|
HS Code |
393160 |
| Name | 3,4-Pyridinedicarboxylic acid |
| Other Names | Quinolinic acid |
| Chemical Formula | C7H5NO4 |
| Molar Mass | 167.12 g/mol |
| Cas Number | 89-00-9 |
| Appearance | White to off-white powder |
| Melting Point | 225-228°C (decomposes) |
| Solubility In Water | Slightly soluble |
| Density | 1.622 g/cm³ |
| Boiling Point | Decomposes before boiling |
| Pka1 | 2.4 |
| Pka2 | 4.2 |
As an accredited 3,4-Pyridinedicarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3,4-Pyridinedicarboxylic acid is provided in a sealed, amber glass bottle with a clear, printed hazard label. |
| Container Loading (20′ FCL) | 20′ FCL container holds tightly sealed, 25kg fiber drums or bags of 3,4-Pyridinedicarboxylic acid, ensuring safe chemical transport. |
| Shipping | 3,4-Pyridinedicarboxylic acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is handled as a stable, non-hazardous solid, typically transported by ground or air freight according to standard chemical shipping regulations. Proper labeling and documentation ensure compliance with safety and environmental guidelines. |
| Storage | 3,4-Pyridinedicarboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep it protected from moisture and direct sunlight. Ensure clearly labeled storage and avoid excessive heat. Use proper personal protective equipment when handling, and follow standard laboratory chemical storage protocols. |
| Shelf Life | 3,4-Pyridinedicarboxylic acid should be stored tightly sealed; shelf life is typically several years under cool, dry conditions. |
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Purity 99%: 3,4-Pyridinedicarboxylic acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity reactions. Melting point 236°C: 3,4-Pyridinedicarboxylic acid with a melting point of 236°C is used in high-temperature catalyst screening, where it maintains structural integrity under thermal stress. Molecular weight 167.12 g/mol: 3,4-Pyridinedicarboxylic acid of molecular weight 167.12 g/mol is used in polymer additive formulation, where it enables precise stoichiometric calculations for consistent product quality. Particle size < 75 µm: 3,4-Pyridinedicarboxylic acid with particle size below 75 µm is used in powder metallurgy applications, where it provides enhanced homogeneity and reactivity in the blend. Stability temperature up to 200°C: 3,4-Pyridinedicarboxylic acid with stability up to 200°C is used in advanced material synthesis, where it resists decomposition during process heating. Water solubility 2.5 g/L: 3,4-Pyridinedicarboxylic acid with water solubility of 2.5 g/L is used in aqueous-phase reaction engineering, where it ensures efficient dissolution and homogeneous reaction mixtures. |
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Not every chemical compound gets the same amount of attention in labs or production halls. Some carve a niche because their structure fits critical functions. 3,4-Pyridinedicarboxylic acid, with its concise six-membered aromatic ring and two strategically placed carboxylic groups, belongs to this select club. As someone who’s spent time hunched over fume hoods and briefing both researchers and purchasing teams, progress doesn’t happen by accident. Chemists look for reliability and consistent performance, especially when investing in starting materials that pave the way for more complex molecules.
In practical use, the model most sought after is the 99% purity crystalline powder, easy to measure and dissolve for lab work. Most standard commercial packs come in moisture-proof, inert containers to keep the acid in workable condition over time. I’ve unpacked more than one poorly sealed reagent in my days, and a spoiled batch frustrates not only plans but budgets. Handling something like this means gloves, clean scoops, and a clear record in the lab notebook for traceability, a habit I developed early thanks to a few stern words from experienced mentors.
There’s a direct line between foundational chemistry and the final dyes, catalysts, or pharmaceutical intermediates seen at scale. 3,4-Pyridinedicarboxylic acid works as a valuable building block to create heterocyclic compounds and specialty polymers. This acid, thanks to the positions of its carboxyls, allows researchers to develop new ligands or chelators for metal complexation, which is a big part of environmental and analytical chemistry. Projects that target new materials—like polymer coatings with resistance to heat or corrosion—often draw on this acid for its predictable reactivity.
From an industry perspective, scale matters. At academic bench scale, a few grams are plenty. In manufacturing, teams order kilograms, sometimes more, depending on throughput and client needs. Whether the goal involves making fine-chemistry intermediates or pharmaceutical scaffolds, it’s vital to use a product whose trace impurity levels and batch consistency line up with regulatory expectations. Labs with proper documentation and trusted lots reduce the risk of failed reactions or impurity spikes downstream.
Over the years, I’ve noticed researchers appreciate the clean separation this acid provides in purification steps. Its solubility profile, neither too sticky nor too soluble, supports crystallization or precipitation steps needed to isolate pure intermediates. This small win matters, especially with budgets tightening and timelines shrinking across both academic and private sectors.
A quick comparison often comes up between 3,4-pyridinedicarboxylic acid and its close relatives, such as the 2,3- and 2,6-substituted forms. Structural differences may sound trivial, but they shape the reactivity, complexation ability, and downstream applications. In my own lab work, switching from a 2,6- to a 3,4-isomer changed both the solubility and final product yield in polymer preparations. Carboxyl group positioning controls whether one gets chelation from both ends or interacts differently with bases and acids.
For those in the pharmaceutical or agrochemical sectors, 3,4-pyridinedicarboxylic acid tends to outperform analogs when it comes to synthesis of active molecules with targeted bioactivity. There’s a reason companies stick with this variant in the search for hit-to-lead compounds—it consistently provides a scaffold that shows both stability and functional group compatibility. It’s not about preference, it’s about performance after months or years of head-to-head trials.
