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HS Code |
149846 |
| Product Name | 2-Bromopyridine-5-Boronic Acid |
| Molecular Formula | C5H5BBrNO2 |
| Molecular Weight | 201.82 g/mol |
| Cas Number | 409537-46-4 |
| Appearance | White to off-white solid |
| Melting Point | 175-177°C |
| Purity | Typically ≥97% |
| Synonyms | 5-Borono-2-bromopyridine; Pyridine-2-bromo-5-boronic acid |
| Smiles | B(O)(O)c1ccc(Br)nc1 |
| Inchi | InChI=1S/C5H5BBrNO2/c7-5-2-1-4(6(9)10)3-8-5/h1-3,9-10H |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Application | Intermediate for Suzuki-Miyaura cross-coupling |
As an accredited 2-Bromopyridine-5-Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Bromopyridine-5-Boronic Acid (1g) is a sealed amber glass vial with a secure screw cap, labeled clearly. |
| Shipping | 2-Bromopyridine-5-Boronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is transported as a hazardous material, complying with relevant chemical safety regulations. Packaging ensures protection from physical damage and leaks. Proper labeling and documentation accompany the shipment to guarantee safe handling and regulatory compliance during transit. |
| Storage | 2-Bromopyridine-5-boronic acid should be stored in a tightly sealed container, protected from light and moisture, and kept at 2–8°C (refrigerated) in a well-ventilated, dry area. Avoid exposure to heat, strong oxidizing agents, and incompatible materials. Ensure proper labeling, and store away from food and incompatible substances to maintain its stability and prevent degradation. |
Applications of 2-Bromopyridine-5-Boronic Acid in Industrial Manufacturing2-Bromopyridine-5-Boronic Acid enables high-value intermediate synthesis across key regulated industries. As a direct manufacturer, we supply this material to established industrial users with robust technical requirements and audit trails. Our application knowledge covers select downstream fields with demonstrated market demand. 1. Pharmaceutical API Intermediate SynthesisInnovator and generic pharmaceutical manufacturers use 2-Bromopyridine-5-Boronic Acid as a critical intermediate for the synthesis of selective kinase inhibitors and targeted oncology products. Its reactivity profile suits Suzuki-Miyaura cross-coupling, enabling complex pyridine motif assembly for orally dosed and parenteral small molecule drugs. Integration must comply with multi-step GMP synthesis and strict residual impurity control, often under ICH Q7 guidelines. Production scale requires validated batch records, controlled chromatographic purity, and reliable supply for lifecycle management. Industry compliance standards
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2. Agrochemical Active Ingredient ManufactureMajor agrochemical formulators and contract synthesis plants rely on 2-Bromopyridine-5-Boronic Acid to assemble novel pyridine-based insecticides and fungicides via Suzuki Coupling and related palladium-catalyzed processes. The boronic acid moiety enables efficient core construction with precision control over isomeric ratios for regulatory dossier batches. Compliance with agrochemical quality systems is essential, with regular audits on trace-level contaminants and data support for global registration files. Industry compliance standards
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3. Electronic Chemical Synthesis for Organic SemiconductorsLeading electronics chemical manufacturers integrate 2-Bromopyridine-5-Boronic Acid into the development of pyridine-functionalized conjugated polymers and small molecule semiconductors for advanced display and sensor technologies. The material supports high-purity, reproducible coupling for OLED, OPV, and OFET component production under ISO-based QC, with downstream purification tailored for electrical and photonic characteristics. Industry compliance standards
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4. Fine Chemical Production for Diagnostic ReagentsSpecialty chemical producers rely on 2-Bromopyridine-5-Boronic Acid for constructing labeled pyridine derivatives as key building blocks in the synthesis of advanced diagnostic reagents. Applications include covalent attachment of fluorophores or biotin for enzyme immunoassays, where high chemical purity and low trace contaminant levels are audited under supplier qualification programs. The boronic acid group allows for modular substitution strategies in late-stage diagnostic probe production. Industry compliance standards
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As a chemical manufacturer deeply engaged with the practical challenges of specialty intermediates, we’ve seen demand rise for heterocyclic boronic acids, especially in research and pharmaceutical development. One standout in our product line remains 2-Bromopyridine-5-Boronic Acid, a molecule that offers unique benefits for coupling reactions and building advanced materials. Its CAS number and fine structural parameters are well known to dedicated chemists, so here we'll focus on what makes our approach to this product different and how years of hands-on work go into each lot we deliver.
