(E)-4-(((3aR,4R,5R,7S,8S,9R,9aS,12R)-5-(2-((2-(diethylamino)ethyl)thio)acetoxy)-3,8-dihydroxy-4,7,9,12-tetramethyl-7-vinyldecahydro-4,9a-propanocyclopenta[8]annulen-2-yl)oxy)-4-oxobut-2-enoic acid
Tiamulin EP Impurity I is a fully characterized chemical compound used as a reference standard of API Tiamulin. The standard offered is compliant with regulatory guidelines. Tiamulin EP Impurity I is used for analytical method development, method validation (AMV), and Quality Controlled (QC) applications during synthesis and formulation stages of drug development and serves as a reference standard for traceability against pharmacopeial standards (USP or EP). Axios Research products are intended for analytical purposes only and are not for human use. CAS -
