This impurity is related to Escitalopram Impurity 12 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.
       
      
        Escitalopram Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
       
      
        Chemical Name:(2S,3S)-4-((S)-1-(4-cyano-2-(hydroxymethyl)phenyl)-4-(dimethylamino)-1-(4-fluorophenyl)butoxy)-2-hydroxy-3-((4-methylbenzoyl)oxy)-4-oxobutanoic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Escitalopram Molecular Formula: C32H33FN2O8
Molecular Weight: 592.6
Storage: Store in a cool, dry place.