6-Isopropoxypyridine-3-boronic acid

    • Product Name: 6-Isopropoxypyridine-3-boronic acid
    • Chemical Name (IUPAC): (6-propan-2-yloxypyridin-3-yl)boronic acid
    • CAS No.: 1233243-44-7
    • Chemical Formula: C8H12BNO3
    • 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

    508714

    Product Name 6-Isopropoxypyridine-3-boronic acid
    Cas Number 1133055-75-2
    Molecular Formula C8H12BNO3
    Molecular Weight 180.00 g/mol
    Appearance White to off-white solid
    Melting Point 120-124°C
    Purity Typically >97%
    Synonyms 6-(Propan-2-yloxy)pyridine-3-boronic acid
    Chemical Class Boronic acid derivative
    Smiles CC(C)OC1=NC=C(C=B(O)O)C=C1
    Solubility Soluble in DMSO, methanol
    Storage Conditions Store at 2-8°C, protect from moisture

    As an accredited 6-Isopropoxypyridine-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 25g `6-Isopropoxypyridine-3-boronic acid` comes in a sealed amber glass bottle with reagent specifications and safety labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 6-Isopropoxypyridine-3-boronic acid: Securely packed drums or bags, moisture-protected, safely palletized, compliant with chemical transport regulations.
    Shipping 6-Isopropoxypyridine-3-boronic acid is shipped in tightly sealed containers, protected from moisture and light, and handled under cool, dry conditions. Packaging complies with chemical safety standards to prevent leakage or contamination. Appropriate hazard labeling and documentation accompany the shipment to ensure safe and compliant transport according to regulatory guidelines.
    Storage 6-Isopropoxypyridine-3-boronic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and store it under an inert atmosphere, such as nitrogen or argon, to prevent oxidation or hydrolysis. Avoid sources of ignition and incompatible substances like strong oxidizing agents. Store at 2-8°C for optimal stability.
    Shelf Life 6-Isopropoxypyridine-3-boronic acid should be stored cool and dry; shelf life is typically 2 years if unopened and properly stored.
    Application of 6-Isopropoxypyridine-3-boronic acid

    Purity 98%: 6-Isopropoxypyridine-3-boronic acid with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it enables high-yield synthesis of substituted pyridine derivatives.

    Melting point 174-177°C: 6-Isopropoxypyridine-3-boronic acid with a melting point of 174-177°C is used in pharmaceutical intermediate manufacturing, where it ensures thermal stability during reaction processes.

    Particle size <50 µm: 6-Isopropoxypyridine-3-boronic acid with particle size <50 µm is used in solid-phase synthesis applications, where it promotes rapid dissolution and reaction kinetics.

    Moisture content <0.5%: 6-Isopropoxypyridine-3-boronic acid with moisture content <0.5% is used in API development, where it maintains product integrity and prevents hydrolysis during formulation.

    Stability up to 120°C: 6-Isopropoxypyridine-3-boronic acid stable up to 120°C is used in chemical process scale-up, where it provides consistent reactivity under elevated temperature conditions.

    HPLC purity ≥98%: 6-Isopropoxypyridine-3-boronic acid with HPLC purity ≥98% is used in fine chemical synthesis, where it ensures minimal byproduct formation and high product selectivity.

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    Certification & Compliance
    More Introduction

    6-Isopropoxypyridine-3-boronic Acid: Focused Innovation in Boronic Acid Synthesis

    Across decades in boronic acid manufacturing, compound consistency and product purity matter more than any catalog buzzword. In our own experience, the complexities of building functional boronic acids often get overlooked by those who simply trade the finished product. Synthesizing 6-Isopropoxypyridine-3-boronic acid requires careful control around every step, from meticulous raw material selection to precisely monitored reactor conditions. Customers who use this molecule know how even minor differences at the manufacturing stage shape downstream transformations in pharmaceutical, agrochemical, or materials research settings. That’s something only a hands-on chemical producer can stand behind.

