2-((8R,9S,13S,14S,17R)-17-hydroxy-13-methyl-3-oxo-2,3,4,6,7,8,9,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)acetonitrile; (17?)-17-Hydroxy-3-oxo-19-norpregn-5(10)-ene-21-nitrile
Dienogest EP Impurity I is a fully characterized chemical compound used as a reference standard of API Dienogest. The standard offered is compliant with regulatory guidelines. Dienogest EP Impurity I 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 - 65928-65-6
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