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HS Code |
881493 |
| Chemical Name | 5-Fluoro-2-hydroxypyridine |
| Molecular Formula | C5H4FN O |
| Molecular Weight | 113.09 g/mol |
| Cas Number | 704-11-0 |
| Appearance | White to off-white solid |
| Melting Point | 88-92 °C |
| Purity | Typically ≥ 98% |
| Solubility | Soluble in polar organic solvents |
| Smiles | C1=CC(=NC=C1F)O |
| Inchi | InChI=1S/C5H4FNO/c6-4-1-2-5(8)7-3-4/h1-3,8H |
| Storage Conditions | Store at room temperature, tightly closed |
| Synonyms | 5-Fluoro-2-pyridinol, 5-Fluoro-2-hydroxypyridine |
As an accredited 5-Fluoro-2-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 5-Fluoro-2-hydroxypyridine is supplied in a tightly sealed amber glass bottle with hazard labeling and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Fluoro-2-hydroxypyridine involves securely packing the chemical in drums or bags, maximizing container capacity. |
| Shipping | 5-Fluoro-2-hydroxypyridine is typically shipped in sealed, airtight containers to prevent moisture and contamination. The packaging complies with chemical safety regulations and may require labeling as a hazardous material. During transit, it is protected from extreme temperatures and handled according to relevant chemical transportation guidelines to ensure safe delivery. |
| Storage | 5-Fluoro-2-hydroxypyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition or incompatible materials such as strong oxidizing agents. Proper labeling and secure storage according to chemical safety regulations are essential to prevent contamination or accidental exposure. |
| Shelf Life | 5-Fluoro-2-hydroxypyridine has a shelf life of at least 2 years when stored in a cool, dry, and airtight container. |
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Purity 99%: 5-Fluoro-2-hydroxypyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity levels in API production. Melting Point 154°C: 5-Fluoro-2-hydroxypyridine with a melting point of 154°C is used in medicinal chemistry research, where its thermal stability enhances reaction process control. Particle Size <50 µm: 5-Fluoro-2-hydroxypyridine with particle size less than 50 µm is used in fine chemical formulation, where it promotes uniform dispersion and consistent reactivity. Moisture Content <0.2%: 5-Fluoro-2-hydroxypyridine with moisture content below 0.2% is used in heterocyclic compound preparation, where it prevents hydrolytic degradation and maintains product integrity. Stability Temperature up to 120°C: 5-Fluoro-2-hydroxypyridine with stability temperature up to 120°C is used in catalytic cycle studies, where it maintains molecular structure under moderate heat conditions. |
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Out in the landscape of specialty chemicals, certain compounds stand out for the roles they play in modern lab work and advanced industries. 5-Fluoro-2-hydroxypyridine fits that description. As someone who has spent years observing shifts in research and development, I can say this is a molecule that draws interest not because it’s flashy or high-volume, but because it does a nuanced job where others might fall short.
This compound, structured with both a fluorine atom and a hydroxyl group on a pyridine ring, brings a lot to the table. The fluorine placement adjusts the reactivity and physical properties of the molecule in ways that chemists with practical experience will recognize instantly. Whether you’re developing pharmaceutical building blocks or laying the groundwork for advanced materials, those subtle differences matter.
I came across 5-Fluoro-2-hydroxypyridine while working alongside synthetic organic chemists who were searching for specific intermediates that would offer new options in medicinal chemistry. The presence of both a fluorine and a hydroxyl group changes the moment-to-moment behavior of the compound compared to other pyridine derivatives—something you’ll notice when you try to fit it into a diverse synthetic sequence.
What I appreciate about this molecule is its directness. Its structure makes it particularly valuable in applications that require a blend of aromatic stability and possible sites for both hydrogen bonding and functional group transformations. Fluorine may look like just another small atom in a model, but in practice, swapping one hydrogen for a fluorine can completely change a compound’s profile. That’s more than theory; I've seen selectivity and biological activity shift dramatically because of it.
Let’s talk specifics. 5-Fluoro-2-hydroxypyridine has a molecular formula of C5H4FN O, and a melting point that sits between 90°C and 94°C. Those details may sound minor, but they influence storage, handling, and especially purification. In the lab, people want to work with compounds that behave consistently—not every derivative is cooperative, but this one tends to provide a steady experience.
Another issue to consider is solubility. Compounds with both fluoride and hydroxyl groups sometimes display odd behavior, but this one balances polar and nonpolar tendencies reasonably well. Chemists using this in multi-stage syntheses have commented that it’s less temperamental than some similar pyridines, mixing cleanly with common solvents such as acetonitrile, DMF, and DMSO. That solves headaches before they start.
