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Isobutylene





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Isobutylene (or2-methylpropene) is a hydrocarbon with the chemical formula (CH3)2C=CH2. It is a four-carbon branched alkene (olefin), one of the four isomers of butylene. It is a colorless flammable gas, and is of considerable industrial value.[3]

Isobutylene
Skeletal formula of isobutylene
Ball-and-stick model of isobutylene
Ball-and-stick model of isobutylene
Space-filling model of isobutylene
Space-filling model of isobutylene
Names
Preferred IUPAC name

2-Methylprop-1-ene

Other names

2-Methylpropene
Isobutene
γ-Butylene
2-Methylpropylene
Methylpropene

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChemSpider
ECHA InfoCard 100.003.697 Edit this at Wikidata
EC Number
  • 204-066-3

PubChem CID

RTECS number
  • UD0890000
UNII
UN number 1055
InLiquefied petroleum gas: 1075

CompTox Dashboard (EPA)

  • InChI=1S/C4H8/c1-4(2)3/h1H2,2-3H3 checkY

    Key: VQTUBCCKSQIDNK-UHFFFAOYSA-N checkY

  • InChI=1/C4H8/c1-4(2)3/h1H2,2-3H3

  • CC(=C)C

Properties[1]

Chemical formula

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)

Magnetic susceptibility (χ)

-44.4·10−6cm3/mol
Hazards[2]
GHS labelling:

Pictograms

Flam. Gas 1Press. Gas

Signal word

Danger

Hazard statements

H220

Precautionary statements

P210, P377, P381, P403
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 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. propaneInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
4
0
Flash point flammable gas

Autoignition
temperature

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 checkY☒N ?)

Infobox references

Production

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Polymer and chemical grade isobutylene is typically obtained by dehydrating tertiary butyl alcohol (TBA) or catalytic dehydrogenationofisobutane (Catofin or similar processes).[4] Gasoline additives methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE), respectively, are produced by reacting methanolorethanol with isobutylene contained in butene streams from olefin steam crackers or refineries, or with isobutylene from dehydrated TBA. Isobutylene is not isolated from the olefin or refinery butene stream before the reaction, as separating the ethers from the remaining butenes is simpler. Isobutylene can also be produced in high purities by "back-cracking" MTBE or ETBE at high temperatures and then separating the isobutylene by distillation from methanol.

Isobutylene is a byproduct in the ethenolysisofdiisobutylene to prepare neohexene:[5]

(CH3)3C-CH=C(CH3)2 + CH2=CH2 → (CH3)3C-CH=CH2 + (CH3)2C=CH2

Uses

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Isobutylene is used in the production of a variety of products. It is alkylated with butane to produce isooctane or dimerized to diisobutylene (DIB) and then hydrogenated to make isooctane, a fuel additive. Isobutylene is also used in the production of methacrolein. Polymerization of isobutylene produces butyl rubber (polyisobutylene or PIB). Antioxidants such as butylated hydroxytoluene (BHT) and butylated hydroxyanisole (BHA) are produced by Friedel-Crafts alkylationofphenols with isobutylene.

tert-Butylamine is produced commercially by amination of isobutylene using zeolite catalysts:[6]

NH3 + CH2=C(CH3)2 → H2NC(CH3)3

Applications are found in the calibration of photoionization detectors.

Safety

edit

Isobutylene is a highly flammable gas.

See also

edit

References

edit
  1. ^ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed.), Merck, 1989, ISBN 091191028X, 5024.
  • ^ Isobutene, International Chemical Safety Card 1027, Geneva: International Programme on Chemical Safety, April 2000
  • ^ Geilen, Frank M.A.; Stochniol, Guido; Peitz, Stephan; Schulte-Koerne, Ekkehard (2014). "Butenes". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a04_483.pub3. ISBN 978-3527306732.
  • ^ Olah, George A.; Molnár, Árpád (May 2003), Hydrocarbon Chemistry, Wiley-Interscience, ISBN 978-0-471-41782-8.
  • ^ Lionel Delaude; Alfred F. Noels. "Metathesis". Kirk-Othmer Encyclopedia of Chemical Technology. Wiley.
  • ^ Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2000). "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001. ISBN 3527306730.
  • edit

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Isobutylene&oldid=1214842797"
     



    Last edited on 21 March 2024, at 14:39  





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    This page was last edited on 21 March 2024, at 14:39 (UTC).

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