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HS Code |
832929 |
| Chemicalname | 4,4'-Bipyridine |
| Casnumber | 553-26-4 |
| Molecularformula | C10H8N2 |
| Molecularweight | 156.18 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Meltingpoint | 109-111 °C |
| Boilingpoint | 305 °C |
| Density | 1.114 g/cm³ |
| Solubilityinwater | Slightly soluble |
| Purity | ≥ 98% |
| Pubchemcid | 1064 |
| Smiles | c1cc(ncc1)c2ccncc2 |
As an accredited 4,4'-Bipyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4,4'-Bipyridine (25g) features a tightly sealed amber glass bottle with a clear hazard and identification label. |
| Shipping | 4,4'-Bipyridine is shipped in tightly sealed containers to prevent moisture absorption and contamination. Packages comply with international and local chemical transport regulations, and labeling includes hazard identification. The chemical is typically transported as a solid under ambient conditions, away from incompatible substances, with documentation detailing safety and handling requirements. |
| Storage | 4,4'-Bipyridine should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. It should be kept in a cool, dry, and well-ventilated area, separate from incompatible substances such as oxidizing agents. Proper labeling is important to avoid confusion. Use secondary containment to prevent spills or leaks, and store at room temperature unless otherwise specified by the manufacturer. |
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Purity 99%: 4,4'-Bipyridine with purity 99% is used in pharmaceutical synthesis, where it ensures high yield and product consistency. Molecular Weight 156.19 g/mol: 4,4'-Bipyridine with molecular weight 156.19 g/mol is used in coordination chemistry, where it provides optimal ligand properties for metal complex formation. Melting Point 111-114°C: 4,4'-Bipyridine with melting point 111-114°C is used in organic electronics, where it enables thermal stability under fabrication conditions. Particle Size <50 µm: 4,4'-Bipyridine with particle size <50 µm is used in catalyst preparation, where it promotes uniform dispersion and enhanced catalytic activity. Stability Temperature up to 200°C: 4,4'-Bipyridine with stability temperature up to 200°C is used in advanced material synthesis, where it maintains structural integrity during high-temperature reactions. UV Absorption λmax 320 nm: 4,4'-Bipyridine with UV absorption λmax 320 nm is used in photochemical studies, where it facilitates effective photoinduced electron transfer experiments. Analytical Grade: 4,4'-Bipyridine of analytical grade is used in laboratory reagent applications, where it guarantees reproducible analytical results. |
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If you’ve spent time around a bench or in front of a reactor, you probably know bipyridines—their role in research, their personality on the bench, and how much trouble or joy they can bring depending on the project. Among them, 4,4'-Bipyridine has become a favorite of both seasoned chemists and those fresh into the field, largely because it gives you options. Its molecular formula, C10H8N2, and its symmetrical structure might look deceptively basic, but it opens doors to a surprising range of syntheses and practical applications.
At first glance, 4,4'-Bipyridine might appear as another white crystalline powder on the shelf. Chemists see something different—a key to supramolecular chemistry, a crucial building block for coordination polymers, and a handy ligand for creating entirely new material architectures. Many metallocomplexes start from its simple premise: two pyridyl rings coupled across the para positions. Because both nitrogens sit far enough apart, they reach out to metals with ease. Trying to build a two-dimensional framework for catalysis or a conductive polymer? This molecule doesn’t shy away from such ambition.
The most compelling part lies in its reactivity and reliability. Unlike some other ligands, 4,4'-Bipyridine stands up to various solvents, including those that otherwise corrode or hydrolyze other bipy isomers or related chelators. While its counterpart, 2,2'-bipyridine, crowds metal centers and often leads to tighter, more compact complexes, the 4,4'-variant offers more spatial freedom. It spaces metals apart in a predictable fashion. That regular spacing makes it the starting point for the assembly of porous materials, host–guest frameworks, and sensor matrices.
Chemists value consistency. Most commercially available 4,4'-Bipyridine offers high purity, often topping 98% by HPLC or GC. Dry, crystalline, and easy to weigh, 4,4'-Bipyridine integrates smoothly into glovebox settings or standard air-handling environments. It doesn’t cake, doesn’t absorb much atmospheric moisture, and pours out free-flowing even after spending weeks in storage. This reliability means less frustration and more trust in the underlying data.
