As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
Cas:116-15-4
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inquiryThe 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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Cas:116-15-4
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inquiryProduct Name: Hexafluoropropylene Synonyms: 1,1,2,3,3,3-hexafluoro-1-propen;1-Propene, 1,1,2,3,3,3-hexafluoro-;1-Propene,1,1,2,3,3,3-hexafluoro-;CF3CF=CF2;Hexafluofoproene;hexafluoro-propen;hexafluoropropene(hfp);hexafluoro-propylen
Cas:116-15-4
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inquiryHangzhou KeyingChem Co., Ltd. exported this product to many countries and regions at best price. If you are looking for the material’s manufacturer or supplier in China, KeyingChem is your best choice. Pls contact with us freely for getting det
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
Zibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
Cas:116-15-4
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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:25kg/drum, or as per your request. Application:Used as Pharmaceutical Intermediates Tr
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inquiryName: Hexafluoropropylene. English synonyms: 3pyrus, Hexafluofoproenex, CF3CF2x Hexafluofoproenetic, CF2CF2x Hexafluofoproeneenex, Hexafluoroflypropene, Perfluoropropafopropyllimel, proenetic, HFP (hexafluoropropylene). CAS: 116-15-4. Molecul
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inquiryAppearance:95%+ Package:R&D,Pilot run Transportation:per client require Port:Express ,Air, Sea
Best quality, Best price and Best service Appearance:Colorless gas Application:1.A variety of fluorine-containing fine chemical products, drug intermediates, fire extinguishing agents, and fluorine-containing polymer materials can also be prepared
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
Best 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
high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
Our clients, like BASF,CHEMO,Brenntag,ASR,Evonik,Merck and etc.Appearance:COA Storage:in stock Application:MSDS/TDS
hexafluoropropylene(Perfluoropropene;1,1,2,3,3,3-hexafluoro-1-propene),cas:116-15-4 from fandachem Application:fine chemical Transportation:by air,by sea,by express
Cas:116-15-4
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inquiryProduct Description Description & Specification Category Pharmaceutical Raw Materials, Fine Chemicals, Bulk drug Standard Medical standard
Cas:116-15-4
Min.Order:1 Kilogram
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inquiryAnsciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:Foil bag; Drum; Plastic bottle Application:Pharma;Industry;Agricultural Transportation:by sea or air Port:any port in China
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inquiry1.Professional synthesis laboratory and production base. 2.Strong synthesis team and service team. 3.Professional data management system. 4.We provide the professional test date and product information ,ex. HNMR ,CNMR,FNMR, HPLC/G
Cas:116-15-4
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inquiryHexafluoropropylene Basic information Product Name: Hexafluoropropylene Synonyms: 1,1,2,3,3,3-hexafluoro-1-propen;1-Propene, 1,1,2,3,3,3-hexafluoro-;1-Propene,1,1,2,3,3,3-hexafluoro-;CF3CF=CF2;Hexafluofop
1. Subsidiary of Institute of Chemistry, Henan Academy of Sciences, national research platform;2. About 30 years’ experience in this field since 1983;3. An experienced R&D team consisting of Doctors and Masters;4. Various types of analytical instrume
