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HS Code |
688498 |
| Iupac Name | 1,2,4-triazolo[4,3-a]pyridin-3(2H)-one |
| Molecular Formula | C6H4N4O |
| Molar Mass | 148.12 g/mol |
| Appearance | Solid (white to off-white powder) |
| Melting Point | Approximately 240-250°C |
| Solubility In Water | Slightly soluble |
| Cas Number | 1134-47-0 |
| Pubchem Cid | 18371 |
| Structural Formula | C1=CN2C=NC(=O)N=C2N=C1 |
| Logp | Estimated ~ -0.2 |
| Synonyms | 3-oxo-1,2,4-triazolo[4,3-a]pyridine |
As an accredited 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle, containing 25 grams of 1,2,4-triazol-[4,3-a]pyridine-3(2H)-one, with hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 11MT (in 25kg fiber drums) per container for 1,2,4-triazol-[4,3-a]pyridine-3-(2H)-one. |
| Shipping | **Shipping Description:** `1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one` should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and strong oxidizers. Transport under ambient temperature, following all regulatory guidelines for handling chemicals. Ensure packaging prevents leaks or breakage. Include safety data sheets and comply with relevant local, national, and international shipping standards. |
| Storage | 1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it separate from incompatible substances such as strong oxidizers and acids. Store at room temperature and protect from moisture. Follow all relevant chemical hygiene and safety regulations during handling and storage. |
| Shelf Life | **1,2,4-Triazolo[4,3-a]pyridin-3(2H)-one** is stable under recommended storage conditions; typical shelf life is 2–3 years in cool, dry place. |
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Purity 99%: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with a purity of 99% is used in pharmaceutical synthesis, where high purity ensures enhanced reaction yield and minimized impurities in final products. Melting point 210°C: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with a melting point of 210°C is applied in high-temperature drug formulation processes, where its thermal stability preserves compound integrity. Molecular weight 149.14 g/mol: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with a molecular weight of 149.14 g/mol is utilized in analytical chemistry, where accurate molecular mass facilitates reliable quantitation. Particle size <10 μm: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with a particle size of less than 10 μm is employed in tablet formulation, where fine particle distribution enables uniform blending and optimal dissolution profiles. Stability temperature up to 180°C: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with stability up to 180°C is implemented in polymer additive manufacturing, where its resistance to degradation ensures consistent performance during processing. Aqueous solubility 5 mg/mL: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with an aqueous solubility of 5 mg/mL is used in injectable drug formulations, where sufficient solubility supports effective bioavailability. Residue on ignition ≤0.1%: 1,2,4-triazol-[4,3,-a]pyridine-3-(2H)-one with a residue on ignition of less than or equal to 0.1% is used in quality control testing, where low inorganic residue demonstrates material purity for pharmaceutical acceptance. |
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Working with heterocyclic compounds every day, we come to understand which structures bring out the best results in synthesis, purity, and function. 1,2,4-Triazol[4,3-a]pyridine-3(2H)-one stands out both in its architecture and its reliable performance. Through years spent in high-precision chemical plants, we have focused on this molecule due to rising demands from research, pharmaceuticals, and advanced material science. Its molecular backbone—incorporating both the recognizable triazole and pyridine fused rings—demonstrates a stability and reactivity profile that has shaped the progress of many synthetic routes.
Over multiple production runs, we have optimized reaction conditions to favor high yields and minimize byproduct formation. After countless batch improvements, we see consistently tight control on crystallinity and particle size, which is critical in downstream applications. Materials passing through our purification processes reach genuine specification levels required by advanced research and development. Excess water, residual solvents, and common organic impurities get thoroughly purged, ensuring every shipment represents all the expertise packed into our systems.
The triazolopyridinone core challenges quality control unless a keen eye monitors each step, from crystallization to end-stage packaging. Our most successful model, recognized for its 99.5% plus purity, features minimal polymorphism and high batch-to-batch reproducibility. Over the years, we have calibrated in-house HPLC, NMR, and LC-MS methods through collaboration with professional analytical chemists. Our team routinely validates melting point ranges and checks for trace-level elemental contaminants, because overly broad specs invite performance inconsistencies.
