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2-Fluoro-5-Methylphenylboronic Acid

    • Product Name 2-Fluoro-5-Methylphenylboronic Acid
    • Alias 2-FLUORO-5-METHYL PHENYL BORONIC ACID
    • Einecs 841-380-8
    • 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

    627688

    Product Name 2-Fluoro-5-Methylphenylboronic Acid
    Cas Number 132979-02-7
    Molecular Formula C7H8BFO2
    Molecular Weight 153.95 g/mol
    Appearance White to off-white solid
    Melting Point 110-115 °C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO, methanol, and ethanol
    Storage Conditions Store at 2-8°C, keep container tightly closed
    Smiles CC1=CC(=C(B(O)O)C=C1)F
    Inchi InChI=1S/C7H8BFO2/c1-5-2-3-6(9)7(4-5)8(10)11/h2-4,10-11H,1H3

    As an accredited 2-Fluoro-5-Methylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-Fluoro-5-Methylphenylboronic Acid, tightly sealed with a white screw cap, labeled.
    Shipping 2-Fluoro-5-Methylphenylboronic Acid is shipped in tightly sealed containers under cool, dry conditions to prevent moisture absorption and degradation. The packaging complies with safety regulations for chemical transport, typically using bottles with secondary containment. Ensure appropriate labeling and documentation; handle with chemical-resistant gloves and eyewear upon receipt.
    Storage 2-Fluoro-5-methylphenylboronic acid should be stored in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from direct sunlight. Store at room temperature or as specified on the product label. Always handle using proper safety precautions, including wearing protective gloves and eyewear.
    Application of 2-Fluoro-5-Methylphenylboronic Acid

    Applications of 2-Fluoro-5-Methylphenylboronic Acid in Industrial Manufacturing

    2-Fluoro-5-Methylphenylboronic Acid is a specialized organoboron compound essential for advanced organic synthesis in pharmaceutical, biopharmaceutical, agrochemical, and electronics sectors. As a manufacturer, we produce this material to meet strict industrial demands for purity and consistency. Below are core application scenarios and requirements documented from real-world industry use.

    1. Active Pharmaceutical Ingredient (API) Synthesis—Aryl Fluorination Intermediates

    Pharmaceutical manufacturers utilize this compound for the Suzuki-Miyaura cross-coupling reaction, introducing aryl fluorine motifs in drug intermediates. Its unique substitution enhances metabolic stability in final APIs, commonly used in oncology, CNS, and antiviral therapeutic classes. Operators incorporate this boronic acid in automated reactor charging, optimizing conversion rates through precise reagent metering, controlled catalyst loading, and continuous process monitoring in compliance with regulated environments.

    Industry compliance standards

    • United States Pharmacopeia (USP) general chapter <1078>
    • Good Manufacturing Practice (GMP; ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) requirements for starting materials
    • FDA 21 CFR 210/211 process validation

    Typical usage ratio

    • 0.85 – 1.10 molar equivalents per limiting substrate, adjusted based on required aryl substitution and process yield. Users often fine-tune catalyst loading in 1–2 mol% range for the palladium catalyst system.

    Downstream process integration

    • Dosed as core building block after substrate activation in glove box environments or automated reactors; enters during hydrogenation or oxidation to advance chloro-, bromo-, or fluoroaryl API frameworks.

    Final product types

    • Targeted kinase inhibitor drug substances
    • Non-sedating antihistamines
    • Novel antiviral compounds
    • Generic API intermediates with fluorinated aromatic rings

    2. Agrochemical Active Compound Manufacturing—Selective Herbicide Precursors

    Major agrochemical formulators apply this boronic acid for the precision synthesis of substituted phenyl rings in modern herbicides and fungicides. Fluorine incorporation aids in producing active molecules with increased field stability and targeted crop selectivity. Technology transfer teams use dry addition or in-situ solution dosing, optimizing the coupling with halogenated partners under mild aqueous-organic conditions to maximize yield while controlling process emissions and trace impurity profiles.

