Shen, Zhengyuan et al. published their research in Macromolecules (Washington, DC, United States) in 2021 | CAS: 112-49-2

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.Synthetic Route of C8H18O4

Effects of Electrolytes on Thermodynamics and Structure of Oligo(ethylene oxide)/Salt Solutions and Liquid-Liquid Equilibria of a Squalane/Tetraethylene Glycol Dimethyl Ether Blend was written by Shen, Zhengyuan;Chen, Qile P.;Xie, Shuyi;Lodge, Timothy P.;Siepmann, J. Ilja. And the article was included in Macromolecules (Washington, DC, United States) in 2021.Synthetic Route of C8H18O4 This article mentions the following:

Gibbs ensemble Monte Carlo simulations for salt-doped oligo(ethylene oxide) (OEO, Mw = 90-266 g/mol) solutions show that the presence of ions leads to significant increases in the cohesive energy d. (ΠCED) and the enthalpy of vaporization for OEO chains but that compensation by entropic contributions leads to only small changes in the Gibbs free energy of transfer and vapor pressure. At the same relative ion concentration (r) and temperature, the ΠCED values of the salt-doped systems order as LiClO4 > LiF > CsClO4 ≈ CsF. Structural anal. indicates significant ion clustering in addition to coordination of cations by OEO chains. After accounting for ion clustering via the van’t Hoff factor, the solvents’ vapor pressures are well described by Raoult’s law. Experiments and simulations for a squalane/tetraethylene glycol di-Me ether blend (xW,OEO = 0.65) show that the addition of LiClO4 does not significantly alter the miscibility gap below 0.95 TCP,free, the critical temperature of the salt-free blend. However, the coexistence curve for the LiClO4-doped system does not close with the usual power-law scaling at T > 0.95 TCP,free as transfer of OEO chains to the squalane-rich phase leads to an increase in r in the OEO-rich phase, which, in turn, makes it a less hospitable environment for squalane. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2Synthetic Route of C8H18O4).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds.Synthetic Route of C8H18O4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem