|
HS Code |
777836 |
| Chemical Name | 2-Vinylpyridine |
| Cas Number | 100-69-6 |
| Molecular Formula | C7H7N |
| Molecular Weight | 105.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 159-161°C |
| Density | 0.978 g/mL at 25°C |
| Flash Point | 51°C (closed cup) |
| Solubility | Slightly soluble in water; soluble in most organic solvents |
| Refractive Index | 1.587-1.589 (20°C) |
| Melting Point | -53°C |
| Odor | Aminic, unpleasant |
| Iupac Name | 1-ethenylpyridine |
As an accredited 2-vinylpyridine monomer factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-vinylpyridine monomer is packaged in a 500 mL amber glass bottle with a secure cap, labeled with safety and hazard information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2-vinylpyridine monomer is typically loaded in 160 x 200kg steel drums per 20-foot full container load (FCL). |
| Shipping | 2-Vinylpyridine monomer must be shipped in tightly sealed containers, protected from light, heat, and moisture. It is typically transported as a hazardous material under UN 3077 (environmentally hazardous substance, solid, n.o.s.). The chemical should be handled with appropriate labeling and documentation, in compliance with local and international shipping regulations. |
| Storage | 2-vinylpyridine monomer should be stored in a tightly sealed container under a nitrogen or inert gas atmosphere, in a cool, dry, and well-ventilated area away from sources of ignition. Protect from direct sunlight and moisture. Storage temperature should be below 4°C to prevent unwanted polymerization. Keep away from oxidizing agents, acids, and heat sources. |
| Shelf Life | 2-Vinylpyridine monomer typically has a shelf life of 6–12 months when stored sealed, cool (≤30°C), and protected from light. |
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Purity 99%: 2-vinylpyridine monomer with purity 99% is used in polymer synthesis for ion-exchange resins, where high purity ensures consistent polymer chain formation and superior ion-exchange capacity. Molecular Weight 105.14 g/mol: 2-vinylpyridine monomer with molecular weight 105.14 g/mol is used in specialty copolymer manufacturing, where precise molecular weight contributes to predictable mechanical and thermal properties. Stability Temperature 40°C: 2-vinylpyridine monomer at stability temperature 40°C is used in latex formulation for adhesives, where thermal stability allows safe processing and storage without premature polymerization. Viscosity 1.1 mPa·s: 2-vinylpyridine monomer with viscosity 1.1 mPa·s is used in emulsion polymerization systems, where low viscosity facilitates optimal mixing and uniform particle size distribution. Melting Point -32°C: 2-vinylpyridine monomer with melting point -32°C is used in low-temperature processable coatings, where the low melting point enables efficient incorporation into cold-processable formulations. Inhibitor Content 100 ppm MEHQ: 2-vinylpyridine monomer containing 100 ppm MEHQ inhibitor is used in transport and bulk storage applications, where stabilized monomer prevents unwanted polymerization during handling. |
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2-Vinylpyridine monomer attracts attention in the world of specialty chemicals because of what it brings to the table for both industrial manufacturing and research labs. The structure—built on a pyridine ring with a vinyl group at the 2-position—allows for a remarkable blend of reactivity and stability, making it a go-to choice for those developing new functional polymers or resins. The purity of this monomer can drive performance, especially in precision applications, such as specialty adhesives, latex processes, or ion-exchange polymers.
Most practitioners in chemical development see the value in liquids with clear, pale-yellow characteristics and minimal moisture. The absence of excessive impurity content, such as unwanted nitrogen bases or peroxides, can make all the difference during sensitive polymerizations. That touch of attention to how the raw material arrives in the lab counts; it sets up everything down the line, from reaction control to final product consistency.
