pregnant-women-protection

Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II

EU. Chemical Agents: Annexes I & II, Directive 92/85/EEC on Pregnant Workers, 28 November 1992 (updated by table 3 of Annex VI to CLP, 5 October 2018)

This list contains a non-exhaustive inventory of substances to which pregnant workers and workers who have recently given birth or are breastfeeding may not be exposed. Employers are obligated to prevent the exposure of these workers to any agents that may have adverse health effects on either mother or child. The inventory originates from Table 3 of Annex VI to the CLP.

Last updated 18 April 2024. Database contains 2100 unique substances/entries.

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Showing 601 - 800 of 2,100 results.

Substance Name	EC No.	CAS No.	CLP (1272/2008) CMRs	ECCAR Directive 2004/37/EC
cobalt lithium nickel oxide	442-750-5	113066-89-0	Carc. 1A	yes	Details
cobalt nickel oxide	620-395-9	12737-30-3	Carc. 1A	yes	Details
cobalt sulfate	233-334-2	10124-43-3	Carc. 1B; Muta. 2; Repr. 1B	yes	Details
cyanofenphos (ISO); O-4-cyanophenyl O-ethyl phenylphosphonothioate	620-377-0	13067-93-1	STOT SE 1		Details
cyclohexylamine	203-629-0	108-91-8	Repr. 2		Details
cycloxydim (ISO); 2-(N-ethoxybutanimidoyl)-3-hydroxy-5-(tetrahydro-2H-thiopyran-3-yl)cyclohex-2-en-1-one	405-230-9	101205-02-1	Repr. 2		Details
daminozide (ISO); 4-(2,2-dimethylhydrazino)-4-oxobutanoic acid; N-dimethylaminosuccinamic acid	216-485-9	1596-84-5	Carc. 2		Details
desmedipham (ISO); ethyl 3-phenylcarbamoyloxyphenylcarbamate	237-198-5	13684-56-5	Repr. 2		Details
di-n-pentyl phthalate	205-017-9	131-18-0	Repr. 1B	yes	Details
di-tert-butyl peroxide	203-733-6	110-05-4	Muta. 2		Details
dialuminium nickel tetraoxide	234-454-8	12004-35-2	Carc. 1A	yes	Details
diammonium 1-hydroxy-2-(4-(4-carboxyphenylazo)-2,5-dimethoxyphenylazo)-7-amino-3-naphthalenesulfonate	422-670-7	150202-11-2	Repr. 2		Details
diammonium nickel bis(sulfate)	239-793-5	15699-18-0	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
diarsenic pentaoxide; arsenic pentoxide; arsenic oxide	215-116-9	1303-28-2	Carc. 1A	yes	Details
diarsenic trioxide; arsenic trioxide	215-481-4	1327-53-3	Carc. 1A	yes	Details
dibenzo[b,def]chrysene; dibenzo[a,h]pyrene	205-878-0	189-64-0	Carc. 1B; Muta. 2	yes	Details
dibenzo[def,p]chrysene; dibenzo[a,l]pyrene	205-886-4	191-30-0	Carc. 1B; Muta. 2	yes	Details
diboron trioxide	215-125-8	1303-86-2	Repr. 1B	yes	Details
dibutyltin di(acetate)	213-928-8	1067-33-0	Muta. 2; Repr. 1B	yes	Details
difenoconazole (ISO); 1-({2-[2-chloro-4-(4-chlorophenoxy)phenyl]-4-methyl-1,3-dioxolan-2-yl} methyl)-1H-1,2,4-triazole; 3-chloro-4-[(2RS,4RS;2RS,4SR)-4-methyl-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-2-yl] phenyl 4-chlorophenyl ether	601-613-1	119446-68-3	Carc. 2		Details
difethialone (ISO); 3-[3-(4'-bromobiphenyl-4-yl)-1,2,3,4-tetrahydronaphthalen-1-yl]-4-hydroxy-2H-1-benzothiopyran-2-one	600-594-7	104653-34-1	Repr. 1B	yes	Details
dimethomorph (ISO); (E,Z)-4-(3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl) acryloyl)morpholine	404-200-2	110488-70-5	Repr. 1B	yes	Details
dimethyl propylphosphonate	242-555-3	18755-43-6	Muta. 1B; Repr. 1B	yes	Details
dimethylsulfamoylchloride	236-412-4	13360-57-1	Carc. 1B	yes	Details
dimoxystrobin (ISO); (2E)-2-{2-[(2,5-dimethylphenoxy)methyl]phenyl}-2-(methoxyimino)-N-methylacetamide; (E)-2-(methoxyimino)-N-methyl-2-[α-(2,5-xylyloxy)-o-tolyl]acetamide	604-712-8	149961-52-4	Carc. 2; Repr. 2		Details
dinickel boride	234-494-6	12007-01-1	Carc. 1A	yes	Details
dinickel diphosphate	238-426-6	14448-18-1	Carc. 1A	yes	Details
dinickel hexacyanoferrate	238-946-3	14874-78-3	Carc. 1A	yes	Details
dinickel orthosilicate	237-411-1	13775-54-7	Carc. 1A	yes	Details
dinickel phosphide	234-828-0	12035-64-2	Carc. 1A	yes	Details
dinickel silicide	235-033-1	12059-14-2	Carc. 1A	yes	Details
dinickel trioxide	215-217-8	1314-06-3	Carc. 1A	yes	Details
