Vinylidene fluoride
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Vinylidene fluoride
structure -
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CAS No:
75-38-7
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Formula:
C2H2F2
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Chemical Name:
Vinylidene fluoride
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Synonyms:
Ethene,1,1-difluoro-;Ethylene,1,1-difluoro-;1,1-Difluoroethene;1,1-Difluoroethylene;Genetron 1132a;Vinylidene fluoride;Vinylidene difluoride;HFC 1132a;R 1132a;CA 16;FC 1132a;Fluorovinylidene;HFO 1132A;1272398-81-8
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CAS No:
Description
Colorless gas; faint ethereal odor. Slightly soluble in water; soluble in alcohol and ether. Vinylidene fluoride is a colorless gas. Faint ethereal odor. Shipped as a liquefied compressed gas.
Characteristics
0
1.24
1,1-Difluoroethylene (or vinylidene fluoride) is a colorless gas which is flammable in the ranges of 5.5 to 21%. It is toxic by inhalation and contact. It is slightly soluble in water and soluble in alcohol and ether. Under prolonged exposure to fire or intense heat the containers may rupture violently and rocket.
0.6 g/cm3
-144 °C
-83 °C
NA (Gas)
1.264
Insoluble
Store gas cylinders in a cool, dry place and use the safety precautions necessary with all compressed gases. High concentrations cause a deficiency of oxygen with the risk of unconsciousness or death.
518 psi ( 21 °C)
2.2 (vs air)
Inhalation-Rat LC 128000 PPM/4 hours
Flammable; decomposes toxic hydrogen fluoride gas in case of heat
21.3%
Nearly odorless
Safety Information
2.1
UN 1959 2.1
3
12
16-7/9
KW0560000
F+,F
Treasury is ventilated, low temperature and dry; stored separately from oxidant
Flammable
Explosive when mixed with air
Chemical stability: Stable under recommended storage conditions.
P210, P261, P271, P304+P340, P312, P377, P381, P403, P403+P233, P405, P501
H220
Vinylidene fluoride Use and Manufacturing
1. The vinylidene fluoride ethane chlorination method uses dry acetylene to react with hydrofluoric acid in the presence of fluorosulfonic acid to produce 1, 1-difluoroethane, which is compressed, fractionated and purified to obtain refined 1, 1-di Ethylene fluoride is fully mixed with chlorine in a quantitative ratio and pyrolyzed at 650-680°C to generate crude vinylidene fluoride, and then compressed, fractionated and purified to obtain refined monomers. 2. Other methods Due to the development of the chlorofluoroalkane substitute industry in recent years, 1, 1, 1-trichloroethane can be used to produce 1, 1-difluoro-1-chloroethane by one-step reaction, and then thermally cracked to remove Hydrogen chloride.
Mainly used as monomer raw material for fluororesin and fluororubber
Computed Properties
Molecular Weight:64.03
XLogP3:1.3
Hydrogen Bond Acceptor Count:2
Exact Mass:64.01245639
Monoisotopic Mass:64.01245639
Heavy Atom Count:4
Complexity:27
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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