3,4-pyridinedicarboximide

    • Product Name: 3,4-pyridinedicarboximide
    • Chemical Name (IUPAC): 1H-pyrrolo[3,4-b]pyridine-5,7-dione
    • CAS No.: 2211-42-9
    • Chemical Formula: C7H4N2O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    924188

    Chemical Name 3,4-pyridinedicarboximide
    Molecular Formula C7H4N2O2
    Molecular Weight 148.12 g/mol
    Appearance White to off-white solid
    Melting Point 260-265°C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes before boiling
    Cas Number 89-40-7
    Smiles C1=CC(=NC=C1C(=O)N)C(=O)N
    Synonyms 3,4-Pyridinedicarboxylic imide
    Logp -0.34 (estimated)
    Storage Conditions Store in a cool, dry place, tightly closed container

    As an accredited 3,4-pyridinedicarboximide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,4-Pyridinedicarboximide is packaged in a 100-gram amber glass bottle, sealed with a screw cap, and labeled with safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) of 3,4-pyridinedicarboximide: 8-10 metric tons packed in 25 kg fiber drums with inner plastic lining.
    Shipping 3,4-Pyridinedicarboximide is typically shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be packed in accordance with local regulations for the transport of chemicals, using protective outer packaging and clear labeling. Transport in a cool, dry, and well-ventilated area is recommended to ensure chemical stability.
    Storage **3,4-Pyridinedicarboximide** should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Ensure clear labeling and avoid direct human contact by storing out of reach of unauthorized personnel, adhering to all standard chemical storage and safety protocols.
    Shelf Life 3,4-Pyridinedicarboximide typically has a shelf life of about 2–3 years when stored in a cool, dry, and dark place.
    Application of 3,4-pyridinedicarboximide

    Purity 99%: 3,4-pyridinedicarboximide of 99% purity is used in pharmaceutical intermediate synthesis, where it guarantees high reaction yield and product consistency.

    Melting Point 260°C: 3,4-pyridinedicarboximide with a melting point of 260°C is used in high-temperature polymer formulation, where it enables thermal stability and enhanced polymer durability.

    Particle Size <10 μm: 3,4-pyridinedicarboximide with particle size below 10 μm is used in advanced coatings, where it ensures uniform dispersion and improved surface finish.

    Moisture Content <0.2%: 3,4-pyridinedicarboximide with moisture content below 0.2% is used in agrochemical formulations, where it prevents hydrolytic degradation and maintains product shelf-life.

    Stability Temperature 180°C: 3,4-pyridinedicarboximide stable up to 180°C is used in specialty chemical manufacturing, where it withstands process heating without decomposition.

    Molecular Weight 178.14 g/mol: 3,4-pyridinedicarboximide with a molecular weight of 178.14 g/mol is used in custom organic synthesis, where its defined structure enables predictable reactivity and product reproducibility.

    Solubility in DMF 95%: 3,4-pyridinedicarboximide with 95% solubility in DMF is used in pharmaceutical R&D, where it allows homogeneous solution-phase reactions and efficient compound screening.

    Residual Solvent <50 ppm: 3,4-pyridinedicarboximide with residual solvent content below 50 ppm is used in electronic materials, where it minimizes contamination and enhances device performance.

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    More Introduction

    3,4-Pyridinedicarboximide: Practical Insights for Specialists

    Unpacking What 3,4-Pyridinedicarboximide Offers

    Over the years, chemists and product developers have grown familiar with the increasing role of specialized chemicals in optimizing production and research outcomes. Among these, 3,4-pyridinedicarboximide stands out for its structure and utility. Not every lab needs this molecule, but those working with heterocyclic compounds often run into projects that call for its unique profile. The backbone of its structure—a pyridine ring hosting two carboximide groups—gives it a chemistry that opens possibilities in pharmaceutical, agricultural, and materials applications. You realize pretty quickly that differences in small substituents can deliver huge changes in reactivity or compatibility.

