08910
2-Amino-4-nitrophenol
≥99.0% (NT)
Synonym(s):
2-Hydroxy-5-nitroaniline
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About This Item
Linear Formula:
H2NC6H3(NO2)OH
CAS Number:
Molecular Weight:
154.12
Beilstein/REAXYS Number:
776533
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
assay
≥99.0% (NT)
mp
140-143 °C (lit.)
143-145 °C
SMILES string
Nc1cc(ccc1O)[N+]([O-])=O
InChI
1S/C6H6N2O3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H,7H2
InChI key
VLZVIIYRNMWPSN-UHFFFAOYSA-N
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
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
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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
2-Amino-4-nitrophenol.
IARC monographs on the evaluation of carcinogenic risks to humans, 57, 167-176 (1993-01-01)
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
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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