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Valaciclovir EP Impurity Q

N° de SZ CAT:SZ-V003017
Número CASNA
Mol.F.C19H25N11O5 
Peso Molecular487.5
Status de FaturaUnder Synthesis

Nome Químico: 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl N-[[(6-oxo-6,9-dihydro-1H-purin-2-yl)amino]methyl]-L-valinate ;

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C([C@@H](NCNC1=NC(NC=N2)=C2C(N1)=O)C(C)C)OCCOCN(C=N3)C4=C3C(NC(N)=N4)=O

Valaciclovir EP Impurity Q is chemically 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl N-[[(6-oxo-6,9-dihydro-1H-purin-2-yl)amino]methyl]-L-valinate ;. Valaciclovir EP Impurity Q is supplied with detailed characterization data compliant with regulatory guideline. Valaciclovir 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 Valaciclovir.

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.

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