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HS Code |
650774 |
| Product Name | 2-Bromopyridine-6-boronic acid pinacol ester |
| Cas Number | 870281-30-0 |
| Molecular Formula | C11H15BBrNO2 |
| Molecular Weight | 283.96 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents such as DMSO, DMF, dichloromethane |
| Storage Temperature | 2-8°C (refrigerated) |
| Smiles | B1OC(C)(C)OC1c2cccc(n2)Br |
| Synonyms | Pinacol 2-bromo-6-pyridylboronate |
As an accredited 2-Bromopyridine-6-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with PTFE-lined cap, labeled; contains 5 grams of 2-Bromopyridine-6-boronic acid pinacol ester. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packed 2-Bromopyridine-6-boronic acid pinacol ester in sealed drums or cartons, ensuring safe international transport. |
| Shipping | 2-Bromopyridine-6-boronic acid pinacol ester is shipped in tightly sealed containers under inert atmosphere, protected from moisture and light. The chemical is classified as hazardous and sent via certified carriers, following all relevant regulations for the transport of chemicals. Temperature control may be maintained to ensure product stability during transit. |
| Storage | 2-Bromopyridine-6-boronic acid pinacol ester should be stored in a cool, dry, well-ventilated area, away from moisture, heat, and direct sunlight. Keep the container tightly closed under an inert atmosphere, such as nitrogen or argon, to prevent hydrolysis or oxidation. Store separately from incompatible materials like strong oxidizers, acids, and bases for safety and stability. |
| Shelf Life | 2-Bromopyridine-6-boronic acid pinacol ester is typically stable for 1-2 years if stored cool, dry, and protected from light. |
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Purity 98%: 2-Bromopyridine-6-boronic acid pinacol ester with purity 98% is used in palladium-catalyzed Suzuki-Miyaura cross-coupling reactions, where high purity ensures superior coupling efficiency and product yield. Stability temperature 25°C: 2-Bromopyridine-6-boronic acid pinacol ester with stability temperature 25°C is used in organoboron reagent storage, where chemical integrity is maintained for long-term synthetic applications. Molecular weight 323.95 g/mol: 2-Bromopyridine-6-boronic acid pinacol ester with molecular weight 323.95 g/mol is used in drug intermediate synthesis, where precise molecular mass supports accurate stoichiometric calculations. Melting point 105–108°C: 2-Bromopyridine-6-boronic acid pinacol ester with melting point 105–108°C is used in solid-phase synthesis, where controlled phase transitions facilitate process reproducibility. Particle size <10 µm: 2-Bromopyridine-6-boronic acid pinacol ester with particle size <10 µm is used in automated reagent dispensing systems, where fine particle distribution enables uniform dosing and reaction consistency. Water content <0.1%: 2-Bromopyridine-6-boronic acid pinacol ester with water content <0.1% is used in moisture-sensitive coupling reactions, where low moisture prevents side reactions and degradation. Solubility in DMSO >50 mg/mL: 2-Bromopyridine-6-boronic acid pinacol ester with solubility in DMSO >50 mg/mL is used in solution-phase combinatorial chemistry, where excellent solubility supports high-concentration screening assays. |
Competitive 2-Bromopyridine-6-boronic acid pinacol ester prices that fit your budget—flexible terms and customized quotes for every order.
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Chemistry has always thrived on connections—the link between gathering quality raw materials and delivering robust intermediates forms the backbone of building blocks in our industry. In our daily work as a chemical manufacturer, we have seen how researchers and process engineers often hit critical walls during synthesis of complex organic structures. A compound like 2-Bromopyridine-6-boronic acid pinacol ester consistently helps them break through. The journey from elemental sources to specialized intermediates rarely runs smooth for anyone, but with the right experience behind the glassware and reactors, reliability becomes part of the product itself.
We typically identify this compound by its CAS number, 870299-39-5. The name alone—long and cumbersome on a label—reflects the multifaceted role the molecule plays in various synthetic steps. The model we produce follows established molecular structure: C11H15BBrNO2. Our process prioritizes consistency, with strict controls on purity and minimization of residuals. Typical batch purities exceed 98%, moisture kept below 0.5%. We achieve these marks using high-vacuum distillation and sealed packaging under inert atmosphere. Every gram we ship comes off our own line, not relabeled, not diverted from a broker.
Multistep synthesis of pharmaceutical targets and advanced materials often hinges on a critical cross-coupling. Over years of serving process chemists and scale-up teams, we noticed a frequent bottleneck starts with aryl bromides and functionalized pyridines. This is where our product makes a genuine difference. The boronic ester moiety teams up with key catalysts in Suzuki-Miyaura reactions. Pyridine-based molecules lay the foundation for a huge range of active pharmaceutical ingredients, crop-protection agents, OLED materials, and specialty polymers.
