|
HS Code |
484976 |
| Productname | 3-Amino-5-pyridinecarboxylic acid |
| Casnumber | 20645-51-8 |
| Molecularformula | C6H6N2O2 |
| Molecularweight | 138.13 |
| Appearance | Off-white to light brown solid |
| Meltingpoint | 200-205°C |
| Solubility | Soluble in water and DMSO |
| Purity | Typically ≥98% |
| Synonyms | 3-Aminonicotinic acid |
| Structure | Pyridine ring with amino group at position 3 and carboxylic acid at position 5 |
| Smiles | C1=CC(=CN=C1N)C(=O)O |
| Inchi | InChI=1S/C6H6N2O2/c7-5-2-1-4(6(9)10)8-3-5/h1-3H,(H2,7,8)(H,9,10) |
As an accredited 3-Amino-5-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g bottle of 3-Amino-5-pyridinecarboxylic acid arrives in a sealed, amber glass container with a tamper-proof cap. |
| Container Loading (20′ FCL) | 20′ FCL loading: 3-Amino-5-pyridinecarboxylic acid packed in fiber drums, palletized, securely loaded to maximize safety and prevent contamination. |
| Shipping | 3-Amino-5-pyridinecarboxylic acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packages are clearly labeled according to safety regulations and include hazard information. The chemical is transported under controlled temperatures, typically at ambient conditions, and handled by certified couriers specializing in laboratory and industrial chemicals. |
| Storage | Store **3-Amino-5-pyridinecarboxylic acid** in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture and direct sunlight. Store at room temperature, and label appropriately. Avoid sources of ignition. Use appropriate personal protective equipment when handling to prevent inhalation or skin contact. |
| Shelf Life | 3-Amino-5-pyridinecarboxylic acid typically has a shelf life of 2-3 years when stored in a cool, dry place, protected from light. |
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Purity 99%: 3-Amino-5-pyridinecarboxylic acid with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Molecular weight 138.13 g/mol: 3-Amino-5-pyridinecarboxylic acid of molecular weight 138.13 g/mol is used in heterocyclic compound development, where it enables accurate stoichiometric calculations and reproducibility. Melting point 218°C: 3-Amino-5-pyridinecarboxylic acid with melting point 218°C is used in high-temperature reaction processes, where it provides enhanced thermal stability and reduces decomposition risk. Particle size <20 μm: 3-Amino-5-pyridinecarboxylic acid with particle size less than 20 μm is used in solid-phase synthesis, where it improves dissolution rate and homogeneous mixing. Stability temperature up to 150°C: 3-Amino-5-pyridinecarboxylic acid with stability temperature up to 150°C is used in polymer modification, where it offers reliable performance under thermal processing conditions. |
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Curiosity and necessity often drive advances in chemistry. After years following developments in specialty chemicals, 3-Amino-5-pyridinecarboxylic acid has really established itself as a trusted staple across many research labs and industrial operations. This compound, recognized by its well-defined chemical formula (C6H6N2O2), sits comfortably among pyridine carboxylic acids but brings a twist: an amino group at the 3-position and a carboxylic acid function at the 5-position. This simple tweak opens up a horizon of reactivity and potential, giving both academic and industrial chemists a reliable platform for new explorations.
Its white to light beige powdery form looks ordinary, but don't let that fool you. One of the features that stands out is the compound’s balance of polarity and modest molecular weight, which simplifies purification steps, especially when compared with larger or more apolar analogs. Few chemicals in this class walk the line between solubility in water and organic solvents so gracefully, and the lack of overpowering odor certainly makes routine handling easier on lab staff. It's also refreshing to work with a compound that doesn't coat every flask in a stubborn, oily residue.
My interest in 3-Amino-5-pyridinecarboxylic acid was first piqued during a long project on medicinal chemistry scaffolds. The compound performed under challenging conditions—strong acids, bases, and moderate heat—without showing a frustrating loss in purity. Whether synthesizing small combinatorial libraries or scaling up batches for pilot drug development, knowing that a key intermediate will consistently yield pure product takes a lot of worry out of big projects.
