2,3-Pyridinedicarboxylic anhydride

    • Product Name: 2,3-Pyridinedicarboxylic anhydride
    • Chemical Name (IUPAC): 1H-pyrrolo[3,4-b]pyridine-1,3,5(2H)-trione
    • CAS No.: 89-25-8
    • Chemical Formula: C7H3NO3
    • Form/Physical State: Crystalline powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    255916

    Compound Name 2,3-Pyridinedicarboxylic anhydride
    Cas Number 552-30-7
    Molecular Formula C7H3NO3
    Molecular Weight 149.10
    Appearance White to off-white crystalline powder
    Melting Point 142-144°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.55 g/cm³
    Pubchem Cid 19914
    Smiles O=C1OC(=O)c2ncccc12
    Inchi InChI=1S/C7H3NO3/c9-6-4-2-1-3-5(8-4)7(10)11-6/h1-3H
    Synonyms Quinolinic anhydride; Pyridine-2,3-dicarboxylic anhydride

    As an accredited 2,3-Pyridinedicarboxylic anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle securely sealed with a plastic screw cap, labelled with hazard symbols and chemical identification for 2,3-Pyridinedicarboxylic anhydride.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2,3-Pyridinedicarboxylic anhydride: Typically 10–12 metric tons, packed in 25 kg fiber drums, securely palletized.
    Shipping 2,3-Pyridinedicarboxylic anhydride is shipped in sealed, moisture-resistant containers with clear hazard labeling. It is kept away from moisture, heat, and incompatible substances during transit. Transportation complies with relevant chemical safety and regulatory guidelines to ensure safe handling and delivery, minimizing risks of exposure or environmental release.
    Storage Store 2,3-Pyridinedicarboxylic anhydride in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong bases, oxidizing agents, and water. Keep away from sources of ignition. Handle under a fume hood and avoid contact with skin and eyes. Properly label storage containers and ensure access to safety data sheets.
    Shelf Life 2,3-Pyridinedicarboxylic anhydride should be stored in a cool, dry place; shelf life is typically 2-3 years if unopened.
    Application of 2,3-Pyridinedicarboxylic anhydride

    Purity 99%: 2,3-Pyridinedicarboxylic anhydride with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels.

    Melting Point 235°C: 2,3-Pyridinedicarboxylic anhydride with a melting point of 235°C is used in high-temperature polymerization processes, where it provides thermal stability during reactive extrusion.

    Molecular Weight 165.12 g/mol: 2,3-Pyridinedicarboxylic anhydride with a molecular weight of 165.12 g/mol is used in organic synthesis as a building block, where it allows precise stoichiometric calculations in multistep reactions.

    Particle Size <10 µm: 2,3-Pyridinedicarboxylic anhydride with particle size below 10 µm is used in catalyst preparation, where it improves dispersion and accelerates reaction kinetics.

    Stability Temperature 180°C: 2,3-Pyridinedicarboxylic anhydride with stability up to 180°C is used in electronic material manufacturing, where it maintains structural integrity under processing conditions.

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    Certification & Compliance
    More Introduction

    Understanding 2,3-Pyridinedicarboxylic Anhydride: A Manufacturer’s Perspective

    The Role of 2,3-Pyridinedicarboxylic Anhydride in Modern Chemistry

    From the ground up, our approach to producing 2,3-pyridinedicarboxylic anhydride reflects years of hands-on experience in fine and specialty chemicals manufacturing. Chemists working in pharmaceutical synthesis, agrochemical development, and advanced material projects often rely on this compound for both its specificity and its performance in targeted reactions. The formula—C7H3NO3—and the purity levels we can ensure, directly influence reaction yields and reproducibility, two pillars of practical chemistry that become clear in large-scale applications.

    Other isomers and related anhydrides exist, but the 2,3-arrangement presents a unique structure that continues to be favored where selectivity and reactivity are key concerns. This particular anhydride’s ring arrangement shapes downstream chemistry in ways that are very different from 2,6- or 3,4-pyridinedicarboxylic anhydride. Researchers and process engineers frequently point out how much more predictable the reaction profile stays when using our 2,3 isomer; fewer side products and greater conversion rates become the norm in practical settings.

    Consistency forms the backbone of our operation. Over the years, our production lines have responded to wide fluctuations in raw material quality and stringencies in customer processes, all while holding to standards that balance cost, performance, and environmental responsibility. Each batch must match not just a paper specification but the demanding expectations of R&D labs aiming for reproducibility, project after project.

    Manufacturing Experience and Product Gallery

    We produce 2,3-pyridinedicarboxylic anhydride as a white to pale yellow solid, typically supplied in flake or fine crystalline form. Moisture sensitivity issues have shaped our packaging protocols over time. We run regular stability trials to verify shelf-life under storage conditions common in most syntheses labs. These details—often beyond what a technical sheet lists—become critical for chemists rotating product out of long-term storage or scaling up previously bench-scale processes.