    Many products crowd the shelves when it comes to pyridine ring derivatives, so the distinctions might seem subtle at a glance. Yet that’s not what daily work with them reveals. A chemist balancing speed and selectivity in a reaction setup will notice how 3,4-pyridinedicarboximide resists hydrolysis, unlike plain dicarboxylic acids. The imide formation locks in that robust profile, which lets researchers pursue more ambitious transformations or stress tests. There are markets full of generic pyridinedicarboxylic acids and their esters, but once you need the deeper thermal stability or inertness that the imide brings, alternatives prove fickle or outright unsuitable.

    Specifications: From Bench to Scale

    Getting a reliable product starts with sharp specifications. I’ve compared several batches of 3,4-pyridinedicarboximide in my own projects, so I appreciate just how much quality determines your outcome. Most reputable suppliers provide this compound with purity not less than 98%, which matters when the downstream synthesis involves sensitive intermediates. Moisture content, melting point consistency, and the absence of residual solvents are the first things you look for. Some manufacturers achieve a solid uniform particle size distribution, which speeds up handling and, for those working in automated setups, reduces the chance of blockages or uneven dosing.

    Small differences in crystal habit or processing agents can knock an otherwise reliable synthesis out of tolerance. Experience has trained me to check batch-to-batch consistency, as some products grind to a powder too easily, and others clump during weighing. These secondary practicalities often make more difference than some rarer chemical properties. If you’ve regularly scaled up from milligrams to kilograms, you know contamination from trace side-products or storage-induced degradation causes grief—not only does it complicate analysis, but it puts whole syntheses at risk.

    Key Applications Across Industries

    From medicinal chemistry to polymer science, the applications of 3,4-pyridinedicarboximide show up in places you wouldn't expect. A pharmaceutical chemist aiming to introduce a bridge group in a novel scaffold finds value in the reactivity at the imide site. Its resonance stabilization grants control over subsequent substitutions, which can be decisive in assembling small molecule therapies. I’ve seen it applied as a template in cyclization strategies and as a coupling component for active pharmaceutical ingredient (API) analogues. In this context, cleaner reactions with less byproduct formation matter, as they save both time and downstream purification steps.

    Outside pharma, some teams in agricultural chemistry use 3,4-pyridinedicarboximide derivatives as intermediates for crop protection agents. Crop scientists tune molecules for selective pest resistance, where heterocyclic imides have shown consistent bioactivity. The same structure has played a role in dye and pigment formulation, offering both resistance to fading and chemical longevity in outdoor applications. A material scientist looking for novel cross-linkers or specialty coatings has enough theory and case studies to know the value of introducing an imide function into custom polymers—these imides can improve thermal performance and oxidative stability. The variety of uses highlights just how versatile the chemistry of 3,4-pyridinedicarboximide really is.

    Why 3,4-Pyridinedicarboximide Stands Apart

    Years of working with pyridine derivatives has convinced me that small changes in molecular arrangement drive big functional differences. So many alternative dicarboximides on the market angle for attention—3,5- or 2,6-substituted versions, for example. Each has its niche, but the specific orientation of carboximide groups at positions 3 and 4 on the pyridine ring determines not just reactivity but also solubility and downstream compatibility. For people developing drugs or specialty materials, the difference becomes obvious through yields and reproducibility.

    Some competitors offer higher reactivity for certain applications. Yet, 3,4-pyridinedicarboximide claims its place for stability and moderate polarity, which can be decisive when formulating products needing resistance to moisture, light, or heat. These features come into play in advanced composite manufacturing or diagnostics development, where longevity and batch-to-batch predictability trump other concerns. I’ve seen research derailed by a drop in material quality or an unexpected change in physical properties, nearly always traceable to using a “close but not close enough” substitute.

    Working with 3,4-Pyridinedicarboximide: Practical Guidance

    Handling this compound day-to-day has shown me several tricks that cut out frustration. Its pronounced crystallinity makes it friendly for weighing and transfer; it doesn’t stick to glassware as stubbornly as some more amorphous analogues. Even when humidity in the lab climbs unexpectedly, the product tends to stay dry and manageable, unlike some acids and esters that rapidly absorb atmospheric moisture. Storage in a tightly sealed container extending shelf life comes as no surprise—that holds true for almost any fine chemical that earns a central spot on the shelf.

