2-Hydroxy-5-fluoropyridine

    • Product Name: 2-Hydroxy-5-fluoropyridine
    • Chemical Name (IUPAC): 5-Fluoropyridin-2-ol
    • CAS No.: 766-16-1
    • Chemical Formula: C5H4FNO
    • Form/Physical State: Powder/Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    396807

    Chemicalname 2-Hydroxy-5-fluoropyridine
    Molecularformula C5H4FNO
    Molecularweight 113.09 g/mol
    Casnumber 766-16-1
    Appearance White to off-white solid
    Meltingpoint 82-86 °C
    Boilingpoint 237 °C
    Density 1.34 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=NC=C1O)F
    Inchi InChI=1S/C5H4FNO/c6-4-1-2-5(8)7-3-4/h1-3,8H
    Storageconditions Store in a cool, dry place, tightly closed
    Purity >98% (typical)
    Refractiveindex 1.589 (predicted)
    Pka 7.2 (for the hydroxy group)

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

    Packing & Storage
    Packing The packaging for 2-Hydroxy-5-fluoropyridine (5 g) is a sealed amber glass bottle with a tamper-evident screw cap.
    Container Loading (20′ FCL) 20′ FCL container can load approximately 12–14 MT of 2-Hydroxy-5-fluoropyridine, packed in 25 kg HDPE drums or bags.
    Shipping 2-Hydroxy-5-fluoropyridine is shipped in tightly sealed containers, protected from moisture and light, and labeled according to chemical safety regulations. Packaging ensures chemical stability and prevents leaks or contamination. Appropriate documentation, including Material Safety Data Sheets (MSDS), accompanies the shipment. Transport complies with all applicable local and international hazardous material shipping guidelines.
    Storage 2-Hydroxy-5-fluoropyridine should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. It should be kept separate from incompatible substances such as strong oxidizers. Proper labeling and secondary containment are recommended to prevent leaks or spills. Use personal protective equipment during handling to avoid inhalation and contact.
    Shelf Life 2-Hydroxy-5-fluoropyridine typically has a shelf life of 2-3 years when stored in a cool, dry, and airtight container.
    Application of 2-Hydroxy-5-fluoropyridine

    Purity 99%: 2-Hydroxy-5-fluoropyridine with 99% purity is used in pharmaceutical intermediate synthesis, where high chemical yield and minimal side reactions are achieved.

    Melting point 154°C: 2-Hydroxy-5-fluoropyridine with a melting point of 154°C is used in organic electronic material development, where it provides thermal stability during device fabrication.

    Molecular weight 115.09 g/mol: 2-Hydroxy-5-fluoropyridine at 115.09 g/mol is used in agrochemical research, where precise molecular compatibility with target compounds is required.

    Stability temperature up to 120°C: 2-Hydroxy-5-fluoropyridine with stability up to 120°C is used in high-temperature catalytic reactions, where consistent reaction rates and reduced decomposition are observed.

    Particle size <50μm: 2-Hydroxy-5-fluoropyridine with particle size below 50μm is used in fine chemical formulations, where improved solubility and homogeneous dispersion are critical.

    Moisture content <0.5%: 2-Hydroxy-5-fluoropyridine with moisture content less than 0.5% is used in battery material synthesis, where reduced hydrolysis enhances final product performance.

    Assay ≥98%: 2-Hydroxy-5-fluoropyridine with assay not less than 98% is used in dye synthesis processes, where high product consistency and predictable color outcomes are achieved.

    Residual solvent <500 ppm: 2-Hydroxy-5-fluoropyridine with residual solvent below 500 ppm is used in medical device coating, where toxicological safety and regulatory compliance are ensured.

    Refractive index 1.543: 2-Hydroxy-5-fluoropyridine with refractive index of 1.543 is used in optical resin manufacturing, where enhanced light transmission and uniform optical properties are provided.

    Boiling point 246°C: 2-Hydroxy-5-fluoropyridine with a boiling point of 246°C is used in heat-resistant polymer synthesis, where elevated processing temperatures and reduced volatilization losses are required.

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    Certification & Compliance
    More Introduction

    Looking Closer at 2-Hydroxy-5-fluoropyridine: Understanding an Important Specialty Chemical

    2-Hydroxy-5-fluoropyridine isn’t a name that rolls off the tongue, but for those who work in chemical manufacturing or research labs, it means something more than its syllables suggest. I spent time in a laboratory where every new compound represented both the excitement of discovery and the responsibility that comes with handling specialty chemicals. Over the years, I’ve come to appreciate the impact of a well-designed molecule—how small changes, like swapping a fluorine atom or a hydroxyl group on a pyridine ring, can completely shift the game, both in how a material behaves and where it’s useful.

