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HS Code |
827144 |
| Chemicalname | 1,2-Bis(2-Pyridyl)Ethylene |
| Casnumber | 17538-11-9 |
| Molecularformula | C12H10N2 |
| Molecularweight | 182.22 g/mol |
| Appearance | Yellow powder or crystals |
| Meltingpoint | 102-106 °C |
| Solubility | Soluble in organic solvents such as chloroform and dichloromethane |
| Smiles | C(=C)(c1ccccn1)c2ccccn2 |
| Inchi | InChI=1S/C12H10N2/c1-3-9-13-7-5-11(1)12(2-4-10-14-8-6-12)2-4-10-14-8-6-12/h1-10H |
| Storageconditions | Store in a cool, dry place, tightly closed container |
| Synonyms | 1,2-Di(2-pyridyl)ethylene |
| Pubchemcid | 320115 |
As an accredited 1,2-Bis(2-Pyridyl)Ethylene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g 1,2-Bis(2-Pyridyl)Ethylene comes in a sealed, amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | **Shipping Description for 1,2-Bis(2-Pyridyl)Ethylene:** This chemical should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Handle with appropriate PPE. Transport according to applicable regulations for hazardous materials. Ensure compliance with all national and international shipping standards, labeling clearly as a laboratory chemical for research use only. |
| Storage | 1,2-Bis(2-Pyridyl)Ethylene should be stored in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Store at room temperature, protected from direct sunlight. Use appropriate chemical storage cabinets if possible, and ensure proper secondary containment to avoid spills or leaks. |
Applications of 1,2-Bis(2-Pyridyl)Ethylene in Industrial ManufacturingAs a specialized manufacturer of 1,2-Bis(2-Pyridyl)Ethylene, we supply this material for established downstream sectors where its molecular structure and chelation properties fulfill precise performance, process, and compliance demands. Below, we detail key industrial applications, illustrating technical standards, practical dosage guidance, process integration, and typical finished product types. 1. Homogeneous Catalysis for Fine Chemical SynthesisThis ligand critically supports homogeneous transition metal catalyst formulations, particularly in multistep synthesis routes including selective oxidations, C–C coupling, and asymmetric transformations for active pharmaceutical intermediate (API) and agrochemical manufacturing. Its electronic characteristics influence selectivity and yield, making it preferred in specialty processes that require consistent, scalable reactivity under regulated environments. Industry compliance standards
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2. Coordination Chemistry Reagent for Analytical StandardsLaboratories and reference standard producers utilize this material as a chelation agent to form stable complexes, serving as model compounds, titration standards, or calibration entities for analytical method development by AAS, UV-vis, or NMR. Its predictable binding behavior allows reproducibility crucial for QC in pharma, environmental, and industrial analytics. Industry compliance standards
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3. Ligand System for Coordination Polymer and MOF FabricationThis compound serves as a key organic linker in synthesizing transition metal-based coordination polymers or metal-organic frameworks (MOFs), applied in gas separation, storage, or catalysis. Control over ligand-to-metal ratio and synthesis conditions impacts framework porosity and functional properties, supporting tailored materials for advanced separations or sensing applications. Industry compliance standards
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4. Metal Chelator for Transition Metal Removal in Electronics and Semiconductor Wet ProcessingDownstream electronics manufacturers employ this chelator as an additive in formulated cleaning and etching solutions. It binds residual transition metals with high specificity, allowing for rigorous part cleanliness and device purity in production lines processing semiconductors, microelectromechanical systems (MEMS), and printed circuits. The dosage and process parameters vary to match metal load and substrate sensitivity, with strict controls for all water and solvent contaminants. Industry compliance standards
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It takes experience on the production floor and an eye on the research to really understand what sets 1,2-bis(2-pyridyl)ethylene apart, so let’s get into it. In our plant, we've spent good years refining how to synthesize and handle this bidentate ligand, known to plenty of chemists as DPEN or BPE. Unlike many other chelating agents or pyridine derivatives, this compound’s ethylene bridge gives it stronger backbone rigidity, allowing for selective binding behavior. Chemists who handle transition metal catalysts have recognized its unique bite angle, which supports reactivity patterns not easily duplicated by other ligands. You’ll see it show up most often as a partner in catalysis or as a building block for more specialized organometallic complexes.
Out on the production floor, the synthesis of 1,2-bis(2-pyridyl)ethylene involves careful stepwise assembly. We start with high-purity 2-pyridyl precursors because even slight upstream impurities can create difficulties downstream, especially during cross-coupling or condensation. Our process avoids excess byproducts and prioritizes reproducibility, since so much rides on consistency when supplying academic labs or pharmaceutical manufacturers. We monitor critical stages in real time—no shortcuts with batch verification. The final product leaves our reactors as a crystalline solid with characteristic bright color, reassuring us we’ve hit the right mark.
We dry and pulverize the compound in dedicated suites. Moisture is a silent enemy here—trace water compromises subsequent reactions. Packing technicians use tamper-evident packaging under inert atmosphere conditions, because we’ve seen too many end users report unexpected degradation when storage jars weren’t properly sealed. We keep particle size distribution tight; it simplifies dissolution for customers and minimizes static cling that can waste product at the lab bench.
