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BCR308

9-Nitroanthracene

BCR®, certified reference material

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About This Item

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

grade

certified reference material

Agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

141-144 °C (lit.)

format

neat

storage temp.

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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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

Legal Information

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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)
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)
Hiromichi Akizawa et al.
Chemical & pharmaceutical bulletin, 52(1), 41-46 (2004-01-08)
A comparative study was conducted to elucidate the mechanism underlying the separation of poly-aromatic-hydrocarbons (PAHs) and related compounds thereof on a column packed with silica gels modified with Ni(II)- or Cu(II)-phthalocyanine derivatives (PCS) (Ni- or Cu-PCS(D) column) and commercially available
M J Dennis et al.
Food additives and contaminants, 1(1), 29-37 (1984-01-01)
A method is described for the sample clean-up and estimation of nitropolycyclic aromatic hydrocarbons (nitro-PAH) in foods. The analysis involves the novel use of a coupled capillary gas chromatograph/thermal energy analyser and provides a detection limit for 1-nitropyrene of 12
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
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