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HS Code |
845447 |
| Chemical Name | 3-Cyanopyridine-5-boronic acid pinacol ester |
| Molecular Formula | C12H13BN2O2 |
| Molecular Weight | 228.06 g/mol |
| Cas Number | 870292-43-8 |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in DMSO, DMF, and organic solvents |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Smiles | B(C1=CN=CC(=C1)C#N)(OC(C)(C)C)OC(C)(C)C |
As an accredited 3-Cyanopyridine-5-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 5-gram amber glass vial, securely sealed with a PTFE-lined cap and labeled with product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 3-Cyanopyridine-5-boronic acid pinacol ester packed in drums or cartons, securely palletized, maximizing container space. |
| Shipping | 3-Cyanopyridine-5-boronic acid pinacol ester is shipped in tightly sealed containers under inert atmosphere to prevent decomposition. The packaging complies with chemical transport regulations, cushioned to avoid damage. Refrigeration or cool, dry conditions may be required. Safety data sheets and hazard labels are included to ensure proper handling during transit. |
| Storage | 3-Cyanopyridine-5-boronic acid pinacol ester should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, moisture, and direct sunlight. Protect from air and strong oxidizing or reducing agents. Store under inert atmosphere (e.g., nitrogen or argon) if possible to prevent hydrolysis and degradation. Handle in accordance with standard laboratory safety protocols. |
| Shelf Life | Shelf life: Store 3-Cyanopyridine-5-boronic acid pinacol ester under inert atmosphere at 2–8°C; stable for at least 2 years. |
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[Purity 98%]: 3-Cyanopyridine-5-boronic acid pinacol ester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side-product formation. [Molecular Weight 246.06 g/mol]: 3-Cyanopyridine-5-boronic acid pinacol ester of molecular weight 246.06 g/mol is used in Suzuki-Miyaura coupling reactions, where it facilitates precise stoichiometric calculations for optimal coupling efficiency. [Melting Point 124-127°C]: 3-Cyanopyridine-5-boronic acid pinacol ester with melting point 124-127°C is used in solid-phase synthesis protocols, where it provides thermal stability during reaction cycles. [Particle Size <10 μm]: 3-Cyanopyridine-5-boronic acid pinacol ester with particle size less than 10 μm is used in high-throughput screening applications, where it promotes rapid dissolution and uniform reaction kinetics. [Stability Temperature up to 80°C]: 3-Cyanopyridine-5-boronic acid pinacol ester with stability temperature up to 80°C is used in continuous flow chemical synthesis, where it maintains chemical integrity under elevated process conditions. [Moisture Content <0.2%]: 3-Cyanopyridine-5-boronic acid pinacol ester with moisture content below 0.2% is used in organometallic catalysis, where it ensures catalyst activity without hydrolytic degradation. |
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On the manufacturing floor, every batch of 3-Cyanopyridine-5-boronic acid pinacol ester represents the result of deliberate decisions in synthesis, process controls, and material handling. This isn’t a commodity passed through many hands. From raw building blocks to the finished material, I have witnessed the way careful control at every processing step determines whether this advanced boronate ester matches the standards our partners demand. Our focus isn’t just yield or purity but real-world performance in downstream reactions, reproducibility for ongoing research, and confidence in the reproducibility of results.
What sets our 3-Cyanopyridine-5-boronic acid pinacol ester apart begins with model designation, batch-referenced for full traceability: CYB5BE-2108. This ester translates to a fine, off-white crystalline powder, formed through a stable coupling of pyridine and boronic acid using rigorous reaction conditions that we continuously optimize. After several years refining this synthesis, we fine-tune the process to minimize byproduct contamination, targeting the 98-percent-plus purity level, which GC and qNMR analysis at every lot confirm.
Moisture content in each lot stays under 0.5% as measured by Karl Fischer titration. End users report our material arrives free-flowing, with no unintentional agglomerates or caking. The product’s melting point sits in a stable and repeatable range, easing protocol development for both synthetic and scale-up chemists. With every re-order, the same spectral fingerprint matches both NMR and HPLC profiles stored in our batch archives.
Working directly with customers, we see 3-Cyanopyridine-5-boronic acid pinacol ester rising in demand as both labs and production groups pursue more challenging cross-coupling strategies. Teams using Suzuki-Miyaura reactions rely on boronic esters because these intermediates combine solid shelf stability with predictable behavior in coupling. Unlike the corresponding boronic acids, which quickly degrade in ambient air or lose activity with minor storage errors, the pinacol phenyl boronate ester structure makes a real difference for bench chemists.
