|
HS Code |
475568 |
| Iupac Name | pyridine-3,4-dicarboxylic acid |
| Molecular Formula | C7H5NO4 |
| Molar Mass | 167.12 g/mol |
| Cas Number | 89-00-9 |
| Appearance | white to off-white crystalline powder |
| Melting Point | 271-273 °C |
| Solubility In Water | slightly soluble |
| Boiling Point | decomposes before boiling |
| Density | 1.54 g/cm³ |
| Pka1 | 2.55 |
| Pka2 | 4.38 |
| Pubchem Cid | 9974 |
As an accredited pyridine-3,4-dicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle labeled "Pyridine-3,4-dicarboxylate," with hazard warnings, lot number, and tightly sealed cap for safety. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Loaded in 25kg bags, 16–18MT per container, securely packed on pallets to prevent damage and contamination. |
| Shipping | Pyridine-3,4-dicarboxylate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport under ambient temperature in accordance with local, national, and international regulations for chemicals. Include appropriate labeling to indicate the chemical name and hazard classification. Ensure packaging is compatible and prevents leaks or spills during transit. |
| Storage | Pyridine-3,4-dicarboxylate should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizing agents. Store in a cool, dry, and well-ventilated area, preferably under inert atmosphere if sensitive to air. Proper labeling and segregation from food and drink are essential. Follow all relevant chemical safety protocols and local regulations. |
| Shelf Life | Pyridine-3,4-dicarboxylate typically has a shelf life of 2–3 years if stored in tightly sealed containers at room temperature. |
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Purity 99%: pyridine-3,4-dicarboxylate with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimized byproduct formation. Melting point 270°C: pyridine-3,4-dicarboxylate with a melting point of 270°C is used in high-temperature catalyst preparation, where it provides thermal stability during process operations. Particle size <50 μm: pyridine-3,4-dicarboxylate with particle size under 50 μm is used in advanced materials engineering, where it enables uniform dispersion and improved material homogeneity. Aqueous solubility 4 g/L: pyridine-3,4-dicarboxylate with aqueous solubility of 4 g/L is used in water-based coating formulations, where it enhances dissolution and film integrity. Stability at pH 7: pyridine-3,4-dicarboxylate with stability at pH 7 is used in bioconjugation processes, where it maintains compound integrity during buffer reactions. Molecular weight 167.12 g/mol: pyridine-3,4-dicarboxylate with a molecular weight of 167.12 g/mol is used in chelating agent manufacturing, where it provides precise stoichiometric control. |
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Some chemicals come with big names and bigger expectations, but few get the down-to-earth respect they deserve. Pyridine-3,4-dicarboxylate doesn’t turn heads at dinner parties, yet its practical role in research labs and industrial processes keeps many operations moving forward. This compound, derived from the pyridine family, brings two carboxylate groups attached at the third and fourth positions on the ring. That might sound technical, but those positions subtly set it apart in a sea of similar molecules and inform the way it behaves in real-world settings.
You don’t have to carry a PhD in organic chemistry to appreciate why a small change in a molecule’s architecture can matter so much. The carboxylate groups on pyridine-3,4-dicarboxylate fall on adjacent carbon atoms, which alters the reactivity profile compared to compounds like pyridine-2,6-dicarboxylate or the well-known pyridine-2,3-dicarboxylate. From my perspective—shaped by years spent troubleshooting in a working lab—this means better control when designing coordination complexes or seeking specific binding motifs in research. In a crowded market of similar molecules, these little shifts make for more predictable outcomes on the bench.
Every chemist has different priorities, but some needs keep surfacing: purity, solubility, consistency. Pyridine-3,4-dicarboxylate in its most widely distributed model shows up as a crystalline powder, usually off-white. Purity tends to fall above 98% in laboratories with proper storage. Water solubility is moderate—a notch below some other di-carboxylates—which shapes how you’d use it in synthetic protocols or preparations. Melting point hovers in the 220-225°C range, which gives it stability without making handling awkward in most settings. What matters to me is not just the numbers but the reliability of those numbers over repeat orders and batches, because most projects depend on small differences, not broad promises.
Pyridine-3,4-dicarboxylate finds a distinct place in practical applications. In synthesis labs, it often winds up as a ligand for coordination chemistry, producing metal-organic frameworks or fine-tuning enzyme mimics. Thanks to its geometry and electron distribution, it interacts with metal ions more selectively than its neighbors. This is less about trend and more about predictable chelation, which anyone at a lab bench can appreciate after a few failed experiments with less cooperative compounds.
