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Zopiclone
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Zopiclone reference materials. Our portfolio includes both pharmacopeial and non-pharmacopeial impurities, metabolites, stable isotope-labeled compounds, and nitrosamine derivatives (N-NO products). These reference standards play a crucial role in pharmaceutical R&D, aiding in formulation development, ANDA/DMF submissions, quality control, method validation, stability studies, and impurity profiling—including the identification and assessment of potentially genotoxic impurities.
Each Zopiclone-related product is rigorously characterized and delivered with a detailed Certificate of Analysis (COA) and comprehensive analytical data to ensure regulatory compliance. Upon request, we also offer EP/USP traceable standards. To maintain the highest quality standards, all materials are subject to periodic re-testing and continuous quality monitoring.
Zopiclone
Zopiclone EP Impurity A
Zopiclone EP Impurity B
Zopiclone EP Impurity C
(R)-Zopiclone
Eszopiclone (S-Zopiclone)
N-Desmethyl Zopiclone HCl
N-Demethyl Eszopiclone HCl
Zopiclone Deschloro Impurity
Di-O-benzoyl-D-tartaric Acid
Zopiclone Impurity 1
Zopiclone Impurity 2
Zopiclone Impurity 3
Zopiclone Impurity 4
Zopiclone Impurity 5
Zopiclone Impurity 6
Zopiclone Impurity 7
Zopiclone Impurity 8
Zopiclone Impurity 9
Zopiclone Impurity 10
Zopiclone Impurity 11
Zopiclone Impurity 12
Zopiclone Impurity 13
Zopiclone Impurity 14
Zopiclone D4
Zopiclone D8 N-Oxide
R-Zopiclone D8
S-Zopiclone D8
Zopiclone D8
