Dabigatran Stage-ll Impurity - Solicitar cotización

Dabigatran Stage-ll Impurity is chemically Ethyl 3-(2-(((4-(ethoxy(imino)methyl)phenyl)amino)methyl)-1-methyl-N-(pyridin-2-yl)-1H-benzo[d]imidazole-5-carboxamido)propanoate oxalate. Dabigatran Stage-ll Impurity is supplied with detailed characterization data compliant with regulatory guideline. Dabigatran Stage-ll Impurity 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 Dabigatran.

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.