dinoterb (ISO); 2-tert-butyl-4,6-dinitrophenol	215-813-8	1420-07-1	Repr. 1B	yes	Details
diphosphoric acid, nickel(II) salt	-	19372-20-4	Carc. 1A	yes	Details
disodium 4-amino-3-[[4'-[(2,4-diaminophenyl)azo][1,1'-biphenyl]-4-yl]azo]-5-hydroxy-6-(phenylazo)naphtalene-2,7-disulphonate; C.I. Direct Black 38	217-710-3	1937-37-7	Carc. 1B; Repr. 2	yes	Details
disodium octaborate anhydrous	234-541-0	12008-41-2	Repr. 1B	yes	Details
disodium octaborate tetrahydrate	602-894-3	12280-03-4	Repr. 1B	yes	Details
disodium tetraborate decahydrate	603-411-9	1303-96-4	Repr. 1B	yes	Details
Disodium tetraborate pentahydrate	601-808-1	12179-04-3	Repr. 1B	yes	Details
disodium tetraborate, anhydrous	215-540-4	1330-43-4	Repr. 1B	yes	Details
disodium {5-[(4'-((2,6-hydroxy3-((2-hydroxy-5-sulphophenyl)azo)phenyl)azo)(1,1'-biphenyl)-4-yl)azo]salicylato (4-)}cuprate(2-); CI Direct Brown 95	240-221-1	16071-86-6	Carc. 1B	yes	Details
Distillates (coal tar), benzole fraction, BTX-rich; Light Oil Redistillate, low boiling [A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).] A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75°C to 200°C (167°F to 392°F).	309-984-9	101896-26-8	Carc. 1B; Muta. 1B	yes	Details
Distillates (coal tar), benzole fraction, distn. residues; Wash Oil [A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150°C to 300 °C (302°F to 572°F) or a semi-solid or solid with a melting point up to 70 °C (158°F). It is composed primarily of naphthalene and alkyl naphthalenes.] A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150°C to 300°C (302°F to 572°F) or a semi-solid or solid with a melting point up to 70°C (158°F). It is composed primarily of naphthalene and alkyl naphthalenes.	310-165-3	121620-46-0	Carc. 1B; Muta. 1B	yes	Details
Distillates (coal tar), light oils, neutral fraction; Light Oil Extract Residues, high boiling [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135o C to 210o C (275°F to 410°F). May also include unsaturated hydrocarbons such as indene and coumarone.] A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135°C to 210°C (275°F to 410°F). May also include unsaturated hydrocarbons such as indene and coumarone.	309-971-8	101794-90-5	Carc. 1B; Muta. 1B	yes	Details
Distillates (coal tar), naphthalene oils, indole-methylnaphthalene fraction; Methylnaphthalene Oil [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).] A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235°C to 255°C (455°F to 491°F).	309-972-3	101794-91-6	Carc. 1B; Muta. 1B	yes	Details
Distillates (coal tar), naphthalene oils, methylnaphthalene fraction; Methylnaphthalene Oil [A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437°F to 491 °F).] A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225°C to 255°C (437°F to 491°F).	309-985-4	101896-27-9	Carc. 1B; Muta. 1B	yes	Details
Distillates (coal tar), pitch; Heavy Anthracene Oil [The oil obtained from condensation of the vapors from the heat treatment of pitch.; Composed primarily of two-to four-ring aromatic compounds boiling in the range of 200 °C to greater than 400 °C (392 °F to greater than 752 °F).] The oil obtained from condensation of the vapors from the heat treatment of pitch. Composed primarily of two- to four-ring aromatic compounds boiling in the range of 200°C to greater than 400°C (392°F to greater than 752°F).	309-855-7	101316-49-8	Carc. 1B	yes	Details
Distillates (petroleum), C7-9, C8-rich, hydrodesulfurized dearomatized; Low boiling point naphtha -unspecified [A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 o C to 130 o C (248 °F to 266 °F).] A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120°C to 130°C (248°F to 266°F).	309-862-5	101316-56-7	Carc. 1B; Muta. 1B	yes	Details
