Tetrafluoroethylene Basic information Product Name: Tetrafluoroethylene Synonyms: TETRAFLUOROETHYLENE;1,1,2,2-Tetrafluoroethylene;C2F4;Ethene,tetrafluoro-;Ethylene,
The above product is Ality Chemical's strong item with best price, good quality and fast supply. Ality Chemical has been focusing on the research and production of this field for over 14 years. At the same time, we are always committed to providi
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inquirySuperior quality, moderate price & quick delivery. Appearance:white powder Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Application:Used as Pharmaceuti
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inquiryProduct Name: Tetrafluoroethylene Synonyms: TETRAFLUOROETHYLENE;1,1,2,2-Tetrafluoroethylene;C2F4;Ethene,tetrafluoro-;Ethylene, tetrafluoro-;ethylene,tetrafluoro-;ethylenetetrafluoride;Fluoroplast 4 CAS: 116-14-3 MF: C2F4
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryBest service,high quality and cheap price. Storage:Keep away from heat,sparks and flames. Package:25kg/50kg/200kg drum or Customer demand Application:Used as pharmaceutical intermediates Transportation:BY sea/air or by courier
R & D enterprises have their own stock in stock Package:1kg Application:pharmaceutical intermediates
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inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
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inquiryTIANFUCHEM--High purity 116-14-3 Tetrafluoroethylene Application:TIANFUCHEM--High purity 116-14-3 Tetrafluoroethylene
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TIANFUCHEM--High purity 116-14-3 TetrafluoroethyleneAppearance:powder Storage:room tempurature Package:As required Application:medical Transportation:By express (Door to door) such as FEDEX, DHL, EMS for small amount. By air(airport to airport) or by
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inquiryGood quality, Competitive price Tetrafluoroethylene 116-14-3 Port:shanghai,ningbo,tianjin,qingdao
Henan Sunlake Enterprise Corporation Our Advantages 1, Any inquiry about ch
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propene
1,1,2,2,3,3-Hexafluoro-cyclopropane
A
polytetrafluoroethylene
B
1,1-difluoro-2-methylcyclopropane
C
Octafluorocyclobutane
D
1,1,2,2-tetrafluoro-3-methylcyclobutane
Conditions | Yield |
---|---|
at 296℃; for 1h; sealed tube in vacuo; | A 16% B 100% C 9% D 21% |
at 296℃; sealed tube in vacuo; | A 16% B 100% C 9% D 21% |
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
A
polytetrafluoroethylene
B
pentafloropropylene
C
1,1,2,2,3,3-Hexafluoro-cyclopropane
D
Octafluorocyclobutane
Conditions | Yield |
---|---|
at 300℃; for 160h; Further byproducts given; | A 28% B 100% C 6% D 12% |
Conditions | Yield |
---|---|
With hydrogen at 336.84 - 736.84℃; Product distribution / selectivity; Gas phase; Inert atmosphere; | 100% |
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
cyclohexene
A
polytetrafluoroethylene
B
pentafloropropylene
C
Octafluorocyclobutane
D
7,7-difluoronorcarane
Conditions | Yield |
---|---|
at 200℃; for 320h; Further byproducts given; | A 14% B 99% C n/a D 47% |
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
cyclohexene
A
polytetrafluoroethylene
B
pentafloropropylene
C
carbon monoxide
D
Octafluorocyclobutane
E
7,7-difluoronorcarane
F
silicon tetrafluoride
Conditions | Yield |
---|---|
With Pyrex tube at 200℃; for 320h; Product distribution; Mechanism; further periods of contact time, other temperatures; | A 14% B 99% C 11% D n/a E 47% F 13% |
Conditions | Yield |
