1,1-Difluoroethane

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1,1-Difluoroethane[1]
Difluoroethane
Difluoroethane
Difluoroethane
Names
IUPAC name
1,1-Difluoroethane
Other names
difluoroethane
Freon 152a
ethylidene difluoride
ethylidene fluoride
HFC-152a
R-152a
DFE
Identifiers
75-37-6 YesY
ChEMBL ChEMBL325493 YesY
ChemSpider 6128 YesY
Jmol 3D model Interactive image
PubChem 6368
RTECS number KI1410000
UNII 0B1U8K2ME0 YesY
  • InChI=1S/C2H4F2/c1-2(3)4/h2H,1H3 YesY
    Key: NPNPZTNLOVBDOC-UHFFFAOYSA-N YesY
  • InChI=1/C2H4F2/c1-2(3)4/h2H,1H3
    Key: NPNPZTNLOVBDOC-UHFFFAOYAM
  • FC(F)C
Properties
C2H4F2
Molar mass 66.05 g/mol
Density 2.7014 g/L @ 25 °C
Melting point −117 °C (−179 °F; 156 K)
Boiling point −25 °C (−13 °F; 248 K)
0.54% @ 0 °C
Vapor pressure 4020 mmHg/536 kPa @ 21.1 °C

5.1 bar/510 kPa @ 20 °C

Viscosity 0.00887 cP (8.87 µPa·s) @ 25 °C
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

1,1-Difluoroethane, or DFE, is an organofluorine compound with the chemical formula C2H4F2. This colorless gas is used as a refrigerant, where it is often listed as R-152a (refrigerant-152a) or HFC-152a (hydrofluorocarbon-152a). As an alternative to chlorofluorocarbons, it has an ozone depletion potential of zero, a lower global warming potential (120) and a shorter atmospheric lifetime (1.4 years).[2] It has recently been approved for use in automobile applications as an alternative to R-134a.[citation needed]

Production

1,1-Difluoroethane is produced by the mercury-catalyzed addition of hydrogen fluoride to acetylene:[3]

HCCH + 2 HF → CH3CHF2

The intermediate in this process is vinyl fluoride, the monomeric precursor to polyvinyl fluoride.

Uses

In addition to serving as a refrigerant, 1,1-difluoroethane is also commonly used in gas duster (commonly thought of as "canned air") and many consumer aerosol products, especially those subject to stringent VOC requirements.

The molecular weight of difluoroethane is 66, making it useful and convenient tool for detecting vacuum leaks in GC-MS systems.

Safety

The practice of deliberately inhaling or “huffing” canned air is extremely dangerous and can be fatal. It caused a fatal cardiac arrhythmia in a 42-year-old man.[4] Several reports of fatal car crashes have been linked to drivers huffing 1,1-difluoroethane.[5][6][7] Because of inhalant abuse, a bitterant is added to consumer canned air products.

In a DuPont study, rats were exposed to up to 25,000 ppm (67,485 mg m−3) for six hours daily, five days a week for two years. This has become the no-observed-adverse-effect level for this substance. Prolonged exposure to 1,1-difluoroethane has been linked in humans to the development of coronary disease and angina.[8]

Though not extremely flammable in gaseous form, 1,1-difluoroethane can burn under some conditions. As such, there is also a warning label present on some gas dusters. When inverted to spray liquid, the boiling fluorocarbon aerosol is easily ignitable, producing a very large blast of flame and extremely toxic gases such as hydrogen fluoride and carbonyl fluoride as combustion products.

See also

References

  1. 1,1-Difluoroethane at Sigma-Aldrich
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