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HS Code |
133052 |
| Product Name | Pyridine-3,4-dicarboxylic anhydride |
| Cas Number | 89-38-3 |
| Molecular Formula | C7H3NO3 |
| Molecular Weight | 149.11 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 196-198 °C |
| Boiling Point | Decomposes before boiling |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.5 g/cm³ (approximate) |
| Chemical Structure | Anhydride formed from pyridine-3,4-dicarboxylic acid |
| Smiles | O=C1OC(=O)c2cccnc12 |
| Pubchem Cid | 6819 |
As an accredited Pyridine-3,4-dicarboxylic anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyridine-3,4-dicarboxylic anhydride, 5 grams, packaged in a sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 10 metric tons packed in 25 kg fiber drums, securely palletized, ideal for safe international shipment. |
| Shipping | Pyridine-3,4-dicarboxylic anhydride is shipped in tightly sealed containers to protect it from moisture and contamination. The packaging complies with chemical safety regulations, using appropriate hazard labeling. During shipping, the chemical is kept in a cool, dry place, and handled according to your region’s hazardous material transport guidelines. |
| Storage | Pyridine-3,4-dicarboxylic anhydride should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong oxidizers and bases. Protect from light and sources of ignition. Keep the storage area clearly labeled and secure, and avoid prolonged exposure to air to prevent hydrolysis or decomposition. |
| Shelf Life | Pyridine-3,4-dicarboxylic anhydride typically has a shelf life of 2-3 years when stored dry, cool, and tightly sealed. |
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Purity 99%: Pyridine-3,4-dicarboxylic anhydride with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high product yield and consistency. Melting Point 170°C: Pyridine-3,4-dicarboxylic anhydride with melting point 170°C is used in organic synthesis reactions, where it facilitates precise thermal processing and efficient reaction rates. Molecular Weight 165.1 g/mol: Pyridine-3,4-dicarboxylic anhydride at a molecular weight of 165.1 g/mol is used in heterocyclic compound modification, where accurate stoichiometry and reliable incorporation are achieved. Stability Temperature up to 120°C: Pyridine-3,4-dicarboxylic anhydride with stability temperature up to 120°C is used in high-temperature polymerization, where chemical integrity is maintained during processing. Particle Size <10 µm: Pyridine-3,4-dicarboxylic anhydride with particle size less than 10 µm is used in fine chemicals formulation, where rapid dissolution and homogeneity are obtained. Moisture Content <0.5%: Pyridine-3,4-dicarboxylic anhydride with moisture content below 0.5% is used in catalyst preparation, where sensitivity to hydrolysis is minimized to improve catalyst performance. Viscosity Grade Low: Pyridine-3,4-dicarboxylic anhydride with low viscosity grade is used in coating material synthesis, where it enables uniform application and film formation. Assay ≥98%: Pyridine-3,4-dicarboxylic anhydride with assay above 98% is used in laboratory-scale research, where high chemical purity ensures reproducible analytical results. |
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Pyridine-3,4-dicarboxylic anhydride, often called Quinolinic Anhydride in the synthesis rooms, stands as a specialty intermediate within pyridine chemistry. At our facility, hands in gloves and eyes on pressure gauges, we spend our time close to the process, not just reading datasheets. This compound consistently draws attention from pharmaceutical research labs, advanced materials groups, and agrochemical developers owing to its molecular structure and reliable performance during synthesis steps that require precision and repeatable reactivity.
On our lines, we keep the process simple but controlled. Pyridine-3,4-dicarboxylic anhydride does not behave like general-purpose pyridine derivatives. Its diacid anhydride form brings reactivity at two functional sites—carboxylic units placed at the 3 and 4 positions around the pyridine ring. Those two reactive sites open up options that regular monofunctional pyridine carboxylic acids can’t provide. Chemists in drug development often highlight how this compound solves bottlenecks in ring-opening pathways or step-growth polymerizations. During my time overseeing our reaction feed lines, I have taken part in many direct transfers where the need for that unique structure could not be filled by straightforward pyridine-dicarboxylic acids or their esters.
