This impurity is related to Avatrombopag Impurity 12 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.
Avatrombopag Impurity 12 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:4-(4-Chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amineCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Avatrombopag Molecular Formula: C17H23ClN4S2
Molecular Weight: 383
Storage: Store in a cool, dry place.