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HS Code |
221099 |
| Chemical Name | 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C12H17B FNO2 |
| Molecular Weight | 237.08 g/mol |
| Cas Number | 1000330-48-8 |
| Appearance | White to off-white solid |
| Purity | Typically ≥97% |
| Melting Point | 51-54°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, chloroform) |
| Smiles | CC1=NC=C(B2OC(C)(C)C(C)(C)O2)C=C1F |
| Inchi | InChI=1S/C12H17BFNO2/c1-8-10(13-15-11(2,3)16-13)5-6-12(14)7-9(8)4/h5-7,13H,1-4H3 |
| Storage Temperature | 2-8°C (refrigerated) |
| Synonyms | 2-Fluoro-6-methyl-3-(pinacolboronate)pyridine |
As an accredited 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 1 gram of 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, sealed, labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine: securely packed drums/pallets, optimized for safe international transit. |
| Shipping | 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is shipped in tightly sealed containers under inert atmosphere, away from moisture and heat. It is packaged according to regulatory standards for organic reagents, ensuring safety during transit. Shipping includes appropriate labeling and documentation for chemical handling and storage requirements. |
| Storage | Store **2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** in a tightly sealed container, under an inert atmosphere (such as nitrogen or argon), and in a cool, dry place away from moisture and direct sunlight. Avoid exposure to air and strong oxidizers. Recommended storage temperature is 2-8 °C (refrigerated). Handle in a well-ventilated area using appropriate personal protective equipment. |
| Shelf Life | Shelf life of 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is typically 2 years when stored properly. |
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Purity 98%: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side product formation. Melting point 90-94°C: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 90-94°C is used in organic coupling reactions, where it enables precise temperature-controlled processing. Molecular weight 263.13 g/mol: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine at a molecular weight of 263.13 g/mol is used in boronic acid cross-coupling reactions, where it supports accurate stoichiometric calculations. Stability temperature up to 120°C: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with stability up to 120°C is used in high-temperature Suzuki-Miyaura reactions, where it maintains structural integrity during prolonged heating. Particle size <50 µm: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size below 50 µm is used in automated solid-dispensing systems, where it facilitates uniform blending and rapid dissolution. Moisture content <0.5%: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with moisture content below 0.5% is used in moisture-sensitive synthesis protocols, where it minimizes hydrolytic degradation. HPLC assay ≥99%: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with an HPLC assay of at least 99% is used in high-precision material synthesis, where it guarantees consistent purity across production batches. Residual solvent <0.1%: 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with residual solvent below 0.1% is used in electronic material manufacturing, where it prevents contamination of sensitive components. |
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Every day, in our manufacturing facility, new molecules bring new opportunities and puzzles. Much of our time goes into getting to know each compound closely—figuring out its quirks, appreciating its value, and understanding the real work it can accomplish in laboratories across the globe. In this line of work, 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine often finds itself in the thick of high-impact synthetic sequences. For chemists refining their Suzuki-Miyaura coupling reactions, this boronic ester stands out for both its chemical structure and practical handling. It’s not just another entry in a catalog page; every batch we make arrives with its own back story—one shaped by the skills of our team, the raw materials we use, and the feedback we get from the bench scientists doing the real discovery.
In any chemical manufacturer’s inventory, you’ll see a growing demand for complex, functionalized pyridines. We pay attention to the chemistries that matter most right now. In medicinal chemistry and agrochemical synthesis, small changes to a core ring produce big jumps in biological properties. 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine delivers a useful combination of fluorine, methyl, and boron substitutions. The fluorine atom on the pyridine ring brings more than electronegativity—it influences binding affinity in drug molecules and frequently moderates metabolic pathways in vivo. The methyl group at the 6-position of the pyridine core alters not only chemical reactivity but also solubility profiles. Add to that the robust 4,4,5,5-tetramethyl dioxaborolane group, and now you have a boronate with shelf stability—even over several months under ambient air.
Making this compound in our factory isn’t a process of automation. Each batch receives attention, driven both by our quality systems and the real-world application data our customers provide. Chemists count on reliable boronate esters to survive shipping and storage before the all-important coupling step. Stories circle back to our lab about reactions that ran for days or nights, where the stability and purity of our boronate were not just convenient but crucial. Shelf-stable doesn’t just mean that the bottle sits around without complaint—it means that the precious, often costly, substitution chemistry on the pyridine ring actually arrives intact, unspoiled and ready to do work.
