Details
High quality purity >99% PERFLUOROOCTANOYL FLUORIDE 335-66-0 for sale
- Molecular Formula: C8F16O
- Molecular Weight: 416.062
- Vapor Pressure: 13.6mmHg at 25°C
- Refractive Index: 1.2770 (589.3 nm 25℃)
- Boiling Point: 123.1 °C at 760 mmHg
- Flash Point: 39.9 °C
- PSA： 17.07000
- Density: 1.696 g/cm3
- LogP: 4.85660
PERFLUOROOCTANOYL FLUORIDE(Cas 335-66-0) Usage
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General Description |
Perfluorooctanoyl fluoride, also known as PFOA, is a synthetic fluorosurfactant and fluorotelomer alcohol used in the production of fluoropolymers such as Teflon. It is a persistent organic pollutant and has been associated with various health risks, including cancer, liver damage, and developmental effects in animals and humans. PFOA is highly soluble in water and does not break down easily in the environment, leading to its widespread contamination of water sources and ecosystems. As a result, many countries and organizations have taken steps to limit or ban the use of PFOA in various consumer products and industrial processes. |
InChI:InChI=1/C8F16O/c9-1(25)2(10,11)3(12,13)4(14,15)5(16,17)6(18,19)7(20,21)8(22,23)24
335-66-0 Relevant articles
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De Pasquale,R.J.
, p. 3025 - 3030 (1973)
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PROCESS IMPROVEMENTS IN THE ELECTROCHEMICAL FLUORINATION OF OCTANOYL CHLORIDE
Prokop, H. W.,Zhou, H-J.,Xu, S-Q.,Wu, C-H.,Chuey, S. R.,Liu, C. C.
, p. 257 - 276 (1989)
The electrochemical fluorination of octa...
EINSTUFIGE HERSTELLUNG HALOGENIERTER CARBONSAUREFLUORIDE AUS DEN FREIEN SAUREN
Schwertfeger, W.,Siegemund, G.
, p. 237 - 246 (1987)
The reaction of per- or polyhalogenated ...
A full-fluorine octanoyl fluorine preparation method (by machine translation)
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Paragraph 0021-0034, (2017/08/19)
The invention relates to a preparation m...
PROCESSES FOR PRODUCTION OF FLUORINE-CONTAINING COMPOUNDS
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Page/Page column 10, (2010/09/05)
This process for producing fluorine-cont...
A Lewis acid catalytic process for preparing fluorocarboxylic acid halides
Behr,Cheburkov
, p. 369 - 372 (2007/10/03)
Selected Group III and Group V Lewis aci...
1,1,2,2-Tetrafluoroethyl-N,N-dimethylamine: A new selective fluorinating agent
Petrov,Swearingen,Hong,Chris Petersen
, p. 25 - 31 (2007/10/03)
The title compound has been prepared in ...
335-66-0 Process route
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111-64-8
n-octanoic acid chloride
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335-35-3
perfluoro-2-butyl-tetrahydrofuran
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-
335-57-9
perfluoroheptane
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-
335-66-0
perfluorooctanoyl fluoride
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335-36-4,11072-16-5
2,2,3,3,4,4,5-heptafluoro-5-nonafluorobutyl-tetrahydro-furan
| Conditions | Yield |
|---|---|
|
In
hydrogen fluoride;
at 5 ℃;
for 77h;
electrochemical fluorination;
|
27.9%
18.1% 11.8% 12.7% |
|
With
hydrogen fluoride;
at 5 ℃;
Product distribution;
electrochemical fluorination, anode potential versus reference electrode 4,3 V; nickel foam anodes and cathodes; effect of substrate concentration; effect of time;
|
|
|
With
hydrogen fluoride;
Product distribution;
electrochemical fluorination;
|
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-
111-64-8
n-octanoic acid chloride
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-
335-35-3
perfluoro-2-butyl-tetrahydrofuran
-
-
335-57-9
perfluoroheptane
-
-
335-66-0
perfluorooctanoyl fluoride
-
-
335-36-4,11072-16-5
2,2,3,3,4,4,5-heptafluoro-5-nonafluorobutyl-tetrahydro-furan
| Conditions | Yield |
|---|---|
|
In
hydrogen fluoride;
at 5 ℃;
for 77h;
Product distribution;
electrochemical fluorination;
|
12.7%
27.9% 18.1% 11.8% |
335-66-0 Upstream products
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335-67-1
Perfluorooctanoic acid
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33496-48-9
pentadecafluorooctanoic anhydride
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592-94-9
octanoic acid fluoride
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335-95-5
sodium perfluorooctanoate
335-66-0 Downstream products
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307-62-0
perfluorotetradecane
-
335-57-9
perfluoroheptane
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2501-01-1
Perfluoro-5,6-dimethyl-4,7-dioxadecane
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109384-71-6
1,2,3,4,5-Pentafluoro-6-pentadecafluoronon-1-ynyl-benzene
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