VINYL FLUORIDE supplier | CasNO.75-02-5

Name
VINYL FLUORIDE
EINECS
CAS No. 75-02-5
Article Data92
CAS DataBase
Density 0,615 g/cm3
Solubility
Melting Point -160,5°C
Formula C2H3 F
Boiling Point -72°C
Molecular Weight 46.0442
Flash Point
Transport Information
Appearance
Safety Confirmed carcinogen. A poison. Mutation data reported. A very dangerous fire hazard. To fight fire, stop flow of gas. When heated to decomposition it emits toxic fumes of F⁻. See also FLUORIDES.
Risk Codes R12;R40;
Molecular Structure
Hazard Symbols Flammable, dangerous fire and explosion risk. Toxic by inhalation. TLV: 2.6 mg(F)/m³.
Synonyms Ethylene,fluoro- (8CI); 1-Fluoroethene; 1-Fluoroethylene; FC 1141; Fluoroethene;Fluoroethylene; Monofluoroethene; Monofluoroethylene; R 1141; Vinyl fluoride
PSA 0.00000
LogP 1.09940

Synthetic route

: 75-37-6
1,1-difluoroethane

: 74-86-2
acetylene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 340℃; other temperatures, other catalysts;	77.5%

: 75-37-6
1,1-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF for 9 - 162h;	29.8%
With hydrogen fluoride; chromium(III) oxide at 245 - 275℃; for 5 - 49h; Catalys was activated in a stream of HF up to 350 C;	13.2%
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF at 200 - 245℃; for 15 - 47.5h;	6%

: 75-37-6
1,1-difluoroethane

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

C: 74-86-2
acetylene

Conditions

Conditions	Yield
With hydrogen fluoride; Guingnet's green at 250 - 400℃; for 10 - 129h;	A 0% B 19.6% C 0%
With hydrogen fluoride; Alpha-chromium oxide obtained from the pyrolysis of ammonium dichromate, treated with HF at 250 - 350℃;	A 0% B 19.3% C 0%
With hydrogen fluoride; Alpha-chromium oxide prepared by the precipitation of chromium hydroxide from chromium nitrate followed by calcination in air at 500 C for 72 hours, treated with HF at 250 - 350℃;	A 0% B 19.9% C 0%

...Expand

: 60-29-7
diethyl ether

: 598-39-0
1,1-difluoro-2-iodoethane

: phenylmagnesium bromide

A: 462-06-6
fluorobenzene

B: 591-50-4
iodobenzene

C: 92-52-4
biphenyl

D: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
Zersetzen des Reaktionsproduktes mit Wasser; Produkt5: Stilben;

...Expand

: 60-29-7
diethyl ether

: 358-97-4
1,2-bromofluoroethane

: phenylmagnesium bromide

A: 108-86-1
bromobenzene

B: 92-52-4
biphenyl

C: 75-02-5
1-fluoroethylene

D: 71-43-2
benzene

Conditions

Conditions	Yield
Zersetzen des Reaktionsproduktes mit Wasser;

...Expand

: 1615-75-4
1-chloro-1-fluoroethane

A: 75-02-5
1-fluoroethylene

B: 75-01-4
chloroethylene

Conditions

Conditions	Yield
at 600℃;

: 624-72-6
1,2-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 103.9 - 201.9℃;
With calcium sulfate at 350℃;

: 359-07-9
2-bromo-1,1-difluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With ethanol; zinc at 50℃;

: 598-39-0
1,1-difluoro-2-iodoethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With diethyl ether; phenylmagnesium bromide
With diethyl ether; magnesium
With diethyl ether; potassium
With diethyl ether; sodium

: 358-97-4
1,2-bromofluoroethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With ethanol; zinc
With diethyl ether; phenylmagnesium bromide
With potassium iodide

: 78-74-0
1,1,2-tribromoethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With bromine; antimony(III) fluoride at 100℃; und Behandeln des Reaktionsprodukts mit Zink in Aethanol;

: 74-86-2
acetylene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With potassium cyanide; hydrogen fluoride; copper(l) cyanide; pyrographite at 160℃;
With hydrogen fluoride; mercury(II) oxide
With hydrogen fluoride; mercury(II) diacetate

