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 02 maggio 2024. Database contains 1679 unique substances/entries.

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Mostrati 1.001 - 1.100 su 1.679 risultati.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
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	603-221-01-3	Carc. 1B
1-(1-naphthylmethyl)quinolinium chloride CIB R634	406-220-7	65322-65-8	613-182-00-7	Carc. 2; Muta. 2
1,5-naphthylenediamine	218-817-8	2243-62-1	612-089-00-9	Carc. 2
1,4-dioxane	204-661-8	123-91-1	603-024-00-5	Carc. 1B
1,4-dihydroxybenzene; hydroquinone; quinol	204-617-8	123-31-9	604-005-00-4	Carc. 2; Muta. 2
1,4-dichlorobut-2-ene	212-121-8	764-41-0	602-073-00-X	Carc. 1B
1,4-dichlorobenzene; p-dichlorobenzene	203-400-5	106-46-7	602-035-00-2	Carc. 2
1,4-Benzenediamine, N,N’-mixed Ph and tolyl derivs.	273-227-8	68953-84-4	612-298-00-5	Repr. 1B
1,4,5,8-tetraaminoanthra; quinone; C.I. Disperse Blue 1	219-603-7	2475-45-8	611-032-00-5	Carc. 1B
1,3-propanesultone; 1,2-oxathiolane 2,2-dioxide	214-317-9	1120-71-4	016-032-00-3	Carc. 1B
1,3-diphenylguanidine	203-002-1	102-06-7	612-149-00-4	Repr. 2
1,3-dichloro-2-propanol	202-491-9	96-23-1	602-064-00-0	Carc. 1B
1,3-butadiene; buta-1,3-diene	203-450-8	106-99-0	601-013-00-X	Carc. 1A; Muta. 1B
1,3-bis(vinylsulfonylacetamido)propane H-604	428-350-3	93629-90-4	616-142-00-7	Muta. 2
1,3,5-tris-[(2S and 2R)-2,3-epoxypropyl]-1,3,5-triazine-2,4,6-(1H,3H,5H)-trione TEPIC-H	423-400-0	59653-74-6	616-091-00-0	Muta. 1B
1,3,5-tris(oxiranylmethyl)-1,3,5-triazine-2,4,6(1H,3H,5H)-trione; TGIC	219-514-3	2451-62-9	615-021-00-6	Muta. 1B
1,3,5-trioxan; trioxymethylene	203-812-5	110-88-3	605-002-00-0	Repr. 2
1,3,5-triazine-2,4,6-triamine; melamine	203-615-4	108-78-1	613-345-00-2	Carc. 2
1,2-epoxybutane	203-438-2	106-88-7	603-102-00-9	Carc. 2
1,2-dimethylhydrazine	-	540-73-8	007-013-00-0	Carc. 1B
1,2-dimethoxyethane; ethylene glycol dimethyl ether; EGDME	203-794-9	110-71-4	603-031-00-3	Repr. 1B
1,2-dihydroxybenzene; pyrocatechol	204-427-5	120-80-9	604-016-00-4	Carc. 1B; Muta. 2
1,2-diethoxyethane	211-076-1	629-14-1	603-208-00-5	Repr. 1A
1,2-dichloropropane; propylene dichloride	201-152-2	78-87-5	602-020-00-0	Carc. 1B
1,2-dichloroethane; ethylene dichloride	203-458-1	107-06-2	602-012-00-7	Carc. 1B
1,2-dibromoethane	203-444-5	106-93-4	602-010-00-6	Carc. 1B
1,2-dibromo-3-chloropropane	202-479-3	96-12-8	602-021-00-6	Carc. 1B; Muta. 1B; Repr. 1A
1,2-bis(2-methoxyethoxy)ethane; TEGDME; triethylene glycol dimethyl ether; triglyme	203-977-3	112-49-2	603-176-00-2	Repr. 1B
1,2-benzenedicarboxylic acid; di-C7-11-branched and linear alkylesters	271-084-6	68515-42-4	607-480-00-6	Repr. 1B
1,2-benzenedicarboxylic acid; di-C6-8-branched alkylesters, C7-rich	276-158-1	71888-89-6	607-483-00-2	Repr. 1B
1,2-benzenedicarboxylic acid, dipentylester, branched and linear	284-032-2	84777-06-0	607-426-00-1	Repr. 1B
1,2-benzenedicarboxylic acid, dihexyl ester, branched and linear	271-093-5	68515-50-4	607-710-00-5	Repr. 1B
1,2,5,6,9,10-hexabromocyclododecane	221-695-9	3194-55-6	602-109-00-4	Repr. 2; Lact.
