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165794

Sigma-Aldrich

3-Aminobenzenesulfonic acid

97%

Synonyma:

Metanilic acid

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About This Item

Lineární vzorec:
H2NC6H4SO3H
Číslo CAS:
121-47-1
Molekulová hmotnost:
173.19
Beilstein/REAXYS Number:
473264
EC Number:
204-473-6
MDL number:
MFCD00065345
UNSPSC Code:
12352100
PubChem Substance ID:
24850147
NACRES:
NA.22

assay

97%

form

powder

mp

>300 °C (lit.)

solubility

ethanol: very slightly soluble(lit.)
methanol: very slightly soluble(lit.)

SMILES string

Nc1cccc(c1)S(O)(=O)=O

InChI

1S/C6H7NO3S/c7-5-2-1-3-6(4-5)11(8,9)10/h1-4H,7H2,(H,8,9,10)

InChI key

ZAJAQTYSTDTMCU-UHFFFAOYSA-N

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General description

3-Aminobenzenesulfonic acid undergoes microbial desulfonation to 3-aminophenol by Pseudomonas sp. strain S-313.

Application

3-Aminobenzenesulfonic acid was used in the synthesis of cytocompatible sulfonated polyanilines. It was used in fabrication of novel glucose biosensor having large active surface area and excellent conductivity.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Osvědčení o analýze (COA)

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Sulfanilic acid sodium salt hydrate 97%

Sigma-Aldrich

251283

Sulfanilic acid sodium salt hydrate

Sodium 3-nitrobenzenesulfonate 98%

Sigma-Aldrich

225193

Sodium 3-nitrobenzenesulfonate

D Zürrer et al.
Applied and environmental microbiology, 53(7), 1459-1463 (1987-07-01)
Sulfur-limited batch enrichment cultures containing one of nine multisubstituted naphthalenesulfonates and an inoculum from sewage yielded several taxa of bacteria which could quantitatively utilize 19 sulfonated aromatic compounds as the sole sulfur source for growth. Growth yields were about 4
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Chemistry (Weinheim an der Bergstrasse, Germany), 27(12), 4108-4114 (2020-12-23)
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Biosensors & bioelectronics, 150, 111901-111901 (2019-11-27)
Molecularly imprinted polymers (MIPs) have been developed to replace antibodies for the recognition of target molecules (such as antigens), and have been integrated into electrochemical sensing approaches by polymerization onto an electrode. Electrochemical sensing is inexpensive and flexible, and has
Yanyin Yang et al.
Macromolecular rapid communications, 32(12), 887-892 (2011-05-19)
We report here that by good design, polyaniline (PANI) can be cytocompatible and formed into usable scaffolds for bio-medical applications. By adjusting the ratio of two monomers, aniline (AN) and metanilic acid (MA), a series of copolymers with different sulfonation
Kai-Hsi Liu et al.
Biosensors, 10(3) (2020-03-04)
Molecularly imprinted polymers (MIPs) can often bind target molecules with high selectivity and specificity. When used as MIPs, conductive polymers may have unique binding capabilities; they often contain aromatic rings and functional groups, which can undergo π－π and hydrogen bonding
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