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Merck
CN

D193011

2,4-Dinitroaniline

98%

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About This Item

Linear Formula:
(O2N)2C6H3NH2
CAS Number:
Molecular Weight:
183.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-553-5
Beilstein/REAXYS Number:
982999
MDL number:
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Product Name

2,4-Dinitroaniline, 98%

InChI key

LXQOQPGNCGEELI-UHFFFAOYSA-N

InChI

1S/C6H5N3O4/c7-5-2-1-4(8(10)11)3-6(5)9(12)13/h1-3H,7H2

SMILES string

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

assay

98%

contains

≤15% water

mp

176-178 °C (lit.)

Quality Level

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signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk

WGK 3

flash_point_f

435.2 °F - closed cup

flash_point_c

224 °C - closed cup

Regulatory Information

危险化学品
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José Raul Herance et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 11(22), 6491-6502 (2005-08-12)
Zeolites are suitable microporous hosts for positively charged organic species, but it is believed that they cannot adsorb organic anions. Pure Meisenheimer complex, derived from reduction of 2,4-dinitroaniline with NaBH4, was adsorbed inside faujasite cavities. Evidence for the internal incorporation
C Bolognesi et al.
Bollettino della Societa italiana di biologia sperimentale, 56(23), 2480-2485 (1980-12-15)
The DNA damage induced by in vivo administration of: 2,4-dinitroaniline, ortho-toluidine and para-toluidine, was determined using alkaline filter elution of DNA. The target organs for ultimate carcinogens produced in mice appear to be the liver and the kidney. The damage
Xiaojia Huang et al.
Journal of chromatography. A, 1216(20), 4354-4360 (2009-04-03)
A simple and sensitive method for the determination of polar aromatic amines (PAAs) was developed using stir bar sorptive extraction (SBSE) coupling to high-performance liquid chromatography. A hydrophilic poly(vinylimidazole-divinylbenzene) (VIDB) monolithic material was prepared and acted as SBSE coating. The
[Experimental study of the effect of 2,4-dinitroaniline on embryogenesis].
S E Khipko et al.
Gigiena truda i professional'nye zabolevaniia, (6)(6), 47-49 (1982-06-01)
H B Matthews et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(1), 1-10 (1986-01-01)
The disposition and metabolism of 2,4-dinitroaniline was studied in male F-344 rats following oral and i.v. administration. Gastrointestinal absorption was near complete and was not affected by dose (10-90 mumol/kg). Following either oral or i.v. administration, dinitroaniline was rapidly distributed

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