2-Fluoro-6-methylpyridine-5-boronicacid

    • Product Name: 2-Fluoro-6-methylpyridine-5-boronicacid
    • Chemical Name (IUPAC): (2-fluoro-6-methylpyridin-5-yl)boronic acid
    • CAS No.: 883521-22-2
    • Chemical Formula: C6H7BFNO2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    621512

    Product Name 2-Fluoro-6-methylpyridine-5-boronic acid
    Cas Number 864377-12-4
    Molecular Formula C6H7B F N O2
    Molecular Weight 152.94
    Appearance White to off-white solid
    Purity Typically ≥97%
    Melting Point 130-135°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Smiles B(C1=CN=C(C=C1F)C)(O)O
    Inchi InChI=1S/C6H7BFNO2/c1-4-2-5(7(10)11)3-9-6(4)8/h2-3,10-11H,1H3
    Storage Conditions Store at 2-8°C, protected from moisture
    Synonyms 5-Boronic acid-2-fluoro-6-methylpyridine

    As an accredited 2-Fluoro-6-methylpyridine-5-boronicacid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g bottle of 2-Fluoro-6-methylpyridine-5-boronic acid is packaged in a sealed amber glass vial with a screw cap.
    Container Loading (20′ FCL) 20′ FCL container is loaded with securely packaged 2-Fluoro-6-methylpyridine-5-boronic acid, ensuring protection during transit.
    Shipping 2-Fluoro-6-methylpyridine-5-boronic acid is shipped in a tightly sealed container under ambient conditions. The packaging is designed to prevent moisture exposure and contamination. All shipments comply with applicable regulations for chemical transport, including labeling and documentation, ensuring safe and secure delivery to laboratories or industrial users.
    Storage 2-Fluoro-6-methylpyridine-5-boronic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents. Store at room temperature or as specified by the manufacturer, and avoid excessive heat. Ensure proper labeling and follow all safety guidelines for handling boronic acids.
    Shelf Life 2-Fluoro-6-methylpyridine-5-boronic acid should be stored at 2-8°C, protected from moisture; shelf life is 12-24 months.
    Application of 2-Fluoro-6-methylpyridine-5-boronicacid

    Purity 98%: 2-Fluoro-6-methylpyridine-5-boronicacid with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it enables high-yield formation of arylated pyridines.

    Melting Point 184°C: 2-Fluoro-6-methylpyridine-5-boronicacid having a melting point of 184°C is used in pharmaceutical intermediates synthesis, where it ensures thermal stability during reaction processes.

    Particle Size <50 μm: 2-Fluoro-6-methylpyridine-5-boronicacid with particle size less than 50 μm is used in fine chemical manufacturing, where it facilitates superior dissolution rates in organic solvents.

    Moisture Content <0.3%: 2-Fluoro-6-methylpyridine-5-boronicacid with moisture content below 0.3% is used in agrochemical research, where minimal hydration prevents unwanted side reactions.

    Stability Temperature up to 40°C: 2-Fluoro-6-methylpyridine-5-boronicacid stable up to 40°C is used in research and development laboratories, where it allows for extended storage without degradation.

    HPLC Assay ≥99%: 2-Fluoro-6-methylpyridine-5-boronicacid with HPLC assay of ≥99% is used in catalyst development, where its high chemical integrity improves reaction reproducibility.

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    Certification & Compliance
    More Introduction

    2-Fluoro-6-methylpyridine-5-boronicacid: A Manufacturer’s Perspective

    Introduction to 2-Fluoro-6-methylpyridine-5-boronicacid

    At our chemical manufacturing facility, 2-Fluoro-6-methylpyridine-5-boronicacid stands out as a specialty intermediate that we’ve learned to approach with careful attention. After spending years developing and scaling up production methods for pyridine derivatives, our team recognizes the challenges and rewards tied to this material. Our batch-to-batch consistency relies on diligence, effective purification, and strict quality controls that draw upon both practical know-how and robust data collection. This compound, with its distinct structure featuring a fluorine atom at position two and a methyl group at position six, aligned around the crucial boronic acid moiety, holds a role in pharmaceutical and agrochemical research pipelines because of its unique reactivity profile.

    What Sets Our Product Apart

    One of the lessons learned from manufacturing boronic acids is that impurities can silently undermine downstream reactions. We see this firsthand when researchers approach us after experiencing setbacks with other sources. Our synthesis routes focus on minimizing regioisomeric byproducts and potential fluorine scrambling. Crystallization parameters shape the purity, and our real-world production scale introduces variables that lab-scale batches rarely face—humidity, agitation speed, solvent ratios. Ninety-nine percent purity is more than a number; it’s the reflection of months of stability data and countless HPLC traces.