    Our in-process controls continuously track trace impurities, unreacted starting material, and isomeric purity, responding to subtle shifts in synthesis parameters as needed. Such control doesn’t emerge from standard operating procedures alone; it follows years spent refining protocols based on actual customer feedback and troubleshooting. NMR, HPLC, and titrimetric analysis guide each lot from raw reactant to finished anhydride, cutting off the risk of surprises at the user’s bench. This isn’t simply quality assurance—it’s a process of active collaboration with partners who run high-stakes reactions.

    The finished anhydride responds reliably in reactions including condensation, ring-opening amidation, or as an intermediate in heterocycle synthesis. As demand grew in high-throughput screening applications, we adapted our process to guarantee every shipment stays within a narrow melting point range and meets pre-defined, practical purity standards. We choose this route, after seeing firsthand that batch-to-batch consistency cuts down failure investigations in customer labs.

    Where 2,3-Pyridinedicarboxylic Anhydride Fits Best

    The specific positioning of the carboxylic groups in this compound makes it valuable for introducing distance-controlled functionalities onto a pyridine core. Coordination chemists prize this arrangement because it enables formation of chelating ligands with predictable, tunable properties. Over the years, customers in catalysis have achieved stronger, more defined binding through this particular isomer as opposed to others. In practice, that means tighter control over ligand-field strength, altered electronic properties, and more robust metal complexes—characteristics that often spell the difference between mediocre and excellent catalytic cycles.

    Pharmaceutical groups often approach us seeking this specific anhydride for its reactivity profile. Compared to the 2,6-analog, the 2,3 isomer opens up reaction pathways in nitrogen-containing heterocycles that would otherwise remain blocked. Hands-on experience with its clean hydrolysis to the corresponding dicarboxylic acid also matters; process chemists rarely have patience for scavenging messy byproducts or unpredictable yields. By listening to customer experiences and adjusting our filtration and drying steps, we help ensure downstream reactions require less re-work, supporting higher-value target molecule syntheses.

    Agrochemical discovery efforts expanded the role of 2,3-pyridinedicarboxylic anhydride on our production line. Esterification and amidation strategies unlock new candidate molecules from this intermediate, and the pathway control gained over certain pests and diseases would not arise without such selectivity. Not every pyridine-based anhydride supports the same transformations. We’ve seen time and again how this anhydride helps organizations fine-tune molecular frameworks for improved field performance.

    Practical Handling, Storage, and Packaging Choices

    Over time, simple packaging modes have proven unreliable for moisture-sensitive chemicals. Early adopters of our product gave immediate feedback—clumped, hydrolyzed, or yellowed product presented frustrating obstacles in the middle of time-pressured project work. As a result, we invested in airtight, layered packaging, nitrogen blanketing, and environmental monitoring during storage and loading. These practices took hold because they worked. Returning customers report fewer problems and more predictable outcomes in their first, second, and even third runs with material stored over months.

    High-purity production means less concern about unwanted byproducts in scale-up operations. Choosing a manufacturer with tight in-line controls over purity, isomer distribution, and water content can simplify downstream purification even before any reaction starts. In our own early days, it took trial and error to balance drying temperature, filtration speed, and the grind size of crystalline product to cut waste and enhance stability. Time taught us that hands-on touch in every batch run reduces the need for post-reception processing by the end user.

    Shipping chemicals with documented, measured stability profiles isn't just a paperwork exercise. It reflects an operational philosophy where real-world user feedback drives improvements. Transporting 2,3-pyridinedicarboxylic anhydride, especially internationally, teaches lessons about customs unpredictability, shipment delays, and temperature variation. Our team built secondary containment, traceable monitoring, and batch-by-batch documentation to address real shipping hazards—rather than build from a hypothetical risk assessment. The result: more responsive support, less unexpected spoilage, and a reduced learning curve for new users.

    Distinguishing 2,3-Pyridinedicarboxylic Anhydride From Other Pyridine-Based Anhydrides

    Some customers new to pyridinedicarboxylic anhydride chemistry mistake 2,6- or 3,4-isomers for interchangeable raw materials. After troubleshooting project setbacks and synthesis failures, the distinctions become glaring. Isomeric placement of carboxylic groups controls access of nucleophiles, determines ligand geometry, and tunes electron density on the pyridine ring. Flattening these specifics in raw material selection leads to unpredictable reactivity, lower yields, and cumbersome purification.

    We ran side-by-side tests comparing our 2,3-pyridinedicarboxylic anhydride to the 2,6 variant in model condensation and amide-forming reactions. The number of unintended side products shot up each time the wrong isomer entered the process. The 2,3 structure supports more constrained ring closures and a tighter transition state, which greatly influences rates and selectivity. Seasoned chemists do not need a textbook to observe this: the difference shows up in LC patterns and NMR spectra. Our commitment to offering only the 2,3 isomer for these use cases arose from these hands-on, data-backed insights, not mere desk research.

    In ligand synthesis, geometric considerations matter more every year. As more applications in advanced catalysts and electronic materials surfaced, customers returned looking for specific isomer control and documented reactivity. Bulk suppliers may treat all anhydrides as broadly interchangeable, but end users learning through trial know that not all pyridinedicarboxylic anhydrides will deliver on targeted, functional properties of newer, more sensitive materials.

