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Featured Results:
 Isobutene : Carcinogenic Potency Database
Isobutene: Carcinogenic Potency Database
potency.berkeley.edu
 
Isobutylene
Isobutylene.png
Isobutylene2.png
Isobutylene3.png
IUPAC name
Other names Isobutene
γ-Butylene
2-Methylpropylene
Identifiers
CAS number 115-11-7 Yes check.svgY
PubChem 8255
EC number 204-066-3
UN number 1055
In Liquefied petroleum gas: 1075
RTECS number UD0890000
SMILES
InChI
ChemSpider ID 7957
Properties[1]
Molecular formula C4H8
Molar mass 56.11 g mol−1
Appearance Colorless gas
Density 0.5879 g/cm3, liquid
Melting point

−140.3 ºC

Boiling point

-6.9 °C, 266 K, 20 °F

Solubility in water Insoluble
Hazards[2]
EU Index 601-012-00-4
EU classification Extremely flammable (F+)
R-phrases R12
S-phrases (S2), S9, S16, S33
NFPA 704
NFPA 704.svg
4
1
0
 
Flash point flammable gas
Autoignition
temperature
465 °C (869 ºF)
Explosive limits 1.8–9.6%
Related compounds
Related butenes 1-Butene
cis-2-Butene
trans-2-Butene
Related compounds Isobutane
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Isobutylene (or 2-methylpropene) is a hydrocarbon of significant industrial importance. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene. At standard temperature and pressure it is a colorless flammable gas.

Contents

[edit] Uses

Isobutylene is used as an intermediate in the production of a variety of products. It is reacted with methanol and ethanol in the manufacture of the gasoline oxygenates methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE), respectively. Alkylation with butane produces isooctane, another fuel additive. Isobutylene is also used in the production of methacrolein. Polymerization of isobutylene produces butyl rubber (polyisobutylene). Antioxidants such as butylated hydroxytoluene (BHT) and butylated hydroxyanisole (BHA) are produced by Friedel-Crafts alkylation of phenols using isobutylene.

[edit] Manufacture

Isobutylene can be isolated from refinery streams by reaction with sulfuric acid, but the most common industrial method for its production is by catalytic dehydrogenation of isobutane.[3] In the 1990s, the production of isobutylene increased dramatically as the demand for oxygenates such as MTBE grew. Key manufacturers of this product are Texas Petrochemicals and Lyondell in North America.

[edit] Safety

Isobutylene is a highly flammable gas and presents an explosion danger. Usually stored as a compressed gas, if released it may produce an oxygen-deficient atmosphere that presents an asphyxiation hazard.[2]

[edit] See also

[edit] References

  1. ^ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed.), Merck, 1989, ISBN 091191028X , 5024.
  2. ^ a b Isobutene, International Chemical Safety Card 1027, Geneva: International Labour Organization, April 2000, http://www.inchem.org/documents/icsc/icsc/eics1027.htm 
  3. ^ Olah, George A.; Molnár, Árpád, Hydrocarbon Chemistry, Wiley-Interscience, ISBN 978-0471417828 .

[edit] External links




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