: 17003-27-9
1-fluoro-1-nitro-ethane

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With (thermolysis) at 300 - 340℃; Kinetics;

: 593-60-2
Vinyl bromide

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 593-60-2
Vinyl bromide

A: 2366-31-6
(Z)-1-bromo-2-fluoroethylene

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With F at 0℃; under 112.5 Torr; Mechanism;

: 392-56-3
Hexafluorobenzene

: 74-85-1
ethene

A: 75-02-5
1-fluoroethylene

B: 653-34-9
2,3,4,5,6-pentafluorostyrene

C: 363-72-4
Pentafluorobenzene

D: 106-99-0
buta-1,3-diene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
Mechanism; Irradiation;	A 8 % Chromat. B 24 % Chromat. C 12 % Chromat. D 7 % Chromat. E 19 % Chromat.

...Expand

: 187737-37-7
propene

A: 2229-07-4
methyl radical

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With fluorine under 0.8 Torr; Mechanism; Product distribution; Irradiation; study of the branching ratio and radical products under multi-photon ionization conditions; other reagents and products;

: 74-84-0
ethane

A: 2229-07-4
methyl radical

B: 2025-56-1
ethyl radical

C: 74-85-1
ethene

D: 75-02-5
1-fluoroethylene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
With fluorine photoelectron spectrum of the product mixture; the ethyl radical was investigated;

...Expand

: 74-85-1
ethene

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 74-85-1
ethene

: 13453-52-6
monofluorocarbene

A: 2465-56-7
methylene

B: 593-53-3
Methyl fluoride

C: 75-02-5
1-fluoroethylene

D: 406-33-7
1-fluoropropene

E: 74-86-2
acetylene

Conditions

Conditions	Yield
In gas Rate constant; Thermodynamic data; Ambient temperature; Irradiation; ΔH;

...Expand

: 74-85-1
ethene

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
With F In gas at -100℃; under 1E-07 Torr; Mechanism; Thermodynamic data; other temperatures, other collision energies; potential energy barrier to F atom addition to C2H4;
With F at -71.15 - 24.85℃; Kinetics; Substitution;

: 74-85-1
ethene

A: 75-02-5
1-fluoroethylene

B: 28761-00-4
β-Fluoroethyl radical

Conditions

Conditions	Yield
With fluorine In gas at 1226.9 - 2226.9℃; Rate constant;

: 762-49-2
2-fluoroethyl bromide

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
Mechanism; Irradiation;
Decomposition; Photolysis;

: 75-01-4
chloroethylene

: 344-07-0
1-chloro-2,3,4,5,6-pentafluorobenzene

A: 75-02-5
1-fluoroethylene

B: 5488-71-1
tetrafluorobezyne

Conditions

Conditions	Yield
at 21.9℃; Irradiation;

...Expand

: 430-51-3
1-fluoro-2-propanone

A: 74-84-0
ethane

B: 74-85-1
ethene

C: 353-36-6
1-fluoroethane

D: 624-72-6
1,2-difluoroethane

E: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 26.9℃; under 840 Torr; Rate constant; Product distribution; Irradiation; bath gas: He; further bath gases; further pressure;

...Expand

: 453-14-5
1,3-difluoro-propan-2-one

A: 593-53-3
Methyl fluoride

B: 624-72-6
1,2-difluoroethane

C: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 101.9 - 202.9℃; under 2.3 - 7.5 Torr; Irradiation;

...Expand

: 79-35-6
1,1'-dichloro-2,2'-difluoroethene

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

C: 1691-13-0
1,2-difluoroethene

D: 74-86-2
acetylene

Conditions

Conditions	Yield
With monosilane under 5 Torr; Mechanism; Product distribution; Irradiation; wave length 944.2 cm-1, ratio SiH4/C2Cl2F2 = 9.0;

...Expand

: 79-35-6
1,1'-dichloro-2,2'-difluoroethene

A: 75-02-5
1-fluoroethylene

B: 74-86-2
acetylene

Conditions

Conditions	Yield
With monosilane under 5 Torr; Mechanism; Product distribution; Irradiation; wave length 1033.5 cm-1, ratio SiH4/C2Cl2F2 = 9.6;

