|
HS Code |
188358 |
| Name | 2-Ethenylpyridine |
| Molecular Formula | C7H7N |
| Molar Mass | 105.14 g/mol |
| Cas Number | 100-69-6 |
| Appearance | Colorless to pale yellow liquid |
| Density | 0.980 g/mL at 25°C |
| Boiling Point | 157-159°C |
| Melting Point | -64°C |
| Flash Point | 44°C |
| Refractive Index | 1.581 at 20°C |
| Solubility In Water | Slightly soluble |
| Synonyms | 2-Vinylpyridine |
| Odor | Acrid, unpleasant |
As an accredited 2-Ethenylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL amber glass bottle with a secure screw cap, labeled “2-Ethenylpyridine,” displaying hazard symbols and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Ethenylpyridine: Typically loaded in sealed steel drums or IBCs, totaling approximately 16-20 metric tons per container. |
| Shipping | 2-Ethenylpyridine should be shipped as a hazardous chemical. It must be transported in tightly sealed containers, compliant with regulations for flammable liquids (UN 1993, Class 3). Package securely to prevent leaks and use appropriate labeling. Avoid heat, sparks, and open flames. Ship with proper documentation and safety data sheet (SDS). |
| Storage | 2-Ethenylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep it separate from oxidizing agents, acids, and bases. Store under inert atmosphere (e.g., nitrogen) if possible, and protect from light. Use appropriate chemical-resistant containers and follow all standard laboratory chemical storage guidelines. |
| Shelf Life | 2-Ethenylpyridine typically has a shelf life of 12 months when stored in a cool, dry, and well-sealed container. |
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Purity 99%: 2-Ethenylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and minimized by-product formation. Molecular Weight 105.13 g/mol: 2-Ethenylpyridine with molecular weight 105.13 g/mol is used in specialty polymer production, where it allows precise molecular architecture control. Melting Point −50°C: 2-Ethenylpyridine with a melting point of −50°C is used in low-temperature copolymerization processes, where it facilitates stable monomer incorporation. Stability Temperature 120°C: 2-Ethenylpyridine with stability temperature up to 120°C is used in high-temperature resin manufacturing, where it enhances process safety and product durability. Viscosity 1.2 cP: 2-Ethenylpyridine with viscosity 1.2 cP is used in inkjet ink formulations, where it achieves optimal flow properties and print resolution. Particle Size <10 µm: 2-Ethenylpyridine with particle size less than 10 µm is used in advanced catalyst supports, where it maximizes reactive surface area for catalysis. Water Content <0.05%: 2-Ethenylpyridine with water content less than 0.05% is used in electronic chemical manufacturing, where it minimizes hydrolytic degradation risks. Refractive Index 1.541: 2-Ethenylpyridine with refractive index 1.541 is used in optical polymer production, where it supports precise light transmission characteristics. GC Assay ≥98%: 2-Ethenylpyridine with GC assay ≥98% is used in agrochemical synthesis, where it ensures consistency in active ingredient formulation. Density 0.976 g/mL: 2-Ethenylpyridine with density 0.976 g/mL is used in solvent blends for coatings, where it contributes to predictable application viscosity. |
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In the world of specialty chemicals, certain compounds carve out a strong presence because people working on real-world problems see their value. 2-Ethenylpyridine belongs among them. Built on a pyridine ring with a vinyl side chain sitting on the second position, this molecule grabs the attention of everyone from synthetic chemists to polymer engineers. I first learned about it in a polymer lab, where researchers sought new ways to bridge organic and inorganic systems. The molecule’s ability to join with a wide range of partners drives its adoption across multiple industries.
The structure of 2-Ethenylpyridine empowers scientists to follow different branches of investigation. Its vinyl group unlocks pathways for addition polymerization, leading to specialty plastics and resins. And its pyridine core often enables strong interactions with metals and other chemicals. By combining these properties, 2-Ethenylpyridine opens the door to custom materials with features not easily found in commodity chemicals.
