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HS Code |
388273 |
| Chemical Name | 3-(1H-Imidazol-4-Yl)Pyridine |
| Molecular Formula | C8H7N3 |
| Molecular Weight | 145.16 g/mol |
| Cas Number | 10050-89-8 |
| Appearance | White to off-white solid |
| Melting Point | 163-167 °C |
| Smiles | c1cc(cnc1)c2cncn2 |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% (varies by supplier) |
As an accredited 3-(1H-Imidazol-4-Yl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, white label with black text, 5 grams, chemical name, CAS number, hazard symbols, supplier logo. |
| Shipping | 3-(1H-Imidazol-4-yl)pyridine is shipped in accordance with standard chemical regulations. It is packaged in tightly sealed containers to prevent moisture and contamination. Shipments are handled by certified carriers, accompanied by appropriate safety and hazard documentation. Ensure storage in a cool, dry place upon receipt. Handle using suitable personal protective equipment. |
| Storage | Store 3-(1H-Imidazol-4-yl)pyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as acids and oxidizing agents. Protect from moisture, direct sunlight, and sources of ignition. Label the container clearly and ensure it is kept in a designated chemical storage area, following appropriate safety protocols and local regulations. |
Applications of 3-(1H-Imidazol-4-Yl)Pyridine in Industrial ManufacturingAs a direct producer of 3-(1H-Imidazol-4-Yl)Pyridine, we support several specialized industrial segments that benefit from this heterocyclic building block’s unique structural features. Our material consistently achieves high purity specifications required for advanced synthesis, making it integral to downstream applications where precise molecular performance directly affects product quality, regulatory compliance, and processing efficiency. The following industrial scenarios highlight how true operators employ this compound with a focus on safe, consistent, and compliant manufacturing practices. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers routinely use 3-(1H-Imidazol-4-Yl)Pyridine as a selective intermediate when constructing imidazole-based active pharmaceutical ingredients, especially in the development of kinase inhibitors and anti-infective agents. After detailed process route selection, formulators incorporate this raw material during stepwise heterocycle formation and subsequent functionalization stages, where a controlled addition provides critical molecular specificity. Quality control laboratories closely monitor impurity profiles and reaction kinetics, as the final compound’s pharmacological profile and regulatory acceptability depend on upstream raw material consistency. Industry compliance standards
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2. Advanced Heterocyclic Catalyst Ligand ProductionSpecialty chemical enterprises utilize this pyridine-imidazole motif to design custom ligands for homogeneous catalysis, specifically in cross-coupling and C–H activation reactions. Technical teams engineer complex metal coordination frameworks using this building block for precise tuning of electron density and steric properties, directly influencing catalyst selectivity, recyclability, and substrate compatibility in pilot and commercial batch reactors. Industry compliance standards
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3. Agrochemical Active Ingredient PrecursorAgrochemical formulators apply 3-(1H-Imidazol-4-Yl)Pyridine as a precursor in selective fungicide and plant growth regulator syntheses where nitrogen-heterocycle functionalities impart target-specific bioactivity. Process engineering teams leverage its reactivity to enable controlled ring substitution or fusion with bioactive scaffolds, ensuring potent field efficacy and regulatory acceptance while maintaining process reproducibility across multi-ton batches. Industry compliance standards
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4. Electronic Material Precursor for OLEDsElectronics material manufacturers integrate this compound into the development of functional organic layers for OLED and advanced display technologies. Its rigid aromatic structure and tailored electron-donor properties suit the creation of hole-transport and host materials, where chemical engineers employ it to construct molecular frameworks promising high mobility, long device lifetime, and precise interface compatibility—crucial factors during OLED mass production and QC release testing. Industry compliance standards
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5. Specialty Analytical Reagents and Reference StandardsManufacturers of advanced analytical solutions rely on this pyridine derivative as a structural standard and reagent for HPLC, LC-MS/MS, and elemental analysis calibration, particularly in research settings targeting trace nitrogen-heterocycle quantification. Production teams verify lot traceability and matrix compatibility, while QC teams document analytical performance according to industry and laboratory accreditation demands. Industry compliance standards
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Over the years of manufacturing specialty heterocyclic chemicals, we’ve constantly seen requests for reliable, high-purity 3-(1H-imidazol-4-yl)pyridine. The labs want consistency, and the scale-up engineers want a process that doesn’t slow down under scale. This compound has steadily gained ground in the research and pharma community, not only because of its structure but also due to its flexibility in synthesis. The molecule—a bridge between the imidazole and pyridine families—opens possibilities across medicinal chemistry and advanced materials.
