Aciclovir EP Impurity I | CAS 1797832-75-7 - Solicitar cotización

Aciclovir EP Impurity I is chemically 2-Amino-7-[[2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethoxy]methyl]-1,7-dihydro-6H-purin-6-one (as per EP) ; 2-Amino-9-({2-[(2-amino-6-oxo-1,6-dihydro-7H-purin-7-yl)methoxy]ethoxy}methyl)- 1,9-dihydro-6H-purin-6-one (as per USP). It is also known as Aciclovir 7,9'-Diguanyl Analog (USP). Aciclovir EP Impurity I is supplied with detailed characterization data compliant with regulatory guideline. Aciclovir EP Impurity I 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 Aciclovir.

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.