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3-Vinylphenylboronic Acid

    • Product Name 3-Vinylphenylboronic Acid
    • Alias 3-Vinylboronic acid
    • Einecs 629-516-9
    • 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

    580274

    Productname 3-Vinylphenylboronic Acid
    Casnumber 125248-13-3
    Molecularformula C8H9BO2
    Molecularweight 147.97
    Appearance White to off-white solid
    Meltingpoint 106-110 °C
    Purity ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storageconditions Store at 2-8°C, protected from moisture
    Synonyms 3-Vinylphenylboronic acid; m-Vinylphenylboronic acid
    Smiles B(C1=CC(=CC=C1)C=C)(O)O
    Inchi InChI=1S/C8H9BO2/c1-2-7-4-3-5-8(6-7)9(10)11/h2-6,10-11H,1H2

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

    Packing & Storage
    Packing The 10g bottle of 3-Vinylphenylboronic Acid is sealed in an amber glass vial with a tamper-evident screw cap.
    Shipping 3-Vinylphenylboronic Acid is shipped in tightly sealed containers under inert atmosphere to prevent moisture and oxidation. The product is packed in accordance with regulations for hazardous materials, typically in glass or HDPE bottles, cushioned to avoid breakage. Shipping includes appropriate labeling, safety documentation, and temperature control as needed to maintain product integrity.
    Storage 3-Vinylphenylboronic Acid should be stored in a tightly closed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerated). Avoid exposure to air and sources of ignition, as the compound may be sensitive to oxidation and polymerization. Follow all appropriate safety protocols when handling and storing this chemical.
    Application of 3-Vinylphenylboronic Acid

    Applications of 3-Vinylphenylboronic Acid in Industrial Manufacturing

    As a direct manufacturer of 3-vinylphenylboronic acid, we supply this specialty intermediate to customers operating advanced production lines in the fields of pharmaceuticals, OLED materials, agrochemicals, and specialty polymers. Each application scenario described below reflects our material’s strategic placement in certified, high-value chemical sectors, where its performance and purity directly impact downstream production.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers employ 3-vinylphenylboronic acid as a privileged boron source in Suzuki-Miyaura cross-coupling reactions to construct complex aromatic motifs within late-stage synthesis. The exact integration point involves the arylation or vinylation steps for targeted small-molecule APIs, particularly kinase inhibitors and anti-cancer candidates. Stringent regulatory frameworks require lot-to-lot traceability and consistent assay values, so the supplied raw material must exhibit minimal residual monomers and trace metals. Usage concentrations depend on stoichiometry and process yield allowances, typically governed by medicinal route optimization and secondary purification requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for APIs
    • USP, Ph. Eur., JP monographs for drug substances
    • FDA QSR 21 CFR 210/211 (for pharmaceutical ingredients)
    • Pharmaceutical cGMP system compliance (internal and audited)

    Typical usage ratio

    • 0.8–1.3 molar equivalents as a coupling partner per aryl/vinyl halide, adjusted during route optimization for yield and impurity profile control

    Downstream process integration

    • Charged at the Suzuki-Miyaura coupling stage following deprotection/isomerization, with in situ Pd(0) catalysis; typically introduced in anhydrous polar aprotic media under nitrogen or argon atmosphere

    Final product types

    • Small-molecule anti-cancer drugs (e.g., kinase inhibitors with aryl boronate-derived motifs)
    • CNS-active pharmaceutical compounds
    • Immunomodulatory agents containing substituted biaryls

    2. OLED Emitter and Host Material Manufacturing

    In the OLED industry, downstream producers utilize 3-vinylphenylboronic acid to construct boron-containing emitters and electron-transport building blocks via cross-coupling steps in the liquid phase. Purity standards demand ultra-trace analysis for halides, residual metals, and water content, as these directly affect charge-transport and device lifetime. Usage amounts differ between emitter and host resin syntheses, with fine-tuning based on target electronic behaviors and solubility in polymer blend formulations. The acid typically enters as a protected or directly coupled monomer during the monomer build-up stage preceding functional layer casting.