1,2,4-triazole	206-022-9	288-88-0	613-111-00-X	Repr. 1B
1,2,3-trichloropropane	202-486-1	96-18-4	602-062-00-X	Carc. 1B; Repr. 1B
1,2,3,4,5,6-hexachlorcyclohexanes with the exception of those specified elsewhere in this Annex	210-168-9	608-73-1	602-042-00-0	Carc. 2
1,1-dichloroethylene; vinylidene chloride	200-864-0	75-35-4	602-025-00-8	Carc. 2
1,1,2-trichloroethane	201-166-9	79-00-5	602-014-00-8	Carc. 2
(Z)-2-methoxymino-2-[2-(tritylamino)thiazol-4-yl]acetic acid	431-520-1	64485-90-1	607-525-00-X	Carc. 2
(S)-4-hydroxy-3-(3-oxo-1-phenylbutyl)-2-benzopyrone	226-907-3	5543-57-7	607-056-00-0	Repr. 1A
(S)-2,3-dihydro-1H-indole-2-carboxylic acid [S]-2-INDOLINE CARBOXYLIC ACID	410-860-2	79815-20-6	607-330-00-X	Repr. 2
(RS)-1-{1-ethyl-4-[4-mesyl-3-(2-methoxyethoxy)-o-toluoyl]pyrazol-5-yloxy} ethyl methyl carbonate; tolpyralate	701-225-3	1101132-67-5	607-755-00-0	Carc. 2; Repr. 2
(R, S)-2-amino-3,3-dimethylbutane amide	447-860-7	144177-62-8	612-279-00-1	Repr. 2
(R)-α-phenylethylammonium(-)-(1R, 2S)-(1,2-epoxypropyl)phosphonate monohydrate PHENETHYLAMMONIUM SALT OF FOSFOMYCIN	418-570-8	25383-07-7	015-178-00-5	Repr. 2
(R)-5-bromo-3-(1-methyl-2-pyrrolidinyl methyl)-1H-indole UK-111,975	422-390-5	143322-57-0	613-201-00-9	Repr. 2
(R)-4-hydroxy-3-(3-oxo-1-phenylbutyl)-2-benzopyrone	226-908-9	5543-58-8	607-056-00-0	Repr. 1A
(methylenebis(4,1-phenylenazo(1-(3-(dimethylamino)propyl)-1,2-dihydro-6-hydroxy-4-methyl-2-oxopyridine-5,3-diyl)))-1,1'dipyridinium dichloride dihydrochloride CARTASOL GEEL M-GL CONC.; CARTASOL GELB M-GL FLÜSSIG (ZUBEREITUNG); CARTASOL GELB M-GL KONZ.; CARTASOL YELLOW M-GL CONC.; HM 2580	401-500-5	118658-99-4	611-099-00-0	Carc. 1B
(isooctanoato-O)(neodecanoato-O)nickel	284-347-5	84852-35-7	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(isononanoato-O)(neodecanoato-O)nickel	287-592-6	85551-28-6	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(isononanoato-O)(isooctanoato-O)nickel	287-471-8	85508-46-9	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(isodecanoato-O)(isooctanoato-O)nickel	285-909-2	85166-19-4	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(isodecanoato-O)(isononanoato-O)nickel	284-348-0	84852-36-8	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(E)-3-[1-[4-[2-(dimethylamino)ethoxy]phenyl]-2-phenylbut-1-enyl]phenol CP-166,221	428-010-4	82413-20-5	604-073-00-5	Carc. 2; Repr. 1B
(E)-2-butenal; (E)-crotonaldehyde	204-647-1	123-73-9	605-009-00-9	Muta. 2
(6R-trans)-1-((7-ammonio-2- carboxylato-8-oxo-5-thia-1- azabicyclo-[4.2.0]oct-2-en-3- yl)methyl)pyridinium iodide	423-260-0	100988-63-4	613-162-00-8	Muta. 2
