Lovastatin EP Impurity B (Sodium salt)

Lovastatin EP Impurity B (Sodium salt) is chemically 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. It is also known as Lovastatin Hydroxy Acid ; Mevinolinic Acid . Lovastatin EP Impurity B (Sodium salt) is supplied with detailed characterization data compliant with regulatory guideline. Lovastatin EP Impurity B (Sodium salt) 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.