Tetraethylene glycol
Structural formula | ||||||||||||||||
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General | ||||||||||||||||
Surname | Tetraethylene glycol | |||||||||||||||
other names |
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Molecular formula | C 8 H 18 O 5 | |||||||||||||||
Brief description |
colorless and odorless liquid |
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External identifiers / databases | ||||||||||||||||
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properties | ||||||||||||||||
Molar mass | 194.23 g mol −1 | |||||||||||||||
Physical state |
liquid |
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density |
1.12 g cm −3 |
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Melting point |
−6 ° C |
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boiling point |
327 ° C |
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Vapor pressure |
0.01 hPa (20 ° C) |
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solubility |
miscible with water |
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Refractive index |
1.4593 (20 ° C) |
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safety instructions | ||||||||||||||||
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Toxicological data | ||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . Refractive index: Na-D line , 20 ° C |
Tetraethylene glycol is a chemical compound from the group of glycol ethers .
Extraction and presentation
Tetraethylene glycol is obtained as a by-product in the synthesis of di- and triethylene glycol from ethylene oxide and ethylene glycol in the presence of acids or in the production of ethylene glycol by hydrolysis of ethylene oxide.
properties
Tetraethylene glycol is a very difficult to ignite, not very volatile, colorless and odorless liquid that is miscible with water. It is less hygroscopic than mono- and diethylene glycol and can only be mixed to a limited extent with alcohols, ketones and alkanolamines in any ratio and with diethyl ether.
use
Tetraethylene glycol is used as a plasticizer for cell glass and nitrocellulose lacquers, as a drying agent for natural and industrial gas, as a heat transfer fluid or humectant for cork. It is a starting material for the production of synthetic resins , plasticizers, emulsifiers and adhesives, especially of tetraethylene glycol di (meth) acrylates by esterification . Tetraethylene glycol is also used as a solvent and lubricant for dyeing and printing textiles, as a lubricant for rubber and as an extractant for aromatics and is a component in printing inks, soldering aids and hydraulic oils . It is used in pharmaceutical and cosmetic preparations and cleaning agents. In organic chemistry, tetraethylene glycol is suitable for the production of crown ethers , as a precursor to linkers in combinatorial chemistry and for the immobilization of biomolecules.
Individual evidence
- ↑ a b c d e f g h i j k Entry for CAS no. 112-60-7 in the GESTIS substance database of the IFA , accessed on September 6, 2015(JavaScript required) .
- ↑ a b c d Entry on tetraethylene glycol. In: Römpp Online . Georg Thieme Verlag, accessed on September 6, 2015.