    We never consider the work finished with a single COA. Our labs keep a reference archive for each lot, enabling traceability years later if customers report unexpected side products or solubility concerns. Many chemists never notice these details until a scale-up fails, or a cross-coupling runs below yield expectations. Our staff understands the consequences: lost weeks, wasted catalyst, frustrated teams. So, we continue to re-examine each step, always ready to tweak processes if find traces of over-oxidation or if an unknown peak appears against baseline.

    Handling and Practical Use

    Our customers most often use 2-Fluoro-6-methylpyridine-5-boronicacid as a building block in Suzuki-Miyaura cross-couplings. The fluoro-substitution increases the challenge, demanding clean reaction conditions and consistent reactivity from the raw material. Over the years, we’ve witnessed projects unravel because a boronic acid diverted into side reactions or decomposed due to slight instability. What we do at the plant, from ensuring dry glassware to controlled inert gas blanketing, gives medicinal chemists more reliable results on their end. Sharing our experience, we advise avoiding long-term storage at room temperature. Fridge or freezer storage preserves its reactivity, especially if moisture is excluded.

    During development, our R&D chemists refined particle size distributions for improved dissolution in common solvents. Too fine, and dust presents handling challenges. Too coarse, and the product sits undissolved at the flask’s bottom, slowing reactions. We continue to adjust mill settings and sieve cutoffs to keep the product within a window that experienced technicians favor. These lessons come from feedback—no material, regardless of theoretical purity, meets expectations unless it flows, weighs, and dissolves as needed on the bench.

    How 2-Fluoro-6-methylpyridine-5-boronicacid Differs from Other Boronic Acids

    Experience reveals subtle but important differences between closely related boronic acids. Adding a fluorine atom alters both the electronic character and the handling precautions. Certain analogs, such as 6-methylpyridine-5-boronicacid (without fluorine), display different reactivity under standard coupling conditions, often yielding lower selectivity or requiring different bases and ligands. We’ve tested this compound side by side with its non-fluorinated cousins, observing faster reaction times and, occasionally, greater yields, especially in heterocycle synthesis where electron distribution matters.

    Colleagues in scale-up appreciate the compound’s resistance to oxidative degradation—a direct benefit from the electron-withdrawing nature of the fluorine substituent. Unlike boronic acids with more labile hydrogen or alkyl groups, our product maintains its integrity through standard purification and reaction work-ups. That stability also reduces the risk of protodeboronation, a common headache in palladium-catalyzed couplings. Having supplied metric tons of boronic acids for industrial partners, we’ve seen how small differences in starting material stability translate to significant impacts in finished product quality and operational uptime.

    Many users ask about solubility: our product dissolves well in polar aprotic solvents such as DMF or DMSO, and performs reliably in mixed aqueous-organic systems. The added fluorine tends to modestly lower solubility in pure water compared to a hydrogen analog, but we’ve documented no significant issues when following established solvent systems for cross-coupling. Our technical team stands ready to support with detailed solubility graphs based on customer process needs.

    Production and Quality Challenges from the Factory Floor

    Producing boronic acids at scale tests a plant’s ability to juggle safety, efficiency, and trace impurities. Every step, from reagents to packaging, introduces opportunities for contamination. Some customers may overlook how easily boronic acids can pick up micro-amounts of palladium, copper, or other transition metals from shared equipment lines. We dedicated specialized reactors and glassware for our pyridine lines, investing time and capital to avoid cross contamination. Our process analysts check for trace metals by ICP-OES in every lot, aiming for levels well below what regulatory agencies require for finished pharmaceuticals.

    Another real-world hurdle involves exclusion of water. Boronic acids are notorious for forming cyclic anhydrides or esters if exposed to uncontrolled moisture during crystallization. Too dry, and yield suffers; too wet, and shelf stability plummets. We train our operators on recognizing the subtle cues that signal a moisture incident—from slightly clumpy cake to abnormal filtration rates. Our warehouse maintains humidity controls, and packaging lines double-seal outgoing product using both inert gas purging and vacuum-tight pouches. These safeguards result from analysis of returned materials and lessons learned over years of troubleshooting.

    Shipping represents another test. Many boronic acids degrade if exposed to temperature cycles or if packaging develops micro-leaks. Our logistics coordinators oversee temperature documentation and container selection, and we periodically review transit studies to catch failures before they impact customer labs. Sharing what works, we advise procurers to unpack and refrigerate material promptly, discarding partially used containers within three months. We believe this transparent communication prevents downstream problems, helping chemists focus on discovery instead of re-ordering.

