Isobutylene

Isobutylene
Names
IUPAC name
2-Methylpropene
Other names
Isobutene
γ-Butylene
2-Methylpropylene
Methylpropene
2-Methylprop-1-ene
Identifiers
115-11-7 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:43907 N
ChemSpider 7957 YesY
ECHA InfoCard 100.003.697
EC Number 204-066-3
PubChem 8255
RTECS number UD0890000
UNII QA2LMR467H YesY
UN number 1055
In Liquefied petroleum gas: 1075
Properties[1]
C4H8
Molar mass 56.106 g/mol
Appearance Colorless gas
Density 0.5879 g/cm3, liquid
Melting point −140.3 °C (−220.5 °F; 132.8 K)
Boiling point −6.9 °C (19.6 °F; 266.2 K)
Insoluble
Hazards[2]
GHS pictograms
GHS signal word DANGER
H220
P210, P377, P381, P403
Extremely flammable (F+)
R-phrases R12
S-phrases (S2), S9, S16, S33
NFPA 704
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g., propane Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
4
1
0
Flash point flammable gas
465 °C (869 °F; 738 K)
Explosive limits 1.8–9.6%
Related compounds
Related butenes
 1-Butene
cis-2-Butene
trans-2-Butene
Related compounds
 Isobutane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Isobutylene (or 2-methylpropene) is a hydrocarbon of industrial significance. 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.

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.

Manufacture

Polymer and chemical grade isobutylene is typically obtained by dehydrating tertiary butyl alcohol or catalytic dehydrogenation of isobutane.[3] Gasoline oxygenates MTBE and ETBE are generally produced by reacting methanol or ethanol with isobutylene contained in butene streams from olefin steam crackers or refineries. Isobutylene is not isolated before the reaction as separating the ethers from the remaining butenes is simpler.

Safety

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

See also

References

  1. ↑ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed.), Merck, 1989, ISBN 091191028X, 5024.
  2. 1 2 Isobutene, International Chemical Safety Card 1027, Geneva: International Programme on Chemical Safety, April 2000
  3. ↑ Olah, George A.; Molnár, Árpád, Hydrocarbon Chemistry, Wiley-Interscience, ISBN 978-0-471-41782-8.
This article is issued from Wikipedia - version of the 11/16/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.