|
HS Code |
914230 |
| Chemical Name | 2-Benzylpyridine |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.22 g/mol |
| Cas Number | 6937-35-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 292 °C |
| Density | 1.057 g/cm³ |
| Refractive Index | 1.615 |
| Flash Point | 141 °C |
| Solubility In Water | Insoluble |
| Smiles | c1ccc(cc1)Cc2ccccn2 |
As an accredited 2-Benzylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-Benzylpyridine, 100g," with chemical details, hazard symbols, batch number, and manufacturer's logo. |
| Container Loading (20′ FCL) | 2-Benzylpyridine is typically shipped in 20′ FCL containers, securely packed in sealed drums or IBCs, ensuring safe bulk transport. |
| Shipping | 2-Benzylpyridine is shipped in tightly sealed containers, typically made of glass or chemical-resistant plastic, to prevent leakage and contamination. Packaging follows international regulations for hazardous chemicals, ensuring protection from light, moisture, and physical damage. Proper labeling with hazard warnings is included, and transport is conducted via certified carriers specializing in chemical logistics. |
| Storage | 2-Benzylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition or direct sunlight. It should be kept separately from incompatible substances such as strong oxidizing agents. Store at room temperature and ensure proper labeling. Use secondary containment to prevent leaks or spills and minimize exposure to moisture. |
| Shelf Life | 2-Benzylpyridine has a shelf life of 2-3 years when stored in a cool, dry place, tightly sealed, and protected from light. |
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Purity 98%: 2-Benzylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high substrate specificity and product yield are achieved. Molecular weight 183.25 g/mol: 2-Benzylpyridine of molecular weight 183.25 g/mol is used in heterocyclic compound research, where precise stoichiometric calculations enable consistent reaction scalability. Melting point 34-36°C: 2-Benzylpyridine with melting point 34-36°C is used in organic synthesis reactions, where ease of handling and reproducible solid phase properties are ensured. Solubility in ethanol: 2-Benzylpyridine with high solubility in ethanol is used in solution-phase catalyst testing, where homogeneous mixture formation increases catalytic efficiency. Stability at 25°C: 2-Benzylpyridine stable at 25°C is employed in chemical storage systems, where long-term compound integrity and reduced degradation are maintained. Impurity ≤0.2%: 2-Benzylpyridine with maximum impurity of 0.2% is used in analytical standards preparation, where accurate quantification and reproducibility are required. Boiling point 285°C: 2-Benzylpyridine with boiling point 285°C is used in high-temperature organic transformations, where thermal resilience and reaction completeness are achieved. Density 1.08 g/cm³: 2-Benzylpyridine with density 1.08 g/cm³ is used in material compatibility assessments, where predictable phase behavior and miscibility are established. |
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For many years, 2-Benzylpyridine has held a steady place in the toolkit of both researchers and professionals working with fine chemicals. It’s a compound that connects academic labs and industrial production floors, showing up in countless syntheses thanks to its unique structure. The molecule consists of a benzyl group attached to the second position of a pyridine ring, giving it a particular set of properties that set it apart from similar pyridine derivatives.
My introduction to 2-Benzylpyridine came early in my career. I remember mixing reagents for a synthetic route targeting a more complex nitrogen-containing compound. Among the bottle labels, 2-Benzylpyridine carried a weight of familiarity. This compound is not a household name, but walk into any synthetic organic lab, and it’s likely you’ll spot it on the shelf. Over the years, its use has expanded, reflecting the evolving needs of research and production.
Chemists care a lot about molecular structure. The benzyl group attached to the pyridine ring at the 2-position creates a specific electron environment, which changes how the molecule participates in reactions compared to its close relatives like 3- or 4-benzylpyridine. In practice, this means pathways for synthesis can be more selective, and certain side reactions occur with less frequency.
The specifications most often discussed revolve around its purity and physical state. In my experience, high-purity 2-Benzylpyridine arrives as a clear, almost colorless to pale yellow liquid, free of the kind of haze or particulate matter that sometimes plagues similar chemicals. Consistency matters more than people often admit. Impurities complicate workups, especially when downstream reactions rely on the reactivity of that nitrogen atom in the pyridine.
Most suppliers offer it at technical grade or higher, with purity levels usually above 98 percent. That extra fraction of a percent in purity can mean fewer headaches during final product isolation. Heavy users—think large-scale pharmaceutical firms—often source from companies that guarantee batch-to-batch reliability. On a smaller scale, grad students and postdocs in synthetic labs tend to appreciate a fresh, well-sealed bottle that behaves as promised, especially when deadlines approach.
