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 24 aprile 2024. Database contains 1679 unique substances/entries.
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206-382-7
334-88-3
006-068-00-8
Carc. 1B
215-481-4
1327-53-3
033-003-00-0
Carc. 1A
215-116-9
1303-28-2
033-004-00-6
Carc. 1A
-
74195-78-1
028-033-00-6
Carc. 1A
239-793-5
15699-18-0
028-017-00-9
Carc. 1A; Muta. 2; Repr. 1B
422-670-7
150202-11-2
607-504-00-5
Repr. 2
-
-
612-151-00-5
Carc. 1B; Muta. 2; Repr. 2
technical product - reaction mass of 4-methyl-m-phenylene diamine (EC No 202-453-1) and 2-methyl-m-phenylene diamine (EC No 212-513-9)
234-454-8
12004-35-2
028-057-00-7
Carc. 1A
203-733-6
110-05-4
617-001-00-2
Muta. 2
205-017-9
131-18-0
607-426-00-1
Repr. 1B
218-961-1
2303-16-4
006-019-00-0
Carc. 2
237-198-5
13684-56-5
616-113-00-9
Repr. 2
200-024-3
50-29-3
602-045-00-7
Carc. 2
216-485-9
1596-84-5
607-757-00-1
Carc. 2
619-020-1
94361-06-5
650-032-00-X
Repr. 1B
261-043-0
57966-95-7
616-035-00-5
Repr. 2
269-855-7
68359-37-5
607-253-00-1
Lact.
642-974-5
400882-07-7
607-733-00-0
Carc. 2
405-230-9
101205-02-1
606-147-00-2
Repr. 2
203-629-0
108-91-8
612-050-00-6
Repr. 2
200-636-0
66-81-9
613-140-00-8
Muta. 2; Repr. 1B
427-230-8
5571-36-8
606-131-00-5
Repr. 1B
206-992-3
420-04-2
615-013-00-2
Carc. 2; Repr. 2
202-704-5
98-82-8
601-024-00-X
Carc. 1B
224-030-0
4170-30-3
605-009-00-9
Muta. 2
The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38°C (100°F).
274-566-4
70321-80-1
648-138-00-6
Carc. 1B
The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).
The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5°C (41°F).
274-565-9
70321-79-8
648-100-00-9
Carc. 1B
The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41°F).
A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.
292-605-3
90640-84-9
648-098-00-X
Carc. 1B
A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464°F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.
The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.
292-606-9
90640-85-0
648-043-00-X
Carc. 1B
The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.
A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200°C to 325°C (392°F to 617°F).
263-047-8
61789-28-4
648-099-00-5
Carc. 1B
A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).
The distillate of coal tar produced by the high temperature carbonization of bituminous coal. It consists primarily of aromatic hydrocarbons, tar acids and tar bases.
232-287-5
8001-58-9
648-101-00-4
Carc. 1B
The distillate of coal tar produced by the high temperature carbonization of bituminous coal. It consists primarily of aromatic hydrocarbons, tar acids and tar bases.
227-424-0
5836-29-3
607-059-00-7
Repr. 1B
200-598-5
64-86-8
614-005-00-6
Muta. 1B
233-334-2
10124-43-3
027-005-00-0
Carc. 1B; Muta. 2; Repr. 1B
620-395-9
12737-30-3
028-043-00-0
Carc. 1A
This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77332.
269-051-6
68186-89-0
028-043-00-0
Carc. 1A
261-346-8
58591-45-0
028-043-00-0
Carc. 1A
442-750-5
113066-89-0
028-058-00-2
Carc. 1A
233-402-1
10141-05-6
027-009-00-2
Carc. 1B; Muta. 2; Repr. 1B
268-169-5
68016-03-5
028-057-00-7
Carc. 1A
231-589-4
7646-79-9
027-004-00-5
Carc. 1B; Muta. 2; Repr. 1B
200-755-8
71-48-7
027-006-00-6
Carc. 1B; Muta. 2; Repr. 1B
208-169-4
513-79-1
027-010-00-8
Carc. 1B; Muta. 2; Repr. 1B
231-158-0
7440-48-4
027-001-00-9
Carc. 1B; Muta. 2; Repr. 1B
The product obtained by filtration of coal mineral matter and undissolved coal from coal extract solution produced by digesting coal in a liquid solvent. A black, viscous, highly complex liquid combination composed primarily of aromatic and partly hydrogenated aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic and other aromatic oxygen compounds and their alkyl derivatives.