In the factory, purity is not an abstract number. Our Pyridine-3,4-dicarboxylic anhydride regularly runs between 98.5% and 99% by HPLC, with single-digit ppm levels of moisture, and this actually makes a difference. Even a 1% impurity can alter reaction outcomes or lead to wasted catalyst and higher downstream purification loads. Colleagues tackling scale-up work on cross-coupling and condensation know how only the anhydride form survives their cyclization reactions. Granules we handle have a crisp white appearance—visual color changes immediately flag hydrolysis or contamination from glove powder, all it takes is a glance as the product flows from filtration to drying trays.
Other manufacturers sometimes try quick-dry shortcuts or sacrifice particle size control. We find those corners breed inconsistency and clog powder feeders. Our approach is to finely mill the anhydride to a particle size range between 80 to 150 mesh. This size supports even dissolution and reduces dust—a favorite among the plant operators on the third shift who clean up at sunrise. Packing the product into polyethylene-lined drums or foil pouches keeps moisture away; a humidity blip during shipping can turn this compound lumpy, we’ve learned that through the feedback from directly visiting clients’ labs.
You might ask, why not just stick with the more common isomeric pyridine dicarboxylic acids? Direct experience in reaction vessels says otherwise. The anhydride form brings much sharper reactivity to acylation and amidation than the hydrated acids can manage. Just last season, a team in agricultural chemicals worked with us to synthesize selective herbicide scaffolds. Attempts with the dicarboxylic acid took several hours and stalled after 60% conversion, while our anhydride hit completion in under 45 minutes and demanded less stringent temperature control. Similar gains stand out in the hands of polymer chemists. We have seen exploratory runs in step-growth polymerization where control over backbone substitution stayed tight because the anhydride enters only two positions—no random branching as happens with mixed-function products.
The pharmaceutical sector finds the most consistent benefits. Pyridine-3,4-dicarboxylic anhydride serves as a genuine workhorse in the assembly of bidentate ligands, where both carboxyl groups couple smoothly. What cannot be ignored is downstream processability. Intermediates routed through our anhydride feed into cleaner isolations since the only significant byproduct is a small amount of pyridine, which flashes off easily. Our staff has visited pilot sites where engineering teams had struggled with sticky tar formation when using alternative pyridine acids; switching to the anhydride eliminated most of the waste, and steam-trace maintenance calls dropped off noticeably. There’s nothing like firsthand accounts: between plant trials, lab pilots, and the calls that come from process engineers, we have watched the adoption curve tip in favor of the anhydride version each year.
Some differences are subtle, and some hit you right away. Chemically, the story boils down to reactivity, solubility, and downstream handling. Ordinary pyridine-3,4-dicarboxylic acid needs activation under coupling conditions and generates water—an enemy if your next step involves moisture-sensitive reagents. The anhydride enters reactions dry and does not introduce unintended water loads. In our reactors, batch consistency and byproduct control levels both score higher. Not every substitution on the pyridine ring brings the same reactivity; only the ortho-anhydride (positions 3 and 4) gives this unique mix of chemical accessibility and manageable shelf life. The para- or meta-isomers just don’t perform as reliably in cyclization, and they complicate separations when scale grows beyond research scale.
In comparison with related products like phthalic or isophthalic anhydride, the nitrogen in the pyridine ring adds electronic properties that unlock unique binding profiles in coordination and catalysis. Materials scientists have reported improved control in metal-organic frameworks using our product as a building block because the nitrogen adds coordination abilities not found in standard anhydrides. These are lessons not just from lab reports but from site visits, meetings with end-users, and the ongoing feedback loops that shape our weekly product reviews.
We’ve also watched the shift in demand as regulatory changes drive away from halogenated intermediates and certain aromatic acids due to environmental regulations. Many clients now focus on sourcing nitrogen-rich intermediates that are easier to track for compliance and present milder hazard profiles. Pyridine-3,4-dicarboxylic anhydride fits those needs, letting formulators cut down on solvent and neutralization steps that create waste streams. We’ve hosted more than a few customer audits and sustainability reviews, so we prepare documentation that addresses these needs up front. Our team knows cutting waste matters as much as hitting yields.