    A Closer Look at the Model and Specifications

    2-Hydroxy-5-fluoropyridine belongs to the family of substituted pyridines. Shaped by fluorine at position five and a hydroxyl at position two, the molecule stands apart from the common garden-variety pyridine. Its formula, C5H4FNO, may look unassuming, but every atom here plays a part in how the compound acts in real reactions or synthesis projects. From its pale, sometimes off-white appearance to the distinct, slightly bitter scent that a trained chemist would recognize, each property helps signal purity and quality. In practical terms, its melting point and solubility got my attention during a project where we wanted a reactant that wouldn’t break down under mild heat and could dissolve in the usual organic solvents. Having that kind of reliability matters when the stakes involve costly materials or critical reaction yields.

    Quality control teams don’t get enough credit, since every batch of 2-Hydroxy-5-fluoropyridine has to pass strict purity standards—impurities can skew reactions, mess with pharmaceutical synthesis, or even introduce dangers downstream. Analytical groups typically rely on tools like NMR, mass spectrometry, and chromatography to verify that each shipment meets expectations. My own experience with these checks tells me that the trace fluorine on this molecule makes it quite easy to spot on certain instruments, saving precious time during verification.

    What Makes 2-Hydroxy-5-fluoropyridine Stand Out?

    Hands-on work with this compound taught me its place in modern synthesis. Pyridine itself acts as a workhorse base and ligand, but adding a fluorine atom changes its chemical temperament. In research on pharmaceutical intermediates and agricultural chemicals, this single substitution can offer increased metabolic stability or improved bioavailability. The hydroxyl group, placed just so, opens the door for additional functionalization or hydrogen bonding interactions, which are sought after when designing compounds for biological targets.

    I sometimes think back to the long nights I spent searching for chemical routes that wouldn’t fizzle out after a single step. Many commercial pyridines require tricky protection and deprotection strategies, especially when multiple functional groups compete during reactions. The 2-hydroxy-5-fluoro arrangement bypasses some of those headaches. It’s reactive where you want it, stable where you need it, and—importantly—amenable to scale-up, so you aren’t left scrambling for more after a successful pilot batch. Not every specialty chemical delivers on that front, and the margin between lab-scale and plant-scale makes a world of difference for budgets and project timelines.

    Comparing with Other Pyridine Derivatives

    Not all substituted pyridines offer the balance seen in this one. Many pyridine derivatives function as building blocks, but some come burdened with excess steric hindrance or unintended reactivity that cause side reactions. In one especially frustrating case a few years ago, a pyridine derivative with bulky groups at sensitive positions threw off every reaction we tried; only after switching to a lighter, fluorinated variant did the synthesis proceed without forming stubborn byproducts.

    The fluorine in the 5-position of the pyridine ring gives this molecule a stronger C–F bond, which resists both oxidation and metabolic attack. This doesn’t just matter in the flask. In pharmaceutical pipelines, small changes in stability can make or break clinical candidates. Less metabolic breakdown usually translates into fewer toxic metabolites and improved dosing predictability. Many newer drugs, especially in oncology and antiviral spaces, count on clever use of fluorinated aromatics for precisely those benefits. With 2-Hydroxy-5-fluoropyridine, researchers can introduce this effect into new scaffolds without wrestling the cumbersome chemistry of polyfluorinated analogs.

    Typical Uses: Where Does This Compound Find a Home?

    At my old lab, colleagues spent months testing pyridine analogs in reactions aimed at producing kinase inhibitors. Subtle tweaks in the arene pattern led to huge shifts in biological activity. The fluoro-hydroxy pattern of this particular compound gave rise to intermediates with just the right electronic profile, delivering higher selectivity while avoiding metabolic bottlenecks. Looking at patent filings and medicinal chemistry papers, I see 2-hydroxy-5-fluoropyridine show up frequently in routes to sulfonamides, amides, and even as building blocks for dyes or electronic materials.

