27326-65-4

Basic information

• Product Name: 2-(2-PYRIDYL)ETHYLTRIMETHOXYSILANE
• Synonyms: B-TRIMETHOXYSILYLETHYL-2-PYRIDINE;2-(2-PYRIDYL)ETHYLTRIMETHOXYSILANE;2-TRIMETHOXYSILYLETHYL-2-PYRIDINE;2-(TRIMETHOXYSILYLETHYL)PYRIDINE;2-(2-Trimethoxysilylethyl)-pyridine;Trimethoxy(2-Pyridin-2-Ylethyl)Silane
• CAS NO: 27326-65-4
• Molecular Formula: C10H17NO3Si
• Molecular Weight: 227.33
• Mol File: 27326-65-4.mol

Chemical Properties

• Boiling Point: 103 °C
• Flash Point: >110°C
• Appearance: /
• Density: 1,06 g/cm3
• Vapor Pressure: 0.0462mmHg at 25°C
• Refractive Index: 1.4755
• PKA: 5.87±0.12(Predicted)
• CAS DataBase Reference: 2-(2-PYRIDYL)ETHYLTRIMETHOXYSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-PYRIDYL)ETHYLTRIMETHOXYSILANE(27326-65-4)
• EPA Substance Registry System: 2-(2-PYRIDYL)ETHYLTRIMETHOXYSILANE(27326-65-4)

Safety Data

• Statements: 34-36/37/38-41
• Safety Statements: 23-26-36/37/39-45
• RIDADR: 1760
• TSCA: No
• Hazardous Substances Data: 27326-65-4(Hazardous Substances Data)

Usage

Uses

Used in Coatings Industry:
2-(2-Pyridyl)ethyltrimethoxysilane is used as a surface modifier for enhancing the adhesion and durability of coatings on various substrates. Its reactivity with specific functional groups allows for improved bonding between the coating and the substrate, resulting in a more robust and long-lasting finish.
Used in Adhesives Industry:
In the adhesives industry, 2-(2-Pyridyl)ethyltrimethoxysilane is used as an adhesion promoter to improve the bonding strength between different materials. Its ability to form covalent bonds between organic and inorganic materials contributes to the development of high-performance adhesives with increased resistance to environmental factors.
Used in Organic Synthesis:
2-(2-Pyridyl)ethyltrimethoxysilane is used as a crosslinking agent in organic synthesis, enabling the formation of covalent bonds between molecules. This property is valuable in the development of new materials and advanced composites, where enhanced chemical resistance and structural integrity are desired.
Used in Material Development:
2-(2-Pyridyl)ethyltrimethoxysilane is used as a valuable tool in the development of new materials and advanced composites. Its ability to bond to a variety of substrates and facilitate the formation of covalent bonds between organic and inorganic materials allows for the creation of innovative materials with improved properties and performance.

InChI:InChI=1/C10H17NO3Si/c1-12-15(13-2,14-3)9-7-10-6-4-5-8-11-10/h4-6,8H,7,9H2,1-3H3

Upstream product

• 100-69-6 2-vinylpyridine 
• 2487-90-3 trimethoxysilane 
• 67-56-1 methanol 
• 17082-69-8 2-trichlorosilylethylpyridine 

Relevant articles and documents

ORGANOSILICON COMPOUND, MAKING METHOD, ADHESIVE COMPOSITION, AND ARTICLE

An organosilicon compound having a hydrolyzable silyl group and pyridine ring in the molecule is provided. A composition comprising a polymer having an isocyanate, epoxy or acid anhydride in admixture with the organosilicon compound is shelf stable.

Tailoring photoluminescence properties in ionic nanoparticle networks

To investigate the original and promising luminescence properties of ionic nanoparticle networks (INN), various material compositions were investigated. In this work, the linker used to network the silica nanoparticles was varied; numerous substituted or non-substituted imidazolium, pyrazolium and pyridinium linkers are presented. Photoluminescence experiments on the INN hybrid materials revealed strong emission bands over a broad range in the visible region of the light spectrum. Varying the aromatic linker between the imidazolium units induced clear shifts of the emission maxima up to 100 nm, as a consequence of π-π stacking interactions. Steric hindrance and inductive effects of the substituents, introduced on the aromatic units, also strongly influenced the luminescence properties of the materials by modifying the π-π stacking between the imidazolium rings. Small and wide-angle X-ray scattering (SAXS, WAXS) experiments revealed a clear trend between the obtained structural parameters (short-range order parameter and distance of the aromatic units within the hybrid material) and the luminescence quantum yields of the INN materials. Inducing luminescence: Interesting luminescence properties were observed in ionic nanoparticle networks containing no luminophore. "Playing" with the nanoparticle linker allowed tailoring of the excitation and emission wavelength over a broad range. A clear trend between the obtained structural parameters (obtained from small-angle X-ray scattering experiments) and the luminescence quantum yields of the ionic nanoparticle network materials could be evidenced (see figure).