302-682-8
94114-47-3
648-143-00-3
Carc. 1B
The product obtained by filtration of coal mineral matter and undissolved coal from coal extract solution produced by digesting coal in a liquid solvent. A black, viscous, highly complex liquid combination composed primarily of aromatic and partly hydro-genated aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic and other aromatic oxygen compounds and their alkyl derivatives.
The substantially solvent-free product obtained by the distillation of the solvent from filtered coal extract solution produced by digesting coal in a liquid solvent. A black semi-solid, composed primarily of a complex combination of condensed-ring aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic compounds and other aromatic oxygen compounds, and their alkyl derivatives.
302-683-3
94114-48-4
648-144-00-9
Carc. 1B
The substantially solvent-free product obtained by the distillation of the solvent from filtered coal extract solution produced by digesting coal in a liquid solvent. A black semi-solid, composed primarily of a complex combination of condensed-ring aromatic hydrocarbons, aromatic nitrogen compounds, aromatic sulfur compounds, phenolic compounds and other aromatic oxygen compounds, and their alkyl derivatives.
433-460-1
210880-92-5
613-307-00-5
Repr. 2
204-385-8
120-32-1
604-093-00-4
Carc. 2; Repr. 2
A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350°C (662°F). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.
269-782-0
68333-26-6
649-020-00-7
Carc. 1B
A complex combination of hydrocarbons obtained by treating catalytic cracked clarified oil with hydrogen to convert organic sulfur to hydrogen sulfide which is removed. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 °C (662 °F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.
A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350°C (662°F). This stream is likely to contain 5 wt. % or more of 4- to 6-membered condensed ring aromatic hydrocarbons.
265-064-6
64741-62-4
649-011-00-8
Carc. 1B
A complex combination of hydrocarbons produced as the residual fraction from distillation of the products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly greater than C20 and boiling above approximately 350 °C (662 °F). This stream is likely to contain 5 wt. % or more of 4-to 6-membered condensed ring aromatic hydrocarbons.
245-119-0
22605-92-1
028-054-00-0
Carc. 1A; Muta. 2; Repr. 1B
242-161-1
18283-82-4
028-054-00-0
Carc. 1A; Muta. 2; Repr. 1B
426-020-3
51229-78-8
612-251-00-9
Repr. 2
604-318-6
142891-20-1
616-107-00-6
Carc. 2
207-803-7
495-54-5
611-151-00-2
Muta. 2
264-409-8
63681-54-9
611-152-00-8
Muta. 2
282-432-1
84196-22-5
611-152-00-8
Muta. 2
208-545-8
532-82-1
611-152-00-8
Muta. 2
278-290-5
75660-25-2
611-152-00-8
Muta. 2
281-549-5
83968-67-6
611-152-00-8
Muta. 2
