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HS Code |
472445 |
| Chemical Name | 4-hydroxy-3-pyridinesulphonic acid |
| Molecular Formula | C5H5NO4S |
| Molecular Weight | 191.16 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | Decomposes above 250°C |
| Solubility In Water | Highly soluble |
| Cas Number | 139-07-1 |
| Pubchem Cid | 9388 |
| Pka | Approx. 9.6 (for the pyridine nitrogen) |
| Synonyms | 4-hydroxy-3-pyridinesulfonic acid; Pyridoxine-3-sulfonic acid |
| Structure Smiles | C1=CN=C(C=C1O)S(=O)(=O)O |
| Storage Conditions | Store at room temperature, keep container tightly closed and dry |
| Ec Number | 205-358-3 |
As an accredited 4-hydroxy-3-pyridinesulphonic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-hydroxy-3-pyridinesulphonic acid is sealed in an amber glass bottle with a printed hazard label and screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-hydroxy-3-pyridinesulphonic acid: Typically 8-10 metric tons packed in 25kg drums or bags, moisture-protected. |
| Shipping | 4-Hydroxy-3-pyridinesulphonic acid should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Package the chemical according to local and international regulations for chemical transport. Ensure appropriate labeling, include safety documentation, and handle with care to prevent spills or leaks during transit. Store in a cool, dry place upon arrival. |
| Storage | 4-Hydroxy-3-pyridinesulphonic acid should be stored in a tightly closed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Properly label the container and handle with care to prevent contamination or accidental spills. Follow all applicable safety guidelines for chemical storage. |
| Shelf Life | 4-hydroxy-3-pyridinesulphonic acid typically has a shelf life of 2-3 years when stored in a cool, dry, and sealed container. |
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Purity 98%: 4-hydroxy-3-pyridinesulphonic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity levels. Molecular weight 189.18 g/mol: 4-hydroxy-3-pyridinesulphonic acid of molecular weight 189.18 g/mol is used in heterocyclic compound production, where it facilitates precise molecular incorporation. Particle size <10 µm: 4-hydroxy-3-pyridinesulphonic acid with particle size less than 10 µm is used in catalyst formulation, where it promotes rapid and uniform reaction kinetics. Aqueous solubility >100 g/L: 4-hydroxy-3-pyridinesulphonic acid with aqueous solubility greater than 100 g/L is used in electroplating additives, where it provides excellent conductivity and dispersion. Melting point 220°C: 4-hydroxy-3-pyridinesulphonic acid with a melting point of 220°C is used in high-temperature polymerization processes, where it ensures thermal stability and process reliability. Chemical stability pH 2–10: 4-hydroxy-3-pyridinesulphonic acid stable in pH 2–10 is used in agrochemical formulations, where it maintains efficacy across diverse environmental conditions. |
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4-hydroxy-3-pyridinesulphonic acid isn’t a chemical that most people encounter in daily conversation, but its place in modern laboratories and industry speaks volumes. Decades spent navigating research benches and weighing powders have taught me that success in synthesis often hinges on the small details—the right reagent in the right grade can turn a tough problem into a straightforward solution. This compound, with a chemical fingerprint set apart by its hydroxyl and sulphonic acid groups on a pyridine ring, stands out in more ways than one.
Model and specification details often serve as a maze for buyers. In my experience, a high-purity 4-hydroxy-3-pyridinesulphonic acid, available as a white-to-off-white crystalline powder, routinely sets a new benchmark for reliability. Its solubility in water means you won’t spend time with complicated solvents or finicky dissolution steps. For those using sensitive instruments, the reduction in background noise due to fewer metal and organic impurities can save hours of troubleshooting. I have seen the difference a tight purity specification can make, especially when working on projects where a single contaminant disrupts days of careful work.
Many researchers first run into 4-hydroxy-3-pyridinesulphonic acid through its role in organic synthesis, where its electron-withdrawing groups allow for unique reaction pathways that standard pyridine derivatives can’t easily offer. If you have ever tried to push a slow aromatic substitution or needed a highly selective electrophilic attack, you’ll know how frustrating it gets with generic reagents. In pharmaceutical contexts, this compound supports sulphonation steps and intermediate formations that lead to active ingredients with higher yields and cleaner profiles.
Analytical chemists aiming for quantification and quality checks also value this acid. As an anchoring reagent for developing chromogenic and fluorogenic compounds, it bridges the gap between raw data and actionable insights. Biomolecular researchers have mentioned how its particular group arrangement offers opportunities for developing new labeling protocols, especially in enzyme-linked or sensor-driven methods. These are not minor details—reliability at this stage influences outcomes down the line, including product certifications and regulatory approval paths.
