Vortioxetine

Vortioxetine Impurities & Reference Standards

Vortioxetine is recognized as an active pharmaceutical ingredient (API) that supports formulation development, process validation, and quality assurance in drug manufacturing. The compound carries the molecular formula C17H20N2S, corresponding to a molecular weight of 284.4 g/mol. Vortioxetine 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 Vortioxetine 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.