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BCR081R

5-Methylchrysene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C19H14
Número de CAS:
3697-24-3
Peso molecular:
242.31
Beilstein:
2048519
Número MDL:
MFCD00215919
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329774213

grado

certified reference material

Agency

BCR®

fabricante / nombre comercial

JRC

técnicas

HPLC: suitable
gas chromatography (GC): suitable

aplicaciones

environmental
pharmaceutical (small molecule)

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

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

Clave InChI

GOHBXWHNJHENRX-UHFFFAOYSA-N

Nota de análisis

For more information please see:
BCR080R

Información legal

BCR is a registered trademark of European Commission

Palabra de señalización

Danger

Frases de peligro

H302,H318,H351,H410

Clasificaciones de peligro

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

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

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C E Afshar et al.
Carcinogenesis, 17(11), 2507-2511 (1996-11-01)
The three-dimensional structure of the product of the reaction of a diol epoxide of the carcinogen 5-methylchrysene with methanol has been determined by an X-ray diffraction analysis. The diol epoxide used to obtain this compound contains a stereochemically hindered bay
K Peltonen et al.
Chemical research in toxicology, 4(3), 305-310 (1991-05-01)
Eight deoxyribonucleoside adducts formed from reactions of syn-5-methylchrysene 1,2-dihydrodiol 3,4-epoxide with DNA or with nucleotides were characterized spectroscopically. The adducts arose from both cis and trans opening of the epoxide ring at C4 by the amino group of either deoxyadenosine
Toshiaki Yoshioka et al.
Journal of bioscience and bioengineering, 126(1), 126-130 (2018-03-04)
Polycyclic aromatic hydrocarbons (PAHs) are carcinogenic substances that are mainly generated during heating in food; therefore, the European Union (EU) has regulated the amount of benzo[a]pyrene and PAH4 in various types of food. In addition, the Scientific Committee on Food
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
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