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Phthalylsulfathiazole

CAS No.
85-73-4
Chemical Name:
Phthalylsulfathiazole
Synonyms
PST;SULFATHALIDINE;Phthalysulfathiazole;N4-PHTHALYLSULFATHIAZOLE;ST1A1;SIAT8D;TSPST1;ST8SIA4;Talidine;Thalinil
CBNumber:
CB2405964
Molecular Formula:
C17H13N3O5S2
Molecular Weight:
403.43
MDL Number:
MFCD00005318
MOL File:
85-73-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 00:27:08

Phthalylsulfathiazole Properties

Melting point 198-204°C
Boiling point 371.31℃[at 101 325 Pa]
Density 1.4235 (rough estimate)
vapor pressure 0Pa at 25℃
refractive index 1.6390 (estimate)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Practically insoluble in water, freely soluble in dimethylformamide, slightly soluble in acetone and in ethanol (96 per cent).
pka 3.40±0.36(Predicted)
form Solid
color White to Light Yellow
biological source rabbit
Water Solubility 400mg/L at 28℃
Merck 14,7377
BRN 359901
Major Application pharmaceutical (small molecule)
InChI 1S/C17H13N3O5S2/c21-15(13-3-1-2-4-14(13)16(22)23)19-11-5-7-12(8-6-11)27(24,25)20-17-18-9-10-26-17/h1-10H,(H,18,20)(H,19,21)(H,22,23)
InChIKey PBMSWVPMRUJMPE-UHFFFAOYSA-N
SMILES OC(=O)c1ccccc1C(=O)Nc2ccc(cc2)S(=O)(=O)Nc3nccs3
LogP -2 at 28℃
CAS DataBase Reference 85-73-4(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 6875L5852V
ATC code A07AB02
NIST Chemistry Reference Phthalylsulfathiazole(85-73-4)
EPA Substance Registry System Benzoic acid, 2-[[[4-[(2-thiazolylamino)sulfonyl]phenyl]amino]carbonyl]- (85-73-4)
UNSPSC Code 41116107
NACRES NA.41

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Health Hazard (GHS08)Environment (GHS09)
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H412
Precautionary statements  P273-P501
Safety Statements  24/25
RIDADR  3249
WGK Germany  WGK 3
RTECS  TH8575000
TSCA  TSCA listed
HazardClass  6.1(b)
PackingGroup  III
HS Code  29350090
Storage Class 11 - Combustible Solids
Hazard Classifications Aquatic Chronic 3
Toxicity LD50 i.p. in mice: 920 mg/kg (Mattis)
REACH Registrations Inactive
NFPA 704
0
0 1

Phthalylsulfathiazole price More Price(38)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P1500000 Phthalylsulfathiazole European Pharmacopoeia (EP) Reference Standard 85-73-4 100 mg $175 2026-04-30 Buy
Sigma-Aldrich HPA051126 Anti-ST8SIA4 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution 85-73-4 100μL $667 2026-04-30 Buy
Sigma-Aldrich HPA049500 Anti-SULT1A1 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution 85-73-4 100μL $607 2026-04-30 Buy
Sigma-Aldrich HPA036437 Anti-St8Sia4 Antibody Produced In Rabbit Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution 100 μL $667 2026-04-30 Buy
Sigma-Aldrich WH0006817M1 Monoclonal Anti-SULT1A1 antibody produced in mouse clone 1F8, ascites fluid 85-73-4 200μL $406 2025-07-31 Buy
Product number Packaging Price Buy
P1500000 100 mg $175 Buy
HPA051126 100μL $667 Buy
HPA049500 100μL $607 Buy
HPA036437 100 μL $667 Buy
WH0006817M1 200μL $406 Buy

Phthalylsulfathiazole Chemical Properties, Uses, Production

Chemical Properties

White or yellowish-white, crystalline powder.

Originator

Sulfathalidine, MSD, US,1946

Uses

Phthalylsulfathiazole is a sulfonamide antibacterial drug with similar and stronger effects than Sulfaguanidine and Succinylsulfathiazole. It is rarely absorbed orally and slowly decomposes in the intestine to release Sulfathiazole and exert intestinal antibacterial effects, and is used in the treatment of dysentery, colitis, and gastroenteritis.

