(8R,9S,10R,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-7,8,9,11,12,13,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,6(2H,10H)-dione;13-Ethyl-17-hydroxy-18,19-dinorpregn-4-en-20-yne-3,6-dione;6-Oxo Norgestrel(+/-)-6-Keto Norgestrel; (6-Keto Levonorgestrel)
Levonorgestrel EP Impurity J 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 J 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 - 1175109-63-3
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