    Industry compliance standards

    • ISO 9001:2015 quality management for agrochemical production
    • FAO/WHO specification guidelines on technical active ingredients
    • Globally Harmonized System (GHS) for labeling and transport
    • REACH Regulation (EC 1907/2006) for raw material registration

    Typical usage ratio

    • 0.9 – 1.5 equivalents compared to electrophilic halide, based on the reactivity of active centers and scale-up process optimization. Adjustments made for reaction throughput and process solvent system.

    Downstream process integration

    • Added at the coupling stage of heterocyclic ring formation; enters during batch or continuous stirred-tank reactor cycles; complements other arylation reagents in multi-step herbicide synthesis.

    Final product types

    • Fluorinated phenyl-substituted herbicide actives
    • Leaf-selective fungicidal ingredients
    • Crop-specific pesticide precursors
    • Advanced safener development batches

    3. OLED Material Production—Organic Semiconductor Synthesis

    Electronic component manufacturers employ this boronic acid as a coupling agent for introducing stable fluorinated aromatic units in emitter and host materials for OLED displays. This targeted substitution achieves improved charge transport and lifetime in blue and deep-blue layers. The raw material is charged under inert atmosphere and integrated into multi-step synthesis involving palladium-catalyzed coupling, followed by vacuum purification and inline UV/Vis QC analysis.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics chemicals
    • IEC 62474 material declaration protocol
    • JIS C 61290-1 (semiconductor chemical purity)
    • REACH Annex XVII for handling and reporting SVHC content

    Typical usage ratio

    • Typically 1.05 – 1.20 molar ratio relative to halogenated organic precursor, determined by stoichiometry of target semiconducting oligomers. Utilized in pilot campaigns at 10–150 g per batch for color-specific emitter synthesis.

    Downstream process integration

    • Added into the Suzuki coupling step for the formation of extended π-conjugated molecules; processed under nitrogen or argon jacketed reactors; purification by column chromatography or vacuum distillation.

    Final product types

    • Blue and deep-blue OLED emitting layers
    • Fluorinated host materials for high-performance displays
    • Organic semiconducting coatings for thin-film transistors
    • Printed flexible circuitry elements

    4. Fine Chemical Intermediate for Specialty Fragrance Compounds

    Fragrance industry producers incorporate this compound in the production of advanced aromatic intermediates used for high-value synthetic fragrances. The boronic acid introduces both a methyl and fluoro group to the phenyl core, enhancing structural stability and providing unique olfactory notes. Chemists perform the coupling reactions under strict batch records, balancing metal catalyst residues and minimizing unreacted intermediates. Stringent roadmap audits ensure batch-to-batch reproducibility and compliance with IFRA and consumer safety requirements.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • ISO 22716:2007 (Cosmetic GMP)
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • REACH compliance for non-pharma fine chemicals

    Typical usage ratio

    • Used at 0.6 – 1.0 equivalents per aldehyde or halide substrate, depending on target molecule and desired purity. Process tuned for maximizing conversion while controlling off-odor impurities.

    Downstream process integration

    • Engaged during initial aromatic substitution, followed by hydrogenation, methylation, and fractional distillation; integrated with multi-step patch synthesis for specialty notes.

    Final product types

    • Synthetic tonalide base notes
    • Fluorinated musk fragrance intermediates
    • Stabilizer molecules for premium perfumery blends
    • Intermediate blocks for commercial aroma chemicals
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    Certification & Compliance
    More Introduction

    2-Fluoro-5-Methylphenylboronic Acid: Insight From the Production Floor

    What We See in the Workshop

    Every batch of 2-Fluoro-5-Methylphenylboronic Acid coming out of our reactors reflects hours of focus and tested method. Sitting at a steady balance between technical challenge and practical payoff, this compound (CAS: 352303-67-4) proves itself a staple for researchers and industrial players working in pharmaceuticals, agrochemical intermediates, and cross-coupling chemistry. Its chemical structure incorporates both the fluoro and methyl group on the phenyl ring, which isn't just a textbook detail. Those groups shape its reactivity, solubility, and downstream behaviors, something evident when monitoring crystallization from mother liquor, or when the NMR peaks finally settle as expected.

