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 srpnja 2024. Database contains 1679 unique substances/entries.

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Prikazano 501 - 550 od 1.679 rezultata.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
Alkanes, C1-4, C3-rich; Petroleum gas	292-456-4	90622-55-2	649-114-00-8	Carc. 1A; Muta. 1B
Alkanes, C12-26-branched and linear	292-454-3	90622-53-0	649-242-00-4	Carc. 1B
Hydrocarbons, C4; Petroleum gas	289-339-5	87741-01-3	649-113-00-2	Carc. 1A; Muta. 1B
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).] 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	649-378-00-4	Carc. 1B; Muta. 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).
(isononanoato-O)(neodecanoato-O)nickel	287-592-6	85551-28-6	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
Solvent naphtha (coal), xylene-styrene cut; Light Oil Redistillate, intermediate boiling	287-502-5	85536-20-5	648-007-00-3	Carc. 1B; Muta. 1B
Solvent naphtha (coal), coumarone-styrene contg.; Light Oil Redistillate, intermediate boiling	287-500-4	85536-19-2	648-008-00-9	Carc. 1B; Muta. 1B
Solvent naphtha (coal), light; Light Oil Redistillate, low boiling	287-498-5	85536-17-0	648-006-00-8	Carc. 1B; Muta. 1B
alkanes, C14-17, chloro; chlorinated paraffins, C14-17	287-477-0	85535-85-9	602-095-00-X	Lact.
alkanes, C10-13, chloro; chlorinated paraffins, C10-13	287-476-5	85535-84-8	602-080-00-8	Carc. 2
(isononanoato-O)(isooctanoato-O)nickel	287-471-8	85508-46-9	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
(2-ethylhexanoato-O)(isononanoato-O)nickel	287-470-2	85508-45-8	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
nickel(II) neodecanoate	287-469-7	85508-44-7	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
nickel(II) isodecanoate	287-468-1	85508-43-6	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
chrysoidine C10-14-alkyl derivatives; benzenesulfonic acid, mono-C10-14-alkyl derivatives, compounds; with 4-(phenylazo)-1,3-benzenediamine	286-946-7	85407-90-5	611-153-00-3	Muta. 2
(isodecanoato-O)(isooctanoato-O)nickel	285-909-2	85166-19-4	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
2-ethylhexanoato-O)(neodecanoato-O)nickel	285-698-7	85135-77-9	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
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°C to 548°C (579°F to 1018°F). Likely to contain 5 % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.] 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°C to 548°C (579°F to 1018° F). Likely to contain 5% or more of 4- to 6- membered condensed ring aromatic hydrocarbons.	285-555-9	85117-03-9	649-039-00-0	Carc. 1B	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 °C to 548 °C (579 °F to 1018 °F). Likely to contain 5 % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.
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).] 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 minus 20°C to 190°C (-4°F to 374°F).	285-512-4	85116-61-6	649-336-00-5	Carc. 1B; Muta. 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).
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).] 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	649-335-00-X	Carc. 1B; Muta. 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).
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 66o C to 121o C (151°F to250°F).] 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	649-377-00-9	Carc. 1B; Muta. 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).
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).] 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	649-309-00-8	Carc. 1B; Muta. 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).
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 °C to 400o°C (401°F to 752°F).] A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurized thermal 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° C to 400°C (401°F to 752°F).	285-505-6	85116-53-6	649-443-00-7	Carc. 1B	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 °C to 400 °C (401 °F to 752 °F).
Petrolatum (petroleum), alumina-treated; Petrolatum [A complex combination of hydrocarbons obtained when petrolatum is treated with Al2O3 to remove polar components and impurities. It consists predominantly of saturated, crystalline, and liquid hydrocarbons having carbon numbers predominantly greater than C25.] A complex combination of hydrocarbons obtained when petrolatum is treated with Al2O3 to remove polar components and impurities. It consists predominantly of saturated, crystalline, and liquid hydrocarbons having carbon numbers predominantly greater than C25.	285-098-5	85029-74-9	649-256-00-0	Carc. 1B	A complex combination of hydrocarbons obtained when petrolatum is treated with Al2O3 to remove polar components and impurities. It consists predominantly of saturated, crystalline, and liquid hydrocarbons having carbon numbers predominantly greater than C25.
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).] 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	648-084-00-3	Carc. 1B; Muta. 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).
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.] 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	648-096-00-9	Carc. 1B; Muta. 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.