Despite a growing crowd of pyridine derivatives, few can match this molecule’s clean reaction behaviors and reliable performance in both laboratory and semi-industrial scenarios. Large-scale users, such as those in agrochemical research, often mention the savings in downstream purification or catalyst loading—that’s an area not to underestimate. Having purity specs that routinely exceed 98% by HPLC saves long hours and extra solvents that pile up all too quickly. Time and labor do cost money, so cutting down on rework and retesting translates directly to leaner budgets and happier teams.
Placing the amino group at the 3-position and the carboxylic acid at the 5-position isn’t arbitrary. From my experience and what’s reported in literature, this arrangement creates a unique anchor point for both peptide chemistry and metal complex catalysis. Chemists appreciate how readily this molecule forms amide or ester bonds, paving the way for building blocks used in pharmaceuticals, advanced materials, and even niche ligands for transition metal complexes.
In medicinal chemistry, 3-Amino-5-pyridinecarboxylic acid slots right into heterocyclic frameworks. The pyridine ring provides aromatic stability while the functional groups allow selective activation or protection. There’s comfort in choosing a building block that’s been tried and tested for stability across pH, and one where functional group transformations follow clear, reliable pathways.
On the side of materials science, engineers have found a use for this compound when tailoring surface properties or preparing ion-exchange materials. The acid and base character of the molecule promote anchoring to metal oxides or activated polymers, which broadens the range of experimental setups or end-uses. This isn’t always obvious until you’ve spent time troubleshooting failed surface coatings or patchy thin films with less cooperative molecules.
Chemists often look for substitutes across a family of analogs, but the differences can make or break a process. I’ve noticed that 3-Amino-5-pyridinecarboxylic acid sidesteps some persistent pitfalls seen with other pyridinecarboxylic acids. Compounds like isonicotinic acid or nicotinic acid, while useful, have fewer vectors for further synthetic modification. The unique arrangement in the 3-amino-5-carboxy configuration allows for denser functionalization without crowding the ring or inviting side reactions, especially for sensitive medicinal chemistry campaigns.
Many chemists lament stubborn byproducts from adjacent functional groups or the stubbornness of leaving groups during acylations. In practice, the electron-donating nature of the 3-amino group counters the ring’s electron deficiency, smoothing out many organic transformations. That means fewer headaches trying to drive reactions to completion or needing elaborate purification steps to separate nearly co-eluting byproducts.
Users in peptide synthesis often swap out comparable building blocks, but few match the balance of reactivity and predictability this acid offers. Even in high-load, automated systems, the solid performance under SPPS conditions (solid-phase peptide synthesis—those who’ve spent days at the bench push-buttoning know the struggle) can shave precious hours off troubleshooting cycles.
Supply chain uncertainty plagues many specialty chemicals, but reliable sourcing of 3-Amino-5-pyridinecarboxylic acid hasn’t seen the same wild swings. Part of the reason stems from robust synthetic routes, typically starting with pyridine derivatives widely available on the global market. Lately, interest has grown in greener synthesis routes. Catalytic hydrogenation and using water as a solvent have both been explored with some success, pointing to a future where preparing this compound might avoid the harsh reagents or heavy metals often associated with specialty amines or carboxylic acids.
Waste reduction becomes another talking point once you witness how much solvent and starting material go into less efficient syntheses. Where other pyridine carboxylic acids might run into low recoveries due to challenging separations, 3-Amino-5-pyridinecarboxylic acid generally comes out without excessive sidestreams, which simplifies both compliance and process validation for companies with tough regulatory environments. Any researcher who’s wrestled with solvent disposal limits or fines for improper waste can appreciate that.
It's also worth highlighting that the molecule’s stability lets distributors ship and store it without special cold-chain or light-protective measures, cutting both costs and energy use during supply. These differences make a tangible impact both on the budget sheet and in day-to-day logistics inside labs and warehouses.
No product comes without challenges. For all its stability, 3-Amino-5-pyridinecarboxylic acid can show gradual hydrolysis under highly basic or acidic aqueous conditions if left for extended periods. Routine storage in dry, closed containers solves most of those problems, but in fast-moving production settings, occasionally an open container sits a bit too long or moisture creeps in. Lab managers often benefit from straightforward reminders on container sealing and environmental controls to protect yields and avoid contamination.
