Sulfathiazole sodium

Base Information

• Chemical Name: Sulfathiazole sodium
• CAS No.: 144-74-1
• Molecular Formula: C9H8N3NaO2S2
• Molecular Weight: 277.303
• Hs Code.: 2935009090
• Mol file: 144-74-1.mol

Synonyms:Benzenesulfonamide,4-amino-N-2-thiazolyl-, monosodium salt (9CI);Sodium norsulfazole;Sodium sulfathiazolate;Norsulfazole soluble;Sodium sulfathiazole;Soluble norsulfazole;Solublesulfathiazole;Soluthiazomide;Sulfathiazole sodium salt;Sulphathiazole sodium;2-(p-Amino-N-sodiobenzenesulfonamide)thiazole;2-(p-Aminobenzenesulfonamido)thiazole sodium salt;2-Sulfanilamidothiazolesodium salt;Norsulfazol sodium;Sodium 2-sulfanilamidothiazole;Norsulfazole sodium;Norsulfazole sodium salt;

Chemical Property of Sulfathiazole sodium

Chemical Property:

• Vapor Pressure: 2.35E-09mmHg at 25°C
• Melting Point: 175oC (form a); 202oC (form b)
• Boiling Point: 479.5 °C at 760 mmHg
• Flash Point: 243.8 °C
• PSA: 112.91000
• LogP: 3.04690
• Solubility.: H2O: soluble50mg/mL

Purity/Quality:

99% ^*data from raw suppliers

Sulfathiazole sodium salt ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36-24/25-23

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Uses: Sulfathiazole sodium salt is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA). It can also be used in biological study of thermotherapy and sulfonamide antibiotics deciphered Cyanobacteria and Proteobacteria microbiome in huanglongbing-affected Citrus paradise and Citrus limon.

Technology Process of Sulfathiazole sodium

There total 1 articles about Sulfathiazole sodium which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ sulfathiazole sodium (144-74-1)

Guidance literature:

Reference yield: 90.0%

copper (II)-fluoride + sulfathiazole sodium (144-74-1) → Cu2(sulfathiazolato)4 (72446-92-5)

Guidance literature:

In methanol; pptn. on addn. of Cu-salt to warm soln. of 2 equiv. ligand (stirring); collection (filtration), drying; elem. anal.;

DOI:10.1021/ic960968p

Reference yield: 88.6%

cobalt(II) chloride hexahydrate + sulfathiazole sodium (144-74-1) → Co(II)(sulfathiazolate)2(H2O)4 + Co(II)(sulfathiazolate)2(H2O)3

Guidance literature:

In water; aq. soln. of CoCl2 was added to 2.2 equiv. of S-compd. in H2O, stirring at room temp.; standing for 4 d, solid was centrifuged off, washed with H2O several times, dried (vac., away from light), elem. anal.; liq. was stood for 7-12 d, crystals were centrifuged off, washed with H2O several times, dried (vac., away from light), elem. anal.;

DOI:10.1016/j.poly.2004.12.017

Downstream raw materials:

Cremothalidine

Cu₂(sulfathiazolato)4

Cd(H₂NC₆H₄SO₂N(C₃H₂NS))2

Co(H₂NC₆H₄SO₂N(C₃H₂NS))2

Refernces