    Industry compliance standards

    • IEC 62321 for hazardous substance screening in electronics
    • ISO 9001:2015 for total quality management in specialty materials
    • Restriction of Hazardous Substances (RoHS) Directive (when required in end products)
    • OEM customer-specific material purity specifications (sub-ppm clarity on transition metals and residual halides)

    Typical usage ratio

    • 0.5–2.0% w/w in monomer batches for functional layer synthesis, adjusted for charge-transport efficiency and device emission wavelength tuning

    Downstream process integration

    • Introduced during Grignard or Suzuki coupling of conjugated skeleton and boron atom incorporation, prior to the purification and casting of emitting or transport layers

    Final product types

    • Green, red, and blue OLED emitter molecules
    • Electron transport layer (ETL) resins incorporating triarylboron units
    • Host matrix polymers for high-efficiency OLED display panels

    3. Agrochemical Active Ingredient Synthesis

    Leading crop protection manufacturers implement 3-vinylphenylboronic acid in precision heterocycle assembly for next-generation herbicides and fungicides. The compound participates in advanced cross-coupling reactions to enable the formation of complex, bioactive aromatic segments within selective agrochemicals. Compliance emphasizes minimized trace contamination to preserve ecological balance and regulatory acceptance. Usage rates in downstream synthesis are dictated by desired coupling ratios and the agrochemical’s targeted aromatic substitution pattern. Integration into the process commonly occurs just before endgame molecular closures, under strictly inert process conditions and with careful control of exothermicity.

    Industry compliance standards

    • ISO 9001:2015 for crop chemical production
    • Global GAP for sustainable agriculture inputs
    • Relevant FAO/WHO pesticide specifications
    • REACH (EC No 1907/2006) for European market agrochemicals

    Typical usage ratio

    • 0.95–1.2 molar equivalents per halogenated intermediate; calculated based on reactant feedstock assay and process yield optimization

    Downstream process integration

    • Reacted at the penultimate synthetic stage via palladium-catalyzed C–C coupling, immediately preceding ring-closure or final functionalization reaction and downstream purification

    Final product types

    • Aromatic heterocyclic herbicide actives
    • Fungicidal agents with boron-linked aryl chains
    • Crop protection intermediates destined for further downstream elaboration

    4. Specialty Functional Polymer Synthesis

    Producers of advanced functional polymers utilize 3-vinylphenylboronic acid as a comonomer or reactive intermediary in the synthesis of boron-containing resin systems. The addition of the monomer imparts specific functional groups that support molecular recognition, self-healing behavior, or fluorescence-quenching attributes. Processing involves meticulous dosing relative to the main chain monomer and real-time monitoring of conversion efficiency during the polymerization reaction. Regulatory controls concern occupational exposure and potential migratory monomer risks when targeting applications such as medical diagnostics or electronic encapsulants. Exact loading levels depend on target cross-link density and finished polymer properties.

    Industry compliance standards

    • ISO 14001 environmental management for specialty chemical synthesis
    • RoHS and SVHC (Substances of Very High Concern under REACH) restrictions when used in electronics
    • USP Class VI biocompatibility (for diagnostic and contact medical applications)
    • ISO 10993 if intended for medical device integration

    Typical usage ratio

    • 0.5–3.0 mol% in total monomer feed, calculated relative to desired degree of functionalization and monitored for conversion yield

    Downstream process integration

    • Added as a discrete component to bulk or solution polymerization setups, typically post-monomer purification and just prior to chain-growth initiation; monitored via NMR or GC/MS for reaction endpoint

    Final product types

    • Self-healing polymer networks for functional coatings
    • Boron-fluorescent diagnostic chips and sensing films
    • Electronic encapsulant resins with boron-linked aryl groups
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    Certification & Compliance
    More Introduction

    Introducing 3-Vinylphenylboronic Acid: Direct from the Manufacturer

    What 3-Vinylphenylboronic Acid Brings to Modern Chemistry

    Working in the chemical industry brings daily opportunities to see how specific molecules can open the door to better research and smoother production. Among the specialty intermediates we handle, 3-Vinylphenylboronic Acid stands out for its unique balance of reactivity and selectivity. Manufacturing this compound gives a clear view into its value for advanced organic synthesis. Many customers look for a dependable supply of this boronic acid due to its vinyl group, which readily participates in coupling reactions, and its clean phenyl backbone, which enables scientists to craft tailored molecules for pharmaceutical or material science work.

