|
HS Code |
219943 |
| Name | Pyridine-3-sulfonic acid |
| Cas Number | 636-73-7 |
| Molecular Formula | C5H5NO3S |
| Molecular Weight | 159.16 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 184-188°C |
| Solubility In Water | Soluble |
| Pka | approximately 1.4 |
| Boiling Point | Decomposes before boiling |
| Smiles | C1=CC(=CN=C1)S(=O)(=O)O |
| Synonyms | 3-Pyridinesulfonic acid |
As an accredited pyridine-3-sulfonic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyridine-3-sulfonic acid, 100g, supplied in a tightly sealed amber glass bottle with hazard labeling and tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine-3-sulfonic acid: Typically packed in 25kg bags, 16-18MT per 20′ FCL, palletized or non-palletized. |
| Shipping | **Pyridine-3-sulfonic acid** should be shipped in tightly sealed, appropriately labeled chemical containers. It must be protected from moisture and stored in a cool, well-ventilated area. During transport, follow all applicable regulations for hazardous materials. Use secondary containment to prevent leaks and ensure upright positioning to avoid spills. |
| Storage | Pyridine-3-sulfonic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizers or bases. Protect the container from moisture and direct sunlight. Properly label the storage vessel, and ensure suitable spill containment. Store at room temperature and follow all local regulations for chemical storage. |
| Shelf Life | Pyridine-3-sulfonic acid typically has a shelf life of 2–3 years if stored in a cool, dry, tightly sealed container. |
|
Purity 98%: Pyridine-3-sulfonic acid with a purity of 98% is used in pharmaceutical intermediate synthesis, where enhanced yield and product selectivity are achieved. Melting Point 225°C: Pyridine-3-sulfonic acid with a melting point of 225°C is used in high-temperature organic reactions, where thermal stability ensures consistent reaction progress. Particle Size <50 microns: Pyridine-3-sulfonic acid with particle size below 50 microns is used in heterogeneous catalysis, where increased surface area improves catalytic efficiency. Aqueous Solubility 120 g/L: Pyridine-3-sulfonic acid with an aqueous solubility of 120 g/L is used in electroplating baths, where uniform dissolution improves metal deposition quality. Stability Temperature up to 160°C: Pyridine-3-sulfonic acid with stability up to 160°C is used in polymer modification processes, where chemical integrity is maintained under process conditions. Moisture Content <0.5%: Pyridine-3-sulfonic acid with moisture content less than 0.5% is used in peptide coupling reactions, where minimized hydrolysis enhances product purity. Molecular Weight 173.16 g/mol: Pyridine-3-sulfonic acid with a molecular weight of 173.16 g/mol is used in analytical standards preparation, where accurate quantification is facilitated. Thermal Decomposition Above 240°C: Pyridine-3-sulfonic acid with thermal decomposition above 240°C is used in high-energy material synthesis, where stability minimizes unwanted degradation. |
Competitive pyridine-3-sulfonic acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Pyridine-3-sulfonic acid, also known as 3-pyridinesulfonic acid, brings something extra to bench chemistry and industrial manufacturing. The molecular formula, C5H5NO3S, puts it in a category of organic sulfonic acids with a defined structure and straightforward chemical reactivity. Many people in laboratories and production spaces appreciate the product for one main reason: its sulfonic acid group sits directly on the third position of the pyridine ring. That small shift within the ring changes a lot about what it can do in real life. The model people recognize most often shows a white, sometimes off-white, crystalline powder, with a melting point that typically falls above 200°C, indicating stability for a range of chemical processes.
In my days working between bench-top discoveries and scaling up in industry, I have seen this compound earn its spot as a partner in many reactions. It is not just another sulfonic acid. The specific placement of the sulfonic group helps with nuance—control over acidity and reactivity in ways that the more commonly used p-toluenesulfonic acid or benzenesulfonic acid can’t reach. In synthesis, for those looking for a mild acid with a touch of nucleophilic capability, pyridine-3-sulfonic acid lets you move away from highly aggressive mineral acids that risk ruining sensitive components. A clear solution is important, but so is being able to nudge a reaction rather than slam it home. Pyridine-3-sulfonic acid gives you that choice.
Comparing pyridine-3-sulfonic acid to the more popular benzenesulfonic acid or toluenesulfonic acid isn’t just about looking at numbers in a table. The aromatic ring on the pyridine offers a nitrogen atom, which changes electron distribution. That in turn shifts both acidity and behavior. Acid strength sits in a middle space—strong enough for practical applications but rarely so harsh that everything else needs redesigning to protect substrates. This balance means smoother runs, less cleanup from side reactions, and fewer headaches when moving from gram to kilogram quantities in industry. There are people who will always reach for the classics—sulfuric, methane sulfonic—but once they start with pyridine-3-sulfonic acid, they find options that keep more delicate substrates intact.
