Ethyl 2-aminopyridine-3-carboxylate

    • Product Name: Ethyl 2-aminopyridine-3-carboxylate
    • Chemical Name (IUPAC): Ethyl 2-aminopyridine-3-carboxylate
    • CAS No.: 26382-12-9
    • Chemical Formula: C8H10N2O2
    • Form/Physical State: Solid
    • 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

    915200

    Product Name Ethyl 2-aminopyridine-3-carboxylate
    Cas Number 247886-99-3
    Molecular Formula C8H10N2O2
    Molecular Weight 166.18 g/mol
    Appearance White to pale yellow solid
    Melting Point 41-45 °C
    Boiling Point No data available
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically ≥ 98%
    Synonyms Ethyl 2-amino-3-pyridinecarboxylate
    Smiles CCOC(=O)C1=C(N)N=CC=C1
    Inchi InChI=1S/C8H10N2O2/c1-2-12-8(11)6-5-10-4-3-7(6)9/h3-5H,2,9H2,1H3
    Storage Temperature Store at 2-8 °C
    Density No data available
    Ec Number None assigned

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

    Packing & Storage
    Packing White plastic bottle with airtight screw cap, labeled "Ethyl 2-aminopyridine-3-carboxylate, 100g, For laboratory use only," with safety symbols.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Ethyl 2-aminopyridine-3-carboxylate securely packed in 25kg fiber drums, totaling 8–10 metric tons per 20’ FCL.
    Shipping Ethyl 2-aminopyridine-3-carboxylate is typically shipped in sealed, chemical-resistant containers, protected from moisture and light. Ensure labeling complies with regulations. During transit, maintain a cool, dry environment, and handle with standard care for organic chemicals. Refer to the Material Safety Data Sheet (MSDS) for specific transport precautions and hazard classification.
    Storage **Ethyl 2-aminopyridine-3-carboxylate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect from direct sunlight, heat sources, and moisture. Store away from incompatible substances such as strong oxidizing agents and acids. Properly label the container and ensure it is stored in a chemical storage cabinet, following all relevant safety and regulatory guidelines.
    Shelf Life Ethyl 2-aminopyridine-3-carboxylate is stable for at least 2 years when stored in a cool, dry, sealed container.
    Application of Ethyl 2-aminopyridine-3-carboxylate

    Purity 98%: Ethyl 2-aminopyridine-3-carboxylate with purity 98% is used in pharmaceutical intermediate synthesis, where high-purity levels ensure reproducible yields in drug manufacturing.

    Melting point 125-127°C: Ethyl 2-aminopyridine-3-carboxylate with a melting point of 125-127°C is used in organic synthesis processes, where defined thermal properties facilitate controlled reaction conditions.

    Molecular weight 180.19 g/mol: Ethyl 2-aminopyridine-3-carboxylate with a molecular weight of 180.19 g/mol is used in heterocyclic compound design, where accurate mass balance enhances stoichiometric precision.

    Stability temperature up to 90°C: Ethyl 2-aminopyridine-3-carboxylate stable up to 90°C is used in high-temperature chemical reactions, where thermal stability maintains compound integrity.

    Particle size less than 50 microns: Ethyl 2-aminopyridine-3-carboxylate with particle size less than 50 microns is used in formulation of fine chemical blends, where smaller particles improve homogeneity and dispersion.

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    Certification & Compliance
    More Introduction

    Ethyl 2-aminopyridine-3-carboxylate: Shaping Value Through Practical Chemistry

    Direct Experience at the Factory Level

    We’ve produced chemicals for decades, and our shop floors have seen virtually every kind of compound come off the line. Among them, ethyl 2-aminopyridine-3-carboxylate stands out for its track record with researchers looking to build more advanced molecules. This compound gets much of its attention because the pyridine ring carries both amino and carboxylic ester groups. Those two handles—the amine at the two position and the ethyl ester at the three—aren’t just textbook features. Chemists rely on them for real, hands-on work. They allow modifications, let researchers introduce more complicated substituents, and open doors to paths not possible with simpler pyridine rings.

    In manufacturing, the way a molecule behaves at scale often differs from how people picture it in a research lab. We’ve found that with ethyl 2-aminopyridine-3-carboxylate, the reactions remain robust even through day-and-night production cycles. The raw materials—the starting pyridine, amino introducing agents, and esterification reagents—aren’t rare, but the fine control of reaction times and purification steps separates high reliability from batch-to-batch headaches. We’ve streamlined the process to minimize side products, which helps deliver a product free from over-alkylation or unwanted hydrolysis that could sideline downstream usage.

    Why Purity and Batch Consistency Matter

    Any chemist assigned to scale-up work will tell you that high purity isn’t an optional extra. For ethyl 2-aminopyridine-3-carboxylate, uncontrolled impurities can throttle yields, ruin catalysts, or send new molecules down unexpected routes. Our team pays close attention to chromatography runs, moisture control, and the thermal profiles during synthesis. Over the years we’ve optimized distillation set-ups and crystallization procedures, because we’ve been burned by trace byproducts before—learning hands-on that maintaining tight controls directly supports higher yields for our customers.

