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HS Code |
655646 |
| Product Name | 2-Fluoropyridine-4-boronic acid pinacol ester |
| Molecular Formula | C11H15BFNO2 |
| Molecular Weight | 223.06 g/mol |
| Cas Number | 933746-36-6 |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Boiling Point | No data available (decomposes) |
| Melting Point | 62-66°C |
| Solubility | Soluble in organic solvents such as DMSO, THF, and dichloromethane |
| Storage Temperature | 2-8°C, protected from light and moisture |
| Smiles | B1(OC(C)(C)C(C)(C)O1)c2ccnc(F)c2 |
| Inchi | InChI=1S/C11H15BFNO2/c1-10(2)15-11(3,4)16-12(14)8-5-6-13-9(7-8)14/h5-7,10H,1-4H3 |
As an accredited 2-Fluoropyridine-4-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5g of 2-Fluoropyridine-4-boronic acid pinacol ester is supplied in a sealed amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | 20′ FCL contains securely packed drums of 2-Fluoropyridine-4-boronic acid pinacol ester, ensuring moisture protection and safe chemical transport. |
| Shipping | 2-Fluoropyridine-4-boronic acid pinacol ester is shipped in tightly sealed containers under inert atmosphere to prevent moisture and air exposure. It is packed with appropriate hazard labeling and cushioning for protection during transit. Standard shipping uses temperature-controlled conditions if required, complying with all relevant chemical transport regulations. |
| Storage | 2-Fluoropyridine-4-boronic acid pinacol ester should be stored in a cool, dry, and well-ventilated area, tightly sealed in its original container. Protect from moisture, heat, and direct sunlight. Store away from strong oxidizers and acids. Recommended storage temperature is 2–8°C (refrigerated). Ensure containment in an inert atmosphere, such as under nitrogen or argon, to prevent hydrolysis or degradation. |
| Shelf Life | 2-Fluoropyridine-4-boronic acid pinacol ester is stable at room temperature, with a typical shelf life of 2 years when sealed. |
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Purity 98%: 2-Fluoropyridine-4-boronic acid pinacol ester with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low by-product formation. Molecular weight 237.07 g/mol: 2-Fluoropyridine-4-boronic acid pinacol ester with molecular weight 237.07 g/mol is used in Suzuki-Miyaura cross-coupling reactions, where it facilitates precise stoichiometric calculations. Melting point 52–56°C: 2-Fluoropyridine-4-boronic acid pinacol ester with a melting point of 52–56°C is used in solid-phase organic synthesis, where it allows for controlled processing conditions. Particle size ≤50 µm: 2-Fluoropyridine-4-boronic acid pinacol ester with particle size ≤50 µm is used in automated synthesis systems, where it promotes efficient dissolution and mixing. Stability at 25°C: 2-Fluoropyridine-4-boronic acid pinacol ester stable at 25°C is used in chemical storage and transport, where it prevents degradation and preserves reactivity. Water content ≤0.5%: 2-Fluoropyridine-4-boronic acid pinacol ester with water content ≤0.5% is used in moisture-sensitive catalyst systems, where it reduces hydrolysis and maintains catalytic activity. HPLC purity ≥98%: 2-Fluoropyridine-4-boronic acid pinacol ester with HPLC purity ≥98% is used in high-precision ligand synthesis, where it supports reproducible reaction outcomes. Residue on ignition ≤0.1%: 2-Fluoropyridine-4-boronic acid pinacol ester with residue on ignition ≤0.1% is used in fine chemical manufacturing, where it minimizes contamination in end-products. |
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In the world of chemical manufacturing, progress means keeping one foot in proven methods and the other in new ideas. Years in the lab and on the production floor have taught us that the right starting material often makes a world of difference, especially for chemists chasing yield, purity, and reliability. That’s the driving reason behind our work on 2-fluoropyridine-4-boronic acid pinacol ester. It’s not just another molecule on a product list; it reflects hard-earned lessons learned from scale-up headaches, reactivity challenges, and a growing demand for reproducibility.
We produce this compound under the designation 2-FP4BA-PE, which has become a reliable standard on our own shop floor and in partner labs. Each batch comes as a solid with consistent melting behavior in the expected range for pinacol esters—no unexplained variance, no off-colors or clumps. Our team uses single-point GC and NMR to track trace impurities, putting all data on a sample’s journey from start to finish. Moisture and trace metal content often get overlooked elsewhere—our QC team checks both before a drum or bottle leaves the facility.
At our plant, the reaction sequence uses fluoride-safe glassware and low-extractable stoppers to prevent contamination. After boron coupling, rigorous crystallization ensures particle uniformity. The final solid is easy to handle, even in high-throughput automated setups. Each drum comes with a batch-specific data sheet summarizing purity levels, trace halide analysis, and lot history. Specifications are not generic—they reflect typical needs from pharmaceutical scale-up teams, medicinal chemists tinkering on new NCE scaffolds, and process developers exploring Suzuki cross-coupling.
