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Chlorphenamine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Chlorphenamine 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 Chlorphenamine-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.
Chlorphenamine Maleate
Chlorphenamine EP Impurity A (2HCl)
Chlorphenamine EP Impurity B
Chlorphenamine EP Impurity C
Chlorphenamine EP Impurity D
Dexchlorpheniramine EP Impurity A
Chlorphenamine EP Impurity A (Dimaleate)
Dexchlorpheniramine EP Impurity B
Chlorphenamine EP Impurity C Maleate
Chlorphenamine EP Impurity D Maleate
Chlorphenamine N-Oxide
Pheniramine Maleate
Chlorphenamine di-N-Oxide
Didesmethyl chlorpheniramine maleate
S-Chlorpheniramine Maleate
R-Chlorpheniramine Maleate
Dexchlorpheniramine N-Oxide
2-chloro-N,N-dimethylethan-1-amine HCl
Chlorphenamine Impurity 1
Chlorphenamine Impurity 2
Chlorpeniramine EP Impurity A
Chlorpeniramine EP Impurity C
Chlorpeniramine EP Impurity D
Nitroso Dexchlorpheniramine maleate
N-Nitroso Chlorphenamine EP Impurity C
