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BCR307

2-Nitronaphthalene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C10H7NO2
CAS Number:
581-89-5
Molecular Weight:
173.17
Beilstein:
2046354
EC Number:
209-474-5
MDL number:
MFCD00004055
UNSPSC Code:
41116107
PubChem Substance ID:
329773816
NACRES:
NA.24
Pricing and availability is not currently available.

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

Signal Word

Danger

Hazard Statements

H228,H350,H411

Hazard Classifications

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

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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.
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
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)
1-nitronaphthalene.
IARC monographs on the evaluation of carcinogenic risks to humans, 46, 303-312 (1989-01-01)
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