The backbone of our 2-Bromopyridine-5-Boronic Acid process relies on careful selection of pyridine derivatives and stringent quality control on bromination and borylation steps. Our chemists understand the impact even low levels of palladium, iron, or copper residuals can have on downstream reactions. From the earliest pilot batches, we've pushed for reliable analytical verification—HPLC, NMR, mass spectrometry—and do not settle for superficial purity indicators. Our finished product achieves purity well above 98%, although purity alone isn’t the end of the story. Trace metal analysis and the absence of water content actually influence how well the boronic acid performs in Suzuki couplings. This fact gets overlooked by those who focus only on headline numbers, and it’s feedback from experienced users that guides these refinements.
We craft each batch to be practical. Powder morphology, solubility profile in common organic solvents, and minimal degradation under ambient handling play big roles in laboratory efficiency. For gram-to-kilogram scale runs, researchers benefit from repeatable behavior, so we’ve dialed in parameters such as mean particle size and bulk density that affect weighing, dissolution rates, and filtration performance. Loss on drying and melting range checks are always completed, not just for paperwork but because slight variance here can impact storage or scale-up. We run short-term stability tests during humid summer months, and all packaging lines use moisture-resistant materials to keep the integrity sharp for several months after delivery.
Most of our customers rely on 2-Bromopyridine-5-Boronic Acid for Suzuki and other palladium-catalyzed cross-couplings. These are not just science-fair demonstrations; downstream compounds often move towards high-value therapeutic candidates or functional materials. Our direct customers often share feedback from dozens of runs, giving us insights on improving purification or minimizing side products. It’s this collaborative cycle that leads to improvements in yield and consistency for academic and industrial teams alike. Pyridine derivatives pose distinct challenges in some metal-catalyzed reactions, especially in the presence of heteroatoms that can poison catalysts or promote side reactions. We've adapted our synthesis and purification workflow in response to reports from process chemists—such as tighter filtration, or double re-crystallizations—because we understand how frustrating troubleshooting can get when materials misbehave just ahead of a deadline.
Unlike plain phenylboronic acid or other less functionalized pyridine boronic acids, 2-Bromopyridine-5-Boronic Acid brings more reactivity and versatility. The bromine not only provides a useful handle for further substitution, but also introduces a predictable electronic effect across the ring, giving synthetic chemists extra options for regioselective reactions. Our manufacturing process keeps halide content tightly controlled, which helps minimize the generation of unwanted side products down the line. Comparing to 3-bromo or 4-bromo analogs, the substitution pattern on 2-Bromopyridine-5-Boronic Acid brings recognizable differences you notice right away during cross-coupling: varied insertion rates, different by-product profiles, and, in some Suzuki-type workflows, changes in the need for base equivalents or ligand adjustments. These subtle trends get built into our lot traceability plan, and we record them alongside every release, so those preparing scale-up runs can plan effectively.
It would be easy just to ship the product in bulk jars, but our experience tells us this shortcut can lead to waste. Anyone who handles hundreds of grams at a bench or production floor knows how fast boronic acids can cake or degrade if not packed properly. We invest in lined containers and low-humidity fills to extend shelf life as long as possible. Field returns provide useful data: even small visual changes in color or flow properties can alert us to oxygen ingress or moisture exposure. It is not just about keeping paperwork in order; it's about real savings and reliable results for end-users.
Years of feedback from process chemists and pilot plant engineers have shaped our current approach. Some years back, several partners reported foaming or poor dispersion during preps, so we refined our crystallization protocol to manage crystal habit and avoid fines that create static issues. Others had trouble redissolving the material after short-term storage, leading us to adjust drying profiles for both lower bound water and minimal lattice stress. Each tweak comes from actual runs, not just textbook theory. Reliability and trust only come from seeing similar results, lot after lot, across varying scale and reaction conditions.
We devote a good share of our QC resources to tracking even subtle batch-to-batch differences. This means that every lot receives identification and purity checks beyond what regulations demand. NMR fingerprinting, for example, allows us to spot even trace isomers or byproducts that sometimes escape routine HPLC screening. As equipment improves and customer expectations climb, we upgrade our protocols, too. In the last two years, more emphasis has been placed on impurity profiling, especially targeting nitro and halide residues that could interfere directly with expensive metal catalysts down the chain. These extra layers of control make a visible difference, especially for those scaling projects for regulatory submissions or commercial production.
