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Leflunomide
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Leflunomide 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 Leflunomide-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.
Leflunomide
Leflunomide EP Impurity A
Leflunomide EP Impurity B
Leflunomide EP Impurity C
Leflunomide EP Impurity D
Leflunomide EP Impurity E
Leflunomide EP Impurity F
Leflunomide EP Impurity G
Leflunomide EP Impurity H
Teriflunomide-E Isomer
Ethyl 3-methylisoxazole-4-carboxylate
Leflunomide Metabolite Ethyl Analog
Leflunomide Related Compound (Methyl 5-methyl-1,2-oxazole-3-carboxylate)
3-Trifluoro Isomer
5-Methylisoxazole-3-carboxylic-d4 Acid
Leflunomide Impurity 1
Leflunomide Impurity 2
Ethyl 5-Methylisoxazole-4-Carboxylate
