Tadalafil EP Impurity A | CAS 171596-27-3 - Solicitar cotización

Tadalafil EP Impurity A is chemically (6R,12aS)-6-(1,3-Benzodioxol-5-yl)-2-methyl-2,3,6,7,12,12a-hexahydropyrazino[1′,2′:1,6]pyrido[3,4-b]indole-1,4-dione (as per EP) ; 6R,12aS)-6-(1,3-Benzodioxol-5-yl)-2,3,6,7,12,12a-hexahydro-2-methyl-pyrazino[1′,2′:1,6]pyrido[3,4-b]indole-1,4-dione (as per USP). It is also known as cis-Tadalafil ; 6R,12aS diastereomer (USP). Tadalafil EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Tadalafil 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 Tadalafil.

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.