|
HS Code |
827368 |
| Product Name | 3,4-Pyridinedicarboxylic anhydride |
| Molecular Formula | C7H3NO3 |
| Molecular Weight | 149.10 g/mol |
| Cas Number | 89-25-8 |
| Appearance | White to off-white solid |
| Melting Point | 142-146 °C |
| Boiling Point | 362.7 °C at 760 mmHg |
| Density | 1.545 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Synonyms | Quinolic anhydride; Pyridine-3,4-dicarboxylic anhydride |
| Structure | Anhydride form of pyridine-3,4-dicarboxylic acid |
| Smiles | O=C1OC(=O)c2cccnc12 |
| Inchi | InChI=1S/C7H3NO3/c9-6-3-1-2-8-4-5(6)7(10)11/h1-4H |
As an accredited 3,4-Pyridinedicarboxylic anhydride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tight-seal cap, labeled “3,4-Pyridinedicarboxylic anhydride” and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL typically holds 10,000–12,000 kg of 3,4-Pyridinedicarboxylic anhydride, packed in 25 kg fiber drums, securely palletized. |
| Shipping | 3,4-Pyridinedicarboxylic anhydride should be shipped in tightly sealed containers, clearly labeled, and protected from moisture. Transport in accordance with local, national, and international regulations for hazardous chemicals. Store and ship in a cool, dry place, ensuring proper documentation and handling to prevent accidental release or exposure during transit. |
| Storage | 3,4-Pyridinedicarboxylic anhydride should be stored in a tightly sealed container, protected from moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong bases and oxidizing agents. Minimize exposure to air and humidity to prevent hydrolysis. Label storage containers properly and handle under a fume hood if possible to avoid inhalation. |
| Shelf Life | Shelf life of 3,4-Pyridinedicarboxylic anhydride: Store tightly sealed, cool, and dry; stable for up to 2 years under proper conditions. |
|
Purity 99%: 3,4-Pyridinedicarboxylic anhydride with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity product formation. Molecular weight 165.11 g/mol: 3,4-Pyridinedicarboxylic anhydride of molecular weight 165.11 g/mol is used in preparing specialty heterocyclic compounds, where it offers reproducible stoichiometric control. Melting point 111°C: 3,4-Pyridinedicarboxylic anhydride with melting point 111°C is used in fine chemical production, where it facilitates efficient solid-phase reactions and easy purification. Particle size ≤ 50 μm: 3,4-Pyridinedicarboxylic anhydride with particle size ≤ 50 μm is used in high-throughput screening assays, where it enables rapid dissolution and uniform dispersion. Thermal stability up to 180°C: 3,4-Pyridinedicarboxylic anhydride with thermal stability up to 180°C is used in polymer modification processes, where it maintains structural integrity under elevated processing temperatures. Hydrolytic stability: 3,4-Pyridinedicarboxylic anhydride featuring hydrolytic stability is used in manufacturing long-lived polymeric materials, where it prevents premature degradation during synthesis. Assay (HPLC) ≥ 98%: 3,4-Pyridinedicarboxylic anhydride with assay (HPLC) ≥ 98% is used in analytical reference standards, where it ensures reliable and accurate quantitative analysis. Low moisture content < 0.5%: 3,4-Pyridinedicarboxylic anhydride with low moisture content < 0.5% is used in moisture-sensitive organic reactions, where it minimizes side reactions and maintains process efficiency. |
Competitive 3,4-Pyridinedicarboxylic anhydride prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Working as a manufacturer in the fine chemicals industry means developing a strong grasp of how unique intermediates like 3,4-Pyridinedicarboxylic anhydride shape downstream innovation. This compound, also known in research circles as 3,4-pyridine-dicarboxylic anhydride or quinolinic anhydride, is not something that turns up in commodity trade catalogs. It occupies a more specialized niche, and those who work with it up close appreciate how its properties and reactivity influence targeted synthesis rather than bulk processing.