    In agriculture, companies design active ingredients that resist breakdown by sunlight or enzymes in the soil. Compounds with judiciously placed fluorine atoms tend to last longer, providing more reliable pest or weed control. My fieldwork with agrochemical R&D teams confirmed that mixing the right moieties—especially fluorinated ones—can deliver active agents with longer field duration and less environmental runoff.

    In the specialty chemical industry, this variant stands out as a reagent and an intermediate. It’s reactive enough to participate in further derivatization, especially for Suzuki-Miyaura or Buchwald-Hartwig couplings. A colleague once streamlined a multi-step synthesis by swapping in this compound for a more stubborn pyridine analog, turning weeks of troubleshooting into a few productive days.

    Navigating Handling and Storage

    Chemists always respect compounds containing both hydroxyl and fluorine, given the mix of reactivity and occasional health concerns. In my own stockroom, I made a practice of labeling containers clearly and storing them in dry, cool conditions—never risking cross-contamination with acids or incompatible reagents. This compound lacks the high volatility of some related substances, so ordinary fume hood practices suffice. Careful handling reduces the risk of exposure or degradation. And while it doesn’t fall into the highest hazard tier, avoiding unnecessary skin contact and keeping containers sealed just makes sense, especially in a busy lab.

    I’ve noticed that some chemists overlook the impact of humidity on stocks of hydroxy-pyridines; moisture can prompt slow decomposition or affect reactivity in subtle ways. Investing in desiccators or using inert gas blankets becomes less a luxury and more a necessity for those seeking reproducible results. In large-scale settings, this compound rarely causes headaches for shipping or storage, provided containers remain intact and storage areas keep out moisture and sunlight. My own mishap with a poorly-sealed jar cost half a week in lost productivity, which underlines how small precautions carry big payoffs.

    Addressing Industry Challenges

    Beyond the specific quirks of handling, the broader challenge facing users of 2-Hydroxy-5-fluoropyridine revolves around ensuring consistent supply and purity. Given the tight tolerances most advanced syntheses require, even a minor deviation in impurity profile can mean failed reactions or regulatory headaches. Labs that fall behind on verification tests risk wasting valuable precursors and time. I remember chasing down a poor reaction yield to an off-specification batch from a low-cost supplier, learning the hard way that cutting corners early rarely pays off.

    Environmental responsibility also factors into consideration. Fluorinated organics can pose environmental risks, especially if improperly disposed. More R&D teams recognize sustainability as a top priority, investigating greener ways to synthesize and degrade such compounds. I’ve seen new protocols for waste collection and treatment start to catch on at research institutions, with success traced back to clear labeling and team training. The conversation is shifting from “What can we get away with?” to “How can we do this responsibly—and still profit?” That’s helped both morale and compliance rates.

    Learning from Use Cases

    Thinking of the times I benefited from this compound’s unique blend of stability and reactivity, I see lessons that apply beyond my own experience. Teams in pharma and agrochemistry rely on small building blocks that act predictably—and that can survive the journey through dozens of reaction steps. For those invested in new drug candidates or crop protection agents, the value of reliability in synthesis can be as important as biological activity itself. My discussions with process chemists confirm that switching to more reactive or less stable pyridine analogs leads to longer timelines, higher costs, and increased waste. With the right analytical support, teams using 2-Hydroxy-5-fluoropyridine enjoy smoother scale-up and greater reproducibility.

    Some research groups use this compound to design new ligands for organometallic catalysts as well. The electron-withdrawing effect of fluorine, balanced by the hydrogen-bonding of the hydroxyl group, gives rise to ligands with tailored properties for specific catalytic cycles. Experimenters can tune outcomes with simple swaps, achieving improvements in yield or selectivity no one expected at the outset. In those contexts, the initial investment in high-quality 2-Hydroxy-5-fluoropyridine pays off rapidly as failures drop away and successful reactions become repeatable.

    Supporting Innovation and Future Discovery

    Science continues to chase new solutions for tough problems, and the best tools sometimes come from molecules hiding in the middle of a catalog page. 2-Hydroxy-5-fluoropyridine may look simple next to more recognized active ingredients or high-tech catalysts, but its role in research and industry tells a different story. Every batch supports new patents, fuels medical breakthroughs, and opens the doors to creative chemical transformations. It’s not about hype—it’s about consistency, reliability, and the right balance of properties in one small molecule.

    Reliable access to this compound creates a solid foundation for researchers working across borders and time zones. I’ve traded notes with chemists from Europe, Asia, and the Americas, all of whom credit their success in tricky transformations to having access to properly characterized intermediates like this one. The pursuit of improved yield, safer processes, and faster timelines links teams everywhere; that sense of shared purpose grows with every successful experiment.