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inquiryBaiFuChem is a Professional chemical raw material supplier in China, our main products include Biochemical , Pharma Intermediate and Organic chemical etc. BaiFuChem have wealth of products,experience , expertise and state-of-the-art
Our company is committed to the research and development, production and sales of bulk drugs and their intermediates, fine chemicals.Appearance:See details Storage:Room temperature Package:See details Application:Pharmaceutical intermediates Transpor
Cas:116-15-4
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inquirysub/micron to mesh powders (near/spheres, whiskers, flake, fiber, porous) and grain/ball, thin/ thick metal / alloys pieces / parts, thin and thick (particle) film materials /target, and custom-made crystals, substrates/parts. In the industries and a
high quality and competitive priceAppearance:colorless Storage:dry,cool Package:UN drum Application:intermediate Transportation:FOB or CIF
.Name:Hexafluoropropylene(Othernames:Perfluoropropene;1-Propene,1,1,2,3,3,3-hexafluoro-)2.MF:C3F63.Usage:Itisoneoftheimportantfluorinatedmonomerwithhi…Appearance:GAS Storage:storage in cool and dry place,far away Package:800kg/800L, 1000kg/1000L cyli
Cas:116-15-4
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inquiryConditions | Yield |
---|---|
With silicon carbide at 450 - 850℃; for 3.33333E-05h; | 96.5% |
at 760 - 860℃; unter vermindertem Druck; | |
at 700℃; bei der thermischen Zersetzung; |
Conditions | Yield |
---|---|
In further solvent(s) decomposition on boiling in dibutyl ether;; | A 76% B 6% |
In further solvent(s) decomposition on boiling in dibutyl ether;; | A 76% B 6% |
Conditions | Yield |
---|---|
In diethyl ether warming from -78 to 20°C and heating under reflux, 1 hour;; | 70.5% |
In diethyl ether warming from -78 to 20°C and heating under reflux, 1 hour;; | 70.5% |
perfluoro-2-methylpentan-3-one
A
perfluoropropylene
B
perfluoropropanoyl fluoride
Conditions | Yield |
---|---|
With cesium fluoride at 250℃; for 2h; Product distribution; | A 68% B n/a |
ethyl heptafluoroisobutyrate
phenyllithium
A
perfluoropropylene
B
benzoic acid ethyl ester
C
perfluoroisopropyl phenyl ketone
Conditions | Yield |
---|---|
In diethyl ether at -110℃; for 0.166667h; C6H5Li added to ester; | A n/a B n/a C 65% |
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% |
1,2-dibromohexafluoropropane
A
1-bromo-1,1,2,3,3,3-hexafluoro-propane
B
perfluoropropylene
C
1,1,1,2,3,3-hexafluoropropane
D
2-bromo-1,1,1,2,3,3-hexafluoro-propane
Conditions | Yield |
---|---|
With tri-n-butyl-tin hydride for 1.5h; Product distribution; Heating; | A 53% B 3% C 14% D 21% |
Conditions | Yield |
---|---|
at 195 - 600℃; under 75.7576 Torr; Temperature; Pressure; Pyrolysis; | A 50.3% B 28.9% |
methane
Octafluorocyclobutane
A
polytetrafluoroethylene
B
perfluoropropylene
C
Vinylidene fluoride
D
2,3,3,3-tetrafluoro-propene
E
1,1,2-trifluoroethylene
Conditions | Yield |
---|---|
at 250 - 800℃; under 150.015 Torr; for 0.000175h; Temperature; | A 45.8% B 7.4% C 10.4% D 8.4% E 9.5% |
perfluorocetane
A
polytetrafluoroethylene
B
perfluoropropylene
C
Octafluorocyclobutane
Conditions | Yield |
---|---|
at 195 - 550℃; under 75.7576 Torr; Temperature; Pressure; Pyrolysis; | A 36.1% B 42.7% C 6.1% |
2-chloroundecafluoro-2-methyl-3-pentanone
A
perfluoropropylene
B
perfluoropropanoyl fluoride
C
perfluoro-2-methylpentan-3-one
Conditions | Yield |
---|---|
