(8R,9S,13S,14S,17S)-13-ethyl-3-methoxy-4,6,7,8,9,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-ol;Levonorgestrel Impurity; (±)-3-Methoxy-18-methylestra-2,5(10)-dien-17?-ol;13-Ethyl-3-methoxygona-2,5(10)-dien-17?-ol;
Levonorgestrel EP Impurity Q 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 Q 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 - 1038-28-4
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