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BCR311

6-Nitrobenzo[a]pyrene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C20H11NO2
Número de CAS:
63041-90-7
Peso molecular:
297.31
Beilstein:
2472924
Número MDL:
MFCD00215956
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
329773820
NACRES:
NA.24

grado

certified reference material

Agency

BCR®

fabricante / nombre comercial

JRC

técnicas

HPLC: suitable
gas chromatography (GC): suitable

Formato

neat

temp. de almacenamiento

2-8°C

cadena SMILES

[O-][N+](=O)c1c2ccccc2c3ccc4cccc5ccc1c3c45

InChI

1S/C20H11NO2/c22-21(23)20-16-7-2-1-6-14(16)15-10-8-12-4-3-5-13-9-11-17(20)19(15)18(12)13/h1-11H

Clave InChI

NMMAFYSZGOFZCM-UHFFFAOYSA-N

Descripción general

6-Nitrobenzo[a]pyrene belongs to the class of nitrated-polycyclic aromatic hydrocarbons, found to be persistent in the environment. It is produced from direct sources such as diesel, gasoline exhaust and by the gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs) with oxides of nitrogen.

Nota de análisis

For more information please see:
BCR311

Información legal

BCR is a registered trademark of European Commission

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

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B S Hass et al.
Mutation research, 171(2-3), 123-129 (1986-08-01)
The mononitro-substituted isomers of benzo[a]pyrene (B[a]P), 1-, 3- and 6-nitrobenzo[a]pyrene (NB[a]P), are environmental pollutants and are metabolized to mutagens in Salmonella by rat-liver homogenate postmitochondrial supernatant (S9) fractions. In this study, activation of these compounds to mutagens was investigated using
M Sala et al.
Carcinogenesis, 8(4), 503-507 (1987-04-01)
Two nitroaromatics, 6-nitrobenzo[a]pyrene (6-N-BaP) and 6-nitrochrysene (6-N-CRY), and the corresponding parent hydrocarbons, benzo[a]pyrene (BaP) and chrysene (CRY), were studied in in vitro transformation assays with Syrian hamster embryo (SHE) cells, BALB/3T3 and C3H10T1/2 mouse cell lines. The three cell systems
G C Millner et al.
Journal of toxicology and environmental health, 19(4), 519-530 (1986-01-01)
The fungal metabolism of the potent mutagenic and carcinogenic nitropolycyclic aromatic hydrocarbon (nitro-PAH) 6-nitrobenzo[a]pyrene (6-NO2-BaP) was investigated. Cunninghamella elegans was incubated with 6-NO2-BaP for periods ranging between 1 and 7 d, and the metabolites formed were separated by high-performance liquid
Binary mixtures containing isomers of nitrobenzo[a]pyrene induce greater-than-additive mutational responses in Salmonella typhimurium. I. Analysis by the total concentration-proportional mixture model.
B S Hass et al.
Mutation research, 190(4), 247-252 (1987-04-01)
C Raha et al.
Research communications in chemical pathology and pharmacology, 58(1), 63-74 (1987-10-01)
6-Nitrobenzo (a) pyrene (6-NBaP) is an environmental contaminant. In bacterial mutagenesis assays, 6-NBaP requires rat liver S9 enzymes for its activity. Chemical characterization of metabolites of 6-NBaP produced by male rat liver microsomes showed them to be ring-hydroxylated (both mono-
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