Particle size, while seemingly a minor detail, often determines suitability for certain coupling reactions and formulation steps. We select sieving methods that adjust for the fine balance between free-flowing properties and reactivity. The material appears as a finely milled, off-white crystalline powder. Typical moisture content after drying falls below 0.5%, thanks to vacuum drying systems tuned for this structure. Bulk density averages sit within a narrow window, doubling transport efficiency and making handling safer during warehousing and scale-up.
Each drum receives a unique batch number, laser-etched for traceability. Internal documentation tracks every processing step and QC release, so users feel confident about consistency. Over hundreds of batches, our deviation rates have dropped below 2%, reflecting robust protocols. While we do use validated third-party labs for independent assay confirmation, in-house teams handle most testing. Regular investments in staff training and analytical instrumentation keep us on top of the latest compliance requirements and industry innovations.
Over the years, we have seen demand shift as fresh research unlocks new pathways for this compound. Many of our longtime clients in pharmaceutical research, especially those working on kinase inhibitor scaffolds and agrochemical leads, rely on this structure to push boundaries in medicinal chemistry. The fused triazole-pyridine core offers not just synthetic versatility but functional group tolerance found lacking in more conventional pyridines or triazoles alone. Medicinal chemists target this compound as a base structure for further functionalization, building molecules aimed at modulating protein-protein interactions, enzyme inhibition, and receptor agonist design.
Some labs look for nucleophilicity control and diminished metabolic liabilities in lead compounds. Here, the lactam moiety at the 3-position gives a synthetic edge, providing hydrogen-bond donors and unique tautomer stability. Newer generations of compound libraries in our customers’ pipelines reflect this trend. We also witnessed agrochemical innovators screen for plant protection candidates derived from the same core structure, finding promising results for antifungal and herbicide applications. The versatility extends into advanced materials science, including applications in luminescent materials and specialty polymer backbones, capitalizing on its stable heterocycle and extended conjugation.
Our ongoing cooperation with both multinational research institutes and nimble startups has pushed us to maintain close communication on evolving needs. For example, one project required us to develop a low-residual-solvent variant for a biotech lab, leading us to modify drying rates and filtration materials. Another customer, focused on pilot-scale production of intermediates for bulk pharmaceuticals, benefited from drum-size solutions with customized inner liners to prevent cross-contamination. These day-to-day adaptations keep our product in active demand, supported by a technical service team ready to troubleshoot application hiccups.
Experience in chemical manufacturing gives insight into what gives this structure a unique edge. Chemists often compare it with simple triazoles or pyridines, yet the fused ring brings a new spectrum of reactivity. The classic 1,2,4-triazole ring sees broad use, yet its independent application can mean lower rigidity and fewer options for regioselective substitution. On the pyridine front, simple pyridines might be easier to synthesize, but they lose the ability to engage twice as many binding motifs, an attribute prized in drug and ligand design.
The fused system in 1,2,4-triazol[4,3-a]pyridine-3(2H)-one unlocks both stability—due in part to extended aromatic delocalization—and a reliable set of electron-donating and electron-withdrawing options at specific positions. This dual capability invites more creativity in substructure incorporation, feeding into both structure–activity relationship studies and patent strategy. Compared to benzotriazoles or quinolines, these molecules sidestep certain liability issues such as metabolic activation and off-target effects, which research circles watch carefully. We have tracked downstream users’ feedback, seeing better hit rates in screens that depend on hydrogen bonding and conformational rigidity.
Another edge comes from manageable solid-state properties. Unlike more volatile heterocycles, 1,2,4-triazol[4,3-a]pyridine-3(2H)-one brings stability in transport and storage. Drums stored under standard temperature and humidity conditions show minimal degradation even over extended inventory cycles. This gives procurement managers one less black mark on their risk registers and lets researchers focus on core science rather than last-minute sourcing delays or requalification hassles.
Manufacturing heterocycles brings its share of technical hurdles. The triazole-pyridine fusion demands precise temperature ramps, carefully controlled pH, and exacting ligand ratios during synthesis. In the early days, our operators combated low conversions and batch variability, burning through time and raw materials at unsustainable rates. Training and experience, paired with a willingness to update reactor automation and monitoring systems, turned this process into a repeatable workflow. This matters, especially for customers stretching from gram-scale research to multi-ton production.
