Atorvastatin EP Impurity Mixture (E & H) - Request Quote

Atorvastatin EP Impurity Mixture (E & H) is chemically 5-(4-Fluorophenyl)-1-(2-((2R,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)ethyl)-2-isopropyl-N,4-diphenyl-1H-pyrrole-3-carboxamide (3S,5S)-7-(2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl)-3,5-dihydroxyheptanoate. It is also known as Mixture of SZ-A037009 & SZ-A037093. Atorvastatin EP Impurity Mixture (E & H) is supplied with detailed characterization data compliant with regulatory guideline. Atorvastatin EP Impurity Mixture (E & H) 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 Atorvastatin.

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.