Organic synthesis stands out. Sulfonation reactions, oxidative transformations, and as a catalyst or co-catalyst, this compound always offers a steady hand. It’s particularly useful when the goal involves forming sulfonate esters, which often serve as leaving groups for nucleophilic substitution reactions. Here, the built-in stability of the pyridine ring, along with the less extreme acidity, lets you keep reaction conditions milder. Researchers choosing between different sulfonic acids frequently look for something that won’t force them to degrade or rearrange their starting materials. In protection-deprotection strategies, a lot of routes use pyridine-3-sulfonic acid because it’s strong enough to act and gentle enough not to destroy what you’ve worked hard to build.
I can remember days working through libraries of small molecule analogs, where a single misstep with an acid reagent meant going back to square one. I watched colleagues rely mostly on highly acidic reagents—many times those made a mess out of protected alcohol or amine groups. Pyridine-3-sulfonic acid became a quiet favorite because it would allow for clean separation by filtration, rarely colored batch solutions, and was surprisingly forgiving in reactions that needed a bit of water present. This product also made purification, such as recrystallization, less frustrating. The crystalline form doesn’t smell sharp or pose serious handling difficulties, making it a staple for both multi-step synthesis projects and scale-up work.
In manufacturing environments, fine chemicals and pharma intermediates demand consistent quality and reproducibility. Pyridine-3-sulfonic acid’s stability and straightforward reactivity allow for batch processes and continuous flow chemistry setups. Producers value how its medium-strength acidity offers flexibility—reaction times may be a little longer than with strong acids, but the upside comes in less equipment corrosion, fewer byproducts, and more stable product yields. A facility running oxidative coupling or arylation routes can keep glassware or metal reactors in better shape over time. Maintenance teams quietly like that, and so do accountants tallying savings on the back end.
Purity levels usually reach above 98%, which sets minds at ease for people who measure every input down to the last decimal. The crystalline powder flows well, dissolves in water or common polar solvents, and—unlike some sticky or oily products—lets you measure consistently even in humid conditions. Shelf life, when kept in well-sealed, dry conditions, stretches out. Most people appreciate being able to pull a bottle off the shelf after months, finding that it hasn’t clumped together or formed lumps, which is more than can be said for many other acids that suck in moisture or begin to brown. Laboratory inventory managers often comment on the ease of stock rotation and the reliable color-form signals purity in check-ins.
No one wants surprises at the lab bench or on the plant floor. Pyridine-3-sulfonic acid carries a chemical odor typical of its class, but it doesn’t send people running from the room or require over engineered ventilation. Regular gloves, lab coats, and eye protection have always sufficed in my work. Its dust flows easily, which means careful transfer is important, but it avoids the strong, persistent odors or heavy fumes that make some sulfonic acids infamous among new technicians. Disposal procedures follow standard protocols for organic sulfonic acids, and wastewater treatments handle its breakdown without added infrastructure. From an environmental standpoint, lower amounts needed for many reactions mean smaller waste streams, a point that starts gaining ground for companies keeping a close eye on sustainability. While it’s not labeled as benign, it’s a definite step up from using harsher acids with persistent toxicity and corrosive residues.
Scientific literature and patent filings reflect a clear trend over the past decade: pyridine-3-sulfonic acid appears more frequently as a catalyst and auxiliary in synthetic routes for pharmaceuticals, agrochemicals, and specialty dyes. Several peer-reviewed studies, especially those focusing on regioselective sulfonations, give it credit for minimizing unwanted rearrangements and maximizing yields of targeted products. In patent files, companies often mention pyridine-3-sulfonic acid in the context of improved process economics—fewer purification steps, less solvent waste, more robust batch performance. Industry trade publications echo what I have seen on the ground: those switching to pyridine-3-sulfonic acid report reductions in both downtime from corrosion and maintenance as well as improved consistency in product quality. These aren’t just claims to boost marketing; you find these results in footnotes, batch reports, and final annual audits that drive process improvement reviews.
Something has shifted over the past several years in both research and manufacturing. Academic departments and commercial labs chase new synthetic methods, and there’s a steady push to do more with less waste and less risk. Safety officers set new rules about volatile acids, while chemists working under those rules seek alternatives that won’t tie their hands. Pyridine-3-sulfonic acid lands squarely in that search. It gives experimenters a middle ground between the strong, aggressive acids and the weaker sulfonic acid derivatives that may fall short in driving key reactions. For chemists aiming to scale up a promising bench discovery, being able to switch to a more controllable acid during scale-up lets them keep projects moving forward without unexpected pitfalls. Academic publications now frequently mention it in Supporting Information, and forwarded process development reports often describe how swapping in pyridine-3-sulfonic acid allowed them to meet updated safety or green chemistry requirements.
