Sumatriptan EP Impurity A

Sumatriptan EP Impurity A is chemically 1-(3-(2-(Dimethylamino)ethyl)-2-((3-((dimethylamino)methyl)-1H-indol-5-yl)methyl)-1H-indol-5-yl)-N-methylmethanesulfonamide. It is also known as Sumatriptan USP Related Compound A. Sumatriptan EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Sumatriptan EP Impurity A 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 Sumatriptan.

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.