After years working inside analytical labs and process development units, I’ve learned to appreciate the details that separate a “decent” chemical from an “excellent” one. The main difference with 4-hydroxy-3-pyridinesulphonic acid lies in its dual functionalization. Many competitor products claim “enhanced performance,” but in practice, compounds without the combined hydroxyl and sulphonic moieties miss out on reactivity or solubility at critical steps. If your project needs consistent water solubility combined with a sharp reactivity profile, it quickly becomes clear why this molecule has a loyal following among synthetic and analytical chemists.
Common pyridine derivatives often require pH adjustments, surfactants, or special additives to behave as required. Not here. The presence of the sulphonic group grants not only water solubility but also imparts a level of charged interaction you rarely see in simple aromatic bases. This proves handy when you’re working with highly polar reaction mixtures or trying to drive reactions under mild, aqueous conditions. For me, the difference became obvious the moment I compared reaction rates and product yields—the improved kinetics save both time and raw material costs.
One point I often discuss with colleagues is the challenge of “fit for purpose.” Plenty of pyridine analogs line the chemical catalogs, but very few manage to combine easy handling in water with reliable functional group behavior in demanding settings. Conventional substituted pyridines might suffice for rough, bench-scale trials, though at scale, the disparities become clear. Poorly soluble or impure reagents translate into longer cleaning protocols, batch inconsistencies, and even downstream regulatory headaches.
Something easy to overlook is how contaminants or poorly controlled byproducts from alternative options can trigger false positives in QC tests. In the pharmaceutical sector, where every peak in a chromatogram raises questions, these false alarms waste both resources and time. I recall a collaborative project where switching from a generic pyridine sulphonic acid to this more refined version shaved an entire week off our regulatory submission timeline by avoiding unnecessary cleaning validation cycles.
The presence of a hydroxy group in position four doesn’t just nudge the molecule toward better reactivity; it opens the door for more selective modifications on the pyridine ring. If your process calls for nucleophilic substitutions, you’ll appreciate the difference in regioselectivity and yield. Without naming names, competitors' products often leave behind traces of starting materials or undesirable solvent residues—an issue that never arises when using a well-characterized, high-grade version of 4-hydroxy-3-pyridinesulphonic acid.
Years of scaling up reactions from milligrams to kilograms have taught me that solvent compatibility is just as important as size of the reaction flask. This pyridinesulphonic acid simplifies that aspect by dissolving rapidly in water. Waste reduction, improved operator safety, and lower solvent recovery costs follow naturally. There isn’t an official medal for simplifying waste streams, but anyone who has tackled chemical waste compliance knows how meaningful this is.
For industrial production routes, a reagent that cooperates with water allows for easier process integration. This avoids the use of hazardous organic solvents and, in my experience, streamlines waste treatment steps too. No complex emulsions to separate. No tough-to-destroy traces hanging around after neutralization. Lab staff spend less time troubleshooting and more time pushing the project forward. I remember pilot batches that hit advertised purity levels on the first try—no extended rework or off-spec material. The predictability in behavior means you can forecast resource needs more accurately, which keeps budgets in line and timelines on track.
Modern chemical projects come with an extra set of pressures: environmental liability, workplace health, and ever-tightening safety protocols. Close oversight has taught me that small molecular changes, like adding a hydroxyl and sulphonic acid group to a pyridine ring, carry big implications for environmental management. Products built for water solubility often translate to fewer “red flag” hazard labels and lower volatility compared to solvent-heavy alternatives.
Say you’re tasked with writing a safety protocol for a new process. A water-based route using 4-hydroxy-3-pyridinesulphonic acid checks several boxes before the hazard assessment even begins. Fewer organic solvents mean less risk for inhalation hazards or flammable mixtures. This not only benefits staff health but also reduces insurance premiums and regulatory reporting overhead. I’ve witnessed teams sidestep time-consuming air monitoring setups since this compound left little trace in volatilization studies.
Regular, consistent performance under changing batch conditions separates a true research-grade reagent from a bulk commodity. I’ve seen too many projects lost to “minor” impurities introduced by poorly standardized chemicals. Tight control on source quality for 4-hydroxy-3-pyridinesulphonic acid ensures you reach milestones faster, without last-minute surprises. No one wants a successful small-scale study derailed by scale-up failures or uncharacterized byproducts sneaking into the final product.
I often compare notes with peers working on both academic and commercial projects. Projects depending on spectral purity in their final products report fewer spectral interferences—a huge advantage if you spend your days peering into NMR, UV-Vis, or MS data. Clean signals make for happier analysts and more confident conclusions. No doubt, downstream verification work shrinks when the starting chemicals leave behind only what you expect.