    The Experience Behind Making 3-Vinylphenylboronic Acid

    Producing specialty boronic acids requires more than following a formula. 3-Vinylphenylboronic Acid, with the model number typically referenced as 90000-90-5, presents specific challenges in its synthesis. Factory teams handle sensitive manipulations of boronate derivatives and must ensure the vinyl group remains intact without unwanted side reactions or isomerization. Over years of hands-on production, these procedures have been refined, and careful process controls are in place to prevent contamination and maintain consistency. Our direct experience with upstream purification allows us to offer this product at a purity that suits demanding research programs.

    Specifications Reflecting Direct Manufacturing Knowledge

    From raw input to the finished crystalline solid, nothing is left to chance on the production line. 3-Vinylphenylboronic Acid often appears as a white to light beige solid, and best results come when purity consistently exceeds 98%. Every batch is checked by NMR and HPLC, since even minor impurities can throw off delicate coupling steps in downstream chemistry. Water content remains low, given the hydrolytic sensitivity of boronic acids, and trace metal analysis backs up reliability for Suzuki coupling or other palladium-catalyzed protocols.

    Size options match regular laboratory and industrial needs, usually offered in grams for research, but scaling up to kilograms is part of standard operation for experienced chemical manufacturers like us. Neither transportation nor storage is overlooked; we keep careful supervision over the process, since boronic acids can degrade if exposed to moisture or air for too long. This diligence sets direct manufacturers apart from third-party distributors—consistent monitoring and timely restocking has become second nature to the entire production and logistics team.

    Usage Rooted in Lab and Plant Experience

    Ask a chemist what draws them to 3-Vinylphenylboronic Acid, and coupling reactions will be one of the first uses they mention. It’s not just the Suzuki reaction—though this product is a staple in those transformations—but also applies to many other transition metal-catalyzed processes, including Negishi and Stille types. While traders often describe these reactions abstractly, a manufacturer sees the intense demand from contract research organizations, pharmaceutical discovery groups, and polymer labs who rely on highly reactive boronic acids to introduce vinyl functions into aromatic systems.

    Customers in the agrochemical sector come to us for a steady supply of this compound, since vinyl functional groups help open development routes to crop protection candidates. University labs, always hunting for robust building blocks, tend to favor our lots for their clean spectra and ease of handling. By delivering directly, we gain immediate feedback on how the acid behaves both in small-scale flask work and in pilot-scale production, so any issues get fixed at the source before they can hold up a project.

    Differences That Matter in Performance and Handling

    Every manufacturer claims a specialty compound is unique, but not all boronic acids deliver the same experience, even with similar basic attributes. Take 3-Vinylphenylboronic Acid compared to closely related isomers; the position of the vinyl group changes its electronic properties and reaction outcomes. Para-vinyl and ortho-vinyl isomers may look comparable on paper, but switching positions on the aromatic ring shifts the selectivity of coupling reactions and the physical handling of the powder. Only after working with both do you appreciate the subtleties: the meta (3- position) gives a better balance of accessibility and functionalization range.

    Subtle differences show up during crystallization, drying, and storage. For example, some boronic acids clump or cake after a few weeks at room temperature, but the 3-vinyl variant tolerates regular laboratory conditions as long as basic packaging precautions are in place. From a direct manufacturer's perspective, proper bottling and stabilization make the difference between an easily handled product and a frustrating, sticky solid that resists weighing on an analytical balance. People who order directly from manufacturers avoid the degradation issues that crop up in goods kept too long on distributors’ shelves.

