Sigma-Aldrich S9876 Sulfathiazole 100 gr
Kategori
Marka
Stok Kodu
LB.SA.S9876-100G
Kısa Bilgi
Synonym(s): 2-Sulfanilamidothiazole, 4-Amino-N-(2-thiazolyl)benzenesulfonamide, N1-(2-Thiazolyl)sulfanilamide Empirical Formula (Hill Notation): C9H9N3O2S2 CAS Number: 72-14-0 Molecular Weight: 255.32 Beilstein: 226178 EC Number: 200-771-5 MDL number: MFCD00005319 PubChem Substance ID: 329824636 NACRES: NA.24
| Sigma-Aldrich S9876 Sulfathiazole 100 gr |
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Synonym(s): 2-Sulfanilamidothiazole, 4-Amino-N-(2-thiazolyl)benzenesulfonamide, N1-(2-Thiazolyl)sulfanilamide
Empirical Formula (Hill Notation): C9H9N3O2S2
CAS Number: 72-14-0
Molecular Weight: 255.32
Beilstein: 226178
EC Number: 200-771-5
MDL number: MFCD00005319
PubChem Substance ID: 329824636
NACRES: NA.24
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PROPERTIES
grade analytical standard
Quality Level 100
Agency EPA 1694
form powder
technique(s) HPLC: suitable, gas chromatography (GC): suitable
mp 200-202 °C (lit.)
application(s) clinical testing
SMILES string Nc1ccc(cc1)S(=O)(=O)Nc2nccs2
InChI 1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)
InChI key JNMRHUJNCSQMMB-UHFFFAOYSA-N
DESCRIPTION
General description
Sulfathiazole is a broad-spectrum antibacterial drug,[1] belonging to the class of sulfonamides, used in veterinary and human medication for the treatment of infections. It is also involved in promoting growth of livestock and fish.[2]
Application Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support. Sulfathiazole is used as an analytical reference standard for the quantification of the analyte in meat,[3][2] and honey[1] samples using different chromatography techniques.
Packaging
100, 250 g in poly bottle
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, Chlamydia
Mode of Resistance: Alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis. |