Based on our hands-on production, the material consistently weighs in with a purity above 98% as checked by HPLC and GC, meeting expectations for both R&D and industrial users. The model we produce, referred to in most catalogs as “1,2-bis(2-pyridyl)ethylene, batch 07-XX,” reflects only those lots that have cleared full analytical profiling. We hold spectral data—NMR, FTIR, and mass spec—on file, and our on-staff chemists personally compare new batches against trusted benchmarks. Consistency isn’t just a word here; it’s the only reason our product list survives on the market.
Shipping protocols originated from lessons we learned shipping this compound to humid climates. We include desiccant sachets in every drum, so even after weeks in transit, users report negligible clumping or caking at the bottom. We don’t make claims about magical shelf-lives. With proper storage—sealed, dry, out of direct sunlight—the powder remains within spec for hundreds of days. In labs lacking controlled atmospheres, product integrity drops as moisture creeps in, pointing to a simple solution: make airtight closure a habit.
Our biggest customers use this compound as a ligand for transition metal catalyzed cross-coupling. With its two pyridine rings and ethylene bridge, it creates a pocket for nickel, palladium, and copper centers. Professions in synthetic chemistry appreciate its role in facilitating Suzuki-Miyaura and Heck-type reactions. Researchers have demonstrated that complexes built with this ligand sometimes outperform phosphine ligands in select transformations, something we’ve followed closely in collaboration with partner labs.
Beyond catalysis, there’s a practical side: companies focused on materials science use our 1,2-bis(2-pyridyl)ethylene to template metal-organic frameworks and related architectures. This compound fits nicely into grid-like assemblies, where the nitrogen donors click into place with metallated nodes. Some customers, especially those investigating nanostructured arrays, praise the geometric control that these ligands provide versus single-site pyridine donors. In the past, we fielded requests from electronics R&D facilities eager to see if the compound could tune optical or electronic properties—the answer is yes, when inserted correctly into larger frameworks.
Pharmaceutical research groups buy this compound for its behavior in rigidification of molecular scaffolds. We know from talking to customers that its ability to chelate metal ions selectively improves hit rates in metallodrug discovery, and also helps stabilize otherwise tricky intermediates during organic syntheses. We keep an eye on literature reports and patent filings, watching for any new applications so we can advise on optimized protocols in our technical bulletins.
Over the years, chemists have designed dozens of bidentate ligands for catalysis and complex assembly. 1,2-bis(2-pyridyl)ethylene’s most common competitors are 2,2'-bipyridine and 1,10-phenanthroline. In our hands, the ethylene linkage makes a visible difference. While 2,2'-bipyridine offers flexibility and accommodates a wider range of metal centers, that same flexibility reduces selectivity in some catalytic cycles. By comparison, the rigid scaffold in our compound consistently leads to sharper selectivity, which is key in stereospecific reaction workflows.
1,10-phenanthroline remains highly popular, but its fused ring system can have solubility issues in certain nonpolar solvents. In contrast, 1,2-bis(2-pyridyl)ethylene dissolves more evenly in both polar aprotic and select nonpolar solvents. We have customers reporting faster dissolution and clearer reaction mixtures, making isolation of target compounds less labor-intensive. In the final step, cleaner separation often means higher yields, which every process chemist values.
Traditional phosphine ligands such as triphenylphosphine still command mindshare for many organometallic reactions, yet they suffer from air-sensitivity and, in some cases, environmental impact concerns. 1,2-bis(2-pyridyl)ethylene is more stable to oxygen and moisture, lessening risks in open-flask handling. This compound won’t solve every problem, but its lower sensitivity supports longer shelf life and easier inventory management, especially for resource-limited teaching and development labs.
Our journey with 1,2-bis(2-pyridyl)ethylene started a decade ago, working alongside academic pioneers who needed kilogram lots for the first time. Back then, market options often meant fluctuating purity, off-spec lots, or product arriving in leaky packaging. That inspired us to invest in refining our process, even down to in-house glassware repair for specialized reaction rigs. Sourcing directly from manufacturer means direct access to application experience—no need to guess about solubility quirks, batch-to-batch drift, or how to re-dissolve caked powder after long storage. Our support chemists troubleshoot side-by-side with clients, instead of sending generic email advice.
We review customer feedback as a critical part of our process improvement. For example, a materials chemistry outfit found that a minor trace impurity consistently interfered with a low-scaling step in their process. We rolled out additional purification in the final crystallization, fixed the problem, and followed up with analytical reports to confirm. Real-world feedback loops like this shape our production—unlike distributors that don’t see the factory floor, our team knows where each improvement lands.
Manufacturing organic ligands with nitrogen heteroatoms involves safety risks most end-users rarely see. Our plant uses vented hoods, containment protocols, and round-the-clock scrutiny from safety officers. We learned through fire drills that no glove or mask can take the place of proper engineering controls. Chlorinated solvents and strong bases, needed at some synthesis steps, demand overhead monitoring and robust employee training. We don’t just post the paperwork on the wall; lead operators walk the line every morning before shift starts.
