This impurity is related to Risedronate 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.
Risedronate EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:[(3RS,6RS and 3R,6S-meso)-2,5-dihydroxy-2,5-dioxo-3,6-bis[(pyridin-3-yl)methyl]-1,4,2?5,5?5-dioxadiphosphinane-3,6-diyl]bis(phosphonic acid)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Risedronic Acid Molecular Formula: C14H18N2O12P4
Molecular Weight: 530.2
Storage: Store in a cool, dry place.