Valaciclovir Impurity-I

Proudly synthesized by Manasa Life Sciences a leading industry manufacturer and supplier our high-purity Valaciclovir Impurity-I acts as an essential Valacyclovir impurity I reference standard for active pharmaceutical ingredient (API) stability profiling. This compound is thoroughly cataloged by its specific chemical name 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate, CAS 102728-64-3, molecular formula C₁₀H₁₃N₅O₄, and Molecular weight 267.2g/mol, providing absolute clarity for Valaciclovir impurity-I identification. To satisfy strict USFDA and EMA regulatory compliance, our quality assurance team utilizes state-of-the-art HPLC, LCMS, NMR, and Fourier-transform IR systems to confirm its structural integrity against Valacyclovir EP impurity I standard limits. Meeting all Valaciclovir impurity I specification demands under ICH guidelines, this premium standard is produced under strict GMP controls, managed via GDP documentation, and shipped alongside an inspection-ready CoA and user-protective MSDS.