Escitalopram

Escitalopram Impurities & Reference Standards

Escitalopram is recognized as an active pharmaceutical ingredient (API) that supports formulation development, process validation, and quality assurance in drug manufacturing. With molecular formula C20H21FN2O and molecular weight 324.39 g/mol, its physicochemical identity is well characterized. Escitalopram impurity reference standards are used to support assay development, purity testing, and stability studies in line with global pharmacopoeial requirements (ICH, USP, BP, EP). Our Escitalopram reference standards are provided with full documentation — Certificate of Analysis (CoA), HPLC chromatographic data, and spectral characterization — to support pharmaceutical R&D and GMP manufacturing.