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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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
D I Metelitza et al.
Journal of inorganic biochemistry, 98(1), 1-9 (2003-12-09)
The steady-state kinetics of the horseradish peroxidase (HRP)-catalyzed oxidation of 3,3',5,5'-tetramethylbenzidine (TMB) has been studied in the presence of 2-amino-4-nitrophenol (ANP), gallic acid (GA) or 4,4'-dihydroxydiphenylsulfone (DDS) and their polydisulfides poly(ADSNP), poly(DSGA), poly(DSDDS) at 20 degrees C in 10 mM
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
T A Robert et al.
Journal of chromatography, 344, 177-186 (1985-11-08)
Eleven groups of six ICR mice were dosed orally with 22.5 mg/kg 2,4-dinitrophenol. Groups were sacrificed at 0, 0.5, 1, 2, 4, 6, 9, 12, 24, 48, and 96 h post-treatment and plasma was collected for analysis of dinitrophenol, 2-amino-4-nitrophenol
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