Glycol ethers are a class of chemical compounds consisting of alkyl ethers that are based on glycols such as ethylene glycol or propylene glycol. They are commonly used as solvents in paints and cleaners. They have good solvent properties while having higher boiling points than the lower-molecular-weight ethers and alcohols.
History
editThe name "Cellosolve" was registered in 1924 as a United States trademark by Carbide & Carbon Chemicals Corporation (a division[1] of Union Carbide Corporation) for "Solvents for Gums, Resins, Cellulose Esters, and the Like". "Ethyl Cellosolve" or simply "Cellosolve" consists mainly of ethylene glycol monoethyl ether and was introduced as a lower-cost solvent alternative to ethyl lactate. "Butyl Cellosolve" (ethylene glycol monobutyl ether) was introduced in 1928, and "Methyl Cellosolve" (ethylene glycol monomethyl ether) in 1929.[2][3]
Types
editGlycol ethers are designated "E-series" or "P-series" for those made from ethylene oxide or propylene oxide, respectively. Typically, E-series glycol ethers are found in pharmaceuticals, sunscreens, cosmetics, inks, dyes and water-based paints, while P-series glycol ethers are used in degreasers, cleaners, aerosol paints and adhesives. Both E- and P-series glycol ethers can be used as intermediates that undergo further chemical reactions, producing glycol diethers and glycol ether acetates.[citation needed] P-series glycol ethers are marketed as having lower toxicity than the E-series.
Health impacts
editThis section needs more reliable medical references for verification or relies too heavily on primary sources. (February 2024) |  |
Most glycol ethers are water-soluble, biodegradable and only a few are considered toxic.[citation needed]
In the early 1990s, studies found higher than expected rates of miscarriages among women who worked in semiconductor plants, which was traced back to glycol ethers[which?] used in the photoresist substances that coat semiconductors.[4]
One study suggests that occupational exposure to glycol ethers is related to low motile sperm count,[5] a finding disputed by the chemical industry.[6]
Subclasses
editSolvents
edit- Ethylene glycol monomethyl ether (2-methoxyethanol, CH3OCH2CH2OH)
- Ethylene glycol monoethyl ether (2-ethoxyethanol, CH3CH2OCH2CH2OH)
- Ethylene glycol monopropyl ether (2-propoxyethanol, CH3CH2CH2OCH2CH2OH)
- Ethylene glycol monoisopropyl ether (2-isopropoxyethanol, (CH3)2CHOCH2CH2OH)
- Ethylene glycol monobutyl ether (2-butoxyethanol, CH3CH2CH2CH2OCH2CH2OH), a widely used solvent in paintings and surface coatings, cleaning products and inks
- Ethylene glycol monophenyl ether (2-phenoxyethanol, C6H5OCH2CH2OH)
- Ethylene glycol monobenzyl ether (2-benzyloxyethanol, C6H5CH2OCH2CH2OH)
- Propylene glycol methyl ether, (1-methoxy-2-propanol, CH3OCH2CH(OH)CH3)
- Diethylene glycol monomethyl ether (2-(2-methoxyethoxy)ethanol, methyl carbitol, CH3OCH2CH2OCH2CH2OH)
- Diethylene glycol monoethyl ether (2-(2-ethoxyethoxy)ethanol, carbitol cellosolve, CH3CH2OCH2CH2OCH2CH2OH)
- Diethylene glycol mono-n-butyl ether (2-(2-butoxyethoxy)ethanol, butyl carbitol, CH3CH2CH2CH2OCH2CH2OCH2CH2OH)
- Dipropyleneglycol methyl ether
- C12-15 pareth-12 a polyethylene glycol ether used as an emulsifier in cosmetics
Dialkyl ethers
edit- Ethylene glycol dimethyl ether (dimethoxyethane, CH3OCH2CH2OCH3), a higher boiling alternative to diethyl ether and THF, also used as a solvent for polysaccharides, a reagent in organometallic chemistry and in some electrolytes of lithium batteries
- Ethylene glycol diethyl ether (diethoxyethane, CH3CH2OCH2CH2OCH2CH3)
- Ethylene glycol dibutyl ether (dibutoxyethane, CH3CH2CH2CH2OCH2CH2OCH2CH2CH2CH3)
Esters
edit- Ethylene glycol methyl ether acetate (2-methoxyethyl acetate, CH3OCH2CH2OCOCH3)
- Ethylene glycol monoethyl ether acetate (2-ethoxyethyl acetate, CH3CH2OCH2CH2OCOCH3)
- Ethylene glycol monobutyl ether acetate (2-butoxyethyl acetate, CH3CH2CH2CH2OCH2CH2OCOCH3)
- Propylene glycol methyl ether acetate (1-methoxy-2-propanol acetate)
References
edit- ^ History - Union Carbide Company (Year 1920)
- ^ Benninga, H. (1990). A history of lactic acid making: a chapter in the history of biotechnology. Dordrecht [Netherlands]: Kluwer Academic Publishers. p. 251. ISBN 0-7923-0625-2. OCLC 20852966.
- ^ Union Carbide later registered "Cellosolve" as a trademark for "ETHYL SILICATES FOR USE AS BINDERS IN INVESTMENT CASTINGS AND IN ZINC-RICH PRIMERS" (Reg. Number 1019768, September 9, 1975), but allowed it to expire.
- ^ Calma, Justine (Dec 8, 2023). "The fight to clean up the toxic legacy of semiconductors". The Verge. Retrieved 5 January 2024.
- ^ Nicola Cherry; Harry Moore; Roseanne McNamee; Allan Pacey; Gary Burgess; Julie-Ann Clyma; Martin Dippnall; Helen Baillie; Andrew Povey (2008). "Occupation and male infertility: glycol ethers and other exposures". Occup. Environ. Med. 65 (10): 708–714. doi:10.1136/oem.2007.035824. PMID 18417551.
- ^ Peter J Boogaard; Gerard M H Swaen (2008). "Letter to the editor on a recent publication titled "Occupation and male infertility: glycol ethers". Occup. Environ. Med. Archived from the original on 2011-07-24.