Velpatasvir Glycine Dimer Impurity - Solicitar cotización

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