Definition

ChEBI: Phthalylsulfathiazole is a sulfonamide incorporating 2-carboxybenzamido and 1,3-thiazol-2-yl moieties that is a broad-spectrum antibiotic indicated in the treatment of dysentery, colitis, gastroenteritis and intestinal surgery. It is a sulfonamide, a member of 1,3-thiazoles, a dicarboxylic acid monoamide and a sulfonamide antibiotic. It derives from a phthalic acid.

Preparation

It may be prepared by the interaction of sulfathiazole and phthalic anhydride in equimolar proportions.
It exerts its bacteriostatic effect in the gastro-intestinal tract. It has been found to be twice as active as sulfaguanidine in the treatment of bowel irregularities. It is often effective in watery diarrhoeas and ulcerative colitis. It is also used in the pre-operative treatment of patients undergoing surgery of the intestinal tract. It may also be recommended in the treatment of acute bascillary dysentry of the Sonne, Flexner and Shiga species.

Manufacturing Process

5 g of phthalic anhydride was added to a boiling suspension of 10 g of sulfathiazole in 100 cc of alcohol. The mixture was then refluxed for 5 minutes after the addition was complete at which time all of the solids were in solution. The solution was then cooled and diluted with an equal volume of water, The white solid precipitate which formed was filtered and recrystallized from dilute alcohol, yielding 2-N4-phthalylsulfanilamidothiazole,which decomposes above 260°C, according to US Patent 2,324,015.

brand name

Canidis-anti-diarr;Carbidiar;Carbotalin;Colicitina;Coliclase;Crematalil;Diacolin;Direver;Disenterol;Ef-micin;Enterocalme;Entero-hermes;Entero-red;Enterosteril;Entero-toxan;Esteraplidin mag;Eugeniteed;Fitazil;Ftalil-tiazol;Ilentazol;Inrestibla strepto;Iodentero-neomicina;Logical;Massotalil;Neo-sulfazon;Novosulfina;Phtazol;Septiftalil;Syptan;Talisulfazol;Tamil;.

Therapeutic Function

Antibacterial (intestinal)

World Health Organization (WHO)

Phthalylsulfathiazole, a sulfonamide anti-infective agent, was introduced in 1946 for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing bacterial resistance and their replacement by antibiotics which are generally more active and less toxic. Although phthalylsulfathiazole, which is poorly absorbed from the gastrointestinal tract, is no longer recommended in some countries, it continues to be used in others for the treatment of local intestinal infections, including bacterial dysentery, and for pre-operative bowel preparation.

Flammability and Explosibility

Non flammable

Biological Activity

Sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (SULT1A1) is a phenol sulfotransferase with thermostable activity. The members of sulfotransferase family localize to cytoplasm and catalyze the sulfate conjugation of hormones, xenobiotic compounds, drugs and neurotransmitters.

Mode of action

Phthalylsulfathiazole is of low inherent toxicity. Besides, it also enjoys an additional plus point for being only slightly absorbed by the intestinal mucosa ; and, therefore, may be safely administered in comparatively large doses in the management and treatment of bacillary infections of the intestine. The drug is not absorbed orally and is mostly employed for ulcerative colitis.

85-44-9
72-14-0
85-73-4
Synthesis of Phthalylsulfathiazole from Phthalic anhydride and Sulfathiazole

Phthalylsulfathiazole Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 289)
Supplier Tel Email Country ProdList Advantage
Creasyn Finechem(Tianjin) Co., Ltd. 022-83946278 13820372920 sales@creasyn.com China 968 68
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
3B Pharmachem (Wuhan) International Co.,Ltd. 18930552037 3bsc@sina.com China 15813 69
future industrial shanghai co., ltd 400-0066400 13621662912 sales@jonln.com China 1989 65
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61
Shanghai Longsheng chemical Co.,Ltd. 58099637 13585536065 sales@shlschem.com China 9880 59
XiaoGan ShenYuan ChemPharm co,ltd 15527621225; 15527621225 1791901229@qq.com China 6744 52
Shandong Xiya Chemical Co., Ltd 13355009207 13355009207 3007715519@qq.com China 18722 57

