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Sulfapyridine

Base Information Edit
  • Chemical Name:Sulfapyridine
  • CAS No.:144-83-2
  • Molecular Formula:C11H11N3O2S
  • Molecular Weight:249.293
  • Hs Code.:29350010
  • European Community (EC) Number:205-642-7
  • NSC Number:757329,41791,4753
  • UNII:Y5V2N1KE8U
  • DSSTox Substance ID:DTXSID3026067
  • Nikkaji Number:J5.831I
  • Wikipedia:Sulfapyridine
  • Wikidata:Q3976827
  • NCI Thesaurus Code:C66570
  • Metabolomics Workbench ID:43165
  • ChEMBL ID:CHEMBL700
  • Mol file:144-83-2.mol
Sulfapyridine

Synonyms:Sulfapyridine;Sulphapyridin;Sulphapyridine

Suppliers and Price of Sulfapyridine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Usbiological
  • THAP11
  • 100ug
  • $ 539.00
  • Usbiological
  • Sulfapyridine
  • 500ul
  • $ 523.00
  • Usbiological
  • Sulfapyridine
  • 100g
  • $ 247.00
  • TRC
  • Sulfapyridine
  • 250mg
  • $ 325.00
  • TCI Chemical
  • Sulfapyridine >98.0%(HPLC)(T)
  • 25g
  • $ 41.00
  • SynQuest Laboratories
  • Sulfa pyridine 98.0%
  • 100 g
  • $ 68.00
  • Sigma-Aldrich
  • Sulfapyridine VETRANAL?, analytical standard
  • 250mg
  • $ 47.50
  • Sigma-Aldrich
  • Sulfapyridine European Pharmacopoeia (EP) Reference Standard
  • $ 190.00
  • Sigma-Aldrich
  • Sulfapyridine European Pharmacopoeia (EP) Reference Standard
  • s2159100
  • $ 190.00
  • Sigma-Aldrich
  • Sulfapyridine ≥99.0%
  • 100g
  • $ 183.00
Total 97 raw suppliers
Chemical Property of Sulfapyridine Edit
Chemical Property:
  • Appearance/Colour:white or yellowish-white crystalline powder 
  • Vapor Pressure:3.9E-09mmHg at 25°C 
  • Melting Point:191-193 °C 
  • Refractive Index:1.674 
  • Boiling Point:473.5 °C at 760 mmHg 
  • PKA:pKa 8.48(H2O t = 25 I = 0.05) (Uncertain) 
  • Flash Point:240.2 °C 
  • PSA:93.46000 
  • Density:1.432 g/cm3 
  • LogP:3.19960 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly) 
  • Water Solubility.:<0.1 g/100 mL at 22℃ 
  • XLogP3:0
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:3
  • Exact Mass:249.05719778
  • Heavy Atom Count:17
  • Complexity:331
Purity/Quality:

99% *data from raw suppliers

THAP11 *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 22-24/25-36-26 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N
  • Description Sulfapyridine is a sulfonamide antibiotic with antibacterial and anti-inflammatory activities. It is also a metabolite of sulfasalazine formed through bacterial conversion in the colon. It is active against strains of Y. enterocolitica and Salmonella (MICs = 3.1-25 and 25-100 μg/ml, respectively), as well as S. aureus (MBC = 0.8 μM). It is an inhibitor of recombinant P. carinii dihydropteroate synthetase (DHPS; IC50 = 0.18 μM). Sulfapyridine scavenges peroxyl radicals in an oxygen radical absorbance capacity (ORAC) assay. It inhibits histamine release induced by compound 48/80 from isolated rat peritoneal mast cells in a dose-dependent manner. Sulfapyridine (1 μg/kg) also inhibits compound 48/80-induced systemic allergic reaction in rats. Formulations containing sulfapyridine have previously been used in the treatment of dermatological conditions and ulcerative colitis.
  • Uses Used in treatment of dermatitis herpetiformis; antibacterial. antibacterial, dermatitis herpetiformis therapy
Technology Process of Sulfapyridine

There total 24 articles about Sulfapyridine 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:
Guidance literature:
With iron; ammonium chloride; In methanol; at 80 ℃; for 3h; Temperature; Solvent;
Guidance literature:
With sodium hydroxide; water;
DOI:10.1039/jr9410000009 DOI:10.1021/ja01859a040
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