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Sulfathiazole

Product Name
Sulfathiazole
CAS No.
72-14-0
Chemical Name
Sulfathiazole
Synonyms
ST;NORSULFAZOLE;Sulphathiazole;Norsulfazol;SULFATHIAZOL;Sulfathiazloe;Sulzol;Duatok;Dulana;m&b760
CBNumber
CB6133470
Molecular Formula
C9H9N3O2S2
Formula Weight
255.32
MOL File
72-14-0.mol
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Sulfathiazole Property

Melting point:
200-202 °C (lit.)
Boiling point:
479.5±47.0 °C(Predicted)
Density 
1.4629 (rough estimate)
refractive index 
1.6560 (estimate)
storage temp. 
2-8°C
solubility 
0.5g/l
pka
7.2(at 25℃)
form 
Solid
color 
White
Water Solubility 
Insoluble (<0.1 g/100 mL at 21 ºC)
Merck 
14,8943
BRN 
226178
Stability:
Stable. Incompatible with strong oxidizing agents.
InChIKey
JNMRHUJNCSQMMB-UHFFFAOYSA-N
CAS DataBase Reference
72-14-0(CAS DataBase Reference)
NIST Chemistry Reference
Sulfathiazole(72-14-0)
EPA Substance Registry System
Sulfathiazole (72-14-0)
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
3249
WGK Germany 
2
RTECS 
WP2360000
TSCA 
Yes
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29350090
Hazardous Substances Data
72-14-0(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

H412Harmful to aquatic life with long lasting effects

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P273Avoid release to the environment.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
8.21112
Product name
N1-2-Thiazolylsulfanilamid
Purity
for synthesis
Packaging
5G
Price
$36.4
Updated
2024/03/01
Sigma-Aldrich
Product number
8.21112
Product name
N1-2-Thiazolylsulfanilamid
Purity
for synthesis
Packaging
250g
Price
$113
Updated
2024/03/01
Sigma-Aldrich
Product number
46902
Product name
Sulfathiazole
Purity
VETRANAL?, analytical standard
Packaging
250mg
Price
$62.1
Updated
2024/03/01
Sigma-Aldrich
Product number
1636504
Product name
Sulfathiazole
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
350mg
Price
$436
Updated
2024/03/01
TCI Chemical
Product number
S0272
Product name
Sulfathiazole
Purity
>98.0%(HPLC)(T)
Packaging
25g
Price
$78
Updated
2024/03/01
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Sulfathiazole Chemical Properties,Usage,Production

Chemical Properties

white to cream powder

Originator

Tiazol,C. and C.

Uses

Antibacterial.This compound is a contaminant of emerging concern (CECs).

Uses

Sulfonamide antibacterial.

Definition

ChEBI: A 1,3-thiazole compound having a 4-aminobenzenesulfonamido group at the 2-position.

Manufacturing Process

116 parts 4-acetamidobenzolsufonyl chloride (prepared from acetanilide and chlorosulfonic acid) was mixed with 100 parts 2-aminothiasole in 1000 parts water by cooling and stirred for some hours. The bis-amide obtained was filtered off and re-crystallized from 50% ethanol to give bis-(pacetylaminobenzolsulfo)- 2-aminothiazol with MP: 129°C.
10 parts above bis-amide was heated with 10% sodium hydroxide solution for 0.5 hour on water bath. On cooling and filtration the alkaline solution was acidified with glacial acetic acid. The amide obtained was cleared by recrystallized from water to give N1-2-thiazolylsulfanilamide; MP: 202°-203°C.

brand name

Argazol;Bucosol;Chemiovis;Coryza;Crionil;Csp 500;Csp-250;Edifeno;Femakzem;Formotablin antidiarreico;Gyne-sulf;Gyn-sulf;Neosutrin;Polvos wilfe;Pomada wilfe;Prothiazol;Septex cream no. 2;Streptacillin;Sulfa-orzon;Sulfazol;Sulfhatose;Sulfintestin;Sulfopyrol;Sulfour;Sulfzol;Sulnac;Sulphatriad;Tampovagan pss;Thiadyl;Thiuramide;Tiadyl;Trimeto;Trisulpha;Trysul;Tylasul;Ufa 902-duo;Vetoprim mi;Wintrazol.

