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3-(1H-Imidazol-4-Yl)Pyridine

    • Product Name 3-(1H-Imidazol-4-Yl)Pyridine
    • Alias Imidazo[4,5-b]pyridine
    • Einecs 629-541-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 3-(1H-Imidazol-4-Yl)Pyridine

    Applications of 3-(1H-Imidazol-4-Yl)Pyridine in Industrial Manufacturing

    As 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 Synthesis

    Pharmaceutical 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

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF Monographs (where applicable for downstream APIs)
    • European Pharmacopoeia production guidelines
    • 21 CFR Part 211 (GMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 0.5–2.0 molar equivalents relative to core scaffold; optimized per synthetic step and scale-up yield targets

    Downstream process integration

    • Introduced at intermediate condensation stage after initial ring construction; purified via crystallization or preparative HPLC prior to final API coupling

    Final product types

    • Small-molecule anti-cancer drugs (e.g., kinase inhibitors)
    • Antiviral and anti-infective agents (imidazole-derivatives)
    • Investigational clinical trial substances requiring clear impurity traceability

    2. Advanced Heterocyclic Catalyst Ligand Production

    Specialty 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

    • REACH registration for downstream application
    • ISO 9001 Quality Management System in chemical synthesis
    • Chemical Producers Association (CPA) Environmental & Process Safety Guidelines

    Typical usage ratio

    • 0.05–0.15 molar equivalents relative to transition metal, based on stoichiometry of ligand-to-metal complexation and activity needs

    Downstream process integration

    • Employed in chelation steps during ligand formation; added after primary backbone preparation directly into the ligand assembly reactor, followed by coordination to metal centers

    Final product types

    • Bidentate/tridentate ligands for palladium, ruthenium, and copper complexes
    • Homogeneous catalysts for pharmaceutical and agrochemical intermediates synthesis
    • Catalyst performance enhancers for olefin polymerization

    3. Agrochemical Active Ingredient Precursor

    Agrochemical 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

    • FAO/WHO Specification for Pesticide Ingredients
    • ISO 17025 (Laboratory Accreditation for Residual Testing)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products Authorization)
    • China GB 2763 Maximum Residue Limits guidance (for export-focused products)

    Typical usage ratio

    • 5–15% w/w of total synthetic mass depending on the designed target molecule and yield optimization at pilot and production scales

    Downstream process integration

    • Added during the active ingredient core assembly, typically after initial halogenation and before side-chain derivatization; followed by purification through extraction or chromatographic separation

    Final product types

    • Triazole-based fungicides
    • Imidazole-functionalized plant growth stimulants
    • Nitrogen-heterocycle intermediates for custom agrochemical formulations

    4. Electronic Material Precursor for OLEDs

    Electronics 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

    • RoHS Directive (EU) 2011/65
    • IEC 62474 (Material Declaration for Electronic Industry)
    • ISO 14001 (Environmental Management in Electronic Component Manufacturing)

    Typical usage ratio

    • 0.3–3.0% by mass within organic host matrix, adjusted according to emission profile and film-forming property requirements

    Downstream process integration

    • Incorporated at organic synthesis step for host or transport material creation; purified through repeated recrystallization and introduced into spin-coating or vapor deposition feed solutions

    Final product types

    • OLED hole-transport layers
    • Fluorescent and phosphorescent host materials
    • Advanced thin-film display modules (TV, mobile, automotive displays)

    5. Specialty Analytical Reagents and Reference Standards

    Manufacturers 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

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • USP Reference Standard Guidelines
    • GLP (Good Laboratory Practice, OECD Principles)

    Typical usage ratio

    • 1–10 μg/mL as calibration standard concentration in analytical solution; precise concentration chosen to match assay sensitivity and detection requirements

    Downstream process integration

    • Formulated as a neat or diluted standard; packaged under inert gas to prevent decomposition and distributed for direct use in analytical test method development

    Final product types

    • Heterocycle reference standards for HPLC/LC-MS quantification
    • Certified analytical reagents for research and quality assurance laboratories
    • Traceability solutions for impurity identification in pharmaceutical and chemical raw materials
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    Certification & Compliance
    More Introduction

    Introducing 3-(1H-Imidazol-4-Yl)Pyridine: Insights from the Factory Floor

    Direct from the Line: What We See in Every Batch

    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.

    The Essential Structure: More Than Just Another Heterocycle

    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.

    From Lab to Kilo Scale: A Manufacturer’s View of Reliability

    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.

    Why Purity Matters in Real-World Chemistry

    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.

    A Chemical with Versatility: Where We See It Used

    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.

    Handling Real-World Logistics

    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.

    What Sets It Apart from Related Products

    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.

    Working with Chemists: Meeting Unusual Demands

    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.

    Building for the Future: Sustainability and Process Improvements

    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.

    Listening and Adapting: Feedback Directs Our Choices

    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.

    Traceability and Documentation: Supporting Regulatory Demands

    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.

    Practical Storage and Handling: Tips from Day-to-Day Production

    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.

    Solubility and Reactivity Observations from Production

    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.

    Learning from Setbacks: Batch Recovery and Improvements

    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.

    The Difference Direct Manufacturing Makes

    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.

    Supporting Research and Scalability Goals

    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.

    Meeting Tougher Standards: Aiming for Trace Consistency

    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.

    Keeping Pace with Industry Trends

    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.

    Final Thoughts from the Factory

    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.