Distillates (petroleum), carbon-treated light paraffinic; Gasoil — unspecified [A complex combination of hydrocarbons obtained by the treatment of a petroleum oil fraction with activated charcoal for the removal of traces of polar constituents and impur ities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C28.] A complex combination of hydrocarbons obtained by the treatment of a petroleum oil fraction with activated charcoal for the removal of traces of polar constituents and impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C12 through C28.	309-667-5	100683-97-4	Carc. 1B	yes	Details
Distillates (petroleum), heavy steam-cracked; Cracked gasoil [A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250 °C to 400 °C (482 °F to 752 °F).] A complex combination of hydrocarbons obtained by distillation of steam cracking heavy residues. It consists predominantly of highly alkylated heavy aromatic hydrocarbons boiling in the range of approximately 250°C to 400°C (482°F to 752°F).	309-939-3	101631-14-5	Carc. 1B	yes	Details
Distillates (petroleum), hydrodesulfurized full-range middle; Heavy Fuel oil [A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150°C to 400°C (302 °F to 752 °F).] A complex combination of hydrocarbons obtained by treating a petroleum stock with hydrogen. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150°C to 400°C (302°F to 752°F).	309-863-0	101316-57-8	Carc. 1B	yes	Details
Distillates (petroleum), hydrodesulfurized middle coker; Cracked gasoil [A complex combination of hydrocarbons by fractionation from hydrodesulfurised coker distillate stocks. Is consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200 °C to 360 °C (392 °F to 680 °F).] A complex combination of hydrocarbons obtained by fractionation from hydrodesulphurised coker distillate stocks. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C21 and boiling in the range of approximately 200°C to 360°C (392°F to 680°F).	309-865-1	101316-59-0	Carc. 1B	yes	Details
Distillates (petroleum), intermediate paraffinic, carbon-treated; Gasoil — unspecified [A complex combination of hydrocarbons obtained by the treatment of petroleum with activated charcoal for the removal of trace polar consti tuents and impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C36.] A complex combination of hydrocarbons obtained by the treatment of petroleum with activated charcoal for the removal of trace polar constituents and impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C36.	309-668-0	100683-98-5	Carc. 1B	yes	Details
Distillates (petroleum), intermediate paraffinic, clay-treated; Gasoil — unspecified [A complex combination of hydrocarbons obtained by the treatment of petroleum with bleaching earth for the removal of trace polar constituents and impurities. It consists predomi nantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C36.] A complex combination of hydrocarbons obtained by the treatment of petroleum with bleaching earth for the removal of trace polar constituents and impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C16 through C36.	309-669-6	100683-99-6	Carc. 1B	yes	Details
divanadium pentaoxide; vanadium pentoxide	215-239-8	1314-62-1	Muta. 2; Carc. 1B; Repr. 2	yes	Details
dodemorph (ISO); 4-cyclododecyl-2,6-dimethylmorpholine	216-474-9	1593-77-7	Repr. 2		Details
emamectin benzoate (ISO); (4''R)-4''-deoxy-4''-(methylamino) avermectin B1 benzoate	605-015-1	155569-91-8	STOT SE 1		Details
epoxiconazole (ISO); (2RS,3SR)-3-(2-chlorophenyl)-2-(4-fluorophenyl)-[(1H-1,2,4-triazol-1-yl)methyl]oxirane	406-850-2	133855-98-8	Carc. 2; Repr. 1B	yes	Details
erionite	620-440-2	12510-42-8	Carc. 1A	yes	Details
ethidium bromide; 3,8-diamino-1-ethyl-6-phenylphenantridinium bromide	214-984-6	1239-45-8	Muta. 2		Details
ethyl 1-(2,4-dichlorophenyl)-5-(trichloromethyl)-1H-1,2,4-triazole-3-carboxylate HOE 70542	401-290-5	103112-35-2	Carc. 1B	yes	Details
ethyleneimine; aziridine	205-793-9	151-56-4	Carc. 1B; Muta. 1B	yes	Details
