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Iohexol
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Iohexol 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 Iohexol-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.
Iohexol
Iohexol EP Impurity A
Iohexol EP Impurity B
Iohexol EP Impurity C
Iohexol EP Impurity D
Iohexol EP Impurity E
Iohexol EP Impurity F
Iohexol EP Impurity G
Iohexol EP Impurity H
Iohexol EP Impurity I
Iohexol EP Impurity J
Iohexol EP Impurity K
Iohexol EP Impurity L
Iohexol EP Impurity M
Iohexol EP Impurity N
Iohexol EP Impurity O
Iohexol EP Impurity P
Iohexol EP Impurity Q
Iohexol USP Related Compound C
