Tenofovir Impurity 110 - Solicitar cotización

Tenofovir Impurity 110 is chemically ((1-(6-((((9-(2-((hydroxy(((isopropoxycarbonyl)oxy)methoxy)phosphoryl)methoxy)propyl)-9H-purin-6-yl)amino)methyl)amino)-9H-purin-9-yl)propan-2-yl)oxy)(hydroxy(methoxy)phosphoryl)methylene diisopropyl bis(carbonate) (1:1). Tenofovir Impurity 110 is supplied with detailed characterization data compliant with regulatory guideline. Tenofovir Impurity 110 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 Tenofovir.

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.