    Scale-Up Parameters and Customization Based on Customer Feedback

    Lab-scale experiments do not always translate easily to industrial reactors—this fact has shaped our own manufacturing development time and again. When synthesis protocols move from 100-gram test runs to multi-kilogram lots, thermal transfer, agitation, and filtration behave unpredictably if the starting material quality varies. By refining process parameters for 2,3-pyridinedicarboxylic anhydride manufacture, our technical team resolved issues like batch-to-batch color changes, variable particle sizes, and inconsistent solubility profiles—problems that can short-circuit a scale-up campaign for customers downstream.

    Fielding requests for customized packaging and particle size distribution, our plant operators learned that one-size-fits-all solutions drag down overall performance. Project goals in heterocycle synthesis, complex ligand design, or even specialized dye manufacture call for intentional planning at every step—beginning with the raw material itself. Such requests, whether for specific mesh sizing, tailored impurity levels, or added drying steps, drove us to revisit and upgrade reactor configurations, material transfer techniques, and even HVAC logic in our plants.

    Some researchers run screening campaigns needing many small lots, while contract manufacturers demand seamless, multi-ton transport options. By actively drawing on field reports—what chemists actually encountered, not just what technical papers theorized—our team built flexible production and delivery models. Real scalability rests on adaptability, not just raw output. Again and again, it becomes clear that knowledge gained from direct customer collaboration pushes our quality and responsiveness ahead, leaving commodity suppliers behind.

    Environmental Safeguards and Responsible Production Strategy

    Our experience manufacturing 2,3-pyridinedicarboxylic anhydride confirmed early on that waste management and emissions controls are not simply regulatory check-boxes—they directly affect product consistency and community relationships. Anhydride processes can release acid mist and generate organic solvent waste. Tightening vent capture, using closed-loop solvent recovery, and investing in PID-monitored neutralization systems grew naturally from a desire to avoid local complaints and unplanned shutdowns, not just to please auditors.

    Years ago, a sudden change in local wastewater limits forced us to modify both our mother liquor neutralization and filtration processes. The result was not only regulatory compliance, but increased recovery rates and lower operating costs—gains that get passed on in product pricing and purity guarantees. Open disclosure to our customers about these changes built credibility, especially with R&D partners whose own green chemistry mandates shaped their reagent acceptance policies.

    We support requests for environmental documentation including batch carbon footprint estimates, process water optimization figures, and records of solvent recapture. This reporting framework—which we continually refine—sprang from our team’s lived experience, not outside mandates. It drives down waste, reduces energy inputs, and meets growing demands for transparent, responsible sourcing in specialty chemical manufacturing.

    Application Insights and Long-Term Collaboration

    In every major project where 2,3-pyridinedicarboxylic anhydride is chosen as a key building block, long-term collaboration between chemist and manufacturer raises success rates. Examples from pharmaceutical and fine chemical synthesis highlight how early discussions about scale, solvent interactions, and byproduct risks head off expensive surprises down the line. We maintain open, technical lines of communication with users through initial pilot phases, scaling up to full production and post-delivery support. This longstanding habit emerged as a direct reaction to recurring challenges in the early years—when missed details or rushed shipments could send an entire project back to square one.

    Under competitive project deadlines, research teams regularly need overnight answers about batch trace data, alternate shipment routes during border delays, and product handling protocols for new regulatory environments. We shape our service response around these real-world bottlenecks. Chemists value this experience-driven support—because every hour lost recovering a failed reaction, or every kilogram of spoiled reagent, cuts directly into project momentum and costs.

    Trusted supplier–user relationships in specialty chemical production depend on understanding both the granular demands of process chemistry and the bigger-picture project context. Experience tells us that users return, not just for that first delivery, but for ongoing collaboration on troubleshooting, customizations, or application expansion. Honest discussion of successes and setbacks defines the basis for continued partnership.

    Final Reflections: Experience as the Guiding Principle

    Decades of manufacturing 2,3-pyridinedicarboxylic anhydride have brought daily reminders that the difference between reliable raw material and a recurring research problem lies in lived experience, transparency, and a continuous improvement mindset. Customers need insight—not just a certificate of analysis. Our role grows beyond routine specifications to one of active engagement and iterative support, rooted in the lessons found only in true plant-floor production and field troubleshooting.

    We see equipment upgrades, new filtration techniques, and smarter packaging strategies take root following regular, candid feedback from users at the laboratory bench and in the production suite. It’s this shared knowledge, built through ongoing conversations and a willingness to adapt, that shapes not just our anhydride offering, but a broader standard of partnership in the specialty chemical world.

    2,3-Pyridinedicarboxylic anhydride represents more than a reagent or a formula. It marks the cumulative learning and everyday problem-solving that persist in chemical manufacturing. Tuning production from the manufacturer’s perspective is a living process—one that benefits most from the honesty, regular feedback, and ongoing engagement of the users who bring our material to life in world-changing applications.