(8R,9S,13S,14S,17R)-13-ethyl-17-ethynyl-17-hydroxy-4,6,7,8,9,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3(2H)-one; 13-Ethyl-17-hydroxy-18,19-dinor-17α-pregn-5(10)-en-20-yn-3-one; (17a)-13-Ethyl-17-hydroxy-18,19-dinorpregn-5(10)-en-20-y n-3-one
Levonorgestrel EP Impurity B 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 B 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 - 19914-67-1
Related products
(S)-2-Amino-3-(3,5-diiodo-4-(4-methoxyphenoxy)phenyl Propanoic Acid
M.F.
M.W. 539.11
CAT# AR-L13658
CAS# 94345-95-6