With cesium fluoride In diethylene glycol dimethyl ether for 1h; Product distribution; Heating; | A n/a B n/a C 38% |
heptafluoro-butyric acid iodoamide
A
HFC-227ca
B
perfluoropropylene
C
1,1,2,2,3,3-Hexafluoro-cyclopropane
Conditions | Yield |
---|---|
With sodium hydroxide byproducts: NH3; boiled in 30% NaOH for 5h; | A 38% B n/a C n/a |
With NaOH byproducts: NH3; boiled in 30% NaOH for 5h; | A 38% B n/a C n/a |
perfluorocetane
A
polytetrafluoroethylene
B
perfluoropropylene
C
octafluoro-1-butene
D
Octafluorocyclobutane
Conditions | Yield |
---|---|
at 195 - 450℃; under 75.7576 Torr; Temperature; Pressure; Pyrolysis; | A 32.5% B 16.5% C 9.2% D 8.2% |
perfluoroallylfluorosulphate
perfluoropropylene
Conditions | Yield |
---|---|
With Trimethyl borate; sulfur trioxide at 25℃; for 168h; | 30% |
With cesium fluoride In 1,2-dimethoxyethane at 20℃; | 25.5% |
sodium cyanide
perfluoroallylfluorosulphate
A
fluorosulfonyl fluoride
B
perfluoropropylene
C
methyl fluorosulfonate
D
2,2,3,4,4-pentafluorobut-3-ene nitrile
E
2,3,3-trifluoroacryloyl fluoride
F
sulfur dioxide
Conditions | Yield |
---|---|
In acetonitrile at -10 - 4.4℃; for 4.5h; Temperature; Inert atmosphere; | A n/a B n/a C n/a D 27% E n/a F n/a |
perfluoroallylfluorosulphate
tetra-n-butylammonium cyanide
A
fluorosulfonyl fluoride
B
Carbonyl fluoride
C
perfluoropropylene
D
2,2,3,4,4-pentafluorobut-3-ene nitrile
E
silicon tetrafluoride
Conditions | Yield |
---|---|
In dichloromethane at -20 - 20℃; for 4h; Solvent; Inert atmosphere; | A n/a B n/a C n/a D 22% E n/a |
Conditions | Yield |
---|---|
With hydrogen; NiCl2 on activated carbon at 250 - 300℃; for 0.00161111 - 0.00305556h; | 21.6% |
sodium cyanide
Triethylene glycol dimethyl ether
perfluoroallylfluorosulphate
A
fluorosulfonyl fluoride
B
perfluoropropylene
C
hydrogen cyanide
D
Dimethyl ether
E
ethanedinitrile
F
methyl fluorosulfonate
G
methyl-pentafluoroallyl ether
H
2,2,3,4,4-pentafluorobut-3-ene nitrile
I
2,3,3-trifluoroacryloyl fluoride
J
sulfur dioxide
K
fluorosulphonic acid
L
silicon tetrafluoride
Conditions | Yield |
---|---|
at -10 - 60℃; for 2.5h; Temperature; Inert atmosphere; | A n/a B n/a C n/a D n/a E n/a F n/a G n/a H 18% I n/a J n/a K n/a L n/a |
trifluoromethan
A
polytetrafluoroethylene
B
carbon tetrafluoride
C
freon-218
D
perfluoropropylene
E
Hexafluoroethane
Conditions | Yield |
---|---|
With activated carbon supported potassium at 799.84℃; under 750.075 Torr; Pyrolysis; Inert atmosphere; | A 16.1% B n/a C n/a D 14.4% E n/a |
Conditions | Yield |
---|---|
at 300℃; Reaktion des Natrium-Salzes; | |
at 235℃; Reaktion des Kalium-Salzes; | |
at 275℃; Reaktion des Barium-Salzes; |
Conditions | Yield |
---|---|
at 300 - 320℃; Reaktion des Silber-Salzes.Pyrolysis; |
heptafluorobutyric Acid
A
perfluoropropylene
B
perfluorobutyryl fluoride
C
heptafluorobutyric anhydride
Conditions | Yield |
---|---|
Pyrolyse von Lithium-, Calcium-, Strontium-, Blei- und Aluminium-Salz.Pyrolysis; |
Conditions | Yield |
---|---|
at 25℃; |
Conditions | Yield |
---|---|
With acetic acid; zinc at 25℃; | |
With ethanol; zinc |
Conditions | Yield |
---|---|
at 700℃; Pyrolysis; |
polytetrafluoroethylene
A
perfluoropropylene
B
Hexafluoroethane
C
perfluoroisobutylene
D
Octafluorocyclobutane
Conditions | Yield |
---|---|
at 600℃; Dimerisierung.Pyrolysis; | |
at 650℃; Dimerisierung.Pyrolysis; |
polytetrafluoroethylene
A
perfluoropropylene
B
octafluoro-2-butene
Conditions | Yield |
---|---|
at 700℃; | |
at 700℃; |
Conditions | Yield |
---|---|
With ethanol; zinc at 40℃; | |
With ethanol; zinc at 100℃; unter Druck; |
perfluoropropylene
