| Identification | More | [Name]
1H,1H,2H,2H-PERFLUOROOCTYLTRIMETHOXYSILANE | [CAS]
85857-16-5 | [Synonyms]
1H,1H,2H,2H-PERFLUOROOCTYLTRIMETHOXYSILANE
(TRIDECAFLUORO-1,1,2,2-TETRAHYDROOCTYL)TRIMETHOXYSILANE
Perfluorooctyltrimethoxysilane
trimethoxy(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)silane
1H,1H,2H,2H-Perfluorooctyltrimethoxysilane 97%
1H,1H,2H,2H-Perfluorooctyltrimethoxysilane97%
trimethoxytridecafluorooctylsilane
1,1,1,2,2,3,3,4,4,5,5,6,6-Tridecafluoro-8-(trimethoxysilyl)octane
2-(Tridecafluorohexyl)ethyltrimethoxysilane | [EINECS(EC#)]
288-657-1 | [Molecular Formula]
C11H13F13O3Si | [MDL Number]
MFCD00153261 | [Molecular Weight]
468.28 | [MOL File]
85857-16-5.mol |
| Hazard Information | Back Directory | [Chemical Properties]
liquid | [Uses]
1H,1H,2H,2H-Perfluorooctyltrimethoxysilane, a functional material widely used to make material surface water-repellent[1]. Fluorosilane 1H,1H,2H,2H-perfluorooctyltrimethoxysilane could be coated onto the surface of BaTiO3 nanofibers by chemical reaction, which enhances their dispersion in poly(vinylidene fluoride) matrix[2]. | [Flammability and Explosibility]
Nonflammable | [Synthesis]
1H,1H,2H,2H-Perfluorooctyltrimethoxysilane (PFOT) could be synthesized by a two-step method: after the hydrosilylation of trichlorosilane and 1H,1H,2H-perfluoro-1-octene (HPFO), the resulting product was then subjected to the alcoholic reaction with sodium methoxide to get the PFOT[1]. | [References]
[1] Xianhong Zhang . "High dielectric constant and low dielectric loss hybrid nanocomposites fabricated with ferroelectric polymer matrix and BaTiO3 nanofibers modified with perfluoroalkylsilane." Applied Surface Science 305 (2014): Pages 531-538.
[2] Feihong Ye. "Effect of reaction conditions on one-step preparation of 1H,1H,2H,2H-Perfluorooctyltrimethoxysilane by catalytic hydrosilylation over RuCl3·3H2O catalysts." Journal of Industrial and Engineering Chemistry 110 (2022): Pages 405-413. |
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