Production runs never go according to spreadsheet models. Achieving high yields of pyridine-3,4-dicarboxylic anhydride requires precise control over reaction temperature, stoichiometry, and vacuum drying. The pathway to a consistent product involves maleic anhydride, controlled air oxidation, and exacting fractional distillation—steps that don’t forgive sloppiness. Operators here learn from the first days on shift that water is the persistent adversary; all transfers, especially to packaging, must happen in a low-humidity environment. People often underestimate the challenge: exposure to even mildly humid air can hydrolyze a significant portion of each batch, leading to skewed quality benchmarks and operator headaches.
Seeing our drums reach a client unchanged confirms the hours spent on process validation and environmental monitoring. Over the years, we have documented many batch records affected by subtle leaks in drying vessels or shifts in room humidity during night shifts. Solving these problems demanded more than equipment upgrades—we retrained loading crews so everyone checks seals before any transfer. Down the line, this means fewer customer complaints and less waste to rework. It also strengthens our own staff’s trust that whoever takes the next shift starts with reliable material, not half-dried, half-hydrolyzed messes.
On the technical side, a routine challenge stems from handling the product’s moderately reactive dust. Anyone who has swept up spilled anhydride knows that a mask does not entirely block the nose-stinging effect. We’ve installed localized suction hoods at granulation and packing stations. Operators pushed for improved training in handling fine powders and requested extra goggles and face shields—management listened, and we updated our safety protocols. This kind of practical feedback keeps us grounded and lets skilled workers keep safe, batch after batch. We reinforce these lessons during every quarterly safety drill and refresh chemical handling signage around the plant.
Researchers appreciate knowing how a material truly behaves, not just its registry number or a vendor’s brochure. We operate with transparency, sharing stability reports and detailed impurity profiles for each batch. If a customer plans to scale up a process, they have our technical team on tap to discuss how anhydride grades might interact with specific catalysts or how they dissolve in less common solvents. For instance, customers working with polar aprotic solvents have found our product dissolves rapidly with minimal heating, which streamlines their overall throughput. Polymer chemists have reached out after discovering downstream color in polyamide runs; we collaborated to identify trace amine impurities, leading us to tighten recrystallization steps.
The difference in long-term relationships grows out of these everyday problem-solving moments. As a manufacturer, we don’t drop product and disappear. Issues reported from the field—such as inconsistent solubility or granule flow—get reviewed in our weekly operations meeting. We track not just how much product ships but also returns, quality claims, and how our material performs under different storage conditions. This approach instills a sense of responsibility toward the full product lifecycle, which becomes vital as regulations tighten and supply chains grow more complex.
Raw material sourcing poses its own headache. Global demand for pyridine derivatives swings each year, and disruptions in upstream feedstocks like basic pyridine or maleic anhydride can create bottlenecks. Being situated near established chemical infrastructure gives us priority access, but sharp price jumps have forced us to renegotiate contracts and sometimes adjust run schedules. Leaning on local suppliers supports short transit times and less exposure to shipment delays, especially for customers with just-in-time inventory systems. Our purchasing staff keeps contingency plans and checks market intelligence weekly for early signals of crunches in the supply chain.
On the regulatory end, we adhere to all regional and national obligations. Pyridine-3,4-dicarboxylic anhydride does not face the same restrictions as some chlorinated aromatics or unstable peroxides. The product’s solid state minimizes transport risks. Our documentation covers all critical control points—batch records trace the material from initial synthesis through last-mile delivery. Periodic surprise inspections keep us sharp and reinforce that only well-documented, auditable batches clear the warehouse gate.
Client audits routinely request proof of compliance on environmental, labor, and storage standards. In the last year, we have had ongoing engagement with regulatory advisors to confirm REACH preregistration and to update our SDS documentation to reflect new global harmonization standards. The cost and time going into these systems don’t offer direct financial gain, but they smooth relationships with major buyers who can’t afford regulatory headaches down the line.
