5-Trifluoromethyl-pyridine-3-boronic acid

    • Product Name: 5-Trifluoromethyl-pyridine-3-boronic acid
    • Chemical Name (IUPAC): [5-(Trifluoromethyl)pyridin-3-yl]boronic acid
    • CAS No.: 877399-50-3
    • Chemical Formula: C6H5BF3NO2
    • 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

    374344

    Product Name 5-Trifluoromethyl-pyridine-3-boronic acid
    Cas Number 851386-49-3
    Molecular Formula C6H5BF3NO2
    Molecular Weight 192.92
    Appearance White to off-white solid
    Purity Typically ≥97%
    Melting Point 120-124°C
    Solubility Soluble in DMSO, methanol
    Smiles B(O)(O)c1cncc(C(F)(F)F)c1
    Inchi InChI=1S/C6H5BF3NO2/c8-6(9,10)4-3-5(7(12)13)1-2-11-4/h1-3,12-13H
    Storage Temperature 2-8°C (refrigerated)
    Synonyms 3-Boronic acid-5-(trifluoromethyl)pyridine

    As an accredited 5-Trifluoromethyl-pyridine-3-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Plastic screw-cap vial, amber colored, labeled clearly with "5-Trifluoromethyl-pyridine-3-boronic acid, 1 g" and hazard information.
    Container Loading (20′ FCL) Container loading (20′ FCL) for 5-Trifluoromethyl-pyridine-3-boronic acid ensures secure, bulk transport with moisture protection and proper labeling.
    Shipping 5-Trifluoromethyl-pyridine-3-boronic acid is shipped in tightly sealed containers to prevent moisture and air exposure. Packaging complies with chemical safety regulations, including labeling and hazard identification. The chemical is shipped as a solid under ambient conditions, with appropriate documentation, and handled as a standard laboratory chemical, ensuring safe delivery and storage.
    Storage 5-Trifluoromethyl-pyridine-3-boronic acid should be stored in a tightly sealed container, protected from air and moisture. Store at 2–8°C in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizing agents. Minimize exposure to light. Handle under an inert atmosphere if prolonged storage is anticipated to prevent degradation or hydrolysis.
    Shelf Life 5-Trifluoromethyl-pyridine-3-boronic acid typically has a shelf life of 1–2 years when stored cool, dry, and protected from light.
    Application of 5-Trifluoromethyl-pyridine-3-boronic acid

    Purity 98%: 5-Trifluoromethyl-pyridine-3-boronic acid with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it provides high selectivity and efficient biaryl compound synthesis.

    Melting point 124–128°C: 5-Trifluoromethyl-pyridine-3-boronic acid with a melting point of 124–128°C is used in pharmaceutical intermediate preparation, where it ensures stable processing conditions.

    Particle size < 75 microns: 5-Trifluoromethyl-pyridine-3-boronic acid with particle size less than 75 microns is used in automated synthesis platforms, where it enables rapid dissolution and homogeneous reaction mixtures.

    Moisture content < 0.5%: 5-Trifluoromethyl-pyridine-3-boronic acid with moisture content under 0.5% is used in sensitive organometallic processes, where it prevents undesirable hydrolysis and maintains product yield.

    Stability temperature up to 60°C: 5-Trifluoromethyl-pyridine-3-boronic acid stable up to 60°C is used in storage and transport of reagents, where it assures long-term shelf life and reactivity.

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    Certification & Compliance
    More Introduction

    5-Trifluoromethyl-pyridine-3-boronic Acid: Reliable Building Block for Advanced Synthesis

    Our Hands-on Experience with 5-Trifluoromethyl-pyridine-3-boronic Acid

    For nearly two decades, we have been manufacturing advanced boronic acids, including 5-Trifluoromethyl-pyridine-3-boronic acid. We measure success by the feedback we get from process chemists, research labs, and plants who need consistent quality so their work proceeds without interruption. Our familiarity with this class of products comes from years on the front lines: handling everything from scale-up and storage to support in troubleshooting rare synthetic issues. Through it all, 5-Trifluoromethyl-pyridine-3-boronic acid has become a reliable tool in the toolkit of many customers pushing the boundaries of medicinal chemistry, agrochemicals, and specialty materials.

