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 19 aprile 2024. Database contains 1679 unique substances/entries.

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Mostra 1.401 - 1.450 di 1.679 risultati.

Substance Name	EC No.	CAS No.	Index	Classifications	Substance Description	Physical form
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, anthracene-low; Anthracene Oil Fraction [The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.] The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.	292-604-8	90640-82-7	648-104-00-0	Carc. 1B; Muta. 1B	The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.
Anthracene oil, anthracene paste; Anthracene Oil Fraction [The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.] The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.	292-603-2	90640-81-6	648-103-00-5	Carc. 1B; Muta. 1B	The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.
Anthracene oil, anthracene paste, distn. lights; Anthracene Oil Fraction [A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554°F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.] A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290°C to 340°C (554°F to 644°F). It contains chiefly trinuclear aromatics and their dihydro derivatives.	295-278-5	91995-17-4	648-108-00-2	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.
Anthracene oil, anthracene paste, carbazole fraction; Anthracene Oil Fraction [A complex combination of hydrocarbons from the distil lation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662°F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.] A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350°C to 360°C (662°F to 680°F). It contains chiefly anthracene, carbazole and phenanthrene.	295-276-4	91995-16-3	648-107-00-7	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons from the distil lation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.
Anthracene oil, anthracene paste, anthracene fraction; Anthracene Oil Fraction [A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626°F to 662°F). It contains chiefly anthracene, carbazole and phenanthrene.] A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330°C to 350°C (626°F to 662°F). It contains chiefly anthracene, carbazole and phenanthrene.	295-275-9	91995-15-2	648-106-00-1	Carc. 1B; Muta. 1B	A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.
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.
Aniline	200-539-3	62-53-3	612-008-00-7	Carc. 2; Muta. 2
androsta-1,4,9(11)-triene-3,17-dione	433-560-3	15375-21-0	606-134-00-1	Repr. 2
ammoniumpentadeca-fluorooctanoate	223-320-4	3825-26-1	607-703-00-7	Carc. 2; Repr. 1B; Lact.
Ammonium salts of perfluorononan-1-oic-acid	-	4149-60-4	607-718-00-9	Carc. 2; Repr. 1B; Lact.
ammonium perfluorooctanesulfonate; ammonium heptadecafluorooctanesulfonate	249-415-0	29081-56-9	607-624-00-8	Carc. 2; Repr. 1B; Lact.
ammonium nonadecafluorodecanoate	221-470-5	3108-42-7	607-720-00-X	Carc. 2; Repr. 1B; Lact.
ammonium dichromate	232-143-1	7789-09-5	024-003-00-1	Carc. 1B; Muta. 1B; Repr. 1B
ammonium bromide	235-183-8	12124-97-9	035-005-00-7	Repr. 1B; Lact.
amitrole (ISO);1,2,4-triazol-3-ylamine	200-521-5	61-82-5	613-011-00-6	Repr. 2
amisulbrom (ISO); 3-(3-bromo-6-fluoro-2-methylindol-1-ylsulfonyl)-N,N-dimethyl-1H-1,2,4-triazole-1-sulfonamide	672-776-4	348635-87-0	616-224-00-2	Carc. 2