Extract oils (coal), coal tar residual pyrolysis oils, naph thalene oil, distn. residues; Redistillates [Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 o C to 260o C (464°F to 500°F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.] Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240°C to 260°C (464°F to 500°F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.	310-171-6	122070-80-8	Carc. 1B; Muta. 1B	yes	Details
Extract oils (coal), coal tar-residual pyrolysis oils, naphthalene oils; Redistillates [A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225o C to 255o C (437°F to 491°F). Composed primarily of substituted dinuclear aromatic hydrocarbons.] A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225°C to 255°C (437°F to 491°F). Composed primarily of substituted dinuclear aromatic hydrocarbons.	310-170-0	122070-79-5	Carc. 1B; Muta. 1B	yes	Details
Extract residues (coal tar), benzole fraction alk., acid ext.; Light Oil Extract Residues, low boiling [A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195°C (185°F to 383°F).] A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85°C-195°C (185°F-383°F).	309-868-8	101316-63-6	Carc. 1B; Muta. 1B	yes	Details
Extract residues (coal), creosote oil acid; Wash Oil Extract Residue [A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482°F to 536°F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.] A complex combination of hydrocarbons from the base-free fraction from the distillation of coal tar, boiling in the range of approximately 250°C to 280°C (482°F to 536°F). It consists predominantly of biphenyl and isomeric dimethylnaphthalenes.	310-189-4	122384-77-4	Carc. 1B	yes	Details
Extract residues (coal), light oil alk., acid ext., indene fraction; Light Oil Extract Residues, intermediate boiling	309-867-2	101316-62-5	Carc. 1B; Muta. 1B	yes	Details
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	Carc. 1B; Muta. 1B	yes	Details
Extract residues (coal), naphthalene oil, alk., naphthalene-low; Naphthalene Oil Extract Residue [A complex combination of hydrocarbons remaining after the removal of naphthalene from alkali-washed naphthalene oil by a crystallization process. It is composed primarily of naphthalene and alkyl naphthalenes.] A complex combination of hydrocarbons remaining after the removal of naphthalene from alkali-washed naphthalene oil by a crystallization process. It is composed primarily of naphthalene and alkyl naphthalenes.	310-167-4	121620-48-2	Carc. 1B; Muta. 1B	yes	Details
Extract residues (coal), naphthalene oil, alk.; Naphthalene Oil Extract Residue [A complex combination of hydrocarbons obtained from the alkali washing of naphthalene oil to remove phenolic compounds (tar acids). It is composed of naphthalene and alkyl naphthalenes.] A complex combination of hydrocarbons obtained from the alkali washing of naphthalene oil to remove phenolic compounds (tar acids). It is composed of naphthalene and alkyl naphthalenes.	310-166-9	121620-47-1	Carc. 1B; Muta. 1B	yes	Details
Extracts (petroleum), light paraffinic distillate solvent, carbon-treated; Distillate aromatic extract (treated) [A complex combination of hydrocarbons obtained as a fraction from distillation of an extract recovered by solvent extraction of light paraffinic top petroleum distillate treated with activated charcoal to remove traces of polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.] A complex combination of hydrocarbons obtained as a fraction from distillation of an extract recovered by solvent extraction of light paraffinic top petroleum distillate treated with activated charcoal to remove traces of polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.	309-672-2	100684-02-4	Carc. 1B	yes	Details
