Velpatasvir Impurity 47 - Solicitar cotización

Velpatasvir Impurity 47 is chemically Methyl ((S)-1-((2S,5S)-2-(9-(2-((2R,4S)-1-((S)-2-((methoxycarbonyl)amino)-2-phenylacetyl)-4-(methoxymethyl)pyrrolidin-2-yl)-1H-imidazol-4-yl)-1,11-dihydroisochromeno[4',3':6,7]naphtho[1,2-d]imidazol-2-yl)-5-methylpyrrolidin-1-yl)-3-methyl-1-oxobutan-2-yl)carbamate. Velpatasvir Impurity 47 is supplied with detailed characterization data compliant with regulatory guideline. Velpatasvir Impurity 47 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 Velpatasvir.

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.