Anhui Liwei Chemical Co., Limited
Products

3-Fluoro-4-Vinylphenol


    • Product Name 3-Fluoro-4-Vinylphenol
    • Alias 3-Fluoro-4-hydroxy-styrene
    • Einecs 810-021-8
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    149317

    Chemical Name 3-Fluoro-4-vinylphenol
    Cas Number 329735-74-6
    Molecular Formula C8H7FO
    Molecular Weight 138.14
    Appearance Pale yellow to light brown solid
    Boiling Point 262-263 °C
    Melting Point 41-44 °C
    Density 1.19 g/cm3
    Smiles C=CC1=CC(=C(C=C1)O)F
    Inchi InChI=1S/C8H7FO/c1-2-6-3-4-7(10)8(9)5-6/h2-5,10H,1H2

    As an accredited 3-Fluoro-4-Vinylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "3-Fluoro-4-Vinylphenol, 10g." Features hazard symbols, product code, lot number, and supplier information.
    Shipping 3-Fluoro-4-Vinylphenol is shipped in secure, airtight containers to prevent moisture absorption and contamination. The packaging complies with chemical safety regulations, including labeling for hazardous materials. The product is transported at ambient temperature, with appropriate documentation, and in accordance with local, national, and international shipping guidelines for chemicals.
    Storage 3-Fluoro-4-vinylphenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat sources, open flames, and direct sunlight. It should be kept away from incompatible materials such as strong oxidizers. Proper labeling and secondary containment are recommended. Ensure storage in compliance with all local regulations and safety protocols.
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    Certification & Compliance
    More Introduction

    Introducing 3-Fluoro-4-Vinylphenol: Unique Features and Practical Value From the Manufacturer’s Bench

    Real Chemistry in Action: How We Developed 3-Fluoro-4-Vinylphenol

    In the years we’ve spent designing and scaling up fine chemicals for researchers and industry players, few molecules have brought out as much hands-on innovation as 3-Fluoro-4-Vinylphenol. At our facility, the heart of production isn’t backroom theory. It’s reactors humming in tandem, chemists checking yields, and line operators logging data by the hour. Delivering 3-Fluoro-4-Vinylphenol refined our process workflows and pushed the team to think about every reaction variable, every filtration, and every shipment.

    The product, known among specialists as 3-fluoro-4-ethenylphenol or 4-hydroxy-3-fluorostyrene, is not another generic aromatic compound. Its synthesis brings together knowledge of halide substitution, vinyl chemistry, and the subtle impact of fluorine on reactivity. Over time, our setup balanced safety, throughput, and purity because we saw chemists in the field needing a clean, reliable supply. Low byproduct levels were not a luxury—many downstream reactions stall if even minute impurities persist.

    Model and Specifications: More Than a Catalog Number

    We produce 3-Fluoro-4-Vinylphenol under the model “FVPH-345” for batch traceability. Each run batches around 500 grams up to multi-kilo scale, which supports both R&D and pilot-phase development. Customers have direct access to each lot’s certificate of analysis, and we keep spectroscopic data on record for every batch.

    Chemically, the compound weighs in at 138.13 g/mol. It presents as a crystalline powder and remains stable under cool, dry storage. As a phenol derivative, it keeps an active aromatic ring, the influence of the para-positioned vinyl group, and an ortho-positioned fluorine atom. GC-MS and NMR routinely indicate purity >98%. Our customers care less about paper numbers and more about what actually comes in the bottle. We track moisture content and test for trace halide, because these can ruin a controlled Pd-catalyzed coupling, or interfere with library synthesis for pharmaceutical screens.

    What Sets 3-Fluoro-4-Vinylphenol Apart From the Old Standbys?

    In practice, new targets in agrochemical and pharma lead discovery mean researchers crave alternatives to vanilla phenol or unsubstituted styrene. Fluorination opens up possibilities on the electronic tuning of molecules, often increasing metabolic stability and modulating binding affinity for drug targets. We field requests from research teams optimizing the next potential kinase inhibitor or tweaking polymer backbones for better thermal resistance.

    Traditionally, 4-vinylphenol or non-fluorinated analogs stand in as feedstock for polymerization or further functionalization. The strategic placement of fluorine in 3-Fluoro-4-Vinylphenol acts as a switch. It alters reaction rates in cross-couplings and changes the physical properties of any downstream intermediate. The difference shows up not just on NMR—they sweat it out in the fume hood, comparing reaction times, yield reproducibility, and final product profiles.

