|
HS Code |
426007 |
| Chemical Name | Diethyl 2,6-pyridinedicarboxylate |
| Molecular Formula | C13H15NO4 |
| Molecular Weight | 249.26 g/mol |
| Cas Number | 4193-55-9 |
| Appearance | Colorless to pale yellow liquid or solid |
| Boiling Point | 343.8 °C at 760 mmHg |
| Melting Point | 44-46 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.17 g/cm3 |
| Smiles | CCOC(=O)C1=CC=NC(C(=O)OCC)=C1 |
| Refractive Index | 1.487 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Synonyms | Diethyl pyridine-2,6-dicarboxylate |
As an accredited Diethyl 2,6-pyridinedicarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle, tightly sealed with a screw cap, labeled 'Diethyl 2,6-pyridinedicarboxylate,' includes safety and handling instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Approximately 10-12 metric tons of Diethyl 2,6-pyridinedicarboxylate packed in 25 kg fiber drums. |
| Shipping | Diethyl 2,6-pyridinedicarboxylate is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be stored and transported at room temperature, away from incompatible substances. Packaging complies with chemical safety regulations, ensuring protection against leaks or spills during transit. Handle with standard laboratory chemical precautions. |
| Storage | Diethyl 2,6-pyridinedicarboxylate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Ensure proper labeling, and avoid prolonged exposure to air. Store according to standard laboratory chemical safety protocols to prevent degradation and ensure stability. |
| Shelf Life | Shelf life of Diethyl 2,6-pyridinedicarboxylate is typically 2-3 years when stored in a cool, dry, and dark place. |
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Purity 99%: Diethyl 2,6-pyridinedicarboxylate with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting point 58-60°C: Diethyl 2,6-pyridinedicarboxylate with melting point 58-60°C is used in organic laboratory preparations, where controlled solidification improves handling efficiency. Molecular weight 251.25 g/mol: Diethyl 2,6-pyridinedicarboxylate with molecular weight 251.25 g/mol is used in ligand design studies, where precise stoichiometric calculations facilitate accurate complex formation. Stability temperature up to 120°C: Diethyl 2,6-pyridinedicarboxylate with stability temperature up to 120°C is used in catalyst synthesis, where thermal stability allows robust process conditions. Particle size <20 µm: Diethyl 2,6-pyridinedicarboxylate with particle size <20 µm is used in advanced material fabrication, where fine dispersion produces uniform composite materials. Hydrolytic stability: Diethyl 2,6-pyridinedicarboxylate with hydrolytic stability is used in ester exchange reactions, where extended resistance to decomposition maintains reagent integrity. |
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Operating as a manufacturer in fine chemicals, we’ve seen the role of Diethyl 2,6-pyridinedicarboxylate (DEPDC) continue to grow, especially in the context of pharmaceutical intermediates and organic synthesis. This compound, with its molecular structure based on the pyridine ring and a pair of diethyl ester groups at the 2 and 6 positions, brings both reliability and versatility to the table.
The unique arrangement of carboxylate functionalities on the pyridine core gives DEPDC a range of reactivity not seen in many traditional mono-functional esters. In our own operations, we keep a close eye on purity levels—our product routinely exceeds 99 percent by HPLC, which guarantees minimal side reactions during downstream transformations. DEPDC’s melting point and handling properties also contribute to consistent batch quality. Our procedures retain strict control over by-products like trace pyridine or other positional isomers, cementing reproducibility from gram to multi-ton scales.
Manufacturing DEPDC involves a series of precisely monitored esterification and purification steps. Our facilities rely on controlled temperatures, solvent recovery, and thorough impurity screening because contaminants can trigger problems in later synthesis steps. Typically, our product presents as a clear, colorless to pale yellow liquid or crystalline solid, depending on storage and temperature. Moisture content stays below 0.1 percent—something lesser-focused manufacturers sometimes overlook, and which can throw off any moisture-sensitive reactions.
Because downstream users demand reliability, we maintain tight batch records that track starting materials, process conditions, and every measure taken throughout each lot. This transparency came about due to repeated requests for documentation by our regular buyers, particularly those involved in pharmaceutical and OLED (organic light-emitting diode) material production. Labs producing API intermediates benefit most from rigorous lot-to-lot consistency. Over the years, incidents of failed reactions traced to upstream contaminants have made us fanatical about internal controls—from inline filtration to post-synthesis spectral checks.
