tert-Amyl methyl ether

From Wikipedia, the free encyclopedia
Not to be confused with tert-Amyl ethyl ether.
tert-Amyl methyl ether[1][2]
Tert-amyl methyl ether.svg
Amyl methyl ether.png
Names
Preferred IUPAC name
2-Methoxy-2-methylbutane
Other names
tertiary-Amyl methyl ether; TAME; Methoxypentane
Identifiers
3D model (JSmol)
Abbreviations TAME
ChemSpider
ECHA InfoCard 100.012.374 Edit this at Wikidata
UNII
  • InChI=1S/C6H14O/c1-5-6(2,3)7-4/h5H2,1-4H3 checkY
    Key: HVZJRWJGKQPSFL-UHFFFAOYSA-N checkY
  • InChI=1/C6H14O/c1-5-6(2,3)7-4/h5H2,1-4H3
    Key: HVZJRWJGKQPSFL-UHFFFAOYAC
  • O(C(C)(C)CC)C
Properties
C6H14O
Molar mass 102.177 g·mol−1
Appearance Clear, colorless liquid
Density 0.76-0.78 g/mL[3]
Melting point −80 °C (−112 °F; 193 K)
Boiling point 86.3 °C (187.3 °F; 359.4 K)
10.71 g/L at 20 °C
1.3896
Hazards
Flash point −11 °C (12 °F; 262 K)
430 °C (806 °F; 703 K)
Explosive limits 1.0-7.1%
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

tert-Amyl methyl ether (TAME) is an ether used as a fuel oxygenate. TAME derives from C5 distillation fractions of naphtha.[4] It has an ethereous odor.[1] Unlike most ethers, it does not require a stabilizer as it does not form peroxides on storage.[5]

Uses[]

TAME is mostly used as an oxygenate to gasoline. It is added for three reasons: to increase octane enhancement, to replace banned tetraethyl lead, and to raise the oxygen content in gasoline. It is known that TAME in fuel reduces exhaust emissions of some volatile organic compounds.[1]

TAME is also used as a solvent in organic synthesis as a more environmentally friendly alternative to some of the classic ether solvents.[4] It is characterized by a high boiling point (86 °C) and a low freezing point (−80 °C), allowing a wide range of reaction temperatures. TAME can be used as a safe reaction medium (e.g. condensation reactions, coupling reactions, such as Grignard reactions and Suzuki reactions, as well as metal hydride reductions) and as an extraction solvent to replace dichloromethane, aromatics, and other ethers.[6]

Toxicity[]

In an animal toxicology study, inhalation of high concentrations of TAME (4000 ppm) caused central nervous system depression, leading to death in most cases.[7]

See also[]

References[]

  1. ^ a b c "tert-AMYL METHYL ETHER (1,1-DIMETHYLPROPYL METHYL ETHER)". chemicalland21.com. Retrieved 2009-10-20.
  2. ^ National Industrial Chemicals Notification and Assessment Scheme (2001). "t-Amyl methyl ether (TAME)" (PDF). Full Public Reports. Retrieved 2009-10-20.
  3. ^ "tert-Amyl methyl ether". Sigma-Aldrich.
  4. ^ a b Prat, Denis; Wells, Andy; Hayler, John; Sneddon, Helen; McElroy, C. Robert; Abou-Shehada, Sarah; Dunn, Peter J. (2015-12-21). "CHEM21 selection guide of classical- and less classical-solvents". Green Chem. 18 (1): 288–296. doi:10.1039/c5gc01008j. ISSN 1463-9270.
  5. ^ Diaz, Arthur F.; Drogos, Donna L. (2001-11-06). Oxygenates in Gasoline. ACS Symposium Series. 799. American Chemical Society. pp. 138–152. doi:10.1021/bk-2002-0799.ch010. ISBN 978-0841237605.
  6. ^ Author. "INEOS Oligomers Products". www.ineos.com. Retrieved 2017-10-30.
  7. ^ White, Russell D.; Daughtrey, Wayne C.; Wells, Mike S. (December 1995). "Health effects of inhaled tertiary amyl methyl ether and ethyl tertiary butyl ether". Proceedings of the International Congress of Toxicology - VII. Toxicology Letters. 82–83. pp. 719–724. doi:10.1016/0378-4274(95)03590-7. PMID 8597132.
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