The 2-bromo substitution pattern is not accidental. It opens doors for regioselective transformations, allowing succinct installation of diverse functional groups in the 6-position. We are not blind to the synthetic challenges our customers face — there is real relief among chemists when they source a stable, bench-friendly boronic ester instead of unstable boronic acids. In the past, we encountered containers of boronic acids that degraded during shipping or became sticky and hard to weigh in open air. Our pinacol ester form avoids these headaches, granting you robust shelf life and easier handling. Solubility in standard coupling solvents, reduced sensitivity to air and moisture—these come as built-in benefits, not add-ons.
Every project has its unique set of problems, but similar needs keep popping up time after time. Clients in active pharmaceutical development choose our 2-bromopyridine-6-boronic acid pinacol ester for building up pyridine scaffolds, especially those targeting kinase inhibitors and CNS actives. One team came to us after back-to-back failures isolating their boronic acid intermediate; switching to our ester unlocked their process, shortened their reaction times, and improved yields.
Across the electronics space, R&D groups request this compound for functionalizing pyridine monomers. During pilot-scale OLED material synthesis, our boronic ester format provides a well-behaved partner for cross-coupling, avoiding major losses to protodeboronation even under rigorous reaction conditions.
We have seen agrochemical researchers take advantage of the coupling-ready form for assembling diverse combinatorial libraries. Rapid entry to functionalized 2-pyridines gives them a flexible tool for designing structure-activity relationships around new fungicides and herbicides.
Decades ago, boronic acids dominated laboratory catalogs. Still, those of us responsible for production, packing, and logistics learned a tough lesson—boronic acids can be fragile. They absorb water, sometimes degrade to intractable tars, or lose performance in coupling reactions. Shipping those acids halfway across a humid continent often led to more rejected product than usable lots.
The pinacol ester form transformed the scene. We have put in the time to optimize esterification, securing a product that ships globally with only basic precautions. The ester’s lower reactivity towards air and moisture means shelf lives measured in months, not days. Storage needn’t be as tightly controlled, and end-users can take out what they need without feeling rushed or concerned about stability. Chemists tell us the pinacol ester handles well in gloveboxes and basic fume hoods alike.
Our attention to detail rests not just on purity, but also on crystalline form and batch-to-batch uniformity. We have heard the horror stories—clumpy powders, uneven melting points, unexpected color shifts—that result from poorly controlled syntheses. In our facility, every reaction runs under real-time monitoring. We source high-purity pinacol and pyridine intermediates from longtime partners we audit in person. We run extensive spectral (NMR, HPLC, GC-MS) and visual inspection to avoid hidden pitfalls. Ninety-eight percent purity is not the ceiling but the baseline.
Other variant boronic esters exist—neopentyl glycol, for example, sometimes gets proposed as an alternative protecting group. Yet we have observed the pinacol ester offers the best compromise between solubility, stability, and reactivity across most organometallic coupling protocols. Unless prompted by unusual substrate requirements, we continue to recommend the pinacol variant. Such industry experience comes from seeing the same reactions run hundreds of times under both small- and large-scale conditions.
Plenty of suppliers claim to offer specialty intermediates, but only a fraction actually produce them from start to finish. We have invested in dedicated reactors and qualified technical staff to run every stage ourselves. This way, traceability never gets lost. Any questions about residual solvents or impurity profiles get a clear answer—they come directly from our analytical logs and batch cards. We handle questions about process or custom spec modifications without middlemen adding noise to communications.
Trust builds slowly, especially after a single out-of-spec shipment can damage a project’s timeline or break a supply chain. We see researchers returning year after year because their teams value transparency and the ability to request tailored QC documentation. Some customers require extremely low palladium residues; we meet those numbers by employing additional purification and metal-scavenging steps. Feedback matters—a warning about a troublesome impurity or packing issue reaches our production chief the same day, not weeks down the line.
We have worked closely with process development teams to troubleshoot coupling reactions that veered off track with inconsistent boronic acid sources. In Suzuki reactions for high-value targets, a single trace impurity in the intermediate can spell disaster. Our experience tells us even minor deviations—moisture, residual parent pyridine, or non-pinacol boronic components—can reduce product yield or create stubborn by-products. We fine-tune our crystallization steps and maintain routine validation checks for every batch. Many competitors cannot vouch for their product past the broker level; we can provide sample chromatograms, melting point curves, even replicate aliquots from the same production run.
Experience also taught us about the unpredictability of global supply lines. When interruption strikes elsewhere, in-house reserves become invaluable. Our factory keeps adequate safety stock and scales up on flexible notice, so large pilot lots or urgent project restarts avoid delays.