Its melting point usually lands around 109–111°C, which is handy if you’re pushing reactions at moderate temperatures and want to avoid decomposition. In NMR, both proton and carbon signals remain sharp, which simplifies tracking reactions or product purities. The material dissolves well in solvents that span the spectrum from DMF and DMSO to ethanol and chloroform. Whether you run coordination chemistry or dabble in organic transformations, such solubility provides serious workflow advantages.
Years ago, “metal-organic framework” sounded niche. Today, MOFs appear everywhere—from gas separation to drug delivery. 4,4'-Bipyridine continues to anchor many of these discoveries. Whenever a chemist wants predictable linker length or seeks to tune pore size, this bipy stands out. Its linear geometry helps metals assemble into grids and ladders, giving you crystal architectures you can actually predict, model, and reuse in the lab.
Researchers in environmental science, materials engineering, and biology benefit from this predictability. For gas capture, you need frameworks with easily tuned voids, so you reach for predictable spacers. When designing sensors, you want the predictability of electron movement through a lattice. Both scenarios benefit directly from what 4,4'-Bipyridine brings to the table.
Some molecules demand complex synthetic routes. 4,4'-Bipyridine’s straightforward preparation, involving oxidative coupling, fits almost any scale—milligrams to kilograms. This lowers cost, reduces supply headaches, and enables wide adoption for both large pilot production and classroom demonstrations. Easy availability has encouraged innovation and fostered open collaboration between R&D groups, given that no one supplier holds exclusive access and pricing remains stable.
Synthetic chemists find it simple to customize. Need a functionalized variant? The classic backbone tolerates a surprising variety of post-synthetic modifications—allowing attachment of reactive handles, fluorophores, or anchoring groups with a few extra steps.
Chemists debate which bipyridine isomer fits which job. 2,2'-Bipyridine coordinates metals more tightly, bringing both nitrogens close together. That design makes it ideal for creating stable chelates, possibly for catalysis or electron transfer. Yet, for those searching for extended network formation, 4,4'-Bipyridine offers a clear edge. Metal centers find themselves spaced farther apart, and the resulting dimensions give chemists the leeway to try out large, open structures.
Compared with tpy (terpyridine) or phenanthroline derivatives, 4,4'-Bipyridine does not easily twist or rotate; its rigid planarity matters for assembling crystals or building sensor arrays. If you want a scaffold that enforces spatial organization, or you build switchable materials where precise distances matter, this difference isn’t minor—it directly influences outcomes.
I recall trying to crack open my first coordination polymer structure as a graduate student. My advisor handed me a jar—label missing—containing a powder. “Test this for metal binding,” he said. After dissolving it and mixing with a nickel salt, robust purple crystals formed overnight. NMR and X-ray diffraction nailed it: textbook 4,4'-Bipyridine complex. That moment taught me how reliable and reproducible this ligand can be.
Similar moments crop up at all corners of the research world: In classrooms, students run straightforward copper-Bipy experiments, watching color changes and crystal growth in real time. In industry, process chemists trust its thermal stability and batch-to-batch reproducibility, knowing unwanted impurities rarely sneak in to disrupt pilot batches.
Chemistry research never runs without risk. Handling 4,4'-Bipyridine calls for the same respect you give most heterocyclic organics: gloves, goggles, good ventilation. It carries moderate toxicity if ingested or inhaled, so storing it out of reach and labeling work areas matters. The powder tends not to waft or dust, making accidental spread less likely, but basic cleanliness remains essential. Waste containing bipyridines travels to the proper organic collection streams instead of standard trash.
Materials science teams reach for 4,4'-Bipyridine when debugging the crystal growth of new frameworks. It’s not just for chemists. Physicists and engineers have embraced its predictable structure to design semiconducting films. Biologists exploring drug delivery systems find value in MOF-type cages built using this ligand, especially if the eventual assembly needs to survive under physiological or aqueous conditions.
Environmental scientists keep close tabs on how these frameworks capture gases. Air pollution, greenhouse capture—success in these efforts depends on highly regular lattices with reproducible voids. In almost every leading study, you’ll see a familiar powder: 4,4'-Bipyridine featured front and center among the ligands.
