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HS Code |
511306 |
| Product Name | 2-Fluoropyridine-3-boronic acid pinacol ester |
| Cas Number | 1029652-58-9 |
| Molecular Formula | C11H15B F N O2 |
| Molecular Weight | 223.06 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Solubility | Soluble in common organic solvents (e.g., DMSO, DMF) |
| Synonyms | 2-Fluoro-3-pyridylboronic acid pinacol ester |
| Smiles | B1(OC(C)(C)C(C)(C)O1)c2ccnc(C2)F |
| Inchi | InChI=1S/C11H15B F N O2/c1-10(2)15-12(16-11(3)4)9-6-5-8(13)7-14-9/h5-7,10-11H,1-4H3 |
As an accredited 2-Fluoropyridine-3-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 vial containing 1 gram of 2-Fluoropyridine-3-boronic acid pinacol ester, tightly sealed with a PTFE-lined cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packages and ships bulk 2-Fluoropyridine-3-boronic acid pinacol ester in sealed drums, ensuring safe, moisture-free transport. |
| Shipping | 2-Fluoropyridine-3-boronic acid pinacol ester is carefully packed in sealed containers to protect against moisture and contamination. Shipped at ambient temperature, it complies with all relevant chemical transport regulations. Accompanied by a safety data sheet (SDS), it is delivered via certified carriers specialized in handling chemical reagents. |
| Storage | 2-Fluoropyridine-3-boronic acid pinacol ester should be stored in a cool, dry, and well-ventilated area, protected from moisture and direct sunlight. Keep the container tightly closed when not in use. Store under inert gas, such as nitrogen or argon, to prevent hydrolysis and degradation. Avoid exposure to strong oxidizing agents, acids, or bases. Store at recommended temperature (usually 2–8°C) for optimal stability. |
| Shelf Life | 2-Fluoropyridine-3-boronic acid pinacol ester exhibits a shelf life of up to 2 years when stored cool, dry, and sealed. |
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Purity 98%: 2-Fluoropyridine-3-boronic acid pinacol ester with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it enables high-yield synthesis of fluorinated pyridine derivatives. Molecular weight 237.01 g/mol: 2-Fluoropyridine-3-boronic acid pinacol ester with molecular weight 237.01 g/mol is used in pharmaceutical intermediate production, where it ensures precise stoichiometry in synthetic pathways. Melting point 52-54°C: 2-Fluoropyridine-3-boronic acid pinacol ester with melting point 52-54°C is used in solid-phase organic synthesis, where it allows easy handling and storage under ambient conditions. Particle size <50 µm: 2-Fluoropyridine-3-boronic acid pinacol ester with particle size <50 µm is used in catalytic processes, where it promotes enhanced reaction kinetics due to increased surface area. Stability temperature up to 120°C: 2-Fluoropyridine-3-boronic acid pinacol ester stable up to 120°C is used in high-temperature synthesis routes, where it ensures minimal decomposition and consistent product yield. Moisture content <0.5%: 2-Fluoropyridine-3-boronic acid pinacol ester with moisture content <0.5% is used in automated peptide synthesis, where it minimizes hydrolytic side reactions for improved purity. Assay by HPLC ≥97%: 2-Fluoropyridine-3-boronic acid pinacol ester with assay by HPLC ≥97% is used in agrochemical research, where it delivers reproducible batch-to-batch performance in bioactive compound development. Reactivity index high: 2-Fluoropyridine-3-boronic acid pinacol ester with high reactivity index is used in medicinal chemistry, where it accelerates lead compound optimization cycles. |
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We have been manufacturing boronic acid derivatives for over a decade, and over those years, one thing remains clear: the increasing complexity of modern organic synthesis calls for building blocks that deliver both precision and flexibility. Among the many compounds we produce, 2-Fluoropyridine-3-boronic acid pinacol ester has distinguished itself for its unique combination of reactivity and selectivity. Our product, F3P-BAP103, serves as a linchpin for those advancing pharmaceutical research, agrochemical invention, and material science development.
Rising regulatory scrutiny and tighter control over synthetic processes drive many researchers and commercial manufacturers to seek improved alternatives to classic coupling reagents. The 2-fluoropyridine scaffold attracts attention for medicinal chemistry; the selective fluorine atom adjusts electronic distribution without the volatility seen in less stable fluorinated compounds. The boronic acid pinacol ester group opens up clean, high-yield routes via Suzuki-Miyaura cross-coupling, delivering consistent results even in the hands of less-experienced chemists.