    Product Model and Specifications Backed by Practice

    We produce 5-Trifluoromethyl-pyridine-3-boronic acid to practical research scales and support larger projects that require significant bulk. This product is available as white to off-white solid crystals. Through repeated recrystallization and advanced drying techniques, we keep moisture content under stringent control—critical for Suzuki couplings and similar palladium-catalyzed reactions. The assay routinely surpasses 98% (HPLC), with single impurities usually below 0.5%. Our control of organometallic impurities makes isolation and downstream purification easier for our partners. Standard packaging ranges from grams for medicinal chemistry pilots to multi-kg quantities for intermediates manufacture, and we use packaging tested to prevent hydrolysis or decomposition over extended storage.

    Real-world Applications and End-user Feedback

    Chemists in both research and production settings turn to 5-Trifluoromethyl-pyridine-3-boronic acid when they want to introduce both a pyridine ring and a trifluoromethyl group in one step. These two structural elements add distinct electronic and physical properties to molecules—changing everything from lipophilicity to metabolic stability. Pharmaceutical companies trust this compound for fragment-based drug discovery, especially in the design of kinase inhibitors or CNS-active agents. Agrochemical developers also value it, exploiting the stability and bioavailability offered by its fluorinated pyridine backbone. Since introducing this product line, multiple research teams have told us that the purity and ease of handling helped shorten project timelines and reduce batch rejection rates.

    Key Differences Compared to Other Boronic Acids

    5-Trifluoromethyl-pyridine-3-boronic acid offers certain features that set it apart from both simple pyridine boronics and other fluorinated analogs. Not all boronic acids handle moisture the same way. The presence of CF3 on the pyridine ring lowers the tendency to form boroxines, commonly seen with less electron-deficient analogs. Our monitoring of storage stability shows this product keeps well in standard lab conditions for months, a significant advantage for research teams cycling through different targets. In contrast, some of the basic pyridine-3-boronic acids need strict dry-box storage to avoid rapid polymerization.

    Another key difference is in cross-coupling performance. The electronic effects of the trifluoromethyl substituent extend the range of coupling partners, allowing for greater flexibility in ligand and catalyst selection. Process chemists working with competitive libraries have praised this, noting higher yields and fewer byproducts with our product, especially under milder Suzuki-Miyaura conditions. We’ve supplied both simple and highly functionalized boronic acids; only a few, like this one, let reactions proceed smoothly even with more sensitive aryl halides or heterocycles.

    Challenges During Scale-up and Our Practical Solutions

    Manufacturing trifluoromethylated pyridine boronic acids at scale poses a set of headaches that we’ve come to know well. Water control requires not just dry solvents but careful exclusion during workup and packaging. Early on, we observed issues with residual color and variable melting points, so we reworked the process to include two extra purification steps and finer temperature control during isolation. Purity improvements tracked closely with project outcomes: customers reported fewer chromatographic loads and cleaner analytical profiles in their final API intermediates.

    Another lesson learned involves handling losses during filtration. This product does not always behave like standard benzeneboronic acids—its solubility profile in common solvents can complicate filtrations. Our solution involved fine-tuning the stoichiometry and filtration temperatures, opting for specialized glassware that minimizes product loss. We share these handling tips with customers, some of whom switched from other suppliers after facing similar issues without support.

    Insights Gained from Direct Collaboration

    We encourage feedback from every user—as routine as a purchase order or as detailed as a reaction troubleshooting report. One research group working with a novel kinase inhibitor highlighted a persistent side reaction from trace halide contamination. After a joint review of batch records and analytical data, we implemented additional halide trimming steps. Their next delivery met their internal threshold, and the final reaction worked seamlessly. This sort of two-way communication allows us to adapt and drives improvements in the supply chain.

    Other collaborations informed our packaging upgrades: for example, a pharma partner flagged issues with static buildup, which affected their weighing accuracy. After testing multiple solutions, we shifted to anti-static bottles and instruction inserts for safe handling, reducing sample-to-sample variation. These changes may feel small, but they have knocked hours off prep times and prevent costly delays downstream.

    Supporting Sustainable and Safe Use

    Customers regularly ask about the environmental and safety aspects of working with trifluoromethylated boronic acids. We evaluate suppliers for the starting trifluoromethyl-pyridine, and select those with documented emissions reduction practices. Waste streams in our facility go through advanced fluorine-removal treatments. Staff use closed handling systems to avoid unnecessary exposure—an approach that translates to safer treatment of intermediates and waste at customer sites, whether they run kilo-labs or benchtop screens.

    Practical safety comes from years of hands-on practice: we recommend not just PPE, but specific ventilation or glove choices based on our own mishaps and experience. We’ve seen researchers new to boronic acids sometimes underestimate their skin sensitivity, so we include tip sheets based on our staff’s real incidents, encouraging the right precautions from day one. This direct, experience-focused feedback loop shortens the learning curve for new users and helps avoid the errors we made along the way.

