D193011
2,4-二硝基苯胺
98%
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关于此项目
线性分子式:
(O2N)2C6H3NH2
化学文摘社编号:
分子量:
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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signalword
Danger
Hazard Classifications
Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2
存储类别
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
法规信息
危险化学品
此项目有
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
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
[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
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