---|---|
at 300℃; Pyrolysis; | 98% |
Conditions | Yield |
---|---|
With sodium dithionite; Allyl ether; sodium hydrogencarbonate In water; acetonitrile at 20℃; for 0.0833333h; | 97% |
polytetrafluoroethylene
Conditions | Yield |
---|---|
at 630 - 650℃; under 0.6 - 2 Torr; for 0.5h; | 96% |
Conditions | Yield |
---|---|
With high nickel alloy at 420 - 955℃; for 6.94444E-05h; Temperature; | 95.2% |
In gas Product distribution; Irradiation; dependence on pressure and light intensity; | |
Pyrolysis; |
Conditions | Yield |
---|---|
at 300℃; Pyrolysis; | 91.3% |
Conditions | Yield |
---|---|
With sodium; ethyl acetoacetate In ethanol; N,N-dimethyl-formamide at 60℃; for 5h; | 91.2% |
chloroethylene
1,1,2,2,3,3-Hexafluoro-cyclopropane
A
polytetrafluoroethylene
B
Octafluorocyclobutane
C
1,1-difluoro-2-chlorocyclopropane
Conditions | Yield |
---|---|
at 294℃; for 1h; sealed tube in vacuo; | A 91% B 19% C 55% |
Conditions | Yield |
---|---|
In methanol at 50℃; | 91% |
With triethylchlorogermane; hexaethylphosphoric triamide In dichloromethane at -50 - 20℃; | 85% |
With zinc In ethanol |
Conditions | Yield |
---|---|
With Acetyl bromide for 0.0833333h; | A 64% B 91% |
Conditions | Yield |
---|---|
With Allyl ether; sodium; ethyl acetoacetate In ethanol; N,N-dimethyl-formamide at 60℃; for 5h; | 90.5% |
With cadmium In acetonitrile for 2h; | |
at 0℃; Mechanism; Irradiation; other temperatures, other excitation energies; |
pyrographite
trifluorophosphane
A
polytetrafluoroethylene
B
carbon tetrafluoride
Conditions | Yield |
---|---|
In neat (no solvent) react. of C with PF3 in a Ni-tube at 1100°C;; | A 90% B 9% |
Conditions | Yield |
---|---|
byproducts: N2; Irradiation (UV/VIS); irradn. with UV lamp at 25°C (2.5 h); | 90% |
1-dichloromethylene-2,2-difluoro-3,3-bis(trifluoromethyl)cyclopropane
A
polytetrafluoroethylene
B
1,1-dichloro-4,4,4-trifluoro-3-trifluoromethylbuta-1,2-diene
Conditions | Yield |
---|---|
at 550℃; under 2 Torr; Yields of byproduct given; | A n/a B 87% |
Conditions | Yield |
---|---|
In dichloromethane | A 50% B 86% |
1-Chloro-2,2-difluoroethene
A
polytetrafluoroethylene
B
Vinylidene fluoride
C
1,1,2-trifluoroethylene
Conditions | Yield |
---|---|
With hydrogen sulfide Product distribution; Irradiation; added CH3OH or alone; | A 6% B 82% C 12% |
(trifluoro methyl) magnesiumiodide
A
polytetrafluoroethylene
B
difluoro-methylene
C
trifluoromethan
Conditions | Yield |
---|---|
In diethyl ether decomposition under reflux in ether;; | A 6% B n/a C 81% |
In diethyl ether decomposition under reflux in ether;; | A 6% B n/a C 81% |
Tris(trifluormethyl)-difluorphosphoran
A
polytetrafluoroethylene
B
difluoro-methylene
C
1,1,2,2,3,3-Hexafluoro-cyclopropane
Conditions | Yield |
---|---|
120°C (24 h); | A 10% B 10% C 80% |
200°C (10 min); | A 80% B 10% C 10% |
120°C (24 h); | A 10% B 10% C 80% |
200°C (10 min); | A 80% B 10% C 10% |
1,2-dibromo-1,1,2,2-tetrafluoroethane
diethylamine
phosphonic acid diethyl ester
A
polytetrafluoroethylene
B
diethyl-amidophosphoric acid diethyl ester
Conditions | Yield |
---|---|
at 0 - 20℃; Todd-Atterton reaction; | A n/a B 73% |
ethene
1,1,2,2,3,3-Hexafluoro-cyclopropane
A
polytetrafluoroethylene
B
2,2-difluorocyclopropane
C
1,1,2,2-tetrafluorocyclobutane
D
Octafluorocyclobutane
Conditions | Yield |
---|---|
at 300℃; for 4h; sealed tube in vacuo; | A 16% B 68% C 63% D 15% |
trifluoromethyltrimethylsilane
A
polytetrafluoroethylene
B
(difluoromethyl)fluorosilane
Conditions | Yield |
---|---|
With fluorosilane at 102℃; for 2h; | A n/a B 67% |
Conditions | Yield |
---|---|
