Zolmitriptan EP Impurity C | CAS 1350928-05-0 - Request Quote

Zolmitriptan EP Impurity C is chemically (4S,4′S)-4,4′-[[4-(Dimethylamino)butane-1,1-diyl]bis[[3-[2-(dimethylamino)ethyl]-1H-indole-2,5-diyl]methylene]]bis(1,3-oxazolidin-2-one) (as per EP) ; 2,2′-[4-(Dimethylamino)butane-1,1-diyl]bis{5-[(S)-(2-oxooxazolidin-4-yl)methyl]-3-(2-dimethylaminoethyl)indole} (as per USP). It is also known as Zolmitriptan USP Related Compound F ; Zolmitriptan Dimer Impurity; . Zolmitriptan EP Impurity C is supplied with detailed characterization data compliant with regulatory guideline. Zolmitriptan EP Impurity C 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 Zolmitriptan.

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.