Valganciclovir EP Impurity J

Valganciclovir EP Impurity J is chemically (2RS)-2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]-3-hydroxypropyl propanoate (as per EP) ; 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]-3-hydroxypropyl propionate (as per USP). It is also known as Ganciclovir Monopropionate (USP). Valganciclovir EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Valganciclovir EP Impurity J 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 Valganciclovir.

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.