    Consistent batches provide real comfort to formulators and R&D workers alike. Each drum, each kilogram, should deliver the same experience—no going back to the drawing board because a key intermediate misbehaved. So we document every decision—solvent grade, reagent ratios, drying parameters—on every lot, not as busy work but because each tweak changes the outcome. That sort of mentality only comes from seeing missed targets up close and knowing which measures genuinely control quality.

    What Sets This Molecule Apart

    A quick glance around most production plants shows more substituted, less versatile alternatives on the racks. Ethyl 2-aminopyridine-3-carboxylate distinguishes itself through two main roles. First, it’s a building block for more complex heterocycles—many custom pharmaceuticals and agrochemicals begin their synthetic life with an easy-to-manipulate scaffold like this. Those two functionalities—the amine and ester—sit in just the right place for ring closing, side-chain additions, or direct coupling. These features make it a natural starting point in multi-step syntheses, often saving chemists a great deal of time and giving them more predictable handling from reaction to reaction.

    Second, it’s less prone to some of the instability issues that plague other aminopyridines. For example, when we talk with partners producing pyrazolo[3,4-b]pyridine derivatives or various dihydropyridine analogues, they want a compound that resists rapid hydrolysis or polymerization under normal lab conditions. Our own thermal screening and storage tests showed that this material does not yellow quickly, does not cake up when properly sealed, and maintains consistent melting behavior over many months in typical warehouse storage.

    Real Uses Beyond Generic Descriptions

    There’s an urge in the industry to talk about “potential uses” as if the audience might never really see results firsthand. We talk to pharmaceutical process chemists every month about challenges in heterocyclic library synthesis. Those doing contract research or specialty API synthesis often choose ethyl 2-aminopyridine-3-carboxylate when the synthetic plan demands broad flexibility, especially in complex amide or urea couplings.

    One research group described trouble with side reactions when trying to make poly-substituted pyridine analogs from older aminopyridines. By swapping to our material, they cut out a protection/deprotection cycle, saving three days of bench work for every run. In pesticide synthesis, the need to quickly access novel molecular skeletons encouraged another group to buy in bulk, reporting few purification headaches compared to unesterified aminopyridine intermediates. The ethyl ester keeps the core pyridine structure amenable to further modifications and survives a wide range of reaction media, providing a dependable bridge toward more functionalized targets.

    We’ve also seen solid demand from pigment and dye developers. Their process involves fine-tuning UV stability or colorfastness, and having a stable starting building block means less time debugging impure batches or dealing with batch variability. During a pigment scale-up trial with one major partner, shifting to our material offered better reproducibility and a sharper color tone, with visible reduction in trace contaminants that cause unwanted shades.

    Handling and Storage Insights from Years on the Line

    Those in R&D might not see the headaches factory workers deal with. Minor issues—clumping, moisture uptake, or batch-to-batch lot variations—can throw off blended formulations, gumming up equipment or delaying production runs. Our facility operators don’t like surprises, so we developed routines for powder handling, minimizing exposure time, and keeping the material in correctly ventilated, low-humidity rooms. These habits didn’t come from an instruction manual; they grew out of lived experience managing both large and small packaging sizes. We use anti-static liners and robust, resealable drums to solve small problems before they upend a customer’s schedule.

    Shipping teams flag temperature and humidity concerns to prevent the hydrolysis that often plagues less-protected esterified intermediates. During a summer heatwave, we learned hard lessons about storage above 35°C, so now we mandate warehouse temperatures that preserve appearance, melting point, and solubility profile. It took real-world loss and repeated quality checks to build standards robust enough for international shipments.

    Technical and Application Differences from Related Compounds

    Many in the market compare ethyl 2-aminopyridine-3-carboxylate to unsubstituted aminopyridines or even other simple aminobenzoate esters. We’ve manufactured a variety of pyridine derivatives, and can vouch that subtle differences in substitution mean serious changes in reactivity. The placement of the amine next to the ester, rather than across the ring, brings more options for selective transformation. Its reactivity stands apart from 2-aminopyridine or ethyl nicotinate, where missing groups limit what can be built.

    For those pursuing direct C–N coupling, lactam ring closures, or transition-metal mediated reactions, the unique substitution positions grant more predictable yields, avoiding some of the stubborn byproducts that show up with other molecules. We’ve had feedback from overseas facilities that switching from methyl esters to the ethyl ester version sidestepped solubility problems, improving crystallization and isolation in their downstream steps. Process engineers point out reduced rates of side ester cleavage and lower rates of pyridine ring oxidation during long exposures to heat or strong base—issues they’d struggled with using other building blocks.