The cost difference between isomers may seem minor, but recurring supply issues and purification headaches can eat into project budgets. From my experience, investing in the right starting material saves both money and frustration, as separation and purification steps with a less cooperative isomer tend to lead to lost product and extra solvent use. Sustainable chemistry depends as much on picking the right primary ingredients as it does on fancy downstream technologies.
Working with organic acids in a lab or production setting involves a balance between safety and efficiency. 3,4-Pyridinedicarboxylic acid won’t explode, combust spontaneously, or emit strong fumes, but good practices mean gloves, goggles, and covered containers. The crystalline powder can draw moisture from the air, so resealing containers matters. It sounds basic, but every time a boisterous group leaves a chemical exposed, degradation creeps in, and so do unwanted side reactions that affect yields.
In my early days, I remember opening a container only to find clumped solids, which spelled trouble for weighing and mixing. Since then, I always checked desiccant packets and labels before opening a new shipment. For longer-term use, storing the compound in a cool, dry spot away from direct light avoids slow degradation of both the acid and the container itself. Even if the product specification says it will last a year or more, careful storage extends shelf life beyond that.
Disposal also deserves attention. Residues and waste need neutralization before heading to typical drains. Local policies mean lab staff need to track what leaves the site, and unmarked waste creates headaches for everyone. Proper labeling is neither glamorous nor exciting, but it avoids penalties and keeps everyone safe—something I learned the hard way handling a mixed acid waste container during a routine audit.
Talk to any purchasing manager or lab supervisor, and the main complaints revolve around batch variability and incomplete documentation. For ingredients like 3,4-pyridinedicarboxylic acid, missing a certificate of analysis or batch traceability means research timelines get busted or, worse, manufacturing grinds to a halt. There’s no substitute for a product with a transparent supply chain and a proven record of regulatory compliance. Experienced teams source only from suppliers who show test results, lot numbers, and clear documentation, all of which matter more than a small price advantage.
In one project I supported, a poorly documented batch delayed an entire set of pharmaceutical screenings. Waiting for another shipment, with all requisite paperwork, wasted both time and credibility. Since then, I always checked the COA before even opening a container. Documentation isn’t bureaucracy for its own sake—it’s assurance that every gram can be traced from shipment through to final product.
More industries now care about both the origin of chemical ingredients and how they impact downstream waste streams. Regulations shape what enters the market and how it’s handled at disposal. Companies seeking certifications have to prove their supply chains for precursors like 3,4-pyridinedicarboxylic acid are clean and sourced responsibly. In response, trustworthy suppliers share details on their sourcing and production processes, helping buyers meet both internal targets and government requirements.
Calls for increased transparency don’t come out of nowhere. Once, our lab had to account for every chemical, from arrival to end use and waste, to comply with new local regulations. This led to a shift in how we evaluated suppliers—not just on cost and purity, but on the strength and clarity of their supply chain documentation. For chemicals with widespread industrial and research use, having this clarity avoids compliance headaches and supports responsible chemistry.
The role of 3,4-pyridinedicarboxylic acid is set by its history of reliability in synthesis, but its future depends on the creative work of chemists and material scientists. Teams working on novel catalysts or next-generation polymers need access to high-quality starting materials without supply chain hiccups. More collaboration between suppliers and users would help streamline troubleshooting for unexpected issues or application questions.
From my experience helping to source rare building blocks or troubleshoot contaminated batches, fast feedback and open communication with suppliers make all the difference. Direct channels keep both sides nimble if a quality concern appears, or if a project needs a custom batch with tighter impurity specifications. In some cases, joint development agreements ensure both parties update test methods to catch new impurities or meet emerging regulatory guidelines.
Investing in automation for documentation and tracking further strengthens the position of both buyers and suppliers. Automated tracking of lot numbers and expiry dates means less human error and quicker identification of problems. This minimizes downtime and supports the push for data-driven quality control, a lesson I learned over years managing both lab inventory and large-scale production.
Transparency about sustainability is another growing demand, especially from clients who look beyond just technical performance. Sharing details about greener synthesis routes or reduced solvent waste enhances the appeal of established chemicals like this one. In projects where the end clients value environmental profiles, a supplier’s transparency and innovation make a real difference during selection.
3,4-Pyridinedicarboxylic acid might not dominate headlines, but it holds quiet importance across several fields. Its reliability in delivering clean reactions and supporting new discoveries gives it staying power. Distinguishing it from other isomers boils down to small but crucial molecular differences that affect everything downstream—yield, cost, and sometimes regulatory approval.
As the industry landscape shifts, demand for traceable, documented and sustainably produced chemicals grows. Each batch, sourced and handled with care, supports not just today’s projects, but the next wave of innovation that could shape fields as diverse as new materials, life sciences, and sustainable manufacturing. The real story revolves around thoughtful selection, diligent handling, and open lines of trust between suppliers and users.
Thinking beyond fancy terms or buzzwords, what counts is a product that holds up in real work. Talking with researchers, manufacturers, and even students starting out, it all circles back to one thing—the need to deliver accurate, dependable results. That’s where the value of 3,4-pyridinedicarboxylic acid comes into its own, not simply as a chemical, but as a tool for advancing what’s possible in the lab and beyond.
Each time I see a project succeed—whether it’s a complex synthesis route pulled off on schedule or a coating that shows better durability—it’s clear that good chemistry starts at the foundation. The materials we pick at the start shape the quality and success of everything that follows. 3,4-Pyridinedicarboxylic acid, by combining structural versatility with steady supply and clear documentation, takes its place as a trusted partner in the practical pursuit of new solutions.