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HS Code |
366022 |
| Productname | 6-Chloropyridine-3-boronic acid pinacol ester |
| Casnumber | 936047-53-5 |
| Molecularformula | C11H13BClNO2 |
| Molecularweight | 237.49 |
| Appearance | White to off-white solid |
| Meltingpoint | 98-102°C |
| Purity | Typically >97% |
| Solubility | Soluble in organic solvents such as DMSO, DMF, and chloroform |
| Smiles | B1OC(C)(C)C(C)(C)O1c2ccc(Cl)nc2 |
| Inchikey | ZKXWMAOVSXKUHY-UHFFFAOYSA-N |
As an accredited 6-Chloropyridine-3-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 6-Chloropyridine-3-boronic acid pinacol ester is packaged in a sealed amber glass bottle with a tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL container loading of 6-Chloropyridine-3-boronic acid pinacol ester ensures secure, moisture-free transport with robust packaging standards. |
| Shipping | 6-Chloropyridine-3-boronic acid pinacol ester is shipped in tightly sealed containers under a nitrogen or inert atmosphere to prevent degradation. The chemical is packed securely, protected from moisture, heat, and light. Shipping complies with relevant regulations, and appropriate hazard labeling is included to ensure the safe transport of this reagent. |
| Storage | 6-Chloropyridine-3-boronic acid pinacol ester should be stored in a tightly sealed container, under an inert atmosphere (such as nitrogen or argon), and kept in a cool, dry place away from moisture and direct sunlight. Avoid exposure to air and strong oxidizing agents. Recommended storage temperature is 2-8 °C (refrigerated). Ensure proper labeling and handle according to appropriate safety guidelines. |
| Shelf Life | Shelf Life: Stable for at least 2 years when stored in a cool, dry place, tightly sealed, and protected from light and moisture. |
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Purity 98%: 6-Chloropyridine-3-boronic acid pinacol ester with purity 98% is used in Suzuki–Miyaura cross-coupling reactions, where it ensures high product yield and selectivity. Molecular weight 267.48 g/mol: 6-Chloropyridine-3-boronic acid pinacol ester of molecular weight 267.48 g/mol is used in pharmaceutical intermediate synthesis, where precise stoichiometry leads to reproducible compound formation. Melting point 134–137°C: 6-Chloropyridine-3-boronic acid pinacol ester with melting point 134–137°C is used in solid-phase organic synthesis, where thermal stability promotes process reliability. Particle size <50 μm: 6-Chloropyridine-3-boronic acid pinacol ester with particle size less than 50 μm is used in automated synthesis platforms, where fine dispersion improves mixing efficiency and reactivity. Moisture content ≤0.5%: 6-Chloropyridine-3-boronic acid pinacol ester with moisture content ≤0.5% is used in air-sensitive catalytic processes, where low hydration levels reduce side reactions and byproduct generation. Stability temperature up to 80°C: 6-Chloropyridine-3-boronic acid pinacol ester stable up to 80°C is used in heated batch reactors, where thermal resilience ensures consistent catalytic performance. Assay ≥98% (HPLC): 6-Chloropyridine-3-boronic acid pinacol ester with assay ≥98% (HPLC) is used in medicinal chemistry research, where high purity ensures accurate biological evaluation. |
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Chemical manufacturing often means dealing with demanding details every day. Each molecule we produce carries a distinct story. 6-Chloropyridine-3-boronic acid pinacol ester reflects many of these stories. Colleagues and I encounter its nuanced role in active pharmaceutical ingredient (API) synthesis, agrochemical research, and new material development. The journey from raw intermediates to fine-tuned, high-purity boronic esters involves relentless control and craft, not just routines. Every step draws on what we’ve learned in practice about catalysis, crystallization, and purification. The questions customers ask—about yields, about water content, about process impurities—shape what we put into the production design and quality system.
Our model for 6-Chloropyridine-3-boronic acid pinacol ester centers on reliable pyridine ring substitution, specific to the 3-position attachment. The boronic ester brings reactivity that specialists in Suzuki-Miyaura cross-coupling need. Synthetic teams prefer boronic acid pinacol esters to other forms because they persist in air and moisture, making lab life less frantic. Drawing on feedback from chemists, we refine batch schedules for optimal shelf life and storage stability. It’s tough to overstate how critical ease of handling is for bench chemists and pilot plants.