304-236-8
94247-67-3
611-153-00-3
Muta. 2
286-946-7
85407-90-5
611-153-00-3
Muta. 2
279-116-0
79234-33-6
611-152-00-8
Muta. 2
205-923-4
218-01-9
601-048-00-0
Carc. 1B; Muta. 2
239-056-8
14977-61-8
024-005-00-2
Carc. 1B; Muta. 1B
215-607-8
1333-82-0
024-001-00-0
Carc. 1A; Muta. 1B; Repr. 2
-
-
024-017-00-8
Carc. 1B
282-714-4
84332-86-5
607-306-00-9
Carc. 2
202-925-7
101-21-3
006-096-00-0
Carc. 2
239-592-2
15545-48-9
616-105-00-5
Carc. 2; Repr. 2
217-588-1
1897-45-6
608-014-00-4
Carc. 2
204-818-0
126-99-8
602-036-00-8
Carc. 1B
223-003-0
3691-35-8
606-014-00-9
Repr. 1B
200-817-4
74-87-3
602-001-00-7
Carc. 2
200-663-8
67-66-3
602-006-00-4
Carc. 2; Repr. 2
200-830-5
75-00-3
602-009-00-0
Carc. 2
203-472-8
107-20-0
605-025-00-6
Carc. 2
SEL DE VILSMEIER-HAACK
425-970-6
3724-43-4
612-250-00-3
Repr. 1B
444-950-8
99464-83-2
607-667-00-2
Muta. 2
203-480-1
107-30-2
603-075-00-3
Carc. 1A
243-269-1
19750-95-9
650-009-00-4
Carc. 2
228-200-5
6164-98-3
650-007-00-3
Carc. 2
205-601-3
143-50-0
606-019-00-6
Carc. 2
200-349-0
57-74-9
602-047-00-8
Carc. 2
240-408-8
16337-84-1
028-010-00-0
Carc. 1A; Muta. 2; Repr. 1B
200-262-8
56-23-5
602-008-00-5
Carc. 2
211-128-3
630-08-0
006-001-00-2
Repr. 1A
200-843-6
75-15-0
006-003-00-3
Repr. 2
240-286-6
16118-49-3
616-223-00-7
Carc. 2; Repr. 1B
234-232-0
10605-21-7
613-048-00-8
Muta. 1B; Repr. 1B
200-555-0
63-25-2
006-011-00-7
Carc. 2
229-879-0
6804-07-5
613-050-00-9
Carc. 1B
205-087-0
133-06-2
613-044-00-6
Carc. 2
219-363-3
2425-06-1
613-046-00-7
Carc. 1B
232-283-3
8001-35-2
602-044-00-1
Carc. 2
237-366-8
13765-19-0
024-008-00-9
Carc. 1B
241-084-0
17010-21-8
048-005-00-7
Carc. 2
215-147-8
1306-23-6
048-010-00-4
Carc. 1B; Muta. 2; Repr. 2
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Sulfuric acid, cadmium salt, hydrate (3:3:8) EC / List no: 616-572-5 | CAS no: 7790-84-3
Sulfuric acid, cadmium salt (1:1), hydrate EC / List no: 626-360-4 | CAS no: 15244-35-6
233-331-6
10124-36-4
048-009-00-9
Carc. 1B; Muta. 1B; Repr. 1B
show/hide
Monteponite (CdO) EC / List no: - | CAS no: 12139-21-8
215-146-2
1306-19-0
048-002-00-0
Carc. 1B; Muta. 2; Repr. 2
233-710-6
10325-94-7
048-014-00-6
Carc. 1B; Muta. 1B
232-223-6
7790-80-9
048-007-00-8
Carc. 2
244-168-5
21041-95-2
048-013-00-0
Carc. 1B; Muta. 1B
232-222-0
7790-79-6
048-006-00-2
Carc. 1B; Muta. 1B; Repr. 1B
224-729-0
4464-23-7
048-003-00-6
Carc. 2
208-829-1
542-83-6
048-004-00-1
Carc. 2
show/hide
cadmium chloride (CdCl2), hydrate (2:5) EC / List no: 640-998-0 | CAS no: 7790-78-5
233-296-7
10108-64-2
048-008-00-3
Carc. 1B; Muta. 1B; Repr. 1B
208-168-9
513-78-0
048-012-00-5
Carc. 1B; Muta. 1B
231-152-8
7440-43-9
048-011-00-X
Carc. 1B; Muta. 2; Repr. 2
231-152-8
7440-43-9
048-002-00-0
Carc. 1B; Muta. 2; Repr. 2
212-668-2
842-07-9
611-056-00-6
Carc. 2; Muta. 2
220-600-8
2832-40-8
611-055-00-0
Carc. 2