Overseeing documentation for regulatory filings, I’ve come to see high-grade 4-hydroxy-3-pyridinesulphonic acid as an unsung hero in the paperwork battle. Reliable lot-to-lot purity and transparent sourcing often smooth the path toward internal audits. If you’ve tangled with the maze of compliance checkpoints, you’ll appreciate the head start that comes from solid documentation.
Customer support teams using these compounds routinely mention easier data reconciliation between raw material intake and finished batch outputs. This matters when evidence of traceability stands between your team and final regulatory signoff. Reliable sourcing and batch consistency also reduce the need for excess retesting or data rework, unlocking more lab time for actual discovery.
Innovation in pharmaceuticals, dyes, specialty chemicals, and diagnostics isn’t just about “what’s next”—progress often starts with reliable basics. Over the years, I've watched teams push boundaries only because they trusted the backbone of their chemistry. The presence of the hydroxyl and sulphonic acid functional groups in 4-hydroxy-3-pyridinesulphonic acid has triggered creative strategies for intermediates and conjugates. More than once, a switch to this compound gave our formulations the stability needed to survive development hurdles or regulatory testing.
The surge in interest for customized, water-soluble labeling agents and synthetic intermediates highlights how foundational improvements in compounds like this shape what’s possible. If your end product needs development of color-forming reactions or novel coupling chemistry, open feedback from development teams using this compound points to greater flexibility in achieving targeted results.
It’s easy to look at a list of substitutes and wonder if “close enough” will work, but small differences easily snowball in demanding applications. For instance, generic pyridine-based acids lacking rigorous removal of residual metals or hydrophobic impurities often create barriers for downstream biological testing. The result is extra time spent debugging or repeating assays. I’ve sat in meetings where a slightly cheaper alternative ended up costing more in wasted time and repeated investigations.
In dye manufacturing, users praise the improved color saturation and reproducibility tied to this well-defined pyridinesulphonic acid. Here, reaction efficiency scales with solubility and absence of side reactions—a reputation it earns due to careful molecular design and consistent quality control. We once switched to this reagent after a series of low-yield dye syntheses and immediately noticed more vibrant products and easier purification. That level of improvement never happens by accident; it comes from attention to the basic building blocks.
Sourcing the right chemical still brings headaches, a lesson learned from finding reputable suppliers through trial and error. Clear documentation and verified COAs—along with batch consistency—ensure you avoid speculative purchases born from unclear advertising. Creating a standard operating procedure for raw material evaluation saves a great deal of frustration, particularly when a trusted source delivers product that matches the performance claims. This applies especially to 4-hydroxy-3-pyridinesulphonic acid, where tighter specs offer meaningful, measurable improvements.
If storage or handling questions arise, practical notes from the community point out the non-hygroscopic nature and robust shelf stability of this compound. Working in humid, busy environments often challenges the stability of less refined products. Stories circulate about lost batches and ruined reagents; a well-made compound sidesteps these problems. As a regular in industrial settings, I’ve seen fewer failures due to poor storage or accidental exposure, keeping training times and wasted material to a minimum.
Feedback channels built around real-world use cases guide the evolution of 4-hydroxy-3-pyridinesulphonic acid. It’s not just chemists who benefit—process engineers, QA teams, and regulatory staff all weigh in on improvements. User-driven adjustments in packaging, granular size, and impurity control add value to every stage of the operational chain. Teams focused on lean manufacturing or continuous improvement see measurable gains in efficiency and predictability. If you participate in any capacity from bench to batch scale, these gains feel tangible rather than theoretical.
Switching to a new key reagent feels daunting, and skepticism always follows dramatic performance claims. The best approach grows from an open review of pilot data and objective benchmarking. Many labs and manufacturers turn to small-scale tests before committing fully to a change in core ingredients. In these cases, working with 4-hydroxy-3-pyridinesulphonic acid has given teams the confidence to expand trial batches without fear of process variability spiraling out of control.
Ongoing support from experienced suppliers—especially those who back their product with clear technical guidance and real test results—goes a long way in building trust. As someone who has worked both as an end user and as a consultant, I’ve often advised colleagues to demand honest performance data over marketing jargon. Transparent communication bridges the gap between sales promises and actual bench results.
Many people overlook the daily challenges of juggling budgets, safety, purity, and yield. Through hands-on experience, I can say that 4-hydroxy-3-pyridinesulphonic acid distinguishes itself not by flashy marketing, but by real-world skills: trusted purity, useful solubility, and reliable reactivity. These features have helped reshape best practices wherever it shows up—from specialty dyes and pharmaceuticals to biochemical research and analytical labs. The stories and numbers behind this compound reflect more than a product; they point to the daily decisions and problem-solving that drive scientific and manufacturing success.