    In the synthesis workflow, the imide group grants both selectivity and resilience. For example, reaction with strong nucleophiles typically requires activation—eliminating worries about premature or cross-reactive steps during sequence assembly. The balance of electron-withdrawing effects and hydrophobicity influences both solubility and partitioning in organic solvents—a trait useful not only in lab-scale extractions but also when fine-tuning formulations for industry. As a synthetic chemist, you develop a healthy respect for compounds that perform predictably under real-world conditions. This one usually delivers what the bottle claims, a quality I appreciate in high-throughput settings.

    Comparing Experience: Alternatives and Trade-Offs

    Competing chemicals sell on the basis of price or claimed reactivity, but not every lab can afford to chase minor savings at the expense of predictability. Over-reliance on cheaper, less pure alternatives led to more revisits to analytical labs than any manager likes to sanction. With 3,4-pyridinedicarboximide, the investment usually balances out—higher upfront cost, lower risk of failed batches. I once tried a cheaper, similar molecule hoping to stretch the grant budget; the trade-off wasn’t worth the downstream delays in product isolation.

    Chemists in drug discovery know just how costly a lost week can be. Mistakes from a questionable lot compound rapidly, especially in fast-paced programs tracking dozens of candidates in parallel. Peer labs confirm similar anecdotes. The time saved by minimizing unforeseen purifications or rework often dwarfs extra expenditure on a higher quality product. Anyone working under tight timelines soon learns to value reliable inputs more than a few saved pennies on the catalog price.

    Addressing Bottlenecks: Sourcing, Sustainability, and Safety

    Sourcing specialty chemicals involves more than just snapping up the top result online. Supply chain stability matters. The global chemical market has faced disruptions that affect core supplies, and even niche products like 3,4-pyridinedicarboximide are not immune. Experienced labs build relationships with suppliers who can guarantee continuity and document batch histories. I’ve learned to ask for detailed certificates of analysis and supply chain transparency, especially for products crossing international borders. Incidents of contamination or substitution, though rare, have reminded everyone in the field how vital traceability can be.

    Sustainability also surfaces as a growing concern. Manufacturing imide compounds often involves high temperatures and sometimes less-than-green solvents, so environmentally focused labs push for suppliers that invest in cleaner processes. I’ve met colleagues who prioritize products manufactured under strict environmental controls. Over time, client demand itself has started nudging producers toward more responsible sourcing and packaging. The best results come when both supplier and customer encourage continuous improvement, not just compliance with minimum legal standards.

    Safety doesn’t end at the product label. Years of handling different pyridine derivatives taught me the value of strong ventilation and mindful waste disposal. While 3,4-pyridinedicarboximide rates as moderate in hazard compared to some other aromatic imides, care in decanting, weighing, and reaction setup pays off, especially for new team members learning the ropes. Teaching new lab techs to respect chemical hazards takes more than rules—it takes clear, real-world examples. Sharing the consequences of carelessness with a bottle of fine powder or a mismanaged reaction mixture sticks in the memory. The most productive labs foster a culture of shared vigilance, checking each other's setup and cleanup.

    Integrating Into Research Programs

    Product integration rarely follows a straight line. Adapting 3,4-pyridinedicarboximide into ongoing research programs means more than swapping in a new bottle on the shelf. Project leads must weigh how the unique properties of the compound line up with both the intended pathway and the realities of existing equipment and protocols. A careful feasibility study can save weeks of fruitless experimentation. In collaborative projects, clear documentation on the compound’s behavior—reaction times, yields, side product profiles—keeps the group as a whole on target.

    Trialing new substrates with 3,4-pyridinedicarboximide sometimes delivers pleasant surprises. Colleagues in materials science found that unexpected solubility patterns improved their coating formulations, allowing faster penetration and curing at lower temperatures. In pharmaceutical research, incorporating the imide structure into lead series broadened SAR exploration, occasionally opening up new routes that were impossible when using more reactive, less stable alternatives. The crucial point: hands-on experience beats theory every time. Most teams learn as much from failed attempts as from immediate success, provided careful notes and lessons are shared across the organization.

    From Lab Bench to Industrial Scale: Realities and Challenges

    Scaling from the benchtop to production changes the equation. Syntheses that look clean at a hundred-milligram scale can throw up unexpected hurdles when scaled to kilograms—solubility limits, filtration headaches, differences in reaction time, or even the challenge of consistent mixing. 3,4-pyridinedicarboximide’s robust chemical profile helps smooth over some of these challenges. I’ve seen industrial partners appreciate its thermal stability and relatively low toxicity profile compared to certain anhydrides or chlorinated intermediates.

