Abacavir EP Impurity F | CAS 1443421-68-8 - Request Quote

Abacavir EP Impurity F is chemically 6-(Cyclopropylamino)-9-[(1R,4S)-4-[[(1,1-dimethylethyl)oxy]methyl]cyclopent-2-enyl]-9H-purine-2-amine (as per EP) ; 9-[(1R,4S)-4-(tert-Butoxymethyl)cyclopent-2-enyl]-N6-cyclopropyl-9H-purine-2,6-diamine (as per USP). It is also known as O-t-Butyl Derivative Abacavir (USP). Abacavir EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Abacavir EP Impurity F can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Abacavir.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.