2-Bromo-3-methylpyridine-5-boronicacid

    • Product Name: 2-Bromo-3-methylpyridine-5-boronicacid
    • Chemical Name (IUPAC): (2-Bromo-3-methylpyridin-5-yl)boronic acid
    • CAS No.: 874290-64-9
    • Chemical Formula: C6H7BBrNO2
    • 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

    837837

    Product Name 2-Bromo-3-methylpyridine-5-boronic acid
    Cas Number 877399-60-5
    Molecular Formula C6H7BBrNO2
    Molecular Weight 215.84
    Appearance White to off-white powder
    Melting Point 153-156°C
    Purity Typically ≥ 97%
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Storage Conditions Store at 2-8°C, away from moisture and light

    As an accredited 2-Bromo-3-methylpyridine-5-boronicacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g 2-Bromo-3-methylpyridine-5-boronic acid is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Container Loading (20′ FCL) 20′ FCL (Full Container Load): Securely packed drums or bags of 2-Bromo-3-methylpyridine-5-boronic acid, maximizing container capacity.
    Shipping **2-Bromo-3-methylpyridine-5-boronic acid** is shipped in tightly sealed containers, protected from moisture and light. Transport follows standard chemical safety protocols, including appropriate labeling and documentation. The package must comply with local and international regulations for hazardous materials to ensure safety during transit. Temperature-sensitive conditions may be recommended depending on storage requirements.
    Storage **Storage of 2-Bromo-3-methylpyridine-5-boronic acid:** Store in a tightly sealed container, protected from moisture and air. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerated conditions). Avoid exposure to direct sunlight and incompatible substances such as strong oxidizers. Clearly label the container and use appropriate secondary containment to prevent accidental spills or contamination.
    Shelf Life 2-Bromo-3-methylpyridine-5-boronic acid is stable for 1–2 years when stored cool, dry, in tightly sealed containers.
    Application of 2-Bromo-3-methylpyridine-5-boronicacid

    Purity 98%: 2-Bromo-3-methylpyridine-5-boronicacid with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield coupling reactions.

    Molecular weight 215.88 g/mol: 2-Bromo-3-methylpyridine-5-boronicacid of molecular weight 215.88 g/mol is used in Suzuki-Miyaura cross-coupling, where precise mass enables accurate stoichiometry.

    Melting point 155–158°C: 2-Bromo-3-methylpyridine-5-boronicacid featuring a melting point of 155–158°C is used in solid-phase organic synthesis, where controlled phase transitions facilitate purification steps.

    Particle size <50 μm: 2-Bromo-3-methylpyridine-5-boronicacid with particle size below 50 μm is used in catalyst preparation, where increased surface area enhances reactivity.

    Stability up to 80°C: 2-Bromo-3-methylpyridine-5-boronicacid stable up to 80°C is used in elevated-temperature reactions, where thermal stability maintains compound integrity.

    Water content ≤0.2%: 2-Bromo-3-methylpyridine-5-boronicacid with water content not exceeding 0.2% is used in moisture-sensitive synthesis, where low water level prevents hydrolysis.

    Assay ≥98%: 2-Bromo-3-methylpyridine-5-boronicacid with assay not less than 98% is used in medicinal chemistry research, where high purity supports reproducible experimentation.

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    Certification & Compliance
    More Introduction

    2-Bromo-3-methylpyridine-5-boronicacid: Quality Insights from the Production Floor

    Looking Through the Lens of Straightforward Chemistry

    Making 2-Bromo-3-methylpyridine-5-boronicacid is not about following a recipe in a textbook. Years of hands-on adjustments, process revisions, and close tweaks to reaction conditions go into every batch. This compound, with its distinct combination of a bromo group, a methyl group, and a boronic acid moiety attached to the pyridine ring, demands more than a surface-level approach. This isn’t an offbeat product cobbled together because a catalog asks for it. The chemistry of coupling, specificity in substitution, and attention to stability all come through, batch after batch, because we have seen what goes right and what can go wrong in the reactor. In the industry, you cannot afford superficial work—one missed detail, and downstream synthesis will stall or collapse.

    The Production Mindset: Experience over Guesswork

    Our on-site team runs every process step themselves; we do not rely on nameless third parties or jobbers with little stake in the outcome. The starting point is pyridine, one of the more challenging heterocycles to handle—its volatility and strong odor are legends in a production setting. Bromination calls for real sensitivity: too aggressive, and you leave a trail of impurities; too mild, and the conversion lags behind. Methylation isn’t a one-size-fits-all addition either. The boronation step marks the trickiest phase. The pyridine ring resists boronation at some positions, but careful temperature and reagent control, along with constant sample checks, carries us through. Each lot is weighed, dried, and inspected in-house. We do not simply “follow the literature”; we regularly update our conditions based on the lab’s collected process data and real output.