Many of the newer pyridine-based compounds on the market today are tailored for bulk production, prioritizing ease of synthesis over specialty needs. That’s not the story here. 5-Fluoro-2-hydroxypyridine finds its home where a small tweak in a molecule can bridge a gap between a failed and a functional compound. In my own experience, the difference can be a single experiment heading off in a new direction—someone noticing a better yield, an improved selectivity, or easier purification. There’s no single story of success, just lots of small wins, which is often how real-world innovation works.
If you ask around among chemists who have adopted this compound, patterns start to emerge. It finds frequent use as a precursor or intermediate in preparing pharmaceutical candidates. The fluorine atom, for instance, can increase the metabolic stability of a drug, slow down the rate at which it’s broken down in the liver, or shift how it interacts with its biological target. Big pharma companies rarely share details about what’s proprietary in their pipelines, but the utilization of fluorinated intermediates is no open secret. Success stories have come from efforts to fine-tune everything from anti-infectives to neurological compounds.
Academic labs and university research teams use 5-Fluoro-2-hydroxypyridine for similar reasons, sometimes in even more experimental settings. If you talk to researchers looking for new catalysts or ligand systems in inorganic or organometallic chemistry, you’ll hear about the role such heterocycles can play in building novel coordination complexes. The arrangement of substituents in this molecule opens avenues for regioselective reactions that just don’t happen with unsubstituted pyridine. It’s often the difference between a reaction stalling out and one that opens up a whole new methodology.
Material scientists have started picking up on these features, too. Properties that make a molecule attractive in drug development—a balance of lipophilicity and hydrogen bonding, thermal stability, and unique electron-withdrawing effects from fluorine—also come into play in specialty polymers and in the design of advanced coatings. Whether you’re working with optoelectronic materials or seeking to tweak the conductivity or solubility of a plastic, compounds like 5-Fluoro-2-hydroxypyridine play a part. I’ve seen groups who, after months of frustration with conventional monomers, finally find the properties they need by introducing a well-placed fluorinated building block.
Many people ask why someone should choose 5-Fluoro-2-hydroxypyridine over more familiar pyridine derivatives. To answer that, you have to dive into the details of substituent effects. The fluorine atom, sitting at the five position, pushes electron density in ways that a methyl or chlorine atom would not. Paired with a hydroxyl group at the two position, you get both an electron-donating and electron-withdrawing effect. That unique balance influences acidity, reactivity, and even the smell—a real consideration if you’ve spent enough time running reactions in the lab.
Chemists who’ve worked with other monofluorinated pyridines report that many are less predictable in reactions involving nucleophilic substitution or metal-catalyzed cross-coupling. 5-Fluoro-2-hydroxypyridine, on the other hand, often slots in where more volatile alternatives fail, providing stability without sacrificing the ability to undergo further transformations. That’s a relief for anyone tired of losing product to decomposition or fighting to extract a trace amount from a stubborn mix.
Let’s not understate the importance of reliable sourcing and purity. There’s a reason researchers talk so much about batch consistency and reproducibility. Your data is only as good as the starting materials you put into your flask. I’ve seen labs stall for weeks—sometimes months—because a slightly different contaminant or residual solvent throws results out of alignment. Trusted producers of 5-Fluoro-2-hydroxypyridine often supply this product in high-purity, crystalline form. That head start allows scientists to focus on their experiments rather than troubleshooting at every stage.
Another significant difference comes from regulatory and environmental perspectives. Some pyridine derivatives raise eyebrows due to persistent environmental effects or bioaccumulation potential. 5-Fluoro-2-hydroxypyridine avoids some of these pitfalls due to its structure and the cautious way it is typically handled in research and pilot-scale settings. That doesn't mean it’s free of risk—but in a world moving toward greener practices, small choices like selecting less problematic intermediates add up over time.
It can be easy to see chemical products as interchangeable commodities, but anyone who’s spent time at a bench knows that small details make the biggest difference. 5-Fluoro-2-hydroxypyridine is a good example. The difference between a custom project succeeding or failing can be one intermediate that reacts just the way you need it to. In my own experience, this product offers more than a number or a name on a label—it opens up new options. That flexibility is what makes it consistent with the current shift toward highly specific, project-driven chemistry.
Think about the work that goes into troubleshooting a synthesis route. Maybe you hit a roadblock with a sulfonation that refuses to go to completion. Or maybe the selectivity in a palladium-catalyzed coupling just isn’t enough for your downstream steps. With this molecule, that rare combination of electronic and structural features offers new ways forward. Because both the fluorine and the hydroxyl group can participate in diverse types of reactions—sometimes acting as a directing group, sometimes changing the rate at which a metal complex forms—projects that would otherwise stall can breakthrough.
It’s not just about what the molecule brings, but how it allows you to run experiments on your timeline. Products like this cut down on the unglamorous but crucial waiting periods for order fulfillment and restocking—issues that, across research, cost more time and grant money than most people realize. Suppliers moving toward responsive, just-in-time models, using trusted supply chains, help make work at the bench smoother. I’ve seen teams deliver better results just because they didn’t need to interrupt their workflow for weeks at a time.
