This impurity is related to Deferasirox Impurity 21 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.
Deferasirox Impurity 21 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(Z)-3-((4-carboxyphenyl)diazenyl)-4-hydrazinylbenzoic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Deferasirox Molecular Formula: C14H12N4O4
Molecular Weight: 300.3
Storage: Store in a cool, dry place.