It serves as both a building block and a research tool. In organic synthesis, 2-Benzylpyridine works as a starting material for rings, chains, and other aromatic compounds. Medicinal chemists have put it to use in the early stages of discovering molecules with activity against particular targets. Its structure lends itself to straightforward modifications; you can easily add different groups to the benzyl position, or make changes to the pyridine ring itself.
From my own bench work, I saw it turn up most frequently during alkylation reactions. The pyridine nitrogen’s electron-withdrawing properties influence reactivity, making substitution at adjacent positions both more predictable and efficient. Colleagues working in material science once used 2-Benzylpyridine as a ligand in transition metal complexes. They told me the compound helped provide the right balance of stability and reactivity for their catalysts.
Outside of cutting-edge research, 2-Benzylpyridine shows up in the real world, too. It has played a quiet role in manufacturing intermediates for agrochemicals and pharmaceuticals. Even in chemical education, it's valued because students can explore a variety of synthetic techniques using this straightforward starting point.
Ask anyone who synthesizes organic chemicals: impurities and storage conditions take center stage in day-to-day lab life. 2-Benzylpyridine benefits from a degree of shelf stability, especially when kept in a cool, dry environment, well-sealed away from air and light. In less-than-ideal storage, though, it can develop a faint yellow tint and an off-smell, signaling the breakdown of the aromatic system or slow oxidation.
Mistakes made handling or storing 2-Benzylpyridine tend to echo down the line. In the throes of a new project, no one wants to discover by thin-layer chromatography that an impurity has traveled through every stage, all because the original bottle picked up water or dust. For anyone scaling up production, these small details grow in importance, since deviations from the expected result can add cost and burn valuable time.
If you compare 2-Benzylpyridine to other pyridine derivatives, the differences often show up during reactions involving metal catalysts or electrophilic aromatic substitution. The benzyl group offers a convenient handle for further transformation, a feature not present in, say, plain pyridine or methyl-substituted versions. For those working on complex molecule construction, this flexibility often outweighs any added cost.
Global supply networks for fine chemicals aren’t as seamless as they seem from the outside. A single hiccup—a batch that falls out of spec, a shipment delayed by customs, a new regulatory challenge in a producing country—can impact dozens of projects. For specialty chemicals like 2-Benzylpyridine, chemists don’t always have the luxury of swapping in an alternative without cutting corners.
Reliable supply depends on both scale and reputation. Those working in commercial synthesis, whether for active pharmaceutical ingredients or critical intermediates, often contract with suppliers known for transparency. Trusted vendors routinely provide analytical data—high-performance liquid chromatography traces, nuclear magnetic resonance spectra—so users can judge for themselves if the sample meets their needs.
Transparency works both ways. Feedback from end-users floats back to suppliers. If a particular lot of 2-Benzylpyridine leads to failed syntheses, the word spreads quickly, and companies feel the pressure to track down the cause. I’ve watched suppliers respond by tweaking purification steps or improving packaging, often in direct response to complaints from the scientific community.
No discussion of fine chemicals is complete without weighing safety and environmental impact. 2-Benzylpyridine, like most pyridine compounds, carries risks. It should be handled with gloves and eye protection, in a fume hood if possible, given its potential for skin and respiratory irritation. Most labs keep detailed safety data sheets at hand and train new hires to treat even familiar bottles with care.
Waste management enters the conversation quickly in any lab that cares about its footprint. Proper disposal satisfies regulatory requirements but also reflects a deeper commitment to community safety. Where possible, responsible users batch waste for collection rather than pouring it down the drain, keeping solvents and pyridines out of the water supply.
The latest trends in green chemistry encourage researchers to minimize waste and avoid hazardous reagents when better options exist. Some newer protocols even use catalytic amounts of 2-Benzylpyridine, reclaiming and reusing what would have been discarded in decades past. The future points to more sustainable synthesis, with a close focus on both human safety and the broader environment.
Not every pyridine looks or works the same. 2-Benzylpyridine distinguishes itself from its relatives because the benzyl group at the second position creates both a unique chemical reactivity and a handle for synthetic modification. Compare it to unsubstituted pyridine, and the differences become clear during any experiment using nucleophilic aromatic substitution. The benzyl group shifts electronic density across the ring and can direct incoming groups to preferred sites.
