This impurity is related to Zopiclone EP Impurity B 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.
Zopiclone EP Impurity B is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(7RS)-6-(5-Chloropyridin-2-yl)-7-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-one (as per EP) ; 6-(5-Chloropyridin-2-yl)-7-hydroxy-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-one (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Zopiclone Molecular Formula: C11H7ClN4O2
Molecular Weight: 262.7
Storage: Store in a cool, dry place.