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BCR081R

5-Methylchrysene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C19H14
CAS Number:
3697-24-3
Molecular Weight:
242.31
Beilstein/REAXYS Number:
2048519
MDL number:
MFCD00215919
UNSPSC Code:
41116107
PubChem Substance ID:
329774213

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

Cc1cc2ccccc2c3ccc4ccccc4c13

InChI

1S/C19H14/c1-13-12-15-7-3-4-8-16(15)18-11-10-14-6-2-5-9-17(14)19(13)18/h2-12H,1H3

InChI key

GOHBXWHNJHENRX-UHFFFAOYSA-N

Analysis Note

For more information please see:
BCR080R

Legal Information

BCR is a registered trademark of European Commission

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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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T Kuljukka-Rabb et al.
Mutagenesis, 16(4), 353-358 (2001-06-23)
Cultures of a human mammary carcinoma cell line (MCF-7) were exposed to the soluble organic fraction of diesel particle emissions, benzo[a]pyrene (B[a]P) and 5-methylchrysene (5-MeCHR) to study time- and dose-related PAH-DNA binding. The concentrations of 14 PAHs in three extracts
C A Bigger et al.
Carcinogenesis, 11(12), 2263-2265 (1990-12-01)
An SV40-based pS189 shuttle vector, which contained a supF target gene and was replicated in human cells (Ad293), was used to determine the mutational specificity of anti 5-methylchrysene 1,2-dihydrodiol 3,4-epoxide, the active metabolite of the environmentally prevalent carcinogen 5-methylchrysene. The
Stephen S Hecht et al.
Cancer letters, 187(1-2), 87-94 (2002-10-03)
Polycyclic aromatic hydrocarbons (PAH) are an important group of carcinogens that are likely to be involved as one of the causes of lung cancer in smokers and occupationally exposed individuals. Previous studies have shown that benzyl isothiocyanate (BITC), administered by
S Amin et al.
Chemical research in toxicology, 5(2), 237-241 (1992-03-01)
In previous studies, we have observed unexpected structure-tumorigenicity relationships among the dimethylchrysenes. Thus, 5,6-dimethylchrysene and 5,7-dimethylchrysene were only weakly tumorigenic and were significantly less active than 5-methylchrysene. These results were surprising in view of the known route of metabolic activation
D B Reardon et al.
Carcinogenesis, 8(9), 1317-1322 (1987-09-01)
Products of reaction of the racemic anti bay region 1,2-dihydrodiol-3,4-epoxide of 5-methylchrysene with DNA were identified by comparison with the products formed in reactions with individual nucleotides. The latter products, i.e. two deoxyguanosine adducts and four deoxyadenosine adducts, were characterized
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