(6-(4-hydroxy-3-(2-methoxyphenylazo)-2-sulfonato-7-naphthylamino)-1,3,5-triazin-2,4-diyl)bis[(amino-1-methylethyl)ammonium] formate 2691; CARTASOL BRILLANT SCHARLACH K-2GL KONZ.; CARTASOL BRILLANTSCHARLACH K-2GL FLÜSSIG (ZUBEREITUNG); CARTASOL BRILLANTSCHARLACH K-2GL GRANULAT (ZUBEREITUNG); CARTASOL BRILLIANT SCARLET K-2GL; CARTASOL BRILLIANT SCARLET K-2GL CONC.	402-060-7	108225-03-2	611-058-00-7	Carc. 1B
(5-chloro-2-methoxy-4-methyl-3-pyridyl) (4,5,6-trimethoxy-o-tolyl)methanone; pyriofenone	692-456-8	688046-61-9	606-152-00-X	Carc. 2
(4-phenylbutyl)phosphinic acid	420-450-5	86552-32-1	015-198-00-4	Carc. 2
(4-hydrazinophenyl)-N-methylmethanesulfonamide hydrochloride SULPHAZINE	406-090-1	81880-96-8	007-025-00-6	Muta. 2
(4-ethoxyphenyl)(3-(4-fluoro-3-phenoxyphenyl)propyl)dimethylsilane SILANEOPHAN	405-020-7	105024-66-6	014-036-00-X	Repr. 1B
(3-chlorophenyl)-(4-methoxy-3-nitrophenyl)methanone T 1569; T001569	423-290-4	66938-41-8	606-061-00-5	Muta. 2
(3-chloro-2-hydroxypropyl); trimethylammonium chloride ... %	222-048-3	3327-22-8	612-238-00-8	Carc. 2		… %
(3,3'-Dimethyl(1,1'-biphenyl)-4,4'-diyl)diammonium bis(hydrogen sulphate)	265-294-7	64969-36-4	612-081-00-5	Carc. 1B
(2E)-2-cyano-N-[(ethylamino)carbonyl]-2-(methoxyimino) acetamide	-	166900-80-7	616-035-00-5	Repr. 2
(2-ethylhexanoato-O)(isononanoato-O)nickel	287-470-2	85508-45-8	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(2-ethylhexanoato-O)(isodecanoato-O)nickel	284-351-7	84852-39-1	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(2-chloroethyl)(3-hydroxypropyl)ammonium chloride CLETOPROPAMINHYDROCHLORID	429-740-6	40722-80-3	612-246-00-1	Carc. 1B; Muta. 1B
(1R,2S,5S)-2-[(4-chlorophenyl)methyl]-5-propan-2-yl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol	-	115937-89-8	603-237-00-3	Repr. 1B
(1R,2S,5R)-2-[(4-chlorophenyl)methyl]-5-propan-2-yl-1-(1,2,4-triazol-1-ylmethyl)cyclopentan-1-ol	-	115850-69-6	603-237-00-3	Repr. 1B
(1,3,4,5,6,7-hexahydro-1,3-dioxo-2H-isoindol-2-yl)methyl (1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarboxylate	214-619-0	1166-46-7	607-728-00-3	Carc. 2
methyl-phenylene diamine	246-910-3	25376-45-8	612-151-00-5	Carc. 1B; Muta. 2; Repr. 2	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)
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)]	-	-	612-151-00-5	Carc. 1B; Muta. 2; Repr. 2	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)
sodium N-(hydroxymethyl)glycinate; [formaldehyde released from sodium N-(hydroxymethyl)glycinate]	274-357-8	70161-44-3	607-746-00-1	Carc. 1B; Muta. 2	formaldehyde released from sodium N-(hydroxymethyl)glycinate
lead chromate molybdate sulfate red; C.I. Pigment Red 104 [This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77605.] This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77605.	235-759-9	12656-85-8	082-010-00-5	Carc. 1B; Repr. 1A	This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77605.
