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HS Code |
907392 |
| Chemicalname | 5-Ethylpyridine-2,3-dicarboxylic acid |
| Molecularformula | C9H9NO4 |
| Molecularweight | 195.17 g/mol |
| Casnumber | 26733-19-5 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and polar organic solvents |
| Boilingpoint | Decomposes before boiling |
| Pka | Estimated between 2-5 for carboxylic acid groups |
| Synonyms | 5-Ethyl-2,3-pyridinedicarboxylic acid |
| Structuretype | Aromatic heterocycle with carboxylic acid |
As an accredited 5-Ethylpyridine-2,3-dicarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5-Ethylpyridine-2,3-dicarboxylic acid is supplied in a 25g amber glass bottle with a secure, tamper-evident cap. |
| Container Loading (20′ FCL) | 5-Ethylpyridine-2,3-dicarboxylic acid is securely packed in 25kg fiber drums, efficiently loaded into 20′ FCL containers for shipment. |
| Shipping | 5-Ethylpyridine-2,3-dicarboxylic acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically transported at ambient temperature, following standard regulations for chemical handling. Packaging is clearly labeled with appropriate hazard and safety information, ensuring safe delivery and compliance with local and international shipping guidelines. |
| Storage | 5-Ethylpyridine-2,3-dicarboxylic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong oxidizers and bases. Use appropriate chemical storage cabinets and avoid extreme temperatures to maintain stability and prevent decomposition. |
| Shelf Life | Shelf life of 5-Ethylpyridine-2,3-dicarboxylic acid is typically 2-3 years when stored in a cool, dry, and dark place. |
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Purity 99%: 5-Ethylpyridine-2,3-dicarboxylic acid with a purity of 99% is used in pharmaceutical intermediate synthesis, where it enables high-yield target compound formation. Melting Point 230°C: 5-Ethylpyridine-2,3-dicarboxylic acid with a melting point of 230°C is used in high-temperature organic reactions, where it maintains structural integrity during processing. Particle Size 10 µm: 5-Ethylpyridine-2,3-dicarboxylic acid with a particle size of 10 µm is used in catalyst development, where it provides enhanced surface area for improved catalytic activity. Stability Temperature up to 180°C: 5-Ethylpyridine-2,3-dicarboxylic acid stable up to 180°C is used in polymer synthesis, where it ensures consistent material performance during thermal curing. Molecular Weight 195.18 g/mol: 5-Ethylpyridine-2,3-dicarboxylic acid with a molecular weight of 195.18 g/mol is used in structure-activity relationship studies, where it allows precise molecular modeling and docking analyses. Aqueous Solubility 15 g/L: 5-Ethylpyridine-2,3-dicarboxylic acid with aqueous solubility of 15 g/L is used in biochemical assay formulation, where it guarantees homogeneous solution preparation. Analytical Grade: 5-Ethylpyridine-2,3-dicarboxylic acid analytical grade is used in quality control laboratories, where it facilitates reproducible HPLC and NMR analysis results. Low Metal Impurities (<50 ppm): 5-Ethylpyridine-2,3-dicarboxylic acid with low metal impurities (<50 ppm) is used in electronic material manufacturing, where it ensures minimal electrical interference. |
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Years in chemical manufacturing teach you that fine distinctions in molecular structure can completely shift the direction of an application, and 5-Ethylpyridine-2,3-dicarboxylic acid gives a strong example. Shaped by the balance of an ethyl group at the 5-position and two carboxylic acids at the 2 and 3 positions, this compound delivers performance advantages our customers depend on.
We manufacture this molecule with careful control over purity and crystalline consistency. The purity levels necessary for downstream synthesis in pharmaceuticals and advanced materials demand a meticulous process. Consistency in melting point, moisture content, and free acid spectrum signals tight adherence to raw material sourcing, solvent quality, and temperature control. Every batch reflects adjustments based on years of process feedback, lab testing, and operator expertise on the manufacturing floor. For us, there’s no shortcut: impurities in this kind of acid easily translate into end-product rework for our customers.
Lab staff have carried out HPLC and NMR runs on hundreds of sample lots, and one thing always stands out. Any deviation from spec shows up in reactivity changes and can disrupt prolonged synthesis steps. The difference between trusted and untrusted sources is clear—our batches show tight spectral signatures with consistent retention times, no rogue peaks or unexplained by-products. When your end application depends so much on the core building block, such trace-level reliability matters.
