3330-15-2

Basic information

• Product Name: HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER
• Synonyms: HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER;1,1,1,2,2,3,3-heptafluoro-3-(1,2,2,2-tetrafluoroethoxy)-propan;Ether, heptafluoropropyl 1,2,2,2-tetrafluoroethyl;freone1;HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER 97%;Propane, 1,1,1,2,2,3,3-heptafluoro-3-(1,2,2,2-tetrafluoroethoxy)-;Heptafluoropropyl1,2,2,2-tetrafluoroethylether97%;(1,2,2,2-Tetrafluoroethyl)(heptafluoropropyl) ether
• CAS NO: 3330-15-2
• Molecular Formula: C₅HF₁₁O
• Molecular Weight: 286.04
• Mol File: 3330-15-2.mol
• Article Data: 6

Chemical Properties

• Melting Point: 8-9°C
• Boiling Point: 40 °C
• Flash Point: 26-36/37/39
• Appearance: /
• Density: 1.538
• Vapor Pressure: 281mmHg at 25°C
• Refractive Index: 1.2434
• CAS DataBase Reference: HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER(3330-15-2)
• EPA Substance Registry System: HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER(3330-15-2)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: 3265
• HazardClass: IRRITANT
• Hazardous Substances Data: 3330-15-2(Hazardous Substances Data)

Usage

General Description

HEPTAFLUOROPROPYL 1,2,2,2-TETRAFLUOROETHYL ETHER is a chemical compound with the molecular formula C6F13O that belongs to the class of perfluoroethers. It is a colorless, odorless liquid that is non-flammable and stable under normal conditions. It is commonly used as a solvent for various organic compounds in chemical reactions and is also used as a lubricant and heat transfer fluid in industrial applications. Additionally, it has potential applications in the electronics industry as a dielectric fluid and in the pharmaceutical industry as a processing aid. However, it is important to handle and store this chemical with care, as it is considered environmentally hazardous and may have adverse effects on human health if not properly managed.

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

Relevant articles and documents

A NEW METHOD FOR ELIMINATING CARBONYL FLUORIDE FROM α-TRIFLUOROMETHYLATED ACYL FLUORIDES

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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".

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.