lead sulfochromate yellow; C.I. Pigment Yellow 34 [This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77603.] This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77603.	215-693-7	1344-37-2	082-009-00-X	Carc. 1B; Repr. 1A	This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77603.
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 140o C to 215o C (284 °F to 419 °F).] This oil is a complex mixture 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	648-022-00-5	Carc. 1B; Muta. 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).
Light oil (coal), coke-oven; Crude benzole [The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1 292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.] 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	648-147-00-5	Carc. 1B; Muta. 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.
Light oil (coal), semi-coking process; Fresh oil [The volatile organic liquid condensed from the gasevolved in the low-temperature (less than 700 °C (1 292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.] 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	648-156-00-4	Carc. 1B; Muta. 1B	The volatile organic liquid condensed from the gasevolved in the low-temperature (less than 700 °C (1 292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.
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.
Naphtha (coal), distn. residues; Light Oil Redistillate, high boiling [The residue remaining from the distillation of recovered naphtha. Composed primarily of naphthalene and condensation products of indene and styrene.] The residue remaining from the distillation of recovered naphtha. Composed primarily of naphthalene and condensation products of indene and styrene.	292-636-2	90641-12-6	648-009-00-4	Carc. 1B; Muta. 1B	The residue remaining from the distillation of recovered naphtha. Composed primarily of naphthalene and condensation products of indene and styrene.
Extract residues (coal), tar oil alk.; Carbolic Oil Extract Residue [The residue obtained from coal tar oil by an alkaline wash such as aqueous sodium hydroxide after the removal of crude coal tar acids. Composed primarily of naphthalenes and aromatic nitrogen bases.] The residue obtained from coal tar oil by an alkaline wash such as aqueous sodium hydroxide after the removal of crude coal tar acids. Composed primarily of naphthalenes and aromatic nitrogen bases.	266-021-4	65996-87-4	648-027-00-2	Carc. 1B; Muta. 1B	The residue obtained from coal tar oil by an alkaline wash such as aqueous sodium hydroxide after the removal of crude coal tar acids. Composed primarily of naphthalenes and aromatic nitrogen bases.
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.] 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	648-137-00-0	Carc. 1B; Muta. 1B	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.
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 °C to 170 °C (284 °F to 392 °F) according to DIN 52025. Composed primarily of tri-and polynuclear aromatic compounds which also contain heteroatoms.] 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° to 170°C (284°F to 392°F) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.	302-650-3	94114-13-3	648-057-00-6	Carc. 1B	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 °C to 170 °C (284 °F to 392 °F) according to DIN 52025. Composed primarily of tri- and polynuclear aromatic compounds which also contain heteroatoms.
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 o C to 330 o C (518 °F to 626 °F). It consists predomi nantly of dinuclear aromatic and heterocyclic hydrocarbons.] 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	648-080-00-1	Carc. 1B	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 predomi nantly of dinuclear aromatic and heterocyclic hydrocarbons.
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.] 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	648-105-00-6	Carc. 1B; Muta. 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.
