Ivermectin EP Impurity F

A review on method development and validation of Ivermectin by RP-​HPLC
By Parkhe, Sagar B.; Laware, Ravindra B.; Ghogare, Rajashri
From World Journal of Pharmacy and Pharmaceutical Sciences (2020), 9(7), 627-635
 
Determination of imidacloprid and ivermectin in chemical soil barrier by HPLC
By Song, Yu-mei; He, Jian-qiang; Liu, Jie-heng; Ma, Yan-fang
From Huaxue Shiji (2017), 39(8), 850-852, 866
 
Analytical method development and validation for simultaneous estimation of Ivermectin and Fenbendazole in bulk dosage form by RP-​HPLC
By Pradeep, S.; Javali, Chandrashekar
From World Journal of Pharmacy and Pharmaceutical Sciences (2016), 5(4), 1614-1624

Ivermectin EP Impurity F is chemically 5-O,12-Didemethyl-25-de(1-methylpropyl)-12-ethyl-25-(1-methylethyl)-22,23-dihydroavermectin A1a (as per EP). It is also known as 12-demethyl-12-ethyl-H2B1b . Ivermectin EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Ivermectin EP Impurity F 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 Ivermectin.

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.