    How It Differs in Real Reactions

    Working as a direct manufacturer, we've seen that not all boronic acids behave the same on the bench or in the flask. Plenty of clients have come with experiences where close isomers—like 3-Fluoro-5-methyl analogs, or the non-fluorinated methylphenyl boronic acids—underperform or complicate downstream reactions. The fluorine at position two on the ring gives this molecule a stiffer character, changing electron density and making it more suited for certain Suzuki-Miyaura couplings. Where other boronic acids show sluggish transmetalation or bring side reactions at the palladium catalyst, this one tends to offer a cleaner route, fewer byproducts, higher selectivity—notes we see reflected in TLC runs and HPLC readouts, not just in catalog descriptions.

    Clients working at pilot or kilo scale often report stronger yields and simpler purification with this fluorinated derivative. Comparing postage-stamp and full-scale runs, even subtle shifts in aromatic substitution have been enough to shrink loss at filtration, shorten column times, and give crisper endpoint detection during synthesis of specialty ligands, biaryl compounds, or new API intermediates.

    Specification and Quality: What Actually Gets Checked

    In-house labs set the bar for material release at ≥98% purity by HPLC and GC. Moisture content, a frequent troublemaker for this class, sits below 0.5% after proper drying cycles. We avoid metal-powder contamination and residual palladium, which would frustrate downstream chemistry. Melting point, color, residual solvent, and fine dust particles all get real scrutiny under both spectroscopy and visual checks.

    Some external buyers underestimate how much handling matters. Boronic acids love to form hydrates if stored wrong, and we've seen freshly sealed drums in humid seasons drift higher on Karl Fischer. That’s a risk for sensitive coupling reactions, so we keep an eye on packaging, ambient humidity, and proper polymer liners that minimize water ingress. It’s these material realities—not just COA numbers—that help customers trust what comes in, batch after batch. Every operator on our line knows that ease in the lab tomorrow starts with care on the floor today.

    Applications: Beyond Just Another Starting Material

    Universities, biotech startups, and large CDMOs bring 2-Fluoro-5-Methylphenylboronic Acid into their labs with a goal: to build new molecular scaffolds where the subtle influence of a fluorine atom and a methyl group can change an entire candidate’s pharmacokinetics. In pharma, these tweaks can drive up binding affinity, alter metabolic stability, or tune lipophilicity—a small change, but one that might mean the difference between a dropped candidate and a drug that survives phase trials.

    In crop science and agrochemical R&D, the story plays out differently. Younger chemists want to plug in more fluorinated motifs, looking for enhanced pest resistance or stability under UV. We’ve seen purchasing officers shift orders toward this molecule instead of the non-fluorinated boronic acids, citing project data that shows improved conversion and minimal catalyst poisoning in their own hands.

    Anyone doing Suzuki, Stille, or Sonogashira cross-coupling recognizes the comfort in using a material that consistently works, makes purification easier, and avoids stress over unexpected shelf-life decay. That’s a lesson we’ve learned with each invoice; a compound that bolts quickly or brings repeat performance earns its spot on more synthetic benches.

    Production Insights: The Road From Raw to Pure Compound

    Sourcing raw substituted aromatics comes with its own hurdles. We track every barrel of 2-Fluoro-5-methyliodobenzene from trusted suppliers, confirming identity by GC-MS before a single gram goes into our vessels. Scaling up boronic acid synthesis is not just about technical process—temperature control, slow addition of boronate reagents, proper agitation—it’s about anticipating batch-to-batch quirks.

    Our process uses high-strength base, careful phase separation, and slow neutralization to encourage fine, even crystal formation. Waste from boronate hydrolysis can pose environmental load, so we recycle solvents, strip volatile organics, and treat aqueous phases onsite before anything moves toward licensed disposal. Traces of byproduct—bis-boronic acids, biaryl debris, or unreacted starting material—don’t leave unnoticed; control at every step is what separates reliable output from “close enough.”