    Model, Appearance, and Specifications

    We offer 6-Isopropoxypyridine-3-boronic acid as a consistent, crystalline solid, white or faintly off-white in pure form. Years of synthesis optimization led us to a single, tightly-controlled preparation route that avoids batch-to-batch ambiguity. Drawing from process improvements and analytical learnings, we peg minuscule byproduct levels through advanced HPLC and NMR monitoring. Moisture can alter storage or reactivity in air-sensitive transformations, so we focus on delivering every batch in sealed, low-humidity packaging, with a guaranteed moisture level below commonly accepted thresholds.

    Molecular formula: C8H12BNO3
    Molecular weight: 180.00 g/mol
    Purity: Assay typically above 98%. We use our own instrumentation to validate every lot, and keep below 1% total impurities. Direct mass spectral confirmation always accompanies shipment. If customers request, we offer either standard analytical data sets or additional validation—most engineers and scientists appreciate the difference it makes to interact directly with the people behind the instrument.

    Key Usage in Complex Synthesis

    Chemists involved with Suzuki-Miyaura cross-couplings recognize the unique leverage that nitrogen-containing boronic acids offer. In our case, 6-isopropoxypyridine-3-boronic acid’s pyridine motif guides regioselective coupling through both electronic and steric effects. Medicinal chemists lean on this particular boronic acid for creating core scaffolds in kinase and GPCR inhibitor programs, where positional fidelity in the pyridine ring shapes downstream pharmacokinetics. The isopropoxy substituent at the 6-position unlocks tailored solubility profiles and acts as a handy handle for further derivatization. Our experience with project partners in the drug discovery space underscored the problems that arise when even a trace of boroxine or pyridine N-oxide sneaks through—these act as silent disruptors in late-stage assembly, contaminating reaction vessels and wasting costly catalysts. Direct traceability, expert interpretation of characterization data, and real-world exposure to scale-up challenges let manufacturers like us make quick course corrections. Our customers trust us to spot these obscure pitfalls in advance, helping smooth the transition from benchtop to pilot plant.

    Advantages over Standard Boronic Acid Offerings

    Many generic boronic acids lack thoughtful design around substituent effects or molecular orientation. Our team’s background in heterocyclic synthesis lets us anticipate the subtle ways that the 6-isopropoxy group on this pyridine ring interacts with various coupling partners. Comparing this product to general aryl boronic acids, the electronic distribution makes for stronger, more directed metal binding, and improves reliability under Suzuki conditions, even with demanding ligands. Our own comparative studies—inspired by frustrations with inconsistent trial materials—showed distinctly enhanced coupling rates at lower catalyst loadings, and diminished formation of undesired homocoupled bipyridines. Material handled directly from our drums performs more predictably across solvent systems, including challenging aqueous blends where hydrolytic stability becomes a concern.

    Customers who used other suppliers frequently encountered morphology inconsistencies, from oiling out in chromatography to unexpected melting phenomena. Our tighter synthetic process, along with rigorous post-synthesis drying, removes these headaches. We listen to feedback from research chemists and process engineers, tweaking particle size distribution and surface area profiles to ease suspension and transfer between steps. This attention to bulk handling wouldn’t come from a distribution warehouse—it takes lab-scale trial runs, repeated filtration cycles, and thirteen years of listening to what works in a real synthesis suite.

    Sustainable Manufacturing Practices and Waste Minimization

    Manufacturing specialty boronic acids at scale raises unique environmental questions. Solvent streams, especially with pyridine derivatives, present disposal risks and regulatory scrutiny. Over the past decade, we built recycling systems that recover over 80% of our major solvent components, including those with higher boiling points like ethylene glycol dimethyl ether, often used in complex pyridine chemistry. By streamlining workups and implementing closed-loop rinses for reactor cleaning, we trimmed downstream organic waste volumes by almost a third over the last five years.