208-953-6
548-62-9
612-204-00-2
Carc. 2
208-953-6
548-62-9
612-205-00-8
Carc. 1B
219-376-4
2426-08-6
603-039-00-7
Carc. 2; Muta. 2
BUTROXYDIM; ICIA0500
414-790-3
138164-12-2
606-070-00-4
Repr. 2
202-496-6
96-29-7
616-014-00-0
Carc. 1B
203-448-7
106-97-8
601-004-01-8
Carc. 1A; Muta. 1B
255-391-2
41483-43-6
612-288-00-0
Carc. 2
-
34492-97-2
028-003-00-2
Carc. 1A
216-885-3
1689-99-2
608-017-00-0
Repr. 2
260-300-4
56634-95-8
607-427-00-7
Repr. 2
show/hide
3,5-dibromo-4-hydroxybenzonitrile EC / List no: 216-882-7 | CAS no: 1689-84-5
2,6-dibromo-4-cyanophenyl heptanoate EC / List no: 260-300-4 | CAS no: 56634-95-8
2,6-dibromo-4-cyanophenyl butyrate EC / List no: 223-374-9 | CAS no: 3861-41-4
2,6-dibromo-4-cyanophenyl octanoate EC / List no: 216-885-3 | CAS no: 1689-99-2
216-882-7
1689-84-5
608-006-00-0
Repr. 2
200-813-2
74-83-9
602-002-00-2
Muta. 2
209-800-6
593-60-2
602-024-00-2
Carc. 1B
200-825-8
74-96-4
602-055-00-1
Carc. 2
249-205-9
28772-56-7
607-716-00-8
Repr. 1B
233-139-2
10043-35-3
005-007-00-2
Repr. 1B
234-343-4
11113-50-1
005-007-00-2
Repr. 1B
201-245-8
80-05-7
604-030-00-0
Repr. 1B
CGI 784
412-000-1
125051-32-3
022-003-00-6
Repr. 2
201-279-3
80-43-3
617-006-00-X
Repr. 1B
233-118-8
10039-54-0
612-123-00-2
Carc. 2
276-205-6
71957-07-8
028-054-00-0
Carc. 1A; Muta. 2; Repr. 1B
208-832-8
542-88-1
603-046-00-5
Carc. 1A
204-212-6
117-82-8
607-228-00-5
Repr. 1B
203-924-4
111-96-6
603-139-00-0
Repr. 1B
204-211-0
117-81-7
607-317-00-9
Repr. 1B
203-870-1
111-44-4
603-029-00-2
Carc. 2
205-594-7
143-24-8
603-238-00-9
Repr. 1B
202-177-1
92-67-1
612-072-00-6
Carc. 1A
202-110-6
91-95-2
612-239-00-3
Carc. 1B; Muta. 2
201-990-9
90-41-5
612-142-00-6
Carc. 2
207-612-9
485-31-4
609-024-00-1
Repr. 1B
617-373-6
82657-04-3
607-699-00-7
Carc. 2
-
1820573-27-0
607-254-00-7
Lact.
215-133-1
1304-56-9
004-003-00-8
Carc. 1B
show/hide
Copper alloy, Cu 96, Be 2.2-2.8, Ni 1.1 (CDA 827) EC / List no: - | CAS no: 11108-64-8
Phosphoric acid, beryllium salt (2:3) EC / List no: - | CAS no: 13598-26-0
Beryllium sulphide EC / List no: 237-064-6 | CAS no: 13598-22-6
Triberyllium nitride EC / List no: 215-132-6 | CAS no: 1304-54-7
Beryllium telluride EC / List no: 235-451-4 | CAS no: 12232-27-8
Beryllium diboride EC / List no: 235-694-6 | CAS no: 12536-51-5
Steel manufacture, chemicals
This category includes the chemical substances which are manufactured as part of steel and alloy steels. The following list identifies those elements which may exist in steel or which may comprise compounds present in steel or alloy steels. Aluminum, beryllium, boron, calcium, carbon, cerium, chromium, cobalt, copper, hafnium, iron, lanthanum, lead, magnesium, manganese, molybdenum, nickel, niobium, nitrogen, oxygen, phosphorus, selenium, silicon, sulfur, tantalum, tin, titanium, tungsten, vanadium, yttrium, zinc, zirconium.
