![]() Imino (top) and amino (bottom) tautomers | |
Clinical data | |
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AHFS/ Drugs.com | International Drug Names |
ATC code | |
Identifiers | |
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CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.000.701 |
Chemical and physical data | |
Formula | C9H9N3O2S2 |
Molar mass | 255.31 g·mol−1 |
3D model ( JSmol) | |
Melting point | 202 to 202.5 °C (395.6 to 396.5 °F) |
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(verify) |
Sulfathiazole is an organosulfur compound used as a short-acting sulfa drug. [1] Formerly, it was a common oral and topical antimicrobial, until less toxic alternatives were discovered. [2]
Sulfathiazole exists in various forms ( polymorphs). The imine tautomer is dominant in solid samples. [3]
![]() Imino (top) and amino (bottom) tautomers | |
Clinical data | |
---|---|
AHFS/ Drugs.com | International Drug Names |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEBI | |
ChEMBL | |
CompTox Dashboard ( EPA) | |
ECHA InfoCard | 100.000.701 |
Chemical and physical data | |
Formula | C9H9N3O2S2 |
Molar mass | 255.31 g·mol−1 |
3D model ( JSmol) | |
Melting point | 202 to 202.5 °C (395.6 to 396.5 °F) |
| |
| |
(verify) |
Sulfathiazole is an organosulfur compound used as a short-acting sulfa drug. [1] Formerly, it was a common oral and topical antimicrobial, until less toxic alternatives were discovered. [2]
Sulfathiazole exists in various forms ( polymorphs). The imine tautomer is dominant in solid samples. [3]