Extracts (petroleum), light paraffinic distillate solvent, clay-treated; Distillate aromatic extract (treated) [A complex combination of hydrocarbons obtained as a fraction from distillation of an extract recovered by solvent extraction of light paraffinic top petroleum distillates treated with bleaching earth to remove traces of polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.] A complex combination of hydrocarbons obtained as a fraction from distillation of an extract recovered by solvent extraction of light paraffinic top petroleum distillates treated with bleaching earth to remove traces of polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C16 through C32.	309-673-8	100684-03-5	Carc. 1B	yes	Details
Extracts (petroleum), light vacuum gas oil solvent, clay-treated; Distillate aromatic extract (treated) [A complex combination of hydrocarbons obtained by solvent extraction of light vacuum petroleum gas oils treated with bleaching earth for removal of trace polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.] A complex combination of hydrocarbons obtained by solvent extraction of light vacuum petroleum gas oils treated with bleaching earth for removal of trace polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.	309-675-9	100684-05-7	Carc. 1B	yes	Details
Extracts (petroleum), light vacuum, gas oil solvent, carbon-treated; Distillate aromatic extract (treated) [A complex combination of hydrocarbons obtained by solvent extraction of light vacuum petroleum gas oil treated with activated charcoal for the removal of trace polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.] A complex combination of hydrocarbons obtained by solvent extraction of light vacuum petroleum gas oil treated with activated charcoal for the removal of trace polar constituents and impurities. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C13 through C30.	309-674-3	100684-04-6	Carc. 1B	yes	Details
flufenoxuron (ISO); 1-(4-(2-cloro-α, α,α-p-trifluorotolyloxy)-2-fluorophenyl)-3-(2,6-difluorobenzolyl)urea FLUFENOXURON	417-680-3	101463-69-8			Details
flumioxazin (ISO); N-(7-fluoro-3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboximide	600-425-7	103361-09-7	Repr. 2		Details
folpet (ISO);N-(trichloromethylthio)phthalimide	205-088-6	133-07-3	Carc. 2		Details
foramsulfuron (ISO); 2-{[(4,6-dimethoxypyrimidin-2-yl)carbamoyl]sulfamoyl}-4-formamido-N,N-dimethylbenzamide; 1-(4,6-dimethoxypyrimidin-2-yl)-3-(2-dimethylcarbamoyl-5-formamidophenylsulfonyl)urea	605-666-1	173159-57-4	Carc. 2		Details
formic acid, nickel salt	239-946-6	15843-02-4	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
furan	203-727-3	110-00-9	Carc. 1B; Muta. 2	yes	Details
gallium arsenide	215-114-8	1303-00-0	Repr. 1B; Carc. 1B	yes	Details
glyoxal ... %; ethandial ... %	203-474-9	107-22-2	Muta. 2		Details
halosulfuron-methyl (ISO); methyl 3-chloro-5-{[(4,6-dimethoxypyrimidin-2-yl)carbamoyl]sulfamoyl}-1-methyl-1H-pyrazole-4-carboxylate	600-130-3	100784-20-1	Repr. 1B	yes	Details
heazlewoodite	-	12035-71-1	Carc. 1A; Muta. 2	yes	Details
heptachlor epoxide; 2,3-epoxy-1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro-4,7-methanoindane	213-831-0	1024-57-3	Carc. 2		Details
hexachlorobenzene	204-273-9	118-74-1	Carc. 1B	yes	Details
hydrazine bis(3-carboxy-4-hydroxybenzensulfonate) STABO-FIX	405-030-1	148434-03-1	Carc. 1B	yes	Details
hydrazine-trinitromethane	-	14913-74-7	Carc. 1B	yes	Details
hydrazobenzene; 1,2-diphenylhydrazine	204-563-5	122-66-7	Carc. 1B	yes	Details
Hydrocarbon oils, arom., mixed with polyethylene and polypropylene, pyrolyzed, light oil fraction; Heat Treatment Products [The oil obtained from the heat treatment of a polyethylene/ polypropylene reaction mass with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).] The oil obtained from the heat treatment of a polyethylene/polypropylene mixture with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70°C to 120°C (158°F to 248°F).	309-745-9	100801-63-6	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbon oils, arom., mixed with polyethylene, pyrolyzed, light oil fraction; Heat Treatment Products [The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158°F to 248°F).] The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70°C to 120°C (158°F to 248°F).	