: 462-26-0
2-fluoroethyl acetate

A: 74-85-1
ethene

B: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
In toluene at 610℃; Product distribution;

: 462-26-0
2-fluoroethyl acetate

: 75-02-5
1-fluoroethylene

Conditions

Conditions	Yield
at 430.2 - 450.1℃; Rate constant;

: 75-02-5
1-fluoroethylene

: 162291-59-0
RuH(C6H5)(CO)(P(C(CH3)3)2CH3)2

: 878750-74-4
RuF(C2H3)(CO)(P(C(CH3)3)2CH3)2

Conditions

Conditions	Yield
In benzene-d6 byproducts: C6H6; all manipulations under Ar atm.; soln. of Ru compd. reacted with C2H3F at 1 atm for 12 h at room temp.; detected by 31P(1H) NMR spectra;	99%
With methyldi-t-butylphosphine In Cyclohexane-d12 byproducts: C6H6; all manipulations under Ar atm.; soln. of Ru and P compds. reacted in NMR tube with C2H3F at 1 atm for 12 h at room temp.; detected by 31P(1H) NMR spectra;	99%

: 75-02-5
1-fluoroethylene

: 2154-71-4
bis-trifluoromethyl-aminooxyl

: 67329-58-2
C6H3F13N2O2

Conditions

Conditions	Yield
for 21h; Ambient temperature;	98%

: 75-02-5
1-fluoroethylene

: 2714-60-5
tetrakis(trifluoromethyl)diphosphine

: 34250-88-9
1,2-Bis-(bis-trifluoromethyl-phosphanyl)-1-fluoro-ethane

Conditions

Conditions	Yield
50°C (120 h);	96%
Irradiation (UV/VIS); 20°C (94 h);	59%
Irradiation;

: 75-02-5
1-fluoroethylene

: 1357616-33-1
[Ir2H(CO)2(μ-CO)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

A: 1357616-35-3
[Ir2(H)(CO)3(μ-CCH2)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

B: 1357616-37-5
[Ir2(H)2(CO)2(μ-H)(μ-CCHF)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

Conditions

Conditions	Yield
In dichloromethane-d2 (Ar); using Schlenk techniques; charging of NMR tube with (Ir2(CO)3(H)(PEt2CH2PEt2)2)(B((CF3)2C6H3)4), addn. of CD2Cl2, addn. of CFHCH2 via a gastight syringe, vigorous mixing for 30 min; monitoring by NMR, transferring to Schlenk tube, removal of solvent under vac., redissolving in Et2O, addn. of pentane, pptn.; elem. anal.;	A 94% B n/a

...Expand

: 75-02-5
1-fluoroethylene

: 6141-72-6
perfluoro(2,4-dimethyl-3-oxa-2,4-diazapentane)

A: O-[2-(Bis-trifluoromethyl-amino)-1-fluoro-ethyl]-N,N-bis-trifluoromethyl-hydroxylamine

B: O-[2-(Bis-trifluoromethyl-amino)-2-fluoro-ethyl]-N,N-bis-trifluoromethyl-hydroxylamine

Conditions

Conditions	Yield
for 240h; Ambient temperature; in vacuo;	A 93% B 6%

...Expand

: 75-02-5
1-fluoroethylene

: 430-66-0
1,1,2-Trifluoroethan

Conditions

Conditions	Yield
With xenon difluoride; silicon tetrafluoride at 20℃; for 5h; Fluorination;	93%

: 75-02-5
1-fluoroethylene

: 431-94-7
N-chlorobistrifluoromethylamine

A: 35060-90-3
1-(bis(trifluoromethyl)-amino)-2-fluoro-2-chloro-ethane

B: 35060-87-8
1-bis(trifluoromethyl)-amino-2-fluoro-2-chloro-ethane

Conditions

Conditions	Yield
In gas Irradiation (UV/VIS); photolysis for 0.5 h;	A 5% B 91%
In neat (no solvent, gas phase) Irradiation (UV/VIS); photolysis for 0.5 h;	A 5% B 91%
at 25°C for 10 d in dark;	A 7% B 88%

