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

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

Uses

Used in Coatings Industry:
3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE is used as a component in the formulation of coatings for its potential to enhance stability and resistance to high temperatures, which can be beneficial in various applications requiring durable and heat-resistant coatings.
Used in Electronics Industry:
3-(1H,1H,7H-DODECAFLUOROHEPTYLOXY)-1,2-EPOXYPROPANE is used as a material in the electronics industry, potentially for its properties that could contribute to the development of more robust and temperature-resistant electronic components.

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.

An approach to fluorinated surface coatings via photoinitiated cationic cross-linking of mixed epoxy and fluoroepoxy systems

The synthesis and characterisation of four polyfluorinated monoepoxides is described. These fluoroepoxy monomers were cationically polymerised either neat or as mixtures with diglycidylether of bisphenol-A using the initiator system (CH3CH2)3Al/H2O (2/1) or the photoinitiator Ph2I+, PF6-. Contact angle measurements indicated that, in favourable cases, the fluorinated epoxide monomer surface segregated at low loadings to give significant lowering of the surface free energy of photocured films of diglycidylether of bisphenol-A.

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.