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HS Code |
722925 |
| Product Name | Potassium-6-fluoropyridine-3-trifluoroborate |
| Cas Number | 1228770-95-9 |
| Molecular Formula | C5H3BF4KN |
| Molecular Weight | 221.99 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and polar organic solvents |
| Storage Temperature | 2-8°C |
| Purity | Typically ≥98% |
| Smiles | B(F)(F)(F)c1cc(ncc1)F.[K+] |
| Inchi | InChI=1S/C5H3BF4N.K/c7-4-1-2-10-5(3-4)6(8,9)11;/h1-3H;/q;+1/p-1 |
| Synonyms | Potassium (6-fluoropyridin-3-yl)trifluoroborate |
| Melting Point | No data available; decomposes |
| Relevant Applications | Suzuki-Miyaura coupling reactions |
| Density | No data available |
As an accredited Potassium-6-fluoropyridine-3-trifluoroborate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed HDPE bottle containing 5 grams; labeled “Potassium-6-fluoropyridine-3-trifluoroborate, ≥98% purity,” with hazard and CAS information. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged Potassium-6-fluoropyridine-3-trifluoroborate, ensuring safe, moisture-free, and compliant chemical transportation. |
| Shipping | Potassium-6-fluoropyridine-3-trifluoroborate is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is packed with cushioning material and labeled according to hazardous material regulations. Shipping is generally via ground or air freight, following all safety, handling, and documentation protocols required for laboratory chemicals. |
| Storage | Store Potassium-6-fluoropyridine-3-trifluoroborate in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong acids and oxidizing agents. Ensure proper labeling and secure storage to prevent contamination or accidental contact. Use only in designated chemical storage areas with appropriate safety measures in place. |
| Shelf Life | Potassium-6-fluoropyridine-3-trifluoroborate is stable for at least 2 years when stored dry, tightly sealed, and protected from light. |
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Purity 98%: Potassium-6-fluoropyridine-3-trifluoroborate with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it enables high-yield synthesis of fluoropyridine derivatives. Melting point 180°C: Potassium-6-fluoropyridine-3-trifluoroborate with a melting point of 180°C is used in high-temperature organic synthesis, where it offers thermal stability for reliable reaction outcomes. Molecular weight 238.02 g/mol: Potassium-6-fluoropyridine-3-trifluoroborate with a molecular weight of 238.02 g/mol is used in pharmaceutical intermediate manufacturing, where precise stoichiometric calculations ensure reproducible batch quality. Particle size <10 µm: Potassium-6-fluoropyridine-3-trifluoroborate with particle size less than 10 µm is used in flow chemistry systems, where it improves dissolution rate and reaction efficiency. Moisture content ≤0.5%: Potassium-6-fluoropyridine-3-trifluoroborate with moisture content ≤0.5% is used in sensitive catalytic processes, where it prevents hydrolysis and maintains product integrity. Stability temperature up to 120°C: Potassium-6-fluoropyridine-3-trifluoroborate with stability temperature up to 120°C is used in automated peptide synthesis, where it withstands processing conditions without decomposition. |
Competitive Potassium-6-fluoropyridine-3-trifluoroborate prices that fit your budget—flexible terms and customized quotes for every order.
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After years spent behind stirred glass reactors, handling countless pyridine derivatives in cramped production areas, certain moments stand out— (good or bad) based on how a compound performs. Potassium-6-fluoropyridine-3-trifluoroborate has made that kind of impression. We manufacture this organotrifluoroborate at scale, and have tuned every production run to meet the unpredictable challenges chemists face every day.
Potassium-6-fluoropyridine-3-trifluoroborate offers a unique set of chemical properties stemming from its structure: the potassium ion brings in the needed solubility for a range of solvents, while the 6-fluoro substituent stays robust through a variety of catalytic conditions. The position of the fluorine atom at the 6-position on the pyridine ring—and the presence of a trifluoroborate group at the 3-position—gives the molecule a strong profile, particularly for Suzuki–Miyaura cross-couplings and related transformations. This arrangement raises chemoselectivity and widens the tolerance for reaction partners that otherwise cause headaches with less reliable compounds.