In pharmaceuticals, the molecule has cropped up in routes leading to active intermediates for drug development, where subtle differences in structure make or break downstream activities. I’ve seen research teams lean into pyridine-3,4-dicarboxylate when other, closely related products introduce too much unpredictability or side reactions. It doesn’t soak up attention in industry meetings, but it shows up again and again in published protocols and patents where flexibility and consistency mean projects stay funded and products make it out of the lab.
Many newcomers to chemistry think all dicarboxylates are interchangeable—just swap one out for another and expect similar results. That hope rarely lasts long. Pyridine-2,6-dicarboxylate, for example, creates distinctly different coordination geometries with metals, leading to unique crystal structures that simply don’t emerge from the 3,4-isomer. If you’re chasing a certain topology in a metal-organic framework, using the wrong isomer wastes time and resources. Another near neighbor, pyridine-2,3-dicarboxylate, interacts with solvent systems in ways that might seem minor on paper but can become a logistical headache in scale-up or analysis later.
In my own work, swapping out pyridine-3,4-dicarboxylate for other isomers often changed the game entirely—either opening doors for new reactivity or introducing quirks that could throw off an entire week’s worth of effort. It is the small details that separate smooth progress from endless troubleshooting. People hoping to sidestep careful selection on the assumption that “close enough” equals “good enough” usually find themselves chasing their tails in development cycles.
Some days, it’s easy to get lost in data sheets and logistics. Experience in a hands-on lab shows that the value of a substance like pyridine-3,4-dicarboxylate isn’t always obvious in raw specs. Its history in forming stable complexes—useful as tools in catalysis or as probes in biology—warrants attention. For instance, when synthesizing coordination polymers, the compound frequently delivers the right balance between rigidity and flexibility. This trait becomes crucial for tuning physical properties, be it for gas storage, separation membranes, or sensing applications.
In academic research, it has served as an efficient scaffold for building molecular architectures with predictable outcomes. These results have become staples in the chemical literature. Beyond research, real-world sectors like materials science, environmental engineering, and pharmaceutical pre-formulation keep drawing on pyridine-3,4-dicarboxylate’s unique ability to provide robust linkages and repeatable binding sites. Anyone in these fields knows that repeating the same work with slightly different molecules often throws process efficiency or reliability out the window.
A lot has changed since I first measured grams of this compound on a dusty old balance. Increased regulatory expectations from government agencies and end-users put pressure on suppliers to routinely deliver the product free of volatile impurities and with documentation that meets growing scrutiny. Anyone who’s prepared a regulatory submission for new materials understands how frustrating it can feel to hunt down certificates of analysis or track unexpected contaminants back to a manufacturer’s inconsistent process. Considering this, leading sources now run batches through advanced chromatographic and spectroscopic checks. These steps earn trust among buyers who depend on tight process controls, from early-stage R&D teams to full-scale producers.
This atmosphere, with uncompromising compliance standards, also pushes producers to invest in better analytical instrumentation and cleaner production routes. Even a small impurity can create a domino effect in advanced chemistry projects. I’ve seen plenty of cases where one small off-target reaction, thanks to an overlooked trace contaminant, delayed an entire research program and ballooned costs.
My years working with pyridine-based compounds taught me caution. Pyridine rings often raise eyebrows due to bioactivity and persistence in the environment, prompting responsible users to factor environmental management into every purchase and disposal decision. Pyridine-3,4-dicarboxylate doesn’t behave exactly like its parent compound. Its increased polarity makes it somewhat easier to handle regarding containment and cleanup, though the carboxylate groups don’t eliminate all headaches.
Most responsible labs treat it as they would other pyridine derivatives, tracking cleanup protocols tightly, using fume hoods, and collecting solid waste for hazardous disposal. These practices, reinforced by both experience and regulation, help keep labs safe and protect water systems from contamination. Larger facilities sometimes face pressure to prove downstream breakdown byproducts pose minimal risk—another layer to track without cutting corners. As more industries face sustainability reviews or move toward green chemistry principles, these concerns gain urgency.
One thing often overlooked is how pyridine-3,4-dicarboxylate earns its keep through subtle but important performance differences. Many users focus only on price per gram and overlook the unpredictable costs of substitutions that create supply headaches or lead to wasted material. Here, its consistent performance under typical lab conditions adds enough value to justify slightly higher sticker prices compared to more generic di-carboxylates on the market. It has less of a volatility problem, stashes more easily without caking, and stays compatible across a wider pH window than some competing isomers. That translates to fewer ruined reactions and more confidence during method transfer or scale-up.
There’s a lesson in this for anyone who’s ever tried to cut corners: cheapness rarely equals savings if the compound doesn’t perform exactly as the project demands. From my own experience consulting for contract research organizations, the cost of a failed batch—lost hours, wasted reagents, missed milestones—always outweighs the difference between a premium product and a so-called “bargain” substitute.
