Chromatographic purification of some 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors was written by Grahek, R.;Milivojevic, D.;Bastarda, A.;Kracun, M.. And the article was included in Journal of Chromatography A in 2001.Name: 2-(2-(Hexyloxy)ethoxy)ethanol The following contents are mentioned in the article:
The purification of pravastatin, simvastatin and lovastatin in the sodium salt or lactone form and of mevastatin in the lactone form by reversed-phase displacement chromatog. is presented. The mobile phases consisted of water or mixtures of water-methanol and water-acetonitrile. Six different displacers were successfully used. Up to 0.14 g of raw sample per g of stationary phase was loaded on a column packed with silica-based octadecyl phase. Crude substances from 85 to 88% chromatog. purity were purified and at least 99.5% purity was achieved. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Name: 2-(2-(Hexyloxy)ethoxy)ethanol).
2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters perform as high-grade solvents for a broad array of plastics, plasticizers, resins, and lacquers, and are one of the largest classes of synthetic lubricants on the commercial market. Polyesters are important plastics, with monomers linked by ester moieties. Acyl chlorides and acid anhydrides alcoholysis is another way to produce esters. Acyl chlorides and acid anhydrides react with alcohols to produce esters. Anydrous conditions are recommended since both acyl chlorides and acid anhydrides react with water.Name: 2-(2-(Hexyloxy)ethoxy)ethanol
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem