BCR308
9-硝基蒽
BCR®, certified reference material
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经验公式（希尔记法）:
C14H9NO2
化学文摘社编号:
分子量:
223.23
Beilstein:
1877509
EC 号:
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
141-144 °C (lit.)
包装形式
neat
储存温度
2-8°C
SMILES字符串
[O-][N+](=O)c1c2ccccc2cc3ccccc13
InChI
1S/C14H9NO2/c16-15(17)14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H
InChI key
LSIKFJXEYJIZNB-UHFFFAOYSA-N
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一般描述
9-Nitroanthracene 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 PAHs with oxides of nitrogen.
应用
9-Nitroanthracene may be used as a certified reference material for the quantification of the analyte in the following:
- Aerosol samples using direct infusion into an atmospheric pressure photoionization high-resolution mass spectrometer (APPI-HRMS).
- Air and diesel particulate reference materials using pressurized-fluid extraction (PFE) with normal-phase liquid chromatography (LC) followed by gas chromatography coupled to mass spectrometry (GC-MS) in negative ion chemical ionization (NICI) mode.
分析说明
For more information please see:
BCR308
BCR308
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)
Direct target and non-target analysis of urban aerosol sample extracts using atmospheric pressure photoionization high-resolution mass spectrometry
Giorio C, et al.
Chemosphere, 224, 786-795 (2019)
Andrea Alparone et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 89, 129-136 (2012-01-20)
Structure, IR and Raman spectra of 1-, 2- and 9-nitroanthracene isomers (1-NA, 2-NA and 9-NA) were calculated and analyzed through density functional theory computations using the B3LYP functional with the 6-311+G** basis set. Steric and π-conjugative effects determine the characteristic
9-Nitroanthracene.
IARC monographs on the evaluation of the carcinogenic risk of chemicals to humans, 33, 179-185 (1984-04-01)
X B Xu et al.
Biomedical and environmental sciences : BES, 1(1), 83-89 (1988-06-01)
Five commercially available nitropolyclyclic aromatic hydrocarbons (nitro-PAH), namely, 4-nitrobiphenyl, 2-nitrofluorene, 9-nitroanthracene, 1-nitropyrene, and 2,7-dinitrofluorene, were exposed under restricted sunlight in the open air. The direct-acting mutagenicities of the samples after an exposure of 45 days were measured in order to
Byron E Butterworth et al.
International journal of toxicology, 23(5), 335-344 (2004-10-30)
Anthraquinone (AQ) (9,10-anthracenedione) is an important compound in commerce. Many structurally related AQ derivatives are medicinal natural plant products. Examples include 1-hydroxyanthraquinone (1-OH-AQ) and 2-hydroxyanthraquinone (2-OH-AQ), which are also metabolites of AQ. Some commercial AQ is produced by the oxidation
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