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BCR309

6-Nitrochrysene

BCR®, certified reference material

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About This Item

Formule empirique (notation de Hill):
C18H11NO2
Numéro CAS:
7496-02-8
Poids moléculaire :
273.29
Numéro Beilstein :
2134652
Numéro MDL:
MFCD00021179
Code UNSPSC :
41116107
ID de substance PubChem :
329773818
Nomenclature NACRES :
NA.24

Qualité

certified reference material

Agence

BCR®

Fabricant/nom de marque

JRC

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Pf

220 °C (dec.) (lit.)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

[O-][N+](=O)c1cc2c3ccccc3ccc2c4ccccc14

InChI

1S/C18H11NO2/c20-19(21)18-11-17-13-6-2-1-5-12(13)9-10-15(17)14-7-3-4-8-16(14)18/h1-11H

Clé InChI

UAWLTQJFZUYROA-UHFFFAOYSA-N

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Application

6-Nitrochrysene may be used as a certified reference material for the quantification of the analyte in air samples, standard reference material 1649a (urban dust), air and diesel particulate reference materials using gas chromatography-mass spectrometry with negative ion chemical ionization (GC/NICI-MS).

Remarque sur l'analyse

For more information please see:
BCR309

Informations légales

BCR is a registered trademark of European Commission

Pictogrammes

Health hazardExclamation mark
GHS08,GHS07

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Muta. 1B

Code de la classe de stockage

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificats d'analyse (COA)

Lot/Batch Number

Désolés, nous n'avons pas de COA pour ce produit disponible en ligne pour le moment.

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E A Carrasco-Flores et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(3), 509-514 (2004-12-08)
The infrared and Raman spectra of solids and thin solid films of 6-nitrochrysene, its electronic spectra, and resonance Raman scattering (RRS) obtained with UV-laser excitation at 325 nm are reported. The vibrational assignment is supported by ab initio computations at
Yuan-Wan Sun et al.
Chemical research in toxicology, 22(12), 1992-1997 (2009-11-06)
The environmental pollutant 6-nitrochrysene (6-NC) is a powerful mammary carcinogen and mutagen in rats. Our previous studies have shown that 6-NC is metabolized to trans-1,2-dihydroxy-1,2-dihydro-6-nitrochrysene (1,2-DHD-6-NC) in rats and in several in vitro systems, including human breast tissue, and the
J V Pothuluri et al.
Applied and environmental microbiology, 64(8), 3106-3109 (1998-08-04)
The fungus Cunninghamella elegans was used to biotransform 6-nitrochrysene, a mutagen that is a widespread environmental contaminant. After 6 days, 74% of the 3H-labeled 6-nitrochrysene added had been metabolized to two isomeric sulfate conjugates. These conjugates were separated by high-performance
Jacek Krzeminski et al.
Chemical research in toxicology, 24(1), 65-72 (2010-12-01)
Ubiquitous environmental agents [e.g., polynuclear aromatic hydrocarbons (PAHs) and their nitrated derivatives (NO(2)-PAHs)] that are known to induce mammary cancer in rodents are regarded as potential human risk factors for inducing analogous human cancers. Although 6-nitrochrysene (6-NC) is less abundant
Wanli Xing et al.
International journal of environmental research and public health, 17(3) (2020-02-06)
Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) in PM2.5 samples were collected at a roadside monitoring station in Kanazawa, Japan, in every season from 2017 to 2018. Nine PAHs and five NPAHs were determined using high-performance liquid chromatography with fluorescence
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