Out of our range of pyridine-based reagents, the anhydride form of 3,4-pyridinedicarboxylic acid stands out for its reactivity profile. The transformation from dicarboxylic acid to anhydride doesn't just affect the dehydration point; it shifts the whole behavior in coupling and activation reactions. Customers come to us with end goals in material science, polymer chemistry, and pharmaceuticals because they can't always address their needs with other pyridines or carboxylic acids. Experiencing those production campaigns firsthand gives us a clearer sense of why certain features matter.
In the laboratory, 3,4-Pyridinedicarboxylic anhydride often starts as a bridge molecule. During real-world process development, we see its dual anhydride groups display solid reactivity toward amines and alcohols. This proves especially useful for making functionalized heterocycles or linking blocks in specialty polymers. In contrast, using the parent dicarboxylic acid usually requires separate activation steps or harsher conditions, which introduces more variability and often leads to less predictable yields.
On the plant floor, we need to account for the anhydride’s sensitivity to ambient moisture. Its handling is markedly different from more robust pyridine derivatives, so our production teams go the extra mile with dry-room operations and inert-gas handling. Over time, these small adjustments in discipline add up—we can attest to the value behind the anhydride format, as it streamlines coupling routes, minimizes side product formation, and supports higher throughput for our clients’ custom molecules.
Requests for product purification, packaging, or transport usually reflect the high value of this compound relative to its volume. Most users take this compound directly into synthesis steps without storing it for long. This pattern emerged from decades in the industry, as the anhydride releases energy and water upon hydrolysis, which means every shipment needs to meet exacting handling standards. It’s not simply about regulatory compliance; product integrity protects research outcomes as much as it ensures worker safety.
Among our customers—who typically include advanced R&D labs, material science innovators, and pharmaceutical API developers—there’s an awareness of purity that comes from hands-on experience. Purities in the 98%+ range are almost seen as baseline, and requests often specify HPLC or NMR quality control. The physical appearance, a white or off-white crystalline solid, tells a trained eye a lot. Small traces of yellowing or moisture pickup tend to be flagged immediately. Our packing teams regularly choose sealed glass or HDPE bottles, often flushed with inert gas if requested, so users receive material that maintains original reactivity right through to the bench.
Within our own facility, we've refined lot sizes to balance the fine line between demand and shelf-life. The anhydride’s propensity to absorb water means that extra bulk packaging leaves it vulnerable. Smaller aliquots and fresh production runs allow us to guarantee each lot meets initial test certificate values. Unlike mass-market chemicals, compromises in storage and supply chain timing are not an option here. End users expect each gram to perform consistently, and we hold ourselves accountable for that continuity, batch after batch.
Chemists who’ve relied on other pyridine analogs or carboxylic anhydrides recognize the small but crucial differences with 3,4-Pyridinedicarboxylic anhydride. Taking the example of succinic anhydride or phthalic anhydride—both widely available and easy to work with—there’s a clear difference in aromaticity and electronic effects. Our product’s pyridine ring brings extra rigidity and electron-deficient reactivity, making it more attractive for heterocycle synthesis and as a precursor for active pharmaceutical ingredients where nitrogen plays a key role.
In-house trials demonstrate that switching from an aliphatic to this heteroaromatic anhydride ramps up selectivity toward nucleophilic substitution. Customers find that the position of the anhydride groups on the pyridine ring determines what downstream transformations are possible—something that can’t be replicated by just swapping in other dicarboxylic anhydrides. The ortho relationship (positions 3 and 4) encourages formation of certain ring closures or sidechain linkages that can be unpredictable or outright unavailable with para or meta arrangements.
Another difference we witness often is in process safety and emissions control. While some aromatic anhydrides bring concerns about off-gassing or decomposition, 3,4-Pyridinedicarboxylic anhydride remains relatively stable under well-maintained dry conditions but reacts quickly when needed. That fine balance between shelf stability and in-reaction responsiveness comes up often in direct feedback from process chemists. They know they are not dealing with a generic acid or bulk anhydride—they depend on our attention to these features for process repeatability and product confidence.
