This impurity is related to Tenofovir Impurity 35 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.
Tenofovir Impurity 35 is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:((hydroxy((((R)-1-(6-(methyleneamino)-9H-purin-9-yl)propan-2-yl)oxy)methyl)phosphoryl)oxy)methyl isopropyl carbonateCountry of Origin: India Product Category: Impurity Reference StandardAPI NAME: Tenofovir Molecular Formula: C15H22N5O7P
Molecular Weight: 415.3
Storage: Store in a cool, dry place.