(8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-1,7,8,9,10,11,12,13,14,17-decahydro-3H-cyclopenta[a]phenanthrene-3,6(2H)-dione; 13-ethyl-17-hydroxy-18,19-dinor-17α-pregna-4,15-dien-20-yne-3,6-dione; 6-keto-gestodene
Gestodene EP Impurity E is a fully characterized chemical compound used as a reference standard of API Gestodene. The standard offered is compliant with regulatory guidelines. Gestodene EP Impurity E 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 - 2143949-52-2
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