Aciclovir EP Impurity Q
| VS CAT No | VS-A017013 |
| CAS No | NA |
| Mol.F. | 2(C9H13N5O4) |
| Mol.Wt. | 2(255.2) |
| Inv. Status | Custom Synthesis |
Chemical Name: 2-Amino-9-[[2-(hydroxyethoxy) methoxy]methyl]-1,9-dihydro-6H-purin-6-one and 2-amino-9-[[2-(hydroxymethoxy)ethoxy]methyl]-1,9-dihydro-6H-purin-6-one (as per EP)
Shipping Temperature: Ambient
Country of Origin: India
Smiles: O=C1NC(N)=NC2=C1N=CN2COCOCCO.O=C3NC(N)=NC4=C3N=CN4COCCOCO
Aciclovir EP Impurity Q is chemically 2-Amino-9-[[2-(hydroxyethoxy) methoxy]methyl]-1,9-dihydro-6H-purin-6-one and 2-amino-9-[[2-(hydroxymethoxy)ethoxy]methyl]-1,9-dihydro-6H-purin-6-one (as per EP). Aciclovir EP Impurity Q is supplied with detailed characterization data compliant with regulatory guideline. Aciclovir EP Impurity Q 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.