Reactive thiol (–SH) group enables covalent bonding with metals, sulfur-cured elastomers, and inorganic surfaces.
Three hydrolyzable methoxy groups ensure strong siloxane network formation with glass, silica, and metal oxides.
Excellent hydrolytic stability in anhydrous or low-moisture formulations prior to application.
Low volatility and favorable handling characteristics compared to mercaptosilanes with ethoxy or chloro substituents.
Enables improved adhesion, dispersion, and interfacial reinforcement in hybrid organic–inorganic systems.
Tire tread compounds for enhanced silica–rubber coupling in high-performance passenger and truck tires.
Adhesion promoters in rubber-to-metal bonding systems (e.g., engine mounts, vibration dampers).
Surface modification of fillers such as precipitated silica, fumed silica, and glass fibers for composites.
Functionalization of nanoparticles and mesoporous materials for catalysis and sensing applications.
Hybrid sol–gel coatings requiring dual reactivity toward both organic polymers and inorganic substrates.
| Chemical Type | Organofunctional alkoxysilane |
| IUPAC Name | (3-Mercaptopropyl)trimethoxysilane |
| Product Form | Clear, colorless to pale yellow liquid |
| Appearance | Homogeneous liquid, free from visible particles or phase separation |
| Density (20 °C) | 1.05–1.07 g/cm³ |
| Refractive Index (20 °C) | 1.432–1.436 |
| Flash Point (PMCC) | ≈ 95 °C |
| Solubility | Miscible with common organic solvents (e.g., ethanol, acetone, toluene); hydrolyzes in water |
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