    Troubleshooting and Real-World Handling Advice

    Even a high-purity 5-Trifluoromethyl-pyridine-3-boronic acid batch can sometimes behave unpredictably—clumping, sticking, or taking on moisture during transfer. We maintain a technical support line, and encourage teams to call us the same day issues appear. Tapping into decades of first-hand process experience, we offer practical suggestions: pre-cooling spatulas, using specific solvent pre-washing methods, or leveraging temperature ramps during transfers. Customers have often solved recurring problems after just a few calls with our technical team, as we share what’s worked—or failed—based on what we’ve personally seen.

    Scaling reactions above 100 grams often brings new complications, and the product’s behavior can diverge from that seen at bench scale. We attend scale-up trials on-site whenever possible, providing step-by-step input that saves time and reduces expensive batch failures. In more than a few cases, academic labs have reached out for advice after a challenging scale-up, only to return for additional material once their procedures stabilized—often crediting our shared hands-on approach for their saved time and reduced troubleshooting efforts.

    Continuous Improvement in Quality and Supply

    Supply chain disruptions, variable pricing, and unexpected grading have become all too common. We have learned to invest in upstream relationships, qualifying only those producing high-integrity starting materials and holding regular joint audits. This focus on reliable sourcing allows us to give customers real visibility on anticipated lead times and catch any changes in quality before they threaten a larger campaign. With specialized fluorinated building blocks, we see that corners cut upstream almost always show up as headaches downstream.

    We run stability and compatibility studies internally, and update customers well before any observed batch drift. This helps partners plan their campaigns with confidence, knowing that substitutions or scaling changes on our end come fully validated. To strengthen long-term confidence, each lot ships with extended analytical reports including full chromatograms—not just summary numbers—so that chemists on the receiving end see real data, not just a certificate.

    Role in Custom Synthesis and Diverse Synthetic Challenges

    As customers’ chemistry grows more sophisticated, demand for unique building blocks like 5-Trifluoromethyl-pyridine-3-boronic acid continues to expand. We coordinate closely with R&D teams exploring less common reaction conditions: microwave synthesis, continuous flow, or even organocatalysis. Our team documents how this boronic acid behaves under non-standard conditions—both what works and where additional drying or in situ preparation proves necessary. This record-keeping has fed back into commercial process development, leading to more efficient and reproducible applications in material science and drug discovery programs.

    Some of the more rewarding collaborations arise when we act as a sounding board for new synthetic methodologies. A recent case involved a customer shifting from conventional cross-coupling to a nickel-catalyzed process intended for greener, lower-waste production. Our role included providing clean, multiple-kg lots and sharing analytical support on the side-products seen for the first time with this new route. These shared findings advanced the project and improved our own process by highlighting previously unseen impurity pathways, which we then worked to minimize in-house.

    Benefits to End-users—Drawn from Practice, Not Theory

    Adopting 5-Trifluoromethyl-pyridine-3-boronic acid has allowed industrial and academic labs to streamline target synthesis routes while controlling for unwanted side-products often introduced by less stable analogs. Research participants tell us that yields and selectivities stay within tight windows, enabling faster milestones whether the goal is moving a candidate into IND-enabling studies or producing the next crop protection molecule. Even teams pursuing high-throughput screening of new chemical entities have noted fewer failed runs and more consistent library builds with this product, as compared to broader boronic acid classes which display greater batch-to-batch performance swings.

    The user experience matters. Where some products require elaborate pre-drying or extra care in inert atmosphere handling, this compound takes less time to prep and integrate, due to its relative stability and predictable reactivity. Directly from our facility into the hands of those driving the next round of innovation, our 5-Trifluoromethyl-pyridine-3-boronic acid has proven its worth as a robust and trustworthy chemical building block.

    Ongoing Commitment and Shared Progress

    Building reliable, functional boronic acids requires attention to every detail, from raw materials sourcing to packaging and customer support. Our direct experience has made clear which process choices truly impact the quality and usability of 5-Trifluoromethyl-pyridine-3-boronic acid. Feedback shapes not only our production methods but also tailored support for unique customer needs. Only through dialogue, trial and error, and a shared goal of better chemistry have we built a product line trusted by innovators worldwide.

    We welcome continued partnership with those aiming to push the boundaries of molecular innovation. 5-Trifluoromethyl-pyridine-3-boronic acid stands as one of the strongest testaments to quality through hands-on expertise, careful refinement, and unbroken lines of collaboration from lab bench to production floor.