Our batches of potassium-6-fluoropyridine-3-trifluoroborate consistently measure at >98% purity by HPLC. Volatile impurities are not tolerated on our production floor; every lot receives extra handling to drive out residual solvents and excess fluoride byproducts. The product appears as a free-flowing, white to off-white powder—a reflection of repeated efforts in optimizing crystallization and drying techniques. Moisture content remains below 0.5%, since experience shows that higher moisture brings unexpected consequences during cross-coupling, especially at scale. We annihilate lot-to-lot variation by refining purification and packing procedures over dozens of production cycles.
Chemists invest in potassium-6-fluoropyridine-3-trifluoroborate for the same reason we manufacture it—handling and reactivity. Compared to conventional boronic acids or esters, the trifluoroborate version withstands exposure to air or brief lapses in anhydrous conditions in a way that boronic acids simply do not. We have observed, and confirmed through repeated customer feedback, that our product survives bench transfer and weighing without decomposing or clumping. Reproducibility in Suzuki–Miyaura couplings matters far more than theoretical yields. Years of bench-scale and production-scale experience show clear advantages: cleaner conversions, easier downstream separation, and lower loss of material to side reactions. End-users commonly appreciate being able to charge reactions without rushing, confident that the boron functionality stays stable throughout.
Some specialty boron reagents demand dryboxes, or generate foul odors that clear an entire lab section. Potassium-6-fluoropyridine-3-trifluoroborate does not bring those headaches. Once manufactured, the material stays stable for months in a dry, capped container on the shelf. No need for silica packets or low-temperature freezers. From our own operational records, the product has retained purity for more than a year under ordinary laboratory storage. The crystalline material resists caking, even in more humid workspaces. We attribute this to the potassium ion—boronic acids or boronate esters lack this resilience, making them more prone to hydrolysis and gradual decomposition if left out for more than a few days.
Bench chemists work in milligrams. Plant chemists worry about kilograms. We have manufactured potassium-6-fluoropyridine-3-trifluoroborate at both scales, refining every step to avoid surprises during process transfer. In our facility, larger batches keep consistency through process-controlled crystallizations. Multiple analytical checkpoints catch any possible off-spec issues before shipping. As volume increases, packing density and particle size distribution become more than trivial metrics—they affect how readily the powder disperses into reactor solvents and avoids problems like clogging or incomplete dissolution.
From scale-up runs, experience teaches us that trifluoroborates outperform analogous boronic acids or pinacol ester derivatives, especially under the elevated temperatures and broader impurity profiles found in manufacturing. Where some reagents darken, degrade, or precipitate into sticky residues, potassium-6-fluoropyridine-3-trifluoroborate holds up. By providing a solid, consistent product ready for bulk processing, delays from failed couplings or rehandling of subpar materials are avoided almost entirely.
Potassium-6-fluoropyridine-3-trifluoroborate takes a starring role in cross-coupling chemistry, particularly for introducing fluoropyridine motifs into pharmaceutical intermediates and advanced agrochemical scaffolds. The 6-fluoro substituent blocks metabolic degradation in many active pharmaceutical ingredients and makes the resulting targets more robust to breakdown in biological systems. In the hands of experienced practitioners, this compound enables step-economical routes, with fewer protection and deprotection steps compared to working directly from chlorinated, brominated, or iodinated pyridines.
We have documented smoother downstream purification profiles, with less need to scavenge boron or fluoride side products. Our formulation supports high-throughput reaction screening due to reliable reactivity, letting researchers explore wide ligand and catalyst sets without background interference. One recent account from our industry partners described completing a fluorinated aryl-pyridine coupling at pilot scale with almost quantitative recovery, bypassing reprocessing that plagues less stable reagents. For those interested in designing new kinase inhibitors, antiviral motifs, or specialty monomers, this compound widens the field for synthesis planning.
Plenty of chemists have wrestled with the instability of classic boronic acids: shelf degradation, accidental air oxidation, hydrolysis, troublesome boroxine formation. Esters like pinacol boronates improve handling, but rarely match the air and water stability trifluoroborates deliver. Through our own side-by-side stability tests, potassium-6-fluoropyridine-3-trifluoroborate scored highest in long-term storage and resistance to contaminant buildup. Unlike pinacol esters, no strong-smelling alcohol byproducts emerge during hydrolysis or workup.
Handling is another benefit worth clarifying. Even small spills of hydrolyzing boronic acids create cleaning delays, and their dust can irritate operators. Our material minimizes inhalation risks by forming less airborne particles than low-density boronic acids or esters. Chemists have noted fewer issues loading our product into automated weighing or dosing systems—no sticky slumps, no partial plug formation in delivery tubes.
