|
HS Code |
512373 |
| Compoundname | 3-Pyridineboronic acid pinacol ester |
| Casnumber | 185982-75-4 |
| Molecularformula | C11H16BNO2 |
| Molecularweight | 205.07 |
| Appearance | White to off-white solid |
| Meltingpoint | 64-67°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, dichloromethane, and ethanol |
| Storageconditions | Store at 2-8°C, protected from moisture and light |
| Smiles | B(C1=CC=CN=C1)OC(C)(C)C(C)(C)O |
| Synonyms | 3-Pyridylboronic acid pinacol ester; Pyridin-3-ylboronic acid pinacol ester |
As an accredited 3-Pyridineboronicacidpinacolester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 3-Pyridineboronic acid pinacol ester comes in a sealed amber glass bottle with a white screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 3-Pyridineboronicacidpinacolester is loaded in securely sealed drums or bags, optimized for safe, stable transport. |
| Shipping | 3-Pyridineboronic acid pinacol ester is shipped in tightly sealed containers to prevent moisture and air exposure, typically under inert atmosphere. It is packed following hazardous material guidelines, ensuring protection from light and physical damage, and complies with relevant transportation regulations for flammable solids. Proper labeling and documentation accompany each shipment. |
| Storage | 3-Pyridineboronic acid pinacol ester should be stored in a tightly sealed container, protected from moisture and air, in a cool, dry, and well-ventilated area. Avoid exposure to heat and direct sunlight. Store away from incompatible substances, such as strong oxidizing agents. For best stability, keep under inert gas (e.g., nitrogen or argon) and avoid prolonged storage once opened. |
| Shelf Life | 3-Pyridineboronic acid pinacol ester typically has a shelf life of 2 years when stored tightly sealed, protected from moisture and light. |
|
Purity 98%: 3-Pyridineboronicacidpinacolester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels. Melting Point 80–84°C: 3-Pyridineboronicacidpinacolester with melting point 80–84°C is used in Suzuki-Miyaura coupling reactions, where it provides predictable handling and reproducible reactivity. Molecular Weight 205.05 g/mol: 3-Pyridineboronicacidpinacolester with molecular weight 205.05 g/mol is used in organic electronics manufacturing, where it enables precise stoichiometric calculations for material formulation. Particle Size <20 µm: 3-Pyridineboronicacidpinacolester with particle size <20 µm is used in catalyst preparation, where it offers rapid dissolution and efficient reaction kinetics. Stability Temperature up to 120°C: 3-Pyridineboronicacidpinacolester stable up to 120°C is used in automated synthesis processes, where it maintains structural integrity under elevated temperatures. Water Content <0.5%: 3-Pyridineboronicacidpinacolester with water content <0.5% is used in moisture-sensitive cross-coupling reactions, where it minimizes hydrolysis and maximizes product conversion. |
Competitive 3-Pyridineboronicacidpinacolester prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Making 3-Pyridineboronicacidpinacolester takes more than off-the-shelf chemistry and generic batch processing. Since early in our plant’s history, we have focused on organic boron compounds—a space full of subtle challenges. This boronic ester in particular draws on our long-standing expertise in boronic acid controls, selective boronation, and pinacol protection, because every successful Suzuki coupling or heteroaromatic synthesis starts with raw material you can trust.
We produce 3-Pyridineboronicacidpinacolester (CAS: 103978-85-6) in dedicated facilities that handle boronates and pyridine derivatives with specialized attention to storage, inert handling, and strict quality checkpoints. We see first-hand how minor process slips can introduce off-odors, yellowing, or instability in low-molecular-weight pyridine esters. Our commitment: we control water activity to below 0.1%, minimize oxygen exposure, and purify in deoxygenated environments so the final ester remains a free-flowing, off-white crystalline powder well suited for demanding reaction conditions. Our model routinely delivers content over 98.5% by HPLC, with boron content and pinacol integrity confirmed by both titration and NMR, because we know trace hydrolysis or oxidative breakdown jeopardizes scale-up and reproducibility for our partners.
Few molecules pack as much practical punch in the lab as this pyridine boronate pinacol ester. In our experience, it stands out for several reasons. Its aromatic boronic ester group remains robust in coupling and cross-coupling chemistries, repeatedly powering through dozens of batch cycles during kilogram syntheses—testimony to its stability in the face of air and trace moisture. Unlike many boronic acids that decompose or polymerize under mild conditions, the pinacol ester form protects the active species, helping researchers reliably join pyridyl motifs to aryl, vinyl, or alkynyl groups in palladium-mediated reactions. We work closely with process chemists who share that cleaner reactions, easier filtration, and reduced need for scavenging agents all begin with a pure and stable boronate ester.
