2-((8S,9R,10S,11S,13S,14S,16R,17S)-9-fluoro-11,16,17-trihydroxy-10,13-dimethyl-3-oxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl acetate; Triamcinolone 21-Acetate; (11?,?16?)?-21-?(Acetyloxy)?-?9-?fluoro-?11,?16,?17-?trihydroxy-?pregna-?1,?4-?diene-?3,?20-?dione; 9-Fluoro-11?,16?,17,21-trihydroxypregna-1,4-diene-3,20-dione 21-Acetate
Triamcinolone EP Impurity B is a fully characterized chemical compound used as a reference standard of API Triamcinolone. The standard offered is compliant with regulatory guidelines. Triamcinolone EP Impurity B 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 - 3859-65-2
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