    Customers used to working with small-scale or academic sources regularly comment on the difference in handling and reproducibility. The commercial batches we run, designed for larger-scale users, focus on easy dissolution in a wide range of polar solvents and low static, which comes only after you perfect hours of rotary evaporation, fine-powder handling, and post-synthesis drying.

    Handling and Storage Onsite

    Experience has shown that even small lapses in storage compromise boronic acids. Early on, we found high-performance PE-lined drums and extra desiccant packets guarded against the product pulling in wet air, preventing shifts in melting point or off-color during long-term storage. Labs working in climates with variable humidity learn quickly that room-temperature storage without desiccant can spoil weeks of scale-up work.

    Care in logistics has paid off repeatedly for both us and downstream users. Regular checks on drum seals, fast tracked shipping, and tracking temperature logs through the supply chain reduce the headaches that come with returns, claim disputes, or frantic phone calls before deadline coupling runs. Over several years, this has tightened both our release process and customer confidence, something we didn’t fully appreciate without time on the ground watching those first kilo-scale lots ship out.

    The R&D Perspective: Customers Driving Our Process

    One truth from years in custom manufacturing: new applications drive what happens at the plant as much as any internal decision. Years ago, orders for 2-Fluoro-5-Methylphenylboronic Acid clustered near catalogue scale—grams up to a few hundred grams for classwork or patent filings. That changed with pharmaceutical teams chasing new SAR studies on heteroaryl scaffolds and wanting reliable kilo or multi-kilo supply, not just a “research grade” option. With every new project came tighter specs: lower ppm levels of residual iodine, stricter HPLC purity, specific limits on trace metals.

    This led us to push beyond off-the-shelf boronate routes. Our chemists adjusted workup conditions, tested alt drying protocols, and invested in finer detection for organics left over after workup. Several spinouts and process tweaks later, the analytical team and plant operators finally met those tougher specs routinely. This process wasn’t just investment—it was driven by feedback and a steady contraction of quality tolerances.

    A direct link between manufacturer and customer has made a difference in shaping this product's reputation. We spend time on tech transfer calls, run sample batches when customers need extra assurance, and adapt packing and documentation as single-site facilities move into split operations overseas. This direct feedback keeps the molecule competitive and the plant tuned to new requirements.

    2-Fluoro-5-Methylphenylboronic Acid Versus Other Boronic Acids

    It’s tempting to view all arylboronic acids as interchangeable, but real-world results say otherwise. In the context of high-throughput screening or lead synthesis in pharmachem labs, our team has seen clear differences in reaction rates, byproduct formation, and downstream workup between this fluorinated methyl derivative and others like 4-methylphenylboronic acid or 3-fluoro derivatives.

    The difference in electron withdrawal from ortho-fluorine, coupled with methyl at position five, means tighter control over coupling selectivity. In practice, end users report less clogging during catalyst-loaded flow chemistry, lower foaming in solvent exchange, and more robust shelf-life under ambient conditions. If regular phenylboronic acid is standard chalk, this derivative draws sharp lines where chemistry needs precision.

    In some comparative runs, we’ve seen the non-fluoro analogs stall during certain halide activation steps, resulting in lower yields or less efficient catalyst cycling. Working with teams that run hundreds of reactions per month, the net cost savings show up not only in reagent price, but in reduced rework, faster HPLC cleanups, and higher throughput. Feedback from industrial users keeps confirming: changing the substitution pattern, even slightly, alters the entire downstream map from isolation to formulation.

    Observations on the Growing Demand Curve

    Several years back, forecasts for boronic acid growth pointed toward gradual increases. Now, with fluorinated aromatics making regular appearances in medicinal chemistry and branding around new API designs, demand has leapt. Tracking volumes year-on-year, we’ve scaled up to offer reliable drum quantities, not just bottle lots. Every new industry report pushes more attention toward high-purity, differentiator molecules—our production planners see requests shifting from schedule fill-ins to long-term supply agreements.

