This impurity is related to Cilostazol Impurity 19 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.
Cilostazol Impurity 19 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:5-(5-Chloropentyl)-1-cyclohexyl-1H-tetrazoleCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cilostazol Molecular Formula: C12H21ClN4
Molecular Weight: 256.8
Storage: Store in a cool, dry place.