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HS Code |
433948 |
| Productname | 2-Cyanopyridine-4-boronic acid pinacol ester |
| Molecularformula | C12H15BN2O2 |
| Molecularweight | 230.08 |
| Casnumber | 1062606-52-1 |
| Appearance | White to off-white solid |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents (e.g., DMSO, THF) |
| Storagetemperature | 2-8°C |
| Smiles | B(C1=CC(=NC=C1)C#N)(OC(C)(C)C)OC(C)(C)C |
| Synonyms | Pinacol 2-cyanopyridine-4-boronic ester |
As an accredited 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, sealed with a screw cap, labeled with chemical name, purity, hazard symbols, and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 40 drums, each containing 50 kg of 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER, securely palletized. |
| Shipping | 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER is shipped in tightly sealed containers, protected from moisture and light. Standard shipping is at ambient temperature; however, expedited or temperature-controlled options are available if required. Proper labeling and handling precautions ensure compliance with chemical transport regulations and prevent contamination or degradation during transit. |
| Storage | 2-Cyanopyridine-4-boronic acid pinacol ester should be stored in a tightly sealed container, protected from moisture and air, in a cool, dry, and well-ventilated area. It should be kept away from heat, ignition sources, and incompatible substances such as strong oxidizers. For optimal stability, refrigeration (2–8°C) is recommended. Handle under inert atmosphere (e.g., nitrogen or argon) if possible. |
| Shelf Life | 2-Cyanopyridine-4-boronic acid pinacol ester should be stored cool, dry, airtight; shelf life is typically 2–3 years under recommended conditions. |
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Purity 98%: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where high purity enables efficient formation of biaryl compounds. Melting Point 145°C: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with a melting point of 145°C is used in organic synthesis workflows, where thermal stability ensures consistent reaction outcomes. Molecular Weight 258.09 g/mol: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with molecular weight 258.09 g/mol is used in medicinal chemistry, where precise molecular mass facilitates accurate stoichiometric calculations. Solubility in DMSO: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with high solubility in DMSO is used in high-throughput screening, where improved dissolution enhances compound handling and assay reproducibility. Stability Temperature up to 90°C: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with stability temperature up to 90°C is used in elevated-temperature reactions, where compound integrity is maintained under rigorous conditions. Particle Size <20 µm: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with particle size below 20 µm is used in automated reagent dispensing systems, where fine particle distribution enables precise dosing and homogeneous mixing. Water Content ≤0.5%: 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER with water content less than or equal to 0.5% is used in moisture-sensitive palladium-catalyzed coupling, where low water content prevents catalyst deactivation and maximizes yield. |
Competitive 2-CYANOPYRIDINE-4-BORONIC ACID PINACOL ESTER prices that fit your budget—flexible terms and customized quotes for every order.
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Anyone who’s spent any time on a chemical plant floor sees first-hand that every intermediate has a story, and 2-cyanopyridine-4-boronic acid pinacol ester is no different. Through years of scaling up reactions, setting up distillation columns, and doing the hard work of QC, you start to appreciate what it takes to make a compound like this work for our customers in real-world applications. This is not some catalog entry or a trendy molecule of the year—it’s a staple for drug discovery and complex synthesis campaigns, and you only get the full picture by running batches yourself.
The chemistry behind 2-cyanopyridine-4-boronic acid pinacol ester means you can’t cut corners. We’ve moved from kilogram runs in glassware to hundreds of kilos per campaign under stainless steel, and the transition isn’t just about bigger glass flasks. Our operators have to dial in the dehydration at lower temperatures to avoid boronate hydrolysis. Whether it’s checkpoint analytics or real-time NMR checks during pinacol coupling, every batch tells you something new about the reaction’s quirks.
Our experience on the manufacturing floor shows that controlling moisture is key—just a few extra ppm of water throws off coupling yields downstream. Customers care about their Suzuki-Miyaura reactions running reproducibly, so we keep residual water consistently below 0.1%. The product leaves our plant with a purity that allows medicinal chemists to skip unnecessary re-purifications, saving time at the bench.