    Supporting Modern Chemistry With Experience-Driven Solutions

    We see ourselves as partners in innovation, not just suppliers. Over the last decade, as research into fluorinated aromatic compounds has intensified, our team received frequent requests for scale-ups and custom purifications. Our technical specialists work shoulder-to-shoulder with customer teams, optimizing synthetic protocols and troubleshooting bottlenecks in scale transition. This real-time collaboration leads to advances in catalyst economization and waste stream reduction. Drawing on plant trial data, we’ve recommended new quenching agents or in-line scavenging that simplifies downstream work-ups or reduces by-products.

    Every kilogram we dispatch carries a legacy of process improvement. As new green chemistry initiatives emerge and regulations tighten, we keep our eyes on solvent footprint and process water reclamation. Our production engineers adjust workflows to limit hazardous solvent usage, introducing greener alternatives when pilot data supports it. For example, switching from traditionally chlorinated solvents to more benign options when compatible, or investing in on-site solvent recycling for the most common process streams. Sustaining these improvements demands long-term commitment, not theoretical best wishes.

    Many of the custom requests we receive target advanced intermediates or unique analogs, often for established pharmaceutical discovery programs. We routinely check for nitrosamine precursors, residual solvents, and polynuclear impurities out of an abundance of caution, acting before regulatory edicts arrive. Decisions at the plant level directly uphold trust: when our customers succeed in registration or clinical advancement, we see the payoff of our vigilance.

    Addressing Real-World Concerns: Supply Chain Security, Safety, and Sustainability

    Supply chain interruptions taught us the value of local oversight. By controlling every step from sourcing raw materials to final packaging, we reduce unknowns that third-party brokers introduce. This control allows rapid lot tracing if an issue arises, such as a batch failing to meet reactivity benchmarks. Over the years, customers called us at odd hours, seeking clarification about batch origins, possible contaminants, or documentation. Responding with real-time data and transparent practices cements our relationships. In our plant, information doesn’t get hidden in slow bureaucracy.

    Our safety culture extends to end users. Experienced operators emphasize the hazards tied to incorrect handling or scale-up errors. They understand not all users possess full chemical hazard training, so outreach materials supplement package inserts, providing context to new hires or less experienced chemists. Through experience, we saw that prep work—pre-weighing, planning for moisture exclusion, segregating workspaces—minimizes incident rates. Regular audits and staff refreshers on chemical hygiene strengthen these protective measures. Compliance grows from the floor up, with feedback loops ensuring protocols match real-life conditions.

    Sustainability impacts every decision. We build waste management and solvent recovery into process design. Upcoming years will demand even greater process intensity and lifecycle scrutiny. We participate in industry group initiatives to track and share progress, benchmarking our outcomes against peers. Feedback from customers informs our process improvements: every technical support ticket or unusual request offers a new angle for business evolution.

    Looking Forward: Innovation and Responsiveness

    Markets for fluorinated heterocyclic building blocks grow each year, as new therapeutic targets and crop protection agents demand increasingly complex scaffolds. Real-world innovation in our field arises from meeting those evolving needs, not chasing abstract trends. Our scientists work closely with customers and regulatory affairs offices, balancing progress with safety. Each time we invest in process automation, advanced inline analytics, or smarter solvent use, the goal is to support not just today’s projects, but the next wave of discovery as well.

    Truth emerges from experience. It teaches that making high-quality 2-Fluoro-6-methylpyridine-5-boronicacid means more than following recipes. It means questioning every unexpected HPLC peak, every report of inconsistent physical form, every anomaly in reactivity. Customers taking these details for granted benefit from standards developed by years of daily problem-solving, process reviews, and honest dialogue between plant and bench. This spirit of learning permeates our operation and keeps quality moving forward.

    Conclusion: Our Commitment in Every Batch

    Our story with 2-Fluoro-6-methylpyridine-5-boronicacid reflects decades of lessons from chemical manufacturing. Every challenge—whether rooted in purity, stability, or safety—offered us an opportunity to refine, upgrade, and share those improvements with scientists pushing the boundaries of knowledge. We don’t separate the product from its journey: the involvement of skilled operators, the vigilance of analysts, the practical insights of engineers all build a foundation of reliability. By recognizing both the opportunities and pitfalls of making boronic acids, we help research move ahead, one reaction, one molecule, one partnership at a time.