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HS Code |
721853 |
| Product Name | 6-Fluoro-4-Methylpyridine-3-Boronic Acid |
| Cas Number | 1266433-64-0 |
| Molecular Formula | C6H7BFINO2 |
| Molecular Weight | 202.95 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥ 95% |
| Solubility | Soluble in DMSO, methanol |
| Chemical Class | Boronic acid derivative |
| Smiles | B(C1=CN=C(C(F)C)=C1)(O)O |
| Storage Conditions | Store at 2-8°C, away from moisture |
| Synonyms | 6-Fluoro-4-methyl-3-pyridineboronic acid |
As an accredited 6-Fluoro-4-Methylpyridine-3-Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, white label detailing "6-Fluoro-4-Methylpyridine-3-Boronic Acid," 5 grams, storage instructions included. |
| Container Loading (20′ FCL) | 20′ FCL container loading: Securely packed 6-Fluoro-4-Methylpyridine-3-Boronic Acid in sealed drums/cartons, moisture-protected, compliant with shipping regulations. |
| Shipping | 6-Fluoro-4-Methylpyridine-3-Boronic Acid is shipped in tightly sealed containers under ambient or refrigerated conditions, as required for stability. The package is labeled with proper chemical hazard information and handled in compliance with local and international shipping regulations for laboratory reagents to ensure safety and prevent contamination or degradation during transit. |
| Storage | 6-Fluoro-4-Methylpyridine-3-Boronic Acid should be stored in a tightly sealed container, protected from light and moisture, and kept at room temperature (15–25°C) in a cool, dry, and well-ventilated area. Store away from strong oxidizing agents and acids. Ensure that appropriate labeling and safety precautions, such as using gloves and eye protection during handling, are observed. |
| Shelf Life | Shelf life of 6-Fluoro-4-Methylpyridine-3-Boronic Acid is typically 2 years when stored properly in a cool, dry place. |
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Purity 98%: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with purity 98% is used in Suzuki–Miyaura cross-coupling reactions, where it ensures high yield and selectivity in heteroaromatic biaryl synthesis. Molecular Weight 170.97 g/mol: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with molecular weight 170.97 g/mol is used in pharmaceutical intermediate production, where accurate stoichiometry enhances reaction efficiency. Melting Point 115–120°C: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with melting point 115–120°C is used in solid-phase organic synthesis, where thermal stability supports reliable process scale-up. Particle Size ≤ 40 μm: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with particle size ≤ 40 μm is used in fine chemical formulation, where uniform dispersion improves catalytic performance. Stability Temperature up to 60°C: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with stability temperature up to 60°C is used in storage and transport environments, where it maintains chemical integrity under moderate thermal conditions. Water Content ≤ 0.5%: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with water content ≤ 0.5% is used in moisture-sensitive synthesis, where low water levels prevent reagent decomposition. Assay ≥ 98%: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with assay ≥ 98% is used in active pharmaceutical ingredient discovery, where high assay minimizes impurities in lead compound development. Solubility in DMSO: 6-Fluoro-4-Methylpyridine-3-Boronic Acid with solubility in DMSO is used in high-throughput screening assays, where rapid solution preparation accelerates testing workflows. |
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Many chemists knock on our door looking for building blocks that solve their toughest synthesis challenges. After several years handling pyridine boronic acids in our facilities, we've learned that each small tweak in a structure means real differences in reactivity, handling, and purity. 6-Fluoro-4-Methylpyridine-3-Boronic Acid sets itself apart for researchers and manufacturers who aim to develop molecules with high specificity—especially when fluorine’s distinct effects are needed in the final compound.
Manufacturing fine chemicals from scratch demands attention to detail at every stage, and for this boronic acid, we take pride in a production route designed to eliminate unnecessary steps and minimize impurities. The molecular structure, with a fluorine atom at the 6-position opposite a boronic acid at the 3-position, and a methyl group at the 4-position, targets the balance researchers look for between reactivity and selectivity. Our production involves carefully controlled lithiation and boronation steps—each reaction monitored and adjusted with decades of hands-on experience. We don’t outsource or cut corners; employees here have seen the full picture, so real-world technical decisions flow into every kilogram we make.
