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Vinyl Trifluoroacetate

    • Product Name Vinyl Trifluoroacetate
    • Alias vinyl trifluoroacetate
    • Einecs 212-234-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of Vinyl Trifluoroacetate

    Applications of Vinyl Trifluoroacetate in Industrial Manufacturing

    Vinyl 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 Synthesis

    In 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

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP-NF Monographs (where relevant)
    • European Pharmacopoeia (Ph. Eur.) protocols for API purity
    • FDA cGMP 21 CFR Part 210/211

    Typical usage ratio

    • 0.5–5 mol% of total reactant input, with adjustment based on desired fluorination level and process yield

    Downstream process integration

    • Fed during stage-specific synthesis as a reagent for nucleophilic substitution, vinylation, or as a protected group introduction, followed by purification and intermediate isolation

    Final product types

    • Pharmaceutical intermediates bearing trifluoromethyl substituents
    • Trifluoroacetic acid derivatives for further synthetic transformation
    • Bioactive precursors for oncology and CNS small molecules

    2. Agrochemical Active Ingredient Manufacturing

    Agrochemical 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

    • FAO/WHO International Code of Conduct on Pesticide Management
    • US EPA Pesticide Registration regulations (40 CFR Parts 152-180)
    • EU Regulation (EC) No 1107/2009 concerning plant protection products
    • ISO 17025 laboratory testing for product registration

    Typical usage ratio

    • 0.2–2.5 wt% of batch, optimized to maintain desired fluorine content without excess unreacted monomer

    Downstream process integration

    • Introduced in the core structure assembly or post-condensation functionalization, usually in the vinylation or acylation step under controlled temperature and pressure

    Final product types

    • Fluorinated herbicide actives (e.g., trifluralin derivatives)
    • Fungicidal compounds with trifluoroacetyl moieties
    • Precursor intermediates for insecticidal agents

    3. Specialty Fluoropolymer Modification

    Fluoropolymer 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

    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • ASTM D3307 for Perfluoropolymer Resins
    • REACH (EC 1907/2006) registration for downstream substance use
    • RoHS Directive (2011/65/EU) for polymer materials in electrical applications (as applicable)

    Typical usage ratio

    • 0.5–3 mole% comonomer feed, calculated based on required functional group density in polymer chain

    Downstream process integration

    • Metered into the polymerization reactor either as a solution or neat, enabling copolymerization with tetrafluoroethylene or hexafluoropropylene under inert atmosphere

    Final product types

    • Chemically modified PTFE and FEP fluoropolymers
    • Fluorinated copolymer resins for wire coating
    • Membrane materials with defined fluorine content for fuel cells

    4. Fine Chemical Intermediate for Laboratory and Pilot Scale Synthesis

    Chemical 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

    • ISO 17034 Reference Material Producer Accreditation
    • GLP (Good Laboratory Practice) OECD Guidelines
    • Analytical validation as per ICH Q2(R1)
    • Local hazardous chemicals management policies

    Typical usage ratio

    • 0.1–1 mmol per scale-up cycle or defined by substrate stoichiometry in research processes

    Downstream process integration

    • Charged in Schlenk lines or automated synthesis modules after pre-drying, often as a key step for trifluoroacetylation or as a masked group during multi-step transformations

    Final product types

    • Reference standards for analytical quality control
    • Labeled intermediates for isotopic tracing
    • Synthons for medicinal chemistry and crop protection research

    5. Electronic Chemicals for Photolithography

    Manufacturers 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

    • SEMI Standards for Chemicals (SEMI C93, C94)
    • IEC 62474 for declarable substances in electronic chemicals
    • ISO 9001:2015 for photochemical supply
    • RoHS and REACH compliance for manufacturing environment

    Typical usage ratio

    • 0.3–1.2 wt% of resist formulation, adjusted based on film thickness and lithographic resolution targets

    Downstream process integration

    • Added in solution to resist polymer mixture prior to solvent removal, then processed by spin-coating and UV curing for device fabrication

    Final product types

    • Photolithography resists for microelectronics
    • Etch mask materials for integrated circuit manufacturing
    • High-resolution patterning agents for display technology

    6. Surface-Active Agents for Performance Coatings

    Producers 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

    • ISO 12944-6 Protective Paint Systems Evaluations
    • ASTM D2486 Scrub Resistance of Wall Paints
    • VOC content regulation per EU Directive 2004/42/EC
    • REACH Annex XVII for fluorinated surfactants

    Typical usage ratio

    • 0.05–0.5 wt% in coating formulation, dosage based on substrate type and hydrophobic finish requirements

    Downstream process integration

    • Fed into pre-polymer matrix synthesis or as a post-polymerization surface treatment agent, with additional solvent or catalyst as necessary

    Final product types

    • Anti-graffiti coatings for infrastructure
    • Industrial equipment anti-corrosion paints
    • Water- and oil-repellent finishes for automotive or aerospace use
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