Working hands-on with this compound, its pale solid form signals both purity and practical safety. We keep careful control of contaminants and trace metals, because sensitive catalytic reactions can stumble with even minor impurities. The pinacol ester group guards the boronic acid moiety, blocking the hydrolysis that plagues boronic acids during shipping or even in damp storage rooms. Over years, we learned moisture tests and vacuum drying cycles make all the difference between a shelf-stable product and a risky, degraded lot. Measurement of water by Karl Fischer titration and high-resolution analysis of organoboron content set our quality standards.
A common question from process teams: why not just order the parent boronic acid? It comes down to performance in the hands of people doing the coupling reactions. Under Suzuki conditions, pinacol esters dissolve much easier and stir in solution more evenly, so reactions start and finish with better reproducibility. This pays off in R&D efficiency as well as manufacturing predictability.
Every time we ship 6-Chloropyridine-3-boronic acid pinacol ester, engineers remember the headaches with alternatives. Similar pyridine boronic acids sometimes clog transfer lines or cake inside drums, triggering delays and batch losses. The pinacol ester format sets this model apart in usability, with far smoother re-dissolution in typical cross-coupling solvents like THF and dioxane. Our factory trials proved that transition metal catalysts tolerate this material better, avoiding the insoluble aggregates that slow reaction rates.
Some manufacturers opt for methyl or ethyl boronate versions to cut costs, but these esters can hydrolyze quickly. We’ve seen firsthand that residual parent alcohols generate byproducts or foul up downstream purification. Through continual testing—HPLC, NMR, metal check—we maintain a high standard for the pinacol variant. That translates into less risk for chemists scaling up or moving between development sites.
Pharmaceutical companies approach us for this specific compound to build core scaffolds for kinase inhibitors and antiviral candidates. The regulators gauge residual impurities with precision, so we manufacture and test each batch accordingly. This has led us to invest in dedicated reactor trains, glovebox loading, and extra analytical controls. Our teams work directly with process chemists at client labs to troubleshoot coupling yields or byproduct formation, not just supply kilograms. Some stories from the floor: calibrating conditions for scale-up at 10-100 kg batches, adjusting for substrate compatibility, helping to recover more product when purification steps proved stubborn.
Agrochemical firms use this building block to create selective fungicide and insecticide leads. Here, timelines run brisk, and robust, reliable materials make all the difference in quickly moving from discovery scale to pilot trials. Caked boronic acids delay projects, but this pinacol ester delivers the on-demand solubility and reactivity they need for rapid SAR (structure-activity relationship) screening.
Even in the materials science arena, our partners utilize 6-Chloropyridine-3-boronic acid pinacol ester to tailor new ligands for metal-organic frameworks or specialized polymers. The ability to consistently couple and extend pyridyl groups opens up real innovation in catalysis and sensor tech. Our longstanding relationship with research teams comes from years of troubleshooting storage life, decomposition during reactions, and even issues in waste handling.
Fine chemical manufacture demands tight process windows. To maximize yield for this ester, we select pyridine starting materials from vetted upstream suppliers and then check every incoming drum by gas chromatography. Chlorination and subsequent lithiation steps require close monitoring—minor deviations throw off the regioselectivity or yield. Reactor temperature profiles matter; a degree or two impacts reaction selectivity. Throughout this process, plant chemists keep interaction with the boronating reagents as safe as possible, using high-vent scrubbers and fallback neutralization for any leftover active species.
Crystallization protocols define both purity and process simplicity. We cycled through over twenty solvent combinations to identify ones that maximize solid yield and ease of filtration without introducing impurities or new solubility headaches in final formulation. Each step adds new choices in process control that come only from practice, not textbook theory—things like paddle speed for batch mixing and the dropwise addition of pinacol under nitrogen.
After purification, packaging and storage conditions become another battleground. We train warehouse staff on humidity control to avoid caking or decomposition while drums wait in inventory. Every shipping season, changes in ambient temperature challenge our handling protocols, so improvements happen from direct lessons on the plant floor. By working alongside logistics, technical service, and customers, our team closes the loop from manufacturing line to lab bench.