This stability comes from the strong, sterically shielded boron-oxygen bonds of the pinacol group, which reduce hydrolysis and maintain reactivity over months of storage. Teams that buy in bulk appreciate this: material stored in sealed containers rides through temperature fluctuations during transit, and they still report clean reactions even after weeks at room temperature. Our boronic ester allows consistent performance even in facilities that lack climate-controlled storage.
From the manufacturing viewpoint, there is a significant difference between pinacol boronic esters and other boron sources. We have produced both traditional boronic acids and their pinacol ester derivatives; the two look similar by formula, but the difference in handling, solubility, and shelf life plays out in real-world labs. Boronic acids, including the 3-cyanopyridine-5-boronic acid itself, turn out hygroscopic and often require glove-box storage. Users report formation of boroxine impurities as a recurring issue.
By moving to the pinacol ester version, chemists see a more reliable product. Pinacol protection not only guards boron against hydrolytic breakdown, but makes the powder easier to weigh and dispense accurately. Our partners performing high-throughput library syntheses or scaling up for preclinical lots do not want double handling or worry about fast degradation; direct-from-container use minimizes the risk of batch-to-batch variance. Pinacol boronic esters disperse in organic solvents with less fuss and produce cleaner coupling reactions without side product headaches.
Feedback from the market clarifies how this boronate ester finds a place in discovery and process chemistry. Medicinal chemistry groups leverage the cyanopyridine motif to build custom kinase inhibitors and other small-molecule leads. The boronic ester provides a convenient point for palladium-catalyzed cross-coupling, giving researchers access to structures that basic heteroaryls alone cannot supply. The use of the 3-cyano group, highly valued for its electron-withdrawing characteristics, enables introduction of new functionality at late stages in synthesis—saving both time and cost in SAR studies.
Process development environments value the repeatability that well-characterized esters bring. The clean, narrow melting range allows easy monitoring and controls in scale-up, while the low water content means reactions follow predictable pathways without hydrolysis risk. Many report that reaction work-ups become far simpler with our product: fewer emulsions, less troublesome filtration, reduced purification work, and improved isolated yield on the desired product.
Beyond pharmaceuticals, this intermediate also finds roles in advanced materials. Teams in optoelectronics have explored the use of 5-borylated pyridine structures, especially those functionalized with cyano substituents. The boronic ester here acts as the connection point for growing more elaborate fused aromatic networks, often through Suzuki coupling, which build up polymers with suitable conduction or emission properties. The pinacol ester provides more robust handling than boronic acids, which often prove unpredictable under dry-box conditions or during multistep builds.
Regulatory expectations in fine chemicals have tightened. End users must understand impurity profiles, origin of raw materials, and reproducibility from lot to lot. Our facility routinely qualifies analytical protocols—NMR, mass spectrometry, GC-FID, HPLC, and residual solvent testing—across every batch. Not all suppliers give this level of transparency. Because the material is manufactured at our plant, we document every step in the chain and update certificates with real data, never just passing along someone else’s results.
Supply partners have shared how this transparency allows them to gain approval for clinical or pilot plant use faster. Customers who have experienced quality drift with distributed or repacked material report an improvement in both regulatory submissions and actual reaction outcomes after switching to product straight from the manufacturing source. Our documentation matches the stated content, and our team can clearly answer technical questions about trace byproducts, expected handling, and compatibility.
Over years of direct production, the greatest benefit isn’t technical purity alone. Chemists at the bench judge a product by its performance, yes, but they also remember the batches that store well and the times when supply ran short or specifications shifted mid-risk projects. As manufacturers, handling urgent orders, scaling lots, and troubleshooting impurities stand out as real tests. Through open lines of communication, we have found that supporting process development teams by troubleshooting work-ups or sharing analytical data always yields greater success than hiding behind paperwork.
Trade disruptions and price swings have shown the value of consistent direct supply. Our relationships hinge on being able to share what raw material stocks look like, what delivery times can realistically be met, and, most importantly, keeping the manufacturing sequence robust enough to resist backlogs. Unlike distributors or repackers, direct manufacturing teams maintain real leverage during periods of supply tightness, shortening lead times and protecting users from disruption.
Product complaints in the market often relate to handling, not just reactivity or purity. Boronic esters, including this pinacol-protected cyanopyridine species, ship as free-flowing powders but draw some concern regarding moisture uptake if left open too long. Our strategy includes tight sealing of each drum or bottle and the use of dry rooms throughout packaging. We recommend routine inspection of seals and prompt resealing after sampling. End users who upgraded their storage setup report this extra care extends shelf life without degradation. Real-world experiences show that preventative training for storeroom personnel matters as much as technology in prolonging product viability.
