380-34-7

Basic information

• Product Name: 1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER
• Synonyms: DAIKIN T-8302;1,1,1,2,3,3-HEXAFLUOROPROPYL ETHYL ETHER;1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER;1,1,2,3,3,3-HEXAFLUORO-3-ETHOXYPROPANE;1,1,2,3,3,3-Hexafluoropropyl ethyl ether 97%;1,1,2,3,3,3-Hexafluoropropylethylether97%;Ethyl 1,1,2,3,3,3-Hexafluoropropyl Ether;Propane,1-ethoxy-1,1,2,3,3,3-hexafluoro-
• CAS NO: 380-34-7
• Molecular Formula: C5H6F6O
• Molecular Weight: 196.09
• Mol File: 380-34-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 71 °C
• Appearance: /
• Density: 1.321
• Vapor Pressure: 288mmHg at 25°C
• Refractive Index: 1.305
• CAS DataBase Reference: 1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER(380-34-7)
• EPA Substance Registry System: 1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER(380-34-7)

Safety Data

• Hazard Codes: Xi
• Statements: 11-36/37/38
• Safety Statements: 16-26-36
• RIDADR: 3271
• HazardClass: IRRITANT
• PackingGroup: II
• Hazardous Substances Data: 380-34-7(Hazardous Substances Data)

Usage

General Description

1,1,2,3,3,3-Hexafluoropropyl ethyl ether is a chemical compound with the molecular formula C5H5F6O. It is a colorless liquid with a faint odor, and it is insoluble in water but soluble in organic solvents. 1,1,2,3,3,3-HEXAFLUOROPROPYL ETHYL ETHER is primarily used as a solvent and as a processing aid in the production of fluorinated polymers and resins. It is also used as a heat transfer fluid, a refrigerant, and in other industrial applications. 1,1,2,3,3,3-Hexafluoropropyl ethyl ether is considered to be relatively inert and non-reactive, and it is generally regarded as safe for use in these applications with proper handling and storage. However, it is important to follow safety guidelines and regulations for the use of this chemical.

InChI:InChI=1/C5H6F6O/c1-2-12-5(10,11)3(6)4(7,8)9/h3H,2H2,1H3

Upstream product

• 116-15-4 perfluoropropylene 
• 64-17-5 ethanol 
• 141-52-6 sodium ethanolate 
• 754-34-7 1,1,1,2,2,3,3-heptafluoro-3-iodo-propane 

Downstream Products

• 399-92-8 2,3,3,3-tetrafluoropropionic acid ethyl ester 
• 16519-02-1 diethyl 2-methyl-2-fluoromalonate 
• 685-88-1 fluoromalonic acid diethyl ester 

Relevant articles and documents

Synthesis and use of partially fluorinated dialkyl ethers derived from hexafluoropropylene

A procedure was developed for preparing partially fluorinated dialkyl ethers by the reaction of hexafluoropropylene with aliphatic and polyfluorinated alcohols in the presence of KOH. On treatment with concentrated sulfuric acid, these ethers form alkyl esters of acids, and on treatment with KOH, alkenyl ethers.

Method for removing unsaturated impurities in 1, 1, 2, 3, 3 and 3 - hexafluoropropyl hydrofluoroether crude product

The invention provides a method of removing 1. [] The hydrofluoroether impurities, pentafluoropropylene hydrofluoroether, and, 1 1 pentafluoropropylene 2 hydrofluoroether 3 impurities 3 can 3 - be well separated to provide, hexafluoropropyl hydrofluoroether product 1 having a 1 2 purity of 3 3 - at least. 1 2 1, 2, 3, 3, 3 - 3 1 1 3 3 - 99% 3 3 - 2 3The method does not use dangerous chemical, greatly improves the operation safety, does not generate waste harmful to the environment, and can be regenerated and reused by the adsorbent silica gel column. Cost is reduced, and resources are saved.

Palladium(0)-catalyzed hydroalkoxylation of hexafluoropropene: Synthesis of hydrofluoroethers under neutral conditions

No vinyl ether by-products are formed in the palladium(0)-complex catalyzed hydroalkoxylation of hexafluoropropene (see scheme). Saturated hydrofluoro-ethers are selectively synthesized with alcohols or phenols under neutral conditions in the presence of