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Contents

   



(Top)
 


1 Production  





2 Applications  





3 Gallery  





4 References  





5 Appendix  














Octafluorocyclobutane






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From Wikipedia, the free encyclopedia
 


Octafluorocyclobutane
Structural formula of octafluorocyclobutane
Ball-and-stick of the octafluorocyclobutane molecule
Names
Preferred IUPAC name

Octafluorocyclobutane

Other names

Freon-C-318, perfluorocyclobutane

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

1909266
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.705 Edit this at Wikidata
EC Number
  • 204-075-2
E number E946 (glazing agents, ...)

Gmelin Reference

131113

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C4F8/c5-1(6)2(7,8)4(11,12)3(1,9)10 ☒N

    Key: BCCOBQSFUDVTJQ-UHFFFAOYSA-N ☒N

  • InChI=1/C4F8/c5-1(6)2(7,8)4(11,12)3(1,9)10

    Key: BCCOBQSFUDVTJQ-UHFFFAOYAW

  • C1(C(C(C1(F)F)(F)F)(F)F)(F)F

Properties

Chemical formula

C4F8
Molar mass 200.03 g/mol
Appearance colourless gas
Density 1.637 g/cm3 at −5.8 °C (liquid)

9.97 kg/m3 at −6 °C and 1 atm (gas)
8.82 kg/m3 15 °C and 1 atm (gas)

Melting point −40.1 °C (−40.2 °F; 233.1 K)
Boiling point −5.8 °C (21.6 °F; 267.3 K)

Solubility in water

0.016 vol/vol (1.013 bar and 20 °C)
Viscosity 109e-6 Poise (1.013 bar and 0 °C)
Hazards
GHS labelling:

Pictograms

GHS04: Compressed GasGHS09: Environmental hazard

Signal word

Warning

Hazard statements

H280, H411

Precautionary statements

P273, P391, P410+P403, P501

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

Octafluorocyclobutane, or perfluorocyclobutane, C4F8, is an organofluorine compound which enjoys several niche applications. Octafluorocyclobutane is a colourless gas and shipped as a liquefied gas. It is the perfluorinated analogue of cyclobutane whereby all C–H bonds are replaced with C–F bonds.

Production[edit]

Octafluorocyclobutane is produced by the dimerization of tetrafluoroethylene and the reductive coupling of 1,2-dichloro-1,1,2,2-tetrafluoroethane.[1]

Applications[edit]

In the production of semiconductor materials and devices, octafluorocyclobutane serves as a deposition gas and etchant.[2] It has also been investigated as a refrigerant in specialised applications, as a replacement for ozone depleting chlorofluorocarbon refrigerants. Exploiting its volatility and chemical inertness, octafluorocyclobutane may be found in some aerosolized foods. It is listed by the Codex Alimentarius under number 946 (E946 for EU). It is investigated as a possible replacement for sulfur hexafluoride as a dielectric gas.

Gallery[edit]

References[edit]

  1. ^ Siegemund, Günter; Schwertfeger, Werner; Feiring, Andrew; Smart, Bruce; Behr, Fred; Vogel, Herward; McKusick, Blaine (2002). "Fluorine Compounds, Organic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_349. ISBN 978-3527306732..
  • ^ "Octafluorocyclobutane (RC318)". Gas Encyclopaedia. Air Liquide. Retrieved May 15, 2013.
  • Appendix[edit]

    Its critical point is at 115.3 °C and 2.79 MPa.


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Octafluorocyclobutane&oldid=1186238062"

    Categories: 
    Fluorocarbons
    Aerosol propellants
    Refrigerants
    Dielectric gases
    Cyclobutanes
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    This page was last edited on 21 November 2023, at 20:36 (UTC).

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