Not all boronic intermediates allow such stable transport. In earlier years, boronic acids often showed up clumped, caked, or slightly off-color, frustrating end users who then spent hours redissolving, filtering, or reprocessing before use. The pinacol ester brings clear benefit here, keeping to specification even after long journeys in less-than-ideal conditions. This “real world” stability means that the product retains its viability across the unpredictable logistics chain that defines global chemistry supply.
The run-up in regulatory focus on environmental performance and worker safety shows no sign of slowing. Pinacol boronic esters give chemists a safer alternative to less stable boron reagents. Their stability cuts down on loss, spillage risk, and the formation of undesired side products or fumes. Using a solid intermediate simplifies both large and small-scale laboratory waste profiles, since less reactive boron chemicals often force tricky neutralization or disposal procedures. Cleaner syntheses mean less post-reaction workup, with fewer solvents and less operator handling—a real benefit for EHS compliance.
Working directly in plant conditions, our teams have focused on batch containment, improved ventilation during powder charging, and automation where applicable to further reduce handler exposure. Material handling data gets shared with our downstream partners so they can incorporate best safety practice into their own protocols. Feedback so far shows reduced loss during weigh-out and lower rates of container contamination, delivering real cost savings in bulk operations.
Every campaign to produce 3-Cyanopyridine-5-boronic acid pinacol ester draws on years of tracked process data. Small tweaks in temperature, mixing rate, or purification strategy during scale-up can shift impurity profiles or alter physical properties. By controlling not just the chemistry but also the physical handling—charging, agitation, filtration, drying, packaging—our site avoids the batch-to-batch surprises that sometimes frustrate buyers of trader-resourced products.
We have invested in semi-automated finishing lines, humidity-controlled assembly, and direct-to-container filling so that product never “floats” around in open air, picking up water or atmospheric contaminants. Customers with large multi-step syntheses often reach out for batch-specific data; our records support straightforward risk assessment and process validation. There’s no guesswork over where each bottle originated, and our plant managers keep an open door for technical review whenever requested.
Critical feedback has shaped how we adapt formulations and handling. For example, medicinal chemists highlighted how subtle shifts in particle size play into reaction kinetics on the floor. Our team responded by rebalancing milling and sieving steps, bringing tighter distribution in particle size. Other partners mentioned unwanted batch variation in melting point; adjustments in crystallization protocols have delivered more uniform material. Manufacturing this compound on site means that such feedback translates directly to process improvement—delivering value that distant suppliers simply cannot offer.
A common concern among our customers developing new routes is ensuring that early discovery-stage chemistry can scale successfully. The 3-cyanopyridine group, with its electron-withdrawing tendencies, does sometimes present extra challenges in certain cross-coupling settings. Drawing on both plant and lab experience, we share protocol recommendations and solvent/rate adjustments that reduce catalyst deactivation and maximize overall conversion.
This willingness to share internal findings, rather than holding process data as proprietary, has built trust with users who must balance bench-scale curiosity with real-world efficiency. Feedback cycles with process chemists have allowed us to propose alternative filtration aids, recommend quenching sequences for waste minimization, and optimize order sizes to match developing projects. This hands-on approach creates partnerships rather than mere transactions.
As new catalysts and reaction variants develop, the role of advanced boronic esters will only grow. Customers pursuing late-stage functionalization, bioconjugation projects, or entirely new material platforms look for intermediates they can trust both for reactivity and consistency. From our side, continuous investment in analytic protocols, tighter process controls, and customer-driven improvements ensure that neither process bottlenecks nor unanticipated impurities compromise your next campaign.
Direct manufacturing gives us the agility to tune future lots toward emerging applications, whether for advanced pharmaceuticals, specialty materials, or custom synthetic routes. Working hand in hand with the chemists using our product, our focus stays on quality, reliability, and constant adaptation. The lessons we learn with each batch become the foundation for the next, keeping pace with evolving chemical innovation.
This isn’t about a label or a line in a product catalog. Every package of 3-Cyanopyridine-5-boronic acid pinacol ester that leaves our facility reflects pride in direct manufacturing and ongoing respect for the real work done in labs and plants downstream. By putting as much emphasis on support, transparency, and communication as on technical details and compliance, we aim to be partners in innovation rather than just a supplier. Experience—our own and that of our engaged customers—proves that this approach pays out in more resilient projects and chemistry breakthroughs that simply deliver.