adamantane-1,3-dicarboxylic acid
5-(1,1,2,3,3,3-Hexafluoro-propyl)-adamantane-1,3-dicarboxylic acid
Conditions | Yield |
---|---|
In acetic acid at 20℃; for 20h; Product distribution; Irradiation; var. time, var. temp., var. solvents, var. absorbed dose; | 100% |
In acetic acid at 70℃; for 20h; Irradiation; | 100% |
perfluoropropylene
1,2-diamino-benzene
2-(α-hydro-tetrafluoroethyl)benzimidazole
Conditions | Yield |
---|---|
With potassium fluoride In N,N-dimethyl-formamide | 100% |
With diethylamine In ethyl acetate at 7 - 12℃; for 1.25 - 2.5h; | 85% |
In ethyl acetate at 75℃; under 3000.3 - 9750.98 Torr; for 18h; Solvent; Autoclave; | 75% |
Conditions | Yield |
---|---|
With ozone at -33.15 - 16.85℃; | 100% |
palladium(0)bis(tricyclohexylphosphine)
perfluoropropylene
Conditions | Yield |
---|---|
In toluene at 20℃; under 2660.18 Torr; for 0.5h; Inert atmosphere; Autoclave; regioselective reaction; | 100% |
Conditions | Yield |
---|---|
With palladium/alumina; hydrogen at 59 - 121℃; under 1125.11 Torr; Pressure; Temperature; | 99.9% |
With hydrogen; Pd on alumina; corundum at 105 - 140℃; under 750.075 Torr; Product distribution / selectivity; | 95.2% |
With palladium Hydrogenation; |
perfluoropropylene
2,2,3,3-tetrafluoropropanol
1,1,1,2,3,3-hexafluoro-3-(2,2,3,3-tetrafluoropropoxy)propane
Conditions | Yield |
---|---|
With potassium hydroxide In water at 50 - 60℃; under 3000.3 - 3750.38 Torr; Inert atmosphere; Autoclave; | 99.8% |
With potassium hydroxide at 20 - 40℃; | 87% |
With potassium hydroxide | |
With potassium hydroxide In acetonitrile cooling; |
Conditions | Yield |
---|---|
With potassium fluoride; trifluoroacetic anhydride In diethylene glycol dimethyl ether | A 99.6% B n/a |
Conditions | Yield |
---|---|
With bromine at 100℃; Cooling with acetone-dry ice; | 99.41% |
With bromine at 20℃; for 19h; | 95% |
With bromine for 19h; | 95% |
Conditions | Yield |
---|---|
With potassium hydroxide at 20 - 40℃; | 99% |
With potassium hydroxide | |
(i) NaN3, (ii) Br2, aq. NaBr, (iii) Hg; Multistep reaction; |
porassium hydrogen difluoride
perfluoropropylene
Perfluoro pentanoyl fluoride
B
1,1,1,2,4,4,5,5,6,6,7,7,7-tridecafluoro-2-trifluoromethyl-heptan-3-one
Conditions | Yield |
---|---|
With potassium fluoride In diethylene glycol dimethyl ether | A n/a B 99% |
Conditions | Yield |
---|---|
Stage #1: perfluoropropylene With trimethylaminealane In benzene-d6 at 20℃; under 760.051 Torr; for 0.0833333h; Inert atmosphere; Schlenk technique; Stage #2: With trimethylaminealane In benzene-d6 at 40℃; for 72h; Inert atmosphere; Schlenk technique; | 98.7% |
With trimethylamin alane In benzene-d6 at 40℃; for 90h; | 98% |
With diisobutylaluminium hydride In diethylene glycol dimethyl ether at 20℃; for 19h; | 94.5% |
With palladium on activated charcoal; hydrogen at 120℃; Catalytic behavior; Reagent/catalyst; | |
With palladium on activated charcoal; hydrogen In neat (no solvent) at 120℃; under 750.075 Torr; |
Conditions | Yield |
---|---|
With potassium fluoride; 18-crown-6 ether In acetonitrile at 130℃; under 11026.1 Torr; for 4h; Temperature; Reagent/catalyst; Pressure; Flow reactor; Industrial scale; | 98.43% |
cesium fluoride In acetonitrile at 0℃; | 95% |
With Tetrakis(dimethylamino)ethylen for 24h; Ambient temperature; | 88% |
perfluoropropylene
perfluoropropanoyl fluoride
perfluoro-2-methylpentan-3-one
Conditions | Yield |
---|---|
With iron(III) trifluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave; | 98.2% |
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 95℃; under 1875.19 Torr; | |
