Bisacodyl EP Impurity E

Stability indicating analysis of bisacodyl by partial least squares regression, spectral residual augmented classical least squares and support vector regression chemometric models: A comparative study
Ibrahim A.Naguib
Bulletin of Faculty of Pharmacy, Cairo University Volume 49, Issue 2, December 2011, Pages 91-100
 
Solubility of Bisacodyl in Pure Solvent at Various Temperatures: Data Correlation and Thermodynamic Property Analysis
Yüfang Wu,* Chengmeng Wu, Suyue Yan, and Bin Hu
J. Chem. Eng. Data 2020, 65, 1, 43–48
 
Determination of Bisacodyl and its Hydrolysis Products in Bisacodyl Formulations by High-Performance Liquid Chromatography
Syed Laik Ali
Fresenius Z. Anal. Chem. 299, 124 126 (1979)
 
Development and Validation of Three Stability-Indicating Methods for Determination of Bisacodyl in Pure Form and Pharmaceutical Preparations
Fadia H Metwally, Mohammed Abdelkawy, Ibrahim A Naguib
Journal of Aoac international, Volume 90, Issue 1, 1 January 2007, Pages 113–127

Bisacodyl EP Impurity E is chemically 2-[(RS)-[4-(Acetyloxy)phenyl](pyridin-2-yl)methyl]phenyl acetate (as per EP) ; (2-[(4-Acetoxyphenyl)(pyridin-2-yl)methyl]phenyl acetate) (as per USP). It is also known as Bisacodyl USP Related Compound E. Bisacodyl EP Impurity E is supplied with detailed characterization data compliant with regulatory guideline. Bisacodyl 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 Bisacodyl.

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.