50285-18-2

Usage

Uses

Used in Chemical and Manufacturing Industries:
1,1,1,2,2,3,4,5,5,5-decafluoro-3-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-4-(trifluoromethyl)pentane is used as a solvent for various chemical processes, taking advantage of its stability and resistance to heat and chemicals.
Used in Refrigeration Industry:
1,1,1,2,2,3,4,5,5,5-decafluoro-3-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-4-(trifluoromethyl)pentane is utilized as a refrigerant due to its ability to maintain stability under a wide range of temperatures and its resistance to environmental degradation.
Used in Polymer and Fluorinated Material Production:
1,1,1,2,2,3,4,5,5,5-decafluoro-3-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-4-(trifluoromethyl)pentane is employed in the production of polymers and other fluorinated materials, where its unique properties contribute to the development of specialized products.
It is important to handle and dispose of 1,1,1,2,2,3,4,5,5,5-decafluoro-3-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]-4-(trifluoromethyl)pentane properly due to potential environmental and health risks associated with the presence of fluorine.

InChI:InChI=1/C9F20/c10-1(4(13,14)9(27,28)29,2(11,5(15,16)17)6(18,19)20)3(12,7(21,22)23)8(24,25)26

Upstream product

• 30320-27-5 perfluoro(4-methyl-3-isopropyl-2-pentene) 
• 30320-26-4 1,1,1,4,5,5,5-heptafluoro-3-(pentafluoroethyl)-2,4-bis(trifluoromethyl)pent-2-ene 
• 93683-27-3 perfluoro-2,4-dimethyl-3-ethylpent-3-yl radical 
• 122432-73-9 perfluoro-3-ethyl-2,4-dimethylpent-1-ene 
• 122432-74-0 perfluoro-2-isopropyl-3,3-dimethylbut-1-ene 
• 116-15-4 perfluoropropylene 

Downstream Products

• 76-18-6 2-Chloro-F-propane 
• 677-69-0 perfluoroisopropyl iodide 
• 60340-52-5 1,1,1,2,2,3,4,5,5,5-decafluoro-3-iodo-4-trifluoromethyl-pentane 
• 76-16-4 Hexafluoroethane 
• 335-14-8 perfluoro-2,3-dimethylpentane 
• 354-97-2 2-Pentafluoraethyl-4-trifluormethylperfluorpentan 
• 118909-44-7 perfluoro-2,3,4-trimethylpentane 
• 75-73-0 carbon tetrafluoride 
• 50285-19-3 1,1,1,2,2,4,5,5,5-nonafluoro-3-pentafluoroethyl-3,4-bis-trifluoromethyl-pentane 
• 120615-52-3 perfluoro-2,3,3,4-tetramethylpentane 

Relevant academic research and scientific papers

Spectroscopic observation of charge transfer complex formation of persistent perfluoroalkyl radical with aromatics, olefin, and ether

Charge transfer interaction of a persistent perfluoroalkyl radical, perfluoro-3-ethyl-2,4-dimethyl-3-pentyl (PFR-1), with benzene and methyl substituted benzenes (toluene, m-xylene, mesitylene), 1-decene, and diethyl ether was investigated by UV-vis spect

Synthesis of a persistent perfluoroalkyl radical by electrochemical fluorination

A persistent perfluoroalkyl radical, perfluoro-3-ethyl-2,4-dimethyl-3-pentyl, was synthesized by the electrochemical fluorination of a mixture of hexafluoropropene trimers in the presence of a large amount of sodium fluoride.

DIRECT GAS-PHASE CATALYTIC FLUORINATION OF PARTIALLY FLUORINATED ORGANIC COMPOUNDS

The fluorination of a wide range of polyfluorinated organic compounds with molecular fluorine in the gas phase in a layer of NiF2/support as catalyst was investigated.It was shown that the selectivity of fluorination of the series of fluoroolefins, acid fluorides, polyfluoroalkanes, and hydrogen-containing ethers can be greatly increased.The developed method was used on an industrial scale in the production of perfluorinated liquids.

Photoinduced Fluorination of Hexafluoropropene Trimers: Synthesis of Branched Perfluoroalkanes

Hexafluoropropene trimers, perfluoro-3-ethyl-2,4-dimethylpent-2-ene (1) and perfluoro-3-isopropyl-4-methylpent-2-ene (2) reacted with fluorine under u.v. irradiation to give the new and highly branched perfluoroalkanes perfluoro-2,3,3,4-tetramethylpentane (7) and perfluoro-2,3,4-trimethylpentane (8) through a mechanism involving the elimination-readdition of CF3 groups.Compound (7), which is very bulky, can be easily cleaved at 200 deg C to give two perfluoro radicals capable of initiating the polymerization of vinylic monomers.