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Key Documents

101664

Sigma-Aldrich

4-Chloro-2-nitroaniline

99%

Synonym(s):

1-Amino-4-chloro-2-nitrobenzene

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About This Item

Linear Formula:
ClC6H3(NO2)NH2
CAS Number:
Molecular Weight:
172.57
Beilstein:
512436
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

autoignition temp.

964 °F

mp

117-119 °C (lit.)

functional group

chloro

SMILES string

Nc1ccc(Cl)cc1[N+]([O-])=O

InChI

1S/C6H5ClN2O2/c7-4-1-2-5(8)6(3-4)9(10)11/h1-3H,8H2

InChI key

PBGKNXWGYQPUJK-UHFFFAOYSA-N

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Related Categories

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

375.8 °F

Flash Point(C)

191 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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H M Chopade et al.
Journal of toxicology and environmental health, 12(2-3), 267-282 (1983-08-01)
The disposition and metabolism of 14C-labeled 4-chloro-2-nitroaniline (CNA) was studied in male F344 rats following oral or intravenous (iv) administration. The gastrointestinal absorption of CNA was found to be near complete and was not affected by the dose in the
D Cottalasso et al.
La Medicina del lavoro, 82(3), 253-260 (1991-05-01)
The toxicity of 4-chloro-2-nitroaniline (4C2NA) and 2-chloro-4-nitroaniline (2C4NA) was investigated on isolated rat hepatocytes following 1-3 hours of exposure to 0.2 and/or 2 mM of these xenobiotics. The higher of the two concentrations appeared to induce a statistically significant loss

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Protocol for GC Analysis of Anilines on Equity®-5

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