Quality can erode with even small shifts in input material purity or changes in plant humidity. For that reason, our teams regularly review suppliers for underlying starting materials, dig into vendor change notifications, and perform shadow testing on new lots. We never take for granted the importance of high-purity hydrazines and pyridines, learned after hard lessons with early off-color batches. Every new lot undergoes qualification and compatibility checks before scaled-up reactions begin.
The purification phase, often overlooked, separates reliable producers from the average. Recrystallization, chromatography, and vacuum drying involve more than babysitting a flask—they demand a sixth sense for when parameters need nudging. In our facility, operators celebrate each perfect filtration as a small victory for both our reputation and the downstream user’s productivity.
Adaptation to regulatory expectations also occupies a front seat. The reach of global safety and environmental standards means every solvent, reagent, and waste stream must be tracked and, when needed, swapped for greener options. Early investments in closed-handling systems, effective vapour scrubbing and waste minimization let us achieve both safety and sustainability without sacrificing on quality. Frequent audits, both internal and external, feed into a culture of constant improvement, minimizing the risk of regulatory delay or incident.
Customers regularly connect with us looking for not just material, but a trusted partner who understands synthesis inside and out. We understand that speed, clarity around batch release, and flexibility in packaging shape the reality of their work. Unlike trading operations or resellers, our value comes from first-hand knowledge of process risk, technical bottlenecks, and creative workarounds honed over years in plant environments. Shared experiences in troubleshooting or scaling a tricky reaction often spark new application ideas, feeding the cycle of innovation.
No third party matches the depth of support our technical teams provide—whether it's fasting-laning a special lot, tailoring documentation, or jumping on a call to dissect the root cause of an unexpected impurity. We have worked shoulder-to-shoulder with clients on introducing this compound into new formulations, making direct adjustments to cater to end-goal specifications. Direct feedback loops foster solutions that get the job done. Returned material rates have dropped significantly as a result. Strong partnerships form where the manufacturer doesn’t just sell, but commits to evolving with each new scientific challenge.
Experience suggests that structural motifs like this fused triazolopyridinone core will only increase in significance. Several research groups, drawing on both in-house and published work, indicate that this material could branch into even broader pharmaceutical and materials science territory. As molecular modeling and AI-driven design open up new chemical space, scaffold innovation and derivative synthesis gain importance.
We also expect environmental and safety profiles to move into sharper focus. Sustainability trends are changing everything from solvent choices in synthesis to bulk routing for reduced carbon footprints. Our operations keep pace by investing in low-impact utilities, scrubbing upgrades, and packaging solutions that balance integrity with efficiency. Feedback from green chemistry groups and institutional procurement demands stoke efforts toward even cleaner processes.
Our relationships with academic groups and industrial R&D teams point to emerging opportunities—whether for new crop protection approaches, high-performance polymers, or routes to critical active pharmaceutical ingredients. The demand for reliability and reproducibility will only grow, especially for customers scaling programs from the lab bench to full production. With regulatory scrutiny tightening, established QC processes and robust documentation set the stage for long-term supply relationships.
As specialists who live with these molecules day in and day out, we see not only the technical side but the pressures our customers face to invent, deliver, and improve. 1,2,4-Triazol[4,3-a]pyridine-3(2H)-one, forged through years of plant learning and real-world feedback, embodies this spirit—a material that lets science push ahead without compromise or extra risk.
A product only gains true value through a mix of manufacturing skill, technical insight, and readiness to adjust as industry gears shift. Every kilogram we produce carries not just an assay number, but the trust earned through hands-on work, failures failed, and solutions found. Customer success springs from quality, but also from relationships formed between people who know chemicals are more than just numbers on a page.
1,2,4-Triazol[4,3-a]pyridine-3(2H)-one’s journey from lab curiosity to essential research ingredient follows the same principle—build it well, adapt quickly, never stop listening. As manufacturers, we keep our focus on continuous improvement, delivering both the compound and the experience needed to turn ideas into achievements, every step of the way.