(1S,8R,9S,10S,13S,14S,17R)-17-acetyl-6-chloro-1-(chloromethyl)-10,13-dimethyl-3-oxo-2,3,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl acetate; (1α)-17-(acetyloxy)-6-chloro-1-(chloromethyl)-Pregna-4,6-diene-3,20-dione
Cyproterone Acetate EP Impurity C 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 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 - 17183-98-1
