Aciclovir EP Impurity I

Aciclovir EP Impurity I

VS CAT No VS-A017007
CAS No 1797832-75-7
Mol.F. C14H16N10O4
Mol.Wt. 388.3
Inv. Status Custom Synthesis

Chemical Name: 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)

Synonym: Aciclovir 7,9'-Diguanyl Analog (USP)

Shipping Temperature: Ambient

Country of Origin: India

Smiles: O=C1NC(N)=NC2=C1N(COCCOCN3C=NC4=C3N=C(N)NC4=O)C=N2

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. Vsquare products are for analytical purpose only and not for human use.