(8S,13S,14S)-13-methyl-1,2,6,7,8,12,13,14,15,16-decahydrospiro[cyclopenta[a]phenanthrene-3,2'-[1,3]dioxolan]-17(4H)-one; Estra-5(10),9(11)-diene-3,17-dione 3-Ethylene Ketal; 3,3-(Ethylenedioxy)estra-5(10),9(11)-dien-17-one; Cyclic 3-(1,2-Ethanediyl Acetal)-estra-5(10),9(11)-diene-3,17-dione
Dienogest EP Impurity L 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 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 - 5571-36-8
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