3-Amino-4-pyridinecarboxylic acid

    • Product Name: 3-Amino-4-pyridinecarboxylic acid
    • Chemical Name (IUPAC): I am sorry, but you did not provide the name or structure of the product. Please provide the name or structure of the chemical product you are referring to.
    • CAS No.: ''
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    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    Specifications

    HS Code

    774812

    Cas Number 7421-38-5
    Molecular Formula C6H6N2O2
    Molecular Weight 138.13
    Iupac Name 3-Aminopyridine-4-carboxylic acid
    Appearance White to off-white powder
    Melting Point 300 °C (dec.)
    Solubility In Water Slightly soluble
    Synonyms 3-Aminoisonicotinic acid
    Pka 2.66 (carboxylic acid), 5.21 (amino group)
    Smiles NC1=CN=CC(=C1)C(=O)O
    Inchi InChI=1S/C6H6N2O2/c7-5-3-8-2-4(1-5)6(9)10/h1-3H,7H2,(H,9,10)
    Ec Number 231-011-4

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

    Packing & Storage
    Packing White plastic bottle labeled "3-Amino-4-pyridinecarboxylic acid, 100g, CAS: 81335-77-7," sealed with a screw-top lid for safety.
    Container Loading (20′ FCL) 20′ FCL container loading for 3-Amino-4-pyridinecarboxylic acid includes securely packed, labeled drums or bags, maximizing space and ensuring safe transport.
    Shipping 3-Amino-4-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. Standard shipping is via ground or air, compliant with relevant chemical transport regulations. Packaging ensures no leakage or contamination, and documentation includes safety data sheets and hazard classifications when applicable. Handle with appropriate personal protective equipment.
    Storage 3-Amino-4-pyridinecarboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Store at room temperature, ideally between 2–8°C. Handle with appropriate personal protective equipment to avoid inhalation, ingestion, or contact with skin and eyes.
    Shelf Life 3-Amino-4-pyridinecarboxylic acid is stable for at least 2 years when stored in a cool, dry, well-sealed container.
    Application of 3-Amino-4-pyridinecarboxylic acid

    Purity 99%: 3-Amino-4-pyridinecarboxylic acid with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and contaminant-free drug development.

    Melting Point 245°C: 3-Amino-4-pyridinecarboxylic acid with a melting point of 245°C is used in solid-phase peptide synthesis, where thermal stability supports high-temperature reaction conditions.

    Molecular Weight 138.13 g/mol: 3-Amino-4-pyridinecarboxylic acid of 138.13 g/mol is applied in combinatorial chemistry, where defined molecular mass facilitates accurate stoichiometric calculations.

    Particle Size <10 μm: 3-Amino-4-pyridinecarboxylic acid with particle size below 10 μm is used in formulation of specialized pharmaceutical tablets, where uniform dispersion improves content uniformity.

    Water Solubility 12 mg/mL: 3-Amino-4-pyridinecarboxylic acid featuring water solubility of 12 mg/mL is used in aqueous drug solution preparations, where enhanced solubility ensures higher bioavailability.

    Stability Temperature Up to 110°C: 3-Amino-4-pyridinecarboxylic acid stable up to 110°C is used in thermal processing of active pharmaceutical ingredients, where it prevents degradation and maintains chemical integrity.

    HPLC Grade: 3-Amino-4-pyridinecarboxylic acid of HPLC grade is utilized for analytical reference standards, where high purity guarantees reliable chromatographic analysis.

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    Certification & Compliance
    More Introduction

    3-Amino-4-pyridinecarboxylic Acid: A Closer Look at Its Role and Value

    Insight into a Specialized Chemical

    Every now and then, chemistry introduces a compound that quietly supports work across different fields, and 3-Amino-4-pyridinecarboxylic acid is one of those behind-the-scenes players. Known to chemists by its formula C6H6N2O2, this compound stands out among pyridine derivatives because of its unique structure: a pyridine ring with both an amino and a carboxylic acid group, each sitting in places that matter for reactivity and performance. Workers in pharmaceutical labs, agricultural research, and even materials science rely on this molecule more often than many might imagine. Its careful balance of functional groups opens up reactions and pathways rarely available with more common analogs.

