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Leucine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Leucine 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 Leucine-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.
Leucine EP Impurity A
Leucine EP Impurity B
Leucine EP Impurity C
Leucine EP Impurity D
Leucine EP Impurity E
Leucine Impurity 1
Leucine Impurity 2
N-Fmoc-D-leucine
D-Proline-N-Fmoc
Leucine Impurity 5
L-tert-Leucine
Leucine Impurity 6
Leucine Impurity 7
Leucine Impurity 8
Leucine Impurity 9
Leucine Impurity 10
leucine Enkephalin
N-Nitroso Leucine Impurity
Fmoc-D-Cys(Trt)-OH