Fluorinated pyridines offer a unique toolkit. Teams in biotech or crop science rarely find the perfect scaffold without a few rounds of trial and error—structure-activity relationships demand exploration in every direction. This compound, with its fluorine and methyl patterning, introduces a twist to core heterocycles, offering nuanced shifts in electron density. In practice, we have watched researchers tune kinase inhibition or tweak receptor binding simply by moving a substituent from the 4- to the 6-position of the pyridine. Altering a methyl group or incorporating a seldom-used boronate sometimes unlocks activity in unexpected places.
Inside the factory, our chemists understand how moisture content, lot-to-lot color shifts, and subtle impurities create headaches at scale. Batch after batch, the challenge isn’t just purity alone, but also minimizing side products likely to linger from the aryl lithium or palladium-catalyzed steps in the synthesis. Many competitors offer catalog compounds with technical specifications—a minimum 96% purity, trace boronic acid residue, HPLC retention times listed in a line. Our work never stops at paper numbers. We test batch stability by exposing vials to room light, lab air, or elevated heat, because in the real world, those are the conditions bottles live through. Feedback loops with R&D teams and process scale-up groups help us stay ahead of pitfalls—whether that’s unexpected crystallization during transit or residual traces affecting downstream analytics.
Interest in boronic esters of this type often spikes as new heterocyclic drugs enter discovery pipelines. Many modern kinase inhibitors, anti-infective agents, and CNS-targeting compounds exploit pyridine cores due to their ability to act as hydrogen bond acceptors or fit within protein pockets. Adding a fluorine, in particular, can modulate pKa, electron density, and lipophilicity. Those of us in manufacturing see real impact—from pilot plant runs to custom kilo projects—because each order serves a new generation of chemists pursuing the next big idea.
This molecule supports Suzuki couplings that need both mild conditions and robust yields. Not every aryl boronate stands up to moisture or slight temperature drifts. We have refined our synthesis and purification to deliver material that remains a free-flowing, easy-to-handle solid, resisting the tendency of some boronic acids to clump or cake over time. Packaging in moisture-resistant containers preserves both material integrity and morale in the busy med chem lab. It’s a small touch that comes directly from hands-on experience: nobody wants to chisel a lump out of a bottle while deadlines for SAR studies loom.
Chemists making complex molecules often have choices among several building blocks. Why pick 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine and not a plain 2-pyridyl boronic ester, or its difluoro cousin? The answer runs deeper than simple price differences or catalog listings. Strategic fluorination can mean the difference between a clinical candidate and a failed lead. Our customers tell us that swapping fluorine onto the 2-position shifts binding interactions subtly, but enough to pop onto a hit list after weeks of screening. The 6-methyl further tweaks metabolic stability—a detail often missed in early-stage screens but vital to scale-up and animal studies.
Compared to 2-pyridyl boronic acids, which can be air-sensitive and prone to hydrolysis, the dioxaborolane ester provides enhanced handling and longer bench life. Growing demand for functionalized boronates (especially from process chemistry groups avoiding troublesome protodeboronation) keeps us tuning both process yields and analytical controls. Our team devotes considerable toil into minimizing residual metal contamination, peroxide byproducts, and unwanted regioisomers. These details might look minor in a specification sheet, but they shape every downstream reaction, purification, and analysis.
In a manufacturer’s lab, it’s easy to see where real challenges crop up. Subtle steps—like controlling the lithiation at the correct position on the fluoropyridine ring or maintaining reagent temperature profiles—make all the difference in yield and purity. From the start, we emphasize high-quality raw materials. The tedium of dried glassware, nitrogen atmosphere gloveboxes, and carefully titrated butyllithium improves batch reproducibility. Those steps cost extra hours, but quality upstream pays off downstream. Our chemists obsess over limiting exposure to moisture at every stage, because small leaks translate directly to lost product and, worse, unpredictable impurity profiles. Careful work with NMR and LC/MS lets us track impurities at the ppm level and root out culprits that common QC might miss.
By focusing on the synthetic pain points in both core and scale-up reactions, we’ve learned to anticipate where most production stalls occur. Sometimes a customer requests a single kilogram; other times, it’s tens or hundreds. We adjust our lot sizes, cooling regimes, drying protocols, and handling instructions so that nobody finds themselves with unusable material because of an avoidable processing slip. These practices grow not just from SOPs, but from factory-floor troubleshooting and unglamorous details like real-time monitoring of vacuum oven loadings. We appreciate every aspect of the supply process—down to how powders settle in liners and the effects of vibration on packaging during international shipping.