    We see one of the main distinctions: regular 4-vinylphenol rapidly oxidizes and polymerizes without careful handling, forcing users to compromise on storage and process routines. Our fluorinated version maintains greater oxidative resilience, extending product shelf life and allowing for higher success rates in planned reactions. We’ve listened to reports from those who tried running the same coupling with standard versus fluorinated phenol. Fewer retries, less downtime, fewer surprise impurities on LC-MS readouts. That matters, not just for bench scientists but for project timelines and budgets.

    Experiences From Our Production Floor: Challenges and Insights

    Early on, producing this material at gram scale didn’t match the demands of scale-up campaigns. Fluorine compounds can foul up glassware, accelerate corrosion in stirrers, or drop out in side-streams nobody anticipated. Our team tested a dozen reaction vessels, watching for trace leaching or yield loss. Not every batch succeeded. Failed runs told us more than successful ones: aggressive control over base strength and solvent composition trimmed side reactions, slashed waste, and prevented sticky residues that shut down lines.

    Years of practical work led us to optimize extraction sequences and storage, keeping phenol vapor emission low and product granularity consistent. Handling fluorinated intermediates safely drove investments in better ventilation and gloves, so our operators and the end users both trust the integrity of the container—no seepage, no contamination from residual solvents or organometallics.

    We've eliminated several unwanted adducts by fine-tuning reaction temperatures and swapping from traditional bases to milder alternatives where possible. Customers notice fewer isolated impurities, which supports cleaner downstream chemistry. Recipes that fail at the academic scale often need this kind of re-route, because bench-top assumptions fall apart in reactors ten times larger.

    Why 3-Fluoro-4-Vinylphenol Attracts Synthetic Chemists and Engineers

    From what we’ve seen, demand for this specialty compound arrives from both pharma and advanced materials labs. Medicinal chemists use the vinyl handle to graft on new substituents, assembling phenolic ethers and biaryl linkages. The fluorine on the ring often heightens resistance against oxidative metabolism, so lead compounds stay active longer in preclinical models. There’s a tangible payoff: every extra day of shelf life on a key intermediate means budgets go further and workflows run more smoothly. Some of our partners even report improvements in their in vitro screening pools after switching from non-fluorinated to fluorinated analogs.

    Polymer scientists come for the same molecular features but use them differently. The overlay of both a phenol and a vinyl gives flexibility in synthesizing block copolymers, surfactants, or adhesives where small changes in structure spell big performance jumps. Compared to simple styrenes, this compound’s balance of rigidity and reactivity opens up new monomer design strategies. We’ve seen users push glass transition temperatures higher, or add controlled sites for post-polymerization derivatization—all from switching a single atom in the precursor structure.

    Ion-exchange resin engineers occasionally call for this molecule, too. The unique arrangement enables denser site functionalization and introduces new electronic properties that affect selectivity and throughput. We’ve sent batches specifically for column packing studies, noting how adsorption-desorption equilibria shift once a fluorine atom tips the overall polarity balance.

    Supporting Real-World Problem Solving

    Reproducibility takes more than a guaranteed COA number. Reliable lab performance draws on the whole production setup: workers refine process conditions, QC techs test every output, and sales support liaises with end users to guide troubleshooting. Customers share results, stumble across weird byproducts, and let us know when tricky conversions pop up. Through regular feedback channels, our team tracks case studies of substitution reactions, hydrogenations, and polymerizations in which a small shift in purity or moisture content makes or breaks a whole experiment.

    Chemists working with precious metal catalysts know that uncontrolled halide, acid, or moisture in their starting materials can undermine expensive runs. Through our hands-on collaboration with process chemists, we’ve reduced background signals in downstream NMRs and LC/GC, supporting both reliable scale-up and new reaction development. User feedback often points us toward process refinements that wouldn’t show up in controlled, highly specific lab trials. In one recurring issue, a pharma group reported variability in vinyl coupling efficiency depending on after-sales storage—so we updated guidance, insulated packing better, and increased in-house shelf-life monitoring with periodic reanalysis beyond the standard expiry window. Our supply chain now supports cold-chain logistics for sites with elevated storage needs, reducing waste for programs with staggered project pipelines.

    3-Fluoro-4-Vinylphenol in the Broad Research Landscape

    The growth of fluoroaromatic chemistry in discovery pipelines has shifted the ingredient toolkit for fine chemists. Many biologically active molecules now feature small, targeted fluorine substitutions, and the need for scalable, cleanly made building blocks matters more than abstract supply chains. Years back, large-scale fluorinated intermediates could bottleneck process development because conventional suppliers offered only small lots, intermittent supply, or inconsistent purity. Supporting new compound series required round-after-round of working with purchasing teams to minimize non-compliance risk—largely due to off-specification starting material. These headaches push companies to seek closer relationships with primary producers, cutting dependence on shadowy intermediaries with uncertain material provenance.