at 160℃; under 750.075 Torr; for 10h; Gas phase; |
Conditions | Yield |
---|---|
With sodium for 1.5h; | 98% |
With 1,4-diaza-bicyclo[2.2.2]octane; dmap; DBN; 1,8-diazabicyclo[5.4.0]undec-7-ene In 1-methyl-pyrrolidin-2-one at 50℃; for 0.00277778h; | 95.9% |
With potassium hydroxide |
Conditions | Yield |
---|---|
cesium fluoride on NaF at 250℃; for 5h; | 98% |
cesium fluoride on NaF at 190℃; | 95% |
cesium fluoride on NaF at 190℃; | 95% |
perfluoropropylene
Conditions | Yield |
---|---|
With IOSO2F Ambient temperature; | 98% |
perfluoropropylene
5-Hydroxy-2-(4-nitrophenylazo)pyridine
[5-(1,1,2,3,3,3-Hexafluoro-propoxy)-pyridin-2-yl]-(4-nitro-phenyl)-diazene
Conditions | Yield |
---|---|
With potassium carbonate In acetonitrile at 22 - 36℃; for 0.5h; | 98% |
Conditions | Yield |
---|---|
In toluene at 20℃; under 2660.18 Torr; for 0.5h; Inert atmosphere; Autoclave; regioselective reaction; | 98% |
perfluoropropylene
1,3-bis(2,6-diisopropylphenyl)dihydroimidazol-2-ylidene
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; under 1277.21 Torr; Glovebox; Schlenk technique; Sealed tube; | 98% |
Conditions | Yield |
---|---|
at 50℃; for 5h; | 98% |
Conditions | Yield |
---|---|
With oxygen at 60℃; Temperature; | 98% |
perfluoropropylene
ethene
1,1,2-trifluoro-2-(trifluoromethyl)cyclobutane
Conditions | Yield |
---|---|
With 4-tert-Butylcatechol at 320 - 350℃; for 5h; Inert atmosphere; | 97.9% |
at 250℃; for 18h; |
perfluoropropylene
2,5-dichlorophenol
1,1,2,3,3,3-hexafluoropropoxy-2,5-dichlorobenzene
Conditions | Yield |
---|---|
With sodium hydroxide In dimethyl sulfoxide at 25℃; under 2250.23 Torr; Solvent; Reagent/catalyst; Temperature; Pressure; | 97.7% |
methanol
perfluoropropylene
1,1,2,3,3,3-hexafluoroisopropyl methyl ether
Conditions | Yield |
---|---|
With 1,3-bis-(diphenylphosphino)propane In acetonitrile at 80℃; under 1500.15 - 6000.6 Torr; for 20h; Reagent/catalyst; Solvent; Pressure; Temperature; Autoclave; | 97.7% |
perfluoropropylene
trifluoroacetyl fluoride
trifluoromethyl(perfluoroisopropyl)ketone
Conditions | Yield |
---|---|
With 15-crown-5; cobalt(II) fuoride In acetonitrile at 80℃; for 10h; Reagent/catalyst; Autoclave; | 97.5% |
With liquid phase catalyst Cat15 at 60℃; for 3h; Reagent/catalyst; Autoclave; Inert atmosphere; | 95.3% |
With potassium fluoride In diethylene glycol dimethyl ether at 100 - 110℃; for 8h; Autoclave; | 70% |
potassium fluoride In N,N-dimethyl-formamide at 80℃; for 11.17h; Product distribution / selectivity; | 54 - 84 %Chromat. |
With activated carbon BAU-A-2 supported 20 wtpercent CsF In neat (no solvent) at 65 - 130℃; under 1875.19 Torr; |
Carbonyl fluoride
perfluoropropylene
1,1,1,2,4,5,5,5-octafluoro-2,4-bis(trifluoromethyl)pentan-3-one
Conditions | Yield |
---|---|
With nickel(II) fluoride; 18-crown-6 ether In acetonitrile at 90℃; for 10h; Autoclave; | 97.2% |
With cesium fluoride In acetonitrile |
perfluoropropylene
2,2,3,4,4,4-hexafluoro-1-butanol
CF3CFHCF2CH2OCF2CFHCF3
Conditions | Yield |
---|---|
Stage #1: perfluoropropylene; 2,2,3,4,4,4-hexafluoro-1-butanol With potassium carbonate In acetonitrile at 40℃; Stage #2: With potassium hydrogen difluoride; adogen 464 In diethylene glycol dimethyl ether at 110℃; for 24h; | 97% |
Conditions | Yield |
---|---|
With hydrogenchloride In diethyl ether; acetonitrile at 20℃; under 3863.02 Torr; | 97% |
Conditions | Yield |
---|---|
Stage #1: perfluoropropylene; 4-isopropenylphenol With triethylamine at 40℃; for 3h; Stage #2: With calcium carbonate at 40℃; for 2h; | 96.7% |
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