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Captopril
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Captopril 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 Captopril-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.
Captopril
Captopril EP Impurity A
Captopril EP Impurity B
Captopril EP Impurity C
Captopril EP Impurity D
Captopril EP Impurity E
Captopril EP Impurity F
Captopril EP Impurity G
Captopril EP Impurity H
Captopril EP Impurity I
Captopril EP Impurity J
Captopril EP Impurity L
Captopril EP Impurity M
Captopril EP Impurity N
Captopril EP Impurity O
Captopril Methyl Ester
Captopril Ethyl Ester
D-Captopril
Captopril Related Compound 1
Captopril Related Compound 2
Captopril Related Compound 3
Captopril Related Compound 4
Captopril Related Compound 5
Captopril Related Compound 6
Captopril Related Compound 7
Captopril Related Compound 8
Captopril Impurity 1
