This impurity is related to Zoledronic Acid EP Impurity A 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.
Zoledronic Acid EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:[1-(2-Hydroxy-2,2-diphosphonoethyl)-1H-imidazol-3-ium-3-yl]acetateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Zoledronic Acid Molecular Formula: C7H12N2O9P2
Molecular Weight: 330.1
Storage: Store in a cool, dry place.