2943-73-9

Usage

Uses

Used in Adhesives Industry:
n-Decyltriethoxysilane is used as a coupling agent to enhance the adhesion between organic materials and inorganic surfaces, such as glass, metal, and ceramics. Its strong bonding capabilities improve the overall performance and durability of adhesive products.
Used in Coatings Industry:
As a chemical additive, n-Decyltriethoxysilane is employed in the coatings industry to improve the adhesion, water resistance, and chemical resistance of coatings. This results in a more durable and long-lasting finish for various applications, including automotive, architectural, and industrial coatings.
Used in Crude Oil Industry:
n-Decyltriethoxysilane is used in the crude oil industry as a chemical additive to improve the efficiency of oil extraction and transportation. Its ability to bond with both organic and inorganic materials helps reduce friction and prevent the formation of deposits, leading to smoother and more efficient oil recovery processes.
Used in Glass Fibers Industry:
In the glass fibers industry, n-Decyltriethoxysilane is used as a coupling agent to improve the adhesion between glass fibers and polymer matrices. This enhances the mechanical properties and durability of glass fiber-reinforced composites, making them suitable for various applications, such as automotive, aerospace, and construction materials.
Used in Filler Treatment Industry:
n-Decyltriethoxysilane is used as a chemical additive in the filler treatment industry to improve the dispersion and adhesion of fillers in polymer matrices. This results in enhanced mechanical properties, thermal stability, and overall performance of the filled polymers.
Used in Polymer Modification Industry:
As a chemical additive, n-Decyltriethoxysilane is employed in the polymer modification industry to improve the compatibility, adhesion, and overall performance of polymer blends and composites. This leads to the development of new materials with tailored properties for various applications.
Used in Printing Industry:
In the printing industry, n-Decyltriethoxysilane is used as a chemical additive to improve the adhesion of inks to various substrates, such as paper, plastic, and metal. This results in better print quality, durability, and resistance to environmental factors.
Used in Elastomers Industry:
n-Decyltriethoxysilane is used in the elastomers industry as a chemical additive to improve the adhesion, mechanical properties, and overall performance of elastomeric materials. This enhances their suitability for various applications, including automotive, industrial, and consumer products.
Used in Sealants Industry:
As a chemical additive, n-Decyltriethoxysilane is employed in the sealants industry to improve the adhesion, flexibility, and durability of sealant formulations. This results in better sealing performance and longer-lasting seals for various applications, such as construction, automotive, and industrial sealing.
Used in Textiles Industry:
In the textiles industry, n-Decyltriethoxysilane is used as a chemical additive to improve the adhesion, water resistance, and overall performance of textile materials. This enhances their suitability for various applications, including clothing, upholstery, and industrial textiles.
Used in Thermoplastics Industry:
n-Decyltriethoxysilane is used in the thermoplastics industry as a chemical additive to improve the compatibility, adhesion, and overall performance of thermoplastic materials. This leads to the development of new materials with tailored properties for various applications, including automotive, packaging, and consumer products.
Used in OLED Industry:
n-Decyltriethoxysilane is used as an intermediate in the production of organic light-emitting diodes (OLEDs) due to its ability to form strong bonds with inorganic surfaces and its compatibility with organic materials. This contributes to the development of more efficient and durable OLED devices.
Used in Pharmaceutical Industry:
As an intermediate, n-Decyltriethoxysilane is employed in the pharmaceutical industry for the synthesis of various drug compounds. Its unique properties enable the development of new drugs with improved efficacy and reduced side effects.
Used in Cosmetics Industry:
n-Decyltriethoxysilane is used as an intermediate in the cosmetics industry for the formulation of various cosmetic products. Its ability to bond with both organic and inorganic materials allows for the development of innovative and effective cosmetic formulations.

InChI:InChI=1/C16H36O3Si/c1-5-9-10-11-12-13-14-15-16-20(17-6-2,18-7-3)19-8-4/h5-16H2,1-4H3

Upstream product

• 872-05-9 1-Decene 
• 998-30-1 Triethoxysilane 
• 64-17-5 ethanol 
• 13829-21-5 n-decyltrichlorosilane 
• 78-10-4 tetraethoxy orthosilicate 
• 17049-50-2 n-decyl magnesium bromide 

Relevant academic research and scientific papers

N,N-Dimethylformamide-protected Fe2O3 Combined with Pt Nanoparticles: Characterization and Catalysis in Alkene Hydrosilylation

We report a combination of N,N-dimethylformamide (DMF)-protected Fe2O3 nanoparticles (NPs) and Pt NPs for the hydrosilylation of various industrially relevant alkenes and tertiary silanes. The DMF-protected Fe2O3 and Pt NPs catalysts were characterized by transmission electron microscopy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy. The catalyst of DMF-protected Fe2O3 NPs combined with Pt NPs can be recycled for five cycles by a simple extraction using hexane/DMF. The developed combination Fe2O3/Pt NPs catalyst is effective up to the 1-kilogram scale.

High catalytic activity and selectivity in hydrosilylation of new Pt(II) metallosupramolecular complexes based on ambidentate ligands

Two new air- and water-stable Pt(II) metallosupramolecular complexes based on ambidentate ligands have been designed, synthesized and fully characterized. The structure of complexes has been determined by various analytical techniques including NMR spectroscopy and TOF-MS. Additionally, the single crystal structure of 2 was determined by X-ray diffraction. The catalytic activity of these complexes in hydrosilylation has been investigated, establishing that both have similar high activity and selectivity within a broad scope of structurally distinct olefins and hydrosilanes.

