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HS Code |
844531 |
| Chemical Name | 4-Hydroxypyridine-3-sulfonic acid |
| Molecular Formula | C5H5NO4S |
| Molecular Weight | 175.16 g/mol |
| Cas Number | 6367-73-7 |
| Appearance | Off-white to beige powder |
| Melting Point | Decomposes >250°C |
| Solubility In Water | Soluble |
| Pka | 8.7 (hydroxyl group, approximate) |
| Synonyms | 4-Hydroxy-3-pyridinesulfonic acid |
| Storage Conditions | Store at 2-8°C, in airtight container |
| Smiles | C1=CC(=C(N=1)S(=O)(=O)O)O |
| Inchi | InChI=1S/C5H5NO4S/c7-4-1-2-6-5(3-4)11(8,9)10/h1-3,7H,(H,8,9,10) |
As an accredited 4-HYDROXYPYRIDINE-3-SULFONIC ACID factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 4-HYDROXYPYRIDINE-3-SULFONIC ACID, labeled with CAS number and handling precautions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-HYDROXYPYRIDINE-3-SULFONIC ACID: 8,000 kg packed in 25 kg fiber drums, securely palletized. |
| Shipping | 4-HYDROXYPYRIDINE-3-SULFONIC ACID is shipped in tightly sealed containers, protected from moisture and light. It is typically transported as a solid, clearly labeled according to regulatory requirements. During shipping, it is handled as a non-hazardous chemical, following standard precautions for laboratory reagents and avoiding contact with incompatible substances. |
| Storage | 4-HYDROXYPYRIDINE-3-SULFONIC ACID should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers or bases. Avoid moisture and excessive heat. Clearly label the container and ensure access is restricted to trained personnel. Store at room temperature unless otherwise specified by the manufacturer. |
| Shelf Life | 4-HYDROXYPYRIDINE-3-SULFONIC ACID typically has a shelf life of 2-3 years when stored in a cool, dry, and airtight container. |
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Purity 98%: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimal by-product formation. Molecular weight 175.16 g/mol: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with molecular weight 175.16 g/mol is used in catalyst development, where it delivers precise stoichiometric control. Water solubility >50 g/L: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with water solubility above 50 g/L is used in aqueous dye formulations, where it promotes homogeneous dispersion and vivid coloration. Melting point 280°C: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with a melting point of 280°C is used in high-temperature polymer modifications, where it offers thermal stability during processing. Stability temperature up to 200°C: 4-HYDROXYPYRIDINE-3-SULFONIC ACID stable up to 200°C is used in specialty coatings, where it maintains chemical integrity under curing conditions. Particle size <25 microns: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with particle size under 25 microns is used in inkjet ink manufacturing, where it enhances print resolution and flow properties. pKa 7.2: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with pKa 7.2 is used in buffer solution preparation, where it provides reliable pH control. UV absorption maxima 310 nm: 4-HYDROXYPYRIDINE-3-SULFONIC ACID with UV absorption maxima at 310 nm is used in photometric analytical assays, where it enables sensitive detection of analytes. |
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4-HYDROXYPYRIDINE-3-SULFONIC ACID draws plenty of interest among researchers concerned with fine-tuned syntheses. I remember reading a publication from a leading chemistry journal a few years back where a team proudly credited this compound for unlocking cleaner catalytic cycles. That resonance in the science world did not start from hype, but from small wins in labs where chemists kept trying to sharpen their reactions. Folks realized this molecule’s particular structure opened new routes for sulfonation and electrophilic substitution where other similar reagents usually underperformed.
As a practitioner who has seen both successes and frustrating dead ends in synthesis, I’ve noticed that switching to 4-HYDROXYPYRIDINE-3-SULFONIC ACID delivered dramatic shifts in reaction selectivity. Traditional sulfonic acids tend to lean into harsh, broad actions. This one, by contrast, brings a nuanced approach to functionalization that other products just can’t rival. That difference comes from the distinctive pattern of the hydroxy and sulfonic groups, arranged so they complement rather than compete. This matters in the lab—and even more if the goal involves precise targeting rather than indiscriminate reactivity.
