64-7 Bertrandite (Be4(OH)2O(SiO3)2) EC / List no: 235-299-9 \| CAS no: 12161-82-9 Triberyllium nitride EC / List no: 215-132-6 \| CAS no: 1304-54-7 Beryllium oxyfluoride EC / List no: - \| CAS no: 63990-88-5 Hexakis[μ-(acetato-O:O')]-μ4-oxotetraberyllium EC / List no: 242-785-4 \| CAS no: 19049-40-2	-	-	004-002-00-2	Carc. 1B
benzophenone	204-337-6	119-61-9	606-153-00-5	Carc. 1B
benzo[k]fluoranthene	205-916-6	207-08-9	601-036-00-5	Carc. 1B
benzo[j]fluoranthene	205-910-3	205-82-3	601-035-00-X	Carc. 1B
benzo[e]pyrene	205-892-7	192-97-2	601-049-00-6	Carc. 1B
benzidine based azo dyes; 4,4'-diarylazobiphenyl dyes, with the exception of those specified elsewhere in this Annex	-	-	611-024-00-1	Carc. 1B
benz[e]acephenanthrylene	205-911-9	205-99-2	601-034-00-4	Carc. 1B
benz[a]anthracene	200-280-6	56-55-3	601-033-00-9	Carc. 1B
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°C to 220°C (212°F to 428°F) according to DIN 52025.] 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°C to 220°C (212°F to 428°F) according to DIN 52025.	309-958-7	101794-76-7	648-075-00-4	Carc. 1B	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 °C to 220 °C (212 °F to 428 °F) according to DIN 52025.
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 °C to 220 °C (212°F to 428°F) according to DIN 52025.] 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°C to 220°C (212°F to 428°F) according to DIN 52025.	309-956-6	101794-74-5	648-073-00-3	Carc. 1B	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 °C to 220 °C (212 °F to 428 °F) according to DIN 52025.
Aromatic hydrocarbons, C20-28, polycyclic, mixed coal-tar pitch-polyethylene pyrolysis-derived; Pyrolysis Products [A complex combination of hydrocarbonsobtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numberspredominantly in the range of C20 through C28 and having a softening pointof 100°C to 220°C (212°F to 428°F) according to DIN 52025.] 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°C to 220°C (212°F to 428°F) according to DIN 52025.	309-957-1	101794-75-6	648-074-00-9	Carc. 1B	A complex combination of hydrocarbonsobtained from mixed coal tar pitch-polyethylene pyrolysis. Composed primarily of polycyclic aromatic hydrocarbons having carbon numberspredominantly in the range of C20 through C28 and having a softening pointof 100 °C to 220 °C (212 °F to 428 °F) according to DIN 52025.
anthraquinone	201-549-0	84-65-1	606-151-00-4	Carc. 1B
Anthracene oil; Anthracene oil [A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 °C to 400 °C (572°F to 752°F). Composed primarily of phenanthrene, anthracene and carbazole.] A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300°C to 400°C (572°F to 752°F). Composed primarily of phenanthrene, anthracene and carbazole	292-602-7	90640-80-5	648-079-00-6	Carc. 1B	A complex combination of polycyclic aromatic hydrocarbons obtained from coal tar having an approximate distillation range of 300 °C to 400 °C (572 °F to 752 °F). Composed primarily of phenanthrene, anthracene and carbazole.
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 approxi mately 325 °C to 365 °C (617 °F to 689 °F). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.] 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°C to 365°C (617°F to 689°F). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.	295-274-3	91995-14-1	648-046-00-6	Carc. 1B	A complex combination of hydrocarbons from the base-freed fraction obtained from the distillation of coal tar and boiling in the range of approxi mately 325 °C to 365 °C (617 °F to 689 °F). It contains predominantly anthracene and phenanthrene and their alkyl derivatives.
Alkanes, C12-26-branched and linear	292-454-3	90622-53-0	649-242-00-4	Carc. 1B
acrylonitrile	203-466-5	107-13-1	608-003-00-4	Carc. 1B
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 °C to 290 °C (500°F to 554°F).] 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°C to 290°C (500°F to 554°F).	309-851-5	101316-45-4	648-041-00-9	Carc. 1B	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 °C to 290 °C (500 °F to 554 °F).

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