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BCR305

1-Nitropyrene

BCR®, certified reference material

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10 MG
$337.00

$337.00

Estimated to ship onMay 02, 2025

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10 MG
$337.00

About This Item

Empirical Formula (Hill Notation):
C16H9NO2
CAS Number:
5522-43-0
Molecular Weight:
247.25
Beilstein/REAXYS Number:
1882811
EC Number:
226-868-2
MDL number:
MFCD00004138
UNSPSC Code:
41116107
PubChem Substance ID:
329773814
NACRES:
NA.24

$337.00

Estimated to ship onMay 02, 2025

Request a Bulk Order

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

153-155 °C (lit.)

format

neat

storage temp.

2-8°C

SMILES string

[O-][N+](=O)c1ccc2ccc3cccc4ccc1c2c34

InChI

1S/C16H9NO2/c18-17(19)14-9-7-12-5-4-10-2-1-3-11-6-8-13(14)16(12)15(10)11/h1-9H

InChI key

ALRLPDGCPYIVHP-UHFFFAOYSA-N

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General description

1-Nitronaphthalene, belonging to the class of nitrated-polycyclic aromatic hydrocarbons, is persistent in the environment. It is produced from direct sources such as diesel, gasoline exhaust and gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs) with oxides of nitrogen.[1]

Analysis Note

For more information please see:
BCR305

Legal Information

BCR is a registered trademark of European Commission

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H351

Hazard Classifications

Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

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Wen-Cheng Chu et al.
Chemical research in toxicology, 22(12), 1938-1947 (2009-12-08)
Cytochrome P450 1a1 (Cyp1a1) is a phase I xenobiotic-metabolizing enzyme, the expression of which is mainly driven by the aryl hydrocarbon receptor (AhR). Cyp1a1 messenger (m)RNA is labile. Our study indicates that 1-nitropyrene (1-NP) highly induced Cyp1a1 protein expression, although
Takayuki Kameda et al.
Environmental science & technology, 45(8), 3325-3332 (2011-03-17)
The formation of hydroxynitropyrene (OHNP) via a photochemical reaction of 1-nitropyrene (1-NP) was demonstrated using a UV irradiation system. The photoreaction of 1-NP in methanol gave products that were hydroxy-substituted at position 1 and mononitro-substituted at positions 2, 3, 5
Ning Tang et al.
Chemosphere, 107, 324-330 (2014-02-11)
Airborne particulates were collected at a background site (Wajima Air Monitoring Station; WAMS) on the Noto Peninsula, Japan from January 2006 to December 2007. 1-, 2-nitropyrenes (1-, 2-NPs) and 2-nitrofluoranthene (2-NFR), in the particulates were determined with a sensitive HPLC
Jyan-Gwo J Su et al.
Toxicology, 244(2-3), 257-270 (2008-01-22)
It is reported that diesel exhaust particles contain more 1-nitropyrene (1-NP) than benzo[a]pyrene (B[a]P), both of which are potent carcinogenic compounds. In this study, we show that 1-NP is more potent in reducing cell viability than B[a]P, pyrene, nitrobenzene, and
Rafael Arce et al.
The journal of physical chemistry. A, 112(41), 10294-10304 (2008-09-20)
1-Nitropyrene (1NPy) is the most abundant nitropolycyclic aromatic contaminant encountered in diesel exhausts. Understanding its photochemistry is important because of its carcinogenic and mutagenic properties, and potential phototransformations into biologically active products. We have studied the photophysics and photochemistry of
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