Ebastine EP Impurity A

Green HPTLC-densitometric approach for simultaneous determination and impurity- profiling of ebastine and phenylephrine hydrochloride
Amal M. Abou Al-Alamein, Mohamed K. Abd El-Rahman, Ezzat M. Abdel-Moety, Esraa M. Fawaz
Microchemical Journal Volume 147, June 2019, Pages 1097-1102
 
Using an innovative Quality-by-Design approach for development of a stability indicating UHPLC method for ebastine in the API and pharmaceutical formulations
Alexander H. Schmidt a,∗, Imre Molnár
Journal of Pharmaceutical and Biomedical Analysis 78–79 (2013) 65–74
 
Development and Validation of a Stability-Indicating Liquid Chromatographic Method for Estimating Olmesartan Medoxomil Using Quality by Design
Sarwar Beg, Gajanand Sharma, O.P. Katare, Shikha Lohan, Bhupinder Singh
Journal of Chromatographic Science, Volume 53, Issue 7, August 2015, Pages 1048–1059
 

Ebastine EP Impurity A is chemically Diphenylmethanol. It is also known as Benzhydrol ; . Ebastine EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Ebastine EP Impurity A 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 Ebastine.

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.