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 1.351 - 1.400 su 1.679 risultati.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
benzyl(diethylamino)diphenylphosphonium 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxyphenyl)propan-2-yl]phenolate	479-100-5	577705-90-9	015-204-00-5	Repr. 1B
benzyl violet 4B; α-[4-(4-dimethylamino-α-{4-[ethyl(3-sodiosulphonato benzyl)amino] phenyl}benzylidene)cyclohexa-2,5-dienylidene(ethyl)ammonio]toluene-3-sulphonate	216-901-9	1694-09-3	650-010-00-X	Carc. 2
benzyl 2,4-dibromobutanoate B2,4DBB	420-710-8	23085-60-1	607-376-00-0	Repr. 2
benzophenone	204-337-6	119-61-9	606-153-00-5	Carc. 1B
Benzol forerunnings (coal); Light Oil Redistillate, low boiling [The distillate from coke oven light oil having an approximate distillation range below 100 o C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.] 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	648-003-00-1	Carc. 1B; Muta. 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.
benzo[rst]pentaphene	205-877-5	189-55-9	601-090-00-X	Carc. 1B; Muta. 2
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
benzo[a]pyrene; benzo[def]chrysene	200-028-5	50-32-8	601-032-00-3	Carc. 1B; Muta. 1B; Repr. 1B
benzidine; 1,1'-biphenyl-4,4'-diamine; 4,4'-diaminobiphenyl; biphenyl-4,4'-ylenediamine	202-199-1	92-87-5	612-042-00-2	Carc. 1A
benzidine sulphate	244-236-4	21136-70-9	612-070-00-5	Carc. 1A
benzidine based azo dyes; 4,4'-diarylazobiphenyl dyes, with the exception of those specified elsewhere in this Annex	-	-	611-024-00-1	Carc. 1B
Benzidine acetate	252-984-8	36341-27-2	612-070-00-5	Carc. 1A
benzene	200-753-7	71-43-2	601-020-00-8	Carc. 1A; Muta. 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
bentazone (ISO); 3-isopropyl-2,1,3-benzothiadiazine-4-one-2,2-dioxide	246-585-8	25057-89-0	613-012-00-1	Repr. 2
benomyl (ISO);methyl 1-(butylcarbamoyl)benzimidazol-2-ylcarbamate	241-775-7	17804-35-2	613-049-00-3	Muta. 1B; Repr. 1B
benfuracarb (ISO); ethyl N-[2,3-dihydro-2,2-dimethylbenzofuran-7-yloxycarbonyl(methyl)aminothio]-N-isopropyl-β-alaninate	617-356-3	82560-54-1	006-088-00-7	Repr. 2
benfluralin (ISO); N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-toluidine	217-465-2	1861-40-1	612-295-00-9	Carc. 2; Repr. 2
BBP; benzyl butyl phthalate e	201-622-7	85-68-7	607-430-00-3	Repr. 1B
Barium diboron tetraoxide	237-222-4	13701-59-2	056-005-00-3	Repr. 1B
azobenzene	203-102-5	103-33-3	611-001-00-6	Carc. 1B; Muta. 2
azamethiphos (ISO); S-[(6-chloro-2-oxooxazolo [4,5-b]pyridin-3(2H)-yl) methyl] O,O-dimethyl thiophosphate	252-626-0	35575-96-3	613-338-00-4	Carc. 2
azafenidin (ISO); 2-(2,4-dichloro-5-prop-2-ynyloxyphenyl)-5,6,7,8-tetrahydro-1,2,4-triazolo[4,3-a]pyridine-3(2H)-one	620-425-0	68049-83-2	611-140-00-2	Repr. 1B
avermectin B1a (purity ≥ 80 %)	265-610-3	65195-55-3	606-143-00-0	Repr. 2
Asbestos, tremolite	616-473-7	77536-68-6	650-013-00-6	Carc. 1A
Asbestos, grunerite	601-801-3	12172-73-5	650-013-00-6	Carc. 1A
Asbestos, chrysotile	-	132207-32-0	650-013-00-6	Carc. 1A
Asbestos, anthophyllite	616-472-1	77536-67-5	650-013-00-6	Carc. 1A
Asbestos, actinolite	616-471-6	77536-66-4	650-013-00-6	Carc. 1A
Asbestos fibres show/hide Asbestos, tremolite EC / List no: 616-473-7 \| CAS no: 77536-68-6 Asbestos, chrysotile EC / List no: 601-650-3 \| CAS no: 12001-29-5 Asbestos, amosite EC / List no: 601-801-3 \| CAS no: 12172-73-5 Asbestos, actinolite EC / List no: 616-471-6 \| CAS no: 77536-66-4 Asbestos, crocidolite EC / List no: 601-649-8 \| CAS no: 12001-28-4 Asbestos, anthophyllite EC / List no: 616-472-1 \| CAS no: 77536-67-5	-	-	650-013-00-6	Carc. 1A
arsenic acid and it salts with the exception of those specified elsewhere in this Annex	-	-	033-005-00-1	Carc. 1A
Aromatic hydrocarbons, C9-12, benzene distn.; Light Oil Redistillate, high boiling	295-551-9	92062-36-7	648-013-00-6	Carc. 1B; Muta. 1B
Aromatic hydrocarbons, C8; Light Oil Redistillate, high boiling	292-694-9	90989-38-1	648-010-00-X	Carc. 1B; Muta. 1B
Aromatic hydrocarbons, C8-9, hydrocarbon resin polymn. by-product; Light Oil Redistillate, high boiling [A complex combination of hydrocarbons obtained from the evaporation of solven 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 o C to 215 o C (248 °F to 419 °F).] 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	648-012-00-0	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons obtained from the evaporation of solven 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).
Aromatic hydrocarbons, C8-10; Low boiling point naphtha -unspecified	292-695-4	90989-39-2	649-403-00-9	Carc. 1B; Muta. 1B
Aromatic hydrocarbons, C8, catalytic reforming-derived; Low boiling point cat-reformed naphtha	295-279-0	91995-18-5	649-310-00-3	Carc. 1B; Muta. 1B
Aromatic hydrocarbons, C7-8, dealkylation products, distn. residues; Low boiling point naphtha — unspecified	292-698-0	90989-42-7	649-379-00-X	Carc. 1B; Muta. 1B
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).] 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	649-311-00-9	Carc. 1B; Muta. 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).
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 o C (1 500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.] 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	649-321-00-3	Carc. 1B; Muta. 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.
Aromatic hydrocarbons, C6-10, C8-rich; Light Oil Redistillate, low boiling	292-697-5	90989-41-6	648-005-00-2	Carc. 1B; Muta. 1B
Aromatic hydrocarbons, C6-10, acid-treated, neutralized; Low boiling point naphtha — unspecified	268-618-5	68131-49-7	649-357-00-X	Carc. 1B; Muta. 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.
antu (ISO); 1-(1-naphthyl)-2-thiourea	201-706-3	86-88-4	006-008-00-0	Carc. 2
antimony trioxide	215-175-0	1309-64-4	051-005-00-X	Carc. 2
anthraquinone	201-549-0	84-65-1	606-151-00-4	Carc. 1B

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