    Key regions—North America, Europe, driving parts of East Asia—raise the bar each cycle on specifications. Where one customer may accept 97% by HPLC, another seeks ≥99% and documented residual solvents below 0.1%. Tight supply means close relationships matter. We’ve weathered short-lived booms and dips, but steady, predictable supply draws customers away from spot-buying and toward ongoing partnerships.

    From our vantage on the production side, this product’s success story connects to how early, open technical exchanges foster trust. The closer collaboration with clients, the more quickly our workflows adapt to new needs—be it specialized documentation for regulatory filings, fresh packaging formats, or nimble scale-ups for late-stage development programs.

    Solving the Handling and Safety Puzzle

    Boronic acids—especially those with active functional groups—require careful attention from both us and users. Years back, we saw repeated issues with friable powders leading to airborne dust, raising both safety and loss concerns. We responded by investing in finer, controlled milling equipment and installing local exhaust for each bagging operation. Simple procedural changes, like antistatic gear on operators and automated weighing, have dropped near-miss events and minimized batch-to-batch handling variation.

    We train crews to spot off-color product, caking, or even subtle textural changes that might signal early hydration or contamination. It’s one thing to have a process specification; it’s another to maintain vigilance lot after lot, each weighed and packed by real people who know what good material should look and feel like. This way, clients downstream pick up drums that pour clean, contain crystals not lumps, and never throw off the next step.

    Long-term partners also benefit from our digital tracking system: every shipment gets full traceability through the plant, with cross-referenced data tied to every operator, process step, and lab check. Working as a manufacturer, not a repacker, means we control every variable from raw input to finished good—the accountability pays off in customer calls, where real answers matter more than canned responses.

    Looking at the Future: Improving and Scaling Up

    We don’t see process development as done once a molecule hits spec. Recent investments include new reactor coatings to prevent trace ingress of foreign metal, inline FTIR for faster release decisions, and improved solvent recycling to hit higher eco-standards. Requests from development partners spur us to run pilot campaigns, record impurity profiles, and map new parameters that tighten up both cost and compliance.

    The next step for 2-Fluoro-5-Methylphenylboronic Acid lies not just in more output, but in offering tailored support for high-complexity projects in advanced intermediates or late-stage drug development. Our team fields regular questions about custom specs or advanced analytical profiles, and we view these as opportunities to push our process to the next level. On the ground, new orders lead directly to new trials, shorter cycle times, and longer production runs—practical signs of a market evolving fast.

    As regulatory requirements globally keep ratcheting higher, our in-house team watches horizon scanning for potential new impurity risks, assurance documentation, and packaging improvements. Every step that improves safety, logistics, and consistent quality builds the reputation not just of this one product, but of our broader offering to every chemist, process engineer, or project team who depends on us for key raw materials.

    Why Direct Manufacturing Makes a Difference

    Speaking from the floor, the difference between direct production and supply through third-party warehouses shows up in both small details and major results. End-users making mission-critical products want no compromise on detail. Our regional sales engineers and support staff relay real project problems straight back to the plant: flagging lot-specific quirks, sharing new purification challenges, and transferring real user stories. That real loop closes quickly, leading to faster tweaks and less paperwork clog, compared to waiting through layers of reps, labs, or endless email chains.

    The kind of trust we see comes from accountability, traceability, and hands-on technical support—not just a label stuck to a drum. For each kilogram pressed out of the dryer, we know exactly who set the scales, ran the HPLC, checked the last batch record. This chain of knowledge underpins every delivery, making sure our batches don’t just meet “spec,” but work better in real hands, under real production conditions.

    Final Reflections From the Team

    Every day on the plant floor brings its own problems to solve—from shifting supply chains, balancing solvent recovery, smoothing out QA trends, to responding to a client’s new analytical spec. Watching the rise of 2-Fluoro-5-Methylphenylboronic Acid from niche toolbox option to mainstream reagent, we see the difference that direct production focus brings. The real value shows up not in glossy catalogs, but in reliable results, fewer last-minute headaches, and the steady confidence that comes from knowing the person on the other end of the line isn’t just reading a datasheet—they’re making sure each batch worth using.