EC / List no: 266-048-1 | CAS no: 65997-19-5
Zinc beryllium silicate EC / List no: - | CAS no: 39413-47-3
Beryllium EC / List no: 231-150-7 | CAS no: 7440-41-7
Disodium tetrafluoroberyllate EC / List no: 237-630-2 | CAS no: 13871-27-7
Beryllium diiodide EC / List no: 232-119-0 | CAS no: 7787-53-3
Beryllium diammonium tetrafluoride EC / List no: 238-948-4 | CAS no: 14874-86-3
Octadecanoic acid, beryllium salt EC / List no: - | CAS no: 16687-38-0
Phosphoric acid, beryllium salt EC / List no: 252-356-3 | CAS no: 35089-00-0
Beryllium oxyfluoride EC / List no: - | CAS no: 63990-88-5
Beryllium carbonate EC / List no: 236-030-8 | CAS no: 13106-47-3
Beryllium phosphide (BeP2) EC / List no: - | CAS no: 1268721-56-7
Diethylberyllium EC / List no: 208-823-9 | CAS no: 542-63-2
Tetraberyllium boride EC / List no: 235-695-1 | CAS no: 12536-52-6
Aluminium alloy, Al,Be EC / List no: 603-236-8 | CAS no: 12770-50-2
Beryllium fluoride EC / List no: 232-118-5 | CAS no: 7787-49-7
Beryllium hydrogen phosphate (1:1) EC / List no: - | CAS no: 13598-15-7
Beryllium hydroxide EC / List no: 236-368-6 | CAS no: 13327-32-7
Nitric acid, beryllium salt, tetrahydrate EC / List no: 690-699-4 | CAS no: 13510-48-0
Beryllium, bis(carbonato(2-))dihydroxytri- EC / List no: - | CAS no: 66104-24-3
Beryllium zinc silicate EC / List no: 247-151-0 | CAS no: 25638-88-4
Bis(pentane-2,4-dionato-O,O')beryllium EC / List no: 233-513-5 | CAS no: 10210-64-7
Beryllium selenide EC / List no: 235-450-9 | CAS no: 12232-25-6
Beryllium acetylide EC / List no: 208-050-7 | CAS no: 506-66-1
Bertrandite (Be4(OH)2O(SiO3)2) EC / List no: 235-299-9 | CAS no: 12161-82-9
Hexakis[μ-(acetato-O:O')]-μ4-oxotetraberyllium EC / List no: 242-785-4 | CAS no: 19049-40-2
Beryllium orthosilicate EC / List no: 239-251-8 | CAS no: 15191-85-2
Beryllium nitrate trihydrate EC / List no: - | CAS no: 7787-55-5
Beryllium nitrate EC / List no: 237-062-5 | CAS no: 13597-99-4
Silicic acid, beryllium salt EC / List no: 261-293-0 | CAS no: 58500-38-2
Beryllium sulphate EC / List no: 236-842-2 | CAS no: 13510-49-1
Beryllium sulfate tetrahydrate EC / List no: 629-461-1 | CAS no: 7787-56-6
Beryllium dibromide EC / List no: 232-115-9 | CAS no: 7787-46-4
Beryllium chloride EC / List no: 232-116-4 | CAS no: 7787-47-5
Beryllium hexaboride EC / List no: 235-657-4 | CAS no: 12429-94-6
Beryllium di(acetate) EC / List no: 208-850-6 | CAS no: 543-81-7
Beryllium diboride EC / List no: 235-443-0 | CAS no: 12228-40-9
Beryllium phosphide EC / List no: 261-137-1 | CAS no: 58127-61-0
-
-
004-002-00-2
Carc. 1B
231-150-7
7440-41-7
004-001-00-7
Repr. 2
278-305-5
75768-65-9
015-205-00-0
Repr. 1B
479-100-5
577705-90-9
015-204-00-5
Repr. 1B
216-901-9
1694-09-3
650-010-00-X
Carc. 2
B2,4DBB
420-710-8
23085-60-1
607-376-00-0
Repr. 2
204-337-6
119-61-9
606-153-00-5
Carc. 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.
