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NONAFLUOROHEXYLTRICHLOROSILANE, with the molecular formula C6F9Cl3Si, is a colorless liquid chemical compound known for its highly repellent properties. It is utilized in various applications due to its ability to create water and oil-resistant surfaces, and it serves as a precursor for the production of fluorine-containing polymers and materials.

78560-47-1

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78560-47-1 Usage

Uses

Used in Surface Treatment Industry:
NONAFLUOROHEXYLTRICHLOROSILANE is used as a hydrophobic surface treatment agent for creating water and oil-resistant surfaces, enhancing the durability and performance of treated materials.
Used in Electronics Industry:
In the electronics industry, NONAFLUOROHEXYLTRICHLOROSILANE is used as a component in the formulation of protective coatings, which are essential for safeguarding electronic components from environmental factors and ensuring their longevity.
Used in Polymer and Material Production:
NONAFLUOROHEXYLTRICHLOROSILANE is used as a precursor in the production of specialty fluorine-containing polymers and materials, contributing to the development of advanced materials with unique properties for various applications.
However, due to its potential environmental and health hazards, it is crucial to follow careful handling and disposal practices when working with NONAFLUOROHEXYLTRICHLOROSILANE to minimize risks and ensure safety.

Check Digit Verification of cas no

The CAS Registry Mumber 78560-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,5,6 and 0 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78560-47:
(7*7)+(6*8)+(5*5)+(4*6)+(3*0)+(2*4)+(1*7)=161
161 % 10 = 1
So 78560-47-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl3F9Si/c7-19(8,9)2-1-3(10,11)4(12,13)5(14,15)6(16,17)18/h1-2H2

78560-47-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name trichloro(1,1,2,2,3,3,6,6,6-nonafluorohexyl)silane

1.2 Other means of identification

Product number -
Other names Silane,trichloro(3,3,4,4,5,5,6,6,6-nonafluorohexyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:78560-47-1 SDS

78560-47-1Relevant academic research and scientific papers

Catalyst for use in production of epoxide, method for producing the catalyst, and method for producing epoxide

-

, (2008/06/13)

To provide an epoxide-production-use catalyst that is suitably used for producing an epoxide by partial oxidation of an unsaturated hydrocarbon, a catalyst in accordance with the present invention is obtained by fixing gold fine particles to a carrier containing an oxide containing at least one of titanium and zirconium, and has an acid quantity of not more than 0.1 mmol/g determined by the NH3-TPD method. Such a catalyst for epoxide producing use can be produced by, for instance, fixing gold fine particles to a carrier having an acid quantity of not more than 0.15 mmol/g. The catalyst for epoxide producing use arranged as above is preferably used as a catalyst in partial oxidation of an unsaturated hydrocarbon to produce a corresponding epoxide.

Process for preparing fluoroalkyl-containing organosilicon compounds, and their use

-

, (2008/06/13)

Fluoroalkyl organosilicon compounds are prepared by reacting fluoroolefins with organosilicon compounds that contain at least one H--Si group, in the presence of a Pt(0) complex catalyst. Further, fluoroalkylalkoxy organosilicon compounds are prepared by esterifying fluoroalkyl organosilicon compounds. The process proceeds uniformly under mild conditions with high yields and selectivities.

Syntheses and Reactions of Metal Organics. XVIII. Syntheses of (1H,1H,2H,2H-Polyfluoroalkyl)trimethoxysilanes and Surface Modification of Glass Plate

Yoshino, Norio,Yamamoto, Yasushi,Hamano, Katsumi,Kawase, Tokuzo

, p. 1754 - 1758 (2007/10/02)

Four silane coupling agents, (1H,1H,2H,2H-polyfluoroalkyl)trimethoxysilanes ((1H,1H,2H,2H-henicosafluorododecyl)trimethoxysilane, C10F21C2H4Si(OCH3)3, (1H,1H,2H,2H-heptadecafluorodecyl)trimethoxysilane, C58F17C2H4Si(OCH3)3, (1H,1H,2H,2H-tridecafluorooctyl)trimethoxysilane, C6F13C2H4Si(OCH3)3, and (1H,1H,2H,2H-nonafluorohexyl)trimethoxysilane, C4F9C2H4Si(OCH3)3), were prepared by the hydrosilylation of trichlorosilane with the corresponding 1H,1H,2H,-polyfluoro-1-alkene in the presence of hydrogen hexachloroplatinate-(IV), followed by reaction with sodium methoxide.The surface modification of glass plate was attempted using these products.From measurements of the contact angles θ (deg) of water and oleic acid against a modified glass plate surface, the coupling agents were found to have high modification ability.The modification produced a glass surface with high oxidation resistance.

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