Customers in our industry expect more than just a reagent—they need partners who understand why a particular boronic ester matters. In recent years, pharmaceuticals backed by pyridine rings have surged in value. Adding a fluorine atom to the mix creates new opportunities but can also introduce synthetic hurdles. At our facility, most chemists regard 2-fluoropyridine-4-boronic acid pinacol ester as a workhorse, a bridge between innovation and practicality.
The pinacol ester format offers a blend of chemical stability and coupling versatility. Some prefer the acid, but boronic acids tend to absorb moisture, turn gummy, or degrade on the bench during short-term storage. Pinacol esters resist hydrolysis much longer, tolerate shipping across continents, and work well in glovebox or open-air conditions. Our customers in scale-up and process optimization have told us how a stable boronic ester saves time, minimizes batch failures, and reduces reprocessing.
In medicinal chemistry, the 2-fluorine position can unlock SAR data rapidly. It enables the design of molecules with unique electronegativity profiles or metabolic stability, which remain hard to reach using classical building blocks. Many top-selling therapies contain mono-fluorinated pyridines—this molecule fits squarely into those pipelines.
Our own research and feedback from partners show the most common use for 2-fluoropyridine-4-boronic acid pinacol ester remains the Suzuki-Miyaura reaction. For anyone tuning aryl-aryl or aryl-heteroaryl coupling, this ester brings clear advantages. The pinacol group acts as a protective moiety, holding the boron center stable while enabling smooth transmetalation under normalized conditions.
Some manufacturers cut corners by offering technical or crude grades. We have learned, through direct setbacks early in our scale-up phase, that a higher purity product pays dividends. In cross-coupling runs, side-product build-up often stems from impurities or inconsistent batch content—problems reduced by greater attention to raw input and process control.
2-fluoropyridine-4-boronic acid pinacol ester also features prominently in diverging synthetic routes. Peptide-drug conjugates, fluorinated biaryl scaffolds, and library synthesis efforts all benefit from its reactivity. Several custom projects have used our material for regioselective arylation or assembly of drug candidates resistant to metabolic oxidation. Open-well microplate protocols, automated parallel synthesis, and even multi-liter scale reactions proceed smoothly with this compound, thanks to its predictable melting, stability in bulk form, and absence of volatile breakdown products.
Chemists often debate the merits of various boron reagents. Common options include boronic acids, potassium or cesium trifluoroborates, and pinacol esters. From our experience, the pinacol ester strikes an ideal balance—its handling properties sidestep shipping headaches and lab workflow bottlenecks.
Compared with boronic acids, the pinacol ester demonstrates greater resistance to moisture. It stores well in ambient conditions and seldom forms sticky residues, saving precious minutes in sample prep. Trifluoroborate salts show unique benefits for some aqueous phase coupling, but they invite solubility and mixing concerns on scale-up. With the 2-fluoropyridine-4-boronic acid pinacol ester, users avoid these drawbacks while enjoying a longer shelf-life.
Uptime matters in industrial labs. We regularly compare our material against technical-grade offerings and lower-purity equivalents. Lower purity boron reagents can contribute to side-reaction build-up or incomplete couplings. We routinely see our customers increase throughput, boost yields, and cut out reprocessing steps. Many report more reproducible kinetics and a shortened development cycle.
Each batch of our pinacol ester product also carries a low trace metal burden, the result of diligent process hooks during manufacturing. Metals like palladium, iron, and copper function as essential tools in cross-coupling, yet persistent residual metals can interfere in catalytic cycles or downstream bioassays. Our cleaning and process validation aim to minimize this risk, improving reliability for end-users working at various scales.
Our team supports many customers at early-stage pharma R&D, where every gram is counted and timelines remain tight. One major client needed kilogram quantities for a scale-up of a pyridine-containing intermediate. They struggled with inconsistent reactions using traditional boronic acids sourced from outside vendors, leading to frequent re-crystallizations and delayed downstream steps.
After switching to our 2-fluoropyridine-4-boronic acid pinacol ester, their process ran cleaner, with fewer out-of-spec drums. Product isolation became easier, and their analysts saw sharper NMR and HPLC signals. Fewer byproducts, less time spent troubleshooting—resulting in several weeks shaved off the project timeline. Hearing such outcomes reaffirms our commitment to hands-on process control, rather than relying on commodity approaches.
A separate development focused on producing a fluorinated building block for agrochemical screening libraries. Researchers found that using our pinacol ester, rather than the acid or the potassium salt, provided improved consistency in their microwave-assisted high-throughput reactions. Staff mentioned reduced downtime from clogged lines and easier downstream purification. From gram to pilot scale, this feedback keeps us looking for ways to optimize every batch.
Manufacturing boron reagents—especially fluorinated, heteroaromatic ones—tests the rigor of process design, supply chain reliability, and end-to-end traceability. We stick to time-tested, validated steps but challenge assumptions based on real-world results. At each stage, research and feedback drive our improvements.
