Novel bovine serum album and 尾-cyclodextrin-based mixed chiral stationary phase for the enantioseparation in capillary electrochromatography was written by Tang, Weiyang;Lu, Yao;Row, Kyung Ho;Baeck, Sung Hyeon;Zhang, Yifan;Sun, Genlin. And the article was included in Microchemical Journal in 2022.HPLC of Formula: 83799-24-0 The following contents are mentioned in the article:
A capillary was co-immobilized with mixed 尾-cyclodextrin and bovine serum album by chem. covalent coupling as the chiral stationary phase for the enantioseparation of proton-pump inhibitors in capillary electrochromatog. The chromatog. parameters including buffer concentration, pH value, organic modifier, and applied voltage were optimized. The separation performance of the developed column was evaluated by enantiosepg. omeprazole, lansoprazole, pantoprazole, and esomeprazole with extremely high resolutions of 5.21, 7.11, 6.39, and 4.75, resp. Moreover, the mixed chiral stationary phase exhibited a broader range and could sep. more than 10 chiral analytes compared to the single-selector column. The relative standard deviations of the day-to-day and column-to-column repeatability were less than 4%, demonstrating excellent stability of the fabricated column. An open tubular capillary immobilized with the bovine serum album and 尾-cyclodextrin as the chiral stationary phase is a promising prospect for separating chiral drugs in capillary electrochromatog. because of the combination of the enantioselectivities of both individual selectors. This study involved multiple reactions and reactants, such as 2-(4-(1-Hydroxy-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butyl)phenyl)-2-methylpropanoic acid (cas: 83799-24-0HPLC of Formula: 83799-24-0).
2-(4-(1-Hydroxy-4-(4-(hydroxydiphenylmethyl)piperidin-1-yl)butyl)phenyl)-2-methylpropanoic acid (cas: 83799-24-0) belongs to piperidine derivatives. The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper its spicy taste. Industrially, piperidine is produced by the hydrogenation of pyridine, usually over a molybdenum disulfide catalyst. Pyridine can also be reduced to piperidine via a modified Birch reduction using sodium in ethanol.HPLC of Formula: 83799-24-0
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem