Names | |
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IUPAC name
Fluoroethene
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Other names
Vinylfluoride, Fluoroethylene, Monofluoroethylene, Vinyl fluoride monomer, VF, R 1141, UN 1860 (inhibited)
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Identifiers | |
3D model (Jmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.000.757 |
EC Number | 200-832-6 |
KEGG | |
PubChem CID
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RTECS number | YZ7351000 |
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Properties | |
C2H3F | |
Molar mass | 46.04 g/mol |
Appearance | Colorless gas |
Odor | faint, ethereal |
Density | 0.636 g/cm3 |
Melting point | −160.5 °C (−256.9 °F; 112.6 K) |
Boiling point | −72.2 °C (−98.0 °F; 201.0 K) |
Slightly soluble | |
Vapor pressure | 25.2 atm (370.4 psi) |
Hazards | |
EU classification (DSD)
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Extremely flammable (F+) |
R-phrases | R12 |
S-phrases | S9, S16, S33 |
NFPA 704 | |
385 °C (725 °F; 658 K) | |
Explosive limits | 2.6 - 21.7% |
US health exposure limits (NIOSH): | |
PEL (Permissible)
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none |
REL (Recommended)
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TWA 1 ppm C 5 ppm |
IDLH (Immediate danger)
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N.D. |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Vinyl fluoride is an organic halide with the chemical formula C2H3F. It is a colorless gas with a faint etherlike odor. It is used as the monomeric precursor to the fluoropolymer polyvinylfluoride.
It was first prepared in 1901 by Frédéric Swarts, the Belgian chemist who was the first to prepare CFCs in 1892. Swarts used the reaction of zinc with 1,1-difluoro-2-bromoethane. It is produced industrially by two routes, one being the mercury-catalyzed reaction of acetylene and hydrogen fluoride:
It is also prepared from 1,1-chlorofluoroethane:
Vinyl fluoride is classified as an IARC Group 2A carcinogen (likely to cause cancer in humans).
Its critical point is at 54.8 °C (328 K) and 5.24 MPa. Molecular dipole moment is 1.4 Debye and heat of vaporization is 361 kJ/kg.