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Ganciclovir Impurity – I

2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]propane-1,3-diyl dipropanoate

Chemical Name 2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]propane-1,3-diyl dipropanoate
CAS No. 86357-20-2
Molecular Formula C15H21N5O6
Molecular Weight 367.36
Chemical Structure 2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]propane-1,3-diyl dipropanoate Structure
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Ganciclovir Impurity – I

Ganciclovir Impurity – I is a known related substance / impurity of Ganciclovir, as listed in the EP reference standard. Chemically, it is described as 2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]propane-1,3-diyl dipropanoate. It has the molecular formula C15H21N5O6 and a molecular weight of 367.36 g/mol. It serves as a critical reference material for identifying and quantifying related substances during Ganciclovir manufacturing and stability testing. Available with a Certificate of Analysis (CoA) as a high-purity reference standard suitable for HPLC and LC-MS applications.

Ganciclovir impurities reference standards are useful in pharmaceutical research. They are useful in product development, ANDA and DMF filing, Quality control (QC), method validation, and stability studies. It is also useful in the identification of unknown impurities and the assessment of genotoxic potential.

We are the BHAVANISH LIFE SCIENCES specializes in manufacturing and supplying of Ganciclovir impurities that meet specific pharmacopeial standards (USP/EP/BP/IP) as well as process-related impurities.

This related products or Impurities are thoroughly characterized. Supplied with detailed COA & analytical data Like NMR / MASS / HPLC / GC / IR / TGA / Potency / Structure elucidation data (SER Report) meeting regulatory compliance.

BHAVANISH LIFE SCIENCES provides this compound for research and development and Analytical testing use only, and is not meant for human consumption. With product information including CAS number, molecular formula, molecular weight details.

BHAVANISH LIFE SCIENCES in providing high-quality impurity standards to support pharmaceutical companies in maintaining drug safety and efficacy.

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