2,6-Difluoropyridine-3-boronic acid

    • Product Name: 2,6-Difluoropyridine-3-boronic acid
    • Chemical Name (IUPAC): (2,6-difluoropyridin-3-yl)boronic acid
    • CAS No.: 1224845-89-7
    • Chemical Formula: C5H4BF2NO2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    604474

    Product Name 2,6-Difluoropyridine-3-boronic acid
    Cas Number 732023-54-4
    Molecular Formula C5H4BF2NO2
    Molecular Weight 158.90 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 129-134°C
    Solubility Soluble in DMSO, methanol
    Smiles B(C1=C(N=CC(F)=C1F))(O)O
    Inchi InChI=1S/C5H4BF2NO2/c7-3-1-4(6(11)12)5(8)9-2-3/h1-2,11-12H
    Synonyms 2,6-Difluoro-3-pyridineboronic acid
    Storage Temperature 2-8°C (Refrigerated)
    Hazard Statements May cause irritation

    As an accredited 2,6-Difluoropyridine-3-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed 5-gram amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Container Loading (20′ FCL) 20′ FCL container is loaded with securely packaged 2,6-Difluoropyridine-3-boronic acid, ensuring safe, moisture-free, and efficient transport.
    Shipping 2,6-Difluoropyridine-3-boronic acid is shipped in tightly sealed containers, protected from moisture and light. Standard transportation follows regulations for organic chemicals, with careful labeling and documentation. Packages include appropriate hazard symbols if required and are cushioned to prevent breakage. Temperature-sensitive shipping may be used based on safety data sheet recommendations.
    Storage **2,6-Difluoropyridine-3-boronic acid** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. It should be kept at 2–8 °C (refrigerator conditions) and segregated from incompatible substances such as strong oxidizers. Proper labeling and secondary containment are recommended to prevent accidental exposure and contamination.
    Shelf Life 2,6-Difluoropyridine-3-boronic acid is stable for two years, if stored tightly sealed, dry, and protected from light.
    Application of 2,6-Difluoropyridine-3-boronic acid

    Purity 98%: 2,6-Difluoropyridine-3-boronic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency.

    Molecular Weight 172.93 g/mol: 2,6-Difluoropyridine-3-boronic acid of molecular weight 172.93 g/mol is used in Suzuki coupling reactions, where it provides consistent product yield.

    Melting Point 162–165°C: 2,6-Difluoropyridine-3-boronic acid with a melting point of 162–165°C is used in organic electronics research, where it offers stable processing conditions.

    Particle Size ≤75 µm: 2,6-Difluoropyridine-3-boronic acid with particle size ≤75 µm is used in fine chemical manufacturing, where it enhances reaction homogeneity.

    Stability Temperature up to 50°C: 2,6-Difluoropyridine-3-boronic acid stable up to 50°C is used in material development, where it maintains compound integrity during storage.

    Water Content ≤0.5%: 2,6-Difluoropyridine-3-boronic acid with water content ≤0.5% is used in catalyst formulation, where it minimizes unwanted side reactions.

    Analytical Grade: 2,6-Difluoropyridine-3-boronic acid at analytical grade is used in laboratory validation studies, where it guarantees reproducible analytical results.

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    Certification & Compliance
    More Introduction

    2,6-Difluoropyridine-3-boronic Acid: A Closer Look from the Manufacturing Floor

    Every batch of 2,6-Difluoropyridine-3-boronic acid that leaves our facility carries the effort and attention of those who truly understand both the science and the needs of chemists downstream. Manufacturing isn’t just about following a formula. It’s about control – of moisture, particle size, purity, and, above all, reliability batch to batch. Too many overlook the tangible and subtle differences between what comes from the source and what has passed through layers of middlemen. That difference becomes obvious, especially when you see results repeat every time.

    What Drives Demand for This Molecule?

    Chemists and process engineers ask for 2,6-Difluoropyridine-3-boronic acid for a reason. The presence of both fluorines on the pyridine ring creates electronic and steric effects especially useful in fine chemical and pharmaceutical development. Those working on production-scale synthetic routes often gravitate toward boronic acid building blocks for their stability and compatibility with standard cross-coupling methodologies. The 2,6-difluorosubstitution pattern doesn’t frequently occur by accident in nature, so synthesis on a large scale demands precision and consistency at every step.

    We get frequent requests from medicinal chemists looking to introduce fluorinated motifs into heterocyclic scaffolds. These modifications typically alter drug metabolism, lipophilicity, and receptor interactions. If you’re developing kinase inhibitors or small-molecule probes for disease targets, you probably have this compound, or one of close kin, on your project list. On the manufacturing side, anticipating upcoming demand in these spaces means the work begins long before purchase orders arrive. From sourcing raw materials to end-point analysis, this compound doesn’t leave room for shortcuts.

    Our Approach to Manufacturing and Quality

    We assemble the process for 2,6-Difluoropyridine-3-boronic acid with a focus on impurity profiles and repeatability. The critical step often comes in introducing the boronate moiety under controlled conditions to the difluorinated pyridine ring. Starting material selection, reaction temperature, and handling of intermediates each determine the final outcome. We rely heavily on in-process analytics – not just final COA – because batch variation can creep in from the smallest detail.

