| | Identification | Back Directory |  | [Name] 
 PHTHALYLSULFACETAMIDE
 |  | [CAS] 
 131-69-1
 |  | [Synonyms] 
 Tamid
 TSC-80
 Talecid
 Rabalan
 Kalacet
 Thalajen
 Thalamyd
 Thalisul
 Thalocid
 Talsigel
 Talsutin
 Sterathal
 Sulphalyl
 Talasulfa
 Enterocid
 Enterosulfon
 Talicetimida
 Ftalicetimida
 Enterosulfamid
 Enterosulphamid
 TSC-80 Medicated
 PHTHALYLSULFACETAMIDE
 Phthalylsulfacetimide
 Phthalylthioacetamide
 Phthaloylsulfacetamide
 Phthalylsulphacetamide
 LABOTEST-BB LT00438470
 BENZOICACID,2-[[[4-[(ACETYLA
 PHTHALYLSULFACETAMIDE USP/EP/BP
 phthalylsulfacetamidecrystalline
 N-(o-Carboxybenzoyl)sulfacetamide
 N1-ACETYL-N4-PHTHALYLSULFANILAMIDE
 4'-(Acetylsulfamyl)phthalanilic acid
 4'-(ACETYLSULFAMOYL)PHTHALANILIC ACID
 Phthalanilic acid, 4'-(acetylsulfamoyl)-
 N(Sup1)-Acetyl-N(sup4)-phthalylsulfanilamide
 N-(4-ACETYLSULFAMOYL-PHENYL)-PHTHALAMIC ACID
 N-(4-(acetylsulphamoyl)phenyl)phthalamic acid
 Phthalylsulfacetamide,Bacterial,Inhibitor,inhibit
 4'-(Acetylsulfamyl)phthalanilic acidosetile Pink BN
 2-[[4-(acetylsulfamoyl)phenyl]carbamoyl]benzoic acid
 2-[[4-(ethanoylsulfamoyl)phenyl]carbamoyl]benzoic acid
 2-((4-(N-Acetylsulfamoyl)phenyl)carbamoyl)benzoic acid
 2-((4-[(Acetylamino)sulfonyl]anilino)carbonyl)benzoic acid
 2-[[[4-[(acetylamino)sulfonyl]phenyl]amino]carbonyl]-benzoicaci
 2-([[4-([ACETYLAMINO]SULFONYL)PHENYL]AMINO]CARBONYL)BENZOIC ACID
 |  | [EINECS(EC#)] 
 205-035-7
 |  | [Molecular Formula] 
 C16H14N2O6S
 |  | [MDL Number] 
 MFCD00020275
 |  | [MOL File] 
 131-69-1.mol
 |  | [Molecular Weight] 
 362.36
 | 
 | Hazard Information | Back Directory |  | [Uses] 
 antibacterial
 |  | [Definition] 
 ChEBI: Phthalylsulfacetamide is a member of benzamides.
 |  | [Brand name] 
 Talsigel (Bristol-Myers Squibb); Thalamyd
(Schering) [Name previously used: Phthalylsulphacetamide.].
 |  | [storage] 
 Store at -20°C
 |  | [Purification Methods] 
 It is prepared by hydrolysis of N-acetamidosulfophenylpthalimide by boiling for 3hours in 15% aqueous KOH followed by treatment with Norit, filtration and acidification with AcOH. Crystallise the phthalamide from hot H2O or EtOH [Jain et al. J Indian Chem Soc 24 174 1947]. Itis antibacterial.[Beilstein 14 III 2073.]
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