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Merck

BCR306

1-Nitronaphthalene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
86-57-7
Molecular Weight:
173.17
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329773815
EC Number:
201-684-5
Beilstein/REAXYS Number:
1867714
MDL number:
MFCD00003913

Product Name

1-Nitronaphthalene, BCR®, certified reference material

InChI key

RJKGJBPXVHTNJL-UHFFFAOYSA-N

InChI

1S/C10H7NO2/c12-11(13)10-7-3-5-8-4-1-2-6-9(8)10/h1-7H

SMILES string

[O-][N+](=O)c1cccc2ccccc12

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

304 °C (lit.)

mp

53-57 °C (lit.)

density

1.223 g/mL at 25 °C (lit.)

format

neat

storage temp.

2-8°C

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Analysis Note

For more information please see:
BCR306

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.

Legal Information

BCR is a registered trademark of European Commission

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Flam. Sol. 2

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, 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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Determination and comparison of nitrated-polycyclic aromatic hydrocarbons measured in air and diesel particulate reference materials
Bamford AH, et al.
Chemosphere, 50 (5), 575-587 (2003)
Ching Yu Lin et al.
Proteomics, 6(3), 972-982 (2006-02-03)
Naphthalene and 1-nitronaphthalene are ambient air pollutants, which undergo P450-dependent bioactivation in the lung. Reactive metabolites of naphthalene and 1-nitronaphthalene covalently bind to proteins, and the formation of covalent adducts correlates with airway epithelial cell injury in rodent models. These
Gregory L Baker et al.
Toxicological sciences : an official journal of the Society of Toxicology, 77(1), 135-141 (2003-11-06)
The mechanisms of toxicant-mediated lung injury and repair are influenced by the considerable spatial heterogeneity that exists within the conducting airways of the lungs. As a result of this heterogeneity, significant differences and similarities in gene expression are observed throughout
Kara R Schmelzer et al.
Environmental health perspectives, 114(9), 1354-1360 (2006-09-13)
Ambient air is polluted with a mixture of pulmonary toxicants. Previous studies indicate that prior exposure to atmospheric oxidant pollutants such as ozone may significantly alter the response to other pollutants, such as 1-nitronaphthalene (1-NN) . 1-NN, a component of
Bridget Boland et al.
The Journal of pharmacology and experimental therapeutics, 310(2), 546-554 (2004-04-15)
Studies in rodents have demonstrated the importance of cytochrome P450 monooxygenases in generating reactive metabolites that produce Clara cell injury. Pulmonary P450 activities in rodents are much higher than those in primates, raising the issue of relevance of rodent data
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