    Hydrolytic byproducts, boron-containing wastes, and off-spec intermediates never leave our site untreated. We use multi-stage decomposition beds, designed in-house, to break down redundant borate fractions and oxidize residual impurities. What this means for buyers is a product rooted in well-managed chemistry—one that isn’t just washed up at the finish line, but thoughtfully built from the start. The growing environmental push across our sector calls for continuous audit and courage to invest in new plant technology. We’ve made it a rule to monitor emission levels beyond lowest legal benchmarks, especially around nitrogen-heterocycle and boron handling. Our transparency extends to providing environmental and safety records to major partners—because clean chemistry and strong partnerships depend on facts, not slogans.

    Process Innovation and Real-World Applications

    From the start, our goal was to build a product that doesn’t just sit on a shelf, but powers real innovation in labs and pilot suites. Our technical staff take pride in benchmarking product performance alongside partner R&D teams. In one collaboration, a leading agrochemical innovator sought to couple a sensitive halopyridine to a bulky heteroaromatic fragment. Early runs with commercial boronic acids led to variable yields—water content swings, paste formation during vacuum filtration, and reaction stalls at the scale-up stage. By working directly with their team, we modified our quenching and isolation steps, delivering a boronic acid batch with tighter microcrystalline structure and less surface moisture. That single tweak unlocked cleaner conversions, reduced solids clumping, and improved downstream filtration yields by 12%.

    Pharmaceutical process groups regularly take on advanced multistep syntheses, where a specific boronic acid sits in the critical path for intermediate construction. Our sales engineers, all with laboratory backgrounds, get called in to dissect failed couplings or troubleshoot catalyst deactivation. Solutions often lie in minor details—a tweak in NMR-detectable boroxine fractions, switching from amber to opaque packaging during summer shipments, or tightening glovebox moisture transfer parameters. Our customers appreciate talking directly with bench chemists and scale-up engineers who know the batch history and can run spectral crosschecks without lengthy third-party delays. This sort of technical exchange lies at the heart of real chemical progress, and defines the difference between manufacturer-driven and catalog-driven supply chains.

    Reliability Through Direct Production Oversight

    Our entire line of precision boronic acids, including 6-Isopropoxypyridine-3-boronic acid, comes from a single integrated plant with unified batch tracking. Each reactor load gets monitored by the same process technicians, who calibrate dosing and temperature profiles based on both historical run data and live process controls. We log real-time analytics, documenting every deviation and corrective action, so each batch record tells the material’s full story.

    This level of control attracts advanced end-users, especially in regulated sectors where QA teams demand more than standard certificates. Process chemists have reached out after encountering poorly characterized material elsewhere, struggling with ambiguous melting points, mixed crystal forms, or inconsistent supplier responsiveness. In one typical scenario, a customer received technical support within hours—our in-house chemists re-ran analytical tests from archival samples and shipped fresh documentation, bridging a critical gap in a high-profile research timeline. These experiences fuel our commitment to blend manufacturing discipline with hands-on service, as every chemist working late nights deserves reliable, truthful support.

    Handling and Downstream Compatibility

    Success with sensitive boronic acids stems from disciplined handling, starting at the production site. We use inert, moisture-controlled lines in all transport stages, preventing inadvertent hydrolysis or oxidation before product reaches the customer’s bench. Solid shipment batches rest in vapor-barrier packaging, with desiccant and humidity indicators for end-user verification.

    Many users in the academic and industrial sectors call out transfer and weighing as a pain point, noting stickiness or dust formation from lesser-refined boronic acids. We spent years adjusting drying and final isolation techniques, targeting a balanced microcrystal that resists aggregation but disperses well into common solvents. These improvements see the most feedback from synthetic chemists running 0.1 to 10-gram couplings, especially when precious catalysts or labeled precursors are involved. No one wants to lose a reaction’s value to last-minute bottlenecks, so we keep our staff available for troubleshooting advice on the ground.

    Downstream, compatibility matters for both solvent choices and metallic catalyst blends. Our technical data, paired with customer reporting, confirms predictable coupling rates in both aqueous and organic adsorbent systems. Studies conducted in partnership with several contract manufacturers found that our material maintained its crystallinity—and thus reactivity—after weeks in standard laboratory conditions, outperforming generic samples subjected to identical protocols. Orders destined for automation or high-throughput QC screens receive tailored batch documentation, ensuring users can trace every characteristic back to its lot-specific historical data.