    Specifications: Not Just Numbers, but a Reflection of Purpose

    Quality for this molecule is more than a purity value on a certificate. Spectral data—NMR, HPLC, and more—come from batch-specific samples. We know the side products that often hide in the shadows: overbrominated derivatives, unmethylated precursors, extra boronic acid condensates. These ghosts show up on the trace analysis and sometimes evade standard testing. Because our team has chased down these contaminants before, our analytical methods go beyond a generic check. We coordinate with customers who bring new demands—sometimes wanting different forms such as free acid or pinacol ester. Each variant needs its own workflow. Internal archives of chromatograms from thousands of past runs shape our procedures. Even color, flow, and solubility can foreshadow how a batch will behave in scale-up reactions. Some users want more granular data, such as heavy metal traces or solvent residue reporting. We leave nothing to guesswork, because the headache of a failed Suzuki coupling will circle back to the quality of our input.

    Digging Into Applications: From Discovery to Scale-Up

    For those in pharmaceutical research, agrochemical synthesis, or fine chemicals, the structure of 2-Bromo-3-methylpyridine-5-boronicacid lines up with current methods in cross-coupling reactions. The boronic acid group opens doors for Suzuki-Miyaura coupling, giving users room to build up complex, bioactive scaffolds that would otherwise be a nightmare to assemble. In the past five years, we have seen this intermediate help speed up the discovery and production of kinase inhibitors, specialized pesticide components, and photonic materials.

    In the R&D trenches, researchers often move from single-gram scale up to tens of kilograms with tight timelines. We have adjusted for that. Delivering kilograms with the same analytical depth as research-grade samples is not just a selling point; it makes or breaks the success of pilot-scale synthesis. Production reliability also means users avoid repeated verification or unnecessary purification steps. Our years operating in this field have taught us that reproducibility beats luxury packaging or elaborate documentation every time.

    How This Compound Really Differs from the Crowd

    Walk down the aisles of chemical offerings, and you’ll be bombarded by a list of similar compounds: bromo-, methyl-, and boronic acid-pyridines in every conceivable combination. For a new eye, these might even look interchangeable. Yet, in actual synthetic sequences, the reaction behavior shifts noticeably between isomers and analogs. We handle orders for a wide set of pyridine-building blocks, and no two behave exactly alike. The 2-bromo-3-methylpyridine-5-boronicacid stands out in its balance—reactivity without runaway side reactions, relative stability for shipping and storage, and flexible application range in cross-coupling. The meta position on pyridine impacts electron density in the ring and subsequent coupling yield.

    We have handled alternative isomers—such as 2-bromo-4-methylpyridine variants, or boronic acids at the 2- or 6-positions. These frequently show different solubility, need variations in catalyst loading, and in some cases, demand special handling to prevent degradation. Some lack commercial stability, forming residues or suffering from shelf-life limitations. Scanning through feedback and failure reports, these differences become stark, especially in time-sensitive projects. Those who tried to substitute an “almost identical” product often reported inconsistent yields, failed purifications, or incompatibility with their ligand/catalyst systems. What looks like a simple switch can cause months of lost research time. Our process for 2-bromo-3-methylpyridine-5-boronicacid involves this experience. We chart the critical profile of this molecule, so users are not blindsided by quirks that only appear mid-way through scale-up.

    Inside the Facility: People and Processes

    No slick ad campaign can replace the reality of a plant running at capacity, with a production team tuned to the nuances of this chemistry. Our staff rotates between the synthesis sections—those who run the bromination, those on methylation, boronation, and the analytics team in the R&D corridor. Crossover of roles is common, leading to a situation where process engineers routinely consult with analysts and sometimes even visit the customer’s lab to troubleshoot. Regular maintenance and audit of glassware, reactors, and support equipment follow a schedule built from firsthand repairs, not only manufacturer specs. Breakdowns and mishaps can’t just be filed away out of view; if a filtration bottleneck holds up a batch, it’s back to the drawing board with the hands that mixed the first charge.

    Raw materials get tracked closely. We have swapped out subpar boronic acid sources after finding batch-based color and odor shifts—details that signaled impurity. Every issue like this is cataloged into our process knowledge, forming a company memory stronger than whatever is in the public literature. Suppliers that once impressed with polished samples lost our trust after just one out-of-spec delivery. This direct impact on final product quality keeps us vigilant. For customers, this translates to predictability across years, not just orders.

    Challenges Out in the Open: Regulatory, Environmental, and Shelf Life

    Working with heterocyclic boronic acids means dealing with regulatory shifts on both import and export ends. A few years ago, changes in hazardous labeling for boronic acids and bromo-pyridines meant retooling our plant labeling procedures, training staff on new documentation, and coordinating with freight forwarders who suddenly faced stricter transportation rules. These compliance shifts brought real costs, not to mention delays. We have reacted by investing in targeted regulatory training and by sourcing packaging materials that can handle evolving labeling requirements without risk. There were times when updates to GHS regulations caught others off guard, but experience in dealing directly with regulatory authorities puts us in a position to pivot quickly, losing less time in the shuffle.

    Environmental controls are another hurdle for this class of chemicals. Pyridine derivatives exhibit a persistent odor that neighbors complain about long after the run ends, and boron compounds—though only slightly toxic—call for containment to avoid wastewater issues. We didn’t wait for problems to snowball; engineering controls, upgraded air handling, and the use of closed systems for high-odor intermediates have kept our output stable and community relations strong. Our operators suggested practical tweaks after running into problems themselves, leading to design changes that no outside consultant could have anticipated. Handling the subtle, day-to-day details of odor containment or effluent treatment is far from glamorous, but it builds trust both internally and in the broader community.