    In the pharmaceutical sector, our direct buyers tell us small changes in fluorine substitution create big shifts in biological activity and absorption rates. The same logic echoes in agrochemical synthesis, where lead optimization studies depend on rapid access to tailored phenol derivatives to probe environmental resistance and crop uptake efficiency. Looking beyond discovery, scale-up chemists need confidence that pilot runs won’t waver in purity or supply. We often provide data packets for regulatory submissions, supporting clients in IND filings and REACH registrations by sharing full analytical records and backing material traceability from raw materials onward.

    Polymers and performance materials also take center stage. For every bottle of 3-Fluoro-4-Vinylphenol, there’s usually a festival of downstream analytics: GPC, DSC, TGA, and tens of pages of notes as researchers optimize reaction blends and tweak surface modification studies. Switch the starting material, and those carefully tuned recipes don’t translate—a hard-learned fact for teams who rely on formulaic purchasing. That’s why many now talk directly to manufacturers, not middlemen. Changes in supply lots, even tiny ones, ripple through workflows that depend on micron-level tweaks.

    Balancing Cost, Quality, and Scale in Today’s Market

    Real-world manufacturing faces competing priorities. Synthetic routes for fluorinated aromatics bring higher direct costs. Specialty raw materials, handling protocols, and safety requirements eat up more of the budget than non-fluorinated analogs. Price sensitivity differs by sector: pharma budgets often tolerate premium costs for top-purity, while polymer houses weigh price per kilo more closely. We’ve tracked our own cost-reduction campaigns. Early processes used exotic reagents and generated higher waste rates. By adjusting reaction conditions and switching to supplier-consistent base stocks, we trimmed direct costs without sacrificing purity, reallocating savings into stricter in-process controls.

    There’s no shortcut for safety in production scaleups. The risk of runaway reactions or impurity carryover increases with batch size—the hazards are more than theoretical. We run aggressive monthly audits of everything from pressure equipment to waste incineration records, embedding a culture where everyone speaks up about process oddities or recurring issues. Quick reporting allows root-cause analysis by teams who understand both bench-level chemistry and how pipes, reactors, and chillers behave in industrial settings.

    The Collaborative Advantage: Real Feedback Shapes Better Chemistry

    Our commitment to long-term partnerships means we gather more than just order volumes. Many clients ask to modify batch size, packaging type, or delivery timeline. Occasional requests arrive for custom particle sizing or different solvent residues, as each downstream process finds its own sticking points. We invite feedback: whether a customer notices a tiny shift in color on opening, or a technician’s TLC shows an unexpected minor spot, such micro-level information helps us tweak purification runs, update process maps, and tune the drying cycle.

    We support toll manufacturing, joint development programs, and technical workshops around handling and integrating specialty phenol derivatives. Open lines of communication give all involved more control over process risk—and more opportunity for product innovation. Chemistry changes fast: having a direct partnership with actual manufacturers gives R&D teams flexibility and speed without compromising on material safety or regulatory compliance.

    Practical Notes and Future Opportunities

    Users often share tips back to us. Some find that storing 3-Fluoro-4-Vinylphenol in argon extends shelf-life, others get better yield on methylations with low ppm water content. Downstream reaction profiles depend on both handling discipline and the initial batch characteristics. We’re quick to swap out lots and even redesign shipping protocols if a customer trial uncovers a solubility hiccup or if certain applications show sensitivity to isomerics or trace metals.

    Functional-group innovation drives chemistry today. Many are rethinking how they design ligands, coupling partners, or material additives in both established and emerging sectors. 3-Fluoro-4-Vinylphenol stands out for those who measure impact by experiment, not just catalog listings. Any time a team finds that subtle switch yields a new property, a longer-lasting product, or a more selective intermediate, we share in that result. Our production lines and R&D tables grow along with this work: supporting the push for new discoveries, cleaner reactions, and safer supply chains.

    Conclusion: A Synthesis Forged in Practice, Not Just on Paper

    Supplying 3-Fluoro-4-Vinylphenol taught us the difference between theory and reality. The chemists and engineers we serve gave us real-world lessons—on trace impurities, failed couplings, and the time-saving value of reliable sourcing—changing both our manufacturing culture and how we support each order. This product, unique in structure and tuned by a single fluorine atom, embodies what happens when manufacturing meets discovery, on the ground and in close partnership with those who use what we make. We look forward to every experiment, every challenge shared, and every improvement realized together.