On the bench, the pure liquid shines with its pungent smell and characteristic appearance. Chemists assess purity with gas chromatography or NMR, looking for clear signals that tell them the main chemical sits unaccompanied by leftover reactants. Over time, suppliers settled on reliable ways to produce batches with high purity, which is critical for laboratory and industrial projects.
Molecularly, 2-Ethenylpyridine carries the formula C7H7N. Its boiling point rests near 157°C, letting users handle it with common glassware and equipment. The material resists water but mixes rapidly with most polar organic solvents. Unlike some pyridine derivatives that carry extra functional groups or substitution patterns, the vinyl group at the second position on the ring makes it behave quite differently from its cousins in both reactivity and downstream application.
Not all pyridine compounds perform the same job. Many fill niche roles as pharmaceuticals or intermediates, but few balance reactivity and selectivity like 2-Ethenylpyridine. The molecule’s structure encourages quick and reliable polymerization once given the right catalyst or initiator. Chemists like having this flexibility in their toolbox. For those working on new copolymers, 2-Ethenylpyridine often becomes the go-to monomer when another chemistry fails.
Other pyridines tend to resist copolymerization or encourage undesirable side reactions. The vinyl group, linked directly to the aromatic ring, smooths the entire chain-building process. Scientists interested in functional coatings, adhesives, and advanced resins find that this compound uniquely bridges the gap between cost-effectiveness and high performance.
The differences with similar products stand out most when work demands both reactivity and aromatic stability. For example, vinylbenzene (styrene) carries a similar vinyl motif but lacks the electron-donating or -withdrawing effects of pyridine’s nitrogen. In practice, this changes the resulting polymers’ behavior significantly—improving solubility profiles and coordination chemistry.
My early encounters with 2-Ethenylpyridine came in university, where researchers tried to fine-tune the coordination between organic monomers and transition metals. In some cases, they needed a backbone for cross-linked networks; in others, a discrete ligand for catalytic complexes. The compound’s dual nature—highly reactive double bond and lone-pair nitrogen—answered questions better than most pyridine derivatives or vinyl compounds.
These days, producers deploy it for more than academic curiosities. A variety of manufacturing operations see the benefit in its combination of rapid polymerization and metal-binding. High-value adhesives owe their unique properties to it. Analytical chemists use it to modify silica surfaces on chromatography columns, allowing for strong retention of target analytes. Specialty coatings that resist harsh environments or adhere to metals often draw their strength from this single molecule.
Researchers lean on 2-Ethenylpyridine when standard vinyl monomers fall short. In copolymer projects aiming for custom ion-exchange resins, the nitrogen in the pyridine ring lets the resulting materials coordinate with transition metals or serve as proton acceptors. This trick delivers separation membranes that filter out unwanted ions or catalyze reactions in water purification systems. The medical device industry, too, sees its benefit in applications needing selective ion binding and chemical resistance.
When launched into radical polymerization, 2-Ethenylpyridine participates with other monomers like acrylonitrile or methyl methacrylate. The resulting copolymers can show enhanced chemical stability, resistance to solvents, and sometimes antimicrobial effects due to the nature of the pyridine ring. In industrial settings, these traits deliver coatings that stand up to harsh solvents or temperature swings. Over years of following conferences and literature, I’ve seen teams share case after case where this compound outperforms more common monomers.
Scientists love 2-Ethenylpyridine for catalyst development. The nitrogen atom not only binds to metals but can modulate electron density, tuning the performance of catalytic centers. In organometallic complexes, it acts as a strong ligand, supporting metals like palladium or platinum. Many published papers detail how researchers use this property to create more selective, active, or robust catalysts for hydrogenation, cross-coupling, or polymerization reactions.
