Cyproheptadine EP Impurity C (HCl)

Development and Validation of Stability Indicating High-Performance Liquid Chromatographic Method for Determination of Cyproheptadine Hydrochloride, its Impurity And Degradation Product
Maha M Abdelrahman, Eglal A Abdelaleem, Nouruddin W Ali, Raghda A Emam
Journal of Chromatographic Science, Volume 59, Issue 2, February 2021, Pages 128–133
 
Application of dummy molecularly imprinted solidphase extraction in the analysis of cyproheptadine in bovine urine
Xesffls Fes1, 2 Lei Ye2 Patricia Regal1 Cristina A. Fente1 Seyed V. Hosseini3 Alberto Cepeda
J. Sep. Sci. 2009, 32, 1740 – 1747

Cyproheptadine EP Impurity C (HCl) is chemically 5-(1-Methylpiperidin-4-yl)-5H-dibenzo[a,d][7]annulen-5-ol Hydrocloride. It is also known as Cyproheptadine Related Compound C ; . Cyproheptadine EP Impurity C (HCl) is supplied with detailed characterization data compliant with regulatory guideline. Cyproheptadine EP Impurity C (HCl) 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 Cyproheptadine.

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.