    Unpacking What Sets It Apart

    Not all pyridinecarboxylic acids are created equal. The amino group at the 3-position and the carboxylic acid at the 4-position bring together nucleophilic and acidic sites on the same ring—something you simply don’t get with plain nicotinic or isonicotinic acid. This mix allows researchers to push synthesis in directions that are closed off by simpler molecules. In practical terms, that means greater options whether working with ligands for metal catalysis, new drug candidates, or even designing molecules to chelate metal ions. There’s a real benefit when a molecule can do double duty across different reactions.

    Specifications That Matter in the Real World

    Most chemists aren’t handling kilograms of this acid in a lab, but even at small scale, purity and consistency go a long way. Labs demand reliable material—often at 98% purity or higher. Minute traces of moisture or residual solvents can derail delicate syntheses. The lot-to-lot consistency of 3-Amino-4-pyridinecarboxylic acid, when sourced from trusted suppliers, makes the workflow smoother. Compared to some other aromatic amino acids, this compound often comes as a free-flowing white powder or small crystals, which makes it simpler to weigh, dissolve, and handle without loss from static or air moisture. Stockroom managers see the value in a product that doesn’t clump up or degrade on the shelf.

    Putting It to Work: Multiple Fields, Real Impact

    Pharmaceutical chemists see this compound as more than a raw material. Its framework supports the synthesis of heterocyclic drugs where functional flexibility is essential. Enzyme inhibitors, receptor antagonists, and chelating agents benefit directly from this combination of amino and acid functionality. Synthetic biology and medicinal research teams keep reaching for it to modify lead compounds, aiming for stronger bioactivity or better selectivity. Long hours at the bench have hammered home one thing: a well-placed amino group in the right ring, supported by a carboxylic acid, can turn a bland molecule into a promising candidate.

    Agrichemical developers also incorporate this compound into formulations when they need a balance of reactivity and stability. Herbicide and pesticide precursors are improved by the extra synthetic handles offered by both the amino and carboxylic acid. The molecule avoids excessive volatility and breaks down less rapidly than some traditional amines. Where regulatory pressure favors lower persistence in the environment, chemists have appreciated the reliability with which 3-Amino-4-pyridinecarboxylic acid delivers predictable outcomes.

    Material scientists find a different set of uses. The structure fits into coordination polymers and ligands, supporting work on sensors or catalysts. Transition metal complexes using this compound as a building block exhibit electronic and structural properties that help fine-tune selectivity and sensitivity in analytical systems. No single molecule solves every problem, but the features of 3-Amino-4-pyridinecarboxylic acid crop up in surprising new materials—sometimes in surprising places, like thin-film deposition or next-gen battery research.

    Comparison Without Hype

    Comparing 3-Amino-4-pyridinecarboxylic acid to more familiar alternatives, like 4-aminopyridine or simple picolinic acid, reveals the value of thoughtful molecular design. Where 4-aminopyridine brings neurological or stimulant activity in biological systems, the added carboxyl group in this product changes the entire range of interactions and reduces the risk of unwanted side reactions. Unlike plain pyridinecarboxylic acids, the amino substitution opens up direct routes for coupling, condensation, or amide bond formation. All these features save steps, money, and time during synthesis.

    The molecule has an edge over others when the application demands both an anchoring site and a basic nitrogen. This versatility keeps it appealing—researchers appreciate not juggling two or three separate reagents just to reach a usable intermediate.

    The Importance of Reliable Sourcing

    From personal experience, there’s no shortcut to quality. Working with poorly characterized samples wastes more than just budget; it kills momentum in a project. Labs investing in high-purity 3-Amino-4-pyridinecarboxylic acid tend to see fewer failed runs and better reproducibility. In large projects, reproducibility underpins credibility—one batch lost to impurities can put months of effort at risk. Teams who test their inputs carefully steer clear of the pitfalls common with lower-grade chemicals. The market often offers cheaper variants, sometimes with trace contaminants or inconsistent crystalline forms, but the savings often disappear once downstream problems crop up.

    A lot of projects, especially in pharmaceutical startups, build their timelines around these materials. Tight schedules leave little room for unexpected hiccups. Unexpected lot variation can shut down a campaign, burn through funding, and, worst, erode trust between chemists and suppliers. The best chemical suppliers understand this, and they invest in better production and analytical controls. From clean HPLC profiles to full NMR and IR confirmation, every step in quality control pays off for end users.

