Δ5(6)-Gestodene; (8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-1,2,4,7,8,9,10,11,12,13,14,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one; 13-ethyl-17-hydroxy-18,19-dinor-17α-pregna-5,15-dien-20-yn-3-one
Gestodene EP Impurity L 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 L 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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