    Shelf life emerges as another point that buyers often underestimate. With boronic acids, hydrolysis and oxidation can start on day one if conditions go off track. We optimized our drying and packaging steps after losing material to poor closure systems and humidity ingress. Now, every outgoing package is checked for two things: water content below our practical upper limit and proper sealing (using real-world, stress-tested closures that survive weeks in transit, not just a short ride across town).

    Tracing the Demand Landscape: What Customers Really Value

    Feedback loops shape our business. Users in pharmaceutical research value certainty; a missed step downstream costs far more than a minor price difference. Contract manufacturers make the largest, recurring orders and expect consistent lots months apart, sometimes through regulatory agency review. Academic researchers, working in grant cycles and publication-driven timelines, sometimes find themselves splitting grams to make budgets stretch—small mistakes in quality force reruns on shoestring funds. We know the weight of these issues because they have landed on our support team’s desk for years.

    Procurement questions come thick and fast. Purchasers often want to know stability under ambient shipment, reactivity trends in different solvents, and tolerance to moisture. Over time, we have also collected performance feedback on dozens of coupling runs, noting catalyst demands and product yield differences depending on batch age or shipping route. This open data loop fuels both our commercial and technical approaches. Our staff rarely forgets a failed batch; lessons from those days become the pressure-test for every improvement in plant and protocol. It’s not a stretch to say much of our progress is built on admission and correction of earlier mistakes.

    Why Supply Chains Matter: Reliability Over Hype

    With shifts in the global chemical market, especially in the last decade, pressure mounts to chase the lowest price or cut corners on QC. Some vendors pass off chemically similar pyridine derivatives under different names, or co-mingle fresh and aged material to stretch resale. These practices only invite new headaches at bench scale and worse, at pilot or production scale. Our approach always comes back to transparency: we never mix batches, every certificate is tied back to original test records, and shipment documentation is drawn up by someone who has handled the drum, not just a clerk in an office. Our repeat buyers appreciate that mistakes do not simply get swept under a marketing rug; they get addressed out in the open, with corrections or compensation when warranted.

    In an era when some operations prioritize speed of sale over reliability, our model sticks to one rule: never sell a lot we wouldn’t use ourselves on our next run. Staff across R&D, production, and logistics have stood in front of skeptical customers to explain product differences and field unexpected questions. That regular, real-world cross-exchange makes all the difference when supply disruptions or technical snags hit.

    Troubleshooting in Real Time: Practical Solutions

    Roadblocks come up when scaling up or fine-tuning synthetic routes with this compound. Sometimes users see variable coupling efficiency, unexplained color changes, or low recovery after chromatography. Our process team offers support based on field data, not theoretical fixes. Early on, we realized that a rise in moisture content during shipping led to color deepening—a small fix in packaging protocol reduced returns dramatically. Another time, trace potassium from a base caused separation issues for one customer; we retooled a washing step to reduce the element, solving a problem that could have simmered unseen otherwise.

    Real partnership with users means openness about what this compound is and what it is not. Some customers want substitutes for very similar boronic acids, searching for faster delivery or lower cost. We guide based on reaction compatibility, not only catalog listings. In our experience, the unique substitution pattern of 2-bromo-3-methylpyridine-5-boronicacid gives specific electronic and steric properties not matched by other variants—this complexity resists one-size-fits-all solutions, especially in scale-up. Those who try short-cuts often find cross-coupling yields cut in half, if the reaction works at all.

    Looking Back, Looking Forward: The Future of Pyridine Boronic Acids

    From the outset, single-site pyridine boronic acids were considered niche. Now, as cross-coupling methods dominate the toolbox of chemical synthesis, this class of intermediates has advanced from luxury reagents to production linchpins. Our team stays focused on incremental improvements: sourcing more robust starting materials, adapting isolation processes for lower waste, and collecting application data from users on emerging coupling technologies. The lab frequently evaluates new ligands and bases to map out changes in reaction profiles. These updates cycle back into training, so each production run gets smarter, not just faster.

    The technical journey continues. More customers are pushing us for greener practices and documentation for environmental audits. We’re answering with better solvent recovery, energy management, and support for green-by-design processes. Not every improvement comes from the top: operators and analysts drive change by living with their process day in and day out—details noticed in practice often feed crucial adjustments.

    Final Thoughts: Trust Forged in Practice

    At the end of the day, supplying 2-bromo-3-methylpyridine-5-boronicacid means standing behind everything that enters and leaves the facility. This molecule’s quirks and its place in synthesis pipelines shape our daily choices and long-term strategy. No abstract chart or glossy brochure can replace what years of problem-solving, process tweaks, and open dialogue with users has taught us. We plan to keep learning from every batch, every customer question, and every challenge that hits the floor—a model that has served us, and those who depend on this chemistry, from the lab shelf to full production scale.