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 °C to 180 °C (86°F to 356°F). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.] The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30°C to 180°C (86°F to 356°F). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.	266-028-2	65996-93-2	648-055-00-5	Carc. 1A; Muta. 1B; Repr. 1B	The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 oC to 180 oC (86oF to 356oF). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.
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.] 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	648-095-00-3	Carc. 1B; Muta. 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.
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°C to 180°C (140°F to 356°F). Composed; primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.] The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40°C to 180°C (104°F to 356°F). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.	269-109-0	68187-57-5	648-076-00-X	Carc. 1B	The residue from the distillation of a mixture of coal tar and aromatic petroleum streams. A solid with a softening point from 40 °C to 180 °C (140 °F to 356 °F). Composed primarily of a complex combination of three or more membered condensed ring aromatic hydrocarbons.
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.] 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	648-125-00-5	Carc. 1B; Muta. 1B	The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.
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.] 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	648-110-00-3	Carc. 1B; Muta. 1B	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.
Extract residues (coal), brown; Coal Tar Extract [The residue from extraction of dried coal.] The residue from toluene extraction of dried brown coal.	294-285-0	91697-23-3	648-064-00-4	Carc. 1B	The residue from extraction of dried coal.
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.] 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	648-126-00-0	Carc. 1B; Muta. 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.
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), 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), 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 190o C to 270o C (374oF to 518oF). Composed primarily of substituted dinuclear aromatics.] 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	648-037-00-7	Carc. 1B; Muta. 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.
Extract oils (coal), coal tar-residual pyrolysis oils, naph thalene oil, redistillate; Redistillates [The redistillate from the fractional distillation of dephe nolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220o C to 230o C (428°F to 446°F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.] 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	648-038-00-2	Carc. 1B; Muta. 1B	The redistillate from the fractional distillation of dephe nolated 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.
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 90o C to 160 o C (194oF to 320 oF). It consists predomi nantly of benzene, toluene and xylenes.] 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	648-014-00-1	Carc. 1B; Muta. 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 predomi nantly of benzene, toluene and xylenes.
Tar acids, coal, crude; Crude Phenols [The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.] The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.	266-019-3	65996-85-2	648-116-00-6	Carc. 1B; Muta. 1B	The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.
Tar bases, coal, crude; Crude Tar Bases [The reaction product obtained by neutralizing coal tar base extract oil with an alkaline solution, such as aqueous sodium hydroxide, to obtain the free bases. Composed primarily of such organic bases as acridine, phenanthridine, pyridine, quinoline and their alkyl derivatives.] The reaction product obtained by neutralizing coal tar base extract oil with an alkaline solution, such as aqueous sodium hydroxide, to obtain the free bases. Composed primarily of such organic bases as acridine, phenanthridine, pyridine, quinoline and their alkyl derivatives.	266-018-8	65996-84-1	648-141-00-2	Carc. 1B; Muta. 1B	The reaction product obtained by neutralizing coal tar base extract oil with an alkaline solution, such as aqueous sodium hydroxide, to obtain the free bases. Composed primarily of such organic bases as acridine, phenanthridine, pyridine, quinoline and their alkyl derivatives.
Extract residues (coal), tar oil alk., carbonated, limed; Crude Phenols [The product obtained by treatment of coal tar oil alkaline extract with CO2 and CaO. Composed primarily of CaCO3, Ca(OH)2, Na2CO3 and other organic and inorganic impurities.] The product obtained by treatment of coal tar oil alkaline extract with CO2 and CaO. Composed primarily of CaCO3, Ca(OH)2, Na2CO3 and other organic and inorganic impurities.	292-629-4	90641-06-8	648-115-00-0	Carc. 1B; Muta. 1B	The product obtained by treatment of coal tar oil alkaline extract with CO2 and CaO. Composed primarily of CaCO3, Ca(OH)2, Na2CO3 and other organic and inorganic impurities.

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