309-748-5	100801-65-8	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbon oils, arom., mixed with polystyrene, pyrolyzed, light oil fraction; Heat Treatment Products [The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils.; It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410°F).] The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70°C to 210°C (158°F to 410°F).	309-749-0	100801-66-9	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C3-6, C5-rich, steam-cracked naphtha; Low boiling point naphtha -unspecified [A complex combination of hydrocarbons obtained by distillation of steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly C5.] A complex combination of hydrocarbons obtained by distillation of steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly C5.	310-012-0	102110-14-5	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C5-rich, dicyclopentadiene-contg.; Low boiling point naphtha -unspecified [A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30o C to 170o C (86°F to 338°F).] A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30°C to 170°C (86°F to 338°F).	310-013-6	102110-15-6	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C6-8, hydrogenated sorption-dearomatized, toluene raffination; Low boiling point naphtha — unspecified [A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80o C to 135o C (176°F to 275°F).] A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80°C to 135°C (176°F to 275°F).	309-870-9	101316-66-9	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C6-rich, hydrotreated light naphtha distillates, solvent-refined; Low boiling point modified naphtha [A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65o C to 70o C (149°F to 158°F).] A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65°C to 70°C (149°F to 158°F).	309-871-4	101316-67-0	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C8-12, catalytic cracker distillates; Low boiling point cat-cracked naphtha [A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approxi mately 140 °C to 210 °C (284°F to 410°F).] A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140°C to 210°C (284°F to 410°F).	309-974-4	101794-97-2	Carc. 1B; Muta. 1B	yes	Details
Hydrocarbons, C8-12, catalytic cracking, chem. neutralized, sweetened; Low boiling point cat-cracked naphtha	309-987-5	101896-28-0	Carc. 1B; Muta. 1B	yes	Details
hydroxylamine dihydrogenphosphate	242-818-2	19098-16-9	Carc. 2		Details
hydroxylammonium hydrogensulfate hydroxylamine sulfate(1:1)	233-154-4	10046-00-1	Carc. 2		Details
hydroxylammonium nitrate	236-691-2	13465-08-2	Carc. 2		Details
hymexazol (ISO);3-hydroxy-5-methylisoxazole	233-000-6	10004-44-1	Repr. 2		Details
imazamox (ISO); (RS)-2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-methoxymethylnicotinic acid	601-305-7	114311-32-9	Repr. 2		Details
ioxynil (ISO) 4-hydroxy-3,5-diiodobenzonitrile	216-881-1	1689-83-4	Repr. 2		Details
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	Repr. 1B	yes	Details
iprovalicarb (ISO); isopropyl [(2S)-3-methyl-1-{[1-(4-methylphenyl)ethyl]amino}-1-oxobutan-2-yl]carbamate	604-209-3	140923-17-7	Carc. 2		Details
isoxaflutole (ISO); 5-cyclopropyl-1,2-oxazol-4-yl α,α,α-trifluoro-2-mesyl-p-tolyl ketone	604-222-4	141112-29-0	Repr. 2		Details
kresoxim-methyl (ISO); methyl (E)-2-methoxyimino-[2-(o-tolyloxymethyl)phenyl]acetate	604-351-6	143390-89-0	Carc. 2		Details
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	Repr. 1A	yes	Details
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	Repr. 1A	yes	Details
lead acetate, basic	215-630-3	1335-32-6	Carc. 2; Repr. 1A	yes	Details
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	Carc. 1B; Repr. 1A	yes	Details
lead diazide; lead azide;lead diazide; lead azide [≥ 20 % phlegmatiser]	236-542-1	13424-46-9	Repr. 1A	yes	Details