METHOD FOR PRODUCING ORGANOSILICON COMPOUND BY HYDROSILYLATION WITH METALLIC-ELEMENT-CONTAINING NANOPARTICLES

An organosilicon compound can be efficiently produced by using metallic element-containing nanoparticles such as a platinum element-containing nanoparticle having a solvent on surface as a catalyst of the hydrosilylation reaction of alkenes.

Careful investigation of the hydrosilylation of olefins at poly(ethylene glycol) chain ends and development of a new silyl hydride to avoid side reactions

Hydrosilylation of olefin groups at poly(ethylene glycol) chain ends catalyzed by Karstedt catalyst often results in undesired side reactions such as olefin isomerization, hydrogenation, and dehydrosilylation. Since unwanted polymers obtained by side reactions deteriorate the quality of end-functional polymers, maximizing the hydrosilylation efficiency at polymer chain ends becomes crucial. After careful investigation of the factors that govern side reactions under various conditions, it was related that the short lifetime of the unstable Pt catalyst intermediate led to the formation of more side products under the inherently dilute conditions for polymers. Based on these results, two new chelating hydrosilylation reagents, tris(2-methoxyethoxy)silane (5) and 2,10-dimethyl-3,6,9-trioxa-2,10-disilaundecane (6), have been developed. It was demonstrated that the hydrosilylation efficiency at polymer chain ends was significantly increased by employing the internally coordinating hydrosilane 5. In addition, employment of the internally coordinating disilane species 6 in an addition polymerization with 1,5-hexadiene by hydrosilylation reaction yielded a polymer with high molecular weight (Mn = 9300 g/mol), which was significantly higher than that (Mn = 2600 g/mol) of the corresponding polymer obtained with non-chelating dihydrosilane, 1,1,3,3-tetramethyldisiloxane.

Thiols make for better catalysts: Au nanoparticles supported on functional SBA-15 for catalysis of Ullmann-type homocouplings

A strategy for arraying small gold nanoparticles on a mesoporous support modified with single-component or mixed self-assembled monolayers is described. The use of mixed surface modifiers allows easy access to a range of surface chemistries and modalities of interaction between nanoparticles and supports. A combination of thiol groups and linear semifluorinated chains effectively stabilized the nanoparticles against aggregation, while preserving their catalytic activity. The thiol-fluorous-supported catalyst was found active in Ullmann-type homocoupling of aryl halides and showed exceptional selectivity in this reaction.

An Easily Accessed Nickel Nanoparticle Catalyst for Alkene Hydrosilylation with Tertiary Silanes

The first efficient and non-precious nanoparticle catalyst for alkene hydrosilylation with commercially relevant tertiary silanes has been developed. The nickel nanoparticle catalyst was prepared in situ from a simple nickel alkoxide precatalyst Ni(OtBu)2?x KCl. The catalyst exhibits high activity for anti-Markovnikov hydrosilylation of unactivated terminal alkenes and isomerizing hydrosilylation of internal alkenes. The catalyst can be applied to synthesize a single terminal alkyl silane from a mixture of internal and terminal alkene isomers, and to remotely functionalize an internal alkene derived from a fatty acid.

Application of polyethyleneglycol (PEG) functionalized ionic liquids for the rhodium-catalyzed hydrosilylation reaction of alkenes

Abstract Rh(PPh3)3Cl-polyethyleneglycol (PEG) functionalized ionic liquids with various anions were used as a catalytic system for the hydrosilylation reaction of alkenes. The influence of the anion of the ionic liquid has been investigated. It was found that the anion has an impact on the catalytic activity and selectivity. [PEG400DIL][PF6]-[Rh(PPh3)3Cl] shows an improved catalytic performance towards the hydrosilylation reaction of alkenes. The scope of alkenes and recycling of the catalytic system have been investigated.

MCM-41-immobilised bidentate nitrogen platinum complex: A highly efficient and recyclable phosphine-free catalytic system for the hydrosilylation of olefins

An MCM-41-immobilised bidentate nitrogen platinum complex (MCM-41-2N-Pt) was very conveniently synthesised from commercially available and cheap 3-(2-aminoethylamino)propyltrimethoxysilane by immobilisation on the mesoporous silica nanoparticles, MCM-41, followed by reaction with potassium chloroplatinite. It was found that the MCM-41-2N-Pt complex is a highly efficient catalyst for the hydrosilylation of olefins with triethoxysilane and can be easily recovered and reused several times without significant loss of activity.

A novel fumed silica-supported nitrogenous platinum complex as a highly efficient catalyst for the hydrosilylation of olefins with triethoxysilane

A novel fumed silica-supported nitrogenous platinum complex was conveniently prepared from cheap γ-aminopropyltriethoxysilane via immobilization on fumed silica in toluene, followed by a reaction with hexachloroplatinic acid. The title complex was characterized by fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). It was found that the complex is an efficient and stable catalyst for the hydrosilylation of olefins with triethoxysilane. The title platinum complex could be separated by simple filtration and reused several times without any appreciable loss in the catalytic activity. Crown Copyright

MCM-41-supported bidentate phosphine rhodium complex: An efficient and recyclable heterogeneous catalyst for the hydrosilylation of olefins

MCM-41-supported bidentate phosphine rhodium complex (MCM-41-2P-RhCl 3) was conveniently synthesized from commercially available and cheapγ-aminopropyltriethoxysilane via immobilization on MCM-41, followed by reacting with diphenylphosphinomethanol and rhodium chloride. It was found that the title complex is a highly efficient catalyst for the hydrosilylation of olefins with triethoxysilane and can be recovered and recycled by a simple filtration of the reaction solution and used for at least 10 consecutive trials without any decreases in activity.