Lopinavir EP Impurity O - Solicitar cotización

Lopinavir EP Impurity O is chemically (1S,3S)-1-[(1S)-1-[[2-(2,6-Dimethylphenoxy)acetyl]amino]-2-phenylethyl]-3-[[(2S)-3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanoyl]amino]-4phenylbutyl(2S)-3-methyl-2-[2-oxotetrahydropyrimidin1(2H)-yl]butanoate (as per EP); (S)-{(2S,3S,5S)-2-[2-(2,6-Dimethylphenoxy)acetamido]-5-[(S)-3-methyl-2-(2-oxotetrahydropyrimidin-1(2H)-yl)butanamido]-1,6-diphenylhexan-3-yl} 3-methyl-2-[2-oxotetrahydropyrimidin-1(2H)-yl]butanoate (as per USP). It is also known as Lopinavir O-Acyl Impurity (USP) . Lopinavir EP Impurity O is supplied with detailed characterization data compliant with regulatory guideline. Lopinavir EP Impurity O 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 Lopinavir.

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.