Hands-on experience with 2-vinylpyridine often reveals how even small tweaks in raw materials show up as measurable differences in the end product. Unlike some other vinyl derivatives—think about styrene or methyl methacrylate, both popular in their own right—2-vinylpyridine delivers a unique combination of chemical reactivity and compatibility with polar and ionic monomers. That basic nitrogen atom on the pyridine ring stands ready to coordinate or interact with acidic or electrophilic species, introducing options others do not offer. The difference comes through clearly in real-world applications—latexes or copolymers built on this platform often display better dye uptake, improved adhesion on polar surfaces, and resistance to chemical aging, down to the backbone.
Plenty of chemists find that working with 2-vinylpyridine provides more than just another route to backbone modification. The presence of the pyridine nitrogen creates sites for further functionalization, post-polymerization modifications, and the formation of complex architectures via controlled radical polymerization. Compare that with a standard vinyl monomer, and the leap in versatility seems pretty obvious. It’s not about redundancy; it’s about opening up routes that simply aren’t possible with simple hydrocarbons or oxygenated vinyl monomers.
Many industrial chemists have tested 2-vinylpyridine in the field of specialty latexes, aiming for coatings and adhesives that need to stick well and hold up under stress. High-performance adhesive formulations often benefit when a portion of the copolymer includes this monomer. Think about structural adhesives for metal–rubber bonding. The lone pair on the nitrogen atom in the pyridine moiety forms coordinative bonds with metal surfaces, so you’re not just relying on mechanical adhesion. Real-world results matter, especially in footwear, automotive, or aerospace assemblies, where failure in bonding leads to direct losses.
Other colleagues have told stories of using this monomer to develop ion-exchange resins suited for water treatment and purification. The nitrogen atom can be protonated, leading to polymers with adjustable basicity. I’ve worked on similar projects in the past, and every time, being able to fine-tune the ion-exchange properties lets you target contaminant profiles that just aren’t reachable with less versatile monomers. Even specialty chromatography, a niche but important field, uses these monomers to create selective interaction sites that grab onto specific molecules, making separations sharper and more reproducible.
Academic labs still find value in 2-vinylpyridine for model studies of living and controlled radical polymerizations. The electron-rich vinylpyridine unit remains more reactive toward common initiators compared to many other vinyl monomers, supporting better incorporation into growing polymer chains under mild conditions. In my own studies, including exploratory block copolymer work, the high reactivity and clean, single-point attachment enabled new architectures that were tough to reach using less functionalized monomers.
Direct experience has shown purity often matters as much as reactivity, especially when scaling up. Most research-grade 2-vinylpyridine comes as a liquid with low water content, minimum levels of stabilizer (like hydroquinone or similar inhibitors), and low traces of pyridine. The color is usually a clear, pale yellow, but color alone only tells part of the story. The key factor is absence of residual precursors, which can poison reaction catalysts or compete in uncontrolled side reactions. Chemical producers typically supply technical data—not for the sake of red tape, but because every fractional percentage of impurity can influence how the chemistry plays out at scale.
Packaging also turns out to make a difference. Small-volume research use prefers glass sealed under inert gas, while industrial customers order in larger, stainless steel drums lined to prevent exposure to light and air. From personal observation, nothing sinks a project faster than an unreliable supply or a batch that arrived having started to polymerize before you even open the lid—stabilization and careful logistics are part of the equation, even if they don’t turn up on most product spec sheets.
2-vinylpyridine fills a gap between low-reactivity monomers and highly functionalized specialty compounds. It lets formulation chemists design tailored polymers and copolymers with basic sites that interact strongly with acids, transition metals, or even simple polar solvents. Water treatment, fuel cell membranes, sensor technology, and controlled drug release all draw value from this functionality.
In my own years of working with specialty polymers, I’ve tried to build both high-adhesion and highly-functional materials for demanding customer specs. Having access to pyridine-based monomers like this one gives options that aren’t available with simple hydrocarbon-based vinyls. Adding just a few percent by weight to a polymer backbone can double the strength of adhesion to metal surfaces, even in humid or salt-rich environments. There aren’t many alternative ways to get that blend of adhesion and chemical resilience.