    Observations on Supply Trends and Chemical Landscape

    Market demand for advanced boronic acids continues to surge, propelled by the relentless drive toward complex molecular architectures. Supply chain issues, unforeseen weather impacts, or regulatory bottlenecks all test the resolve of manufacturers. Direct production oversight and robust inventory practices allowed us to weather recent market fluctuations, with flexibility to ramp output or divert materials to customers facing urgent deadlines. There is no substitute for plant-level understanding—no amount of trading can rescue a project when upstream tanks run dry due to raw materials delays, or when reagent purity drops and jeopardizes a tightly-timed campaign.

    We monitor boronic acid consumption trends by sector: pharma R&D, advanced materials, agrochemical intermediates, and academic research. Each application brings unique purity, particle, and packaging needs, and each demands a depth of expertise to navigate unforeseen complications. The real value in long-term manufacturing relationships lies not just in product delivery, but in solving the day-to-day puzzles chemists encounter, whether they involve shelf-life extension or adapting to emerging green coupling protocols.

    Learning from Real-World Setbacks

    Manufacturers who engage deeply with process chemists and synthetic teams build a unique knowledge base, colored by real problems and practical fixes. In one case, a series of delayed pilot batches raised flags with an overseas client. Their receiving docks reported sticky, partial-cake material—initially traced to excess atmospheric humidity during monsoon shipping. By initiating remote batch tracking and offering humidity-controlled air freight as a direct production solution, future shipments arrived in optimal form.

    Other times, a new academic team would embark on an ambitious project, only to hit a wall with standard commercial boronic acids failing in their new coupling designs. We regularly schedule informal technical reviews, encourage transparent feedback, and bring advice back to our plant teams, reinforcing what technical support in specialty chemicals means. Unlike traders or brokers, manufacturers with feet on the ground can see an entire batch through—from the first flask through to the final package—empowering them to adjust pace, technique, and even raw material sourcing to best serve demanding R&D environments.

    Future Directions in Boronic Acid Chemistry

    6-Isopropoxypyridine-3-boronic acid sits at the intersection of classical organic synthesis and modern molecular design. Real advances come from getting the basics right—controlling impurities, understanding customer use cases, rethinking waste and environmental management—and then building customer trust through proven performance. Our own facility remains committed to routine reinvestment, upgrading analytics, refining process design, and mentoring a new generation of chemical engineers and operators out on the plant floor. These investments compound over time, resulting in a product line tuned for the evolving needs of researchers, industry collaborators, and innovators worldwide.

    We’re open about sourcing, manufacture, and supply constraints, and we keep direct communication channels active by design. Every new inquiry around our pyridine boronic acid gets a considered response, from detailed product performance benchmarking to robust environmental and transportation data. We don’t rely on middlemen or generic catalog copy—our commentary and support draw from first-hand production and laboratory experience, shaped by years of working shoulder-to-shoulder with the chemists who drive molecular progress on the front lines.

    Evidence-Driven Commitment

    At the manufacturing level, real quality takes more than polished paperwork. Certified analytical data earns trust, but supporting thousands of successful couplings in academic, industrial, and pharmaceutical labs backs it up with evidence. Problems arise constantly, and overcoming them comes not from marketing, but from expert teamwork and transparency—explaining why a failed reaction might link to trace contamination, unpredictable solubility, or inconsistent drying methods. Customers recognize the value of speaking to specialists who have run the synthesis in-house, handled the final product, and have invested years troubleshooting organic synthesis at scale.

    We believe any successful specialty chemical—from 6-Isopropoxypyridine-3-boronic acid to more complex boronate esters—should be born from technical craft and pragmatic problem solving, not just specification compliance. Experience, data, and the drive to continually improve define our product quality. Chemists and process engineers who choose our materials gain a direct channel into this expertise, not just for today’s molecule, but for the next generation of chemical breakthroughs.