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BCR308

9-Nitroanthracene

BCR®, certified reference material

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About This Item

실험식(Hill 표기법):
C14H9NO2
CAS Number:
602-60-8
Molecular Weight:
223.23
Beilstein:
1877509
EC Number:
210-021-9
MDL number:
MFCD00001248
UNSPSC 코드:
41116107
PubChem Substance ID:
329773817
NACRES:
NA.24

Grade

certified reference material

Agency

BCR®

제조업체/상표

JRC

기술

HPLC: suitable
gas chromatography (GC): suitable

mp

141-144 °C (lit.)

형식

neat

저장 온도

2-8°C

SMILES string

[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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일반 설명

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.

애플리케이션

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.

분석 메모

For more information please see:
BCR308

법적 정보

BCR is a registered trademark of European Commission

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves, type N95 (US)

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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

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)
Eddy F Plaza-Medina et al.
The journal of physical chemistry. A, 115(5), 577-585 (2011-01-11)
We report results of femtosecond-resolved ex-periments which elucidate the time scale for the primary photoinduced events in the model nitroaromatic compound 9-nitroanthracene. Through time-resolved fluorescence measurements, we observed the ultrafast decay of the initially excited singlet state, and through transient
Mutagens in diesel exhaust particulate. Identification and direct activities of 6-nitrobenzo[a]pyrene, 9-nitroanthracene, 1-nitropyrene and 5h-phenanthro[4,5-bcd]pyran-5-one.
J N Pitts et al.
Mutation research, 103(3-6), 241-249 (1982-03-01)
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