Dabigatran Etexilate EP Impurity F | CAS 1610758-21-8 - Solicitar cotización

Dabigatran Etexilate EP Impurity F is chemically Ethyl 3-[2-[[4-[N′-[[[(2RS)-heptan-2-yl]oxy]carbonyl]carbamimidoyl]anilino]methyl]-1-methyl-N-(pyridin-2-yl)-1H-benzimidazole-5-carboxamido]propanoate (as per EP) ; Ethyl 3-{2-[({4-[N-(heptan-2-yloxycarbonyl)carbamimidoyl]phenyl}amino)methyl]-1-methyl-N-(pyridin-2-yl)-1H-benzimidazole-5-carboxamido}propanoate (as per USP). It is also known as O-(2-Heptyl) Dabigatran Ethyl Ester ; Dabigatran heptane-2-yl analog (USP). Dabigatran Etexilate EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Dabigatran Etexilate EP Impurity F 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.