allyl glycidyl ether; allyl 2,3-epoxypropyl ether; prop-2-en-1-yl 2,3-epoxypropyl ether	203-442-4	106-92-3	603-038-00-1	Carc. 2; Muta. 2; Repr. 2
Alkanes, C4-5; Petroleum gas	270-654-1	68475-60-5	649-196-00-5	Carc. 1A; Muta. 1B
Alkanes, C3-4; petroleum gas	270-653-6	68475-59-2	649-195-00-X	Carc. 1A; Muta. 1B
Alkanes, C2-3; Petroleum gas	270-652-0	68475-58-1	649-194-00-4	Carc. 1A; Muta. 1B
alkanes, C14-17, chloro; chlorinated paraffins, C14-17	287-477-0	85535-85-9	602-095-00-X	Lact.
Alkanes, C12-26-branched and linear	292-454-3	90622-53-0	649-242-00-4	Carc. 1B
alkanes, C10-13, chloro; chlorinated paraffins, C10-13	287-476-5	85535-84-8	602-080-00-8	Carc. 2
Alkanes, C1-4, C3-rich; Petroleum gas	292-456-4	90622-55-2	649-114-00-8	Carc. 1A; Muta. 1B
Alkanes, C1-2; Petroleum gas	270-651-5	68475-57-0	649-193-00-9	Carc. 1A; Muta. 1B
aldrin (ISO)	206-215-8	309-00-2	602-048-00-3	Carc. 2
alachlor (ISO); 2-chloro-2',6'-diethyl-N-(methoxymethyl)acetanilide	240-110-8	15972-60-8	616-015-00-6	Carc. 2
acrylonitrile	203-466-5	107-13-1	608-003-00-4	Carc. 1B
acrylamide; prop-2-enamide	201-173-7	79-06-1	616-003-00-0	Carc. 1B; Muta. 1B; Repr. 2
aclonifen (ISO); 2-chloro-6-nitro-3-phenoxyaniline	277-704-1	74070-46-5	612-120-00-6	Carc. 2
acetochlor (ISO); 2-chloro-N-(ethoxymethyl)-N-(2-ethyl-6-methylphenyl)acetamide	251-899-3	34256-82-1	616-037-00-6	Carc. 2; Repr. 2
acetic acid;naphthalen-2-amine	209-030-0	553-00-4	612-071-00-0	Carc. 1A
acetamiprid (ISO); (1E)-N-[(6-chloropyridin-3-yl)methyl]-N’-cyano-N-methylethanimidamide; (E)-N1-[(6-chloro-3-pyridyl)methyl]-N2-cyano-N1-methylacetamidine	682-791-8	160430-64-8	608-032-00-2	Repr. 2
acetamiprid (ISO); (1E)-N-[(6-chloropyridin-3-yl)methyl]-N'-cyano-N-methylethanimidamide; (E)-N1-[(6-chloro-3-pyridyl)methyl]-N2-cyano-N1-methylacetamidine	603-921-1	135410-20-7	608-032-00-2	Repr. 2
acetamide	200-473-5	60-35-5	616-022-00-4	Carc. 2
acetaldehyde; ethanal	200-836-8	75-07-0	605-003-00-6	Carc. 1B; Muta. 2
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).
abamectin (combination of avermectin B1a and avermectin B1b) (ISO)	615-339-5	71751-41-2	606-143-00-0	Repr. 2
[μ-[carbonato(2-)-O:O']]dihydroxy trinickel	265-748-4	65405-96-1	028-010-00-0	Carc. 1A; Muta. 2; Repr. 1B
[carbonato(2-)] tetrahydroxytrinickel	235-715-9	12607-70-4	028-010-00-0	Carc. 1A; Muta. 2; Repr. 1B
[(tolyloxy)methyl]oxirane; cresyl glycidyl ether	247-711-4	26447-14-3	603-056-00-X	Muta. 2
[(p-tolyloxy)methyl]oxirane	218-574-8	2186-24-5	603-056-00-X	Muta. 2
[(m-tolyloxy)methyl]oxirane	218-575-3	2186-25-6	603-056-00-X	Muta. 2
9-vinylcarbazole	216-055-0	1484-13-5	613-169-00-6	Muta. 2
7-oxa-3-oxiranylbicyclo [4.1.0]heptane; 1,2-epoxy- 4-epoxyethylcyclohexane; 4-vinylcyclohexene diepoxide	203-437-7	106-87-6	603-066-00-4	Carc. 1B; Muta. 2; Repr. 1B
7-methoxy-6-(3-morpholin-4-yl-propoxy)-3H-quinazolin-4-one [containing ≥ 0,5 % formamide (EC No 200-842-0)]	429-400-7	199327-61-2	612-253-01-7	Repr. 1B
6-methoxy-m-toluidine; p-cresidine	204-419-1	120-71-8	612-209-00-X	Carc. 1B
6-hydroxy-1-(3-isopropoxypropyl)-4-methyl-2-oxo-5-[4-(phenylazo)phenylazo]-1,2-dihydro-3-pyridinecarbonitrile ARANCIO DISPERSO 149; C.I. DISPERSE ORANGE 149; DISPERS ORANGE 149; DISPERSE ORANGE 149; ORANGE DISPERSE 149; TERASIL GOLDGELB 2RS	400-340-3	85136-74-9	611-057-00-1	Carc. 1B
6-glycidyloxynapht-1-yl oxymethyloxirane	429-960-2	27610-48-6	603-113-00-9	Muta. 2

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