lead diazide; lead azide;lead diazide; lead azide [≥ 20 % phlegmatiser]	236-542-1	13424-46-9	Repr. 1A	yes	Details
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	Carc. 1B; Repr. 1A	yes	Details
lead(II) methanesulphonate BLEIMETHANSULFONAT; LEAD (II) METHANESULFONATE; LEAD METHANE SULPHONATE; LEAD SALT FP	401-750-5	17570-76-2	Repr. 1A	yes	Details
leucomalachite green; N, N,N',N'-tetramethyl-4,4'-benzylidenedianiline	204-961-9	129-73-7	Carc. 2; Muta. 2		Details
lithium nickel dioxide	620-400-4	12031-65-1	Carc. 1A	yes	Details
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	Carc. 1B	yes	Details
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	Carc. 1B	yes	Details
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	Carc. 1B	yes	Details
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	Carc. 1B	yes	Details
m-bis(2,3-epoxypropoxy)benzene; resorcinol diglycidyl ether	202-987-5	101-90-6	Carc. 1B; Muta. 2	yes	Details
m-phenylenediamine	203-584-7	108-45-2	Muta. 2		Details
maneb (ISO); manganese ethylenebis(dithiocarbamate) (polymeric)	235-654-8	12427-38-2	Repr. 2		Details
mepanipyrim; 4-methyl-N-phenyl-6-(1-propynyl)-2-pyrimidinamine	432-140-7	110235-47-7	Carc. 2		Details
mesotrione(ISO); 2-[4-(methylsulfonyl)-2-nitrobenzoyl]-1,3-cyclohexanedione	600-533-4	104206-82-8	Repr. 2		Details
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	Repr. 2		Details
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	Repr. 2		Details
methyl salicylate	204-317-7	119-36-8	Repr. 2		Details
methylmercuric chloride	204-064-2	115-09-3	Carc. 2; Repr. 1A	yes	Details
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	Carc. 2		Details
millerite	-	1314-04-1	Carc. 1A; Muta. 2	yes	Details
molybdenum nickel oxide	-	12673-58-4	Carc. 1A	yes	Details
molybdenum nickel tetraoxide	238-034-5	14177-55-0	Carc. 1A	yes	Details
molybdenum trioxide	215-204-7	1313-27-5	Carc. 2		Details
monuron (ISO); 3-(4-chlorophenyl)-1,1-dimethylurea	205-766-1	150-68-5	Carc. 2		Details
morpholine-4-carbonyl chloride	239-213-0	15159-40-7	Carc. 2		Details
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	Carc. 2		Details
N,N'-dihexadecyl-N,N'-bis(2-hydroxyethyl)propanediamide QUESTAMIDE H	422-560-9	149591-38-8	Repr. 2		Details
N,N,N',N'-tetraglycidyl-4,4'-diamino-3,3'-diethyldiphenylmethane PFMT 1848	410-060-3	130728-76-6	Muta. 2		Details
N,N,N',N'-tetramethyl-4,4'-methylendianiline	202-959-2	101-61-1	Carc. 1B	yes	Details
N,N-dimethylacetamide	204-826-4	127-19-5	Repr. 1B	yes	Details
N,N-dimethylaniline	204-493-5	121-69-7	Carc. 2		Details
N-(5-chloro-2-isopropylbenzyl)-N-cyclopropyl-3-(difluoromethyl)-5-fluoro-1-methyl-1H-pyrazole-4-carboxamide; isoflucypram	811-438-4	1255734-28-1	Repr. 2		Details
N-2-naphthylaniline; N-phenyl-2-naphthylamine	205-223-9	135-88-6	Carc. 2		Details
n-hexane	203-777-6	110-54-3	Repr. 2		Details
N-methoxy-N-[1-methyl-2-(2,4,6-trichlorophenyl)-ethyl]-3-(difluoromethyl)- 1-methylpyrazole-4-carboxamide; pydiflumetofen	817-852-1	1228284-64-7	Carc. 2; Repr. 2		Details
N-methylformamide	204-624-6	123-39-7	Repr. 1B	yes	Details
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	Carc. 1B; Muta. 1B	yes	Details
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	Carc. 1B; Muta. 1B	yes	Details
Naphtha (petroleum), sweetened light; Low boiling point naphtha -unspecified [A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 o C to 130 o C (68 °F to 266 °F).] A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20°C to 130°C (68°F to 266°F).	309-976-5	101795-01-1	Carc. 1B; Muta. 1B	yes	Details
nickel (II) sulfide	240-841-2	16812-54-7	Carc. 1A; Muta. 2	yes	Details
nickel acetate	239-086-1	14998-37-9	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel bis(dihydrogen phosphate)	242-522-3	18718-11-1	Carc. 1A	yes	Details
nickel bis(phosphinate)	238-511-8	14507-36-9	Carc. 1A	yes	Details
