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Phthalylsulfathiazole
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Phthalylsulfathiazole

CAS: 85-73-4

Ref. 3D-FP40968

1kg
501.00 €
2kg
895.00 €
100g
136.00 €
250g
188.00 €
500g
337.00 €
Estimated delivery in United States, on Tuesday 14 Jan 2025

Product Information

Name:
Phthalylsulfathiazole
Synonyms:
  • (o-Carboxybenzoyl)-p-aminophenylsulfonamidothiazole
  • 2-(N<sup>4</sup>-Phthalylaminobenzenesulfonamide)thiazole
  • 2-(N<sup>4</sup>-Phthalylsulfanilamido)thiazole
  • 2-([4-[(1,3-Thiazol-2-yl)sulfamoyl]phenyl]carbamoyl)benzoic acid
  • 2-[[4-(Methylsulfamoyl)Phenyl]Carbamoyl]Benzoic Acid
  • 2-[[[4-[(2-Thiazolylamino)Sulfonyl]Phenyl]Amino]Carbonyl]Benzoic Acid
  • 2-{[4-(1,3-Thiazol-2-Ylsulfamoyl)Phenyl]Carbamoyl}Benzoic Acid
  • 4-(2-Thiazolylsulfamyl)phthalanilic acid
  • 4′-(2-Thiazolylsulfamoyl)phthalanilic acid
  • AFI-Ftalyl
  • See more synonyms
  • Benzoic acid, 2-[[[4-[(2-thiazolylamino)sulfonyl]phenyl]amino]carbonyl]-
  • Cremothalidine
  • Enteramida
  • Entero-sulfina
  • Entexidina
  • Ftalazol
  • Ftalil-Esteve
  • Ftalil-Septol
  • Ftalysept
  • Intestiazol
  • NSC 66454
  • NSC 683525
  • P-St
  • PST
  • Phtalazol
  • Phthalanilic acid, 4′-(2-thiazolylsulfamoyl)-
  • Phthalazol
  • Phthalidin
  • Phthalylnorsulfazole
  • Phthalylsulfonazole
  • Sulfacetil
  • Sulfaphthalazole
  • Sulfathalidine
  • Sulftalyl
  • Sulphaphthalyl
  • Taleudron
  • Talidine
  • Taloudron
  • Thalazole
  • Thalinil
  • Thalistanin
  • Thalistatyl
  • Thiazole
  • Ultratiazol
Description:

Phthalylsulfathiazole is a metal chelate that has been used as an antimicrobial agent and for the treatment of choroidal neovascularization. It has shown to be effective against infectious diseases such as urinary tract infections, pyelonephritis, and septicemia. Phthalylsulfathiazole is also used for the treatment of calcium pantothenate deficiency, which may be caused by intestinal bacteria. The drug's mechanism of action is not fully understood but it has been shown to bind to the hydroxyl group on DNA polymerase and inhibit its activity. Phthalylsulfathiazole can be synthesized in two ways: 1) Reaction with sodium carbonate and sodium citrate: 2) Reaction with sodium salts and metal ions: The reaction mechanism begins with the addition of metal ions onto the sulfonium salt. This leads to displacement of one chloride ion from the sulfonium salt,

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:
403.43 g/mol
Formula:
C17H13N3O5S2
Purity:
Min. 95%
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
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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