(MixtureofDiastereomers)(1S,3R,7S,8S,8aR)-8-(2-((2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-3,7-dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl2-methyl-3-oxobutanoate
Lovastatin Impurity 2 (Mixture of Diastereomers) is a fully characterized chemical compound used as a reference standard of API Lovastatin. The standard offered is compliant with regulatory guidelines. Lovastatin Impurity 2 (Mixture of Diastereomers) 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 -
