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25291-17-2

  • Product Name(Perfluorohexyl)ethylene
  • Molecular FormulaC8H3 F13
  • Molecular Weight346.091
  • Purity99%
  • AppearanceColorless liquid.
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Product Details

Quick Details

  • CasNo: 25291-17-2
  • Molecular Formula: C8H3 F13
  • Appearance: Colorless liquid.
  • Purity: 99%

Buy Reliable Quality (Perfluorohexyl)ethylene 25291-17-2 Offer with Efficient Delivery

  • Molecular Formula:C8H3 F13
  • Molecular Weight:346.091
  • Appearance/Colour:Colorless liquid. 
  • Vapor Pressure:43.8mmHg at 25°C 
  • Refractive Index:n20/D 1.295(lit.) 
  • Boiling Point:99.5 °C at 760 mmHg 
  • Flash Point:20 ºC 
  • PSA:0.00000 
  • Density:1.52 
  • LogP:4.91120 

(Perfluorohexyl)ethylene(Cas 25291-17-2) Usage

Chemical Properties

clear colorless liquid

Flammability and Explosibility

Notclassified

InChI:InChI=1/C8H3F13/c1-2-3(9,10)4(11,12)5(13,14)6(15,16)7(17,18)8(19,20)21/h2H,1H2

25291-17-2 Relevant articles

Parahydrogen-induced polarization transfer to 19F in perfluorocarbons for 19F NMR spectroscopy and MRI

Plaumann, Markus,Bommerich, Ute,Trantzschel, Thomas,Lego, Denise,Dillenberger, Sonja,Sauer, Grit,Bargon, Joachim,Buntkowsky, Gerd,Bernarding, Johannes

, p. 6334 - 6339 (2013)

Fluorinated substances are important in ...

RADICAL SYNTHESIS OF PERFLUORO-n-HEXYL-2-ETHANOL

Signe, E.,Blancou, H.,Benefice-Malouet, S.,Itier, J.

, p. 289 (1991)

-

SYNTHESE DE PERFLUORO-nHEXYL-2 ETHANOL C6F13C2H4OH PAR REDUCTION ELECTROCHIMIQUE SUR FIBRES DE CARBONE DE PERFLUORO-nHEXYL-2 IODO-1 ETHANE C6H13C2H4I DANS LE SOLVANT N,N DIMETHYLFORMAMIDE

Benefice-Malouet, S.,Blancou, H.,Calas, P.,Commeyras, A.

, p. 245 - 260 (1988)

Electrochemical reduction of 2-perfluoro...

Fluorinated imidazolium salts having liquid crystal characteristics

Zama, Isabella,Gorni, Giacomo,Borzatta, Valerio,Cassani, Maria Cristina,Crupi, Cristina,Di Marco, Gaetano

, p. 749 - 753 (2016)

A family of fluorinated imidazolium salt...

2-(Perfluoroalkyl)ethanols by thermal alkylation of ambidentate lactams with 2-(perfluoroalkyl)-1-iodoalkanes, in the presence of added water. A change in mechanism and stoichiometry of the reaction. Isolation of a water adduct of the lactim ether intermediate

Brace

, p. 6504 - 6516 (1996)

Thermal alkylation of amides by an alkyl...

Quaternary ammonium ionic liquids containing fluorous ponytails: Competitive alkylation and elimination reactions of I(CH2) nRf (n = 2, 3) with tertiary amines

Alhanash, Hana B.,Brisdon, Alan K.

, p. 152 - 157 (2013)

The formation of quaternary ammonium iod...

Study of the alkylation of chlorosilanes. Part III. Synthesis and reactivity of new fluorinated organolithium reagents

Boutevin, B.,Guida-Pietrasanta, F.,Ratsimihety, A.,Caporiccio, G.

, p. 53 - 58 (1995)

The effect of the structure of the fluor...

Method for synthesizing perfluoroalkyl ethylene

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Paragraph 0028-0030, (2018/02/04)

The invention provides a method for synt...

25291-17-2 Process route

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane
2043-57-4,71215-70-8

1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane

1H,1H,2H,2H-tridecafluoro-n-octanol
647-42-7

1H,1H,2H,2H-tridecafluoro-n-octanol

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
25291-17-2

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene

(perfluoro-n-hexyl)ethane
80793-17-5

(perfluoro-n-hexyl)ethane

Conditions
Conditions Yield
With water; lithium chloride; In N,N-dimethyl-formamide; Product distribution; effect of quantity of water and current on electroreduction;
80 % Spectr.
5 % Spectr.
15 % Spectr.
polytetrafluoroethylene
116-14-3,82785-14-6

polytetrafluoroethylene

ethene
74-85-1

ethene

Pentafluoroethyl iodide
354-64-3

Pentafluoroethyl iodide

potassium acrylate
10192-85-5

potassium acrylate

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,14-pentacosafluoro-tetradecyl acrylate
34395-24-9

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,14,14,14-pentacosafluoro-tetradecyl acrylate

1H,1H,2H-perfluoro-1-tetradecene

1H,1H,2H-perfluoro-1-tetradecene

1H,1H,2H,2H-tridecafluoro-n-octanol
647-42-7

1H,1H,2H,2H-tridecafluoro-n-octanol

2-(perfluorodecyl)ethanol
865-86-1

2-(perfluorodecyl)ethanol

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
25291-17-2

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene

1H,1H,2H-perfluorodecene
21652-58-4

1H,1H,2H-perfluorodecene

1H,1H,2H,2H-perfluorobutadecan-1-ol
39239-77-5

1H,1H,2H,2H-perfluorobutadecan-1-ol

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol
678-39-7

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-1-decanol

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-henicosafluorododec-1-ene
30389-25-4

3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,12-henicosafluorododec-1-ene

1H,1H,2H,2H-heptadecafluorodecyl acrylate
27905-45-9

1H,1H,2H,2H-heptadecafluorodecyl acrylate

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-propenoate
17527-29-6

3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl 2-propenoate

1,1,2,2-Tetrahydroperfluorododecyl acrylate
17741-60-5

1,1,2,2-Tetrahydroperfluorododecyl acrylate

Conditions
Conditions Yield
polytetrafluoroethylene; Pentafluoroethyl iodide; copper catalyst; at 80 ℃; under 6000.6 Torr;
ethene; copper catalyst; at 100 ℃; for 3h; under 2250.23 Torr;
potassium acrylate; With 4-methoxy-phenol; hydroquinone; In tert-butyl alcohol; at 180 - 190 ℃; for 6h; Product distribution / selectivity;
 

25291-17-2 Upstream products

  • 2043-57-4
    2043-57-4

    1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-iodooctane

  • 123-39-7
    123-39-7

    N-Methylformamide

  • 16741-46-1
    16741-46-1

    N-isopropylformamide

  • 4938-92-5
    4938-92-5

    N-(2-formylaminoethyl)formamide

25291-17-2 Downstream products

  • 51249-62-8
    51249-62-8

    1,2-Dibrom-1H,1H,2H-perfluorooctane

  • 73609-36-6
    73609-36-6

    (1H,1H,2H,2H-tridecafluoro-octyl)(methyl)dichlorosilane

  • 74-85-1
    74-85-1

    ethene

  • 56523-43-4
    56523-43-4

    7H,8H-hexacosafluoro-tetradec-7-ene