(8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-4,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one;(17?)-13-Ethyl-17-hydroxy-18,19-dinorpregn-5-en-20-yn-3-one; Levonorgestrel EP Impurity P;5(6)-Dehydro-4(5)-dihydro D-(-)-Norgestrel;
Levonorgestrel Impurity P is a fully characterized chemical compound used as a reference standard of API Levonorgestrel. The standard offered is compliant with regulatory guidelines. Levonorgestrel Impurity P 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 - 100021-05-4
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