This impurity is related to Clarithromycin EP Impurity J 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.
Clarithromycin EP Impurity J is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(3R,4S,5S,6R,7R,9R,11S,12R,13S,14R,Z)-6-(((2S,3R,4S,6R)-4-(Dimethylamino)-3-hydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)-14-ethyl-7,12,13-trihydroxy-4-(((2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-10-(hydroxyimino)-3,5,7,9,11,13-hexamethyloxacyclotetradecan-2-oneCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Clarithromycin Molecular Formula: C37H68N2O13
Molecular Weight: 748.94
Storage: Store in a cool, dry place.