We hear from chemists who appreciate how our product stores cleanly for long periods, resists clumping, and avoids variable reactivity even after repeat open-close cycles. Repacking for multi-site deployment does not sap performance, and scale-up teams at larger plants report steady coupling efficiency across multi-kilogram runs. The pinacol ester’s manageable melting point and crystalline profile make it easy to weigh, transfer, and dissolve in common solvents. Project managers often tell us this practical reliability matters as much as price.
We advise users to store the compound in sealed, cool, dry conditions to get the maximum lifespan from the material. Our experience suggests packaged pinacol esters withstand moderate temperature swings and transient exposure to ambient air far better than the boronic acid form. That means reduced waste and fewer surprises during campaign-based synthetic runs.
Maintaining high standards in a specialty intermediate means more than checking off a box at QA. We seek out feedback directly from end-users, not just distributors, to spot bottlenecks or recurring pain points with handling, consistency, or application. Over the years, we've updated our protocols to address residue limits, titer strengths, and drying cycles, all based on concrete field reports and follow-up interviews.
We don't just rely on lab reports—our supervisory chemists keep hands-on involvement at each step, monitoring crystalline morphology, solubility metrics, and packaging durability. We refine our processes with targeted investments in purification columns, solvent recovery, and air filtration, aiming for each year's lots to outperform the last. Unlike pass-through traders, our reputation ties directly to the intermediate’s performance—not just its appearance on a specification sheet.
Customers scaling a procedure from gram to kilo scale often find off-the-shelf material changes character under process pressure: what worked at ten grams falters at two kilos. Our staff work closely with project teams to share histories of similar scale-outs—sharing not just data but practical tweaks in addition protocols, solvent blends, or agitation settings. Access to this body of process knowledge helps avoid common pitfalls, especially on time-sensitive deadlines.
Our plant can tailor batch sizes flexibly, providing consistent supply regardless of whether an order is for a hundred grams in discovery or tens of kilos during development. We discuss openly any limitations in scheduling or precursor availability, so buyers never find themselves blindsided after placing an order. It’s a hands-on, real-world approach suited to research cycles as well as long-term supply contracts.
We know clients making pharmaceuticals and regulated materials need more than technical grade product—they expect material qualification, full traceability, and documentation covering each step. Our plant operates according to consistent good manufacturing practice, with thorough records tracing every raw material batch, worker, and equipment used. Requests for change control or audit trails get our direct response, not a runaround between offices.
International shipments roll out with validated export clearance and documentation. Proprietary impurity control and compliance support help clients navigate unique requirements for APIs, including thresholds for heavy metals, non-volatiles, and specific organic contaminants down to parts-per-million ranges. Our staff invest in regular training and compliance updates to stay aligned with current local and global regulations.
Over two decades, we have seen a difference in customer satisfaction between in-house made intermediates and relabeled batches. Relabeling introduces opportunity for mishandling, documentation mistakes, and inconsistent storage. Direct control from synthesis to packaging solves these subtle but important causes of batch-to-batch variation. Chemists working on critical syntheses—where every reaction run costs money and time—depend on traceable, reliable intermediate so nothing derails downstream steps.
Our operations avoid mixing or blending lots to "average out" quality. Customers looking for precise analytical reference material rely on the fact that each unit sold reflects a continuous process, not a patchwork of leftovers from disparate runs. Full transparency into raw material selection, timing, and handling increases not only trust but practical utility in real experimentation.
Applications continue expanding as demand grows for complex pyridines in high-value sectors. Next-generation small molecules, bioactive compounds, performance monomers—each field presents new requirements for coupling efficiency, purity, or functional group compatibility. We track shifts in catalyst technology, continuous-flow chemistry, and microwave-assisted couplings. Each advancement puts new pressure on intermediate performance and usability.
Using insights from collaborative R&D projects, our production line adapts to keep up with increased throughput and regulatory hurdles. Continuous improvement comes from customer-driven data: feedback on melting profiles, compatibility with novel ligands, or unique solubility requests gets relayed to our technical team. This cycle of information ensures the product stays not only relevant but ahead of shifting market needs, far beyond rote specification compliance.
Success in synthesis often runs on the quality and dependability of intermediates. After years of making, packing, and supporting 2-Bromopyridine-6-boronic acid pinacol ester, we have learned attention to every production detail raises everyone’s results. Chemists tell us this compound saves time, reduces frustration, and gets projects over the finish line—even when complexity spikes. Our own pride as manufacturers arrives through every well-crystallized batch, every on-time delivery, and every detailed technical conversation supporting discovery and process chemistry around the world.