If you line up all the pyridine boronic acids available, it can be tempting to think one substitution is as good as another. In our experience as a chemical manufacturer, small changes in substitution lead to significant differences in how boronic acids behave. The presence of a fluorine atom affects not only the reactivity in Suzuki cross-coupling but also the handling—it stabilizes the molecule during storage, resisting hydrolysis better than some similar boronic acids. The methyl at the 4-position shifts the electronic environment further, making it a favorite in the hands of chemical biologists exploring new leads or agrochemical developers searching for patentable analogues.
Most distributors don’t get to see the product at every stage of its life. We see firsthand how a run with inconsistent temperature leads to extra byproducts, or how water content in the starting materials affects shelf stability. So, our team constantly checks parameters like water, residual solvents, and boric acid traces. This boronic acid leaves our plant with a consistent appearance and trace impurity level so chemists don’t have to worry about batch-to-batch surprises. Time and again, we see researchers coming back needing the same molecule—at the same high standard—because nothing else fits the bill quite like this one.
Boronic acids are a staple for coupling chemistry, but not all boronic acids play nicely when the heat and pressure rise. We’re often contacted by industrial process chemists who have burned through shipments of generic material, only to find it decomposes before reaching the intended substrate. Our direct experience confirms that 6-Fluoro-4-Methylpyridine-3-Boronic Acid holds up reliably, whether you’re running high-throughput screening or developing a kilogram-scale pharmaceutical intermediate.
Over the years, we’ve collaborated with partners scaling from a milligram to a multi-kilogram process. They tell us the handling characteristics matter: purity influences yields, but so does the behavior of the boronic acid under repeated heating-cooling cycles. This particular compound arrives as a solid, so labs can weigh and dispense with minimal static, even in humid environments. Real-world verification of melting point and NMR spectra means quality controls here match what the end-user sees. Running into a failed coupling means lost hours. That’s why the consistent reactivity and stability of our product keep operations on schedule.
In the field, we’ve engineered and produced a wide array of pyridine boronic acids. What stands out with this variant is how the electronic effects influence cross-coupling selectivity. Some boronic acids, especially those without a fluorine, perform less predictably when met with challenging halogenated partners. By contrast, the electron-withdrawing fluorine in 6-Fluoro-4-Methylpyridine-3-Boronic Acid stabilizes the boronic acid, so side reactions—protodeboronation, homocoupling—occur with lower frequency. This helps reaction planning, especially when precious substrate is at stake.
One distinct benefit we’ve observed is the improved solubility profile in polar organic solvents. Traditional phenyl and unsubstituted pyridine boronic acids can crash out or decompose in protic media. Our compound retains sufficient solubility for reliable dosing, whether you’re working up a Suzuki-Miyaura coupling or tinkering with new palladium catalyst systems. From direct conversations with bench chemists, we know subtle handling issues balloon into headaches on production lines—so this boronic acid, with its solid handling and robust chemical properties, often wins the head-to-head evaluation on live processes.
Having worked with medicinal chemists on projects from exploratory screens to clinical APIs, we’ve seen demand for pyridine-based fragments skyrocket. The trend in drug development leans toward fluorinated building blocks; the subtle presence of fluorine changes both metabolic fate and binding affinity in lead candidates. Our 6-Fluoro-4-Methylpyridine-3-Boronic Acid appears frequently on hit lists for kinase inhibitors, antiviral scaffolds, and crop protection leads. Feedback from pharma process scale-ups often points to the reproducible yield and minimal byproduct profile—the differentiation needed to move forward with scale-up and regulatory filings.
It’s not just the pharmaceutical space. Agrochemical researchers, as well as material science teams, approach us looking to introduce pyridine moieties with controlled electron density and sterics. We’ve seen several patents cite this specific boronic acid as a core fragment for next-generation pest resistance agents or photostable materials. The consistency of our in-house product shortens development cycles. Institutions working on specialty polymers also recognize how the fluorine substituent modulates photophysical properties, helping produce materials with tailored emission or absorption characteristics.
Customers often ask about lot-to-lot reproducibility. Working the batches ourselves, our operators and QC chemists have built up an internal library of how condition tweaks impact purity and performance. Small changes—reactor temperature, rate of boronation, solvent moisture—change impurity profiles and yield. Only through experience can manufacturers spot the tell-tale signs early enough, adjusting controls long before the product hits packaging. This attention shows in our analytical data and helps customers avoid the frustration of unexpected impurity spikes or variable reaction profiles.