    Building Long-Term Trust Through Consistency

    Knowing every step that brings 3-Vinylphenylboronic Acid from reactor to research bench matters a great deal. Experienced customers, especially in the pharmaceutical industry, run incoming tests that catch inconsistencies others might miss. We have responded to batch-to-batch challenges—keeping color, melting point, and impurity levels within tight targets. Our technical support team is available to discuss unexpected outcomes in customer reactions and to advise on storage practices, since communication works best from a direct supplier who’s involved at every stage, not a distant salesperson with limited insight into how the product was made.

    Many of our regular partners need confidential run histories, certificates of analysis, and full traceability. Operating as a transparent chemical manufacturer, we document every lot and retain samples for cross-reference. In contrast, resellers sometimes provide outdated data or incomplete support, causing delays at key points in critical research timelines. Over the years we have stepped in for research labs facing uncertain product quality from indirect channels. Consistent supply makes the difference between a timely publication or product launch and endless repeat experiments.

    Supporting Advances in Research and Development

    Direct buyers tend to push the boundaries of what a molecule like 3-Vinylphenylboronic Acid can do. Our pharmaceutical customers work on antineoplastic and anti-infective lead compounds that use the vinyl group to expand chemical diversity. The same compound supports research into new organic electronic materials, where the vinyl linkage can open up fresh architectures for molecular wires or light-emitting systems. We see more universities deploying our product in cross-coupling experiments on combinatorial libraries.

    Because our technical team communicates directly with end users, we have helped troubleshoot reaction setups and offered advice on order of addition, solvent choice, and purification methods for this boronic acid family. In academic collaborations, feedback on purification difficulties or reaction byproducts informs our internal quality targets for the next production scale-up. Whether it’s a graduate student needing milligrams or a process chemist ordering kilos, every user benefits from a supply chain designed by experienced hands.

    Ensuring Reliability in Every Lot

    Unpredictable or slow supply can hold up big discoveries, especially with vinyl-functionalized boronic acids, which are not broadly stocked at most general chemical suppliers. Our experience as a manufacturer shows most issues arise downstream—delays due to repackaging, mishandling in warehouses, and mismatched quality documentation. Problems like off-odors, excess clumping, or stray peaks on mass spectra don’t just frustrate researchers; they set back entire R&D programs.

    By managing all aspects of order fulfillment, from solvent drying and bottling to temperature-controlled shipment, we sidestep many pitfalls that beset indirect supply routes. Routine testing before shipping includes checks beyond minimum standard requirements. We look at sample solubility in DMF, check behavior under common cross-coupling conditions, and interview users who have run scale-ups for feedback. These steps help guarantee that the product performs as it should, every time.

    Building Confidence Through Technical Understanding

    Year after year, our technical and quality teams see new variations in downstream applications. From custom ligand systems to non-traditional catalyst packages in cross-couplings, the needs of researchers using 3-Vinylphenylboronic Acid shift with new literature and patent trends. As suppliers who don’t simply sit on inventory, we see first-hand where handling and purity issues crop up: in the fine differences between similar boronic acids, and in the way trace solvents or storage conditions nudge performance up or down.

    Our role goes beyond shipping goods that meet a published spec sheet. Past experience tells us better performance doesn’t always translate from a bulk chemical purchased through a multiparty chain—often the opposite. Researchers and process chemists value honest answers, including what works, what doesn’t, and what further testing we plan to run on future batches. They understand that only a producer with both lab and pilot plant knowledge can point out the silent problems that undermine a promising reaction or slow down a scale-up.

    Differences in Documentation and Regulatory Assurance

    Manufacturing 3-Vinylphenylboronic Acid means meeting documentation standards not just for general commerce, but for advanced quality programs expected in pharmaceutical and advanced material markets. We keep all synthetic route information documented and can provide certificates of analysis, batch-specific spectra, and impurity profiles with every shipment. Our lab can verify identity and purity by HPLC, NMR, and GC-MS, as requested by regulatory or QA teams. Open communication of process changes keeps long-term clients updated, so there are no surprises during routine audits or product qualification.

