(2aR,3aS,3bS,3cS,5aS,6R,8aS,8bR)-6-acetyl-10-chloro-6-hydroxy-3b,5a-dimethyl-3,3a,3b,3c,4,5,5a,6,7,8,8a,8b-dodecahydrocyclopenta[a]cyclopropa[g]phenanthren-2(2aH)-one; 6-Chloro-6-dehydro-17?-hydroxy-1,2?-methyleneprogesterone; 6-Chloro-17-hydroxy-1?,2?-methylenepregna-4,6-diene-3,20-dione; 1,2?-Methylene-6-chloro-6-17?-hydroxyprogesterone; (1?,2?)-6-Chloro-1,2-dihydro-17-hydroxy-3'H-cyclopropa[1,2]pregna-1,4,6-triene-3,20-dione
Cyproterone Acetate EP Impurity F (Cyproterone) is a fully characterized chemical compound used as a reference standard of API Cyproterone. The standard offered is compliant with regulatory guidelines. Cyproterone Acetate EP Impurity F (Cyproterone) 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 - 2098-66-0