Our waste solvent inventory remains segregated and monitored. Once a year, an external auditor reviews evaporation losses and any irregular emissions. Sloppy release of pyridine compounds into drains could foul community water sources, so we’ve invested in a closed-loop solvent recovery. By reusing and purifying, annual volume of hazardous waste fell more than fifty percent over the past three years. This practice remains company policy not because it’s “green” for marketing, but because repairs and recovery cost less than fines or lost community trust.
In the past, some suppliers packaged this compound in glass jars to save on cost, but we switched to high-barrier polymer bottles and lined metal drums. Dropping breakage rates practically ended lost revenue from shattered containers. Besides, our loaders work faster knowing containers don’t smash when jostled on the dock.
Predicting yearly demand for 1,2-bis(2-pyridyl)ethylene remains a puzzle. Researchers can jump from a small test run to a full synthesis campaign with little warning, pushing lead times and logistical juggling. We prepare buffer stock, but capacity planning requires updates on both new grant funding cycles and emerging technology trends. When a catalyst screen in Europe shows promising results, global orders can spike weeks before downstream suppliers catch up. As a result, we update production scheduling based on customer forecasts, adjusting raw material purchases to buffer against price swings.
Supply chain hiccups can surface from small disruptions. Pyridine feedstock logistics, rail strike delays, or port closures all ripple up the value chain. During the last major global logistics crunch, we re-sourced one intermediate from a regional plant rather than risk a multi-month delay. Built-in redundancy keeps customer lead times steady, so users rarely notice what’s happening behind the scenes.
We’ve learned from every delay and order surge. Our site’s operations managers know to rotate raw material stock ahead of the hot season, preventing degradation or trouble in synthesis. Keeping everything transparent for customers, we share batch production timelines and update certificates of analysis proactively, even before questions arise.
Troubleshooting with end users stays core to our service. Handling 1,2-bis(2-pyridyl)ethylene correctly often separates a clean yield from a frustrating mess. Chemists working in humid areas should only open bottles inside dryboxes. In solution, this compound can act as a scavenger for trace metals, sometimes pulling more than intended; we advise analytical check-ins if purity of the final metal complex matters for the application.
Some researchers have attempted high-temperature catalytic runs above 180°C, only to find unexpected ligand decomposition. Our in-house data recommends keeping temperature controls under 160°C for extended runs, especially during pilot-scale workups. We provide guidance on compatible solvents to ensure that reactivity proceeds as planned, not compromised by side reactions. Methanol or DMF both work for most protocols; limited use of aqueous solvent reduces risk of unwanted hydrolysis.
If precipitation occurs during ligand exchange or metal insertion, slow addition and controlled stirring help avoid clumping. We supply stirring guides in technical sheets, showing RPM ranges and dissolution curves based on empirical testing, not theoretical values. Our customers report that following these aids reproducibility with less trial and error.
We dedicate a section of our plant floor as a pilot lab for next-generation pyridine-based ligands. Real-world testing means running sample batches through new reaction schemes, not just beaker-scale demonstrations. This helps address customer questions before scale-up. If a client asks whether 1,2-bis(2-pyridyl)ethylene can handle a new substrate scope, our applied scientists set up miniature test reactions. Only once we document effects on yield, selectivity, and workup, do we forward feedback.
In the last project, our pilot team worked with a biotech startup exploring nickel complexes for sustainable polymerization. Their process offered a cheap alternative to platinum chemistry, but depended on precise ligand-metal ratios. Our technical staff spent a week in their facility, verifying how batch-to-batch purity impacts catalyst longevity. It turned out minor tweaks in input material improved polymer stability, leading to a joint patent application and a stronger supplier-customer relationship.
On the production side, controlling costs links directly to product quality and market stability. Bipyridine precursors can swing in price depending on global market flux, supply interruptions, or regulatory actions on chemical factories. Over time, establishing long-term purchase agreements with upstream firms created insulation against short-term spikes, keeping offer prices grounded. We prioritize clarity in pricing rather than using temporary “specials” or discounts that could mislead about true production costs.
Chemical manufacturing’s reputation often suffers from perceptions about rising prices or inconsistent quality. Direct engagement—responding to concerns with transparency—keeps misunderstandings rare. Our team hosts quarterly open houses at our factory, letting clients and partners see the process, test the current batch, and review all quality logs. By opening the door literally and figuratively, we reduce friction and clarify any lingering doubts about product reliability.
Supplying 1,2-bis(2-pyridyl)ethylene from the manufacturer’s side brings a mix of routine and constant learning. Chemistry never stays still, and end-user demand steers our investment in both plant equipment and staff know-how. Few compounds blend versatility with robust handling quite like this bidentate ligand, making it a fixture for labs and industries building the next wave of catalysts and advanced materials. Daily, we see our work connect theory to practice—batch by batch, process by process—laying the groundwork for every downstream innovation relying on reliable, high-purity 1,2-bis(2-pyridyl)ethylene.