(9R,10R,13S,17R)-13-ethyl-17-ethynyl-17-hydroxy-6,7,9,10,11,12,13,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3(2H)-one; (17α)-13-Ethyl-17-hydroxy-18,19-dinorpregna-4,8(14)-dien-20-yn-3-one; Norgestrel 8(14)-Dehydro Impurity
Levonorgestrel EP Impurity A is a fully characterized chemical compound used as a reference standard of API Levonorgestrel. The standard offered is compliant with regulatory guidelines. Levonorgestrel EP Impurity A 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 - 1260525-53-8
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