DEPDC mainly finds its use as a building block for several classes of pharmaceuticals and agrochemicals. We started out serving mainly pharma R&D, where the compound participates in constructing polycyclic frameworks, complex ligands, and catalysts. Synthetic chemists value DEPDC for introducing both aromaticity and reactive ester groups in one step. Our largest industrial clients employ it to build fused-ring systems that eventually become anti-inflammatory or neuroactive compounds.
As the crop protection industry expanded, our DEPDC served as an intermediate in designing new herbicides and fungicides. The symmetrical diester structure permits straightforward transformation into pyridine-based amides or acids, both of which appear frequently in proprietary agrochemical libraries. Some of our European customers use DEPDC in ligand synthesis for catalysis, where the electronic effects of the pyridine nucleus improve catalytic efficiency in metal-centered reactions.
From a manufacturing standpoint, environmental responsibility goes beyond simply following regulations. We upgraded our waste streams several years ago to recover ethanol and minimize pyridine emissions. Continuous distillation units allow us to reclaim solvents rather than burn them off. Early on, we handled waste by neutralizing spent acids and base. Now, we recover and reuse these reagents wherever possible, which reduces both costs and landfill. Because DEPDC relies on fairly robust starting materials, most waste consists of neutral esters and low-toxicity by-products.
Every year, our process engineers review effluents and emissions data to identify where further cuts are practical. We follow national and local guidance on chemical exposure, which matters when working directly with pyridine-based structures. Many in the chemical industry still treat solvent recovery as optional, but for us it became a necessity—customers do ask about sustainability practices before committing to new supply contracts.
Having supplied research and production groups since our founding, we repeatedly get asked if there’s any reason to buy high-purity DEPDC vs. commercial or technical grades. The answer has never changed. Lower purity material almost always carries inhibitors, moisture, or unconverted pyridinedicarboxylic acid. That might be fine for non-critical applications or simple esterifications, but in pharma production these residues disrupt purification or lead to hazardous unknowns in drug intermediates.
We’ve seen chemists lose entire batches—hundreds of liters—because of impurities traced to the starting ester. Those losses reflect both lost material and weeks of downtime. Across dozens of campaigns, our customers’ QA feedback convinced us that stringent internal controls and full batch testing aren’t just for regulatory peace of mind. They reduce real-world, expensive risks down the supply chain. Some say high-purity grades add to cost, but in practice, the savings from avoiding failed syntheses more than compensates.
In daily practice, handling DEPDC requires awareness of both its reactivity and its ester content. Those unfamiliar with its properties often treat it as a generic pyridine derivative, but the diester groups open up both nucleophilic and electrophilic chemistry routes. For example, in our pilot plant, we observed that varying the reaction time by as little as 15 minutes could tip product distribution towards unwanted by-products. Fine-tuning temperature curves, solvent ratios, and even agitation speeds pays off in reduced impurity content.
Our technical support team works closely with users to troubleshoot synthesis bottlenecks. That sometimes means running pilot batches at a customer’s chosen scale, to give tailored advice and training on handling, storage, and transfer. DEPDC doesn’t call for exotic storage, but it does need protection from excess moisture and strong bases. Overheating or extended exposure to acidic catalysts can prompt hydrolysis, which is why temperature and pH controls stay front-and-center in our process documentation.
Synthetic chemists often weigh DEPDC against similar compounds like the 2,5- or 2,4-pyridinedicarboxylate esters. We make these variants as well, but advise customers on the key differences upfront. The 2,6-regioisomer places carboxylate esters directly opposite each other, which leads to steric effects not found in other isomers. This influences reactivity with nucleophiles, often giving higher selectivity or improved yields in certain ring-closing reactions. In our own screening of ligation reactions, 2,6-diester systems gave fewer side products and more efficient isolation compared to 2,5-analogs.
DEPDC also stands apart from monoesters like ethyl nicotinate. Monoesters rarely deliver the same level of reactivity and double-functionalization potential. The extra ester group doubles the sites for further modification or serves as a protecting group in sequential syntheses. Over decades, we’ve seen some labs try to shortcut syntheses with mono-functional reagents, only to double back after facing tough purification and lower yields. The diester approach streamlines complex molecule assembly and gives flexibility for route changes during process optimization.
