(8S,9R,10S,11S,13S,14S,16R,17S)-9-fluoro-11,16,17-trihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one; Pretriamcinolone; 9?-Fluoro-11?,16?,17?,21-tetrahydroxypregn-4-ene-3,20-dione; 9?-Fluoro-16?-hydroxyhydrocortisone; NSC 21913; 1,2-Dihydro Triamcinolone
Triamcinolone EP Impurity C 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 C 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 - 337-02-0
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