ChemicalBook >> CAS DataBase List >>Phthalylsulfathiazole

Phthalylsulfathiazole

CAS No.
85-73-4
Chemical Name:
Phthalylsulfathiazole
Synonyms
PST;ST8SIA4;Talidine;Thalinil;MGC34450;MGC61459;Anti-PST;Ftalazol;Taloudron;Thalazole
CBNumber:
CB2405964
Molecular Formula:
C17H13N3O5S2
Molecular Weight:
403.43
MDL Number:
MFCD00005318
MOL File:
85-73-4.mol
MSDS File:
SDS
Last updated:2024-11-19 20:33:22

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
Water Solubility 400mg/L at 28℃
Merck 14,7377
BRN 359901
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)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08,GHS09
Signal word  Danger
Hazard statements  H412
Precautionary statements  P273-P501
Safety Statements  24/25
RIDADR  3249
RTECS  TH8575000
HazardClass  6.1(b)
PackingGroup  III
HS Code  29350090
Toxicity LD50 i.p. in mice: 920 mg/kg (Mattis)
NFPA 704
0
0 1

Phthalylsulfathiazole price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich WH0006817M1 Monoclonal Anti-SULT1A1 antibody produced in mouse clone 1F8, ascites fluid 85-73-4 200μL $524 2024-03-01 Buy
Sigma-Aldrich P1500000 Phthalylsulfathiazole European Pharmacopoeia (EP) Reference Standard 85-73-4 p1500000 $153 2024-03-01 Buy
Sigma-Aldrich HPA053995 Anti-ST8SIA4 antibody produced in rabbit Prestige Antibodies? Powered by Atlas Antibodies, affinity isolated antibody 85-73-4 100μL $580 2024-03-01 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 $580 2024-03-01 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 $547 2024-03-01 Buy
Product number Packaging Price Buy
WH0006817M1 200μL $524 Buy
P1500000 p1500000 $153 Buy
HPA053995 100μL $580 Buy
HPA051126 100μL $580 Buy
HPA049500 100μL $547 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

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( 261)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8812 58
Hebei ZB Gamay Biological Technology Co.,Ltd
+8617330018573 info@zbvet.net China 246 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29791 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21634 55
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418679 +8618949832763 info@tnjchem.com China 2986 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29884 58
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28172 58
Xiamen AmoyChem Co., Ltd
+86-86-5926051114 +8618959220845 sales@amoychem.com China 6383 58
Shanghai Longyu Biotechnology Co., Ltd.
+8619521488211 info@longyupharma.com China 2529 58
Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58

View Lastest Price from Phthalylsulfathiazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Phthalylsulfathiazole pictures 2024-11-19 Phthalylsulfathiazole
85-73-4
US $29.00 / mL 95.58% 10g TargetMol Chemicals Inc.
Phthalylsulfathiazole pictures 2024-11-19 Phthalylsulfathiazole
85-73-4
US $29.00 / mL 95.58% 10g TargetMol Chemicals Inc.
Phthalysulfathiazole  pictures 2024-11-19 Phthalysulfathiazole
85-73-4
US $0.00 / Box 5Box 99% 200 Hebei ZB Gamay Biological Technology Co.,Ltd
4'-(2-THIAZOLYLSULFAMYL)PHTHALANILIC ACID 2-[[[4-[(2-THIAZOLYLAMINO)SULFONYL]PHENYLAMINO]CARBONYL]BENZOIC ACID 2-(N4-PHTHALYSULFANILAMIDO)THIAZOLE 2-(N-PHTHALYLAMINOBENZENESULFONAMIDO)THIAZOLE N4-PHTHALYLSULFATHIAZOLE PST PHTHALYLSULFATHIAZOLE PHTHALYLSULFATHIOZOLE PHTHALYLSULPHATHIAZOLE SULFATHALIDINE 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’-(2-thiazolylsulfamoyl)-phthalanilicaci