| Weight | 130.231 g/mol |
|---|---|
| Formula | C8H18O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Di-tert-butyl ether (6163-66-2)
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- Thermodynamic properties and ideal-gas enthalpies of formation for butyl vinyl ether, 1,2-dimethoxyethane, methyl glycolate, bicyclo[2.2.1]hept-2-ene, 5-vinylbicyclo[2.2.1]hept-2-ene, trans-azobenzene, butyl acrylate, di-tert-butyl ether, and hexane-1,6-diol (Journal of Chemical & Engineering Data, 1996)
- Organic peroxides. LXIII. Formation of di-tert-butyl polyoxides in the reaction of tert-butyl hydroperoxide with iodosobenzene and iodosobenzene diacetate in methylene chloride and in diethyl ether at -80 to +5.deg. (Journal of the American Chemical Society, 1968)
- UV absorption spectra and kinetics for alkyl and alkyl peroxy radicals originating from di-tert-butyl ether (Chemical Physics Letters, 1995)
- Di-tert-butyl containing semifluorinated poly(ether amide)s: Synthesis, characterization and gas transport properties (Journal of Membrane Science, 2013)
- Atmospheric chemistry of di-tert-butyl ether: Rates and products of the reactions with chlorine atoms, hydroxyl radicals, and nitrate radicals (International Journal of Chemical Kinetics, 1996)
- The metabolism of di-(3,5-di-tert.-butyl-4-hydroxybenzyl) ether (Ionox 201) in the rat (Biochemical Journal, 1967)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC(C)(C)OC(C)(C)C
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InChIKeyAQEFLFZSWDEAIP-UHFFFAOYSA-N
- Pubchem - Di-tert-butyl ether
- Wikipedia - di-tert-butyl ether
Di-tert-butyl ether is a tertiary ether that is used as a solvent.
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Di-tert-butyl ether
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