This impurity is related to Amlodipine EP Impurity A is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
       
      
        Amlodipine EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
       
      
        Chemical Name:Phthaloyl Amlodipine; 4-(2-Chlorophenyl)-2-[[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)ethoxy]methyl]-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylic Acid 3-Ethyl 5-Methyl Ester; 4-(2-Chlorophenyl)-3-(ethoxycarbonyl)-5-(methoxycarbonyl)-6-methyl-2-[(2-phthalimidoethoxy)methyl]-1,4-dihydropyridineCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Amlodipine Molecular Formula: C28H27ClN2O7
Molecular Weight: 538.99
Storage: Store in a cool, dry place.