Lazertinib Dimer Impurity - Solicitar cotización

Lazertinib Dimer Impurity is chemically N-((1-(2-((5-Acrylamido-2-methoxy-4-morpholinophenyl)amino)pyrimidin-4-yl)-3-phenyl-1H-pyrazol-4-yl)methyl)-3-((5-((4-(4-((dimethylamino)methyl)-3-phenyl-1H-pyrazol-1-yl)pyrimidin-2-yl)amino)-4-methoxy-2-morpholinophenyl)amino)-N,N-dimethyl-3-oxopropan-1-aminium chloride. Lazertinib Dimer Impurity is supplied with detailed characterization data compliant with regulatory guideline. Lazertinib 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 Lazertinib.

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.