Pricing can sway quite a bit between small-batch, research-grade material and industrial ton-lot purchases. Academic labs with tight funding occasionally feel the pinch—bulk buying groups, flexible supply contracts, and technical support from knowledgeable suppliers all help smooth the road. Sourcing from certified producers with clear impurity profiles ensures the material fits high-stakes applications, like pharmaceutical pilot lots or regulatory studies.
End-users sometimes mention batch-to-batch color differences or slight variations in melting ranges. Regular QC (quality control) testing, paired with clear supplier communication, cuts down on unwelcome surprises. Having spent years monitoring analytical data, I’ve found that open dialogue with trusted vendors lets customers request custom specs, or documentation, up front, which spares disappointment and scrambled project schedules.
Better informatics support and digital integration can transform how 3-Amino-5-pyridinecarboxylic acid gets used and tracked throughout its life cycle. In-house LIMS (laboratory information management systems) now tie purified batch data directly to production records, giving R&D and QA/QC teams faster access to relevant specs and impurity mappings. Suppliers who offer transparent COAs (certificates of analysis) and digital tracing, along with robust customer service, improve trust and consistency.
Chemists and engineers often collaborate most fruitfully when suppliers join the conversation—for instance, offering suggestions on optimal storage, compatible reagents, or troubleshooting persistent side-products. Integrating these relationships into the early planning stage of research or production dramatically reduces midstream pivots or unexpected cost overruns.
Process optimizations—swapping solvents, adjusting pH, or carefully managing reaction temperatures—go a long way. A single client-led tweak, such as using buffered aqueous solutions or switching to recyclable media, has helped customers boost yields and cut down on purification stages. Knowledge sharing among user groups, whether through online forums, peer-reviewed journal publications, or at industry conferences, strengthens both reliability and creative applications.
As science continues to move forward, compounds like 3-Amino-5-pyridinecarboxylic acid remain valuable precisely because they aren’t locked into one narrow niche. New uses keep cropping up—for example, as ligands in next-generation catalytic cycles, as core components in opto-electronic devices, or as linkers in functionalized nanoparticles for bio-imaging. Every seasoned chemist has a story about discovering an unexpected application when digging through older literature or collaborating across disciplines.
Tools that foster innovation—robust analytical support, responsive customer service, and open data sharing—empower creative breakthroughs. For students and researchers entering the field, the accessibility of compounds like this one helps flatten the learning curve and frees up energy for bolder projects. It feels good to work with dependable materials, especially when tackling the kind of experimental challenges that demand both flexibility and rigor.
Educational programs and hands-on workshops can extend comfort and skill using 3-Amino-5-pyridinecarboxylic acid. Emphasizing safety, clear technique, and troubleshooting familiarizes young researchers with the practical rhythms of chemical handling. In my own experience, these learning opportunities consistently yield more confident scientists ready to make the most of valuable reagents and avoid costly errors.
Building a career in chemical sciences means relying on a toolkit packed with trusted, versatile building blocks. 3-Amino-5-pyridinecarboxylic acid earns its place by delivering dependable performance across multiple disciplines. Anyone working at the interface of research and application knows that choosing the right compounds up front clears many roadblocks further down the path.
The difference between success and setbacks in the lab often comes down to the reliability of each step, and this molecule supports that goal with a track record filled with positive feedback from professionals in universities, hospitals, start-ups, and large manufacturers. By seeking out quality production, building strong supplier relationships, and keeping up with new green chemistry approaches, the value of 3-Amino-5-pyridinecarboxylic acid will only grow.
For new researchers considering their first synthetic explorations, or industrial chemists trying to push the limits of process efficiency, having a robust compound like this one makes the journey smoother. Good communication, sensible storage, and thoughtful process planning shape a future where innovation and reliability walk hand in hand. From my own lab adventures and the stories shared by so many colleagues, this is a product that stands up to scrutiny and provides a rock-solid foundation for ongoing discovery.