Comparing 2-vinylpyridine with its close cousin, 4-vinylpyridine, might seem like splitting hairs. The position of the vinyl group affects reactivity and the final polymer’s physical properties. In practice, the ortho position of the vinyl group in 2-vinylpyridine leads to copolymers with higher polarity and, in some cases, steric constraints that favor certain block copolymer architectures. That translates to better selectivity in applications where fine-tuning polymer microstructure is critical, such as stimuli-responsive hydrogels or block copolymer micelles for targeted drug delivery.
Compared to neutral monomers like acrylates or methacrylates, 2-vinylpyridine stands out for its basic nitrogen site. This property makes it suitable for applications that would be impossible with non-ionic monomers. For instance, in pH-sensitive coatings or dispersions, the presence of basic sites allows for response to environmental changes, which can be harnessed in sensor development, smart packaging, or controlled-release capsules. Neutral vinyl monomers just don’t offer that level of adaptability.
Environmental chemists face a changing regulatory reality. Pyridine-based monomers offer targeted reactivity, reducing waste by giving more precision in synthesis. This means fewer side products and safer, more predictable reaction outcomes. Synthetic flexibility also supports green chemistry initiatives. Reactions that would otherwise require post-polymerization functionalization can happen in one step with 2-vinylpyridine, saving time, energy, and raw materials.
Despite the performance benefits, working with this monomer introduces some challenges. It’s classified as a hazardous material: it can be irritating to skin and mucous membranes and needs both careful handling and storage to avoid accidental polymerization or exposure. In scale-up, the monomer may form peroxides over time, which requires regular monitoring during long-term storage. In the lab, I’ve observed some small-scale polymerizations exhibit unpredictable induction periods unless inhibitor levels and thermal history are properly managed.
Industrial users face supply-chain pressures. As global demand for specialty monomers rises, sourcing high-purity material calls for trusted suppliers and predictable logistics. I have been part of projects that foundered due to delays in monomer delivery or unexpected substitutions with lower-purity alternatives, which rippled all the way to product certification failures and contract breaches. The lesson—never assume monomer quality is a given, even if the paperwork looks right. Testing on receipt saves headaches down the line.
Cost also comes up in every conversation. Since pyridine derivatives result from multi-step syntheses and require careful purification, the price per kilogram climbs compared to basic monomers. Many product developers face tough choices balancing performance gains with budget realities. Pilot trials often drive home these points, since the real savings rarely come in the first few batches. When product margins are slim, sometimes the decision goes to alternative materials, though at the price of lost functionality.
Great results often depend on informed handling and a bit of creative process design. Chemists new to 2-vinylpyridine benefit from solid training on material hazards and reactivity. Basic protective measures—chemical-resistant gloves, face shielding, workspaces with local exhaust—go a long way, and regular review of material safety protocols keeps things running smoothly. For most labs, good storage—low light, consistent low temperatures, airtight sealed vessels—blunts the risk of premature polymerization.
On the technical side, recipe design should account for the nitrogen functionality. Choosing comonomers that complement the basicity of 2-vinylpyridine, such as carboxylic acids or other electron-deficient partners, can maximize both yield and property development. Scale-up trials benefit from incremental batch size increases and close monitoring of both process variables and end-of-batch impurity profiles. Automation and in-line monitoring tools give operators the real-time data they need to tweak conditions before issues magnify.
From a strategic point of view, sourcing from reputable producers—companies with a strong track record in both quality and service—brings long-term savings. Upfront savings driven by off-brand material rarely compensate for downstream troubleshooting or rejected lots. Long-term framework agreements and advance orders help avoid last-minute shortages, a factor I’ve found critical in project timelines where every week counts.
