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Temozolomide
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Temozolomide 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 Temozolomide-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.
Temozolomide
Temozolomide EP Impurity D
Temozolomide EP Impurity A
Temozolomide USP Related Compound B
Temozolomide EP Impurity B
Temozolomide USP Related Compound C
Temozolomide EP Impurity C
Temozolomide Impurity
Temozolamide Impurity E
Decarbazine Lactose Adduct
Monomethyl Triaizeno Imidazole Carboxamide
5-Aminoimidazole-4-Carboxamide Lactose Adduct
Temozolomide Impurity 1
Cyanotemozolomide
5-Amino-4-imidazole carboxamide lactose adduct