After years of supplying this compound to leading-edge labs and pilot plants, we have a clear picture of its main uses. In step-growth polymerization, researchers leverage the two anhydride sites to connect bifunctional amines, creating tailored backbones with built-in heterocyclic properties. Our clients have used this pathway for high-thermal-resistance materials and for specialty coatings that benefit from nitrogen-containing aromaticity.
In pharma building blocks, the same reactivity underpins the synthesis of heterocyclic drugs and diagnostic reagents. The nitrogen atom in the pyridine ring not only aids in binding to biological targets but also supports solubilization schemes and metabolic stability. Requests from enzyme inhibitor developers and radiolabeling teams often mention the importance of positioning and activation—features that this compound delivers more consistently than others in the same class.
The feedback that resonates most with our production staff comes from customers trying to minimize hazardous waste and streamline multi-step syntheses. By enabling higher conversions and reducing by-product formation, this anhydride plays a subtle but critical role in more sustainable, cost-effective production campaigns. In our own plant, efforts to optimize downstream cleaning and emissions control draw directly from observing this compound’s behavior in organic and aqueous phases.
Our teams know firsthand that delivering reliable 3,4-Pyridinedicarboxylic anhydride starts with sourcing and handling high-purity starting materials. We select pyridine and dicarboxylic acid feedstocks based on supplier test results, but our QC checkpoints don’t stop there. Every batch undergoes careful drying, reaction, and distillation in equipment reserved for non-basic, high-reactivity chemicals only. Any residue from unrelated processes could compromise purity or trigger off-cycle reactions.
Experience has taught us that the final stages—crystallization, washing, and drying—often determine the degree of customer satisfaction. Users will spot signs of incomplete drying or solvent trace immediately, and so do we. Our crew learned early on that a well-designed filter system, temperature-controlled dryers, and fast transfer to sealed packing all guarantee the stability of the finished product. Mishandling in these areas doesn’t just waste material; it can disrupt whole client projects downstream.
From a safety perspective, our staff applies routines engineered for minimal moisture exposure and ventilation. The anhydride’s tendency to undergo exothermic hydrolysis means regular retraining on procedure, continuous monitoring of humidity, and restricted access to production areas. We share direct handling tips with qualified customers, knowing that pitfalls in bench chemistry often mirror what happens at the manufacturing scale. Feedback loops with R&D teams in both directions help us continuously raise our standards.
In terms of environmental responsibility, handling dicarboxylic anhydrides presents manageable risks compared to more volatile organics, but off-spec waste handling deserves equal vigilance. Unreacted intermediates, spent solvents, and cleaning waste are tracked and minimized through process mapping. Our investment in closed-loop solvent recovery and batch documentation pays off not just in meeting regulations but also by earning the trust of partners who value ecological awareness. Regular audits, both internal and external, spot-check water usage, waste streams, and emissions from every campaign involving this compound.
We encounter a broad spectrum of customer needs. Some specialize in exploratory synthesis, needing only a few grams per trial. Others work on kilogram-scale pilot runs. Both sets of customers often look for technical support on reaction conditions or regulatory compliance—more so than with other reagents. Our technical staff draws on plant-scale practical knowledge for real advice, not canned answers. We believe it’s our role to bridge the disconnect between the upstream realities of making sensitive pyridine derivatives and the downstream pressure of project deadlines.
Issues with shipment delays or out-of-spec material prompt us to investigate with urgency because we understand how crucial timing and reliability are in specialty synthesis. If an end user works in discovery chemistry and suddenly faces a project hold due to missing reagents, innovation gets stifled. So, we back every batch with transparent documentation on batch number, expiry, and test results. That way, partners see the same focus on quality that we want in our own suppliers.
Sometimes, especially with complex multi-step projects, design teams share feedback on particular side reactions or purification difficulties tied to this compound’s reactivity. This information cycles back into our process controls. With hands-on dialogue, we tackle challenges ranging from batch-to-batch consistency to bench procedures for improving reaction outcomes. Mutual trust emerges from responsiveness, not just the base quality of the product.
