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BCR310

3-硝基荧蒽

BCR®, certified reference material

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10 MG
$337.00

$337.00

预计发货时间2025年4月04日详情

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10 MG
$337.00

About This Item

经验公式（希尔记法）:
C16H9NO2
CAS号:
892-21-7
分子量:
247.25
Beilstein:
2216474
MDL编号:
MFCD00085494
UNSPSC代码:
41116107
PubChem化学物质编号:
329773819
NACRES:
NA.24

$337.00

预计发货时间2025年4月04日详情

获取大包装报价

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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相关类别

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.[1]

分析说明

For more information please see:
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)

历史批次信息供参考:

分析证书(COA)

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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
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
R Edenharder et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 35(3-4), 357-372 (1997-03-01)
When 56 flavonoids, 32 coumarins, five naphthoquinones, 12 anthraquinones and five structurally-related compounds were tested for their antimutagenic potencies with respect to mutagenicities induced by 2-nitrofluorene (2-NF), 3-nitrofluoranthene (3-NFA) and 1-nitropyrene (1-NP) in Salmonella typhimurium TA98 distinct structure-activity relationships were
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
F E Evans et al.
Chemical research in toxicology, 7(3), 352-357 (1994-05-01)
The structures of selected phenolic metabolites of 2- and 3-nitrofluoranthene have been analyzed. 1H NMR spectral analysis at 500 MHz using one- and two-dimensional methods proves that the site of hydroxy substitution in two metabolites previously reported as 3-nitrofluoranthen-8-ol and
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