382-34-3

Basic information

• Product Name: 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER
• Synonyms: 1,1,1,2,3,3-Hexafluoro-4-oxapentane;1,1,2,3,3,3-Hexafluoro-1-methoxypropane;HFE-356mec;Methyl1,1,2,3,3,3-Pentafluoropropylether;DAIKIN T-8301;1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER;1,1,1,2,3,3-HEXAFLUOROPROPYL METHYL ETHER;Methyl 1,1,2,3,3,3-hexafluoropropyl ether
• CAS NO: 382-34-3
• Molecular Formula: C₄H₄F₆O
• Molecular Weight: 182.06
• Mol File: 382-34-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 53 °C
• Appearance: /
• Density: 1.419
• Vapor Pressure: 909mmHg at 25°C
• Refractive Index: 1.283
• CAS DataBase Reference: 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER(382-34-3)
• EPA Substance Registry System: 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER(382-34-3)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• RIDADR: UN 3271 3/PG II
• HazardClass: 3
• PackingGroup: II
• Hazardous Substances Data: 382-34-3(Hazardous Substances Data)

Usage

General Description

1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER is a chemical compound with the molecular formula C4H5F6O. It is a clear, colorless liquid that is commonly used as a solvent in various industrial applications. 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER is known for its properties as a non-flammable, high-purity solvent with low toxicity, making it a suitable alternative to traditional organic solvents. It is often used as a cleaning and degreasing agent in electronics manufacturing, as well as a solvent for specialized chemical reactions and extraction processes. Additionally, it is also used as an aerosol propellant in certain consumer products. While it offers numerous industrial applications, proper handling and storage of 1,1,2,3,3,3-HEXAFLUOROPROPYL METHYL ETHER are crucial due to its potential health and environmental risks.

InChI:InChI=1/C4H4F6O/c1-11-4(9,10)2(5)3(6,7)8/h2H,1H3

Upstream product

• 67-56-1 methanol 
• 116-15-4 perfluoropropylene 
• 124-41-4 sodium methylate 

Downstream Products

• 593-53-3 Methyl fluoride 
• 6065-84-5 2,3,3,3-tetrafluoropropionylfluoride 
• 382-93-4 methyl 2,3,3,3-tetrafluoropropanoate 

Relevant articles and documents

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Hydrofluoroether continuous synthetic method

The invention discloses a hydrofluoroether continuous synthetic method which is characterized by comprising the following steps of mixing alcohol, a solvent and a composite catalyst, heating a mixtureto 50 DEG C, then introducing the heated mixture and fluorine-containing olefin into a tubular reactor together for reaction, and separating a reaction liquid to obtain a hydrofluoroether product, wherein the molar ratio of the alcohol, the solvent, the composite catalyst and the fluorine-containing olefin is 1 to (1-5) to (0.1-0.25) to (1-1.5), the reaction temperature is 50-150 DEG C, and the reaction time is 5-25s. By adopting the hydrofluoroether continuous synthetic method provided by the invention, a synthetic process is improved so as to be the hydrofluoroether continuous synthetic method which is simple in synthetic process, large in operation flexibility and low in cost and is environmentally friendly.

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