Z-6333;KBM-7103
Dow Corning;ShinEtsu
Siwin-F331
429-60-7
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3,3,3-Trifluoropropyltrimethoxysilane, designated Siwin-F331 with CAS number 429-60-7, is a fluorine-functional silane coupling agent used primarily as a key intermediate in the production of fluorosilicone materials. The molecule features a trimethoxysilyl group for inorganic surface bonding and a 3,3,3-trifluoropropyl group that imparts low surface energy and fluorochemical properties.
Commercial procurement teams in the fluorosilicone rubber, fluorosilicone resin, and specialty coatings sectors source this material when formulations require oil resistance, solvent resistance, water repellency, and low surface friction characteristics. The product serves as a fundamental building block for fluoro-modified silicone polymers that perform in environments where standard silicones lack sufficient chemical resistance.
Parameter | Specification |
|---|---|
Product Code | Siwin-F331 |
Chemical Name | 3,3,3-Trifluoropropyltrimethoxysilane |
CAS Number | 429-60-7 |
Molecular Formula | C6H13F3O3Si |
Molecular Weight | 218.25 g/mol |
Appearance | Colorless Clear Liquid |
Purity (by GC) | ≥ 98.0% |
Density (25°C, g/cm³) | 1.097 |
Boiling Point (760 mmHg) | 124.4 °C |
Refractive Index (n20/D) | 1.355 |
Flash Point | 29 °C |
Equivalent Models | Z-6333; KBM-7103 |
Equivalent Brands | Dow Corning; ShinEtsu |
Purity is determined by gas chromatography with a minimum threshold of 98.0 percent. All physical property measurements are conducted under controlled laboratory conditions with documented temperature parameters.
The molecular structure of 3,3,3-trifluoropropyltrimethoxysilane consists of a silicon atom bonded to three methoxy groups and one 3,3,3-trifluoropropyl chain. The trifluoropropyl group contains three fluorine atoms on the terminal carbon, creating a strong electron-withdrawing effect and low polarizability that underpin the product's surface-modifying properties.
The trimethoxysilyl group undergoes hydrolysis in the presence of moisture, generating silanol groups that can condense with surface hydroxyls on inorganic substrates or with other silane molecules to form siloxane networks. Hydrolysis proceeds under neutral, acidic, or basic catalysis, with reaction rates varying by pH and temperature.
The trifluoropropyl functional group significantly lowers surface energy when incorporated into polymer systems. Measured water contact angles on treated surfaces typically increase substantially compared to untreated or hydrocarbon-modified surfaces, corresponding to improved water repellency and antifouling performance. Oil repellency and solvent resistance follow similar trends, as the low surface energy fluorinated groups resist wetting by both aqueous and organic liquids.
The primary industrial application of 3,3,3-trifluoropropyltrimethoxysilane is as a critical intermediate in the synthesis of fluorosilicone rubbers (FVMQ). Through hydrolysis and polymerization processes, the silane contributes trifluoropropyl-functional siloxane units to the polymer backbone. Fluorosilicone rubbers incorporating these units combine the temperature flexibility of silicone elastomers with the fuel and oil resistance of fluorocarbon elastomers, making them suitable for aerospace, automotive fuel systems, and petroleum processing sealing applications.
The product serves as a building block for fluorosilicone resins used in high-performance protective coatings. These resins find application in industrial settings requiring resistance to aggressive chemicals, weathering, and UV exposure. Coating formulators use fluorosilicone resins to produce finishes that maintain gloss and barrier properties after extended outdoor service.
In composite and coating formulations, the silane treats the surface of mineral fillers and pigments. The methoxy groups anchor to the filler surface while the trifluoropropyl groups orient outward, modifying the filler-matrix interface. This treatment improves dispersion of fillers in fluoropolymer matrices and enhances the mechanical and barrier properties of the resulting composite.
Architectural and industrial coating manufacturers incorporate the fluoro silane into formulations designed for stain resistance and easy-clean performance. Treated coating surfaces exhibit reduced surface energy, causing water and oily liquids to bead and roll off rather than spread and penetrate. This property benefits exterior building facades, kitchen and bathroom surfaces, and industrial equipment coatings.
In mold release applications for rubber and plastic processing, the fluoro silane provides a low-energy surface that facilitates part removal. The product also functions as an anti-fouling additive in marine and industrial coatings, where reduced surface energy discourages the attachment of biological organisms and environmental contaminants.
The carbon-fluorine bond in the trifluoropropyl group exhibits high bond dissociation energy, contributing to resistance against oxidation, UV radiation, and chemical attack. Fluorosilicone materials formulated with this intermediate maintain performance across a broader range of chemical exposures compared to conventional silicone materials.
In coating and ink formulations, the fluoro silane contributes to improved leveling and flow by reducing surface tension. The fluorinated component migrates to the coating surface during curing, creating a uniform, low-energy surface layer that enhances both aesthetic appearance and functional performance.
Trifluoropropyl-modified silicones demonstrate resistance to thermal degradation and UV-induced property changes. Formulators in outdoor coating and sealant applications select these materials when long-term retention of mechanical properties and appearance is required.
The dual functionality of the molecule promotes adhesion between fluoropolymers and inorganic substrates. The silane bridges the chemical dissimilarity between fluorinated organic polymers and glass, metal, or mineral surfaces, improving bond strength and durability in fluoropolymer coatings and composites.
Standard packaging options for industrial applications include steel drums with appropriate inner linings and intermediate bulk containers (IBCs) for volume shipments. Custom packaging arrangements can be coordinated for enterprise customers with specific logistics or handling requirements.
Store the product in a cool, dry, well-ventilated area away from sources of ignition and direct sunlight. Keep containers tightly sealed to prevent moisture ingress, as the methoxy groups are moisture-sensitive and will undergo gradual hydrolysis upon exposure to atmospheric humidity. Recommended storage temperature ranges from 5°C to 30°C.
The product has a flash point of 29°C, classifying it as a flammable liquid. Handling procedures should follow standard industrial hygiene practices for chemical processing, including appropriate personal protective equipment and grounding of transfer equipment. Material Safety Data Sheet (MSDS) documentation is available upon request for all commercial procurement inquiries.
The methoxy version hydrolyzes more rapidly than the ethoxy version, making it suitable for processes requiring faster reaction kinetics. The ethoxy version generates ethanol as a hydrolysis byproduct rather than methanol, which may be preferred in certain regulatory or formulation contexts. Selection depends on specific processing conditions and end-use requirements.
Yes, the product is compatible with most organic solvent systems used in industrial coating formulations. Typical addition levels range from 0.5 percent to 3.0 percent by weight of total formulation, depending on the desired surface modification effect and pigment/filler loading.
When stored in sealed original containers under recommended temperature and humidity conditions, the product maintains specification compliance for a minimum of 12 months from the date of manufacture. Extended storage may result in gradual viscosity increase due to minor condensation reactions.
Yes, the product is classified as a flammable liquid and must be transported in accordance with applicable dangerous goods regulations. Proper packaging, labeling, and documentation are required for all shipment modes. Specific transport classification details are provided in the Safety Data Sheet.
Higher purity levels contribute to more consistent polymerization kinetics and more uniform polymer chain architecture, which translates to more predictable mechanical and chemical resistance properties in the final fluorosilicone product. The 98.0 percent minimum GC purity specification supports consistent batch-to-batch performance for industrial production.
