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HS Code |
266015 |
| Cas Number | 1187595-85-6 |
| Molecular Formula | C6H7BClNO2 |
| Molecular Weight | 171.39 |
| Appearance | White to off-white solid |
| Melting Point | 90-94°C |
| Purity | Typically ≥ 97% |
| Smiles | CC1=CN=C(C=C1Cl)B(O)O |
| Inchi | InChI=1S/C6H7BClNO2/c1-4-2-5(7(10)11)3-9-6(4)8/h2-3,10-11H,1H3 |
| Solubility | Sparingly soluble in water |
| Storage Temperature | 2-8°C |
As an accredited 2-Chloro-5-methylpyridine-3-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass bottle with a secure screw cap, labeled with product and hazard details. |
| Container Loading (20′ FCL) | 20′ FCL: 2-Chloro-5-methylpyridine-3-boronic acid packed in 25kg drums, total ~12–14MT net weight per container. |
| Shipping | **Shipping Description:** 2-Chloro-5-methylpyridine-3-boronic acid should be shipped in tightly sealed containers, protected from light and moisture. It is typically packed in compliance with chemical safety regulations and labelled appropriately. Transportation should ensure temperature stability and avoid exposure to incompatible substances. Suitable for air, ground, and sea shipment following relevant hazardous material guidelines. |
| Storage | 2-Chloro-5-methylpyridine-3-boronic acid should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong oxidizers. Seal the container tightly and protect from light. Store under inert atmosphere (such as nitrogen or argon) if possible to prevent degradation. Always keep it clearly labeled and in a designated chemical storage area. |
| Shelf Life | 2-Chloro-5-methylpyridine-3-boronic acid is stable for at least 2 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-Chloro-5-methylpyridine-3-boronic acid with 98% purity is used in Suzuki coupling reactions, where it ensures high yield and selectivity of biaryl synthesis. Melting Point 152°C: 2-Chloro-5-methylpyridine-3-boronic acid with a melting point of 152°C is used in pharmaceutical intermediate preparation, where it provides enhanced thermal stability during process scaling. Particle Size <20 μm: 2-Chloro-5-methylpyridine-3-boronic acid with a particle size of less than 20 micrometers is used in homogeneous catalyst systems, where it improves dispersion and reaction kinetics. Stability Temp 40°C: 2-Chloro-5-methylpyridine-3-boronic acid stable up to 40°C is used in long-term reagent storage, where it maintains consistent activity over extended periods. Water Content <0.5%: 2-Chloro-5-methylpyridine-3-boronic acid with water content below 0.5% is used in moisture-sensitive organic synthesis, where it prevents by-product formation and maximizes product purity. Molecular Weight 172.45 g/mol: 2-Chloro-5-methylpyridine-3-boronic acid with a molecular weight of 172.45 g/mol is used in library synthesis for drug discovery, where it enables precise stoichiometric calculations and reproducible results. |
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Over years of producing boronic acid derivatives, the story of 2-Chloro-5-methylpyridine-3-boronic acid stands out for its blend of chemical specificity and practical utility. This compound isn’t just a catalog entry or a line item on a bulk quote sheet. Each batch we manufacture starts from raw materials sourced and tested in-house, handled through strict process controls. What ends up in your hands carries the cumulative lessons of scale, purity, consistency, and the small adjustments that keep each lot in line with real world application needs.
Our standard model, often identified by the CAS number 875777-53-6, features the structural motif many medicinal and agrochemical researchers search for: a chloro-methyl substituted pyridine ring bonded to a boronic acid functional group at the 3-position. In practical terms, this modification offers unique electronic properties, which directly influence reactivity in Suzuki–Miyaura couplings and other palladium-catalyzed cross-coupling reactions. The substitution pattern delivers selectivity and reactivity profiles not seen in other pyridine boronic acids, especially in routes where positional isomerism plays a major role in biological activity or process yields.
We monitor our reaction steps using in-process chromatography and titration, minimizing side-product formation and ensuring product integrity even before the drying phase. Our specifications by experience favor a product with solid purity—typically 98% or greater—as determined by HPLC and confirmed by NMR. Water content never exceeds 1%. Bulk density and particle size remain under observation but vary by request, since end-use requirements differ for each client. The solid isolated from our reactors arrives free flowing, with minimal agglomeration and precisely controlled moisture—a crucial point for storage and long-term stability.