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.] A complex combination of hydrocarbons obtained by the crystallization of the fractional distillates from coal tar. It consists of aromatic and polycyclic hydrocarbons, primarily fluorene and acenaphthene.	284-900-0	84989-11-7	648-042-00-4	Carc. 1B	A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists af aromatic and polycyclic hydrocarbons primarily fluorene and some acenaphthene.
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.] A complex combination of hydrocarbons obtained by the crystallization of the fractional distillates from tar oil. It consists of aromatic polycyclic hydrocarbons, primarily diphenyl, dibenzofuran and acenaphthene.	284-899-7	84989-10-6	648-078-00-0	Carc. 1B	A complex combination of hydrocarbons obtained by the crystallization of tar oil. It consists of aromatic polycyclic hydrocarbons, primarily diphenyl, dibenzofuran and acenaphthene.
Distillates (coal tar), naph thalene oils, naphthalene-low; Naphthalene Oil Redistillate [A complex combination of hydrocarbons obtained by crys tallization of naphthalene oil. Composed primarily of naphthalene, alkyl naphthalenes and phenolic compounds.] 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	648-086-00-4	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons obtained by crys tallization of naphthalene oil. Composed primarily of naphthalene, alkyl naphthalenes and phenolic compounds.
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.] 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	648-124-00-X	Carc. 1B; Muta. 1B	The fraction of tar acids, rich in 3,5-dimethylphenol, recovered by distillation of low-temperature coal tar acids.
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.] 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	648-122-00-9	Carc. 1B; Muta. 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.
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.] 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	648-121-00-3	Carc. 1B; Muta. 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.
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.] 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	648-120-00-8	Carc. 1B; Muta. 1B	The fraction of tar acid rich in 3-and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.
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 rude tar acids.] 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	648-123-00-4	Carc. 1B; Muta. 1B	The fraction of tar acids, rich in 3-and 4-ethylphenol, recovered by distillation of low-temperature coal tar rude tar acids.
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.] 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 mixture of monohydric and dihydric phenols.	284-881-9	84988-93-2	648-111-00-9	Carc. 1B; Muta. 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.
(2-ethylhexanoato-O)(isodecanoato-O)nickel	284-351-7	84852-39-1	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
nickel bis(isononanoate)	284-349-6	84852-37-9	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
(isooctanoato-O)(neodecanoato-O)nickel	284-347-5	84852-35-7	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
4-nonylphenol, branched	284-325-5	84852-15-3	601-053-00-8	Repr. 2
1,2-benzenedicarboxylic acid, dipentylester, branched and linear	284-032-2	84777-06-0	607-426-00-1	Repr. 1B
fatty acids, C 8-18 and C18-unsaturated, nickel salts	283-972-0	84776-45-4	028-054-00-0	Carc. 1A; Muta. 2; Repr. 1B
Margosa, ext. [from the kernels of Azadirachta indica extracted with water and further processed with organic solvents] Extractives and their physically modified derivatives such as tinctures, concretes, absolutes, essential oils, oleoresins, terpenes, terpene-free fractions, distillates, residues, etc., obtained from Azadirachta indica, Meliaceae.	283-644-7	84696-25-3	650-058-00-1	Repr. 2	From the kernels of Azadirachta indica extracted with water and further processed with organic solvents
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 compound and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392°F to 482°F).]- 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	648-085-00-9	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compound and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).
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 o C to 210 o C (302 °F to 410 °F).] 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	648-023-00-0	Carc. 1B; Muta. 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).
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).
chlozolinate (ISO); ethyl (RS)-3-(3,5-dichlorophenyl)-5-methyl-2,4-dioxo-oxazolidine-5-carboxylate	282-714-4	84332-86-5	607-306-00-9	Carc. 2
chrysoidine sulfate; bis[4-(phenylazo)benzene-1,3-diamine] sulfate	282-432-1	84196-22-5	611-152-00-8	Muta. 2
chrysoidine dihydrochloride; 4-(phenylazo)benzene-1,3-diamine dihydrochloride	281-549-5	83968-67-6	611-152-00-8	Muta. 2
2-ethylhexyl[[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]thio]acetate	279-452-8	80387-97-9	607-203-00-9	Repr. 1B

Prikazano 501 - 550 od 1.679 rezultata.

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