    Safety and Handling Insights Not Found on the Label

    Common sense governs safe handling in most labs. Even so, a compound like 3-Amino-4-pyridinecarboxylic acid isn’t something to treat lightly. The aromatic amine group raises questions about allergenicity or toxicity. Standard gloves, goggles, and dust masks manage exposure risk, especially when weighing out powders. Since the product usually has moderate solubility in water and classic organic solvents, spills rarely cause panic, but a cautious hand avoids problems.

    One point easily overlooked: bench chemists occasionally forget that seemingly harmless intermediates can create unexpected fumes if heated or mixed too casually. Well-ventilated fume hoods, regular housekeeping, and a culture of training keep the risk low. The label can only do so much; lab culture fills in the rest. Those who have worked through a lab incident know that a few seconds of patience and preparedness make all the difference.

    Product Stability and Storage Lessons

    Sensible storage habits matter more than any data sheet suggests. The molecule holds up reasonably well under normal conditions, but exposure to direct sunlight or high humidity can trigger slow degradation or discoloration. Storing it in tightly sealed amber glass or HDPE containers, away from heat, keeps it in top condition. Refrigerators work, but aren’t strictly necessary for short-term storage. Oxidation rarely threatens during normal use, yet leaving it open or in contact with strong oxidizers can alter its activity for sensitive reactions.

    Overextended storage, especially in poorly maintained storerooms, catches many labs off guard. Minute hydrates or breakdown products appear over time and crop up during routine analysis, usually when a critical batch stumbles for unexplained reasons. Chemists with years at the bench spot these warning signs quickly—unusual color, clumping, or odd odour often mean it’s time to order fresh stock, rather than risk an expensive synthesis.

    Improving the Supply Chain and User Experience

    Anyone managing a research or production line knows logistics don’t always keep pace with the needs of the lab. Delays, backorders, and out-of-spec materials mean researchers sometimes scramble for alternatives. Direct communication between chemistry teams and suppliers pays off here. Open lines let users flag early problems—caking, packaging failures, or documentation gaps—before they affect projects in progress. Suppliers willing to listen to the voice at the bench often catch small issues before they become obstacles.

    With supply chains strained in recent years, more organizations have begun diversifying sources for fine chemicals. They build relationships with multiple local and international vendors. Sometimes, this approach brings added costs, but the investment blunts the shock of sudden shortages and builds leverage for negotiating better terms or faster turnaround times. It’s the difference between sitting idle and staying productive.

    Real progress comes from supplier partnerships that include regular technical feedback. Instead of just buying a bottle, users benefit from direct support—a conversation about lot history, analytical certificates, or special packaging requests. As chemistry evolves, demands for new grades—like higher purity for regulatory submissions—prompt suppliers to upgrade processes and documentation together with their customers.

    The Ethics and Trust Behind Quality Chemicals

    Not all suppliers operate with the same integrity. In the hunt for affordable materials, cutting corners sometimes ends with mislabeling or subpar products sneaking onto the market. Labs who find foreign substances or byproducts in their 3-Amino-4-pyridinecarboxylic acid don’t just lose a reagent—they put publications, patient safety, and business reputation at risk. This field rewards transparency. Trust grows when suppliers furnish comprehensive data, answer technical questions promptly, and recall problem lots without excuses.

    Modern regulations in Europe, North America, and much of Asia encourage traceability and clear documentation. For critical applications in medicine or diagnostics, sourcing from reliable, audited production lines shifts from a preference to a necessity. Technical teams should expect clear batch records, impurity data, and, where possible, third-party validation. Trust is built from consistent good experience, not words on a marketing sheet.

    Future Directions: Opportunities for Innovation

    Chemists and material scientists never stop seeking better reagents. As demand for more specialized pharmaceuticals and advanced materials rises, so does the need for versatile building blocks like 3-Amino-4-pyridinecarboxylic acid. Current efforts aim to optimize synthesis routes for improved yield and environmental footprint, pushing for greener solvents and reusable catalysts. The chemistry community increasingly values processes that minimize waste and cut energy use.