At the heart of supporting research is accessibility and consistency. Synthetic chemists rarely have time to vet every reagent’s provenance—they need reliable lots that align from bench scale to multi-kilos. Our technical support often fields questions about reaction compatibility, side-chain protecting groups, or tricky solvent systems. Rather than push a sale, we talk shop with researchers about their specific route—their experience informs our next round of product improvement. For example, scale-up runs sometimes show exotherms not obvious at milligram scale, or batch heterogeneity that escapes initial screen. Having a factory team that understands both chemical reactivity and industrial realities makes a difference in outcome.
Handling feedback with humility and detail distinguishes a manufacturer from a catalog seller. When teams struggle with long-term shelf life or spot batch inconsistency after international transit, we dig into root causes—modifying solvent ratios, retooling crystallization steps, or changing drying conditions. These decisions get logged and shared, not just for tracking, but to keep our promise of transparency. We see ourselves as partners in the synthetic journey, bringing our know-how about shipping, storage, recrystallization, and contamination risks into the problem-solving process.
Making multi-functional boronates brings a unique environmental responsibility. Our teams have watched solvents leave the plant doors, remembered where residual reagents landed, and kept tabs on the latest guidance for disposal or recycling. In manufacturing 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, we optimize for minimal waste—a tough ask with modern fluorination chemistry, where reagents can be particularly aggressive. Decisions about solvent switches, water recycling, and reaction condition tweaks reflect both industry best practice and on-the-ground reality. We’ve invested in scrubbers, improved batch quenching, and safer workup protocols because those matter as much to us as they do to staff and customers.
From a safety perspective, every process of handling, storing, and transferring boronates gets reviewed and updated as new information emerges from the literature or our own experiences. At scale, we see the hazards that rarely make it into academic reports—dust generation during powder handling, low-level peroxide formation in prolonged storage, and risk mitigation when handling multi-kg batches of flammable solvents. Our staff gets ongoing training not just because it’s required, but because we’ve experienced the before-and-after difference in incident rates and confidence when people are in the loop about the hazards intrinsic to each new molecule.
Time and again, synthetic teams share their stories with us—a crucial reaction sequence that succeeded with a robust boronate, a shipment that kept integrity despite a long customs hold, a medicinal chemistry campaign that picked up speed because reliable batches showed up on time. We take those stories to heart, using each to re-examine our own logistics and production routines. Being able to trace a product back through each step of its creation is more than a compliance exercise for us. It’s about assuring the next user—never just a customer number but a real person in a real lab—that their starting material won’t let them down in a crunch.
Every detail matters, from the tightness of the cap to the clarity of labeling. We’ve experienced frustration with ambiguous bottle identification and slow responses to technical queries; so our team aims to deliver clarity—not only through product quality but through a willingness to have honest, technical conversations on the nitty-gritty of chemical synthesis. When tweaks or customizations make sense, we accommodate those requests to match developing research or process needs. This flexibility comes from a deep familiarity with both our product and the wide-ranging applications it supports.
In our factory, transparency is not a marketing phrase but a daily habit. QA logs and batch records are open to internal peer review, and customer requests for lot-specific data receive prompt responses. Any mistakes or deviations are acknowledged, tracked, and resolved with urgency—our reputation with researchers and process chemists relies on trust built through years of reliability and openness. In a world where sourcing is complex and supply lines are under pressure, giving users a clear line back to manufacturing helps them plan and troubleshoot. We never pretend away a challenge; instead, we share what we’ve learned and ask for feedback.
This openness extends to intellectual property, regulatory issues, and research partnership. Working with both established pharmaceutical companies and fast-moving biotech startups keeps us sharp. We update our knowledge of compliance requirements with changing local and international guidelines, integrate the latest reporting tools, and prioritize the confidentiality of all client-supplied information—backed by standard industry agreements and plain good practice. We are proud of our role in supporting innovative science without over-promising or hiding behind jargon.
While the demand for specialty boronates like 2-Fluoro-6-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine continues to grow, we keep our focus on listening, learning, and investing in improvement. Whether that means better containment for moisture-sensitive products, adapting packing lines to meet custom requests, or building out data systems for enhanced tracking, each step grows from an ongoing relationship with the research community. We track new developments in reaction methodology and stay close to academic and industrial trends, aiming to provide not just a product, but a partnership that lasts the entire research journey.
Every bottle that leaves our production floor reflects years of cumulative experience—drawing together the skill of our plant chemists, the vigilance of our QC team, the adaptability of our packers, and the insight of the scientists in the field who rely on our materials. Our aim is for this compound, and every other that follows it, to carry forward the best traditions of chemical manufacturing—openness with data, respect for safety, and a long-term commitment to the people using the chemistry to make a difference.