(2S)-2-Methylbutanoic Acid (1S,3S,4aR,7S,8S,8aS)-1,2,3,4,4a,7,8,8a-Octahydro-3,7-dimethyl-8-[2-[(2R,4R)-tetrahydro-4-hydroxy-6-oxo-2H-pyran-2-yl]ethyl]-1-naphthalenyl Ester; (+)-Dihydromevinolin; Dihydrolovastatin; Dihydromevinolin; L 154883; MSD 883; Lovastatin EP Impurity E; Lovastatin USP Related Compound A;4a,5-Dihydro Lovastatin
Lovastatin EP Impurity E 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 E 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 - 77517-29-4
