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:
Assay:
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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Related Categories
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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[Establishment of the MPEL for 2,4-dinitroaniline in water by an experimental computational method].
N Ia Mikhaĭlovskiĭ et al.
Gigiena i sanitariia, (10)(10), 15-18 (1982-10-01)
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
[Screening of new 2,4- and 2,6-dinitroaniline derivates for phytotoxicity and antimitotic activity].
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
O Zelenko et al.
Nucleic acids research, 22(14), 2731-2739 (1994-07-25)
The synthesis and enzymatic characterization of DUPAAA, a novel fluorogenic substrate for RNases of the pancreatic type is described. It consists of the dinucleotide uridylyl-3',5'-deoxyadenosine to which a fluorophore, o-aminobenzoic acid, and a quencher, 2,4-dinitroaniline, have been attached by means
T Azuma et al.
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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