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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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Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
Regulatory Information
危险化学品
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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
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
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
[Screening of new 2,4- and 2,6-dinitroaniline derivates for phytotoxicity and antimitotic activity].
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
Biochemistry, 27(16), 6116-6120 (1988-08-09)
The interaction of M315 with 2,4-dinitrophenyl haptens was studied. 2,4-Dinitroaniline (DNP-NH2) showed maximum affinity to M315 at about pH 4. The pH dependence of the association constant of DNP-NH2 to M315 showed three transitions at pH 4.7, at pH 7.2
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