This impurity is related to Timolol EP Impurity E 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.
Timolol EP Impurity E is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2Z)-4-[(1S)-1-[[(1,1-dimethylethyl)amino]methyl]-2-[[4-(morpholin-4-yl)-1,2,5-thiadiazol-3-yl]oxy]ethoxy]-4-oxobut-2-enoic acid ; (S,Z)-4-({1-(tert-butylamino)-3-[(4-morpholino-1,2,5-thiadiazol-3-yl)oxy]propan-2-yl}oxy)-4-oxobut-2- enoic acid (as per USP)Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Timolol Molecular Formula: C17H26N4O6S
Molecular Weight: 414.5
Storage: Store in a cool, dry place.