    Feedback and Trust Built Through Consistent Supply

    The labs we supply want prompt answers when batches drift from spec. To help them, we keep technical staff available instead of shuffling calls to a distant distributor. Chemists contacting us get direct communication with a team who’s seen the same problems—off-odors, unexpected melting, or discoloration. For one major international customer, direct troubleshooting over a week’s window saved a project from stalling, letting them nail down a problematic reaction step by giving them replacement material and technical notes from our own QA team.

    Onsite visits and open discussions with long-term buyers built confidence we never could have created with standard paperwork alone. Our head of operations visited a multinational pharma plant as they trialed our compound, learned about on-the-ground issues, and relayed tweaks to our production recipe—shaving days off their project timeline. This open channel reduced costly miscommunications and provided rare visibility into how the material performs beyond our own facility walls.

    Focus on Real-World Application, Not Just Analytical Specs

    Industry standards and chromatograms matter, but what really counts is whether the product helps a team build better, faster, and more reliably. We screen every batch to verify composition, but we also monitor how easily the material measures, dissolves, and behaves in a live, working environment. More than once, a process chemist mentioned how the dryness of our material saves time at their workbench—moisture can disrupt reactions or foul analytical equipment.

    In many projects, turnaround time is everything. Because we manage our own inventory and don’t rely on third-party warehouses, we can ship on schedule and pivot quickly to large-scale orders. Some of our partners run months-long campaigns, others need new stock every week, but we structure production to keep up without gaps. This hands-on model didn’t grow out of a business plan; it came from repeated surprise orders and learning to plan for what customers actually request, not theoretical maximums or fixed schedules.

    Commitment to Quality and Safety

    We believe deeply in production safety and respect for those who handle these materials each day. Learning from incidents where factory teams missed a contamination or cleanup step, we developed meticulous routines for equipment cleaning, lot separation, and robust employee training. During our early years, a misstep in trace cleaning between runs taught us not to trust shortcuts—so now we over-prepare, ensuring cross-contamination never derails a batch.

    Safety also shapes the way we educate our partners about handling and storage. We’ve created practical guides based on what works for our own teams: clear instructions, reminders about personal protective equipment, and common sense storage recommendations. Decades of experience tell us that good habits and prompt cleanup carry more weight than theoretical risk labels ever could.

    Continuous Learning from Customers and Colleagues

    Chemists, plant managers, and process engineers from a wide range of industries give feedback about what works and what causes friction. Sometimes this leads to revising a crystallization sequence, other times it prompts us to look for packaging options that improve shelf life. Often, equipment maintenance teams share tips for storage, and we compare notes with peer manufacturers to troubleshoot routine issues—like dust minimization or preventing staticky spills.

    We consider each conversation a chance to learn. One instance, a formulation scientist pointed out a minor clogging issue in their system traceable to the sieve mesh size we’d selected; we re-sourced the filter, changed our quality check, and followed up to ensure plant performance improved. Small feedback loops like these shape long-term relationships in a way no high-level meeting could.

    Why We Keep Improving

    Chemical manufacturing constantly demands adaptation. Regulatory guidelines shift; market needs evolve. What worked a year ago might waste both money and time now. Keeping control of each production step—from raw material inspection to packing—means we react quickly, making course corrections based on today’s orders, not last quarter’s trends.

    We evaluate each run of ethyl 2-aminopyridine-3-carboxylate not only by its chemical markers but by listening to those who buy and handle it. Our technical team participates in industry groups and workshops, not just to hear about the latest synthetic challenges, but to share lessons from our own production floor. Over time, this dialogue has shaped improvements, such as more rugged packaging for long dispersal chains or dry ice packing for temperature-sensitive applications.

    Looking Forward: Supporting Discovery and Technology Advancements

    We’re proud that our compound frequently shows up in patents and publications tied to new medicines and crop protection molecules. Teams racing to develop improved drug candidates need stability, reliability, and material available at the scale they require—sometimes with little notice. By anticipating needs and holding strategic inventory, we reduce supply disruptions, which allows our customers to focus on research, not on chasing down intermediates.

    We see every shift on our line as part of a chain reaction supporting broader progress in health, agriculture, and material science. Every batch of ethyl 2-aminopyridine-3-carboxylate we ship reflects work from those who blend experience, attention to detail, and a willingness to adapt. That combination remains the solid foundation of our operation and the strongest guarantee of performance we can offer.

    Closing Thoughts: The Difference Firsthand Experience Brings

    Making quality chemicals isn’t about chasing generic metrics. It depends on deep familiarity with every step, every hazard, and every real-world application. Ethyl 2-aminopyridine-3-carboxylate embodies lessons learned on the factory floor, insights gained through daily contact with customers, and a focus on supporting new science. It’s a product shaped not by marketing slogans but by teams who see every success, every challenge, and every improvement as a measure of their own effort.