678-39-7

  • Product Name:1H,1H,2H,2H-Perfluoro-1-decanol
  • Molecular Formula:C10H5F17O
  • Purity:99%
  • Molecular Weight:464.122
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Product Details;

CasNo: 678-39-7

Molecular Formula: C10H5F17O

factory and supplier 678-39-7 1H,1H,2H,2H-Perfluoro-1-decanol in stock

  • Molecular Formula:C10H5F17O
  • Molecular Weight:464.122
  • Vapor Pressure:0.000484mmHg at 25°C 
  • Melting Point:50 °C 
  • Refractive Index:1.33 
  • Boiling Point:187.9 °C at 760 mmHg 
  • PKA:14.28±0.10(Predicted) 
  • Flash Point:67.5 °C 
  • PSA:20.23000 
  • Density:1.633g/cm3 
  • LogP:5.37820 

1H,1H,2H,2H-Perfluoro-1-decanol(Cas 678-39-7) Usage

Definition

ChEBI: A fluorotelomer alcohol that is ethanol substituted at position 2 by a perfluorooctyl group.

General Description

1H,1H,2H,2H-Perfluoro-1-decanol (8:2 FTOH) is an 8:2 fluorotelomer alcohol. The quantitative analysis of 8:2 FTOH in soil can be done using GC/MS with instrument detection limit (IDL) of 10fg/L. Studies indicate that hydroxyl radical causes indirect photodegradation of 8:2 FTOH in aqueous media.

InChI:InChI=1/C8H2F12O4/c9-3(10,1(21)22)5(13,14)7(17,18)8(19,20)6(15,16)4(11,12)2(23)24/h(H,21,22)(H,23,24)

678-39-7 Relevant articles

Electrochemical Oxidation of Polyfluoroalkyl Iodides: Direct Anodic Transformation of C8F17CH2CH2I to Amides, Esters, and Ethers

Becker, James Y.,Smart, Bruce E.,Fukunaga, Tadamichi

, p. 5714 - 5720 (1988)

The cyclic voltammetry of polyfluoroalky...

Method for preparing perfluoroalkyl ethanol

-

Paragraph 0026-0032, (2017/11/29)

The invention discloses a method for pre...

Method for preparing perfluoroalkyl alcohol from perfluoroalkyl ethylene

-

Paragraph 0034; 0036, (2017/04/03)

The invention discloses a method for pre...

Unprecedented iron-catalyzed ester hydrogenation. Mild, selective, and efficient hydrogenation of trifluoroacetic esters to alcohols catalyzed by an iron pincer complex

Zell, Thomas,Ben-David, Yehoshoa,Milstein, David

supporting information, p. 4685 - 4689 (2014/05/20)

The synthetically important, environment...

Synthesis of 2-(perfluoroalkyl)ethyl potassium sulfates based on perfluorinated Grignard reagents

Paterová, Jana,Skalicky, Martin,Rybá?ková, Markéta,Kví?alová, Magdalena,Cva?ka, Josef,Kví?ala, Jaroslav

experimental part, p. 1338 - 1343 (2011/02/22)

The first example of nucleophilic substi...

678-39-7 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

2-(perfluorodecyl)ethanol
865-86-1

2-(perfluorodecyl)ethanol

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

1H,1H,2H-perfluorodecene

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

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;
2-(n-perfluorooctyl)ethyl iodide
2043-53-0,71215-70-8

2-(n-perfluorooctyl)ethyl iodide

potassium acrylate
10192-85-5

potassium acrylate

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

1H,1H,2H-perfluorodecene

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

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

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

Conditions
Conditions Yield
With 4-methoxy-phenol; hydroquinone; In tert-butyl alcohol; at 180 - 190 ℃; for 6h; Product distribution / selectivity;

678-39-7 Upstream products

  • 74-85-1
    74-85-1

    ethene

  • 77758-89-5
    77758-89-5

    phenyl(perfluorooctyl)iodonium triflate

  • 2043-53-0
    2043-53-0

    2-(n-perfluorooctyl)ethyl iodide

  • 117068-31-2
    117068-31-2

    (3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluoro-n-decyl)trifluoroacetate

678-39-7 Downstream products

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