Highly reactive thiol (–SH) group enables strong covalent bonding with metals, metal oxides, and sulfur-curable elastomers.
Three hydrolyzable methoxy groups ensure rapid and uniform silanol formation for robust interfacial adhesion to inorganic substrates.
Excellent compatibility with organic polymers, resins, and solvents facilitates easy incorporation into coating, adhesive, and sealant formulations.
Enhances dispersion stability of fillers such as silica and carbon black in rubber compounds, improving mechanical performance.
Acts as an effective coupling agent in hybrid organic–inorganic systems, promoting durable crosslinking under ambient or mild thermal conditions.
Silica-reinforced tire tread compounds to improve wet grip, rolling resistance, and abrasion resistance.
Adhesion promoters for metal-to-rubber bonding in automotive vibration dampers and engine mounts.
Surface modification of glass, silica, and metal oxide nanoparticles for functional composites and coatings.
Hybrid sol–gel precursors in corrosion-inhibiting primers and protective thin-film coatings.
Thiol-functionalized matrix modifiers in dental restorative materials and biomedical device coatings.
| Chemical Type | Organofunctional alkoxysilane |
| Product Form | Liquid |
| Appearance | Colorless to pale yellow clear liquid |
| Molecular Weight | 238.4 g/mol |
| Specific Gravity (25°C) | 1.05–1.07 g/cm³ |
| Refractive Index (25°C) | 1.435–1.445 |
| Flash Point (Tag Closed Cup) | ≈ 95°C |
| Solubility | Miscible with common organic solvents (e.g., ethanol, toluene, acetone); hydrolyzes in water |
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