A self-diffusion study of poly(ethylene-oxide) alkyl alcohols was written by Ambrosone, L.;Costantino, L.;D’Errico, G.;Vitagliano, V.. And the article was included in Journal of Solution Chemistry in 1997.Synthetic Route of C10H22O3 The following contents are mentioned in the article:
The self-diffusion coefficients of HDO and some surfactants in aqueous mixtures at different concentrations, below the critical micelle concentration, have been determined by means of the NMR, spin-echo pulsed field gradient method. The surfactant solutes chosen were ethylene glycol-pentyl alc., diethylene glycol-pentyl alc., ethylene glycol-hexyl alc., diethylene glycol-hexyl alc., triethylene glycol-hexyl alc., tetraethylene glycol-hexyl alc., pentaethylene glycol-hexyl alc. The interactions in solution are studied by analyzing the solute self-diffusion coefficients extrapolated to infinite dilution These values are compared with those of 1-alkanols. The slope of the self diffusion coefficients vs. the solute concentration are correlated with the microscopic friction coefficients A model for interpreting the exptl. data is suggested. This study involved multiple reactions and reactants, such as 2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4Synthetic Route of C10H22O3).
2-(2-(Hexyloxy)ethoxy)ethanol (cas: 112-59-4) belongs to ethers. Esters are widespread in nature and are widely used in industry. In nature, fats are in general triesters derived from glycerol and fatty acids. Esters are responsible for the aroma of many fruits. Esters contain a carbonyl center, which gives rise to 120° C–C–O and O–C–O angles. Unlike amides, esters are structurally flexible functional groups because rotation about the C–O–C bonds has a low barrier. Their flexibility and low polarity is manifested in their physical properties; they tend to be less rigid (lower melting point) and more volatile (lower boiling point) than the corresponding amides. Synthetic Route of C10H22O3
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem