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BCR307

2-Nitronaphthalene

BCR®, certified reference material

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About This Item

Fórmula empírica (notación de Hill):
C10H7NO2
Número de CAS:
581-89-5
Peso molecular:
173.17
Beilstein/REAXYS Number:
2046354
EC Number:
209-474-5
MDL number:
MFCD00004055
UNSPSC Code:
41116107
PubChem Substance ID:
329773816
NACRES:
NA.24

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

65-73 °C

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

[O-][N+](=O)c1ccc2ccccc2c1

InChI

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

InChI key

ZJYJZEAJZXVAMF-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR307

Legal Information

BCR is a registered trademark of European Commission

signalword

Danger

Hazard Classifications

Aquatic Chronic 2 - Carc. 1B - Flam. Sol. 2

Storage Class

4.1B - Flammable solid hazardous materials

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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Certificados de análisis (COA)

Lot/Batch Number

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4-Aminobiphenyl ≥98%

Sigma-Aldrich

A2898

4-Aminobiphenyl

1-Naphthylamine 97%

Sigma-Aldrich

N9005

1-Naphthylamine

9-Fluorenone 98%

Sigma-Aldrich

F1506

9-Fluorenone

J M Sauer et al.
Toxicology, 105(2-3), 237-249 (1995-12-28)
We have previously shown that retinol pretreatment limits the amount of pulmonary injury caused by 1-nitronaphthalene in male Sprague-Dawley rats. The main objective of this study was to determine if retinol pretreatment can protect the lung from the toxicity of
M Watanabe et al.
Mutation research, 301(1), 7-12 (1993-01-01)
Salmonella typhimurium YG1024 is a derivative of S. typhimurium TA98 with a high level of N-hydroxyarylamine O-acetyltransferase (OAT) activity. We have demonstrated that this strain is highly sensitive to the mutagenic actions of N-hydroxyarylamines derived from aromatic amines and nitroarenes.
all-trans-retinol modulation of nitronaphthalene-induced lung and liver injury in male Sprague-Dawley rats.
J M Sauer et al.
Proceedings of the Western Pharmacology Society, 38, 29-31 (1995-01-01)
J C Sasaki et al.
Mutation research, 445(1), 113-125 (1999-10-16)
2-Nitronaphthalene (2NN) has been identified as a mutagenic atmospheric reaction product of naphthalene in the Ames bacterial reversion assay. Recent experiments have shown this nitroarene to be genotoxic in a human lymphoblastoid cell line (MCL-5) transfected with plasmids encoding epoxide
Karolina Pecková et al.
Analytical and bioanalytical chemistry, 381(2), 520-525 (2004-12-31)
The polarographic behaviour of 2-nitronaphthalene was investigated by DC tast polarography (DCTP) and differential pulse polarography (DPP), both at a dropping mercury electrode, and differential pulse voltammetry and adsorptive stripping voltammetry, both at a hanging mercury drop electrode. Optimum conditions
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