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17527-29-6

  • Product Name1H,1H,2H,2H-Perfluorooctyl acrylate
  • Molecular FormulaC11H7F13O2
  • Molecular Weight418.155
  • Purity99%
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Product Details

Quick Details

  • CasNo: 17527-29-6
  • Molecular Formula: C11H7F13O2
  • Purity: 99%

Sale Factory Supply 1H,1H,2H,2H-Perfluorooctyl acrylate 17527-29-6 Cheapest Price

  • Molecular Formula:C11H7F13O2
  • Molecular Weight:418.155
  • Vapor Pressure:0.332mmHg at 25°C 
  • Refractive Index:n20/D 1.338(lit.)  
  • Boiling Point:200 °C at 760 mmHg 
  • Flash Point:73 °C 
  • PSA:26.30000 
  • Density:1.494 g/cm3 
  • LogP:4.84450 

1H,1H,2H,2H-Perfluorooctyl acrylate(Cas 17527-29-6) Usage

Chemical Properties

Colorless liquid

Uses

1H,1H,2H,2H-Perfluorooctyl Acrylate is a semi-volatile fluorinated organic compound found in spring-time polluted Asian and western US air masses.

InChI:InChI=1/C11H7F13O2/c1-2-5(25)26-4-3-6(12,13)7(14,15)8(16,17)9(18,19)10(20,21)11(22,23)24/h2H,1,3-4H2

17527-29-6 Relevant articles

Synthesis and characterization of semifluorinated polymers via group transfer polymerization

Krupers, Maarten J.,Moeller, Martin

, p. 119 - 124 (1997)

Group transfer polymerization (GTP) was ...

Cross-polarization for a fluoropolymer involving multiple spin baths of abundant nuclei

Hazendonk, Paul,Harris, Robin K.,Galli, Giancarlo,Pizzanelli, Silvia

, p. 507 - 513 (2002)

The thermodynamic theory of cross-polari...

-

Boutevin,Rigal,Rousseau,Bosc

, p. 47 - 73 (1988)

Several fluorinated and chlorofluorinate...

METHOD FOR PRODUCING FLUORINE-CONTAINING (METH) ACRYLATE

-

Paragraph 0053-0056; 0059, (2021/03/13)

To provide a method for producing fluori...

Method for preparing fluorinated acrylate from fluorinated alcohol (by machine translation)

-

Paragraph 0035-0038; 0042-0044; 0054-0056, (2020/07/21)

Under the presence of a self-made fluori...

Environmentally friendly preparation method of fluorine-containing acrylate

-

Paragraph 0025, (2019/01/06)

The invention relates to the technical f...

PRODUCTION METHOD OF FLUORINE-CONTAINING (METH)ACRYLIC ACID ESTER

-

Paragraph 0039, (2016/10/07)

PROBLEM TO BE SOLVED: To provide a metho...

17527-29-6 Process route

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;
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

C<sub>14</sub>F<sub>29</sub>CH=CH<sub>2</sub>
104564-28-5

C14F29CH=CH2

C<sub>16</sub>F<sub>33</sub>CH=CH<sub>2</sub>

C16F33CH=CH2

1H,1H,2H,2H-perfluorohexadecan-1-ol
60699-51-6

1H,1H,2H,2H-perfluorohexadecan-1-ol

C<sub>14</sub>F<sub>29</sub>CH<sub>2</sub>CH<sub>2</sub>OCOCH=CH<sub>2</sub>
34362-49-7

C14F29CH2CH2OCOCH=CH2

C<sub>16</sub>F<sub>33</sub>CH<sub>2</sub>CH<sub>2</sub>OCOCH=CH<sub>2</sub>

C16F33CH2CH2OCOCH=CH2

C<sub>18</sub>F<sub>37</sub>CH<sub>2</sub>CH<sub>2</sub>OCOCH=CH<sub>2</sub>
65104-64-5

C18F37CH2CH2OCOCH=CH2

2-(perfluorodecyl)ethanol
865-86-1

2-(perfluorodecyl)ethanol

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;

17527-29-6 Upstream products

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

  • 79-10-7
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  • 814-68-6
    814-68-6

    acryloyl chloride

  • 2043-57-4
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