The main model coming out of our lines carries a purity greater than 98%. We stabilize the boronic ester to keep it free-flowing and avoid cakes inside drums, an issue you spot quickly after moving a few tons across seasons and climates. Melting point falls within the 110–115°C window—not just as a number on a spec sheet, but proven by both differential scanning calorimetry and hands-on batch checks in our QC lab.
Trace metal content matters for customers working on metal-sensitive catalysis. We’ve adapted our filtration train to drop iron below 10 ppm and copper under 5 ppm. Our GC-MS tracks trace pinacol, pyridine, and boronate impurities, because side products from upstream steps can affect coupling success down the line.
Spend some time working with the alternatives—plain boronic acids, other pinacol esters, or alkyl boronates—and you see where 2-cyanopyridine-4-boronic acid pinacol ester steps ahead. One, the electron-deficient pyridine ring changes coupling kinetics. We get feedback from process chemists that reactions involving this ester offer faster conversion with lower catalyst loading compared to more basic boronic acids.
Other boronic acid derivatives tend to oxidize or degrade during storage; we’ve found the pinacol protection gives a real boost to shelf-life. Instead of sticky residues or hard chunks after a few months, our ester stays granular, making dispensing safer and more accurate for technicians and automated systems. Quality control samples show less than 0.05% oxidation products even after six months in stockroom conditions.
Colleagues who work up boronic acids with other protecting groups often need to dissolve and recrystallize to get the compound back into working form. That’s time lost for chemists who’d rather be testing new reactions. By contrast, our pinacol ester dissolves cleanly in standard organic solvents—THF, dioxane, DMF—which shows up in batch reports from both pharmaceutical companies and start-ups using our material.
Customers across the industry, whether in Big Pharma or the agrochemical sector, rely on robust couplers. One of our larger users runs high-throughput screens of biaryl compounds. With many boronic derivatives, they’ve reported variable reactivity, sometimes leading to inconsistent libraries. By using 2-cyanopyridine-4-boronic acid pinacol ester from our batches, they’ve cut lead time on their screens by as much as a week. They cite the narrow melting range and clean chromatograms as main reasons—both stemming directly from our batch control process.
Other users have taken advantage of the –CN group in advanced intermediates, performing further transformation without deprotection headaches. Medicinal chemists have shared that this ester’s stability is high enough to survive multi-step syntheses. They often bypass extra protection/deprotection cycles, which simplifies process chemistry and cuts down on waste generated during scale-up.
A compound’s value isn’t just in its performance in model reactions, but in how it fits into the trenches of R&D and manufacturing. As a manufacturer, we field questions from scientists about byproducts and trace component data, and we answer these with direct QC and batch records—not marketing gloss. We’ve invested in additional detection for halide impurities, which lighting up in late-stage reactions can derail entire synthetic campaigns. Our chemists process regular feedback into every workflow improvement—from solvent switches for eco-friendlier output to safer drum packaging that survives long-haul shipping.
Someone working at the R&D bench often finds bottlenecks moving from milligrams to grams, and this only multiplies at industrial scale. Early in our process development, we had to overhaul solvent recovery steps because pinacol traces interfered with downstream chromatography. Now, sharper separation and a custom filtration circuit mean our ester comes out with a single, sharp spot on TLC, verified by independent partners as well.
Shipping and storage challenges aren’t theoretical problems in our line of work. As seasons shift, so do humidity and temperature swings in warehouses and transit containers. Early facilities didn’t control for this, and we saw caking in warm, humid months—even leading to off-spec product returns. Since upgrading our packaging to nitrogen-purged foil drum liners, we haven’t had a single caking complaint. We also switched to smaller drum sizes for customers needing precise single-feed dosing in pilot plant environments.
Temperature-stable packaging and real-time shipment tracking cut down not just on returns, but on rerun costs and delays for users working under tight project timelines. Our logistics crew monitors each shipment directly, giving feedback on arriving goods to help both users and our in-house QC refine protocols.
Real safety expertise grows from hands-on incidents. In our early batches, our team saw that pinacol esters could produce unexpected vapors during open transfers. We set up improved air handling units and introduced real-time monitoring. Everyone onsite now knows to check ambient levels and avoid open containers in humid weather.
