Esposito, George G. et al. published their research in SAE Journal in 1971 | CAS: 20324-33-8

1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol (cas: 20324-33-8) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Application In Synthesis of 1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol

Rapid analysis of brake fluid uses gas-liquid chromatography was written by Esposito, George G.;Jamison, Robert G.. And the article was included in SAE Journal in 1971.Application In Synthesis of 1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol This article mentions the following:

The volatile compounds making up 70-80% of most hydraulic brake fluid can be identified and determined by gas chromatog. on a 20 weight % Carbowax 20M/Chromosorb W or a 20 weight % diethylene glycol succinate/Chromosorb W column, by using ethylene glycol monoethyl ether acetate internal standard, a thermal conductivity detector, and He carrier gas. Retention data are given for 36 compounds Anal. of a synthetic composition gave [component, weight % added, weight % found]: ethylene glycol monoethyl ether, 25.0, 24.8; methoxybutanol, 10.0, 12.0; diethylene glycol monoethyl ether, 24.0, 23.5; diethylene glycol monobutyl ether, 11.0, 10.7; base lubricant (by difference), 30.0, 29.0. In the experiment, the researchers used many compounds, for example, 1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol (cas: 20324-33-8Application In Synthesis of 1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol).

1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol (cas: 20324-33-8) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Application In Synthesis of 1-((1-((1-Methoxypropan-2-yl)oxy)propan-2-yl)oxy)propan-2-ol

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