Ethyl tert-butyl ether

Ethyl tert-butyl ether

IUPAC name
2-Ethoxy-2-methyl-propane

Other names
Ethyl tert-butyl ether
Ethyl tertiary butyl ether
Ethyl tert-butyl oxide
tert-Butyl ethyl ether
Ethyl t-butyl ether

Identifiers

Abbreviations
ETBE

CAS number

PubChem
12512

EINECS number
211-309-7

RTECS number
KN4730200

SMILES

 
CCOC(C)(C)C

InChI

 
1/C6H14O/c1-5-7-6(2,3)4/h5H2,1-4H3

Properties

Molecular formula
C6H14O

Molar mass
102.17 g mol-1

Appearance
Clear colorless liquid

Density
0.7364 g/cm3

Melting point

-94 °C, 179 K, -137 °F

Boiling point

69-71 °C

Solubility in water
1.2 g/100 g

Hazards

R-phrases
R11 R20

S-phrases
S16

Flash point
-19 °C

Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)

Infobox disclaimer and references

Ethyl tert-butyl ether (ETBE) is commonly used as an oxygenate gasoline additive in the production of gasoline from crude oil. ETBE offers equal or greater air quality benefits as ethanol, while being technically and logistically less challenging. Unlike ethanol, ETBE does not induce evaporation of gasoline, which is one of the causes of smog, and does not absorb moisture from the atmosphere.

Contents

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Synthesis

It is synthesized by mixing ethanol and isobutylene and reacting them with heat over a catalyst.

Ethanol, produced by fermentation and distillation, is more expensive than methanol, which is derived from natural gas. Therefore, MTBE, made from methanol is cheaper than ETBE, made from ethanol. However, (bio)ethanol makes ETBE partially a biofuel, while MTBE is entirely a fossil fuel and introduces a risk to the environment (see the article on MTBE).

See also

  • Methyl tert-butyl ether

References

  1. ^ Merck Index, 11th Edition, 3732.

External links

  • EFOA

Retrieved from “http://en.wikipedia.org/wiki/Ethyl_tert-butyl_ether
Categories: Ethers | Ether solvents | Oxygenates | Pollutants

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