Reactive thiol (–SH) group enables covalent bonding with metals, sulfur-curable elastomers, and gold surfaces.
Three hydrolyzable methoxy groups ensure strong siloxane network formation on silica, glass, and metal oxides.
Excellent coupling efficiency between inorganic fillers and organic polymer matrices in rubber and adhesive formulations.
Low volatility and good storage stability under recommended conditions (cool, dry, inert atmosphere).
Enables improved dispersion of fillers and enhanced interfacial adhesion in high-performance composites.
Silica-reinforced passenger and truck tire tread compounds (especially for low-rolling-resistance tires).
Adhesion promoters in rubber-to-metal bonding systems (e.g., engine mounts, bushings).
Surface functionalization of nanoparticles for catalysis, biosensors, and conductive composites.
Hybrid sol-gel coatings requiring thiol-reactive anchoring on oxide substrates.
Filler treatment for EPDM, NBR, and SBR compounds demanding high tear strength and dynamic performance.
| Chemical Type | Organofunctional alkoxysilane |
| Product Form | Liquid |
| Appearance | Colorless to pale yellow clear liquid |
| Molecular Formula | C6H16O3SSi |
| Functional Groups | Thiol (–SH) and three methoxy (–OCH3) groups |
| Density (20 °C) | Approx. 1.05 g/cm³ |
| Refractive Index (20 °C) | Approx. 1.430–1.440 |
| Storage Conditions | Under nitrogen, in tightly sealed containers at 5–25 °C |
Contact With Us:
E-mail: wangxingqiang@ericwchem.com
Have a Questions? Call Us:
Add:
Building A1, Jiete Industrial Park, Huangpu District, Guangzhou City, Guangdong Province, China