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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:
99-57-0
Molecular Weight:
154.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891168
EC Number:
202-767-9
Beilstein/REAXYS Number:
776533
MDL number:
MFCD00007695
Assay:
96%
Form:
solid
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Quality Level

200

assay

96%

form

solid

mp

140-143 °C (lit.)

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

pictograms

Exclamation mark
GHS07

signalword

Warning

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCM2305
R044569/1V
044569/1
S33050
14512MS

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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
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
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Global Trade Item Number

SKUGTIN
A70402-25G04061833383391
A70402-5G04061833383407