Velpatasvir Hydroxy Impurity - Solicitar cotización

Velpatasvir Hydroxy Impurity is chemically Methyl ((1R)-2-((2S,4S)-2-(4-(11-hydroxy-2-((2S,5S)-1-((methoxycarbonyl)-D-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)carbamate. Velpatasvir Hydroxy Impurity is supplied with detailed characterization data compliant with regulatory guideline. Velpatasvir Hydroxy 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.