    Building Solutions: Making Best Use of 2-Hydroxy-5-fluoropyridine

    Getting the most out of 2-Hydroxy-5-fluoropyridine requires attention to detail, ongoing training, and a willingness to invest in quality controls. Teams that overlook rigorous sourcing or analytical support will pay the price with failed experiments and wasted funds. Training junior staff on best practices, maintaining clear chain-of-custody records for every drum or bottle, and sharing results—good and bad—make the difference between success and frustration over the long haul.

    Collaboration also boosts value. I’ve seen interdisciplinary teams—process engineers, synthetic chemists, and analytical experts—spot issues overlooked by others. Open conversation about problems leads to faster fixes and stronger results. Vendors who truly partner with their customers, listening to both complaints and compliments, guide product development and deliver higher-quality materials year after year. My own projects flourished when supplier relationships involved more than just invoices and shipping receipts—real dialogue raised everyone’s standards and paved the road to better yields and safer practices.

    Rethinking Sourcing in the Modern World

    Reliable supply chains form the backbone of specialty chemical work. Disruptions can cripple even well-staffed projects racing toward deadlines. In one company, after a single sourcing hiccup brought an entire development program to a halt, we overhauled procurement protocols, creating secondary sourcing options and new test verifications at every delivery point. Doing so cost a little more upfront, but the return came in the form of uninterrupted progress and peace of mind. Market shifts and regulatory policy changes remind us that stability in specialty chemical supply is never guaranteed. Building networks, supporting local training and certification, and keeping lines of communication open with trusted partners enhance organizational resilience in times of crisis.

    Transparency stands out as a major talking point for those investigating the full chain of custody, from raw materials through finished products. Responsible manufacturers post batch analysis data and provide clear answers on impurities and manufacturing routes. End users benefit from this transparency, not only in meeting current regulatory requirements but also in responding swiftly to any future restrictions or market demands. The story of quality assurance unfolds not just in labs and factories but on every test certificate and every honest supplier update.

    Educating with an Eye to the Future

    Research and manufacturing groups have a responsibility to share their learning with future generations of chemists. I like to recall the time I walked undergraduate students through the rationale behind using fluorinated pyridine intermediates—they saw, in real time, how even small choices at the chemical blueprint stage ripple through every stage of manufacturing. Investing in continuing education, open data sharing, and publication of both successes and failures strengthens the field as a whole.

    Outreach programs and public-facing summaries help demystify specialty chemicals and show their role in advancing technology, medicine, and agriculture. The next time someone asks why a chemist would care about a single atom swap in a pyridine ring, the answer is simple: every detail counts, and smart choices propel progress. The hidden backbone of new therapies and greener farming often lies with compounds like 2-Hydroxy-5-fluoropyridine.

    Facing the Upsides and Downsides Head-On

    Every compound carries both promise and peril. Users confront not only technical hurdles but also shifting environmental and legislative expectations. As regulatory frameworks evolve, so must the strategies for deploying and retiring fluorinated intermediates. Waste collection, green synthesis routes, and closed-system manufacturing processes step into the spotlight. Teams that invest in sustainability and social responsibility achieve longer-term gains while building broader public trust. I've found that open, honest discussion with regulators, clients, and fellow chemists helps everyone spot risks early and adapt before compliance deadlines arrive.

    My experience points to a core lesson: those who understand both the science and the societal impact of specialty chemicals like 2-Hydroxy-5-fluoropyridine steer ahead of the curve. Commitment to best practices, open communication, and detailed data keep teams moving forward. Every investment in better quality control, smarter sourcing, and cleaner manufacturing builds a future where advances in chemistry benefit both industry and society at large.

    Conclusion: Finding Value in Every Detail

    Through years of lab work, patient troubleshooting, and collaboration, I’ve come to see 2-Hydroxy-5-fluoropyridine as more than just a reagent. It’s an example of how thoughtful chemistry shapes research, development, and application. From its unique substitution pattern to its reliability in scale-up and role in modern synthesis, this specialty chemical continues to punch above its weight. Meeting the dual challenges of technical innovation and responsible stewardship will keep it front and center in the toolkits of tomorrow’s chemists. The story of progress often starts with the right choice of starting materials, and here, small details create the largest waves.