This impurity is related to Cisatracurium EP Impurity Q 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.
Cisatracurium EP Impurity Q is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(1R,2R)-1-[(3,4-Dimethoxyphenyl)methyl]-2-[3-[[5-[[3-[(1R)-1-[(3,4-dimethoxyphenyl)methyl]-6,7-dimethoxy-3,4-dihydroisoquinolin-2(1H)-yl]propanoyl]oxy]pentyl]oxy]-3-oxopropyl]-6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinoliniumCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Cisatracurium Molecular Formula: C52H69N2O12
Molecular Weight: 914.1
Storage: Store in a cool, dry place.