No chemical is without limitations. Pyridine-3-sulfonic acid does not offer the extreme acidity that some processes still require; those looking for mineral acid-level performance may need another solution. High water sensitivity in particular applications can create handling issues—moisture can cause partial hydrolysis in certain reaction environments or complicate product isolation if humidity controls lapse. That said, careful packaging and storage tackle most of the consistency concerns. Bulk buyers use lined barrels or double-sealed bags, keeping the product usable far longer and eliminating the common headaches with cheap packaging that attacks the product before it ever reaches the process area.
Product supply has also been affected by raw material disruptions from global logistics hiccups over the past few years. Reliable sourcing and clear supply chain communication are now part of every project planner’s checklist. Producers who establish direct relationships with suppliers and audit those relationships regularly find fewer production line hiccups. Building those connections grants stability not just in price but in ongoing availability of high-purity material. Customers who put in the effort to create supplier partnerships enjoy steadier flows of product and fewer surprises.
The learning curve with specialty acids often feels long and hard-earned. I have seen new chemists reach for what their training handed them—a bottle of sulfuric or p-toluenesulfonic acid. The first few mishaps teach lessons about harsh acids: ruined product, wasted time, hazardous vapors, and ruined glassware. Pyridine-3-sulfonic acid enters as a lesson learned—a move toward something that handles a range of needs without that narrow “all or nothing” feel. It’s not about chasing novelty but reaching a practical balance between reliable performance, manageable safety risks, and the growing demands for greener, more efficient chemistry.
For those stepping up to large-scale synthesis, quality checks run both ways. Pyridine-3-sulfonic acid behaves predictably during titration and analytical verification—not a flashy advantage, but a critical one. Labs needing easy method validation and traceability appreciate knowing impurities won’t creep in unnoticed. Recrystallization from water, methanol, or ethanol proceeds simply, and the product forms stable, easy-to-handle crystals. Those who need subtle acidity for selective transformations keep coming back to it, while process engineers tasked with reducing byproducts and increasing throughput see running cost differences show up in their metrics over time.
Best practices always pay off: keep the product dry, invest in reliable dispensing tools, and use it in well-ventilated spaces. Changes in environmental regulation suggest moving toward milder, less hazardous options wherever possible. Pyridine-3-sulfonic acid speaks to that shift by offering a controllable acidity and a role in high-yield synthesis routes with less waste. Teams actively training new researchers can take advantage; the compound’s low odor, low volatility, and pleasant appearance give less experienced staff confidence as they build skills—and mistakes turn out less costly.
One path the industry is following aims to keep improving recovery and recycling protocols for organic acids like this one. Technologies now exist to reclaim spent acid streams, separate catalyst residues, and recycle products for multiple runs. Using pyridine-3-sulfonic acid in these set-ups extends not only the product’s value but sharpens process economics. Integrated systems recapture the acid after each batch, cutting down fresh input costs and minimizing environmental discharge. I have seen teams re-use this acid in multi-step campaigns without seeing a dip in the quality of target compounds or downstream process performance, which marks a real-world improvement over acids that degrade after a single use.
Pyridine-3-sulfonic acid doesn’t come with a long list of restrictions or complicated storage rules. Most people need only avoid open containers and wipe up dust before starting the next procedure. Measured amounts dissolve quickly, and because the solution stays clear, it’s easier to monitor reactions and get consistent results from batch to batch. The wide solubility in polar solvents further expands uses, letting teams adapt their methods from water-based to alcohol-based chemistries with little guesswork. As industry standards keep shifting, those who anticipate tighter safety and environmental rules see this compound as a future-proof choice that won’t force expensive retrofits of existing hardware.
Feedback from users—lab technicians, synthetic chemists, and plant managers alike—often focuses on simplicity and reliability. Fewer emergency cleanups, fewer batch failures, and more predictable workflow rhythm. Everyone from bench chemists to project managers wants risk reduction, and this acid checks a lot of boxes without requiring extra paperwork or advanced handling techniques. If a process engineer or synthetic chemist can swap this in for harsher acids and watch yields rise while product color and purity hold steady, they notice. Project retrospectives focus less on troubleshooting acid-related issues, and more on moving discoveries forward.
Pyridine-3-sulfonic acid stands out in the chemical landscape because it fits real needs. Its well-balanced properties give chemists and process engineers breathing room to try new approaches, speed up development, and lower risks. Judging from personal experience and industry patterns, it has earned its place on every crowded reagent shelf. Year after year, as regulatory demands grow and customers measure performance, those who have brought this acid into their process tend to stick with it. This loyalty doesn’t happen by accident—it follows from a clear record of steadier performance, safer handling, and economic value. That’s why, as new challenges face the fine chemical and pharma worlds, pyridine-3-sulfonic acid continues to play a trusted and expanding role, both in discovery and in the large-scale production lines that keep modern life moving.