With dibromodifluoromethane; triphenylphosphine; zinc In N,N-dimethyl-formamide at 20℃; | 67% |
1,2-dibromo-1,1,2,2-tetrafluoroethane
phosphonic acid bis-(2,2,3,3-tetrafluoro-propyl) ester
diethylamine
A
polytetrafluoroethylene
Conditions | Yield |
---|---|
at 0 - 20℃; Todd-Atterton reaction; | A n/a B 65.3% |
polytetrafluoroethylene
Conditions | Yield |
---|---|
With Acetyl bromide In various solvent(s) Ambient temperature; | 64% |
1-chloro-1,1,2,2-tetrafluoro-2-iodo-ethane
Allyl ether
ethyl acetoacetate
A
polytetrafluoroethylene
Conditions | Yield |
---|---|
With sodium In ethanol; N,N-dimethyl-formamide at 60℃; for 5h; | A 63.7% B 19.1% |
perfluorocetane
A
polytetrafluoroethylene
B
perfluoropropylene
C
octafluoro-1-butene
Conditions | Yield |
---|---|
at 195 - 500℃; under 75.7576 Torr; Temperature; Pressure; Pyrolysis; | A 62.4% B 24.3% C 6.2% |
polytetrafluoroethylene
(1,1,2,2-tetrafluoroethyl)trifluorosilane
A
pentafloropropylene
B
1,1,2,2,3,3-Hexafluoro-cyclopropane
C
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
D
silicon tetrafluoride
Conditions | Yield |
---|---|
at 150℃; for 18h; Further byproducts given; | A 5% B n/a C 74% D 100% |
at 200℃; for 10h; Further byproducts given; | A 19% B n/a C 71% D 98% |
Conditions | Yield |
---|---|
With oxygen at 200 - 370℃; for 0.00166667h; Product distribution / selectivity; | 100% |
With triplet molecular oxygen; sulphur hexafluoride under 202.5 - 525.04 Torr; Product distribution; Mechanism; Irradiation; various ratio of all the components; |
Conditions | Yield |
---|---|
With ozone at -33.15 - 16.85℃; | 100% |
polytetrafluoroethylene
allyl(cyclopentadiene)palladium(II)
1,4-bis(dicyclohexylphosphino)butane
(η2-tetrafluoroethylene)Pd(1,4-bis(dicyclohexylphosphino)butane)
Conditions | Yield |
---|---|
In toluene at 20℃; under 760.051 Torr; for 3h; Inert atmosphere; | 100% |
polytetrafluoroethylene
bis(1,5-cyclooctadiene)nickel (0)
1,4-bis(dicyclohexylphosphino)butane
(η2-tetrafluoroethylene)Ni(1,4-bis(dicyclohexylphosphino)butane)
Conditions | Yield |
---|---|
In toluene at 20℃; under 760.051 Torr; for 4.5h; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
With triphenylphosphine In toluene at 20℃; for 0.5h; Autoclave; Inert atmosphere; | 100% |
polytetrafluoroethylene
bis(1,5-cyclooctadiene)nickel (0)
ethene
C40H30F8NiP2
Conditions | Yield |
---|---|
With triphenylphosphine In toluene at 20℃; for 0.25h; Autoclave; Inert atmosphere; | 100% |
polytetrafluoroethylene
bis(1,5-cyclooctadiene)nickel (0)
ethene
triphenylphosphine
Conditions | Yield |
---|---|
In benzene-d6 at 20℃; under 1875.19 Torr; Glovebox; | 100% |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); tricyclohexylphosphine In benzene-d6 at 20℃; under 1875.19 - 3750.38 Torr; for 10h; Glovebox; | 100% |
polytetrafluoroethylene
2,2,3,3,3-pentafluoropropyl alcohol
1,1,1,2,2-pentafluoro-3-(1,1,2,2-tetrafluoroethoxy)propane
Conditions | Yield |
---|---|
With potassium hydroxide In water at 75 - 85℃; under 5250.53 - 6000.6 Torr; Inert atmosphere; Autoclave; | 99.8% |
polytetrafluoroethylene
fluorosulfonyl fluoride
A
bis(pentafluoroethyl)diselane
B
bis(pentafluoroethyl) triselenide
Conditions | Yield |
---|---|
20 atm, 100°C, 3 d; | A 99% B <1 |
polytetrafluoroethylene
A
bis(pentafluoroethyl)diselane
B
bis(pentafluoroethyl) triselenide
Conditions | Yield |
---|---|
10 atm, 100°C, 3 d; | A 99% B <1 |
Conditions | Yield |
---|---|
With pyridine In toluene poured through a soln. of OsO4 in toluene and pyridine at 25°C, few minutes; pptd., solvent removed, dried in vacuo, elem. anal.; | 99% |