    Moisture is an ever-present enemy. Some batches handled under standard atmospheres degrade much faster, and that’s easy to overlook until you’re troubleshooting reactions weeks down the line. Our crew knows how to keep boronic acids as dry as possible during isolation, packaging, and transport, and the difference shows up when customers describe their product behavior down the line.

    Specifications: Built for the Real World, Not the Marketing Brochure

    On paper, the chemical is defined by its molecular formula and purity. In practice, those who work at the bench ask for details: Is this white or off-white? Will it clump in the vial? Does the NMR show minor impurities at the three percent level? We recognize what fast-tracks a project in the real world – that is, minimizing re-purification, dissolution issues, and lot-to-lot variability.

    Our standard model for 2,6-Difluoropyridine-3-boronic acid strikes a balance between purity and usability. We routinely deliver material with HPLC purity above 98%, minimizing co-eluting byproducts. Particle size tends to be fine, which benefits weighing and solubility in most coupling reactions. Odor, color, and flow are strictly watched – small markers of process control nobody should ignore.

    Use in the Lab: Everyday Realities and Solutions

    Every process chemist knows the pain points of boronic acid use. 2,6-Difluoropyridine-3-boronic acid doesn’t dissolve like sugars or salt. For Suzuki couplings, the choice of base and solvent makes a big difference, and we often discuss palladium loading, solubility in dioxane or THF, and the merits of slower vs. faster addition with our customers. The tendency of boronic acids to form cyclic esters or decompose in wet air is real; we keep our product moisture below strict thresholds for this reason.

    Stability during shipping and storage matters. We store our stock under inert gas and package in high-barrier containers. That effort pays off on the client end: material can sit in a drybox for weeks or months without turning messy. Some who have switched from middleman-supplied lots comment on the elimination of mysterious blotchy solids and inconsistent weight readings.

    Scaling up syntheses brings other concerns. Boronic acids sometimes perform well at the milligram level but resist full conversion or clean workup on a larger scale. We routinely test for byproduct carryover and optimize crystallization steps to sidestep these scale-up headaches before they reach the users.

    What Sets This Boronic Acid Apart

    Chemically, the difluoro pattern affects not just reactivity, but also purification and storage. Minor impurities, if left unchecked, feel more acute in downstream reactions. Our in-house methods go beyond catalog values, targeting artifacts from fluorination and boronation steps. If you have worked with mono-fluorinated or non-fluorinated pyridine boronic acids, you’ll notice this compound exhibits less hydrogen bonding, faster elution in many chromatographic systems, and lower propensity to form amorphous clumps.

    From a product development standpoint, we track changes in solvent use and cross-coupling catalysts in the literature. We often communicate with users about the switch from triphenylphosphine Pd(0) systems to more robust ligands like XPhos or SPhos, and how it interacts with our batch characteristics. The extra attention in controlling water content and verifying limited aromatic amines or halide residues makes downstream steps—like scale-up to pilot or manufacturing—more predictable. The middleman perspective misses these small process details.

    Insights from Decades on the Production Line

    Those who have spent enough time at the manufacturing end come to respect the perils of chasing “catalog purity” at the cost of process reliability. Through the years, we have seen the market shift between different sources for raw fluoropyridines, and every change leaves an impact that ripples to the customer. We have invested in diversified sourcing and robust testing of starting materials, because price savings on raw input can turn to loss if an entire batch gets rejected for purity or performance issues months later.

    In the early days, product lot-to-lot shift contributed to endless troubleshooting calls. We systematically improved process monitoring so we could recognize the off-odors, atypical melting profiles, or even color changes that predict trouble. This experience helps chemists skip unnecessary troubleshooting and focus on their actual synthesis.

    Feedback loops matter. Chemists who use our 2,6-Difluoropyridine-3-boronic acid in discovery, analytical development, or scale-up do more than follow a procedure; they notice batch nuances. We make it a point to respond to such input, adjusting process settings, filtration steps, or final drying routines as suggested by users who understand product behavior most acutely.

    Navigating Regulatory and Documentation Needs

    Those who have prepared regulatory filings or supported patent litigation with samples know that documentation is more than boilerplate. Each shipment leaves our facility with full analytical reports, including HPLC, NMR, and residual water or byproduct data. Material traceability is built into our workflow because regulatory clarity always traces back to in-house manufacturing diligence. Being the manufacturer, we answer documentation questions directly, with access to all records and batch histories. This avoids common issues where a distributor is caught between the factory and an asking regulator.

    Each batch history refers to raw material sources lot-for-lot. Analytical records, including HPLC chromatograms and NMR spectra, are stored for years. That system gives regulatory consultants real backing when inquiry arises. For those scaling up toward clinical or commercial API production, such traceability has become essential, not just optional.