...Expand

: 75-02-5
1-fluoroethylene

: 758-43-0
N-bromobis(trifluoromethyl)amine

A: 1-(bis(trifluoromethyl)-amino)-2-bromo-1-fluoro-ethane

B: 25237-12-1
1-bis(trifluoromethyl)-amino-2-bromo-2fluoro-ethane

Conditions

Conditions	Yield
Irradiation (UV/VIS); at 20°C for 16 h;	A 6% B 89%
Irradiation (UV/VIS); at 20°C for 16 h;	A 6% B 89%
for 16h; Ambient temperature;
at 20°C for 12 weeks in dark; ratio of (CF3)2NCH2CHFBr:(CF3)2NCHFCH2Br = 9:1;
at 20°C for 12 weeks in dark; ratio of (CF3)2NCH2CHFBr:(CF3)2NCHFCH2Br = 9:1;

...Expand

: 75-02-5
1-fluoroethylene

: 5764-87-4
N-Jod-bis(trifluormethyl)-amin

A: 35060-93-6
1-bis(trimethylfluoro)-amino-2-fluoro-2-iodo-ethane

B: 35060-88-9
1-(bis(trifluoromethyl)-amino)-2-iodo-1-fluoro-ethane

Conditions

Conditions	Yield
Irradiation (UV/VIS); at 20°C for 1 h; in quartz tube;	A 89% B 7%
	A 2% B 89%
Irradiation (UV/VIS); at 20°C for 1 h; in quartz tube;	A 89% B 7%

...Expand

: 75-02-5
1-fluoroethylene

: 460-96-8
bis(trifluoromethyl)phosphine

: 27393-67-5
2-Fluoroaethyl-bis(trifluoromethyl)phosphin

Conditions

Conditions	Yield
Irradiation (UV/VIS); time of irradiation:44 h;	88%
for 44h; Irradiation;

: 75-02-5
1-fluoroethylene

: 23153-22-2
1,1,1,3-tetrachloro-3-fluoropropane

Conditions

Conditions	Yield
With tetrachloromethane; iron(III) chloride; iron; triethyl phosphate at 120 - 127℃; under 3000.3 - 6750.68 Torr; Autoclave; Inert atmosphere;	86%

: 75-02-5
1-fluoroethylene

: 1357616-33-1
[Ir2H(CO)2(μ-CO)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

: 1357616-37-5
[Ir2(H)2(CO)2(μ-H)(μ-CCHF)(bis(diethylphosphino)methane)2][B(3,5-(CF3)2C6H3)4]

Conditions

Conditions	Yield
With trimethylamine-N-oxide In dichloromethane (Ar); using Schlenk techniques; cooling of flask with soln. of (Ir2(CO)3(H)(PEt2CH2PEt2)2)B((CF3)2C6H3)4 in CH2Cl2 to -80°C, transferringof cooled CH2Cl2 soln. of Me3NO via cannula, addn. of CFHCH2, slow warm ing to room temp., stirring for 1 h; removal of solvent, monitoring by NMR;	83%

: 301224-40-8
Hoveyda-Grubbs catalyst second generation

: 75-02-5
1-fluoroethylene

: (RuCl2(CHF)(4,5-dihydro-1,3-dimesitylimidazol-2-ylidene))2

Conditions

Conditions	Yield
In toluene byproducts: CH2CHC6H4OCH(CH3)2; High Pressure; (N2); exposure of toluene soln. of ruthenium compd. to vinyl fluoride at5 psig, cooling to -4°C, stirring for 3 h; cooling to -35°C for 30 min, filtration, wasing with pentane, drying in vac. for 30 min, stirring with benzene for 5 min, drying in vac. for 5 h, elem. anal.;	81.3%

: 75-02-5
1-fluoroethylene

: 201230-82-2
carbon monoxide

: 814-66-4
2-fluoropropionaldehyde

Conditions

Conditions	Yield
With hydrogen; dodecacarbonyltetrarhodium(0) In toluene at 80℃; under 68 Torr; for 18h;	81%

