A70402
2-Amino-4-nitrophenol
96%
Synonym(s):
2-Hydroxy-5-nitroaniline
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About This Item
Linear Formula:
H2NC6H3(NO2)OH
CAS Number:
Molecular Weight:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-767-9
Beilstein/REAXYS Number:
776533
MDL number:
Product Name
2-Amino-4-nitrophenol, 96%
InChI key
VLZVIIYRNMWPSN-UHFFFAOYSA-N
InChI
1S/C6H6N2O3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H,7H2
SMILES string
Nc1cc(ccc1O)[N+]([O-])=O
assay
96%
form
solid
mp
140-143 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
212.0 °F - closed cup
flash_point_c
100 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
危险化学品
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C P Witte et al.
Applied biochemistry and biotechnology, 69(3), 191-200 (1998-05-16)
The phototrophic bacterium Rhodobacter capsulatus photoreduces 2,4-dinitrophenol to 2-amino-4-nitrophenol, which is further metabolized by an aerobic pathway that is also light-dependent. The catabolism of 2-amino-4-nitrophenol requires O2 and the presence of alternative carbon (C) and nitrogen (N) sources, preferably acetate
2-Amino-4-nitrophenol.
IARC monographs on the evaluation of carcinogenic risks to humans, 57, 167-176 (1993-01-01)
A N Eremin
Prikladnaia biokhimiia i mikrobiologiia, 36(4), 449-457 (2000-09-20)
Characteristics of polydisulfides of gallic acid (PDSG), 2-amino-4-nitrophenol (PDSANP), and biuret (PDSB) depending on the composition of the aqueous medium were studied. In contrast to PDSANP and PDSB, there was oxidation of PDSG with accumulation of products of polydisulfide transformation
E I Karasyova et al.
Biochemistry. Biokhimiia, 66(6), 608-617 (2001-06-26)
The effects of different concentrations of 2-amino-4-nitrophenol (ANP) and of its polydisulfide (poly(ADSNP)) on peroxidase-catalyzed oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) were studied at 20 degrees C in reversed micelles of AOT (0.2 M) in heptane and in mixed reversed micelles of
H Hofer et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 20(6), 921-923 (1982-12-01)
The absorption of 14C-labelled 2-amino-4-nitrophenol (ANP) in two hair dyeing formulations was investigated after application to the skin of rats. After 1 and 5 days, 0.21 and 0.36%, respectively, of the administered radioactivity was absorbed from formulation 1 which contained
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