Therapeutic Function

Antibacterial

World Health Organization (WHO)

Sulfathiazole, a sulfonamide anti-infective agent, was introduced more than 25 years ago 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. The sulfonamides are known to cause serious adverse effects such as renal toxicity, sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Although preparations remain available, use of the drug has been discontinued in many countries.

General Description

White crystalline powder. Is dimorphous: form I is consists of prismatic rods and form II of six-sided plates and prisms. Insoluble in water and soluble in dil aqueous acid and aqueous base.

Air & Water Reactions

May be sensitive to heat, air and light during long-term storage . Insoluble in water.

Reactivity Profile

Sulfathiazole is an amino acid.

Fire Hazard

Flash point data for Sulfathiazole are not available, but Sulfathiazole is probably combustible.

Pharmaceutical Applications

2-Sulfanilamidothiazole. A short-acting compound (half-life c. 4 h) with relatively high activity. Protein binding is c. 75%. Its use has declined because of a high incidence of side effects. It is one of the constituents of triple sulfonamide mixtures, of which local preparations are still available.
Two compounds, phthalylsulfathiazole (sulfathalidine) and succinylsulfathiazole (sulfasuxidine) owe their activity to the slow liberation of sulfathiazole in the bowel. They are poorly soluble and very little is absorbed after oral administration. They were formerly used in the treatment of intestinal infections and in bowel preparation before surgery. They are available in multi-ingredient preparations in some countries.

Biochem/physiol Actions

Sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase.Mode of Action: Inhibits folic acid synthesis in prokaryotes.Anti-microbial Spectrum: Gram positive, Gram negative, ChlamydiaMode of Resistance: Alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.

Safety Profile

Human poison by unspecified route. Experimental poison by intraperitoneal route, Moderately toxic by intravenous, subcutaneous, and parenteral routes. Mildly toxic by ingestion. Human systemic effects by unspecified route: conjunctiva irritation, tubule changes, and allergic skin dermatitis. Experimental reproductive effects. Questionable carcinogen with experimental tumorigenic data, Mutation data reported. When heated to decomposition it emits very toxic fumes of NOx and SOx.

Sulfathiazole Preparation Products And Raw materials

Raw materials

Preparation Products

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Sulfathiazole Suppliers

Wuhan penglei Biotechnology Co., Ltd
Tel
15871464247
Email
1545569349@QQ.COM
Country
China
ProdList
734
Advantage
58
XI'AN RONGBAI BIOTECHNOLOGY CO., LTD.
Tel
029-029-81629930 18165286873
Email
rb@xarbkj.com
Country
China
ProdList
348
Advantage
58
WEITIXIHAUGONG
Tel
0371-53370800 18037197114
Email
2853031799@qq.com
Country
China
ProdList
10005
Advantage
58
Wuhan penglei Biotechnology Co., Ltd
Tel
15871464247 17307245989
Email
3471278124@qq.com
Country
China
ProdList
2307
Advantage
58
Creasyn Finechem(Tianjin) Co., Ltd.
Tel
022-83946278 13820503911
Fax
022-83945176
Email
sales@creasyn.com
Country
China
ProdList
978
Advantage
68
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
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View Lastest Price from Sulfathiazole manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Sulfathiazole 72-14-0
Price
US $0.00/KG
Min. Order
1KG
Purity
98%min
Supply Ability
30tons/month
Release date
2023-01-31
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
Sulfathiazole 72-14-0
Price
US $500.00-300.00/kg
Min. Order
0.0010000000474974513kg
Purity
99%
Supply Ability
5000
Release date
2024-08-23
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Product
2-Ethyl-4-methylimidazole 72-14-0
Price
US $500.00-300.00/kg
Min. Order
0.0010000000474974513kg
Purity
99%
Supply Ability
5000
Release date
2024-08-23

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