This impurity is related to Rivastigmine Hydrogen Tartrate EP Impurity E (Di-p-toluoyl-D-tartaric Acid) 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.
Rivastigmine Hydrogen Tartrate EP Impurity E (Di-p-toluoyl-D-tartaric Acid) is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:3-[(1S)-1-(methylamino)ethyl]phenyl N-ethyl-N-methylcarbamate (2S,3S)-2,3-bis((4-methylbenzoyl)oxy)succinic acidCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Rivastigmine Molecular Formula: C13H20N2O2 : C20H18O8
Molecular Weight: 236.3 : 386.4
Storage: Store in a cool, dry place.