Each run of 3-(1H-imidazol-4-yl)pyridine brings us face to face with the balance of purity and yield. The aromatic nature of the compound, with a pyridine ring connected at the 3-position to an imidazole, lends itself to a wide range of reactivity. At our plant, this translates to rigorous process control, with every reaction step monitored for side-product formation. We fine-tune solvents, temperatures, and reaction times—as one would expect when the customer’s next step relies on robust material. This chemical brings together two pharmacophores: the basicity of pyridine and the hydrogen bonding of imidazole, making it essential in many bioactive scaffolds.
Developing a synthetic route that doesn’t give out at higher volumes takes effort. Having worked through various routes, we’ve settled on a process that provides consistent particle size and a product free of lingering raw material odors. We use recrystallization and controlled drying under vacuum to hit a consistent purity, exceeding 98% by HPLC in standard practice. Our crew notices that off-white crystalline appearance at the end—the sort organic chemists expect—free from haze or particulate matter. Handling the material after final drying, we’ve learned that it stays free-flowing in proper containers and doesn’t agglomerate easily, even in higher humidity conditions.
Chromatograms don’t lie, especially when new research or a clinical project is waiting on data. Downstream chemistry suffers when even trace amounts of unreacted imidazole or pyridine sneak through. It’s tempting sometimes to push speed above all, but experience has taught us that solid purification early on saves a lot of headaches later. A strong batch of 3-(1H-imidazol-4-yl)pyridine should show sharp, defined peaks, with no ghosting or shoulders suggesting impurities. In our facility, we validate each lot by NMR and LC-MS, not because we need to tick boxes, but because failed experiments cost much more than a rerun on our end. Some customers are developing kinase inhibitors or antifungal prototypes using this scaffold. If the building block falls short, downstream screening or scale-up projects run into avoidable problems.
Most of the material we ship goes to medicinal research teams—often pharmaceutical labs working on enzyme inhibitors, receptor modulators, or central nervous system targets. The combination of imidazole and pyridine offers avenues for both hydrogen bonding and aromatic stacking, opening up SAR investigations. Others use it in agrochemical research, linking the core to diverse moieties to craft novel crop protection agents. In our batches destined for universities, we’ve seen chemists try out new synthetic routes or explore catalytic properties involving heterocycles.
Moving from grams to kilograms isn’t just a matter of numbers. Solubility changes, the nature of the solvent system matters more, and package selection comes into play. Over time, we have noticed that sealed, UV-protective containers prevent degradation. 3-(1H-imidazol-4-yl)pyridine doesn’t just evaporate or degrade like some fragile intermediates—it’s stable, though it absorbs moisture if left open. Our warehouse team stores it in dry, dark areas using double-sealed bags, and we urge customers to avoid transferring the product in open air, especially in humid environments.
We also manufacture other imidazole derivatives and pyridyl-based compounds, and comparing them directly always highlights the unique value in this molecule. Substituting an imidazole ring at the 4-position brings a clear difference in basicity and hydrogen bonding ability versus the more common 2-position substitution. In subsequent functionalization steps, the 3-(1H-imidazol-4-yl)pyridine resists unwanted ring opening, providing greater stability under typical synthetic manipulations. Other pyridine-imidazole linkages sometimes degrade on storage or show sensitivity to base—here, stability has been notably higher in our shelf-life studies. Chemists often say this backbone is more accommodating to further elaborations, especially for attaching larger fragments in drug-like molecules.
No batch is quite the same, even under controlled conditions. Sometimes a customer requests a custom salt form, or needs a particularly fine powder for a formulation trial. We work closely with these teams, adjusting crystallization conditions or milling particle size to help their projects along. We’ve supplied lots both on the research milligram scale and larger custom campaigns, noting every adjustment in our process logs. A few years ago, a research team required a product with residual solvent below 100 ppm—a tough specification, but reachable with longer vacuum cycles and fresh desiccants. Real-world manufacturing rewards flexibility and a willingness to tweak the process till it fits.
Sustainable practices matter not only for regulatory reasons but because solvent recovery and waste reduction save money and lower our footprint. Over the last few years, we've replaced several chlorinated solvents in our main process with greener alternatives, and found that 3-(1H-imidazol-4-yl)pyridine maintains its yield and quality with adjusted parameters. This required tweaking reaction temperatures and switching purification protocols, but the end result has been less waste and happier staff. Thermal recycling of spent solvents brings emissions down, and we consistently train our operators to spot ways to reduce raw material input without compromising quality. We see more customers—especially those in Europe and North America—looking for greener supply chains, so we keep pushing in that direction.
Direct feedback from the bench tells us more than any spreadsheet or internal report. We invite chemists to share their results, positive or negative, from trials using our batches. About a year ago, a customer raised an issue with trace heavy metal content picked up during a coupling step; we traced it to a single lot of catalyst and have since introduced more robust incoming QC checks for key reagents. Operators on the floor take pride in batches that meet stricter-than-typical specs, and every change to the process means documenting, inspecting, and adjusting. The upgrades take time, but better reliability keeps relationships strong with users who rely on timely shipments and consistent performance.