Sometimes the molecule’s story runs through electronics or advanced analytical tools. Used as a building block in conducting polymers, 2-Ethenylpyridine can become part of materials that transport charge efficiently while withstanding chemical degradation. Electrochemists use it to create surfaces that facilitate electron transfer between electrodes and electrolytes. Instruments like high-performance liquid chromatography columns gain selectivity when surface-bound with this compound.
Trained operators working with 2-Ethenylpyridine need straightforward handling and consistent quality. Liquid form allows for easy metering and mixing in production-scale processes. Because purity and low water content influence how polymers or catalysts perform, trusted suppliers focus on tight controls during storage and shipment.
Many feedback cycles from chemical manufacturers led to formulation tweaks that reduced odor, minimized impurities, and eliminated exposure risks where possible. Workers find onboarding easier compared to unfamiliar specialty chemicals. That’s worth attention for any operation balancing new chemistry with established workflows.
Anyone familiar with aromatic amines or pyridine-based chemicals knows sharp odors and health hazards can be a concern. 2-Ethenylpyridine is no exception, so responsible practices matter. Labs and plants rely on enclosed handling, fume hoods, and splash protection. I’ve seen companies mandate real-time air monitoring where exposure risks could arise. Although acute toxicity stays low compared to some alternatives, no one ignores proper ventilation and spill response.
Waste management policies usually treat the material and its polymers as non-hazardous once fully reacted, yet unreacted monomer gets the same respect as other vinyl chemicals. Manufacturers often offer reconditioning options to minimize leftover waste. Chemical stewardship encourages recycling containers and tracking usage to avoid leaks or environmental release.
Product development managers and supply chain specialists talk frequently about “fit for purpose” chemicals. 2-Ethenylpyridine remains relevant because it adapts to the changing demands of industry—from small batch research to consistent, high-volume manufacturing. While dozens of monomers arrive and disappear in trend cycles, this one finds repeat business through proven versatility. As end-use markets for electronics, specialty polymers, and analytical instruments grow, it continues claiming a spot on procurement lists.
Despite supply chain fluctuations, confidence in sourcing this specialty chemical stays high. Strong supplier relationships and predictable shipment windows help keep projects on schedule. I’ve heard purchasing teams highlight fewer quality rejections and more batch-to-batch consistency when compared to lesser-known alternatives.
Chemical producers face tighter rules and rising expectations for environmental stewardship. 2-Ethenylpyridine’s downstream uses—especially in membranes or catalysts—often support greener processing by reducing waste or improving energy efficiency. High-performance membranes filter brackish water or remove heavy metals with less chemical input. Advances in catalyst design using this compound allow for lower reaction temperatures, saving energy on a plant-wide scale.
Reducing environmental risk largely depends on responsible shipment and storage. Drum and tote designs resist leaks and make containment easier. Some manufacturers now offer reclaimed or recycled-grade material, targeting non-critical uses where ultra-high purity won’t affect performance.
Sustainability teams in large companies push for traceable sourcing and greener manufacturing processes. Some chemical plants switch solvents or energy sources, shrinking overall carbon footprint for intermediates like 2-Ethenylpyridine. Ongoing academic collaborations search for routes from renewable feedstocks, though commercial scale remains on the horizon.
As older chemists retire, experience with specialty aromatic vinyl compounds passes on through mentoring and documentation. I have seen how hands-on training in safe handling and proper use matters just as much as datasheets or regulatory summaries. Site visits and operator shadowing help younger technicians pick up practical knowledge that textbooks miss.
Workshops at industry conferences often include practical demonstrations focused on materials like 2-Ethenylpyridine. By connecting plant engineers and lab scientists, these gatherings build networks that keep best practices alive. As demand moves into new markets—think flexible electronics or smart filtration—new generations will define how and where the molecule creates value.
Development teams use 2-Ethenylpyridine as a starting point for hybrid materials with unique optical, electrical, or chemical resilience. Research on copolymer blends points to improved compatibility with nanomaterials, including graphene or carbon nanotubes. Results include lighter, stronger composite structures for aerospace and automotive applications.
