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Description
TCI C0251 Ethylene Glycol Mono(4-chlorophenyl) Ether combines a 4-chlorophenyl ring with a hydroxyl-terminated ethylene glycol chain. Its primary alcohol is a convenient reactive handle for esterification, tosylation, or conversion into a leaving group, making the compound useful for installing aryloxyethyl linkers in larger molecules. The balance of polar and nonpolar regions also makes it of interest in surfactant and functional material studies. Store the solid in a cool, dry place in a tightly closed container and review the official TCI Safety Data Sheet before handling.
Scientific References
Doe et al. (1990). Mass transfer of acetylacetone, ethylene glycol mono-n-butyl ether and ethylene glycol monophenyl ether across water-carbon tetrachloride and water-chloroform interfaces. Analytica Chimica Actadoi:10.1016/s0003-2670(00)83923-9
Urbala (2020). Technological aspects of synthesis of poly(ethylene glycol) mono-1-propenyl ether monomers. Polish Journal of Chemical Technologydoi:10.2478/pjct-2020-0028
Li et al. (2009). One-pot synthesis of ethylene glycol and its mono-methyl ether from ethylene using Al-TS-1 catalyst. Catalysis Communicationsdoi:10.1016/j.catcom.2009.07.004
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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