Lovastatin EP Impurity B | CAS 75225-50-2 - Solicitar cotización

Lovastatin EP Impurity B is chemically Sodium (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-Dimethyl-8-[[(2S)-2-methylbutanoyl]oxy]-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate (as per EP) ; Sodium (3R,5R)-7-[(1S,2S,6R,8S,8aR)-2,6-Dimethyl-8-{[(S)-2-methylbutanoyl]oxy}-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]-3,5-dihydroxyheptanoate (as per USP). It is also known as hydroxyacid lovastatin (EP) ; Mevinolinic Acid ; Lovastatin acid. Lovastatin EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Lovastatin EP Impurity B can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Lovastatin.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.