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NONAFLUOROHEXYLTRIMETHOXYSILANE is a chemical compound that features a nonafluoroalkyl group connected to a trimethoxysilane molecule, known for its strong hydrophobic and oleophobic properties, making it an effective repellent for both water and oil-based substances.

85877-79-8

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85877-79-8 Usage

Uses

Used in Surface Coating Industry:
NONAFLUOROHEXYLTRIMETHOXYSILANE is used as a water and oil repellent for surface coatings to provide resistance against water and oil-based substances, enhancing the durability and longevity of coated surfaces.
Used in Textile Industry:
In the textile industry, NONAFLUOROHEXYLTRIMETHOXYSILANE is used as a water and oil repellent to treat fabrics, offering protection against water and oil stains, and improving the overall performance and lifespan of textiles.
Used in Building Materials Industry:
NONAFLUOROHEXYLTRIMETHOXYSILANE is utilized as a water and oil repellent in building materials to protect structures from water and oil damage, ensuring their durability and resistance to environmental factors.
Used in Glass, Ceramics, and Metal Surface Treatment:
NONAFLUOROHEXYLTRIMETHOXYSILANE is used as a surface treatment for glass, ceramics, and metals, providing a durable and long-lasting protective layer that enhances their resistance to water and oil contamination.
Used as a Coupling Agent or Adhesion Promoter in Composite Material Production:
In the production of composite materials, NONAFLUOROHEXYLTRIMETHOXYSILANE serves as a coupling agent or adhesion promoter, improving the bonding and integration of different material components, thus enhancing the overall performance and strength of the composite.
Despite its wide range of applications, it is crucial to handle NONAFLUOROHEXYLTRIMETHOXYSILANE with care and follow proper safety precautions to avoid potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 85877-79-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,8,7 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 85877-79:
(7*8)+(6*5)+(5*8)+(4*7)+(3*7)+(2*7)+(1*9)=198
198 % 10 = 8
So 85877-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H13F9O3Si/c1-19-22(20-2,21-3)5-4-6(10,11)7(12,13)8(14,15)9(16,17)18/h4-5H2,1-3H3

85877-79-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Trimethoxy(1H,1H,2H,2H-perfluorohexyl)silane

1.2 Other means of identification

Product number -
Other names trimethoxy(3,3,4,4,5,5,6,6,6-nonafluorohexyl)silane

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:85877-79-8 SDS

85877-79-8Downstream Products

85877-79-8Relevant academic research and scientific papers

PERFLUORO-ALKYL MODIFIED ORGANIC SILANE

-

Paragraph 0103; 0104, (2017/05/27)

The present invention relates to a method for preparing perfluoroalkyl modified organic silane, and the method for preparing perfluoroalkyl modified organic silane comprises a step for adding a pyrolytic radical initiator and a tin-based organic metal compound to a mixture of a perfluoroalkyl iodide compound and an organic silane having a double bond. The method for preparing perfluoroalkyl modified organic silane suppresses an additive reaction of the pyrolytic radical initiator and smoothens the reduction of iodine, thereby forming perfluoroalkylalkoxy silane at high efficiency and high purity, causes no chlorine gas, which is a toxic gas, thereby making less environmental loading, such as gas purification facilities, and does not use an expensive metal catalyst and hydrogen gas, thereby preparing perfluoroalkyl modified organic silane easily and economically.COPYRIGHT KIPO 2016

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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