View Latest Price from Phthalylsulfathiazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Phthalylsulfathiazole pictures 2026-08-12 Phthalylsulfathiazole
85-73-4
$95.00 1KG 99% 1T Baoji Guokang Healthchem Co., Ltd.
Phthalylsulfathiazole pictures 2026-05-11 Phthalylsulfathiazole
85-73-4
$29.00 97.16% 10g TargetMol Chemicals Inc.
Phthalylsulfathiazole pictures 2026-05-11 Phthalylsulfathiazole
85-73-4
$29.00 97.16% 10g TargetMol Chemicals Inc.
4'-(2-THIAZOLYLSULFAMYL)PHTHALANILIC ACID 2-[[[4-[(2-THIAZOLYLAMINO)SULFONYL]PHENYLAMINO]CARBONYL]BENZOIC ACID 2-(N4-PHTHALYSULFANILAMIDO)THIAZOLE 2-(N-PHTHALYLAMINOBENZENESULFONAMIDO)THIAZOLE PHTHALYLSULFATHIAZOLE PHTHALYLSULFATHIOZOLE PHTHALYLSULPHATHIAZOLE 4-(2-THIAZOLYLSULFAMYL)PHTHALANILIC ACID 95+% 2-[(((4-[(2-Thiozolylamino)sulfonyl]phenyl]amino]carbonyl]benzoic acid 2-[[4-[(2-Thiazolyl)sulfamoyl]phenyl]carbamoyl]benzoic acid N-[4-(2-Thiazolylsulfamoyl)phenyl]phthalamic acid N-[4-(2-Thiazolylsulfamoyl)phenyl]phthalamidic acid Phthalylsulfathiazo Phtalylsulfathiazole (o-Carboxybenzoyl)-p-aminophenylsulfonamidothiazole 2-((4-[(1,3-Thiazol-2-ylamino)sulfonyl]anilino)carbonyl)benzoic acid 2-(n(sup4)-phthalyaminobenzenesulfonamide)thiazole 2-(n(sup4)-phthalyaminobenzenesulfonamido)thiazole 2-(n(sup4)-phthalylsulfanilamido)thiazole 2-(N4-phthalyaminobenzenesulfonamide)thiazole 2-(N4-phthalyaminobenzenesulfonamido)thiazole 2-(N4-phthalylsulfanilamido)thiazole 2-(N4-Phthalylaminobenzenesulfonamide)thiazole 2-(p-N-Phthalylsulfanilyl)aminothiazole 2-(p-Phthalylaminobenzenesulfamido)thiazole 2-[[[4-[(2-thiazolylamino)sulfonyl]phenyl]amino]carbonyl]-benzoicaci 4'-(2-Thiazolylsulfamoyl)phthalanilic acid Talidine Taloudron Thalazole Thalinil Thalistanin Thalistatyl Ultratiazol Anti-ST8SIA4 antibody produced in rabbit MGC34450 MGC61459 ST8SIA4 Anti-MGC34450 Anti-MGC61459 Anti-PST Anti-PST1 Anti-ST8 α-N-acetyl-neuraminide α-2,8-sialyltransferase 4 Anti-HAST1/HAST2 Anti-MGC5163 Anti-ST1A3 Anti-STP1 Anti-sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 N4-PHTHALYLSULFATHIAZOLE VETRANAL, 250 PHTHALYLSULFATHIAZOLE(PST) PhthalylsulphathiazolePhthalylsulphathiazoleBp 2-((4-(N-(Thiazol-2-yl)sulfaMoyl)phenyl)carbaMoyl)benzoic acid Phthalyslsulfathiazole(PST) N4-Phthalylsul 4-(1,3-dioxo-2-isoindolyl)-N-(2-thiazolyl)benzenesulfonamide 4’-(2-thiazolylsulfamoyl)-phthalanilicaci 4’-(2-thiazolylsulfamoyl)phthalanilicacid AFI-Ftalyl