This impurity is related to Citalopram Carboxylic Acid Impurity 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.
Citalopram Carboxylic Acid Impurity is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name: 1-[3-(Dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarboxylic AcidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Citalopram Molecular Formula: C20H22FNO3
Molecular Weight: 343.4
Storage: Store in a cool, dry place.