-
Your RFQ cart is empty!
Mexiletine
Venkatasai is a leading provider of pharmaceutical reference standards, specializing in the supply of high-purity Mexiletine 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 Mexiletine-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.
Mexiletine Hydrochloride
Mexiletine Hydrochloride EP Impurity A
Mexiletine Hydrochloride EP Impurity B
Mexiletine Hydrochloride EP Impurity C
Mexiletine Hydrochloride EP Impurity D
1-(2,6-Dimethylphenoxy)-2-propanone Oxime
1-(2,4-dimethylphenoxy)propan-2-amine
1-(2,5-dimethylphenoxy)propan-2-amine
Mexiletine Cyclic Imine Impurity
Mexiletine Impurity 1
2-Hydroxy-3-methylbenzaldehyde