Long-term customers provide us with the most crucial data—what works and what creates headaches. In the last five years, chemists in material science reported using DEPDC for producing pyridine-based polyesters and functionalized polymers. These can be used in membranes, coatings, or even as matrix components in modern battery systems. We’ve responded to requests for differently denatured solvents and tighter residual solvent limits, actions based on direct partnerships rather than distant regulatory standards.
Pharmaceutical developers continue to ask for customized package sizes to match their campaign volumes, rather than standardized drums designed for distributors. With thousands of kilos moving through our facility each month, we structure logistics to cut down cross-contamination and keep each production order fully traceable. Periodic audits with customer QA groups keep our material aligned with shifting industry needs, especially as regulations and technologies bring new requirements to light.
Scaling up DEPDC production from bench to multi-ton output rarely goes smoothly at first try. Early production runs risk fouling equipment or generating difficult-to-separate impurities unless reactor geometry and mixing are carefully optimized. We had to adapt our synthesis vessels with custom agitation patterns to prevent phase separation and uneven heating. Even minor factors like condenser performance and downstream filtration design made measurable differences in yield and color.
Global supply constraints increase the importance of local raw material sourcing and in-house quality assurance. There have been instances where reliance on imported pyridine caused supply bottlenecks, pushing us to diversify suppliers and build backup stock of critical precursors. Secure, long-term relationships with upstream vendors allow us to avoid disruptions seen in more distributor-heavy supply chains. Ultimately, our customers value the assurance that they can obtain consistent materials regardless of shifting logistics in the market.
Regulatory shifts in recent years—particularly in the pharmaceutical sector—make documentation of process controls, impurity profiles, and handling protocols even more important. We train every production and QA chemist on current requirements, from REACH compliance to accurate impurity mapping. While not every customer asks for full trace data, those sharing regulatory submissions have found our level of record-keeping and batch traceability invaluable for technical files and inspections.
Responding to updates in hazard classification, we proactively apply safety labels and risk management measures. Improved air handling, personnel training, and environmental monitoring form part of our daily plant operations. DEPDC itself poses relatively manageable risks, but good training and equipment design protect both workers and neighboring communities. Third-party periodic inspections confirm our practices, which lets us handle both routine and custom syntheses safely.
As more sectors turn towards renewable and bio-based feedstocks, we actively research bio-alternatives for DEPDC production. Biocatalytic routes and renewable starting materials top our list of priorities. Customers increasingly ask us about the cradle-to-gate environmental impact of our products, spurring investment in better waste reduction and solvent recycling systems.
Digitalization enables real-time tracking of QC results, minimizing shipping delays. Our technical data sheets and batch records are now available as live documents—customers no longer have to wait for paperwork to catch up with shipments. Transparency at each production step builds trust, particularly as more clients require documentation stretching back to the earliest precursor batch.
Years of manufacturing DEPDC taught us that end users benefit from hands-on technical support, especially during new product launches or process scale-ups. Our ability to collaborate directly with chemists and plant engineers sets us apart from impersonal resellers. We make our technical representatives available during lab trials, offer on-site training on safe transfer and storage, and share troubleshooting experience built over decades of production.
Process scale-up brings its own set of challenges, from reaction exotherms to equipment fouling. Our engineers can recommend temperature ramps and solvent management strategies designed from firsthand plant operation. Key insights come not only from literature or reference manuals, but from the cumulative experience of staff who have spent years supervising real-world batch failures and optimizations. This approach reduces customer downtime and maximizes overall value from each order.
Our experience manufacturing Diethyl 2,6-pyridinedicarboxylate confirms that product quality, transparency, and technical expertise remain critical in meeting modern industry needs. As end uses diversify—from high-purity pharmaceuticals to advanced material science—direct dialogue and hands-on support make all the difference. Operating as a chemical manufacturer gives us insights into real-world process challenges, letting us help our customers avoid costly setbacks and reach their goals faster. Investing in process improvement, industry compliance, and environmental responsibility keeps us moving forward year after year, ensuring that every shipment of DEPDC delivers both reliability and performance.