(5α,17α)-13-Ethyl-17-hydroxy-5-Methoxy-18,19-dinorpregn-20-yn-3-one
Levonorgestrel EP Impurity O 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 O 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 - 155683-60-6
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