799-34-8

Basic information

• Product Name: 3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE
• Synonyms: 3-(1H,1H,7H-PERFLUOROHEPTYLOXY)-1,2-PROPENOXIDE;2,2,3,3,4,4,5,5,6,6,7,7-DODECAFLUOROHEPTYL GLYCIDYL ETHER;GLYCIDYL2,2,3,3,4,4,5,5,6,6,7,7-DODECAFLUOROHEPTYLETHER;1H,1H,2H,3H,3H,5H,5H-Perfluoro(1,2-Epoxy-4-oxaundecane);3-(1H,1H,7H-Perfluoroheptyloxy)-1,2-propenoxide 97%;3-(1H,1H,7H-Perfluoroheptyloxy)-1,2-propenoxide97%;3-(1H,1H,7H-Dodecafluoroheptyloxy)-1,2-;2,2,3,3,4,4,5,5,6,6,7,7-Dodeca
• CAS NO: 799-34-8
• Molecular Formula: C₁₀H₈F₁₂O₂
• Molecular Weight: 388.15
• Mol File: 799-34-8.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 97-98 °C4 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: /
• Density: 1.614 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0524mmHg at 25°C
• Refractive Index: n20/D 1.345(lit.)
• CAS DataBase Reference: 3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE(799-34-8)
• EPA Substance Registry System: 3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE(799-34-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 799-34-8(Hazardous Substances Data)

Usage

General Description

3-(1H,1H,7H-Dodecafluoroheptyloxy)-1,2-epoxypropane is a chemical compound that is a member of the family of organic compounds known as ethers. The structure of this compound comprises a three-carbon epoxy group (a ring consisting of two carbon atoms and one oxygen atom) and a seven-carbon chain with attached fluorine atoms. The presence of fluorine atoms can give this compound unique properties, such as enhanced stability and resistance to high temperatures. 3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE could potentially be used in applications ranging from coatings to electronics, however, specific uses depend on associated research and development. The physical, chemical properties, as well as potential hazards or risks associated with this compound would be determined through detailed scientific analysis.

InChI:InChI=1/C7H6ClFO/c8-6-1-5(4-10)2-7(9)3-6/h1-3,10H,4H2

Upstream product

• 335-99-9 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoro-1-heptanol 
• 106-89-8 epichlorohydrin 

Relevant articles and documents

Promising prospects for using partially fluorinated alcohols as O-nucleophilic reagents in organofluoric synthesis

Perfluoroolefins react with isopropyl alcohol under the conditions of radical initiation to form partially fluorinated aliphatic alcohols. The reactions of these alcohols with hexafluoropropylene and compounds containing labile halogen atoms (in particular, with allyl bromide and epichlorohydrin) were studied.

FLUORINE-CONTAINING 2,3-EPOXYPROPYL ETHERS. SYNTHESIS AND SPECTRAL CHARACTERISTICS

Polyfluoroalkyl 2,3-epoxypropyl ethers were prepared by the reactions of fluoro olefins with 2,3-epoxy-1-propanol in presence of potassium fluoride and under the conditions of phase-transfer catalysis. 1H and 19F NMR- and mass-spectral characteristics of the polyfluoroalkyl ethers were determined.