: 56-23-5
tetrachloromethane

: 75-02-5
1-fluoroethylene

: 23153-22-2
1,1,1,3-tetrachloro-3-fluoropropane

Conditions

Conditions	Yield
With iron; triethyl phosphite at 120 - 125℃; under 2999.54 - 6205.94 Torr; for 8h; Temperature; Pressure; Autoclave; Inert atmosphere;	81%

: 75-02-5
1-fluoroethylene

: 754-34-7
1,1,1,2,2,3,3-heptafluoro-3-iodo-propane

: 1,1,1,2,2,3,3,5-octafluoro-5-iodopentane

Conditions

Conditions	Yield
With dibenzoyl peroxide at 110 - 120℃; for 4h; Autoclave;	80%

: 75-02-5
1-fluoroethylene

: 106821-13-0
(2-Chlor-2-fluorethyl)schwefelpentafluorid

Conditions

Conditions	Yield
With pentafluorosulfanyl chloride at -35℃; for 4h; Irradiation;	76%

: 75-02-5
1-fluoroethylene

: 141-75-3
butyryl chloride

: 1-Chloro-1-fluoro-hexan-3-one

Conditions

Conditions	Yield
With iron(III) chloride In dichloromethane at 0℃; for 3h;	76%

: 507-63-1
1-iodoheptadecafluorooctane

: 75-02-5
1-fluoroethylene

A: 89608-43-5
iodo-1H,1H,2H,2H-perfluorodecane

B: 89608-42-4
1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,10,12-Nonadecafluoro-12-iodo-dodecane

Conditions

Conditions	Yield
With ethanolamine; triiron dodecarbonyl In ethanol at 60℃; for 5h;	A 14% B 75%

...Expand

: 75-02-5
1-fluoroethylene

: 75-36-5
acetyl chloride

: 2-chloro-2-fluoroethyl methyl ketone

Conditions

Conditions	Yield
With iron(III) chloride In dichloromethane at 0℃; for 3h;	70%

: 75-02-5
1-fluoroethylene

: 142-61-0
Hexanoyl chloride

: 1-Chloro-1-fluoro-octan-3-one

Conditions

Conditions	Yield
With iron(III) chloride In dichloromethane at 0℃; for 3h;	65%

: 75-02-5
1-fluoroethylene

: C2ClF5O3S

: 2-(2-Chloro-1-fluoro-ethoxy)-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride

Conditions

Conditions	Yield
In various solvent(s) at -110℃; for 18h;	62%

: 75-02-5
1-fluoroethylene

: 758-43-0
N-bromobis(trifluoromethyl)amine

: 371-71-1
Perfluoro-2-azapropen

Conditions

Conditions	Yield
20°C, 12 weeks, darkness;	61%
20°C, 12 weeks, darkness;	61%

: 75-02-5
1-fluoroethylene

: 420-25-7
1-bromo-1-fluoroethylene

Conditions

Conditions	Yield
With boron tribromide In dichloromethane at 20℃; under 1875.19 Torr; for 2h; Solvent; Temperature; Autoclave; Inert atmosphere;	61%

: 75-02-5
1-fluoroethylene

: 515-84-4
Ethyl trichloroacetate

: 77147-44-5
2,2,4-Trichloro-4-fluoro-butyric acid ethyl ester

Conditions

Conditions	Yield
copper(I) chloride In acetonitrile at 150℃; for 6h;	60%

: 23777-40-4
bis(triphenylphosphine)ethylenenickel(0)

: 75-02-5
1-fluoroethylene

: 25037-26-7
CH2CHFNi(P(C6H5)3)2

Conditions

Conditions	Yield
In diethyl ether byproducts: ethylene; react. in ether at room temp.;;	56%
In diethyl ether byproducts: ethylene; react. in ether at room temp.;;	56%

