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Key Documents

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101656

Sigma-Aldrich

2-Chloro-4-nitroaniline

99%

Sinónimos:

1-Amino-2-chloro-4-nitrobenzene

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About This Item

Fórmula lineal:
ClC6H3(NO2)NH2
Número de CAS:
121-87-9
Peso molecular:
172.57
Beilstein/REAXYS Number:
638657
EC Number:
204-502-2
MDL number:
MFCD00007665
UNSPSC Code:
12352100
PubChem Substance ID:
24846548
NACRES:
NA.22

Quality Level

200

assay

99%

autoignition temp.

971 °F

mp

105-108 °C (lit.)

SMILES string

Nc1ccc(cc1Cl)[N+]([O-])=O

InChI

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

InChI key

LOCWBQIWHWIRGN-UHFFFAOYSA-N

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pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H411

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 2

flash_point_f

379.4 °F - closed cup

flash_point_c

193 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCM2545
BCCK5919
BCBS6949V
BCBB0074V
BCBB0074

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Sigma-Aldrich

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Thai Ha Tran et al.
Chemosphere, 201, 425-431 (2018-03-13)
The manganese oxide birnessite adsorbed and catalyzed the transformation of the anthelminthic drug niclosamide (NIS) into 2-chloro-4-nitroaniline (CNA) and 5-chlorosalicylic acid (CSA) at acidic pH. The adsorption of NIS was fitted using a linear isotherm for all conditions and reaction
J Borcherding et al.
Archives of environmental contamination and toxicology, 40(4), 497-504 (2001-08-30)
The Dreissena-Monitor is a biological early warning system for the continuous monitoring of river water quality, based on the valve movements of two groups of 42 zebra mussels (Dreissena polymorpha). Laboratory experiments with Cd, PCP, and 2-chloro-4-nitro-aniline were conducted in
J J Espinosa-Aguirre et al.
Mutation research, 264(3), 139-145 (1991-11-01)
Niclosamide is an anti-helminthic drug susceptible to being metabolized into a bacterial mutagen by the action of enzymes present in the S9 activation mixture. Additional results from genotoxic studies in rodents and humans suggest that the drug is absorbed from
Jimmy Murillo-Gelvez et al.
Environmental science & technology, 53(10), 5816-5827 (2019-05-01)
Nitroaromatic compounds (NACs) are a class of prevalent contaminants. Abiotic reduction is an important fate process that initiates NAC degradation in the environment. Many linear free energy relationship (LFER) models have been developed to predict NAC reduction rates. Almost all
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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