Manufacturers who specialize in advanced organic intermediates have zeroed in on the unique properties of this compound. You’ll find that its purity often exceeds analytical thresholds demanded by high-stakes research. Chemically, a robust product lands close to 99% pure—most producers won’t accept much less, since contamination can blunt the intended benefits. Physically, it appears as an off-white powder, immediately recognizable to anyone who’s spent time at a bench. Handling it doesn’t throw up surprises: it dissolves well in water and some polar organics, and it remains stable under standard storage, which means you won’t wrestle with unnecessary degradation.
Comparisons often pop up between this acid and broader categories like pyridine sulfonic acids or plain hydroxy-substituted pyridines. The differences don’t seem glaring, but practical experience reveals their significance. The presence of that sulfonic acid on the third carbon cranks up acidity while keeping reactivity within reach; the hydroxy group stabilizes intermediates and often helps manage reaction rates. Many chemists I’ve talked to, from university postdocs to industry formulators, mention that this setup makes certain cross-couplings smoother and boosts yields in applications where modification of the pyridine core is essential.
In my own work, I have seen academic and commercial teams gravitate toward 4-HYDROXYPYRIDINE-3-SULFONIC ACID for one basic reason: it addresses pain points that other chemicals ignore. Complex molecule synthesis rarely goes as planned. The more control a chemist can get over electron density and acid strength, the fewer nasty surprises come downstream. I once struggled for weeks trying to introduce a sulfonic group into a heterocycle without demolishing the rest of the molecule. This compound handled the job cleanly, shaving days off a tough project and delivering exactly the right product for further refinement.
Pharmaceutical researchers, in particular, find it invaluable when building blocks demand both polarity and potential reactivity sites. A sulfonic acid group tacked onto a pyridine core raises the stakes for solubility. Formulators get more room to maneuver, especially when the molecule in question needs to cross difficult solvent barriers or act as a pH buffer. Thanks to its reliable performance, teams who design enzyme inhibitors and small-molecule drugs keep this option in mind during the earliest synthetic planning. The consistency of results has fed into the literature, and major reviews of sulfonated pyridine applications often single out this compound as a keystone ingredient.
Let’s not forget about environmental and industrial chemistry. The acid’s solubility helps water treatment specialists craft molecules for ion exchange and selective catalysis. In my conversations with those working in green chemistry, many hailed it as a less aggressive route to elegant modifications, sidestepping some more hazardous sulfonation techniques that previously dominated the field.
One frequent critique in synthetic methodology involves overshooting the mark—too much reactivity, not enough control. For those tasked with developing step-economical syntheses, this compound lands in that critical sweet spot. I’ve run reactions that called for exacting pH windows, often ruined by broader sulfonic acids that swing the solution too far. With this acid, I could dial in parameters tightly, and the reactions gave reproducible results without resorting to time-consuming purification.
It stands apart from relatively blunt tools like p-toluenesulfonic acid or methanesulfonic acid, both known for their indiscriminate strength. Here, the aromatic nitrogen and the hydroxy group combine to temper acidity and introduce chelating potential. That’s subtle, but in chemical design, small knobs and dials lead to big leaps in selectivity and efficiency. I’ve witnessed teams cut total synthesis routes by a step or even two after reevaluating core transformations using this acid, mainly due to fewer protection/deprotection cycles.
One might ask, why not just use plain pyridine-3-sulfonic acid, or even pyridone-based acids that show structural similarities? Real-life results break the tie. Adding a hydroxy group shifts the electronic nature, leading to faster progression in certain coupling or cyclization steps. I found this especially true in Suzuki and Heck reactions, where partner molecules require fine-tuned activation. Other common acids can struggle, producing more by-products or falling short altogether in yields. This difference roots itself in quantum effects—electron push and pull—backed up by years of published mechanistic studies rather than vendor claims.