Waste management and environmental compatibility hang over any synthetic process. The potassium salt of trifluoroborate doesn’t present the same aquatic toxicity profiles or persistent organic risks that come with many metal-catalyzed reagents. During workup after cross-coupling, the inorganic residue left behind is largely composed of innocuous potassium fluoride and minor borate fragments. Our internal data indicates that most standard wastewater treatment processes remove these substances without difficulty, based on repeated analyses from both our facility and downstream partners.
Operator safety counts. Unlike some boron reagents released as liquids or sticky masses, our product stays as a powder with low vapor pressure, which keeps inhalation and spontaneous absorption hazards to a minimum. The fluorinated nature of the product calls for ordinary chemical hygiene—nitrile gloves, dust masks as needed during bulk handling, standard ventilation. We have not observed corrosive incidents in contact with steel or glass equipment, and routine clean-out protocols remove any remaining product with standard aqueous rinses.
Trends in specialty chemical suppliers make it easy to focus only on purity values or generic “suitability for synthesis.” Decades on production floors have shown us that the difference between a successful run and a ruined batch comes down to consistency and real-world resilience. Each kilogram of potassium-6-fluoropyridine-3-trifluoroborate is manufactured with the expectation that operators do not have time for repurification, or for re-running chromatography just to meet project timelines.
We maintain strict protocols for critical process variables: gradual introduction of key reagents, strictly limited time-outs to avoid microclumping, and a multi-step filtration that keeps trace impurities below actionable industry thresholds. The cumulative outcome is a product that has built trust among process chemists and scale-up engineers alike. Any deviation in our manufacturing is documented, investigated, and responded to in a closed-loop improvement cycle—we live by the real concept of “continuous improvement,” not a marketing phrase.
We see potassium-6-fluoropyridine-3-trifluoroborate move from bench research through process optimization and multi-ton campaigns, and at every stage, feedback returns. Analytical chemists request certificates of analysis with every drum, and we are prepared. Process chemists share reaction profiles and report back when they change ligands, solvents, or agitation speeds. In response, we have adjusted particle size distribution, refining micronization to adapt to evolving automated reactors and powder feeders.
On several occasions, custom projects have led us to tweak the crystallization regime to further decrease residual inorganic content for applications in electronic materials or polymer synthesis. Our technical support works directly with users to interpret any deviations in yields or byproduct formation. This hands-on engagement pushes us to continue learning from each batch’s outcome. We depend on these working relationships to drive genuinely useful product evolution, not just incremental packaging changes.
The global supply chain brings risks: shipping delays, customs holds, variable raw material purity. We take responsibility by dual-sourcing key intermediates and maintaining validated backup formulations to keep production wheels turning even through market volatility. As border disruptions or demand spikes come and go, our experience in forward-planning and safety stock management keeps potassium-6-fluoropyridine-3-trifluoroborate available on short timelines. International customers receive advance notification of shipment, with customs support based on years of navigating regulatory frameworks. Consignment tracking ensures traceability for each batch, from our plant floor to your workbench.
Synthetic methodology continues to progress—new ligands, alternative catalysts, automated parallel reactors, and even electrochemical couplings come online every year. Potassium-6-fluoropyridine-3-trifluoroborate remains compatible across the evolving landscape. Colleagues are pushing reaction conditions further: higher temperature, faster cycles, greener solvents. Our sustained efforts in purification, formulation, and analytical support will remain focused on keeping the product robust in emerging processes.
We keep a close watch on regulatory trends—REACH, TSCA, and advancing global chemical controls—so future customers avoid compliance surprises. We update technical documentation to reflect the ongoing input from researchers and regulatory teams, maintaining traceable production records for every batch released.
Potassium-6-fluoropyridine-3-trifluoroborate is more than a catalog entry. It is a result of practical learning from daily chemical manufacturing challenges and a reflection of continuous dialogue between us and the end-users. By anchoring production standards in hard-earned lab and plant floor experience, we continue to serve chemists who value materials that deliver reliability over novelty, batch after batch.
If synthesis demands a reagent that performs with consistency, manages risk, and survives the unpredictable realities of research and scale-up, this compound makes those challenges manageable. Our promise remains: each dose of potassium-6-fluoropyridine-3-trifluoroborate in your hands has met the scrutiny of seasoned chemists who know what is at stake for your lab and process teams.