(1S,3R,7S,8S,8aR)-1,2,3,7,8,8a-Hexahydro-3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl Ester (2Z)-2-Methyl-2-butenoic Acid;O-Des(2-methylbutyryl) O-((Z)-2-methyl-2-butenoyl) Lovastatin
Lovastatin EP Impurity F is a fully characterized chemical compound used as a reference standard of API Lovastatin. The standard offered is compliant with regulatory guidelines. Lovastatin EP Impurity F 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 - 1048973-04-1
Related products
Lovastatin EP Impurity B Sodium Salt
M.F. C₂₄H₃₇O₆. Na
M.W. 421.56 22.99
CAT# AR-L01995
CAS# 75225-50-2
Lovastatin Impurity 1 Sodium Salt
M.F. C₁₉H₂₉O₅. Na
M.W. 337.44 22.99
CAT# AR-L01996
CAS# 132294-94-1
Lovastatin EP Impurity B-d3 Sodium Salt
M.F. C₂₄H₃₄O₆D₃. Na
M.W. 424.58 22.99
CAT# AR-L01997
CAS# 1279029-75-2
Lovastatin EP Impurity C (Dehydro Lovastatin)
M.F. C₂₄H₃₄O₄
M.W. 386.53
CAT# AR-L02009
CAS# 109273-98-5