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HS Code |
283886 |
| Cas Number | 382-40-1 |
| Iupac Name | 1-(2,3,3,3-Tetrafluoroprop-1-en-1-yl)benzene |
| Molecular Formula | C9H7F4 |
| Molar Mass | 192.15 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 126-128 °C |
| Density | 1.176 g/cm³ (at 25 °C) |
| Refractive Index | 1.459 (at 20 °C) |
| Smiles | C=CC(F)(F)C(F)(F)c1ccccc1 |
| Inchi | InChI=1S/C9H7F4/c10-9(11,12)7-6-8-4-2-1-3-5-8/h1-7H |
| Solubility In Water | Insoluble |
As an accredited Perfluoroallylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Perfluoroallylbenzene, 100 g: Supplied in a sealed amber glass bottle with a tamper-evident cap and chemical hazard labeling. |
| Shipping | Perfluoroallylbenzene should be shipped in tightly sealed, corrosion-resistant containers, protected from moisture and direct sunlight. Transport under ambient temperature with proper labeling, as it may be classified as a hazardous substance. Adhere to all relevant regulations for fluorinated organics, and ensure documentation for safe handling during transit. |
| Storage | Perfluoroallylbenzene should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and kept in a cool, dry, well-ventilated area away from heat, flame, and incompatible substances like strong oxidizing agents. Protect from moisture and direct sunlight. Clearly label the storage area and ensure that appropriate chemical safety protocols and personal protective equipment are in place. |
Applications of Perfluoroallylbenzene in Industrial ManufacturingAs a specialized manufacturer of Perfluoroallylbenzene, we supply this high-purity raw material to advanced sectors where fluorinated aromatics enable demanding material properties. Below, we detail main industry segments and technical integration points, illustrating how our partners deploy this molecule in their established production flows. 1. Advanced Fluoropolymer Synthesis for ElectronicsManufacturers use Perfluoroallylbenzene to introduce unique aromatic-perfluoroalkyl structures in high-performance fluoropolymers for electronics. The compound participates in free-radical polymerizations and grafting reactions to tailor insulation and dielectric properties required in microelectronics and specialty cable coatings. Typical integration involves controlled copolymerization with tetrafluoroethylene (TFE) or perfluoroalkyl vinyl ether monomers, where the aromatic unit improves resistance to voltage breakdown and thermal degradation seen in semiconductor isolation and flexible PCBs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Surface Treatment Additives for Anti-Fouling CoatingsIndustrial coating formulators use Perfluoroallylbenzene as a co-monomer or functional additive to deliver ultra-low surface energy in anti-fouling paint systems. The molecule brings both perfluorinated and aromatic activity, improving adhesion between the coating matrix and underlying metals or composites while retaining resistance to biological adhesion in marine and fouling-prone industrial environments. This material primarily enters acrylic or epoxy crosslinkable systems applied by spray or dip processes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Precision Chemical Vapor Deposition Precursors for Optical FilmsCVD operators select Perfluoroallylbenzene as a fluorine-rich precursor in preparation of optical-grade, abrasion-resistant fluoropolymer layers. Its volatility and clean decomposition profile afford high-thickness uniformity for anti-reflective and protective films on glass, optical sensors, and display panels. This material undergoes vapor-phase polymerization under strict reactor controls, enabling tough coatings with controlled refractive index and long-term clarity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Elastomer Modification for Chemical Process EquipmentIn chlor-alkali and acid handling applications, engineers incorporate Perfluoroallylbenzene as a reactive monomer to modify FKM and FFKM elastomer formulations. Its fluorinated aromatic structure imparts higher swelling resistance and reduces permeation of harsh chemicals, resulting in improved service life for seals, valve seats, and gaskets. Materials are processed by conventional elastomer blending and crosslinking, with precise compounding to maintain mechanical strength and elasticity in aggressive operational settings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Ingredient for High-Temperature Lubricant Additive ManufacturingProducers of specialty lubricants use Perfluoroallylbenzene to synthesize high-stability additives for greases and oils operating above 250°C, especially in aerospace and semiconductor manufacturing. The aromatic-perfluoro structure forms the basis for stable fluorinated aryl ethers and oligomers, protecting moving components against oxidation and thermal decomposition. Manufacturers carry out step-growth reactions, isolating functionalized intermediates through fractional distillation and chromatographic purification to ensure batch-to-batch reproducibility. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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