Nonafluorohexyltriethoxysilane
Nonafluorohexyltriethoxysilane Basic information
- Product Name:
- Nonafluorohexyltriethoxysilane
- Synonyms:
-
- NONAFLUOROHEXYLTRIETHOXYSILANE
- Triethoxy(1H,1H,2H,2H-nonafluorohexyl)silane
- 1H,1H,2H,2H-Nonafluorohexyltriethoxysilane Triethoxy(1H,1H,2H,2H-perfluorohexyl)silane
- 1H,1H,2H,2H-Nonafluorohexyltriethoxysilane
- 1H,1H,2H,2H-PERFLUOROHEXYLTRIETHOXYSILANE
- Triethoxy(1H,1H,2H,2H-perfluorohexyl)silane
- Triethoxy(1H,1H,2H,2H-nonafluorohexyl)silane
- Silane,triethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)-
- CAS:
- 102390-98-7
- MF:
- C12H19F9O3Si
- MW:
- 410.35
- Mol File:
- 102390-98-7.mol
Nonafluorohexyltriethoxysilane Chemical Properties
- Boiling point:
- 241.5±40.0 °C(Predicted)
- Density
- 1.240±0.06 g/cm3(Predicted)
- refractive index
- 1.3470 to 1.3510
- storage temp.
- Inert atmosphere,Room Temperature
- form
- clear liquid
- color
- Colorless to Almost colorless
- Specific Gravity
- 1.201
- Hydrolytic Sensitivity
- 7: reacts slowly with moisture/water
- EPA Substance Registry System
- Triethoxy(1,1,2,2,3,3,6,6,6-nonafluorohexyl)silane (102390-98-7)
Nonafluorohexyltriethoxysilane Usage And Synthesis
Chemical Properties
Colorless transparent liquid.
Uses
Nonafluorohexyltriethoxysilane is an organic silane, which can be used as an organic reagent.
Application
Main applications of Nonafluorohexyltriethoxysilane(1H,1H,2H,2H-Perfluorohexyltriethoxysilane)
1) Used as a coupling agent to increase the bonding strength of the fluorine-containing resin and the substrate.
2) Used to prepare water-proof, oil-proof and anti-fouling treatment agents, and it can be used in the protection of water-proof, anti-fouling and weathering of cultural relics, masonry, metal, wood, etc.
3) Used as a finishing agent to reduce the water holding capacity of natural fiber (wool, cotton, leather, etc.) products, and to improve surface water repellency and stain resistance.
4) Used as a water-repellent and antifouling treatment on the surface of glass.
Production Methods
Nonafluorobutyl iodide (NFBI) and triethoxyvinylsilane (TEOVS) were fed into a three-necked flask equipped with a reflux condenser at a molar ratio of 1: 1.1 and then heated to 60 ℃ with stirring. When the internal temperature of the flask was sufficiently heated, azobisbutylnitrile (AIBN), a thermal decomposition radical initiator, was dissolved in an ether-based solvent. Then 0.5 ml/sec was dropped slowly into the stirred flask. After that, when the dropwise addition was completed, the external heating temperature was again set to 60 ℃ and stirred for 6 hours. After that, the internal temperature of the flask was lowered to room temperature (25 ℃), and tributyltin hydride (TBTH) was added to the flask at a rate of 1 ml/sec. After further stirring for 4 hours, distillation under reduced pressure at 1 Torr and 40 ° C yielded Nonafluorohexyltriethoxysilane (1H,1H,2H,2H-Perfluorohexyltriethoxysilane) in 75% yield.
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