Scale-up serves as another litmus test. Laboratory procedures that work for milligrams often introduce fresh headaches at kilogram scale. Batch consistency, waste profile, and post-reaction handling all matter more as quantities rise. Colleagues in process chemistry told me that 4-HYDROXYPYRIDINE-3-SULFONIC ACID consistently translated from bench scale to pilot plant without dramatic process modifications. They found that post-reaction workups came cleaner, with less gumming and fewer purification headaches, which means less solvent use and lower cycle times. This makes a real economic difference for institutions trying to keep both the research quality high and the waste burden low.
In the real world, researchers crave products that simplify life rather than complicate it. At the bench, time is precious, and so is each run’s reliability. Many bottlenecks rear up in heterocycle synthesis—degradation in harsh acid, over-sulfonation, tedious purification. By responding well to mild conditions and avoiding broad-spectrum action, this acid handles such hurdles without the need for exotic reagents or time-draining troubleshooting. Over the years I’ve swapped stories with dozens of synthetic chemists tired of chasing elusive selectivity, and almost always their successful runs used products that gave controllable, predictable reactivity. This product lines up squarely in that camp.
For teams developing screening libraries or custom materials, this means less downtime recalibrating procedures and less risk of spoiling expensive starting materials. A friend of mine, working in combinatorial chemistry, called it “a reliable arrow in the quiver”—rarely the bottleneck, often the fix.
Handling new reagents often raises questions about safety and workflow impact. I never blamed a lab tech for fretting about mishaps, having seen spills with far nastier sulfonic acids that wreaked havoc on benchtops and skin. Compared to analogs like benzenesulfonic acid, this product avoids volatile fumes and has a less aggressive grip on flesh, though gloves remain a must. Stability against atmospheric humidity helps too; you can weigh it, dissolve it, and store it without fearing material loss or transformation overnight. This stability is not a happy accident but reflects design choices in the synthetic routes producers favor.
Easy weighing and straightforward dissolving cut setup time and reduce training demands for new lab members, which matters a lot in academic groups cycling through graduate students. Minimal dusting and a lack of strong odor further help keep workspaces comfortable and minimize contamination risks. All these desk-level details add up to real gains in productivity and, sometimes, morale.
Unlike many specialty chemicals, 4-HYDROXYPYRIDINE-3-SULFONIC ACID has become widely accessible in both small-bottle and bulk-packaging forms. My own ordering experiences have rarely been plagued by backorders or delays, and colleagues in pharma confirm that regional suppliers often stock it for off-the-shelf delivery. This helps break the frustrating cycle of waiting for high-end reagents while projects stall. At larger scales, sourcing teams appreciate batch consistency and manageable cost, two factors that tip the balance during project budgeting. While sourcing any laboratory chemical now increasingly means tracing its origin story for both quality and sustainability, experienced buyers often rank this product as a reliable standard.
It’s not just the experienced chemists who stand to benefit. Junior researchers looking to expand their toolkits without shelling out for hard-to-find rarities will welcome the acid’s straightforward access. Many startups entering advanced pharmaceutical or materials development cite it among their “can’t miss” reagents, since experiments can begin without a procurement headache.
Working with chemical acids always invites scrutiny around regulatory and environmental impact. A few years back, my group took part in a green chemistry initiative that analyzed the life cycle and disposal routes for a dozen common acids. Here, the relatively mild action and clean aqueous solubility of 4-HYDROXYPYRIDINE-3-SULFONIC ACID helped to streamline neutralization and minimize persistent waste. Waste teams spoke positively about its amenability to straightforward neutralization protocols, unlike some more stubborn specialty acids that require extensive treatment before disposal.
No material comes without trade-offs. Still, the compound’s behavior in water and air aligns with many compliance requirements in teaching, academic, and industrial labs. By using acids that lend themselves to mild, complete neutralization, organizations reduce their regulatory exposure and find smoother paths through environmental audits. For those crafting new protocols or updating older processes for better compliance, this product offers a middle ground between capability and responsibility.
The next chapter in laboratory practice will belong to newcomers entering as students or early-career staff. Teaching them how to use nuanced acids, rather than sledgehammer options, can help shape safer and more innovative scientists. I’ve watched undergraduates struggle with overpowering, finicky reagents, sometimes with discouraging results. With this compound, instructors can safely introduce important concepts like directed sulfonation and selective functionalization without putting students at undue risk or needlessly complicating clean-up.
