3330-15-2

Usage

Uses

Used in Chemical Reactions:
HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER is used as a solvent for various organic compounds, facilitating their dissolution and participation in chemical reactions.
Used in Industrial Applications:
In the industrial sector, HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER is utilized as a lubricant and heat transfer fluid, capitalizing on its stable and non-flammable nature to enhance machinery performance and thermal management.
Used in the Electronics Industry:
HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER is employed as a dielectric fluid in the electronics industry, leveraging its insulating properties to improve the performance and safety of electronic devices.
Used in the Pharmaceutical Industry:
HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER is used as a processing aid in the pharmaceutical industry, where it aids in the manufacturing process of drugs, potentially enhancing the efficiency and quality of pharmaceutical products.
Used in Environmental and Health Considerations:
It is important to handle and store HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER with care due to its classification as environmentally hazardous. Proper management is crucial to mitigate potential adverse effects on human health and the environment.

InChI:InChI=1/C5HF11O/c6-1(2(7,8)9)17-5(15,16)3(10,11)4(12,13)14/h1H

Upstream product

• 2062-98-8 perfluoro(2-propoxypropionyl) fluoride 
• 76427-70-8 2,3,3,3-Tetrafluoro-2-(1,1,2,3,3,3-hexafluoro-2-heptafluoropropyloxy-propoxy)-N-hydroxy-propionamidine 
• 428-59-1 Hexafluoropropene oxide 
• 1644-11-7 1,1,1,2,3,3-hexafluoro-2-(heptafluoropropoxy)-3-[(trifluorovinyl)oxy]propane 

Relevant academic research and scientific papers

CONVERSION OF A PERFLUORINATED VINYL ETHER INTO A PARTIALLY FLUORINATED SATURATED ETHER DERIVATIVE

Methods of converting a fluorinated vinyl ether to a saturated partially fluorinated ether, the method comprising: reacting the fluorinated vinyl ether with an amine, ammonia, or combination thereof to form the saturated partially fluorinated ether.

Polyfluorinated ethers: IV.* By-products in the synthesis of polyfluorinated alkyl vinyl ethers in a solvating solvent

By-products formed in the synthesis of perfluoro(propyl vinyl ether), perfluoro(2-propoxypropyl vinyl ether), and methyl perfluoro(4-vinyloxybutanoate) in a solvating solvent have been studied. 1998 MAHK "Hayka/Interperiodica".

Polyfluoroalkyl Polyfluorovinyl Ethers. I. Kinetics and Mechanism of Formation of Perfluoropropyl Perfluorovinyl Ether from Sodium Perfluoro-2-methyl-2-oxahexanoate

The kinetics and mechanism of decarboxylation of sodium perfluoro-2-methyl-3-oxahexanoate have been studied in aprotic (diethylene glycol dimethyl ether) and protic (ethylene glycol) solvents.In the synthesis of perfluoropropyl perfluorovinyl ether, the concurrent formation of 1,3,3,3-tetrafluoroethyl perfluoropropyl ether is thermodynamically more favorable.

SYNTHESES AND DEGRADATIONS OF FLUORINATED HETEROCYCLICS. IV. IMIDOYLAMIDOXIMES, 1,2,4-OXADIAZOLE PRECURSORS

Perfluoroalkylether amidoximes free from amide-contamination were prepared from imidate esters.The amidoximes were stable at 110 deg C; at ca. 170 deg C partial decomposition to 1,2,4-oxadiazoles, admixed with other compounds, took place.Interactions between nitriles and amidoximes at 50 deg C resulted in the formation of imidoylamidoximes; these dissociated readily into their constituents when subjected to higher temperatures.At 70 deg C and above, in the presence of excess nitrile or other ammonia acceptors, the imidoylamidoximes afforded high yields of the corresponding 1,2,4-oxadiazoles.

DIPHOSPHATETRAAZACYCLOOCTATETRAENES. II. PROPERTIES AND DEGRADATIONS

1,5-Bis(diphenylphospha)-3,7-bis(perfluoroalkylether)-2,4,6,8-tetraazacyclooctatetraene and 1,3-bis(diphenylphospha)-5,7-bis(perfluoroalkylether)-2,4,6,8-tetraazacyclooctatetraene were found to decompose at 316 deg C to phospha-s-triazines.The symmetrical arrangement liberated perfluoroalkylether nitrile with concommitant formation of the corresponding diphospha-s-triazine; the unsymmetrical isomer eliminated the (C6H5)2PN unit to give the monophospha-s-triazine.The thermal and oxidative stabilities of the two compounds differed widely with the unsymmetrical isomer being significantly more stable than the symmetrical arrangement.Spectral data pertinent to these results are discussed.Both materials were found to be effective in arresting perfluoroalkylether fluid degradation in oxidizing atmospheres in the presence of metal alloys.