    Meeting Real-World Scale-Up Challenges

    From kilo lab to plant startup, the world of scale-up exposes every hidden flaw in your starting materials. If boronic acids arrive with even a hint of decomposition, side reactions and fouling appear in minutes, not days. Powder flow and moisture uptake—details that sometimes get missed—start to impact reactor charging, stirring, and filtration efficiency. Our team and line operators, having invested hundreds of man-hours perfecting not just the chemistry but also handling, address every new scale-up project as a chance to fine-tune process parameters.

    It gets easy to notice the difference between batches produced in true chemical manufacturing environments and those repackaged or intermediated. Handling parameters, logistics, and even minor details like proper labeling or batch numbering all contribute to successful project execution for the end user. We get calls from process engineers asking about lot numbers, color, and physical form specifics—not because it’s busywork, but because those details make expensive failures less likely.

    Comparing to Other Boronic Acids and Market Offerings

    With years spent on the factory floor, it’s clear that not all boronic acids stack up the same, even when they seem identical on paper. The difluoro substitution at the 2,6-positions on the pyridine brings electronic features that improve stability in air, but at the same time challenge classic purification. Our compounds are manufactured to keep aromatic impurities, non-volatile residue, and trace water consistently below critical cutoffs. Other products from brokers or catalog houses sometimes arrive with yellow tint, inconsistent mass loss on drying, or broad melting points, all of which impact downstream chemistry.

    End users come back not for a name brand, but for predictable results. We made choices early about purification steps—choosing extra passes on column or specialized crystallization techniques—that reward our clients with material that behaves as expected, time after time. Where competing materials have shown subtle but significant drift—off-color product, changes in solubility, or unexpected decomposition—we track and report every trend, adjusting procedures to stay ahead of problems.

    The Human Element: What It’s Like Making and Using This Product

    Manufacturing chemicals at this level of detail isn’t glamorous, but it’s meaningful work. There’s pride when a kilogram batch passes tightest specifications and goes to a customer we’ve known for years. Colleagues on the production floor keep sharp eyes out for changes and subtle hints of trouble: humidity shift during the day, a different scent off the reactor, a suspicious HPLC peak. The experience and vigilance of every operator ultimately show up in the material sent to you.

    Factories like ours keep up with developments in methodology and customer requirements. Requests change; yesterday’s most popular boronic acid is replaced by today’s more demanding analog. We adapt with new in-line drying systems, better logistics partners, and in-house analytics. Every year, feedback from analytical chemists and research groups shapes tweaks both in process and protocols.

    Working with end users rather than brokers means we see the output: the successful reactions, the rare failures, the emerging demands of medicinal chemistry. That connection drives us to improve, batch after batch.

    Challenges and How We Address Them

    Boronic acids, even well-prepared, remain less robust than some common aryl intermediates. Temperature, humidity, and exposure to open air impact shelf life and handling. Over the years, we have added redundant checks and multi-step packaging lines to minimize these risks. Some requests come in for specialized vial sizes or air-exclusion packaging; our flexibility at the plant level lets us accommodate researchers working on everything from milligrams in the lab to multiple kilograms for pilot plants.

    Not every challenge comes from within. Supply chain risk for raw materials and reagents keeps all of us alert. Experience taught us to maintain multiple sourcing partnerships, routinely audit suppliers, and keep strategic safety stock both upstream and downstream of our own process.

    Analytical advancements make it easier to ferret out low-level impurities or stability questions. We maintain a close relationship with labs engaged in method development, and implement suggested improvements. Sometimes even a minor change to starting material filtration saves days down the line: less trouble from occluded water, cleaner chromatograms, and more reliable color consistency.

    The Road Ahead and Innovation in Manufacturing

    The chemistry community keeps changing, and so do the demands on 2,6-Difluoropyridine-3-boronic acid. Users now look for compatibility with emerging cross-coupling catalysts, solvent systems, and even flow chemistry applications. Internal R&D groups evaluate material's compatibility with new protocols, so that the product works in both established and leading-edge synthetic routes. Our recurring interaction with academics, pharma, and specialty chemical innovators allows us to spot trends early, validate new process tweaks, and keep final product in lockstep with customer needs.

    Experience tells us that manufacturing is less about static specs, and more about adapting, learning, and keeping channels open. Problems are inevitable—reactor hiccups, supply delays, or oddball impurity spikes—but our approach leans on decades of hands-on troubleshooting. That expertise means fewer surprises, more value to chemists wrestling with the next tough synthesis, and a better path from raw idea to finished molecule.

    Final Thoughts from the Manufacturing Perspective

    2,6-Difluoropyridine-3-boronic acid is more than just another intermediate. Each bottle reflects the knowledge and commitment of those making it from the ground up. On this end, real insight comes from seeing what happens in the plant, how the material handles in the lab, and the kind of feedback that only comes from years of working closely with the world’s best chemists.

    Those at the factory see every order as another chance to refine. Building real relationships with users keeps us honest—if a batch needs improvement, it happens. If a customer needs a tweak, it goes into production. The result: a product line that grows, evolves, and serves chemists preparing the molecules that improve lives worldwide. This day-in, day-out approach to quality and communication yields material that lives up to the hopes and needs of the scientific community.