Colleagues from the R&D and user sides often highlight the importance of pyridine dicarboxylic acids in heterocyclic chemistry. Having a non-alkylated pyridine-2,3-dicarboxylic acid on hand is useful for basic coupling work; by comparison, introducing the ethyl group at the 5-position extends the range of reactivity. End-users describe tighter control over selectivity, especially in oxidative coupling, crosslinking, or ligand design for transition-metal complexes. We see recurring orders from groups working on functional polymers, specialty chelates, and even drug intermediates that depend on both the hydrophilic and hydrophobic regions of this acid.
The ethyl substitution may seem subtle on paper, but in a glass reactor or a commercial batch, the reactivity and solubility shifts enable new classes of derivatives. Many users find these differences translate into fewer synthesis steps, which adds up to reduced solvent waste and shorter cycle times. Case studies in house have shown time and cost savings in ligand synthesis, where isolating and purifying intermediates runs far smoother with the right substitution pattern. Working closely with formulation chemists and synthetic specialists, we’ve learned to prioritize critical details —a 1% impurity can cripple a process, yet a precise ethyl positioning solves selectivity problems for entire product classes.
Over the years, initial lab requests gave way to orders measured by scale. Whether shipped to process developers at biotech startups, specialty rubber formulators, or researchers at large material science labs, the feedback on our crystalline product has remained the same: they come back for our model of dense, sharp-edged crystals. Our mainstay form consists of white to pale off-white solid free of visible inclusions, permitted trace moisture content well below common industrial targets, and a reproducible particle size. This tunable physical form means less handling loss and less blocking during bulk transfers.
We don’t operate from a generic template. It’s not just a question of formula, but of precise control in drying, milling, and stabilization. Where a trader might accept a faint acrid residual or uneven grain, our line staff double-check for consistency. Storage stability comes into play too: our process avoids introducing solvents that could compromise shelf life or require further drying before use. Minor deviations show up quickly, and operators on our line have learned to flag even a fractional off-color or odor change before releasing any batch.
Comparing 5-ethylpyridine-2,3-dicarboxylic acid against straight pyridine-2,3-dicarboxylic acid or other isomers like the 3,4- or 2,4-dicarboxylic acids reveals firsthand why chemists request it for targeted syntheses. Straightparent pyridinedicarboxylic acids have general value, yet cannot provide the same discrimination in catalytic or chelation environments. The ethyl side group adds a crucial handle for increasing lipophilicity—opening possibilities in heterocyclic drug and polymer design that are simply out of reach for the non-alkylated versions.
From the manufacturing side, purity criteria remain strict for all isomers, but the 5-ethyl substitution means we account for potential side reactions originating from the ethyl group. Our experience with competitive products shows that poorly managed alkylation steps introduce structural isomers and residual alkylating agents. Tight batch records and advanced GC analysis roots out these issues before they ever reach customer hands. The absence of solvents or secondary alkylation by-products is one of our hallmarks. Users often report fewer downstream purification issues and greater batch-to-batch reliability with our manufactured lots.
The biggest interest comes from pharmaceutical synthesis and materials science. Medicinal chemistry teams use our compound for scaffold construction, often as a core fragment in more complex molecules where both acidity and hydrophobic tuning are crucial. The electronic and steric environment created by that ethyl group opens access to entire families of ligands for metal catalysis, something not achievable with the parent acids.
Material scientists rely on our 5-ethylpyridine-2,3-dicarboxylic acid for designing specialty polymers and crosslinkers. Our records show that in polymer modification projects, cyclic intermediates built from this acid resist hydrolytic breakdown and tolerate a wider range of plasticizers. Some teams even exploit the dual acid groups for chelating rare earth metals, leveraging the subtle influence of the ethyl chain on binding stability.
Labs seeking tailor-made performance gravitate to this molecule because it drives fewer side reactions in peptide coupling or esterification steps compared to the unmodified backbone. Years of trial and error with alternative reagents underscore how specific this advantage can be in practice. Often, researchers seeking that edge looked for ways to add functional diversity to a scaffold without introducing excess synthetic complexity. The ethyl group’s position gives that needed control.
Experienced chemists and buyers care about more than cost per kilogram. Traceability, raw material handling, and in-plant quality checks decide the success of later processes. As direct manufacturers, we don’t broker intermediates or rely on spot-market imports. Instead, complete oversight—from sourcing, through reaction, to finished drying—remains internal. Lot data feeds back into continuous improvement, enabling us to spot and address drift instantly. Over the years, we’ve developed relationships with input suppliers who hold to the same standards, eliminating random spikes in impurity from poor feedstock.
