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HS Code |
490893 |
| Chemicalname | Vinyl Trifluoroacetate |
| Molecularformula | C4H3F3O2 |
| Molarmass | 140.06 g/mol |
| Casnumber | 1511-24-4 |
| Appearance | Colorless liquid |
| Density | 1.342 g/mL at 25°C |
| Boilingpoint | 56-58°C |
| Meltingpoint | -52°C |
| Refractiveindex | 1.327 |
| Solubility | Decomposes in water |
As an accredited Vinyl Trifluoroacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Vinyl Trifluoroacetate, 100g, is supplied in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling. |
| Shipping | Vinyl Trifluoroacetate should be shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. Avoid exposure to heat, moisture, and direct sunlight. Label all packages with appropriate hazard symbols and transport according to local, state, and international regulations for flammable and reactive organic chemicals. Handle with proper protective equipment. |
| Storage | Vinyl trifluoroacetate should be stored in a cool, dry, and well-ventilated area, away from heat, open flames, and incompatible materials such as strong bases and oxidizers. Keep the container tightly closed and protected from moisture. Use only approved, corrosion-resistant containers. Proper labeling and secure storage will help prevent accidental exposure or release of vapors. Handle under an inert atmosphere if possible. |
Applications of Vinyl Trifluoroacetate in Industrial ManufacturingVinyl Trifluoroacetate serves as a specialized fluorinated intermediate used by advanced manufacturers to introduce trifluoromethyl and vinyl functionalities into downstream chemical products. Its reactivity profile supports targeted molecular modifications in complex synthesis routes. As a direct producer, we highlight key application segments where this raw material adds value by enabling industrial processes that meet sector-specific regulatory and production standards. 1. Pharmaceutical Intermediate SynthesisIn the pharmaceutical sector, this compound is selected to construct trifluoromethylated building blocks integral for API development, supporting the synthesis of molecules where fluorine content enhances pharmacokinetic profiles. Process chemists incorporate it during late-stage functional group installation or to prepare protected trifluoroacetic acid derivatives, with process control for impurity profiles in cGMP environments. Downstream conversion often entails hydrolysis, coupling, or further vinyl group transformations, strictly monitored through validated analytical protocols. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingAgrochemical formulators utilize this material to synthesize active ingredients where trifluoroacetic moieties deliver improved crop protection characteristics, such as higher metabolic stability and environmental persistence. It functions in selective functionalization steps during actives synthesis, particularly for fluorinated herbicide and fungicide frames. Quality teams validate input ratio based on targeted A.I. load and residual fluorine checks per market-specific regulatory constraints. Industry compliance standards
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3. Specialty Fluoropolymer ModificationFluoropolymer manufacturers introduce this chemical during copolymerization to tailor solubility and thermal characteristics in engineered resins. Its vinyl group reacts under radical or ionic polymerization conditions, allowing incorporation into the polymer backbone or as a reactive side-group. Quality managers ensure dosage precision for targeted copolymer architectures, with process integration generally before melt-processing or emulsion polymerization finalization. Industry compliance standards
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4. Fine Chemical Intermediate for Laboratory and Pilot Scale SynthesisChemical research organizations and custom synthesis producers require high-purity sources of this compound to serve as a reactive intermediate for small-molecule development, ligand design, or as a labeled precursor in isotopic studies. Addition occurs stepwise according to process protocols, often under argon and with in-process monitoring for endpoint determination. Carefully calibrated input drives reproducibility and minimizes side-product formation in complex multi-stage routes. Industry compliance standards
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5. Electronic Chemicals for PhotolithographyManufacturers of advanced electronic photoresists employ this material as a precursor for introducing trifluoroacetyl groups, which enhance etch resistance and fine-line definition in semiconductor fabrication. It is carefully dosed to maintain pattern transfer accuracy, minimizing outgassing and resist profile variability. Input ratio is tightly managed in pilot-scale blending before resist coating, with post-polymerization processing to control feature stability. Industry compliance standards
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6. Surface-Active Agents for Performance CoatingsProducers of specialized coatings incorporate this raw material in the synthesis of surface-modifying additives, leveraging the trifluoroacetyl group to impart chemical durability and hydrophobicity in high-value coatings. Addition is carried out during pre-polymer formation or post-curing surface functionalization, with usage calibrated to achieve specified contact angle and abrasion resistance in the final application. Analytical testing verifies compliance to environmental and material performance requirements. Industry compliance standards
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