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D193011

Sigma-Aldrich

2,4-Dinitroaniline

98%

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About This Item

Linear Formula:
(O2N)2C6H3NH2
CAS Number:
Molecular Weight:
183.12
Beilstein/REAXYS Number:
982999
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
assay:
98%

Quality Level

assay

98%

contains

≤15% water

mp

176-178 °C (lit.)

SMILES string

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

InChI

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

InChI key

LXQOQPGNCGEELI-UHFFFAOYSA-N

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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_germany

WGK 3

flash_point_f

435.2 °F - closed cup

flash_point_c

224 °C - closed cup


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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
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
[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)
S P Ozheredov et al.
TSitologiia i genetika, 43(5), 3-13 (2010-05-13)
The results of Allium-test screening of new 2,4- and 2,6-dinitroaniline derivates on antimitotic activity and phytotoxicity are presented in the work. It is revealed that all studied compounds which are derivates of 2,4-dinitroaniline, 2,6-dinitro-(4-fluoromethyl)-aniline as well as (methylsulfonyl) nitrobenzol, can
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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