slight solubility in chloroform and methanol (with sonication) and is soluble in DMSO and DMF
Stability
No Data Available
Boiling Point
No Data Available
Applications
Escitalopram Impurity 7 is supplied with detailed characterization data compliant with regulatory guideline. Escitalopram Impurity 7 can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Escitalopram.