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Aspirin
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Aspirin 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 Aspirin-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.
Acetylsalicylic Acid EP Impurity A (Aspirin Impurity A)
Acetylsalicylic Acid EP Impurity B (Aspirin Impurity B)
Acetylsalicylic Acid EP Impurity C (Aspirin Impurity C)
Acetylsalicylic Acid EP Impurity D (Aspirin Impurity D)
Acetylsalicylic Acid EP Impurity E (Aspirin Impurity E)
Acetylsalicylic Acid EP Impurity F (Aspirin Impurity F)
Acetylsalicylic Acid Acyl-D-Glucuronide (Aspirin Acyl-D-Glucuronide)
Aspirin Impurity (2-(2,4-Dihydroxybenzoyl)Benzoic Acid)
5-(N-Î’-D-Glucopyranosylamino) Salicylic Acid
Acetylsalicyclic Acid Impurity
Acetylsalicyclic Acid
Salicyl Sulfate Disodium salt
5-Methoxy Carbonyl Salicylamide
Acetylsalicylic Acid Impurity 1