Other analogs—boronic acids, for instance—have a stubborn tendency to self-condense or hydrolyze under ambient conditions. Short shelf life, peaky supply chain stability, and handling headaches force unnecessary distractions from the primary work in the lab. In contrast, our pinacol ester form keeps the molecule intact during storage and shipping. The crystalline powder flows smoothly and resists caking, so you can dispense and scale up batches as you need them, whether you are optimizing a gram-scale route or feeding a reactor for kilo production. We prepare F3P-BAP103 through proprietary processes tuned exclusively for moisture control and purity, resulting in minimal residual reagents and solvent traces.
Having supported hundreds of custom synthesis projects worldwide, we see demand consistently shifting toward boronates that streamline late-stage functionalization. The 2-fluoropyridine motif allows for strategic incorporation of fluorine, a substituent known to strengthen metabolic stability and tune receptor affinity in drug candidates. Paired with a boronic ester, this molecule unlocks a toolkit for aromatic substitution, extension, and derivatization. Consider the scenario of crafting kinase inhibitors or crop protection agents; subtle modifications on the ring influence downstream biological properties without cumbersome protection-deprotection steps. Our customers report fewer side reactions and more reproducible couplings, which is critical as regulatory filings demand reproducibility down to the smallest detail.
Technical staff here conduct regular analysis using both GC and NMR, and we measure purity with every lot. The typical purity exceeds 98%, as confirmed by dual testing. We take pains to avoid volatile contaminants and prioritize low water content since trace water sabotages catalytic cycles in Suzuki cross-couplings. Instead of risking scrap rates or in-process delays, you receive crystalline, dust-free powder, always sealed under inert gas. This direct focus on process quality has reduced complaints to near zero—something we take pride in, since our role as the manufacturer is to shoulder the heavy lifting so innovators in their own industries can focus on developing finished products.
Clients come to us with diverse uses in mind. F3P-BAP103 finds its way into:
We discuss scale-up regularly with process engineers who want to move from bench-scale to pilot-ready production. The high solubility in common organic solvents (THF, dioxane, toluene) supports straightforward transfer from research settings to process tanks. Thermal stability under inert conditions enables both safe storage and high-temperature couplings when synthesis calls for aggressive reaction conditions. Unlike more volatile boronic acids, our pinacol ester’s melting point is sufficiently high to prevent decomposition on storage racks, helping to maintain batch-to-batch uniformity in larger operations.
We have seen a recent wave of new entrants offering similar compounds, but several key differences set F3P-BAP103 apart. For research and production alike, minimizing impurity carryover remains crucial. Our processes utilize controlled crystallization, eliminating difficult-to-separate isomers and residual boron reagents. Tech support backs every shipment, and we routinely provide technical documents derived from our own process know-how, not boilerplate files recycled from suppliers who never see the raw material.
We choose pinacol esterification over alternate boronic ester groups because it not only improves hydrolytic stability but also delivers faster conversion in typical Suzuki reactions. Some products on the market swap in neopentyl glycol or other diols in the esterification step; our internal tests show those alternatives suffer from slower transmetalation rates, occasional gel formation, and lower tolerance to varying water levels. False economies from these variations often show up as unreproducible yields when data moves from small-batch to production environments, so our decision to stick with pinacol comes from both our own lab results and consistent customer feedback.
Many academic and start-up labs work with boronic acids supplied by middlemen who inherit mystery lots from far-off sources. Lot-to-lot consistency evaporates in that situation; unpredictable impurity profiles, puzzling byproducts, and variable color or flow create extra analytical chores for people already under pressure to deliver novel compounds or meet regulatory guidelines. We see these realities not just in competitor anecdotes but in firsthand troubleshooting for customers who struggled with off-brand materials and switched to our supply. Every vessel, reactor, and filtration step in our facility gets run through checks, not to chase paperwork compliance but to secure the purity and reactivity that experienced chemists expect.
Some downstream processes place tight limits on metal residues or foreign ions. We employ in-house purification tools—ion exchange, charcoal treatment, vanguard chromatographic systems—to reduce background contamination. The target product flows through closed-loop feeding systems, which means less ambient exposure and lower risk of extraneous particles or solvent vaporization tainting the batch. We periodically invest in staff training and invite customer feedback, tuning our process to meet specifications not only today but as regulatory or application needs evolve. When customers raise specific concerns—trace manganese or iron, for example—we answer with targeted improvements, taking real-world problems as a catalyst for upgrading processes rather than fixed cost overhead.