Running a modern chemicals production facility brings with it environmental and sourcing responsibilities. For 2-Bromopyridine-5-Boronic Acid, we have worked to transition to greener solvents and more efficient halogen sources. Reusable catalyst systems, smart water management, and closed-loop reactions have significantly reduced waste and improved yield. Part of running a sustainable process is working with supply chains that support purity from the ground up. We don’t take raw material screening lightly; even slight contamination at early stages can echo as persistent impurities months later. It can be tempting to cut corners or swap suppliers, but such moves nearly always produce bigger headaches downstream. Keeping to established, audited sources may cost a little more, but it pays back in smoother batches and less rework.
As demand for tailored heterocyclic intermediates keeps growing, requests shift from just standard grades to high-purity and low-metal specifications. Pharmaceutical teams ask about elemental impurities and solvent trace levels as well as residual bromide ion. Academic labs often want to experiment with novel coupling reactions that push the limits of stability and reactivity. We hear from both camps, and both drive our ongoing product development. Expanded purification options, like additional recrystallization or activated charcoal treatment, came from direct requests. Some customers even bench-test sample lots side-by-side and share comparative NMR or LC-MS data, helping us see beyond basic COA numbers to what actually matters for their work.
Laboratories and scale-up facilities both report that effective packaging cuts risk of exposure and minimizes spills. The pyridine backbone and boronic acid group are generally mild, but the bromine handle demands care. We have documented advice directly from customers on integrating ventilation improvements and batch preparation tricks that stop dusting. Our shipping and technical teams treat these insights with the same seriousness as in-house research because they come straight from those handling production-level quantities day after day. Uncluttered labeling and accessible, language-clear safety documents help users in different geographies meet requirements quickly. When new hazard findings surface, we respond immediately with updates, not just to protocols but to next batch production steps. Backward integration—learning from every misstep and success—defines our safety culture.
No two synthetic campaigns run exactly alike. Some customers run into filtering issues when scaling up, stemming from unexpected particle size distributions. We’ve learned to monitor these closely during batch manufacture so nobody gets caught short. If a run needs a custom granulometry, we can handle it in-house with a tailored milling step. Solubility can shift batch-to-batch, especially when process parameters drift beyond tight control. We keep solvent and buffer compatibility top of mind, regularly trialing all-new lots in both classical and slightly offbeat conditions. Real-world troubleshooting also means staying responsive: if a customer calls in with an unusual NMR blip or unexpected off-color, we dig in as a team and rerun every check.
Many think of boronic acids as commodity-level building blocks. Experience says otherwise for 2-Bromopyridine-5-Boronic Acid: small differences in impurity profile, trace water, or residual solvent have outsized effects on final yields, side product formation, and the headache level during purification. The drive for near-identical experience across lots can only come from direct manufacturer involvement. Every touchpoint—from raw material audit and reaction parameter tracking, to hand-inspected bottling—reflects years of lived learning. We aren’t interested in just hitting spec. The real measure lies in batch records full of user-reported results: cleaner reactions, less TLC troubleshooting, higher isolated yields.
Projects take unpredictable turns, and synthetic pathways often shift mid-campaign based on new results or project pivots. Having access to consistently manufactured, traceable 2-Bromopyridine-5-Boronic Acid makes those pivots less painful. Direct consultation between chemists—ground-level feedback, not just distributor relays—lets us tune specs and batch features for highly individual routes. Whether a team needs single-molecule batches for SAR studies or kilogram lots for scale-up, we pair manufacturing focus with the human connection that truly moves science forward.
Research in heterocycle chemistry and cross-coupling keeps evolving. Our own approach must evolve alongside. Process automation, faster batch tracking, and digital recordkeeping keep the core product safer and more predictable. Continuous investment in analytical tech, including the latest chromatographic and spectroscopic tools, helps us detect changes quicker and respond with improved processes. We commit to not just growing volumes but adding new features, specifications, and support as new chemistries demand. We’re not just content with existing benchmarks—instead, we look forward to shaping new standards for performance, reliability, and real usefulness for bench chemists everywhere.
2-Bromopyridine-5-Boronic Acid holds a vital place in advanced chemistry work, not just for its structure but for the trust users place in every delivered batch. Our unique perspective as a manufacturer comes from a thousand small steps: listening to those running the reactions, learning from setbacks, tuning every protocol, and investing in better tools and people. For anyone needing more than just a product off the shelf, our door remains open for discussion, feedback, and future-oriented solutions.