2-Chloroethanol
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| Template:Longitem | Template:Unbulleted list |
| Template:Longitem | 878139 |
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| EC Number | Template:Unbulleted list |
| Template:Longitem | 25389 |
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| MeSH | Ethylene+Chlorohydrin |
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| RTECS number | Template:Unbulleted list |
| UN number | 1135 |
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| Molar mass | Template:Chem molar mass |
| Appearance | Colourless liquid |
| Odor | ether-like |
| Density | 1.201 g/mL |
| Melting point | Template:Chembox CalcTemperatures |
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| log P | −0.107 |
| Vapor pressure | 700 Pa (at 20 °C) |
| Template:Longitem | 1.441 |
| Template:Longitem | −1.1914 MJ/mol |
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2-Chloroethanol (also called ethylene chlorohydrin or glycol chlorohydrin) is an organic chemical compound with the chemical formula HOCH2CH2Cl and the simplest beta-halohydrin (chlorohydrin).[4] This colorless liquid has a pleasant ether-like odor. It is miscible with water. The molecule is bifunctional, consisting of both an alkyl chloride and an alcohol functional group.[5]
Synthesis and applications
2-Chloroethanol is produced by treating ethylene with hypochlorous acid:[5]
2-Chloroethanol was once produced on a large scale as a precursor to ethylene oxide:
- HOCH2CH2Cl + NaOH → C2H4O + NaCl + H2O
This application has been supplanted by the more economic direct oxidation of ethylene. Otherwise chloroethanol is still used in the production of pharmaceuticals, biocides, and plasticizers.[5] Many of these applications entail its use in installing 2-hydroxyethyl groups.[6] Several dyes are prepared by the alkylation of aniline derivatives with chloroethanol.[7] It is also used for manufacture of thiodiglycol.
It is a solvent for cellulose acetate and ethyl cellulose, textile printing dyes, in dewaxing, refining of rosin, extraction of pine lignin, and the cleaning of machines.
Environmental aspects
Chloroethanol is a metabolite in the degradation of 1,2-dichloroethane. The alcohol is then further oxidized via chloroacetaldehyde to chloroacetate. This metabolic pathway is topical since billions of kilograms of 1,2-dichloroethane are processed annually as a precursor to vinyl chloride.[8]
Safety
2-Chloroethanol is toxic with an LD50 of 89 mg/kg in rats. Like most organochlorine compounds, chloroethanol releases hydrochloric acid and phosgene when burned.
In regards to dermal exposure to 2-chloroethanol, the Occupational Safety and Health Administration has set a permissible exposure limit of 5Script error: No such module "String".ppm (16Script error: No such module "String".mg/m3) over an eight-hour time-weighted average, while the National Institute for Occupational Safety and Health has a more protective recommended exposure limit of a 1Script error: No such module "String".ppm (3Script error: No such module "String".mg/m3) exposure ceiling.[9]
It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.[10]Script error: No such module "Unsubst".
References
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- ↑ Script error: No such module "citation/CS1".
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- ↑ Ethylene chlorohydrin: properties
- ↑ a b c Template:Ullmann
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- ↑ Template:Ullmann
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- ↑ CDC - NIOSH Pocket Guide to Chemical Hazards
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