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MilliporeSigma

BCR309

6-Nitrochrysene

BCR®, certified reference material

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10 MG

$256.00

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About This Item

Empirical Formula (Hill Notation):
C18H11NO2
CAS Number:
7496-02-8
Molecular Weight:
273.29
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329773818
MDL number:
MFCD00021179
Beilstein/REAXYS Number:
2134652

Key Documents

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Product Name

6-Nitrochrysene, BCR®, certified reference material

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

SMILES string

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

InChI key

UAWLTQJFZUYROA-UHFFFAOYSA-N

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

220 °C (dec.) (lit.)

format

neat

storage temp.

2-8°C

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6H-Benzo[cd]pyren-6-one BCR®, certified reference material

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6H-Benzo[cd]pyren-6-one

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

format

neat

format

neat

format

neat

grade

certified reference material

grade

certified reference material

grade

certified reference material

grade

certified reference material

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

manufacturer/tradename

JRC

manufacturer/tradename

JRC

manufacturer/tradename

JRC

manufacturer/tradename

JRC

agency

BCR®

agency

BCR®

agency

BCR®

agency

BCR®

Analysis Note

For more information please see:
BCR309

Application

6-Nitrochrysene may be used as a certified reference material for the quantification of the analyte in air samples,[1] standard reference material 1649a (urban dust),[1] air and diesel particulate reference materials[2] using gas chromatography-mass spectrometry with negative ion chemical ionization (GC/NICI-MS).[1][2]

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
R M Chen et al.
Toxicology letters, 117(1-2), 69-77 (2000-10-18)
The present study has determined the effects of 6-nitrochrysene (6-NC) on human cytochrome P450-dependent monooxygenases in human hepatoma HepG2 cells. Treatment of HepG2 cells with 6-NC increased the activities of microsomal benzo[a]pyrene hydroxylase, 7-ethoxycoumarin and 7-ethoxyresorufin O-deethylases, cytosolic glutathione S-transferase
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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