This impurity is related to Ritonavir EP Impurity T 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.
Ritonavir EP Impurity T is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:2S)-N-[(1S,2S,4S)-1-benzyl-2-hydroxy-4-[[(2S)-3-methyl-2-[[methyl[[2-(1-methylethyl)thiazol-4-yl]methyl]carbamoyl]amino]butanoyl]amino]-5-phenylpentyl]-3-methyl-2-[[methyl[[2-(1-methylethyl)thiazol-4-yl]methyl]carbamoyl]amino]butanamideCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Ritonavir Molecular Formula: C46H66N8O5S2
Molecular Weight: 875.2
Storage: Store in a cool, dry place.