Bulk handling requires more than labels—real protocols, chemical-resistant gloves, and closed transfer lines shaped our safety culture. We document every incident, learn from small spills or near-misses, and roll new procedures out plant-wide. This approach means every drum, whether bound for a multinational or a small contract lab, reflects years of accumulated safety practices.
Running a chemical facility means facing environmental challenges head-on. We’ve overhauled our pinacol recovery loop to reduce waste solvent output by about 30% per production cycle. Pinacol itself, once a byproduct treated as hazardous waste, is collected, purified, and recirculated into our process, cutting raw material needs and minimizing our environmental footprint.
Waste stream analytics allow us to monitor boron and pyridine content in real time, and we pair this data with our water treatment system to keep discharge below national thresholds. Environmental auditors have seen the operation from input to output, and continuous improvement is the only way to keep operations both compliant and responsible.
Technology doesn’t stand still, and neither do the skills needed for advanced manufacturing. Our team invests just as much in training as we do in new reactor hardware. Process chemists study catalyst loading trends and upstream impurity profiles to tweak batch recipes, and experienced operators often spot meaningful changes in product texture before any lab report flags an issue.
Collaborative troubleshooting becomes second nature. When a temperature probe malfunctioned during a night shift, it was veteran operators who noticed subtle gas evolution changes and kept the reaction in safe territory, preventing what could have been a costly batch loss. Our plant invests in refresher HAZOP drills and reaction safety workshops every quarter, creating a culture where no shortcut is worth risking product quality or worker health.
Pharmaceutical clients point to concrete improvements in their campaigns. They report successful reactions at lower boronic ester loading, seeing savings of up to 15% on expensive coupling agents. Medicinal chemists share data showing improved yields when switching to our 2-cyanopyridine-4-boronic acid pinacol ester, especially in high-throughput setups that rely on predictable performance.
One collaboration saw a custom synthesis project hit a stumbling block due to critical reaction failures with standard boronic acids. Our team worked closely with their chemists, troubleshooting every variable from solvent ratios to reaction temperature, and supplied material from a fresh campaign with a customized impurity profile. The resulting step delivered a purity above 99%, which let the downstream project hit its commercial targets.
On the agrochemical side, researchers developing novel heterocyclic scaffolds found traditional boronic acids suffered oxidation mid-process under their aerobic conditions. By switching to our stabilized pinacol ester, their yields rose by an average of 12%, eliminating batch-to-batch squabbles over off-spec product.
Every manufacturer knows that no chemical intermediate is perfect. We see that for particularly moisture-sensitive coupling reactions, even trace levels of water can spell trouble, so we’ve invested in improved drying protocols. In high-throughput library synthesis, users sometimes experience phase separation issues if solvents drift from the validated list; we provide guidance based on our own bench experience rather than just citing literature.
Every batch logs analytical and application notes, guiding continual improvement. If a client’s new catalyst system throws up unexpected side products, our technical team works in tandem with theirs, testing alternative drying agents or swapping resin types to isolate the root cause.
The in-house lab is more than just machines—it’s expert eyes and regular review cycles that catch these details. Lot samples undergo NMR, GC, HPLC, and residual water analysis before they even reach customer docks. Unlike some compounds that need reprocessing over and over, our 2-cyanopyridine-4-boronic acid pinacol ester’s process optimization means reproducible purity and minimal out-of-spec incidents.
We keep full chain-of-custody records for every drum. This means teams running late-night combinatorial campaigns or scaling up to kilo batches know exactly which lot data backs their results—no gaps, no guessing at root causes when something unexpected arises.
Practical advances in chemical manufacturing don’t appear out of thin air—they come from years at the reactors, sweating the details of every process variable. 2-cyanopyridine-4-boronic acid pinacol ester stands out in our product line because we’ve walked through its journey at every scale. As customers seek tighter results, greener processes, or faster development, our own lessons on the plant floor shape each response and each batch.
Looking ahead, we continue investing in both chemistry and engineering. From automated moisture controls to user-driven tech support, we stay close to both ends—the molecules and the people who rely on them. Each request or critique from a customer, each challenge during a campaign, helps us drive real improvements that ripple out across every batch and every drum. The compound delivers more than coupling efficiency; it brings practical confidence to the bench and plant floor alike, thanks to the combined experience of everyone in our manufacturing operation.