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Sulfathiazole
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Sulfathiazole

CAS: 72-14-0

Ref. 3D-FS27944

25g
63.00 €
2kg
803.00 €
100g
105.00 €
250g
187.00 €
500g
273.00 €
Estimated delivery in United States, on Monday 22 Jul 2024

Product Information

Name:
Sulfathiazole
Synonyms:
  • 4-Amino-N-2-thiazolylbenzenesulfonamide
  • 2-(P-Aminobenzenesulfonamido)Thiazole
  • 2-(Sulfanilylamino)thiazole
  • 2-(p-Aminobenzenesulphonamido)thiazole
  • 2-Sulfanilamidothiazole
  • 2-Sulfathiazole
  • 2090 R.P.
  • 4-Amino-N-2-Thiazolyl-Benzenesulfonamide
  • 4-Amino-N-2-thiazolylbenzensulfonamide
  • 4-[(1,3-Thiazol-2-yl)aminosulfonyl]aniline
  • See more synonyms
  • 4-amino-N-(1,3-thiazol-2-yl)benzenesulfonamide
  • Azoquimiol
  • Azoseptale
  • Benzenesulfonamide, 4-amino-N-2-thiazolyl-
  • Chemosept
  • Ciba 3714
  • Cibazol
  • Duatok
  • Dulana
  • Eleudron
  • Enterobiocine
  • Estafilol
  • M and B 760
  • M&B 760
  • N'-2-thiazolylsulfanylamide
  • N-(Thiazol-2-yl)-4-aminobenzenesulfonamide
  • N1-(2-Thiazolyl)sulfanilamide
  • N<sup>1</sup>-(2-Thiazolyl)sulfanilamide
  • Neostrepsan
  • Norsulfasol
  • Norsulfazol
  • Norsulfazole
  • Nsc 31812
  • Nsc 683531
  • Planomide
  • Poliseptil
  • ST
  • Sanotiazol
  • Streptosilthiazole
  • Sulfamul
  • Sulfanilamide, N1-2-thiazolyl-
  • Sulfanilamide, N1-4-thiazolin-2-ylidene-
  • Sulfanilamide, N<sup>1</sup>-2-thiazolyl-
  • Sulfanilamide, N<sup>1</sup>-4-thiazolin-2-ylidene-
  • Sulfanilamidothiazole
  • Sulfanilamine, N1-2-Thiazolyl-
  • Sulfathiazol
  • Sulfathiazole Granule
  • Sulfatiazol
  • Sulfavitina
  • Sulfocerol
  • Sulphathiazole
  • Sulzol
  • Thiacoccine
  • Thiasulfol
  • Thiazamide
  • Thiozamide
  • Wintrazole
  • p-Amino-N-(2-thiazolyl)benzenesulfonamide
Description:

Sulfathiazole is a sulfonamide antibacterial agent with a chemical structure similar to that of the sulfa drugs. It is active against Gram-positive and Gram-negative bacteria, including those resistant to other antibiotics. Sulfathiazole has been shown to be effective against infectious diseases caused by Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, and Salmonella typhi. The mechanism of action of sulfathiazole is not fully understood. One hypothesis is that it inhibits the synthesis of folic acid in bacteria by inhibiting enzymes involved in purine metabolism. This drug also has complex pharmacological effects on human cells because it can inhibit both receptor activity and enzyme activity in complex cellular processes such as protein synthesis and DNA synthesis.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
255.32 g/mol
Formula:
C9H9N3O2S2
Purity:
Min. 95%
Color/Form:
Powder
InChI:
InChI=1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)
InChI key:
InChIKey=JNMRHUJNCSQMMB-UHFFFAOYSA-N
SMILES:
Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
MDL:
Melting point:
Boiling point:
Flash point:
Density:
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EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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