In practice, we see two major user groups: research labs scaling up pharmaceuticals and agrochemical development teams designing new compounds for field and greenhouse trials. The methyl group and chlorine on the pyridine ring give unique steric and electron-donating effects, fine-tuning how the molecule engages in C–C coupling. Researchers confirm that this boronic acid frequently succeeds where the non-methylated variants fail, especially when targeting sites sensitive to polarity, hydrophobicity, or electronic push–pull effects. These properties matter directly in combinatorial chemistry and lead optimization, not simply as an academic curiosity but as a practical lever to improve yield or selectivity in active ingredient synthesis.
As the manufacturer, our focus isn’t just filling orders—it’s building trust with chemists who can’t afford inconsistent results. We never relabel or repackage from upstream traders. Our reactors handle all main steps, from pyridine alkylation through lithiation, borylation, and acid quench. Close attention to each phase allows us to tweak process parameters quickly when customers request tighter impurity profiles or adjusted isolation procedures. This flexibility sets us apart because delayed shipments or out-of-spec batches disrupt downstream R&D pipelines in irreplaceable ways. Shipping a batch with tightly monitored residual solvent and impurity levels isn’t a bonus—our pharmaceutical clients require it, and the feedback loop between our QA labs and synthetic chemists out in the field ensures we never lose sight of what matters at the bench.
Among boronic acids, selectivity boils down to ring substitution. Many manufacturers push generic pyridine boronic acids or opt for the unsubstituted 3-pyridylboronic acid. In our experience, the chloro and methyl groups both offer tangible benefits. Compared to 2-chloro-3-pyridylboronic acid, our product introduces a methyl group that shifts both physical and chemical properties enough to open new synthetic routes. The increased bulk at the 5-position can steer coupling reactions toward desired products, particularly in complex molecule synthesis. For those who have worked with less tailored boronic acids, problems like side reactions or poor yields during late-stage modifications become common. We’ve received direct feedback from customers who’ve switched and noted improved handling, enhanced selectivity, and easier crystallization of downstream products.
In lab and production settings, reactivity can mean the difference between a project that moves ahead and one that stagnates. A boronic acid unstable to air or water leads to shelf waste, failed reactions, or, worse, delays in costly development cycles. Our operators store final product in moisture-tight drums with tamper-evident seals; our standard procedure means no batch leaves the floor unless water and residual solvent content meets spec. This practice isn’t theoretical—it’s shaped by the returns, complaints, and repeat orders we’ve received over time, pushing us toward genuine, not just declared, product reliability. The research teams that approach us after trying trader-sourced lots almost always mention one thing: batch to batch differences. With fine chemical intermediates, those differences translate into work lost or budgets blown.
From the outset, every kilogram we release comes with an analytical package showing trace impurities below action limits. Over the years, we’ve invested in upgraded purification lines and more sensitive analytical equipment because even small changes impact end-use in pharmaceutical actives or crop protection agents. Upgrading to LC-MS and more robust wet chemistry checks has allowed us to certify absence of key regulated impurities like heavy metals or persistent organic pollutants. Our documentation includes those details, not bulked up with generic text, but straight readings and spectral data so reviewers and regulatory agencies see exactly what they’re looking for.
Raw material choices often separate a stable supply from a market hiccup. By sourcing core reagents domestically where possible and working with trusted partners for critical imports, we maintain inventory buffers large enough to absorb most supply shocks. We witness price swings for pyridine and boronic esters, especially in periods of tight demand; careful contract negotiation and vertical integration allow us to pass price stability downstream, not just to promise it. Where possible, we recover and recycle solvents, making use of closed-loop streams that reduce waste. Downstream users increasingly ask about our carbon footprint and recycled input share, and we’re transparent on both counts—reusing mother liquors, minimizing hazardous waste, and tracking emissions at each step.
Pharma process teams typically highlight time to result as their top concern. An impurity-laden or unstable boronic acid can extend a synthesis campaign by weeks. Our customers send us feedback, request tailored lots, or even ask for concurrent shipments of analytical standards alongside bulk material, because their own pipelines cannot absorb unpredictability. Last year, a major research team exploring aromatic amide linkages pointed to a dramatic improvement in enzyme inhibitor selectivity after switching to our 2-chloro-5-methylpyridine-3-boronic acid, highlighting the way small structural tweaks upstream cascade into meaningful biological impact. We keep these stories close, since real output—measured in successful patent filings, tighter SAR, and faster route development—grows out of both the molecule and the reliability behind it.
