13,14-Dehydro Lovastatin; (2S)-2-Methylbutanoic Acid (1S,3R,7S,8S,8aR)-8-[2-[(2R)-3,6-Dihydro-6-oxo-2H-pyran-2-yl]ethyl]-1,2,3,7,8,8a-hexahydro-3,7-dimethyl-1-naphthalenyl Ester; Dehydromonacolin K; L 642257; ?,?-Dehydrolovastatin; Lovastatin EP Impurity C;Dehydro Lovastatin
Lovastatin EP Impurity C (Dehydro Lovastatin) 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 C (Dehydro Lovastatin) 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 - 109273-98-5