    On the instrumentation side, real-time analytics allow for tighter control over purity and composition, improving the feedback loop during manufacturing. Automated purification and packaging systems now deliver lots that withstand longer shipping distances and diverse climates, making the compound accessible to labs worldwide. Technical teams that keep advocating for incremental improvements see reliability and sustainability improve together.

    In research, combinatorial chemistry teams use this molecule as a scaffold: tinkering with its framework to generate libraries of analogs. The approach pays off, producing diverse compounds for screening in pharmaceuticals and agrochemicals. The compound’s flexibility fosters new ways to target pathogens or plant pests through unusual molecular interactions. With continuous innovation at both the industrial and bench level, the value of this compound continues to expand.

    Quality at Every Step Matters

    Years of hands-on lab work have taught many that even small differences in input quality can shape the outcome of big projects. A bottle of 3-Amino-4-pyridinecarboxylic acid that opens cleanly and checks out on the spectrometer sets the stage for productive weeks. Missed contaminants or erratic performance knock confidence, slow down momentum, and eat away at budgets. In highly regulated areas like pharmaceuticals and food safety, documentation, consistency, and clear supplier dialogue are not just best practices—they are requirements.

    Quality isn’t just about the raw numbers on a certificate of analysis. It’s about every step from synthesis to packaging, from shipping to final use. Labs that use careful sample retention and run controls on every batch catch more problems early. They combine trust in suppliers with independent verification—balancing convenience and self-reliance. Over the years, reliable reagents become part of a laboratory’s core culture, supporting innovations others might miss because they spent too long fighting unpredictable materials.

    The Broader Picture: Supporting Innovation Across Sectors

    The applications for 3-Amino-4-pyridinecarboxylic acid span more than the typical research categories. Environmental testing, food analysis, and even chemical education encounter the molecule as part of new detection methods or as a practical example in organic synthesis classes. Its value isn’t just in its rarity or unusual structure, but in how often it solves real problems at the bench and beyond. Teams looking for modularity and adaptability return to this compound because it streamlines synthetic plans and unlocks new chemistry.

    Ask professors or senior chemists about unsung heroes on the shelf, and this molecule will come up again and again. It’s not as famous as caffeine or aspirin, but it enables progress behind the curtain. In one case, it stood in for a protected amino acid in a tough peptide synthesis, saving weeks of protection and deprotection steps. In another, its distinctive ring helped clarify analytical signals in a complex investigation of water contaminants. Experience in the lab shapes respect for certain molecules, and over time, those workhorses become trusted tools.

    Solutions and Steps for Making the Most of 3-Amino-4-pyridinecarboxylic Acid

    Users can get the most out of this compound by investing in staff training, routine sample inspection, and close partnerships with their suppliers. Regularly running small-scale trial reactions after receiving a new lot spots problems before they scale up. Careful documentation—keeping track of lot numbers, storage conditions, and observed physical properties—helps trace issues if they arise. Consultation with suppliers about unusual needs, such as low-metal or pharmaceutical-grade material, clarifies expectations and often opens doors to custom solutions.

    Many labs also find value in cross-validating with in-house analytical techniques—NMR, HPLC, IR, or mass spectrometry—so that material doesn’t enter critical pathways without confirmation. For teams seeking regulatory approval or preparing for audits, early discussions with quality assurance and regulatory experts keep projects on track. Personal experience highlights the value of short feedback loops: quickly flagging any inconsistencies and having candid conversations with suppliers about how and where improvements matter most.

    A broad view of any fine chemical’s journey, from synthesis to final application, creates resilience and confidence. Investing in infrastructure—better analytic capability, robust inventory management, and proper storage—protects against unexpected delays or failures. A culture of openness and a willingness to report problems, even small ones, builds a safety net that benefits both research progress and personal safety.

    Final Thoughts on a Quietly Powerful Molecule

    Few molecules serve as quietly and effectively as 3-Amino-4-pyridinecarboxylic acid. Its mix of both amine and carboxylic acid functionality on a single aromatic ring stands out as a rare and valuable feature. Though it may not command headlines, the compound remains a valued partner across pharmaceutical research, advanced material design, and agricultural innovation. Years of experience, repeated successes, and stubborn reliability have made it a fixture in labs that thrive on innovation and demand trustworthy inputs. The best outcomes trace back to smart sourcing, rigorous testing, open lines of communication with suppliers, and a genuine respect for the chemistry at hand.