The main difference experienced chemists note with this ester comes in reaction reliability. Pinacol boronic esters hold their structure in ambient air far better than free boronic acids, which means fewer worries about polymerization or acid-catalyzed breakdown. This chemical resilience reduces the risk of batch-to-batch variability that often frustrates scale-up teams. We hear from contract developers that pinacol esters simplify their liquid handling protocols and accelerate process development timelines.
Reactivity is another angle. The 6-chloro substitution stabilizes the pyridine boronic ester without blocking cross-coupling efficiency. In head-to-head reaction trials at our facility, this compound consistently outperforms similar non-chloro or ortho-substituted versions in terms of overall yield and ease of purification by column chromatography. Fewer side products means less time in rework.
We’ve seen cases where a switch to this ester form turned a low-yielding sequence into a robust workflow, trimmed days from development time, and saved kilo-scale runs from being scrapped. The confidence that comes from this reliability isn’t just sales talk—it’s a matter of witnessing returned drums, analyzing failed reactions, and re-tuning production.
Every specialty compound brings its headaches. This pinacol ester offers long-term stability under dry conditions, but water remains an ever-present threat. Humidity creeps into storage rooms, and a single rainstorm can spike local moisture levels, risking hydrolysis. That’s why we invested heavily in low-humidity warehouses and supply shipments with desiccant packs. All outgoing batches get a final water test, and we build storage instructions into our routine service calls with major customers.
Odor and dust management also require focus. Pyridine derivatives have a sharp, unmistakable smell and can be irritating to plant staff and researchers. Our solution is rigorous dust collection—vacuum loading, sealed screw conveyors—and periodic air monitoring for comfort and safety. Cleanroom packaging lines run under negative pressure for this reason.
Disposal of even minor spills gets specific guidance since boronic esters shouldn’t just wash into standard drains. Safety data and hands-on training with plant operators paid off, as incident rates dropped and routine handling became more efficient. Teamwork between the synthesis crew and EH&S professionals improved more than any written procedure could enforce.
Most competitors focus only on analytical benchmarks, but real chemical manufacturing is more than a purity number. Repeated customer audits prove that our facility’s attention to traceability and documentation meets the scrutiny of regulators and major multinational clients. Every lot of 6-Chloropyridine-3-boronic acid pinacol ester receives batch-level recording from raw materials sourcing, through synthesis, to final dispensing. This habit, built over years, means that any deviation gets caught sooner—not after a failed downstream trial, but before shipping out.
Feedback loops with users have shaped our process more than any top-down mandate. Each complaint about caked product, late shipments, or unanticipated reaction trends turned into a quality improvement session. We honed particle size control for easier weighing, updated our drying protocols to shave hours off timeline bottlenecks, and even coordinated after-sales troubleshooting with chemists in three continents.
The very chemistry community that gave this molecule its value keeps suggesting new challenges. Recently, demand has spiked for greener solvent-compatible grades to support new cross-coupling platforms. Our R&D teams experiment with crystallization solvents and alternative purification protocols to deliver pinacol esters with lower environmental impact. Some requests focus on micron-scale granular forms for automated dosing equipment—a new frontier that keeps our process engineers innovating.
We also see ever-tighter restrictions on allowable trace metals and organics from regulatory bodies. Compliance means more than annual checkboxes; it leads to investment in ICP-MS and next-generation chromatography setups for rapid testing. We share data back to our clients, building confidence in forward integration and quicker tech transfer between pilot and manufacturing sites.
This specialty boronic ester continues to serve as a foundation in custom ligand design, high-throughput screening libraries, and precision medicine programs. Users rely not just on a product, but on a relationship—years in the making, built on trust and mutual learning. Only by listening closely, adapting batch recipes, and supporting technical questions on reaction scale-up do we fulfill the real promise of this chemical intermediate.
Of all the compounds we produce, 6-Chloropyridine-3-boronic acid pinacol ester stands out for its combination of practical usability and foundational importance in advanced synthesis. Each drum started as a challenge, became a lesson, and now helps chemists build the future of medicine, agriculture, and materials. Trust in this product grew batch by batch, not by shortcut, and reflects all we’ve learned by staying close to the process—from the first reaction flask to the last drum leaving our plant.