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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

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

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
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.
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
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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