Skip to Content
Merck
All Photos(1)

Documents

BCR307

2-Nitronaphthalene

BCR®, certified reference material

Sign Into View Organizational & Contract Pricing
All Photos(1)

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

Looking for similar products? Visit Product Comparison Guide

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Sorry, we don't have COAs for this product available online at this time.

If you need assistance, please contact Customer Support.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service