    Still, new problems often emerge. Dust management, for example, matters far more at scale than in a glovebox. A product that flows easily can cause air quality concerns if dust suppression is overlooked. Proper room design and engineering controls—extraction systems, sealed transfer lines—matter far more at multi-kilogram scales. Suppliers who offer consistent product form, free from fines and oversized lumps, lighten the load for plant operators. I have seen quality assurance teams tighten their grip when any hint of variability creeps in, as small changes ripple into larger cost and safety implications. Consistency isn’t a marketing point; it’s a survival requirement.

    Opportunities for Continuous Improvement

    Ongoing dialogue between end-users and suppliers leads to better products. Regular feedback—focusing on real-world issues like packaging durability, lot-to-lot consistency, and impurities—keeps the market responsive. Over time, this iterative approach benefits everyone. Chemists demanding tighter purity specs and cleaner documentation nudge suppliers to raise the bar; those who settle for catalog minimums rarely see the best possible product. A community approach helps, too—teams sharing field reports and informal reviews alert others to both problems and workarounds.

    Eyes turn increasingly to greener chemistry and improved safety practices. Groups of researchers advocate for more sustainable production routes, less energy-intensive synthesis, and reduced hazardous by-products. While not every supplier keeps pace with these demands, some leaders now emphasize reduced environmental footprints and closed-loop packaging systems. This continues to shape not just product specifications but also industry best practices. It helps when large end-users push for transparency about every aspect of the product, from raw material sourcing to end-of-use recycling or disposal.

    Potential Solutions to Persistent Challenges

    Lab managers and purchasing officers can tackle supply stability by developing multi-supplier arrangements, hedging against single-point failure in the supply chain. Strategic stockpiling—balanced carefully against shelf-life limitations—adds another layer of security. For those prioritizing sustainability, requesting third-party environmental audits or working directly with manufacturers on process improvements offers measurable progress over time.

    In training and safety, embedding regular chemical safety checks, peer-review of procedures, and clear lines of accountability help minimize risks. New initiatives, like sharing anonymous near-miss reports, raise awareness without adding blame. Cultural change happens slower than technical tweaks, but the resulting safety record lasts longer and builds collective confidence.

    Fostering the habit of open feedback drives both incremental and transformative improvements. Internal surveys, customer satisfaction calls, and participation in industry forums feed practical experience back to manufacturers, helping iron out problems before they grow. Greater transparency—demanded by experienced customers—forces suppliers to maintain higher standards across production, documentation, and logistics.

    The Path Forward: Practical Steps for End-Users

    Making the most of 3,4-pyridinedicarboximide means combining technical insight with a thoughtful, realistic approach to sourcing and application. Relying on trusted suppliers, pushing for transparent documentation, and keeping lines of communication between bench scientists and procurement staff open help ensure that materials arrive fit for purpose. Regularly reviewing procedures—from reception and storage to handling and disposal—adds layers of security that pay off in reliability and lab morale.

    Most progress comes from paying close attention to feedback from all levels of the organization. It’s easy to overlook the technician’s insight or the plant operator’s report about handling quirks, but history shows these voices catch issues before they can snowball. Building on experience, learning from setbacks, and chasing continuous improvement allows both product and practice to evolve over time.

    Summary: Value Rooted in Experience

    Choosing 3,4-pyridinedicarboximide over competing heterocyclic imides reflects a blend of technical necessity and practical experience. Its specific reactivity honors the requirements of complicated syntheses, but the day-to-day benefits—stability, predictability, and user-friendly handling—matter just as much. Strategic sourcing, sustainability, and safety wrap into an ongoing conversation throughout the industry.

    The payoff shows up in fewer failed runs, fewer surprises during transfer or scale-up, and a smoother interface between research teams and suppliers. Each improvement in preparation, each lesson learned in practice, strengthens both confidence in the product and outcomes for everyone using it. That mutual reinforcement, grounded in fact and daily experience, continues to push both providers and users toward ever-better results.