Mebendazole EP Impurity E

High-performance liquid chromatographic separation and determination of the process related impurities of mebendazole, fenbendazole and albendazole in bulk drugs
Antony Raj Gomes *, V. Nagaraju
Journal of Pharmaceutical and Biomedical Analysis 26 (2001) 919–927
 
New RP-UPLC method development using QbD approach for determination of mebendazole, quinfamide, its impurities and antioxidants in mebendazole and quinfamide fixed dose combinations (FDC)
Rakesh Chandrakant Prabhu, Arthanareeswari Maruthapillai
Materials Today: Proceedings Volume 40, Supplement 1, 2021, Pages S120-S126

Mebendazole EP Impurity E is chemically N-(6-Benzoyl-1H-benzimidazol-2-yl)carbamic Acid Ethyl Ester; 5-Benzoyl-2-benzimidazolecarbamic Acid Ethyl Ester; (5-Benzoyl-1H-benzimidazol-2-yl)carbamic Acid Ethyl Ester;. It is also known as Mebendazole Ethyl Analog. Mebendazole EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Mebendazole EP Impurity E can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Mebendazole.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.