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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:
Molecular Weight:
173.17
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-684-5
Beilstein/REAXYS Number:
1867714
MDL number:
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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)
R C Paige et al.
The Journal of pharmacology and experimental therapeutics, 295(3), 934-941 (2000-11-18)
To test whether exposure to ozone alters pulmonary cytochrome P450 monooxygenase-mediated metabolism of xenobiotics, rates of 1-nitronaphthalene (1-NN) metabolism were measured in microsomes prepared from trachea, intrapulmonary airways, and distal lung of rats exposed to filtered air (FA) or ozone
Robert M Healy et al.
Environmental science & technology, 46(21), 11813-11820 (2012-09-28)
The chemical composition of secondary organic aerosol (SOA) formed from the photolysis of 1-nitronaphthalene in a series of simulation chamber experiments has been investigated using an aerosol time-of-flight mass spectrometer (ATOFMS). The resulting SOA is characterized by the presence of
Ching Yu Lin et al.
Toxicology, 260(1-3), 16-27 (2009-05-26)
Naphthalene and close structural analogues have been shown to cause necrosis of bronchiolar epithelial cells in mice by both inhalation exposure and by systemic administration. Cancer bioassays of naphthalene in mice have demonstrated a slight increase in bronchiolar/alveolar adenomas in
M Govindarajan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 85(1), 251-260 (2011-10-26)
In this work, the vibrational spectral analysis was carried out by using FT-Raman and FT-IR spectroscopy in the range 100-4000cm(-1) and 400-4000cm(-1) respectively, for 1-nitronaphthalene (C(10)H(7)NO(2)) molecule. The molecular structure, fundamental vibrational frequencies and intensity of the vibrational bands are

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