登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式（希尔记法）:
C14H9NO2
化学文摘社编号:
分子量:
223.23
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
210-021-9
Beilstein/REAXYS Number:
1877509
MDL number:
InChI key
LSIKFJXEYJIZNB-UHFFFAOYSA-N
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
SMILES string
[O-][N+](=O)c1c2ccccc2cc3ccccc13
grade
certified reference material
agency
BCR®
manufacturer/tradename
JRC
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
format
neat
storage temp.
2-8°C
正在寻找类似产品? 访问 产品对比指南
General description
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.
Application
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.
Analysis Note
For more information please see:
BCR308
BCR308
Legal Information
BCR is a registered trademark of European Commission
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
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)
B E Butterworth et al.
Mutagenesis, 16(2), 169-177 (2001-03-07)
Commercial anthraquinone (AQ) (9,10-anthracenedione) is produced by at least three different production methods worldwide: oxidation of anthracene (AQ-OX), Friedel-Crafts technology (AQ-FC) and by Diels-Alder chemistry (AQ-DA), with the final product varying in color and purity. AQ-OX begins with anthracene produced
Application of 9-nitroanthracene as a matrix for laser desorption/ionization analysis of fluorinated fullerenes.
Alexey V Streletskiy et al.
Rapid communications in mass spectrometry : RCM, 18(3), 360-362 (2004-02-03)
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持