355-43-1

  • Product Name:Perfluorohexyl Iodide
  • Molecular Formula:C6F13I
  • Purity:99%
  • Molecular Weight:445.95
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Product Details;

CasNo: 355-43-1

Molecular Formula: C6F13I

Appearance: liquid

factory and supplier 355-43-1 Perfluorohexyl Iodide in stock

  • Molecular Formula:C6F13I
  • Molecular Weight:445.95
  • Appearance/Colour:liquid 
  • Vapor Pressure:21.1mmHg at 25°C 
  • Melting Point:-45 °C 
  • Refractive Index:n20/D 1.329(lit.)  
  • Boiling Point:117.096 °C at 760 mmHg 
  • Flash Point:44.982 °C 
  • PSA:0.00000 
  • Density:2.05 g/cm3 
  • LogP:5.11770 

Perfluoro-1-iodohexane(Cas 355-43-1) Usage

Safety Profile

Explodes in contact with sodium when heated to the boiling point of the iodide. When heated to decomposition it emits toxic fumes of Fí and Ií.

General Description

Perfluorohexyl iodide forms 1:1 complexes with a variety of hydrogen-bond acceptors. It has been grafted onto the isocitronellene/propene copolymer by radical reaction yielding a poly(α-olefin) with fluorinated side chains. The radical addition of perfluorohexyl iodide to vinyl acetate, using azo-bis( isobutyronitrile) (AIBN) as an initiator, has been investigated.

InChI:InChI=1/C6F13I/c7-1(8,3(11,12)5(15,16)17)2(9,10)4(13,14)6(18,19)20

355-43-1 Relevant articles

PARTIALLY FLUORINATED COMPOUNDS

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Paragraph 00113-00114, (2014/07/07)

Described herein is a composition compri...

PROCESS FOR PRODUCTION OF FLUOROALKYL IODIDE

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Paragraph 0070; 0071; 0072, (2013/04/23)

To provide a process for producing a flu...

PRODUCING SHORT CHAIN PERFLUOROALKYL IODIDES

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Page/Page column 3, (2011/12/14)

An improved process for producing perflu...

PROCESS FOR PRODUCING FLUOROALKYL IODIDE TELOMER

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Page/Page column 3-4, (2011/02/25)

A novel process for producing a fluoroal...

355-43-1 Process route

polytetrafluoroethylene
116-14-3,82785-14-6

polytetrafluoroethylene

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
423-39-2

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane

perfluorotetradecyl iodide

perfluorotetradecyl iodide

1-iodoheptadecafluorooctane
507-63-1

1-iodoheptadecafluorooctane

1-iodoperfluorododecane
307-60-8

1-iodoperfluorododecane

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

1-Iodo-perfluorodecane
423-62-1

1-Iodo-perfluorodecane

Conditions
Conditions Yield
copper; at 110 ℃; under 2850.29 Torr;
polytetrafluoroethylene
116-14-3,82785-14-6

polytetrafluoroethylene

Pentafluoroethyl iodide
354-64-3

Pentafluoroethyl iodide

1-iodoheptadecafluorooctane
507-63-1

1-iodoheptadecafluorooctane

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane
423-39-2

1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane

n-perfluorohexyl iodide
355-43-1

n-perfluorohexyl iodide

1-Iodo-perfluorodecane
423-62-1

1-Iodo-perfluorodecane

Conditions
Conditions Yield
at 100 ℃; for 5.13333h; Further byproducts given; Irradiation;
5%
26.9%
15.8%
44.5%
at 100 ℃; for 5h; Irradiation;
34.6%
13.8%
3.2%
40.3%
With copper; at 90 - 100 ℃; for 5h; Product distribution; further reaction times, reagent ratio;
17.2%
10.5%
15.9%
2.4%
copper; at 60 - 140 ℃; under 22502.3 - 33753.4 Torr; Product distribution / selectivity;

355-43-1 Upstream products

  • 116-14-3
    116-14-3

    polytetrafluoroethylene

  • 423-39-2
    423-39-2

    1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane

  • 354-64-3
    354-64-3

    Pentafluoroethyl iodide

  • 4520-08-5
    4520-08-5

    perfluorohexyl radical

355-43-1 Downstream products

  • 335-56-8
    335-56-8

    1-bromo-1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane

  • 355-37-3
    355-37-3

    1,1,1,2,2,3,3,4,4,5,5,6,6-tridecafluorohexane

  • 355-41-9
    355-41-9

    perfluoro-n-hexyl chloride

  • 56734-76-0
    56734-76-0

    α-tridecafluorohexylcyclohexanone

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