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Bilastine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Bilastine 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 Bilastine-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.
Bilastine Impurity A
Bilastine Impurity B
Bilastine N-Oxide
1’-Hydroxy Bilastine
Bilastine Amide Impurity
Bilastine Hydroxy Impurity
Bilastine Impurity 1
Bilastine Impurity 2
Bilastine Impurity 3
Bilastine Impurity 4
Bilastine Impurity 5
Bilastine Impurity 6
Bilastine Impurity 7
trans-Bilastine N-Oxide
cis-Bilastine N-Oxide
Bilastine Impurity 11
Bilastine Impurity 12
Bilastine Impurity 13
Bilastine Impurity 14
Bilastine Nitrosoamine Impurity 1
Bilastine Nitrosoamine Impurity 2
Bilastine Related Compound A
Bilastine Impurity 15
2-(2-(4-Bromophenyl)propan-2-yl)-4,4-dimethyl-4,5-dihydrooxazole
2-(4-(2-(4,4-Dimethyl-4,5-dihydrooxazol-2-yl)propan-2-yl)phenyl)ethan-1-ol
