515221
3-Amino-4-hydroxy-5-nitrobenzenesulfonic acid
97%
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About This Item
Linear Formula:
H2NC6H2(OH)(NO2)SO3H
CAS Number:
Molecular Weight:
234.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Assay
97%
mp
325 °C (dec.) (lit.)
SMILES string
Nc1cc(cc(c1O)[N+]([O-])=O)S(O)(=O)=O
InChI
1S/C6H6N2O6S/c7-4-1-3(15(12,13)14)2-5(6(4)9)8(10)11/h1-2,9H,7H2,(H,12,13,14)
InChI key
RHPXYZMDLOJTFF-UHFFFAOYSA-N
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Yaws CL.
Thermophysical Properties of Chemicals and Hydrocarbons, 100-100 (2014)
Yaws CL.
The Yaws Handbook of Physical Properties for Hydrocarbons and Chemicals, 523-523 (2015)
Jolanta Polak et al.
Microbial cell factories, 9, 51-51 (2010-07-06)
Chemical methods of producing dyes involve extreme temperatures and unsafe toxic compounds. Application of oxidizing enzymes obtained from fungal species, for example laccase, is an alternative to chemical synthesis of dyes. Laccase can be replaced by fungal biomass acting as
M J Pacheco et al.
Journal of hazardous materials, 186(2-3), 1033-1041 (2010-12-21)
The electrochemical oxidation of four aromatic amines, with different substituent groups, 3-amino-4-hydroxy-5-nitrobenzenesulfonic acid (A1), 5-amino-2-methoxybenzenesulfonic acid (A2), 2,4-dihydroxyaniline hydrochloride (A3) and benzene-1,4-diamine (A4), was performed using as anode a boron-doped diamond electrode, commercially available at Adamant Technologies. Tests were run
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