Sustainability considerations increasingly drive material selection. 2-vinylpyridine’s unique functionality makes it possible to develop recyclable or reprocessible polymers, thanks to the ability to chemically “unlock” or modify attached pyridine groups. For coatings or membranes designed with end-of-life in mind, developers can take advantage of the monomer’s reactivity to design deconstruction pathways. In some specialty ion-exchange beads, it’s now possible to recover and regenerate the active material multiple times, a feature that was not feasible with earlier generations of neutral vinyl polymers.
Regulators and certification bodies now push for more data on life cycle assessments, workplace exposure, and emissions. 2-vinylpyridine users address these requirements by investing in closed-system transfer, solvent recycling, and by-product management. Deliberate process engineering goes beyond compliance—it opens up cost savings and makes the process friendlier both to people and the planet. I’ve seen R&D labs shift toward water-based processes, using 2-vinylpyridine in emulsion copolymerizations, reducing the reliance on organic solvents and aligning better with regulatory goals.
The pace of innovation continues to accelerate. Polymer scientists look for monomer backbones that support advanced electronics, specialty membranes for lithium-ion batteries, or biocompatible surfaces. The basic structure of 2-vinylpyridine lets researchers develop next-generation materials, such as conductive composites or nanostructured coatings that respond to environmental triggers.
Ongoing research focuses on copolymerizing 2-vinylpyridine with bio-derived monomers or renewable feedstocks, aiming to build high-performance materials with a smaller carbon footprint. Some labs have successfully integrated this monomer with sugar-based macromolecules, opening up biodegradable or compostable functional materials designed for specialty packaging or slow-release agricultural products.
Smart coatings, self-healing surfaces, and biomedical hydrogels draw on the capability of the pyridine ring to interact with living systems or catalytic sites. Enzyme immobilization or metal chelation relies on the predictable reactivity and spatial arrangement that only specific pyridine-based monomers can offer. For analysts working in these high-tech spaces, the choice often reduces to whether the available monomers can meet the requirements for tunable conductivity, hydrophilicity, and biocompatibility. As synthetic targets grow more demanding, researchers put their faith in building blocks that give both reactivity and adaptability.
People who order and use 2-vinylpyridine usually have a checklist in mind. Stability under storage, reliable supply, ease of purification, and proven results in both research and application count more than just reading through a chemical catalog. I’ve fielded questions ranging from “How sensitive is it to light?” to “Can I use this in medical-grade applications?” Each answer depends on the intended use, the conditions of handling, and the backup support for regulatory and quality documentation.
Some users shy away from pyridine-based monomers out of concern for odor, volatility, or toxicity. With improved packaging and better workplace ventilation, most of these worries shrink in day-to-day practice. Users find that following a clear set of precautions makes regular handling manageable, even for people new to working with specialty monomers. Many companies provide dedicated training or offer consultation for first-time users, encouraging safe and productive use in both R&D and full-scale manufacturing.
Long-term, customer feedback continues to shape which specifications and stabilization packages gain traction. Whether for adhesive performance, water purification, or high-value electronics, the ability to fine-tune polymer composition with 2-vinylpyridine’s functional group remains key. As expectations climb, so does the market for more reliable, higher purity, and more user-friendly material offerings.
In the chemistry community, those interested in new polymer architectures or performance improvements often turn to monomers like 2-vinylpyridine for fresh answers. Groups seeking to build the next generation of environmentally responsive materials or smart coatings know the importance of a monomer’s subtle qualities: the difference between experimental success and “back to the drawing board” can hinge on something as small as a low-level impurity or a missed handling step. Connections between research findings, practical processing, and safe, sustainable use drive both customer trust and industry progress.
Looking into the future, the chemistry underpinning 2-vinylpyridine positions it as more than a specialty item. As innovation marches on, the lessons drawn from hands-on use, careful handling, and a focus on precision will continue to guide its success in demanding and high-value fields. Whether in high-tech, environmental, or classic polymer chemistry, the path from molecule to market owes a good deal to the characteristics that make 2-vinylpyridine stand out among vinyl monomers.