Surface science groups investigate how variations in polymer structure can resist biofouling or support advanced sensor designs. Analytical labs benefit from more precise separations, especially in environmental and pharmaceutical contexts. Each breakthrough builds on years of experience and trust in predictable chemistry.
Workshops and publications from professional societies continue to refine handling techniques for chemicals like 2-Ethenylpyridine. Instead of just reading about protective gear, chemists and technicians now share real accident reports and near-misses to improve collective safety. Safety data sheets form a foundation, yet most experienced hands know the on-the-ground reality includes frequent training, labeled storage, and careful decanting procedures.
For transportation and distribution, qualified carriers reduce the risk of spills, keeping product sealed up from production to customer site. Modern tracking systems let buyers see where shipments are, lowering the risk of loss or contamination. Manufacturers keep close watch on product freshness, marking production dates so that degraded material stays out of the lab or plant.
In my experience, those teams who integrate safety best practices from the ground up rarely see product-related slowdowns or incidents. Consistent training and clear communication protect both people and project timelines.
Buyers sometimes wonder why not just use a cheaper monomer, like styrene or vinyl toluene. The answer lies in the advanced performance possible when switching to 2-Ethenylpyridine. The pyridine ring brings binding sites for transition metals or acids that common vinyl monomers simply don’t have. For projects where binding ability and reactivity must coexist, the extra cost per kilogram routinely pays back in reliability and longevity.
Chemists who evaluate alternatives often come back around to 2-Ethenylpyridine after seeing poor reactivity or chemical resistance with less sophisticated options. Over numerous case studies, the compound shows tight polymer control with fewer side reactions and cleaner product profiles.
Vinylpyridine isomers with substitution at the third or fourth positions shift electronic environments enough to change both reactivity and downstream utility. The second position delivers more predictable polymerization and better functional group accessibility for post-reaction modification.
Beyond established recipes, 2-Ethenylpyridine keeps showing up in ground-breaking patents and experimental projects. Its chemical features spark ideas for new adhesives, resins, and functional coatings. One colleague spent months tuning a photoresist for semiconductor production, and only found repeatable performance after introducing this monomer to balance mechanical strength and chemical development rate.
Academic consortia investigating water purification or controlled-release drugs use it to introduce heterocyclic sites into crosslinked networks. By combining these new properties with scalable production, both startups and established firms see it as a way to bridge the gap between research and marketable products.
Consistent delivery, technical advice, and transparent purity documentation keep 2-Ethenylpyridine a staple among specialty chemicals. Over years, users build trust in suppliers whose products show lot-to-lot repeatability and strong technical support. Early problems—like odor complaints or inconsistent purity—get resolved as suppliers invest in better purification and quality checks.
For researchers or production managers, confidence in the supply chain makes a big difference. Delays and bottlenecks often signal the need for deeper vendor relationships. Product support teams answer technical questions or troubleshoot unexpected results, helping teams reach their targets.
Despite its value, challenges remain. The raw material must avoid contamination for use in high-purity applications, and producers watch for subtle shifts in impurity profiles. As regulations evolve, producers adjust labeling, transport certification, and in some regions, tracking of end-use markets. Customers share feedback about delivery speeds and packaging durability, shaping further improvements in supply chains.
As climate and sustainability pressures rise, companies test out renewable synthesis routes and lower-impact solvents. Academic partnerships aim to discover next-generation derivatives that build on the molecule’s strengths while lowering overall environmental impact. With each year, the field moves closer to scalable, sustainable production models that serve both current markets and new opportunities.
My direct experience with 2-Ethenylpyridine tells me that enduring value grows from a track record of performance and adaptability. The bridge it forms between classic reactive vinyl compounds and functional heterocycles remains unmatched in many advanced applications. Industry keeps finding creative uses—from high-performing polymers to cutting-edge sensing platforms. With careful handling, strong technical support, and a focus on quality, this specialty chemical should remain a valued resource across research, development, and production for years ahead.