With pyridine In pyridine; toluene passing olefine through reagent soln. from toluene, OsO4 and pyridine to olefine, room temp., 2h; pptn.; evapn.; recrystn. (toluene/dichlormethane); elem. anal.; | >99 |
polytetrafluoroethylene
allyl(cyclopentadiene)palladium(II)
1,2-bis-(dicyclohexylphosphino)ethane
(η2-tetrafluoroethylene)Pd(1,2-bis(dicyclohexylphosphino)ethane)
Conditions | Yield |
---|---|
In toluene at 20℃; under 760.051 Torr; for 3h; Inert atmosphere; | 99% |
polytetrafluoroethylene
bis(1,5-cyclooctadiene)nickel (0)
tris(1-methylethyl)phosphine
(η2-tetrafluoroethylene)Ni(triisopropylphosphine)2
Conditions | Yield |
---|---|
In toluene at 20℃; under 760.051 Torr; for 16h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With bis(1,5-cyclooctadiene)nickel (0); tricyclohexylphosphine In toluene at 40℃; under 2280.15 Torr; for 1h; Catalytic behavior; Solvent; Reagent/catalyst; Time; Autoclave; | 99% |
Conditions | Yield |
---|---|
With potassium hydroxide In N,N-dimethyl-formamide at 20℃; under 1520.1 Torr; for 1h; Inert atmosphere; | 99% |
Conditions | Yield |
---|---|
With 1,4-diaza-bicyclo[2.2.2]octane; dmap; DBN; 1,8-diazabicyclo[5.4.0]undec-7-ene at 50 - 70℃; for 0.005h; | 98.9% |
With sodium n-propoxide |
polytetrafluoroethylene
2,2,3,3-tetrafluoropropanol
1,1,2,2-tetrafluoro-3-(1,1,2,2-tetrafluoroethoxy)propane
Conditions | Yield |
---|---|
With potassium hydroxide In water at 75 - 95℃; under 5625.56 - 6000.6 Torr; for 8.5h; Product distribution / selectivity; Inert atmosphere; Autoclave; | 98.5% |
With sodium In 1,4-dioxane | |
With potassium hydroxide In N,N-dimethyl-formamide | |
With potassium hydroxide In water at 20 - 95℃; under 750.075 - 6000.6 Torr; Product distribution / selectivity; Inert atmosphere; Industry scale; Autoclave; |
polytetrafluoroethylene
2,2,2-trifluoroethanol
1,1,2,2-Tetrafluoro-1-(2,2,2-trifluoroethoxy)-ethane
Conditions | Yield |
---|---|
potassium hydroxide In diethylene glycol dimethyl ether; water at 50℃; under 1500.15 Torr; for 4.8h; Product distribution / selectivity; Cooling with liquid nitrogen; | 98% |
potassium hydroxide In Tetraethylene glycol dimethyl ether; water at 50℃; under 1500.15 Torr; for 0.33 - 1.25h; Product distribution / selectivity; Cooling with liquid nitrogen; | 97% |
potassium hydroxide In Tetraethylene glycol dimethyl ether; water at 60℃; under 3750.38 Torr; for 10h; Product distribution / selectivity; | 94% |
polytetrafluoroethylene
dimethyl amine
1,1,2,2-tetrafluoro-N,N-dimethylethan-1-amine
Conditions | Yield |
---|---|
at 20℃; for 12h; | 98% |
at -70℃; |
polytetrafluoroethylene
bis(trifluoromethyl)phosphine
Tetrafluorethylbis-trifluormethyl-phosphin
Conditions | Yield |
---|---|
Irradiation (UV/VIS); time of irradiation:1 h; | 98% |
Irradiation (UV/VIS); time of irradiation:1 h; | 98% |
Irradiation (UV/VIS); time of irradiation:20 h; | 83% |
Irradiation (UV/VIS); time of irradiation:20 h; | 83% |
Irradiation; |
polytetrafluoroethylene
(1,1,2,2-tetrafluoroethyl)trifluorosilane
A
pentafloropropylene
B
1,2,2,3,3-pentafluoro-1-difluoromethylcyclopropane
C
silicon tetrafluoride
D
1,1,2-trifluoroethylene
Conditions | Yield |
---|---|
at 200℃; for 10h; Further byproducts given; | A 19% B 71% C 98% D 8% |
polytetrafluoroethylene
1,10-Phenanthroline
2-methoxy-4-nitrophenol
mesitylcopper(I)
Conditions | Yield |
---|---|
Stage #1: 1,10-Phenanthroline; 2-methoxy-4-nitrophenol; mesitylcopper(I) In tetrahydrofuran at 20℃; Autoclave; Inert atmosphere; Stage #2: polytetrafluoroethylene In tetrahydrofuran at 40℃; under 2660.18 Torr; for 24h; Inert atmosphere; | 98% |
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