The demand for heteroaromatic building blocks has only increased as pharmaceutical discovery explores new chemical space. 3-Pyridineboronicacidpinacolester fits directly into medicinal chemistry flows, from generating kinase inhibitors to assembling complex ligands for metal binding. Our product rarely needs recrystallization or additional purification; we ensure trace metal and halide residues stay far below even strict academic or process development thresholds, so the risk of catalyst inhibition drops significantly. This lets chemists spend their attention on new target design, not troubleshooting raw material variability.
The value of strong process control in manufacturing this compound becomes obvious during quality checks and returns. Suppliers that don’t understand the subtle moisture and oxygen sensitivity of pyridine boronates tend to send out batches with high water content or hidden decomposition byproducts. These flaws show up as sluggish couplings, broad melting point ranges, or colored residues after even routine manipulations. We hear from partners in drug development and materials synthesis that this kind of hidden risk adds cost and uncertainty down the line.
Over the years, we have iteratively refined solvent removal, drying, and packaging protocols, switching to argon-purged drums and triple-sealed aluminum liners for shipment at production scale. Feedback from overseas research teams and toll manufacturers highlighted the need for longer storage stability and more granular batch data. We responded by extending post-release lot monitoring and tracking trace signals that escape routine QC (oxidative byproducts, trace acid, and pinacol impurities at sub-ppm levels). As a direct manufacturer, each lesson gets fed back into batch records and operator training, not lost in translation by third-party brokers.
3-Pyridineboronicacidpinacolester consistently shows its strengths during multiple Suzuki-Miyaura and related cross-coupling cycles. In active pharmaceutical ingredient (API) routes, its high selectivity in connecting pyridine rings under mild base and temperature gives fewer byproducts or rearrangements compared with free boronic acids. Our technicians run on-site demonstration couplings and provide detailed post-run data so partners see how the material performs outside of carefully stage-managed pilot plants.
In catalyst screening, especially for new ligand development, users see that the pinacol ester resists protodeboronation and hydrolysis through long catalyst residence times, extending reaction windows and reducing purification burdens. For those optimizing C–N or C–O bond formations, this stability means less need to dry solvents to extremes, lower base excess, and reduced labor screening secondary scavengers. By controlling for trace transition metal and halide contamination in our upstream process, we stop unwanted side reactions before they start.
Colleagues working in functional materials synthesis use our 3-Pyridineboronicacidpinacolester to introduce pyridinyl units in OLED, liquid crystal, and bioconjugation scaffolds. The product maintains color and purity across these different disciplines, something we trace to the low-level impurity fingerprint that our batch records track over years of runs.
Not all pyridine boronates perform alike, even from legitimate sources. 3-Pyridineboronicacidpinacolester offers unique advantages due to its regiochemistry and boronate protection. Many applications that demand the 3- (meta) pyridyl orientation for biological or electronic properties simply can’t substitute 2- or 4- isomers. The pinacol ester form gives our product an edge over hydrolyzable boronic acids—materials we used to offer for specialty syntheses, but phased out for most clients due to storage and process headaches.
Some appear curious about differences between the pinacol, neopentyl glycol, and MIDA variants of pyridineboronic acid. Each has tradeoffs. Pinacol esters win out for general coupling versatility, ease of deprotection (basic aqueous workup or hydrogen peroxide oxidation), and solubility in common reaction media. MIDA esters suit prodrug or mask-release approaches, but our customers regularly report losses in atom economy and extra synthetic steps. Neopentyl glycol esters bring higher hydrolytic stability under strong acids, but cause phase-separation issues and slow down filtration, especially at plant scale.
Through side-by-side in-house trials, our chemists see that 3-Pyridineboronicacidpinacolester outperforms free boronic acid and MIDA ester analogs by remaining more stable during ambient storage and giving consistently higher coupling yields in well-vetted Suzuki protocols. We’ve logged hundreds of coupling outcomes with different catalyst and base systems, letting us offer detailed support or troubleshooting recommendations based on our own datasets, not isolated literature runs.
Research and manufacturing partners in pharmaceuticals set high bars for both consistency and traceability. They use 3-Pyridineboronicacidpinacolester for fragment-based screening, main core installation, late-stage diversification, and intermediate elaboration. In regulatory filings, every impurity profile, residual solvent, and lot number must align across global sites—a requirement that only direct manufacturers with total process visibility can offer. We update our documentation protocols each quarter, as compliance standards evolve and feedback loops with external QA teams reveal new expectations.
