This impurity is related to Gadobutrol 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.
Gadobutrol EP Impurity A is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2,2'-[4,10-bis[2,3-dihydroxy-1-(hydroxymethyl)propyl]-1,4,7,10-tetraazacyclododecane-1,7-diyl]diacetic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Gadobutrol Molecular Formula: C20H40N4O10
Molecular Weight: 496.6
Storage: Store in a cool, dry place.