Buyers from regulated industries place a premium on chain-of-custody and compliance. We see approval requests from both Japanese and European clients who demand a clear audit trail back to raw material and process conditions. As a manufacturer, providing batch records and analytical data comes as standard, not an upcharge. Our analytical group stays updated on shifts in international inspection regimes, ensuring full transparency without disrupting customer documentation flows.
One recurring challenge for product developers centers on formation of unwanted by-products during scale-up. Solution: tight process control at every stage, enabled by real-time monitoring of critical reaction variables and precise temperature management. We built a system that not only achieves the desired yield but also sharply reduces formation of isomeric and oxidative by-products—common traps with aromatic dicarboxylic acids. Our operators have documented how minor heat spikes or improperly aged solvents throw off selectivity. By tracking issues batch-to-batch, we train teams to respond instantly and prevent long-term drift.
Another common pitfall: moisture uptake and caking during storage or shipment. A decade ago, even small moisture ingress caused delays for peptide synthesis customers who needed rapid, residue-free dissolution. Our solution? Enhanced drying under controlled nitrogen, optimized packaging materials, and logistics partners trained on sensitive goods. Today, we route even bulk orders with real-time temperature and humidity tracking. Problems that once took days to fix now barely rate a speed bump.
Customer feedback cycles—honest, sometimes harsh—help root out process weaknesses. When a pharmaceutical client flagged batch cloudiness, sample tracking pinpointed a non-conforming raw input and solved it before it became a pattern. Open communication between lab, production, and outbound logistics closes the loop. Nothing replaces a hands-on commitment from everyone involved; having seen costly batch rework and disposal from poorly sourced intermediates, we know that trust and dialogue cannot be substituted with generic packaging or boilerplate assurances.
Manufacturing any specialty chemical bears an environmental footprint. We minimize solvent usage at every synthesis step and recover over 80% of process water in a closed-loop system. Scrubbers and carbon filtration on emissions equipment keep our operation within strict air-quality targets—even as we scale up production to meet new demand from green syntheses in Europe and North America. Feedback from environmental compliance inspectors shapes continual upgrades. Responsibility to both operators and the broader community stays central in all process decisions.
Waste management gets direct oversight from senior plant staff. We analyze every outgoing stream for trace contaminants, not just the ones mandated by regulation. The benefits return to us in reduced long-term liability, but equally, our customers see smoother approvals for their end use. Safety briefings and up-skilling operators reinforce a culture of stewardship that spans from the sourcing table to outbound loading docks.
No one understands the quirks of 5-ethylpyridine-2,3-dicarboxylic acid production like the team who synthesizes it day after day. Solving practical problems—like errant color, trace off-odors, or inconsistent crystal form—marks the boundary between direct manufacture and generic supply. For teams pursuing process reliability, access to direct answers and solutions from the original plant makes all the difference. Over the years, we’ve developed tweaks in reactivity, filtration, and handling based directly on feedback from user facilities. Knocking down barriers between lab bench and reactor floor saves resources on both sides.
Buyers who collaborate directly with chemical manufacturers gain advantages rooted in transparency, speed, and communication. Lags in sourcing information, origins, or composition often lead to failed syntheses and costly delay. With direct channels and established feedback loops, our customers gain more than a commodity—they access knowledge and customized adjustment built on years of experience with a highly specialized molecule.
Stepping into the plant at the start of each run, every technician recognizes the cumulative impact of incremental improvement. Our process for 5-ethylpyridine-2,3-dicarboxylic acid reflects that learning, not just from textbooks and journals, but from practical, hands-on problem solving. Customers come back because they see the effect of small details—how a subtle tweak in crystallization or a minute adjustment to reactor dwell can turn an ordinary batch into a standout building block for their innovation.
Working closely with scientists who use this product across industries brings fresh challenges and insights. No batch leaves the door without a conversation about its end-use and the expectations attached. Here, reliability has grown from a decade of listening, adapting, and holding every stage to the highest internal bar. Pride in the quality of our 5-ethylpyridine-2,3-dicarboxylic acid doesn’t come from a marketing slogan: it’s visible in the repeatable results, the transparent records, and the partnerships built year by year.