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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Mostra 301 - 350 di 1.679 risultati.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
hymexazol (ISO);3-hydroxy-5-methylisoxazole	233-000-6	10004-44-1	613-115-00-1	Repr. 2
imazamox (ISO); (RS)-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methoxymethylnicotinic acid	601-305-7	114311-32-9	613-208-00-7	Repr. 2
ioxynil (ISO) 4-hydroxy-3,5-diiodobenzonitrile	216-881-1	1689-83-4	608-007-00-6	Repr. 2
ipconazole (ISO); (1RS,2SR,5RS;1RS,2SR,5SR)-2-(4-chlorobenzyl)-5-isopropyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol	603-038-1	125225-28-7	603-237-00-3	Repr. 1B
iprovalicarb (ISO); isopropyl [(2S)-3-methyl-1-{[1-(4-methylphenyl)ethyl]amino}-1-oxobutan-2-yl]carbamate	604-209-3	140923-17-7	616-232-00-6	Carc. 2
isoxaflutole (ISO); 5-cyclopropyl-1,2-oxazol-4-yl α,α,α-trifluoro-2-mesyl-p-tolyl ketone	604-222-4	141112-29-0	606-054-00-7	Repr. 2
kresoxim-methyl (ISO); methyl (E)-2-methoxyimino-[2-(o-tolyloxymethyl)phenyl]acetate	604-351-6	143390-89-0	607-310-00-0	Carc. 2
lead 2,4,6-trinitro-m-phenylene dioxide; lead 2,4,6-trinitroresorcinoxide; lead styphnate;lead 2,4,6-trinitro-m-phenylene dioxide; lead 2,4,6-trinitroresorcinoxide; lead styphnate (≥ 20 % phlegmatiser)	239-290-0	15245-44-0	609-019-00-4	Repr. 1A
lead 2,4,6-trinitro-m-phenylene dioxide; lead 2,4,6-trinitroresorcinoxide; lead styphnate;lead 2,4,6-trinitro-m-phenylene dioxide; lead 2,4,6-trinitroresorcinoxide; lead styphnate (≥ 20 % phlegmatiser)	239-290-0	15245-44-0	609-019-01-1	Repr. 1A
lead acetate, basic	215-630-3	1335-32-6	082-007-00-9	Carc. 2; Repr. 1A
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 diazide; lead azide;lead diazide; lead azide [≥ 20 % phlegmatiser]	236-542-1	13424-46-9	082-003-01-4	Repr. 1A
lead diazide; lead azide;lead diazide; lead azide [≥ 20 % phlegmatiser]	236-542-1	13424-46-9	082-003-00-7	Repr. 1A
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.
lead(II) methanesulphonate BLEIMETHANSULFONAT; LEAD (II) METHANESULFONATE; LEAD METHANE SULPHONATE; LEAD SALT FP	401-750-5	17570-76-2	082-008-00-4	Repr. 1A
leucomalachite green; N, N,N',N'-tetramethyl-4,4'-benzylidenedianiline	204-961-9	129-73-7	612-281-00-2	Carc. 2; Muta. 2
lithium nickel dioxide	620-400-4	12031-65-1	028-057-00-7	Carc. 1A
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 °C (104 °F.] 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 produces a finished oil with a viscosity in the order of 17cSt to 23cSt at 40°C (104°F).	309-875-6	101316-70-5	649-528-00-9	Carc. 1B	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 °C (104 °F).
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 °C (104 °F).] 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°C (104°F).	309-876-1	101316-71-6	649-529-00-4	Carc. 1B	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 °C (104 °F).
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 °C (104 °F).] 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°C (104°F).	309-877-7	101316-72-7	649-530-00-X	Carc. 1B	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 °C (104 °F).
