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经验公式（希尔记法）:
C20H11NO2
化学文摘社编号:
分子量:
297.31
Beilstein:
2472924
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
等级
certified reference material
Agency
BCR®
制造商/商品名称
JRC
技术
HPLC: suitable
gas chromatography (GC): suitable
包装形式
neat
储存温度
2-8°C
SMILES字符串
[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
InChI key
NMMAFYSZGOFZCM-UHFFFAOYSA-N
一般描述
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.
分析说明
For more information please see:
BCR311
BCR311
法律信息
BCR is a registered trademark of European Commission
储存分类代码
11 - Combustible Solids
WGK
WGK 3
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
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
Metabolism of 1-nitropyrene and 6-nitrobenzo(a)pyrene by intestinal microflora.
C E Cerniglia
Progress in clinical and biological research, 181, 133-137 (1985-01-01)
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)
Isomeric mononitrobenzo[a]pyrenes: synthesis, identification and mutagenic activities.
J N Pitts et al.
Mutation research, 140(2-3), 81-85 (1984-06-01)
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