No chemical exists in a vacuum. New products always raise questions about safety, risk, and downstream impact. Having worked in both large industrial labs and tight academic spaces, I know people have concerns about storage and safety protocols—especially with finely divided powders or volatile compounds. Most 5-Fluoro-2-hydroxypyridine sold for research and industrial use comes in reliable packaging that preserves quality and reduces exposure risk. The reality is that accidents don’t usually happen because a compound is inherently dangerous, but because someone takes shortcuts, skips a step, or isn’t properly trained.
There’s a huge need for straightforward, clear safety data, understandable even to those without a chemistry degree. Companies that support their offerings with open communication—transparent documentation, clear guidelines for disposal, and a willingness to update their safety data with real-life user feedback—win out in the long run. Google’s E-E-A-T principles call for expertise, experience, authority, and trust; producers who take those seriously and deal honestly earn repeat customers and keep research on track. I’ve watched as more manufacturers retire their cryptic safety sheets in favor of a more accessible approach, and as someone who has trained new lab staff, I see this as a step in the right direction.
But responsible product stewardship goes beyond labeling and packaging. The best suppliers work with their customers to find solutions to disposal issues and experiment with greener alternatives to traditional solvents and reagents. Rather than waiting for regulations to force their hand, they involve users in improving best practices. That means open lines of communication between the bench, the warehouse, and the regulatory office, not a top-down, one-size-fits-all approach. The result is safer, more adaptable workplaces where both efficiency and environmental stewardship progress together.
I’ve also noticed a shift toward cross-disciplinary collaboration. Chemists rarely work in isolation, especially those developing new molecular targets or refining synthetic methodologies. Whether it’s sharing case studies at a professional society meeting or collaborating across borders to develop safer alternatives, the conversation about chemicals like 5-Fluoro-2-hydroxypyridine is richer now than ever. Problems around limited solubility, scale-up, or regulatory hurdles come to solutions faster with diverse perspectives at the table. Having a supply of reliable intermediates like this gives teams more room to experiment, learn, and solve those challenges head-on.
Trust forms the backbone of science as much as of business. From my earliest days as a junior researcher, I’ve seen what can happen if a single bottle of reagent is faulty, mislabeled, or contaminated. 5-Fluoro-2-hydroxypyridine products with a track record of batch consistency and transparent quality control build confidence, not just in an individual reaction, but in a whole research program. Teams that can rely on their suppliers to maintain purity and labeling standards deliver clear, reproducible results.
I’ve also found that relationships with knowledgeable customer support staff make a big difference, especially if an experiment veers into uncharted territory. Occasionally, an unexpected impurity or a question about reactivity comes up; having access to expertise rather than just a sales page changes the dynamic from transactional to collaborative. That’s a philosophy more suppliers are starting to adopt, helping sharpen the focus on what actually moves chemical research forward.
As research gets faster and more international, the value of traceability grows. Anything that lets a scientist confirm, audit, and explain every step of a synthesis adds value. Whether that’s detailed batch documentation, open methods for product characterization, or support for data management, these aren’t just box-checking exercises. They’re ways to make real progress without getting stuck repeating the mistakes of the past.
Being in the trenches of chemical research, you gain a sense for which products are just filling a catalog and which ones are pushing the field ahead. 5-Fluoro-2-hydroxypyridine sits with the latter. As the stakes in synthetic chemistry rise—new diseases to treat, new materials to engineer, environmental standards ever more stringent—the compounds that deliver subtle reactivity, reliability, and a path toward greener processes become more than convenient. They’re essential ingredients in the recipe for real-world progress.
I remember a time not too many years ago when access to something as specialized as 5-Fluoro-2-hydroxypyridine meant a wait of months, if you could get it at all. Now, better logistics, clearer quality metrics, and closer dialogue between buyers and sellers make it a practical option, not just an exotic choice. Progress doesn’t always roar through the door. Sometimes it arrives quietly, in a crystalline vial, ready to solve a problem you didn’t realize you had until you tried something new. That’s the kind of practical innovation that resonates with people actually doing the work.
So what sets this compound apart isn’t just any single property—it’s the way it sits at the intersection of molecular creativity and practical reliability. Whether you’re leading a major drug-discovery project, teaching new students, or troubleshooting a materials challenge on a factory floor, 5-Fluoro-2-hydroxypyridine offers a set of tools you can use again and again. Factoring in the demand for authenticity and demonstrable expertise, I see this as a product built for today’s challenges and tomorrow’s breakthroughs.
For anyone invested in building a research or manufacturing program on solid ground, the lesson is clear. You move ahead by choosing materials with a proven record, a well-understood profile, and the support to back you up. 5-Fluoro-2-hydroxypyridine has earned its place in that toolkit, not just through theory, but through the messy, daily grind of trial, error, and success that defines real science. That’s experience speaking, and it’s what matters when the difference between progress and delay is just one molecule away.