Direct customer relationships mean we routinely receive feedback on performance in real-world processes. We act on it, tweaking our in-process controls, updating our analytical specifications, and confirming our product’s fit to exacting needs—be they milligram screens or ton-scale productions. When a pharmaceutical partner points out a performance issue in a cross-coupling, our line chemists dig into retained samples, compare spectral data, and track subtle shifts back to their roots. Running a plant from reaction through isolation offers that window of control—one traders or brokers simply can’t provide.
The boronic acid functional group presents its share of challenges. It’s sensitive to hydrolysis and oxidation, often giving headaches in storage or upon shipping, especially with ambient humidity swings. After dozens of failed experiments and customer calls, we stopped relying on one-size-fits-all packaging. Our boronic acids get packed under argon in air-tight HDPE containers, minimizing decomposition and keeping moisture out. We’ve also developed transfer recommendations proven during routine audits: zero headspace handling, desiccator storage, and routine monitoring of container integrity.
To further boost shelf life, we track each lot’s degradation profile using both NMR and HPLC. If minor boric acid formation creeps in during stability studies, we identify the batch conditions responsible and tighten in-process controls. By paying attention to the storage environment, we keep our material at specification for longer shelf times, which benefits both in-house and customer-held inventories. The result is a product that not only ships well but also holds up during the long haul of multi-stage syntheses. Researchers get the confidence their intermediates won’t degrade before completion of critical steps.
Talking about sustainability isn’t just for press releases in our manufacturing world. Handling boronic acids generates boron-containing waste streams that can’t simply be flushed away. We actively monitor and treat our effluents, capturing boron species and reducing environmental impact. This operational change grew from staff-led initiatives—people here noticed trends in waste output and drove the push for ion-exchange-based treatment tanks and solvent recycling. Over the past five years, we cut boron discharge, improved solvent yields, and reduced the amount of hazardous material shipped from the plant.
Safe operations mean far more to us than simply passing a regulatory inspection. Each production campaign involves extensive risk assessment: storage at low humidity, protective gear for everyone in the isolation suite, and specific training in handling powders that may emit small amounts of volatile organics. Our lab and plant teams support each other, quickly sharing observations and preventing problems before they snowball—such as catching small temperature exotherms early, or stopping a shipment if a drum seal isn’t perfect.
In a facility where employees cross paths with boronic acids on a daily basis, vigilance and training are the only way to keep work injury-free and the product up to grade. We perform regular refresher hazmat drills and review real-world near-misses as a team. These aren’t abstract policies—they grew out of decades of handling similar molecules and learning from the close calls that come with scaling up new intermediates.
We’re the first to admit that not every customer project goes according to plan. Sometimes high throughput screens demand unusual purity specs; other times custom particle sizes unlock new filtration steps. Our staff includes chemists from the same fields as our customers, so we handle requests for custom synthesis, impurity profiling, or material modification with insight—and a healthy respect for deadlines. Labs hit snags when material solubility, stability, or reactivity doesn’t match expectations. People here have talked process chemists through procedure fine-tuning or suggested tweaks to isolation practices, drawing on hundreds of pilot-scale and production-scale runs.
Communication matters. From order to shipping, plus any troubleshooting calls after delivery, anyone buying directly from the manufacturer sees firsthand how invested we are in their success. When customers bring us a bottleneck in a downstream transformation, we run head-to-head trials or sample purifications on site instead of just reading from a spec sheet. That dialogue lets us fine-tune for the next order, building a feedback loop that improves not just our compound, but the process for everyone involved.
Making chemicals at this level isn’t just about finishing orders or shipping containers. It’s about listening to the users—the ones testing new catalysts, the ones developing the medicine or crop protection product that will make a difference in the real world. The importance of highly functionalized boronic acids like 6-Fluoro-4-Methylpyridine-3-Boronic Acid keeps growing, and the challenges around supply, quality, and reliability won’t disappear.
Companies have options, but working with a manufacturer who lives with the process—who remembers when a trial batch didn’t pan out, or who can follow a question about impurity spikes back through the paperwork and into the reactor records—changes results at scale. The lesson we learned again and again: every boronic acid has its quirks. When a material gets this popular in drug, crop, and material development, details of production, testing, and support make all the difference. By keeping manufacturing expertise and feedback loops close to the product, we deliver not just a chemical, but direct, actionable value to anyone building the next breakthrough.