BCR310
3-硝基荧蒽
BCR®, certified reference material
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经验公式（希尔记法）:
C16H9NO2
化学文摘社编号:
分子量:
247.25
Beilstein:
2216474
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
mp
157-159 °C (lit.)
包装形式
neat
储存温度
2-8°C
SMILES字符串
[O-][N+](=O)c1ccc2-c3ccccc3-c4cccc1c24
InChI
1S/C16H9NO2/c18-17(19)15-9-8-13-11-5-2-1-4-10(11)12-6-3-7-14(15)16(12)13/h1-9H
InChI key
PIHGQKMEAMSUNA-UHFFFAOYSA-N
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一般描述
3-Nitrofluoranthene, belonging to the class of nitrated-polycyclic aromatic hydrocarbons, is persistent in the environment. It is produced from direct sources such as diesel, gasoline exhaust and gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs) with oxides of nitrogen.
分析说明
For more information please see:
BCR310
BCR310
法律信息
BCR is a registered trademark of European Commission
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
M A Belisario et al.
Carcinogenesis, 11(2), 213-218 (1990-02-01)
Nitrofluoranthenes (NFs) are mutagenic and carcinogenic environmental pollutants found in incomplete combustion products and urban air particulate. We have studied both oxidative and reductive metabolism in vitro of different NF isomers mediated by subcellular rat liver fractions. Under aerobic conditions
X Tang et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(3-4), 373-378 (1997-03-01)
When 21 vitamins including related compounds haemin, chlorophyllin, chlorophyll, biliverdin and bilirubin, as well as juices from five fruits and 25 vegetables and solvent extracts from the residues of fruits and vegetables were tested for their antimutagenic potencies with respect
J V Pothuluri et al.
Journal of toxicology and environmental health, 42(2), 209-218 (1994-06-01)
We investigated the metabolism of 3-nitrofluoranthene by filamentous fungus, Cunninghamella elegans ATCC 36112. Cunninghamella elegans metabolized about 72% of the 3-nitro[3,4-14C]fluoranthene added during 144 h of incubation to 2 major metabolites. These metabolites were separated by reversed-phase high-performance liquid chromatography
J V Pothuluri et al.
Journal of toxicology and environmental health. Part A, 53(2), 153-174 (1998-01-28)
Metabolism of 2-nitrofluoranthene (2-NFA), one of the most abundant and genotoxic environmental pollutants in air, and of a mixture of 2-nitrofluoranthene and 3-nitrofluoranthene (3-NFA) was studied using (1) the fungus Cunninghamella elegans ATCC 36112 and (2) rat liver microsomes. The
K Horikawa et al.
Carcinogenesis, 12(6), 1003-1007 (1991-06-01)
3,9- and 3,7-Dinitrofluoranthene (3,9- and 3,7-DNF), 3-nitrofluoranthene (3-NF) and benzo[a]pyrene (B[a]P) were tested for pulmonary carcinogenicity by intrapulmonary implantation of the compounds into rat lung. These chemicals were given in various doses as suspensions in beeswax-trycaprylin and the animals were
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