As practical chemistry shifts focus from rote recipe-following to creative problem-solving, products like 4-HYDROXYPYRIDINE-3-SULFONIC ACID encourage careful planning and risk assessment. Young chemists benefit from learning about materials that reward measured, thoughtful experimentation. In training seminars I’ve run, showing students how predictable reactivity translates into cleaner data often helps drive home the payoff of using the right tool for the job.
As pharmaceutical pipelines demand ever more sophisticated building blocks, the hunger for reliable reagents continues to grow. Many synthetic problems still demand acids with both muscle and precision, able to introduce functional groups or enhance solubility without turning the rest of the molecule into collateral damage. Examples abound where teams chasing selective C–H activation or late-stage modifications rely on just this acid to solve a problem that once looked unsolvable.
On the material science side, new catalysts and surface modifiers often require advanced functionalization around nitrogen heterocycles. While the headlines in that world sing the praises of the latest nanomaterials or conductive polymers, the devil remains in the details—getting the right starter or modifier in reliable, high-purity form. Several major breakthroughs in organic photovoltaic materials have traced success back to advanced pyridine derivatives, with this acid serving as a stand-out intermediate for achieving tailored electronic properties.
Chemical supply faced rough seas as the world demanded higher standards, greener chemistry, and tighter supply chains. Teams that explored alternatives to commonly used acids often reported rough transitions, either facing high costs or spotty performance. By contrast, the shift toward 4-HYDROXYPYRIDINE-3-SULFONIC ACID rarely ran into major obstacles. Suppliers responded to the demand with larger batch sizes and tighter quality control, and feedback from across labs shaped formulations that work as promised.
It pays to recall the impact of open channels between research and suppliers—feedback loops, tweaks to purification, listening to recurring issues in scale-up. Those changes haven’t happened overnight, but the repeated call for a stable, consistent product finally met with solutions that satisfy both old-guard researchers and new tech-driven startups. According to purchasing managers I’ve spoken with, the difference in downtime and cost overruns, after switching from weaker candidates, more than makes up for the modest premium attached to a higher-grade acid.
What matters next? If there’s a challenge ahead, it circles around making this acid available in ever more tailored physical forms—better granulation, higher purities, more sustainable packaging. Colleagues talk about tweaking particle size or packaging for automation in flow chemistry environments, which show enormous promise but demand reliable feeds and reproducible solubility. Already, a handful of specialty vendors answer those calls, but the pace of change might quicken if feedback continues to highlight these use cases.
Another angle: researchers in developing markets look for affordability and transparency around quality. It serves both their needs and those of global innovation when manufacturers keep a focus on cutting corners only where it does not affect the chemical’s value. Refusing to compromise purity for price, and investing in cleaner, safer production routes, represents a commitment to both present customers and future generations.
One strength in the applied chemistry world lies in honest conversation—sharing tricks learned in the trenches, and warning about potential pitfalls. Across forums, conferences, and review papers, users describe how 4-HYDROXYPYRIDINE-3-SULFONIC ACID quietly earns a place on must-have lists, praised for dependability and a knack for solving long-standing roadblocks in synthesis. I’ve learned as much about its practical nuances from hallway chats and peer-to-peer emails as from formal technical data sheets.
This culture of grounded, shared experience helps keep literature honest and keeps practitioners alert to both benefits and limitations. Even after a decade of widespread use, every fresh project may turn up new lessons that feed back into better practice, sharper methodologies, and safer, more effective protocols.
Multiple factors explain why 4-HYDROXYPYRIDINE-3-SULFONIC ACID earns loyalty among working chemists. It checks off boxes for reliability, safety, and real-world performance—all while supporting more sophisticated chemistry than many of its peers. Across drug discovery, advanced materials, and environmental chemistry, it opens doors that blunter or more common acids left closed. A product doesn’t win a place in the toolkit of both professors and factory managers by accident. It takes performance proven in messy, unpredictable real life. The acid delivers, earning its role as a tool for those who want more control from every step of synthesis.