    Regulatory demands over time have increased for boronic acid derivatives. Many industrial and research users want advance notice about possible route modifications that might introduce residual process agents or uncommon trace byproducts. Having worked for years as a direct producer, we know the importance of early notification and transparency across every handoff point—logistics, safety, and documentation stay tightly connected, without gaps introduced by detached resellers or traders.

    Improving the Customer’s Research Workflow

    Our work does not stop at production and shipment. Direct contact with research teams has made us careful listeners whenever troubleshooting becomes necessary. Feedback collected through decades of direct sales and technical support has improved packaging, documentation, and the clarity of instructions for handling this sensitive boronic acid. For example, one repeated request from university departments concerned reagent stability after opening. We responded by adjusting seal systems in our bottle caps, reducing air and moisture intrusion.

    Many users also benefit from our hands-on suggestions about storage (preferably in tightly closed bottles, under inert gas, with minimal freeze-thaw cycles) and from batch reservation systems, which allow them to lock in a consistent supply from a single production run. Research teams facing upscaling challenges rely on our advice on solvent compatibility, impurity separation, and coupling protocol optimization—experience gained directly from interacting with their teams rather than reading secondhand reports or suggestion sheets.

    Understanding the Broader Impact of Manufacturing Choices

    Making 3-Vinylphenylboronic Acid at scale requires attention to worker safety, resource use, and environmental sustainability. Years ago, the manufacturing process involved less refined purifications, using more aggressive chemicals and producing more waste. Continuous improvement in purification and solvent recovery means that today, we recover and recycle more than 80% of organic solvents used, with significant reduction in energy intensity per kilogram produced. Waste management systems track every batch from the moment it leaves the reactor to final packing.

    Ongoing investments in safety and environmental controls make a tangible difference for workers and customers alike. Whether adapting containment to reduce dust, switching to less hazardous reagents, or implementing regular environmental assessments, these steps directly improve the product’s reliability and the working conditions in the plant. We believe that manufacturers have a duty to produce clean chemistry—not just clean product.

    Challenges and Solutions Unique to a Manufacturer’s Viewpoint

    Long experience producing boronic acid derivatives teaches hard lessons about the vulnerabilities present in small-scale custom synthesis. Some batches won’t crystallize as planned, and subtle shifts in the vinyl group’s orientation challenge automated purification systems. Scale-up doesn’t always proceed smoothly; solid handling, solubility, and even odor become issues when producing kilograms instead of grams. We fine-tune our protocols—in response to real customer feedback and to internal trial runs that probe the edge cases.

    High-quality boronic acids are in greater demand, but not every batch meets the standards required by advanced research. Our responsibility as a manufacturer is to catch and resolve quality issues before product goes out the door. If a lot falls short, we reprocess or discard it, even at significant cost, to assure the reliability researchers expect. Problems that defeat supply chain traders—like unmonitored degradation, unexpected insolubles, or shipment mistakes—find quick resolution here, where every step stays within our walls.

    Final Thoughts on the Role of the Manufacturer

    Being a direct manufacturer of 3-Vinylphenylboronic Acid brings a different kind of responsibility. Those working on the shop floor, along with the chemists running pilot-scale syntheses, experience the real challenges involved with creating and delivering a compound that advances science. Our direct connection to customers means we witness both the struggles and the breakthroughs that come with using this material in intense research projects. Trust builds from providing a product that not only meets a stated specification, but that actually helps researchers do better science.

    For us, every lot of 3-Vinylphenylboronic Acid represents not just a line on an order form, but an investment in our know-how, facility, and the future of chemical research. As a manufacturer with years behind the process, and direct eyes on every gram produced, we’re committed to building the kind of consistent, responsive relationship with customers that supports long-term innovation. That’s the perspective that sets a manufacturer apart, and it’s the reason we take so much pride in the 3-Vinylphenylboronic Acid we make.