nickel bis(sulfamidate); nickel sulfamate	237-396-1	13770-89-3	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel bis(tetrafluoroborate)	238-753-4	14708-14-6	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel boride	235-723-2	12619-90-8	Carc. 1A	yes	Details
nickel boride (NiB)	234-493-0	12007-00-0	Carc. 1A	yes	Details
nickel chromate	238-766-5	14721-18-7	Carc. 1A	yes	Details
nickel diarsenide	235-103-1	12068-61-0	Carc. 1A	yes	Details
nickel dibromate	238-596-1	14550-87-9	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dibromide	236-665-0	13462-88-9	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dichromate	239-646-5	15586-38-6	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel difluoride	233-071-3	10028-18-9	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dihydroxide	235-008-5	12054-48-7	Carc. 1A; Repr. 1B; Muta. 2	yes	Details
nickel diiodide	236-666-6	13462-90-3	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dilactate	-	16039-61-5	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dinitrate	236-068-5	13138-45-9	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dioxide	234-823-3	12035-36-8	Carc. 1A	yes	Details
nickel diperchlorate; perchloric acid, nickel(II) salt	237-124-1	13637-71-3	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel dipotassium bis(sulfate)	237-563-9	13842-46-1	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel disilicide	235-379-3	12201-89-7	Carc. 1A	yes	Details
nickel dithiocyanate	237-205-1	13689-92-4	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel hydrogen phosphate	238-278-2	14332-34-4	Carc. 1A	yes	Details
nickel hydroxide	234-348-1	11113-74-9	Carc. 1A; Repr. 1B; Muta. 2	yes	Details
nickel monoxide	215-215-7	1313-99-1	Carc. 1A	yes	Details
nickel oxide	234-323-5	11099-02-8	Carc. 1A	yes	Details
nickel potassium fluoride	-	11132-10-8	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel selenate	239-125-2	15060-62-5	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel selenide	215-216-2	1314-05-2	Carc. 1A	yes	Details
nickel sulfide	234-349-7	11113-75-0	Carc. 1A; Muta. 2	yes	Details
nickel telluride	235-260-6	12142-88-0	Carc. 1A	yes	Details
nickel tellurium tetraoxide	239-974-9	15852-21-8	Carc. 1A	yes	Details
nickel tellurium trioxide	239-967-0	15851-52-2	Carc. 1A	yes	Details
nickel tin trioxide; nickel stannate	234-824-9	12035-38-0	Carc. 1A	yes	Details
nickel titanium oxide	235-752-0	12653-76-8	Carc. 1A	yes	Details
nickel titanium trioxide	234-825-4	12035-39-1	Carc. 1A	yes	Details
nickel triuranium decaoxide	239-876-6	15780-33-3	Carc. 1A	yes	Details
nickel tungsten tetraoxide	238-032-4	14177-51-6	Carc. 1A	yes	Details
nickel(II) hydrogen citrate	242-533-3	18721-51-2	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel(II) palmitate	237-138-8	13654-40-5	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nickel(II) selenite	233-263-7	10101-96-9	Carc. 1A	yes	Details
nickel(II) trifluoroacetate	240-235-8	16083-14-0	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nitric acid, nickel salt	238-076-4	14216-75-2	Carc. 1A; Muta. 2; Repr. 1B	yes	Details
nitrofen (ISO); 2,4-dichlorophenyl 4-nitrophenyl ether	217-406-0	1836-75-5	Carc. 1B; Repr. 1B	yes	Details
O, O'-(ethenylmethylsilylene)di[(4-methylpentan-2-one)oxime] ASIL-322; OS-5200	421-870-1	156145-66-3	Repr. 2		Details
O-hexyl-N-ethoxycarbonylthiocarbamate	432-750-3	109202-58-6	Carc. 1B; Muta. 1B	yes	Details
O-isobutyl-N-ethoxy carbonylthiocarbamate	434-350-4	103122-66-3	Carc. 1B; Muta. 1B	yes	Details

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pregnant-women-protection

pregnant-women-protection

Protection of Pregnant and Breastfeeding Workers Directive, Annex I+II

EU. Chemical Agents: Annexes I & II, Directive 92/85/EEC on Pregnant Workers, 28 November 1992 (updated by table 3 of Annex VI to CLP, 5 October 2018)

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Last updated 18 April 2024. Database contains 2100 unique substances/entries.

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