This impurity is related to Escitalopram EP Impurity H 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.
Escitalopram EP Impurity H is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:3-[(1RS)-5-Cyano-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-1-yl]-N,N-dimethylpropan-1-amine N-oxideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Escitalopram Molecular Formula: C20H21FN2O2
Molecular Weight: 340.4
Storage: Store in a cool, dry place.