Compounds like 2-chloro-5-methylpyridine-3-boronic acid face risk of mislabeling or adulteration, especially from supply chains leaning on repackagers without chemical manufacturing experience. Overpacking and storage wear down product integrity over time; only back-to-back synthesis and rapid shipment prevent product shift—both chemically and physically. We tackle this not with slogans, but with process audits and tracking from raw input to final lot. Our operators stay trained on best practices for moisture exclusion and rapid packing, which comes out of direct experience dealing with returns and shelf-life extensions. There’s no shortcut to quality here—a fact that shapes how we hand over control samples, how we design spec sheets, and how we align batch numbers with customer inventory records.
Direct feedback from users experimenting with large-scale coupling reactions led us to optimize particle size and purity even further. By filtering out fines and ensuring a granule distribution that supports rapid dissolution, we’ve boosted consistency batch over batch. On the chemical engineering side, making small changes to solvents or reaction sequence can shave hours from a multi-step coupling process. These tweaks show up as improved throughput and yield in the syntheses of heterocyclic APIs. The methyl group, for instance, acts as a protective blocking group in some applications, lowering unwanted oxidative side reactions. Practical value accumulates not only at the bench, but in cost-of-goods for series production—a fact rarely reflected in literature alone.
Manufacturing doesn’t end at the loading dock. Our technical team, drawn from bench chemists and chemical engineers, remains available for troubleshooting and synthesis advice. Clients often share procedure specifics—solvent choices, microwave conditions, or unusual coupling partners—and get real feedback based on our reaction development experience. We offer not only standard analytical packages, but advice about pre-treatment of coupling partners or on-line monitoring strategies. Our clients know the faces and voices on the other end; the personal connection matters more than boilerplate datasheets. Supporting route scouting or process troubleshooting directly shapes our next generation of product improvements.
Import and export logistics hinge on having documents and declaration protocols in place, since customs scrutiny on boronic acids has risen in recent years. Managing these realities is part of producing, not just selling. Our administrative team works with freight forwarders, regulatory officials, and client-side compliance leads to clear every shipment through customs, with tracking and release timed as tightly as possible to avoid project delays. Changing regulations over controlled substances in some jurisdictions require up-front transparency in both documentation and end-use declarations. We handle these with the seriousness they deserve, because no one benefits when regulatory bottlenecks slow down advanced chemistry work.
Production runs expose us to the full challenge of quality management, waste minimization, and throughput efficiency. Each time we upgrade a filtration line or tweak a crystallization protocol, we chase not just cost reduction, but greater dependability in each drum we ship. Surgical changes—like moving to higher-stability packaging or pre-aliquoted lots for time-sensitive trials—grow out of real feedback, not theory. We’ve experimented with alternative drying techniques and storage configurations based on weather patterns and customer shelf-life concerns. These steps rely on data we accumulate from both internal QC and external feedback, giving our teams insight into what solves problems, not just what looks good on paper.
Real-world synthesis means thinking well past the bench and considering lab safety, operator training, and waste stream management. We take the time to pre-test compatibility with common reagents, packaging stability under a range of climates, and even fire resistance under storage stress. Proper documentation and hazard identification (such as clear labeling for boronic acid reactivity or suitable neutralization protocols) support safer end-use. Factory audits, both internal and customer-initiated, push us to maintain standards higher than the letter of the law. None of these responsibilities are abstract—they’re driven by accident logs, near-misses, and operational experience across many years.
We expect the role of 2-chloro-5-methylpyridine-3-boronic acid to keep growing as demand for complex heterocycles and tailored pyridine derivatives expands. Internal R&D focuses on reaction route shortening, green chemistry options for raw material conversion, and dynamic adjustment of process controls as new requests come in. As user needs shift—from gram quantities for screening libraries to multi-kilogram lots for process validation—we scale up with an eye toward matching custom quality requirements rather than standardized “good enough” chemistry. The project managers in our shop keep documentation live, so new specifications, lot history, and process tweaks get recorded and shared, creating an adaptive response instead of relying on old habits.
Making 2-chloro-5-methylpyridine-3-boronic acid isn’t just about reactors and batch numbers; it’s about sharing accountability and knowledge with the world’s chemists. From raw material selection to shelf-ready delivery, each stage combines craftsmanship with transparency. Those relying on our product—whether they work in a pharma scale-up suite, invent new crop protection agents, or chase the next key SAR breakthrough—count on more than a chemical name. They rely on real, tested, and fully accountable material, batch after batch, without the hidden pitfalls that come from distant, disconnected sourcing. That’s our commitment, shaped by experience and feedback, and it continues to drive every improvement that leaves our production floor.