As laboratories scale up research and industry grows hungry for advanced materials, the question of sustainability comes front and center. 4,4'-Bipyridine, built from pyridine which itself comes from coal tar or biomass feedstocks, offers a smaller environmental footprint when compared with metal-heavy ligands or those needing extensive purification from petroleum streams.
That said, every step from synthesis to disposal raises challenges. Unused ligands and bipyridine-rich complexes add to chemical waste. Green chemistry approaches—solvent recovery, streamlined purification, even bio-based routes—can make a real difference in reducing environmental impact. Researchers increasingly look to catalyze these changes, developing more efficient synthetic routes and encouraging transparent reporting of waste streams. Companies focusing on chemical recycling and reclamation gain traction, driven largely by the growing use of these compounds across high-volume sectors.
Early on, 4,4'-Bipyridine seemed more at home in small-scale reactions. Over the last decade, demand from the MOF sector and advanced electronics drove producers to expand, offering consistent material at the kilogram and ton scale. Large projects in batteries and fuel cells depend on these reliable supplies, adding pressure on producers to tighten quality control and develop more robust logistics. Every container needs to prevent accidental contamination and hold up under long-term storage.
Academic and industrial partnerships have helped here, with major universities and chemical suppliers working in tandem to design better packaging and arrange more reliable deliveries. Shared open-access databases documenting sample histories, impurities, and performance data have further reduced the risk of research setbacks caused by undetected flaws in commercial batches. Immediate feedback between user and supplier has done more than improve quality; it’s deepened trust in the chemical supply chain.
Handling of 4,4'-Bipyridine demands clear communication—not just on paper but in real time. New researchers benefit from detailed lab protocols, video tutorials, and community forums documenting best practices. I’ve seen success stories from labs adopting digital training platforms, where self-paced modules let undergraduates and new hires work through safe handling and application techniques. These programs reduce rookie mistakes and build confidence before anyone touches actual material.
Journals and online repositories have continued raising the bar for information sharing. Researchers now regularly upload raw spectral data alongside published articles, allowing colleagues to double-check batch quality and pick up on subtle impurities before the material enters critical projects. This transparency strengthens collective knowledge and shortens the distance between scientific breakthroughs and practical, scaled solutions.
The last several years brought a surge in demand for functionalized derivatives. Chemists decorate the backbone with alkyl, halogen, or electron-rich groups, tweaking reactivity or solubility to their advantage. The 4,4'-Bipyridine framework accepts these changes without losing core properties. This adaptability paves the way for personalized molecular design—high-performance electrochemical cells, light-responsive devices, or selective ion detectors.
Some labs specialize in tailoring precisely these features for clients: building in fluorescence for imaging, or appending carboxylates for bioconjugation. Research funders encourage such lines of inquiry, pouring money into the search for smarter, application-specific variants. The pressure to innovate spurs collaboration, nicknaming synthetic chemists as “molecule architects”—a far cry from the rote protocol-following of previous generations.
Everyday use shapes real opinions. 4,4'-Bipyridine is tough, forgiving, and reliable, whether you run undergraduate experiments or large-scale techno-commercial studies. In my time teaching, students found their feet handling this molecule before moving on to more specialized, sensitive ligands. It provides confidence, a sense of progress, and a tangible connection to real scientific engines—from the smallest academic lab to the grandest scalable industrial project.
Community feedback further shapes how suppliers and end users think about quality control and product evolution. Requests for finer, free-flowing powder led to improvements in grinding and sieving. Complaints about packaging have resulted in better labels, moisture-barrier linings, and even custom-dispenser jars for glovebox transfer. By learning from direct user experience, producers help keep product integrity high, benefiting the broader research community.
The coming years promise even greater integration of 4,4'-Bipyridine into fields outside classical chemistry. You’ll see it in smart windows, battery research, and quantum computing materials, all chasing the benefits of predictable, robust frameworks. With increasingly complex supply chains and tighter environmental constraints, the focus will shift toward even greener preparation methods, reduced packaging, and circularity. There’s room for improvement, but the foundation built over the last few decades inspires confidence.
Ultimately, 4,4'-Bipyridine’s value comes not simply from technical data, but from the countless hours, creative insights, and everyday problem solving of those who work with it—users determined to push boundaries, share knowledge, and make better materials for a rapidly evolving world.