Home  

Random  

Nearby  



Log in  



Settings  



Donate  



About Wikipedia  

Disclaimers  



Wikipedia





1-Butene





Article  

Talk  



Language  

Watch  

Edit  


(Redirected from 1-butene)
 


1-Butene (IUPAC name: But-1-ene, also known as 1-butylene) is the organic compound with the formula CH3CH2CH=CH2. It is a colorless gas. But-1-ene is an alkene easily condensed to give a colorless liquid. It is classified as a linear alpha-olefin (terminal alkene).[2] It is one of the isomersofbutene (butylene). It is a precursor to diverse products.

1-Butene
Names
Preferred IUPAC name

But-1-ene[1]

Other names

Ethylethylene
1-Butylene
α-Butylene

Identifiers

CAS Number

3D model (JSmol)

  • Interactive image
  • Beilstein Reference

    1098262
    ChEBI
    ChEMBL
    ChemSpider
    ECHA InfoCard 100.003.137 Edit this at Wikidata
    EC Number
    • 203-449-2

    Gmelin Reference

    25205

    PubChem CID

    UNII
    UN number 1012

    CompTox Dashboard (EPA)

    • InChI=1S/C4H8/c1-3-4-2/h3H,1,4H2,2H3 checkY

      Key: VXNZUUAINFGPBY-UHFFFAOYSA-N checkY

    • InChI=1/C4H8/c1-3-4-2/h3H,1,4H2,2H3

      Key: VXNZUUAINFGPBY-UHFFFAOYAZ

    • C=CCC

    • CCC=C

    Properties

    Chemical formula

    C4H8
    Molar mass 56.108 g·mol−1
    Appearance Colorless Gas
    Odor slightly aromatic
    Density 0.62 g/cm3
    Melting point −185.3 °C (−301.5 °F; 87.8 K)
    Boiling point −6.47 °C (20.35 °F; 266.68 K)

    Solubility in water

    0.221 g/100 mL
    Solubility soluble in alcohol, ether, benzene

    Refractive index (nD)

    1.3962
    Viscosity 7.76 Pa
    Hazards
    GHS labelling:

    Pictograms

    GHS02: FlammableGHS04: Compressed Gas

    Signal word

    Danger

    Hazard statements

    H220, H221, H280

    Precautionary statements

    P210, P377, P381, P403, P410+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 −79 °C; −110 °F; 194 K

    Autoignition
    temperature

    385 °C (725 °F; 658 K)
    Explosive limits 1.6-10%

    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

    Reactions

    edit

    Polymerization of but-1-ene gives polybutylene, which is used to make piping for domestic plumbing.[3] Another application is as a comonomer in the production of certain kinds of polyethylene, such as linear low-density polyethylene (LLDPE).[4] It has also been used as a precursor to polypropylene resins, butylene oxide, and butanone.[5]

    Manufacturing

    edit

    But-1-ene is produced by separation from crude C4 refinery streams and by ethylene dimerization. The former affords a mixture of 1-and 2-butenes, while the latter affords only the terminal alkene.[6] It is distilled to give a very high purity product. An estimated 12 billion kilograms were produced in 2011.[7]

    References

    edit
    1. ^ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. pp. 17, 61, 374. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  • ^ "1-BUTENE". chemicalland21.com. Retrieved 22 April 2018.
  • ^ Whiteley, Kenneth S.; Heggs, T. Geoffrey; Koch, Hartmut; Mawer, Ralph L.; Immel, Wolfgang (2000). "Polyolefins". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a21_487. ISBN 978-3527306732.
  • ^ Chum, P. Steve; Swogger, Kurt W. (2008). "Olefin polymer technologies—History and Recent Progress at the Dow Chemical Company". Progress in Polymer Science. 33 (8): 797–819. doi:10.1016/j.progpolymsci.2008.05.003.
  • ^ "1-Butene product overview". shell.com. Archived from the original on 2012-02-10. Retrieved 22 April 2018.
  • ^ "Alphabutol process - Big Chemical Encyclopedia". chempedia.info. Archived from the original on 2017-12-08. Retrieved 22 April 2018.
  • ^ 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.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=1-Butene&oldid=1218070066"
     



    Last edited on 9 April 2024, at 14:53  





    Languages

     


    العربية
    تۆرکجه
    Català
    Čeština
    Deutsch
    Ελληνικά
    Español
    Esperanto
    Euskara
    فارسی
    Français
    Bahasa Indonesia
    Italiano
    Magyar

    Română
    Slovenščina
    Српски / srpski
    Srpskohrvatski / српскохрватски
    Suomi
    ி
    Українська

     

    Wikipedia


    This page was last edited on 9 April 2024, at 14:53 (UTC).

    Content is available under CC BY-SA 4.0 unless otherwise noted.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Terms of Use

    Desktop