Aciclovir EP Impurity G
| VS CAT No | VS-A017006 |
| CAS No | 75128-73-3 |
| Mol.F. | C12H15N5O5 |
| Mol.Wt. | 309.2 |
| Inv. Status | Custom Synthesis |
Chemical Name: 2-[(2-Acetamido-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate (as per EP) ; 2-{[2-(Acetylamino)-6-oxo-1,6-dihydro-9H-purin-9-yl]methoxy}ethyl acetate (as per USP)
Synonym: Acyclovir USP Related Compound G ; Aciclovir N,O-Diacetate ; N,O-Diacetylacyclovir
Shipping Temperature: Ambient
Country of Origin: India
Smiles: CC(OCCOCN1C=NC2=C1N=C(NC(C)=O)NC2=O)=O
Aciclovir EP Impurity G is chemically 2-[(2-Acetamido-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate (as per EP) ; 2-{[2-(Acetylamino)-6-oxo-1,6-dihydro-9H-purin-9-yl]methoxy}ethyl acetate (as per USP). It is also known as Acyclovir USP Related Compound G ; Aciclovir N,O-Diacetate ; N,O-Diacetylacyclovir. Aciclovir EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Aciclovir EP Impurity G 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.