Agrochemicals producers select this intermediate for insecticidal and herbicidal product research, adding pyridine motifs to boost bioactivity or modulate environmental persistence. Feedback centers on the importance of reliable stereochemistry and the ability to support one-pot, telescoped reactions. Materials scientists use it for advanced polymers, where reliable integration sites and predictable decomposition profiles matter more than ever. These disciplines push us to improve our process reproducibility, analytical techniques, and on-demand technical support.
Modern synthetic building blocks must do more than satisfy a single purity endpoint. In our labs, we use a suite of in-house methods—routinely updating our NMR fingerprint libraries, calibrating GC-MS protocols, and running orthogonal boron and nitrogen quantification. We respond to customer requests for custom assay reporting, granular impurity breakdowns, and stability testing under different storage and transport conditions. The move toward continuous process verification and digital batch records sprang from requests by long-term development partners who face tight project timelines and must avoid late-stage surprises.
We run post-shipment stability checks and support customers with troubleshooting guidance that reflects our experience with batch and continuous process quirks. Whenever reaction optimization reveals a rare side impurity, we share full analytical traces, so both sides see root causes and solutions without blame or barriers. Our viewpoint as a manufacturer, not just an order taker, makes two-way learning and ongoing product improvement part of our daily routine.
Benchwork and pilot plant feedback shape our understanding of what makes a boronic ester truly useful. There is no replacement for hands-on trials by colleagues in the field. Some have shared how, in multi-step syntheses, our 3-Pyridineboronicacidpinacolester slashes the number of cycles lost to failed couplings or variable reactivity. Others point to tighter analytical specs making documentation for regulatory or scale-up hassle-free. A few university and startup partners cited grant-winning discoveries made possible by switching away from lower-quality sources prone to byproduct formation and erratic coupling yields.
Throughout years of support, these insights refine our process, packaging, and user communication. From moving away from moisture-sensitive packaging to supporting local supply chain resilience for clients working under tight deadlines, our growth as a direct manufacturer follows the path of the customers who use our product for real innovation.
Safe and responsible use of 3-Pyridineboronicacidpinacolester calls for respect for organic base handling, boron chemistry reactivity, and the unique character of the pyridine ring. Our production and packaging teams follow strict personal protective equipment (PPE) guidelines and operate in under-pressured suites, keeping airborne particle levels in check. Outgoing drums undergo moisture testing at the final fill stage, ensuring that product delivered internationally keeps risk of uncontrolled hydrolysis or exotherms to a minimum. Waste management protocols rely on boron and pyridine recycling where permitted, and inert, sealed batch disposal where required.
As environmental expectations evolve, we collaborate with waste treatment partners and end-users to balance reactivity with minimal downstream risks. Our technical teams are available to discuss best practices for both scale-down and scale-up scenarios, reflecting feedback from users on five continents. Safe handling and disposal practices are integral—not an afterthought—and we update protocols regularly.
Every kilogram of 3-Pyridineboronicacidpinacolester that leaves our plant carries the legacy of process improvement, field testing, and open feedback from the global synthesis community. We invest in modern analytical platforms, traceability tools, and operator training not just to pass audits, but to push the practical performance of our product further. Our staff—including process engineers and advanced organic chemists—conduct internal workshops each quarter, sharing technical lessons and troubleshooting new synthetic challenges. These efforts drive smoother scale-up transfers, fewer out-of-spec batches, and faster turnaround for revised customer needs.
Because we see ourselves as partners to the researchers and production teams we serve, our relationships extend far beyond the initial shipment. We work with pilot plant supervisors, formulation chemists, and procurement leads to stay responsive. Their real-world test results guide new directions in product improvement, driving upgrades in drying, filtration, and batch release procedures. This cycle of learning and improvement never slows—a reality that direct manufacturers experience up close.
In an era of global supply disruptions and ever stricter compliance expectations, the ability to maintain consistent, traceable, high-performance chemical building blocks gives our clients an anchor for their R&D and production timelines. For many, “off-the-shelf” simply does not mean fit-for-purpose. The specialized processes, decades of accumulated lessons, and close-knit technical teams behind our 3-Pyridineboronicacidpinacolester produce a compound that scores high marks not only for purity, but for shelf life, usability, and predictability in complex reactions.
As we look ahead to new applications across pharmaceutical, agrochemical, and advanced materials spaces, our product continues to evolve, shaped directly by those who rely on it for discovery, development, and commercialization. Each partnership, each scale-up run, each successful synthesis informs the next. Our story with 3-Pyridineboronicacidpinacolester reflects what is possible when hands-on manufacturing expertise meets the changing needs of science and industry.