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.
205-877-5
189-55-9
601-090-00-X
Carc. 1B; Muta. 2
205-916-6
207-08-9
601-036-00-5
Carc. 1B
205-910-3
205-82-3
601-035-00-X
Carc. 1B
205-892-7
192-97-2
601-049-00-6
Carc. 1B
200-028-5
50-32-8
601-032-00-3
Carc. 1B; Muta. 1B; Repr. 1B
202-199-1
92-87-5
612-042-00-2
Carc. 1A
244-236-4
21136-70-9
612-070-00-5
Carc. 1A
-
-
611-024-00-1
Carc. 1B
252-984-8
36341-27-2
612-070-00-5
Carc. 1A
200-753-7
71-43-2
601-020-00-8
Carc. 1A; Muta. 1B
205-911-9
205-99-2
601-034-00-4
Carc. 1B
200-280-6
56-55-3
601-033-00-9
Carc. 1B
246-585-8
25057-89-0
613-012-00-1
Repr. 2
241-775-7
17804-35-2
613-049-00-3
Muta. 1B; Repr. 1B
617-356-3
82560-54-1
006-088-00-7
Repr. 2
217-465-2
1861-40-1
612-295-00-9
Carc. 2; Repr. 2
201-622-7
85-68-7
607-430-00-3
Repr. 1B
237-222-4
13701-59-2
056-005-00-3
Repr. 1B
203-102-5
103-33-3
611-001-00-6
Carc. 1B; Muta. 2
252-626-0
35575-96-3
613-338-00-4
Carc. 2
620-425-0
68049-83-2
611-140-00-2
Repr. 1B
265-610-3
65195-55-3
606-143-00-0
Repr. 2
616-473-7
77536-68-6
650-013-00-6
Carc. 1A
601-801-3
12172-73-5
650-013-00-6
Carc. 1A
-
132207-32-0
650-013-00-6
Carc. 1A
616-472-1
77536-67-5
650-013-00-6
Carc. 1A
616-471-6
77536-66-4
650-013-00-6
Carc. 1A
show/hide
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, chrysotile EC / List no: 601-650-3 | CAS no: 12001-29-5
Asbestos, anthophyllite EC / List no: 616-472-1 | CAS no: 77536-67-5
Asbestos, amosite EC / List no: 601-801-3 | CAS no: 12172-73-5
Asbestos, tremolite EC / List no: 616-473-7 | CAS no: 77536-68-6
-
-
650-013-00-6
Carc. 1A
-
-
033-005-00-1
Carc. 1A
295-551-9
92062-36-7
648-013-00-6
Carc. 1B; Muta. 1B
292-694-9
90989-38-1
648-010-00-X
Carc. 1B; Muta. 1B
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).
292-695-4
90989-39-2
649-403-00-9
Carc. 1B; Muta. 1B
295-279-0
91995-18-5
649-310-00-3
Carc. 1B; Muta. 1B
292-698-0
90989-42-7
649-379-00-X
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).
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).
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.
292-697-5
90989-41-6
648-005-00-2
Carc. 1B; Muta. 1B
268-618-5
68131-49-7
649-357-00-X
Carc. 1B; Muta. 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.
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.
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.
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.
201-706-3
86-88-4
006-008-00-0
Carc. 2
215-175-0
1309-64-4
051-005-00-X
Carc. 2
201-549-0
84-65-1
606-151-00-4
Carc. 1B

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