Shipping-sensitive materials around the globe was not always as straightforward as it is now. Not long ago, customs delays or minor moisture infiltration would jeopardize an entire order. Through persistent evolution, we now use multi-layer foil packaging and sealed drums filled with dry nitrogen—not just to tick the specification box, but to meet hard-won lessons from actual rejected shipments and downtime in client facilities. Supply reliability depends not just on robust chemical processes but also on a clear-eyed understanding of logistics, cross-border regulatory paperwork, and regional climate differences.
Sustainability issues also shape our ongoing improvement. Disposal of boron-containing process streams can set off alarms in facilities with less experience handling side-products or waste. Our in-house waste management protocols reclaim and recover boron from spent streams, minimizing environmental impact. Long-term customers share these concerns, asking not just for low-impurity products but also proofs of sustainable sourcing and responsible by-product management. Our familiarity with upstream chemical industries—fluorine, pyridine, and boron supply—gives us insight into supply bottlenecks; diversification of procurement, bulk buying agreements, and fair-pricing contracts help shield our customers from market shocks or scarcity-induced delivery delays.
Users report ease of weighing and dispensing compared to hygroscopic analogs—no clumping in scoops, no need for glovebox acrobatics for simple transfer. High recovery rates after chromatography distinguish pinacol esters made in our process from acid-terminated or liquid forms that may adhere to columns and result in poor isolation. Experienced synthetic chemists recognize the predictability of pinacol-derived boronic esters when developing parallel libraries; more adventurous functional group chemistry becomes possible because the boronic coupling partner displays broad compatibility with both electron-rich and electron-poor coupling partners.
Scale-up specialists ask about solvent compatibility as project budgets move from dozens of milligrams to multi-kilogram lots. Pinacol esters generally handle mild heat and temporary atmospheric exposure without catastrophic hydrolysis. Large batch runs, filtrations, and crystallizations align with standard pharma and agrochemical infrastructure as a result. Having gone through years of shipping and handling reviews, we offer packaging formats that preserve powder integrity right down to the last scoop in the drum. We do not overpromise on shelf life and we strongly encourage regular retesting—never hiding behind an artificial “expiry” window, but rather making sure customers have access to live, lot-specific data upon request.
Medicinal chemistry groups deploy 2-fluoropyridine-3-boronic acid pinacol ester to build up molecular libraries at a pace unthinkable even five years ago. The controlling effect of fluorine on metabolic fate combines with the versatile pyridine core—emerging as the backbone of many targeted therapies aimed at kinases and neural receptors. Our own process optimizations have led to more efficient coupling even in ligand-poor catalytic environments, which shortens route development times and reduces catalyst consumption. Clients synthesizing kinase inhibitors often cite our ester’s reliability in late-stage diversification, where cost per gram becomes secondary to process confidence and time-to-filing for regulatory dossiers.
Outside life sciences, specialty polymer and material researchers need catalytic partners with minimal trace metals and impurities, avoiding unplanned color formation or conductivity anomalies. We work directly with upstream component manufacturers to align purity standards and coordinate delivery schedules, minimizing inventory risk for their own production. Projects in organic electronics, such as OLED precursor synthesis, benefit from the durable boronic ester configuration. Our internal customer records confirm fewer rejected batches as compared to those relying solely on generic boronic acid intermediates.
Continued requests for scale-up support and technical transparency drive new features in our manufacturing pipeline. We keep options open for further customization of esters—exploring possibilities with alternative diols or mixed substitution patterns on the pyridine ring as novel syntheses demand. Data-driven decision-making wins the day: we use our own NMR and HPLC analysis to drive process improvements, not waiting for customer complaints but instead proactively upgrading batch records and control points.
Each season brings new regulatory standards or biotech trends. We remain responsive, ready to adapt packaging, documentation, or even traceability protocols as partners demand. Active knowledge-sharing—updating clients on anticipated trends, upcoming EU or U.S. regulatory changes—keeps all parties ahead of compliance or market disruption. Our vision aligns with providing not just material, but peace of mind built on real-world service and responsive manufacturing.
Over years of direct interaction with advanced research groups and production specialists, we have found that consistency and reliability matter as much as any headline innovation. Chemistry is unforgiving when it comes to impurities, sudden batch failures, or unexpected reactivity changes. 2-Fluoropyridine-3-boronic acid pinacol ester—when manufactured with careful control over raw materials, process conditions, and packaging—proves itself every time it leaves our facility and enters a customer’s workflow. Innovation rests not just on new molecules, but on the steady delivery of trusted building blocks, and our experience supports us in offering this critical reagent to the industries creating tomorrow’s solutions.