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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:
982999
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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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Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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


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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
A L Scher
Journal - Association of Official Analytical Chemists, 68(3), 474-477 (1985-05-01)
A method is described for the determination of the intermediates in D&C Orange No. 17 by reverse phase liquid chromatography. The pigment is dissolved in boiling dioxane and then precipitated. The filtrate is chromatographed by isocratic elution, which is followed
B Striepen et al.
The Journal of cell biology, 151(7), 1423-1434 (2001-01-03)
Apicomplexan parasites harbor a single nonphotosynthetic plastid, the apicoplast, which is essential for parasite survival. Exploiting Toxoplasma gondii as an accessible system for cell biological analysis and molecular genetic manipulation, we have studied how these parasites ensure that the plastid
P Gettins et al.
The Biochemical journal, 197(1), 119-125 (1981-07-01)
Pre-resonance Raman spectroscopy was used to study the interactions of the nitro groups of dinitrophenyl haptens with three dinitrophenyl-binding antibody fragments: M315 Fv, M460 Fab' and X25 Fab'. The observed changes in frequency of modes associated with the nitro moieties
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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