: 75-02-5
1-fluoroethylene

: 98-88-4
benzoyl chloride

: 3-Chloro-3-fluoro-1-phenyl-propan-1-one

Conditions

Conditions	Yield
With iron(III) chloride In dichloromethane at 0℃; for 3h;	50%

: 75-02-5
1-fluoroethylene

: 52548-14-8
2-iodoyl-5-methylbenzoic acid

: C10H9FO2

Conditions

Conditions	Yield
With sodium hydrogencarbonate In dimethyl sulfoxide at 20℃; for 6h; Inert atmosphere; Sealed tube; UV-irradiation; regioselective reaction;	50%

: 75-02-5
1-fluoroethylene

: 874-60-2
4-methyl-benzoyl chloride

: 3-Chloro-3-fluoro-1-p-tolyl-propan-1-one

Conditions

Conditions	Yield
With iron(III) chloride In dichloromethane at 0℃; for 3h;	49%

VINYL FLUORIDE Chemical Properties

Molecular formula: C₂H₃F
Molar mass: 46.04 g/mol
Appearance: Colorless gas with a faint, ethereal odor
Density: 2 g/cm³ (gas); 0.91 g/cm³ (liquid)
Melting point: -160.5 °C (-257 °F)
Boiling point: -72.2 °C (98 °F)
Solubility in water: Slightly soluble
Vapor pressure: 25 500 kPa
Other names: Fluoroethylene, Vinylfluoride, Vinyl fluoride monomer, Monofluoroethylene, VF, R 1141, UN 1860 (inhibited)
Vinyl fluoride(75-02-5) is an organic halide with the chemical formula CH₂＝CHF. It is a colorless gas with a faint etherlike odor.
The Structure of Vinyl fluoride(75-02-5):

VINYL FLUORIDE History

Vinyl fluoride(75-02-5) was first prepared in 1901 by Frédéric Swarts (the Belgian chemist who was the first to prepare CFCs in 1892) using the reaction of zinc with 1,1-difluoro-2-bromoethane. Now it is synthesized by the reaction of acetylene and hydrogen fluoride.

VINYL FLUORIDE Uses

The principal use of Vinyl fluoride(75-02-5) is as the primary component in making polyvinyl fluoride, a polymer of the basic vinyl fluoride monomer.

VINYL FLUORIDE Production

Vinyl fluoride (75-02-5), the monomer for poly(vinyl fluoride), is manufactured by addition of hydrogen fluoride to acetylene:
HC≡CH + HF →CH₂＝CHF

VINYL FLUORIDE Toxicity Data With Reference

1.		otr-rat-ihl		ARTODN Archives of Toxicology. 47 (1981),71.
2.		mnt-mus-ihl		EMMUEG Environmental and Molecular Mutagenesis. 19 (Suppl 20)(1992),5.

VINYL FLUORIDE Consensus Reports

NTP 10th Report on Carcinogens. Reported in EPA TSCA Inventory.

VINYL FLUORIDE Safety Profile

Confirmed carcinogen. A poison. Mutation data reported. A very dangerous fire hazard. To fight fire, stop flow of gas. When heated to decomposition it emits toxic fumes of F⁻. See also FLUORIDES.
Hazard Codes:

F
Risk Statements: 12-40
12: Extremely Flammable
40: Limited evidence of a carcinogenic effect
Safety Statements: 9-16-23-36/37/39
9: Keep container in a well-ventilated place
16: Keep away from sources of ignition - No smoking
23: Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer)
36/37/39: Wear suitable protective clothing, gloves and eye/face protection
RIDADR: 1860
Hazard Note: Flammable
HazardClass: 2.1

VINYL FLUORIDE Standards and Recommendations

ACGIH TLV: TWA 1 ppm; Suspected Human Carcinogen
NIOSH REL: (Vinyl Chloride) TWA 1 ppm; CL 5 ppm/15M
DOT Classification: 2.1; Label: Flammable Gas

Product Name

VINYL FLUORIDE

Synthetic route

VINYL FLUORIDE Chemical Properties

VINYL FLUORIDE History

VINYL FLUORIDE Uses

VINYL FLUORIDE Production

VINYL FLUORIDE Toxicity Data With Reference

VINYL FLUORIDE Consensus Reports

VINYL FLUORIDE Safety Profile

VINYL FLUORIDE Standards and Recommendations

Related Products

Hot Products