(8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-2,3,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-ol;(17?)-13-Ethyl-18,19-dinorpregn-4-en-20-yn-17-ol; Levonorgestrel Impurity D (EP); Levonorgestrel EP Impurity D
Levonorgestrel Impurity D is a fully characterized chemical compound used as a reference standard of API Levonorgestrel. The standard offered is compliant with regulatory guidelines. Levonorgestrel Impurity D 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 - 32419-58-2
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