missing translation for 'onlineSavingsMsg'
Learn More
Please login to your online account to display your discounted pricing

Sulfanilamide, 98%, Thermo Scientific Chemicals

$74.51 - $620.90

Chemical Identifiers

CAS 63-74-1
Molecular Formula C6H8N2O2S
Molecular Weight (g/mol) 172.202
MDL Number MFCD00007939
InChI Key FDDDEECHVMSUSB-UHFFFAOYSA-N
Synonym sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol
PubChem CID 5333
ChEBI CHEBI:45373
IUPAC Name 4-aminobenzenesulfonamide
SMILES C1=CC(=CC=C1N)S(=O)(=O)N
View More Specs

Products 3
Catalog Number Mfr. No. Quantity Price Quantity  
Catalog Number Mfr. No. Quantity Price Quantity  
AAA1300122
View Documents
Thermo Scientific Chemicals
A1300122
100 g
Each for $74.51
 
AAA1300136
View Documents
Thermo Scientific Chemicals
A1300136
500 g
Each for $165.10
 
AAA130010E
View Documents
Thermo Scientific Chemicals
A130010E
2500 g
Each for $620.90
 
Description

Description

Sulfonamide antibacterial Sulfanilamide is an antibacterial and used in the treatment of vaginal yeast infections. It is a competitive inhibitor of dihydropteroate synthestase to block the synthesis of folic acid. It serves as an intermediate for the preparation of 2,6-disubstituted anilines by electrophilic substitution followed by removal of the sulfonamide blocking group by desulfonation with sulfuric acid.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Sulfonamide antibacterial Sulfanilamide is an antibacterial and used in the treatment of vaginal yeast infections. It is a competitive inhibitor of dihydropteroate synthestase to block the synthesis of folic acid. It serves as an intermediate for the preparation of 2,6-disubstituted anilines by electrophilic substitution followed by removal of the sulfonamide blocking group by desulfonation with sulfuric acid.

Solubility
Soluble in water, acetone, ethanol, glycerol, propylene glycol and hydrochloric acid. Insoluble in chloroform, ether, benzene and petroleum ether.

Notes
Incompatible with strong oxidizing agents.
Specifications

Chemical Identifiers

63-74-1
172.202
FDDDEECHVMSUSB-UHFFFAOYSA-N
5333
4-aminobenzenesulfonamide
C6H8N2O2S
MFCD00007939
sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol
CHEBI:45373
C1=CC(=CC=C1N)S(=O)(=O)N

Specifications

63-74-1
1.08
MFCD00007939
511852
sulfanilamide, sulphanilamide, sulfamine, sulphonamide, p-aminobenzenesulfonamide, sulfonylamide, sulfonamide, p-aminobenzenesulfamide, bacteramid, streptasol
FDDDEECHVMSUSB-UHFFFAOYSA-N
4-aminobenzenesulfonamide
5333
172.21
Sulfanilamide
163°C to 168°C
C6H8N2O2S
100 g
14,8925
Soluble in water,acetone,ethanol,glycerol,propylene glycol and hydrochloric acid. Insoluble in chloroform,ether,benzene and petroleum ether.
C1=CC(=CC=C1N)S(=O)(=O)N
172.202
CHEBI:45373
98%
Videos
Safety and Handling

Safety and Handling

GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.

P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c

H315-H319-H335

EINECSNumber : 200-563-4

RTECSNumber : WO8400000

TSCA : Yes

Recommended Storage : Ambient temperatures

SDS
missing translation for 'documents'

missing translation for 'documents'

RUO – Research Use Only