Citalopram
Citalopram Impurities & Reference Standards
Citalopram is recognized as an active pharmaceutical ingredient (API) that supports formulation development, process validation, and quality assurance in drug manufacturing. It has a molecular formula of C20H21FN2O and a molecular weight of 324.39 g/mol. High-purity Citalopram and its related substances / process impurities are essential for analytical method development, method validation, quality control, and regulatory submissions under ICH, USP, BP, and EP guidelines. Citalopram is available as a certified impurity reference standard with CoA, HPLC chromatograms, and spectroscopic data to support analytical method development and regulatory compliance.
Associated Impurities
Citalopram Impurity (Escitalopram Enantiomer)
- CAS No: 219861-53-7
- Mol. F.: C20H21FN2O
Citalopram Impurity – B (Hydroxy Impurity)
- CAS No: 411221-53-9
- Mol. F.: C20H21FN2O