Keeping up with new applications means continuous investment in our process development. We’ve spent years refining catalytic and thermal dehydration steps to maximize yield while minimizing energy input. Innovations from our R&D—such as improved purification columns and hybrid drying techniques—help compress lead times and cut solvent usage. Customers most benefit from our willingness to run pilot studies and scaling trials on request, drawing lessons from each batch run through our line.
One of the more exciting trends in the last several years has been the emergence of customized derivatives and linked intermediates that start with 3,4-Pyridinedicarboxylic anhydride. Some of our downstream partners push boundaries in energy storage materials and organic electronic devices, using the compound’s electron-deficient nature to introduce precise new functionalities into their polymers and resins. We take these early development runs seriously, ensuring confidentiality and sharing insight on process bottlenecks.
We’re also witnessing a rise in demand for greener alternatives and safer precursors. Our ongoing initiative reviewing raw material sourcing and waste minimization stems directly from collaborative input. Besides meeting regulatory standards, these efforts avoid future supply bottlenecks and assure continuity for buyers working to scale bench discoveries into marketable products.
Every shipment of 3,4-Pyridinedicarboxylic anhydride carries a certificate of analysis, including spectral data and impurity cutoffs. The test results reflect our internal threshold, set higher than industry minimums. This high bar is not just lip service. Our team understands how small variations can affect downstream coupling, especially in reactions sensitive to trace impurities. Customers expect candor and reliability—qualities we’ve built up by closing feedback loops and promptly investigating any discrepancies.
During in-house validation, spot testing by HPLC and NMR ensures each batch shows a precise match to reference spectra. If customer labs find outliers or unexpected sidebands, they alert us, and we revisit both our synthesis and QC logs to spot the root cause. Having direct lines of communication between our production leaders and client chemists speeds up troubleshooting and builds the kind of trust that written warranties alone don’t provide.
Lot traceability, backed by thorough documentation, supports not only regulatory needs but also customer research outcomes. Our archive includes historical batch data, process modifications, and deviation investigations. This depth of record-keeping comes from real-world lessons—small oversights in the past led to extensive process reviews until our system reached today’s maturity.
Discussing 3,4-Pyridinedicarboxylic anhydride with real users reveals how much weight they assign to a manufacturer’s expertise. Synthetic methods, even from identical starting materials, can produce subtle differences in anhydride quality and reproducibility. Our approach—handling every step in-house, supported by trained technicians and full analytical backup—safeguards product reliability.
End users routinely ask about process details, confidence in the raw material supply chain, and contingency plans for production interruptions. We draw credibility from over a decade of plant operation, real-time audit history, and investment in continuous staff training. Delivering on these expectations is how we maintain relationships built on more than marketing or branding.
Every successful batch we ship stems from our team’s attention to review, training, and real-world learning. Missteps from prior runs have fueled improvements in both quality and responsiveness. With direct oversight of production and logistics, we resolve logistical delays more quickly and adapt to emerging buyer needs, whether that requires adjusted packaging protocols or tailored analytical support.
As chemists and manufacturers, we work every day with specialty molecules that act as cornerstones in advanced synthesis. 3,4-Pyridinedicarboxylic anhydride reflects the balance of reactivity, reliability, and scale. Its unique position among anhydrides allows creative process design without sacrificing quality or operational safety.
Though not as well-known outside research and production facilities, this compound helps drive advancements in multiple fields. Our role, as experienced manufacturers, is to ensure that when customers open one of our containers, they find the exacting standard required for their needs—every time. Success in this business demands more than technical data sheets or mass-market distribution. It comes from a persistent focus on real-world usability, consistent feedback, and a willingness to adapt processes to keep up with our clients’ requirements.
We appreciate every conversation with our partners because each one highlights new uses, new challenges, and fresh ways to improve. It’s that spirit of direct, practical collaboration—rooted in hands-on production—that gives 3,4-Pyridinedicarboxylic anhydride its enduring value for innovators, researchers, and production teams aiming to take their next project further.