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 °C (212 °F).] 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°C (212°F).	309-874-0	101316-69-2	649-527-00-3	Carc. 1B	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 °C (212 °F).
m-bis(2,3-epoxypropoxy)benzene; resorcinol diglycidyl ether	202-987-5	101-90-6	603-065-00-9	Carc. 1B; Muta. 2
m-phenylenediamine	203-584-7	108-45-2	612-147-00-3	Muta. 2
maneb (ISO); manganese ethylenebis(dithiocarbamate) (polymeric)	235-654-8	12427-38-2	006-077-00-7	Repr. 2
mepanipyrim; 4-methyl-N-phenyl-6-(1-propynyl)-2-pyrimidinamine	432-140-7	110235-47-7	612-229-00-9	Carc. 2
mesotrione(ISO); 2-[4-(methylsulfonyl)-2-nitrobenzoyl]-1,3-cyclohexanedione	600-533-4	104206-82-8	609-064-00-X	Repr. 2
metaflumizone (ISO); (EZ)-2-[2-(4-cyanophe-nyl)-1-(a,a,a -trifluoro-m-tolyl)ethylidene]-[4-(tri-fluoromethoxy)phenyl] carbanilohydrazide [E-iso-mer > 90 %, Z-isomer <10 % relative content]	604-167-6	139968-49-3	616-227-00-9	Repr. 2; Lact.
metconazole (ISO); (1RS, 5RS;1RS, 5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol	603-031-3	125116-23-6	613-284-00-1	Repr. 2
methyl salicylate	204-317-7	119-36-8	607-749-00-8	Repr. 2
methylmercuric chloride	204-064-2	115-09-3	080-012-00-0	Carc. 2; Repr. 1A; Lact.
metosulam (ISO); N-(2,6-dichloro-3-methylphenyl)-5,7-dimethoxy[1,2,4]triazolo[1,5-a] pyrimidine-2-sulfonamide	410-240-1	139528-85-1	616-214-00-8	Carc. 2
millerite	-	1314-04-1	028-006-00-9	Carc. 1A; Muta. 2
molybdenum nickel oxide	-	12673-58-4	028-057-00-7	Carc. 1A
molybdenum nickel tetraoxide	238-034-5	14177-55-0	028-057-00-7	Carc. 1A
molybdenum trioxide	215-204-7	1313-27-5	042-001-00-9	Carc. 2
monuron (ISO); 3-(4-chlorophenyl)-1,1-dimethylurea	205-766-1	150-68-5	006-042-00-6	Carc. 2
morpholine-4-carbonyl chloride	239-213-0	15159-40-7	613-041-00-X	Carc. 2
N, N-dimethylanilinium tetrakis(pentafluorophenyl)borate B1; N,N-DIMETHYLANILINUM TETRAKIS(PENTAFLUOROPHENYL)BORATE; TÉTRAKIS(PENTAFLUOROPHÉNYL)BORATE DE N,N-DIMÉTHYLANILINIUM	422-050-6	118612-00-3	005-010-00-9	Carc. 2
N,N'-dihexadecyl-N,N'-bis(2-hydroxyethyl)propanediamide QUESTAMIDE H	422-560-9	149591-38-8	616-143-00-2	Repr. 2
N,N,N',N'-tetraglycidyl-4,4'-diamino-3,3'-diethyldiphenylmethane PFMT 1848	410-060-3	130728-76-6	612-171-00-4	Muta. 2
N,N,N',N'-tetramethyl-4,4'-methylendianiline	202-959-2	101-61-1	612-201-00-6	Carc. 1B
N,N-dimethylacetamide	204-826-4	127-19-5	616-011-00-4	Repr. 1B
N,N-dimethylaniline	204-493-5	121-69-7	612-016-00-0	Carc. 2
N-(5-chloro-2-isopropylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide; isoflucypram	811-438-4	1255734-28-1	616-239-00-4	Repr. 2
N-2-naphthylaniline; N-phenyl-2-naphthylamine	205-223-9	135-88-6	612-135-00-8	Carc. 2
n-hexane	203-777-6	110-54-3	601-037-00-0	Repr. 2
N-methoxy-N-[1-methyl-2-(2,4,6-trichlorophenyl)-ethyl]-3-(difluoromethyl)- 1-methylpyrazole-4-carboxamide; pydiflumetofen	817-852-1	1228284-64-7	616-234-00-7	Carc. 2; Repr. 2
N-methylformamide	204-624-6	123-39-7	616-056-00-X	Repr. 1B
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).] 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	649-273-00-3	Carc. 1B; Muta. 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).
Naphtha (petroleum), hydrodesulfurised full-range coker; Low boiling point naphtha -unspecified [A complex ombination 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).] A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised 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	649-396-00-2	Carc. 1B; Muta. 1B	A complex ombination 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).

Mostra 301 - 350 di 1.679 risultati.

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