For the 2-fluoropyridine-4-boronic acid pinacol ester, the pinacol protection step benefits from careful stoichiometry, uniform mixing, and rapid filtration. Our chemists monitor by-product profiles using both bench and in-line analytics. Every batch is rigorously inspected for color, texture, and spectral consistency. Customers demand robust, non-hygroscopic products—this feedback loops into continuous process tuning.
Packaging also receives special attention: nobody wants degraded boronic esters arriving at their lab. Our sealed containers maintain a vacuum and block moisture ingress. After years of troubleshooting, we know that even small improvements in packaging materials reduce shipping losses and maintain reproducibility. The best product on paper means little if it doesn’t arrive in ideal condition.
Fluorine modification in pyridine scaffolds offers more than just a metabolic tweak—it transforms physical and biological profiles. Activity against biological targets, permeability through membranes, and resistance to degradation all hinge on small changes in substitution patterns. Medicinal chemists consistently want a robust stock of well-characterized, stable fluorinated boron reagents like this pinacol ester.
We have seen partners push boundaries with our material in serial library synthesis, fragment-based drug discovery programs, and development of next-generation ligands. The simplicity of using a shelf-stable, pure pinacol ester means attention focuses on reaction design, not reactivity patchwork. Automation platforms in discovery chemistry thrive on reliability and minimal hands-on input; our product’s robust handling keeps these efforts on track.
Global collaboration also benefits: researchers working across continents share consistent results when tapping into the same lot. No more failed reactions due to local storage conditions or long transit times—a real advantage in a distributed research landscape.
Moving from gram to kilo-scale, scale-up teams need assurance that their boronic ester will behave just as well at large volumes as it did in microgram batches. We have observed that 2-fluoropyridine-4-boronic acid pinacol ester handles the challenges of mass transfer and thermal gradients with ease. Precise control during recrystallization and drying means the solid’s performance remains unchanged.
Integrating our reagent into continuous flow setups reveals another major advantage: its low melting point and absence of sticky intermediates. Slurry feed remains consistent, pumps don’t clog, and filtration proceeds quickly. We continually support customers adopting these modern platforms, providing documentation on heat transfer, particle sizing, and pressure handling derived from our pilot-scale experience.
With increased regulatory scrutiny, especially in pharma, lot traceability and impurity profiling matter more than ever. Each batch reflects not only chemical purity but an ability to withstand harsh audits—a testament to strict attention at every stage rather than treating process validation as a bureaucratic afterthought.
The global focus on environmental impact and sustainable sourcing pushes chemical manufacturers into a new era. Our responsibility doesn’t end at the reactor: it extends to the energy used in dryers and filtration units, solvent reclamation, and the overall carbon footprint of each shipment. We source pinacol from ISO-certified suppliers, tracking every drum from point of origin. Our wastewater systems employ multi-stage scrubbing to minimize boron content and prevent groundwater contamination.
With 2-fluoropyridine-4-boronic acid pinacol ester, circular resource use goes beyond cliché—recycling solvents, recovering pyridine intermediates, and minimizing halogen emissions protect both community health and long-term viability. The feedback from partners, especially those moving toward green chemistry metrics, helps prioritize improvements in process chemistry, waste reduction, and energy minimization.
Stability, purity, and reproducibility make up the core of quality, but listening to users shapes how those qualities evolve. During pilot program rollouts, we’ve witnessed customers side-step lengthy purification runs simply by having access to a higher grade initial material. A pharmaceutical group aiming for accelerated clinical development selected our pinacol ester after competitor batches repeatedly failed their stress stability trials. Consistency across lots gave them confidence to transfer their process internationally, even as regulatory filings set strict quality boundaries.
Another partner conducting high-throughput screening in agricultural applications used our product across dozens of weekly shipments. The feedback? No batch failures, simpler purification, and better analytical performance—translating into faster candidate identification. In these stories, successful outcomes result not only from a well-made molecule but from a grounded approach to support and documentation; lessons like these inform every new run in the plant.
Every chemical manufacturer faces unexpected outcomes at scale, from lot-to-lot variability to supply interruptions. Our philosophy centers on continuous review—learning from process upsets, testing batches for longer-term storage, and updating process documentation in light of near-miss events. We poll our partners after every major shipment, not relying on assumptions about how people use or store our product.
The evolution of our 2-fluoropyridine-4-boronic acid pinacol ester serves as a case in point. Early feedback exposed issues with crystal morphology affecting filtration—so we re-tuned cooling rates and adjusted seeding protocols. Later, as environmental requirements tightened, we invested in energy recovery systems and expanded analytics for trace impurity screening. Improvements like these stem from staying close to the realities of chemical production, not detached theoretical models.
Today’s chemistry relies on bridging the gap between discovery and delivery. As a manufacturer, our value comes not from fancy labels or marketing, but from reliability and a willingness to adapt. 2-fluoropyridine-4-boronic acid pinacol ester underpins countless reactions—each one a small step forward in pharmaceuticals, agrochemicals, and material innovation. With every batch, we commit to ensuring that chemists find not just a raw material but a foundation for building ideas into results.