(6R,8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-6,17-dihydroxy-6,7,8,9,10,11,12,13,14,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one; (6-beta-Hydroxy Gestodene);6β-Hydroxy Gestodene; 13-Ethyl-6β,17-dihydroxy-18,19-dinor-17α-pregna-4,15-dien-20-yn-3-one pregna-4,15-dien-20-yn 3-one
Gestodene EP Impurity D 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 D 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 - NA
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