Working at the manufacturing level, we know regulatory documentation isn't just paperwork. It’s the roadmap that keeps everyone in sync when audits and quality checks come around. Each drum and bottle leaving our facility carries a complete record—from raw material origin and batch history to analytical data—viewable to customers on request. Our processes align with international standards for traceability, batch release, and sample archiving, which matters for customers preparing regulatory filings or scaling up to GMP runs. Quality teams keep reference samples from each campaign, logging any out-of-spec incident and maintaining transparency. This discipline helps us stand behind our product and supply credible certificates to regulatory bodies as needed.
Years of warehouse management have taught us that simple storage mistakes bring the most headaches. For 3-(1H-imidazol-4-yl)pyridine, exposure to open air sometimes leads to clumping or slight color change. Our team uses 2-layer containment, labeling each shipment with air and moisture warnings. Customers who follow similar routines rarely face issues with shelf-life or product integrity. The compound maintains its quality when stored at room temperature, away from strong light, inside tightly closed containers. Some buyers transfer the material to secondary packaging, but we always recommend checking compatibility to avoid any reactivity or leaching.
Chemists often ask about solvent compatibility or reactivity for downstream use. In our own testing, 3-(1H-imidazol-4-yl)pyridine dissolves readily in common polar aprotic solvents, including DMF and acetonitrile, and remains stable for extended periods. Some derivatization protocols involve basic or acidic conditions; over repeated runs, we've found the molecule resists decomposition unless subjected to harsh acids. Quality issues often arise if a batch encounters oxidants, so we implement antioxidant controls in packaging and recommend users add stabilizers if repackaging for long-term storage. These observations guide our advice and keep new users out of common pitfalls.
Mistakes aren’t rare in manufacturing. A small error—a temperature spike or a mislabeled solvent—can cause an entire run to fall short of desired specs. With 3-(1H-imidazol-4-yl)pyridine, scrap rates fell as we improved operator training and built real-time monitoring into the reactor bay. If a batch ever veers out of spec, we track the root cause and reprocess or discard as needed. Staff reluctance to hide mistakes has built a trust culture that ultimately improves every future lot. Rather than offloading questionable material, we destroy compromised batches, knowing downstream customers stake important projects on what we deliver.
Traders and distributors often focus on turning over volume, but the team on the factory floor owns every step from raw ingredient to final QC. Details matter—whether that's the amount of residual water after drying, the tweaking of pH in the final wash, or the check for residual solvents by headspace GC. Long-term batches of 3-(1H-imidazol-4-yl)pyridine show that care paid upfront—clean reaction glassware and utensils, careful temperature ramps, solvent analysis—brings measurable results in final purity. We follow the same protocols batch after batch, allowing process improvements to build on a solid foundation.
From the point of view of a direct manufacturer, understanding what each customer wants out of their 3-(1H-imidazol-4-yl)pyridine deliveries sharpens how we work. Medicinal chemists running multi-step syntheses need lots free of side impurities that could interact with the next reagent. Process chemists developing scale-up protocols request data on melting point, solubility, and stability in various solvents, so the plant provides actual measurements from working runs, not just literature numbers. We share process insights—such as ideal stirring speeds for suspension-based reactions or safe heating limits—so customers starting projects at the gram scale avoid surprises later. This back-and-forth ultimately shortens timelines and improves project outcomes.
Some users in regulated industries approach us with tighter-than-market specifications. Over time, the team has set up purification steps that exceed standard models—additional washes, extra filtrations, and extended drying times become routine for certain orders. Analytical results—such as chiral purity or ultra-low metal content—have improved by involving production staff in every phase. Realistically, each refinement takes time and cost, but customers in the pharmaceutical and specialty chemical arenas prize reliability enough to justify these investments.
We’ve noticed rising demand for increased documentation, scalable green chemistry routes, and rapid technical support. Deploying LIMS systems in the plant, moving toward fully integrated electronic record keeping, and automating much of the sample management are steps we’ve taken to match evolving needs. The feedback loop from users pushes us to investigate new synthetic methodologies—for example, evaluating continuous flow techniques or biocatalytic processes for producing 3-(1H-imidazol-4-yl)pyridine in the coming years.
Day in, day out, producing 3-(1H-imidazol-4-yl)pyridine comes down to supporting researchers who depend on each clean, reproducible batch. It means taking responsibility for transparency and direct accountability, learning from real-world feedback, and pursuing sustainable improvements. From sourcing raw materials and refining manufacturing protocols to meeting ever-tougher customer and regulatory demands, we approach each campaign as a partnership with the chemists and engineers we serve. Where imidazole and pyridine chemistry goes next, our team stands ready to deliver the foundation.