This impurity is related to Rapidosept EP Impurity G 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.
Rapidosept EP Impurity G is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:1,1'-(oxydimethylene)bis(2,4-dichlorobenzene)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Rapidosept Molecular Formula: C14H10Cl4O
Molecular Weight: 336
Storage: Store in a cool, dry place.