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Sulfathiazole

Sulfathiazole Structure
CAS No.
72-14-0
Chemical Name:
Sulfathiazole
Synonyms
ST;NORSULFAZOLE;Sulphathiazole;Norsulfazol;SULFATHIAZOL;Sulfathiazloe;Duatok;Dulana;m&b760;m+b760
CBNumber:
CB6133470
Molecular Formula:
C9H9N3O2S2
Molecular Weight:
255.32
MOL File:
72-14-0.mol
MSDS File:
SDS
Modify Date:
2024/8/24 19:19:26

Sulfathiazole Properties

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)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335-H412
Precautionary statements  P261-P264-P271-P273-P302+P352-P305+P351+P338
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
NFPA 704
1
2 0

Sulfathiazole price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) S9876 Sulfathiazole 72-14-0 100G ₹5282.6 2022-06-14 Buy
Sigma-Aldrich(India) S9876 Sulfathiazole 72-14-0 250G ₹21260.3 2022-06-14 Buy
Sigma-Aldrich(India) 8.21112 N1-2-Thiazolylsulfanilamid for synthesis 72-14-0 5G ₹3080.01 2022-06-14 Buy
Sigma-Aldrich(India) 8.21112 N1-2-Thiazolylsulfanilamid for synthesis 72-14-0 250G ₹11250.01 2022-06-14 Buy
Sigma-Aldrich(India) 46902 Sulfathiazole VETRANAL?, analytical standard 72-14-0 250MG ₹4633.1 2022-06-14 Buy
Product number Packaging Price Buy
S9876 100G ₹5282.6 Buy
S9876 250G ₹21260.3 Buy
8.21112 5G ₹3080.01 Buy
8.21112 250G ₹11250.01 Buy
46902 250MG ₹4633.1 Buy

Sulfathiazole Chemical Properties,Uses,Production

Chemical Properties

white to cream powder

Uses

Sulfonamide antibacterial.

Definition

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

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.

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

Global( 455)Suppliers
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SYNOVA CHEMICALS +91-9920741772 +91-9920741772 Mumbai, India 428 58 Inquiry
Valens Molecules +91-040-23417926 +91-4023417926 Hyderabad, India 10 58 Inquiry
Ishita Drugs And Industries Ltd +91-7226995614 +91-7226995613 Telangana, India 47 58 Inquiry
Sachem 91-9810014878 Delhi, India 75 58 Inquiry
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TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
Pharmaffiliates Analytics and Synthetics P. Ltd +91-172-5066494 Haryana, India 6773 58 Inquiry
4-amino-n-2-thiazolyl-benzenesulfonamid Azoquimiol Azoseptale Benzenesulfonamide, 4-amino-N-2-thiazolyl- Cerazol Cerazol (suspension) cerazol(suspension) Cerazole Chemosept Ciba 3714 ciba3714 Cibazol Coco-Thiazole Duatok Dulana Eleudron Enterobiocine Estafilol Formosulfathiazole M&B 760 m&b760 M+B 760 m+b760 n(1)-2-thiazolyl-sulfanilamid N(Sup1)-(2-Thiazolyl)sulfanilamide n(sup1)-2-thiazolyl-sulfanilamid n(sup1)-2-thiazolylsulfanilamide Neostrepsan Norsulfasol Planomide Poliseptil RP 2090 rp2090 Sanotiazol Septozol Streptosilthiazole Sulfamul Sulfanilamide, N(sup1)-2-thiazolyl- Sulfanilamide, N1-2-thiazolyl- 2-SULFANILAMIDOTHIAZOLE 2-(SULFANILAMINO)THIAZOLE 2-(4-AMINOBENZENESULFONAMIDO)THIAZOLE 2-(P-AMINOBENZENESULFONAMIDO)THIAZOLE Sulfanilamide, N1-4-thiazolin-2-ylidene- Sulfanilamidothiazole Sulfathiazole(form1) Sulfathiazole(form3) sulfathiazone Sulfavitina Sulfocerol Sulzol Thiacoccine Thiasulfol Thiozamide USAF sn-9 usafsn-9 Wintrazole SULFATHIAZOLE