Despite its strengths, pyridine-3,4-dicarboxylate comes with challenges. Its relatively low commercial volume sometimes leads to supply hiccups. This shortage can hit hardest in academic settings or smaller startups that lack the buying clout of big pharma or national labs. Short-term price spikes ripple through research budgets, delaying experiments or forcing painful substitutions. If more chemical suppliers recognized real-world demand and improved supply chain stability, fewer teams would find themselves scrambling to adjust protocols on short notice.
Another practical issue lies in custom synthesis. Occasionally, end-users need tweaks—such as anhydrous versions, micronized particles, or specific counter-ions for salt forms. Current supply channels often lack agility, focusing on standard lots over bespoke preparations. This disconnect leads some researchers to take synthesis in-house or settle for less-than-ideal inputs. Investing in modular production facilities and listening to feedback from users could close that gap and support new discoveries.
Solid, dependable compounds rarely grab headlines, but innovation leans on those quiet workhorses. Pyridine-3,4-dicarboxylate’s track record in helping develop new catalysts and constructing robust frameworks illustrates a broader truth. Most breakthroughs stem from building on the known and reliable before daring the new and risky. In practice, a researcher can bank on this molecule’s predictable behavior, freeing up energy to explore more variable or experimental aspects of a project without wasting cycles second-guessing the basics.
From my time in process development, teams tended to hit roadblocks less often with materials that brought transparency—documented purity, reproducible reactivity, known safety margins. Whether you’re scaling up a new polymer or designing prototype sensors, dependability beats flashiness every time.
Improvements don’t just rest with end-users learning to ask the right questions. Suppliers carry much of the responsibility for ensuring that pyridine-3,4-dicarboxylate arrives on time, in specification, and with traceability. In my work with purchasing departments, nothing frays trust faster than an unexplained batch variation or missing quality paperwork. Companies that invest in transparent supply chains—batch-level testing, clear documentation of synthetic routes, open answers about impurities or side-products—become partners, not just vendors. More widespread adoption of lot-based barcoding and supporting digital records could streamline troubleshooting and keep labs running smoothly.
Meanwhile, producers can work toward environmental benchmarks by seeking greener precursors and minimizing solvent waste. These changes require upfront investment but build a foundation for longer-term relationships with industries driving toward sustainability targets. Inviting more feedback loops between producers and laboratories would speed up this process. Instead of viewing the product as a background commodity, treating it as an integral component of the discovery process raises the bar for everyone involved.
One area ripe for growth involves closing the gap between academic research and commercial practice. Academic labs often push the boundaries of pyridine-3,4-dicarboxylate chemistry, uncovering new uses in pharmaceuticals or materials. Far too frequently, those advances stall when transitioning to scaled production, as industrial partners hit supply or consistency snags. By creating better partnerships—joint working groups, open-access protocols, collaborative quality control projects—researchers and engineers could streamline progress from bench to plant.
I’ve witnessed the frustration of seeing a promising new reaction fail on first scale-up, often because an assumed “standard material” from the catalog actually arrived with unseen quirks or impurities. More cross-sector collaborations, supported by shared data systems and regular check-ins, could prevent wasted effort and encourage shared learning. Both sides stand to gain from transparency and a more open feedback culture.
Access to solid technical support remains an essential factor in getting the most out of pyridine-3,4-dicarboxylate. Over the years, the quality of supplier-provided data has improved—digests now carry melting points, solubility charts, and impurity profiles. Still, many end-users benefit from hands-on troubleshooting tips, real-world applications, and heads-up warnings about common incompatibilities. Hosting regular workshops or publishing detailed case studies could close that knowledge gap.
Developing a shared space for user reports—anonymized, thoughtfully moderated, and searchable—could help researchers avoid repeating common mistakes. Suppliers might also provide follow-up surveys or channels for feedback, helping clarify which tweaks and support services matter most in practice. This moves the conversation past static documentation and into dynamic exchange—a growth point for the next era of reagent distribution.
What sets pyridine-3,4-dicarboxylate apart isn’t sheer novelty or headline-grabbing reactivity. The story here revolves around reliability, subtlety, and a track record of performance in lab and industry alike. It brings real value for those willing to look past the basic spec sheet and match their needs to the molecule’s strengths. The market and the science behind this compound keep evolving, and so do needs for supply chain transparency, environmental management, and technical training. Suppliers who step up to these challenges, and end-users who ask sharp questions, will shape standards moving forward. In my experience, those partnerships—not just the chemistry—push projects across the finish line.