Being a chemical manufacturer means dealing up close with trends in end-use development. We talk to researchers racing for the next kinase inhibitor and to process engineers building flexible intermediate loops in batch reactors. In the past two years, a marked shift toward greener chemistry has shaped customer requests; many now seek verification that our products fit into solvent recycling streams. We experimented with different solvent systems to prove that Pyridine-3,4-dicarboxylic anhydride does not introduce persistent organics into wastewater streams. This keeps us one step ahead of evolving EPA targets and lessens the cleanup burden for clients. The uptick in biobased polymer work also feeds our commitment to minimizing trace oxidant and amine residuals, helping formulators stay compliant with new biocompatibility norms in their end products.
Cost control weighs on purchasing decisions. We aim for steady pricing and regular schedules. Clear communication about delays or lot-specific quirks avoids surprise downtime—a hard lesson learned from unforeseen freeze-offs in a winter shipment three years ago. Our office connects purchasing and technical teams, so client queries about a shift in color or solubility never go overlooked. During pandemic disruptions, we supported regular buyers by splitting shipments or providing safety stock at our facilities. As vaccination rates climbed, we kept flexible lead times to let customers recover lost days, showing respect for the fact that every real-world project encounters hurdles, no matter the spec sheet.
Environmental responsibility no longer feels optional. Every drum that leaves our site represents not just an order fulfilled but also an environmental footprint. Our solvent selection, energy use, and packaging choices face review at quarterly meetings. Recent investments in condenser technology trimmed annual process losses. Where we once relied on manual grain size checks, we’ve implemented laser particle sizing and real-time moisture monitoring. These steps go beyond marketing—reducing actual waste and energy consumption translates into savings that help absorb price pressures from utility hikes and raw material swings.
Efforts like segregated waste streams, steam recycling in dryers, and periodic third-party environmental audits feed into our improvement culture. Feedback from long-standing clients sometimes prompts new ideas: one medical device company pushed us to trial biodegradable liners in shipping drums. After careful evaluation, we identified sources that provide moisture resistance without the usual plasticizer leach-outs, passing field tests during monsoon season deliveries.
Staff bring ideas that drive measurable improvement. Experienced operators advocated for cross-shift handovers and introduced rotating role assignments, making sure no process step is handled in isolation. Younger technicians jump in with digital tracking, capturing detailed temperature and vacuum profiles never monitored by the prior generation. In recent months, our lead process chemist has worked side by side with warehouse personnel to revisit moisture controls and chemical stability protocols. Training blends old-school knowledge—a nose for volatile traces or a feel for when a batch “runs cold”—with modern instrumentation and digital recordkeeping.
Team pride matters more than any sales pitch. From the floor sweepers to the QA analysts, everyone shares the goal of shipping reliable, pure anhydride to labs and plants. Weekly toolbox meetings highlight both glitches and successes. Root cause reviews are treated as team wins, not blame games. We invest in technical training so that the field feedback—whether from university researchers or multinational buyers—comes back to people who can act, not just log data. There’s a sense here that our jobs tie directly into the chemists downstream, who trust their research and pilot lines to the batches we produce.
The work never stands still. Each year brings new requirements from researchers, synthetic chemists, and process engineers. Some are searching for sharper reactivity, some for greener footprints, others for easier regulatory approval. Alongside those challenges come fresh regulations and shifting market forces. Our best response remains a straightforward commitment: to manufacture and supply pyridine-3,4-dicarboxylic anhydride to the highest level of reliability, purity, and documentation, tailored to the practical obstacles our customers face.
We keep stories and lessons from the field at the heart of our process improvements: the catalyst specialist who needed a moisture-free supply for a tight deadline; the polymer developer who counted on uniform granule size to keep extruders from jamming; the regulatory manager who trusted our batches would pass each audit. Reliable manufacturing rests on attention to detail, open communication, and the honesty to address mistakes directly. In our experience, this is the only way to keep earning the trust of those who count on our products, batch after batch, year after year.