3-Benzylpyridine or 4-Benzylpyridine have their own uses, often less suited for site-selective chemistry. Substitution at the 2-position typically offers more versatility, which explains its preference among those who design intricate, multi-step syntheses. Even methyl- or ethyl-substituted pyridines lack the same degree of functionalization potential.
Straightforward syntheses often favor more reactive or volatile pyridines. But for those stepwise approaches aiming at tailor-made molecules—especially ones destined for pharmaceutical products—having a benzyl group ready for simple further modification makes 2-Benzylpyridine a logical first choice.
Every so often a new study or application places 2-Benzylpyridine in an unexpected spotlight. Recently, I came across a publication exploring its role in designing ligands for metal-catalyzed cross-coupling reactions, where the positioning of the benzyl group changed the selectivity of C–H activation. These kinds of incremental advances reveal how established chemicals find new purpose as understanding deepens.
Within pharmaceutical R&D labs, 2-Benzylpyridine’s profile aligns with current efforts to construct libraries of molecules targeting everything from cancer cells to novel antibiotics. Speed remains a priority, but reliable starting materials count for just as much as fast-moving automation platforms and algorithms. Experienced chemists rely on a handful of go-to intermediates, and this compound sits near the top of many lists.
Changing environmental regulations and growing pressure to minimize resource use have also influenced how 2-Benzylpyridine is sourced and employed. Manufacturers take these cues seriously; several now embrace lower-impact synthetic routes for its production, cutting down on hazardous byproducts and using renewable feedstocks where possible. This push echoes broader shifts in the chemical industry, where profit and stewardship increasingly go hand in hand.
Trust forms the backbone of good science. No one wants to gamble their thesis or a million-dollar production run on inconsistent chemicals. That’s why analysis at every stage matters. For 2-Benzylpyridine, suppliers usually back up shipments with detailed certificates of analysis. These documents include results from gas chromatography and mass spectrometry, confirming both identity and purity.
I recall a case where a colleague’s final product kept showing impurities no one could account for. After weeks retracing every step, the culprit turned out to be a degraded bottle of 2-Benzylpyridine. Testing revealed oxidation products that subtly shifted the properties of downstream materials. The lesson stuck with everyone in the lab: quality in, quality out.
Some experienced chemists run their own checks, especially when embarking on a sensitive synthesis. A quick NMR or GC analysis offers peace of mind. In high-stakes pharmaceutical development, every reagent gets this scrutiny. Small investments in testing up front shield teams from bigger losses later, whether measured in wasted time or regulatory setbacks.
Seasoned professors often use 2-Benzylpyridine as a teaching tool. The molecule’s structure encourages conversations about aromaticity, functional group reactivity, and synthetic design—core concepts for any aspiring organic chemist. Undergraduate labs introduce students to hands-on techniques using chemicals like this, making abstract textbook principles concrete.
As students learn to weigh, mix, and react real compounds, they gain an appreciation for both the opportunities and headaches that face professional chemists every day. Small mishaps—an evaporated solvent, a mixed-up label, a slightly off color—help instill the habits and caution that serve them well later. Teachers, for their part, value reliable access to high-quality starting materials so students get consistent, instructive results.
Scientists share their findings widely at conferences, in group meetings, and through publications. Details about the quirks of 2-Benzylpyridine—what works, what doesn’t, ways to purify a stubbornly impure batch—make the rounds just as quickly as grand discoveries. This culture of sharing underpins steady progress, transforming scattered anecdotes into a body of working knowledge.
As fields such as medicinal chemistry and materials science push the boundaries of what can be built in a laboratory, chemicals like 2-Benzylpyridine stand in the background. They seldom make headlines but enable much of the innovation we rely on for new products, smarter drugs, and better materials.
Balancing access with responsibility falls to both suppliers and users. Companies providing reliable, ethically sourced 2-Benzylpyridine play a part in making cutting-edge research possible. Scientists in labs, from graduate students to senior researchers, hold an equal share of responsibility in using and disposing of it safely.
As the chemical market responds to concerns around transparency and sustainability, expect continued evolution in sourcing, manufacturing practices, packaging, and supply chain management. The days of anonymous brown bottles with minimal information are giving way to a more open, connected era. Certificates of analysis, QR-coded tracking, and real-time updates from vendors build trust and streamline everyday lab tasks.
Demand for flexibility and reliability hasn’t faded; if anything, it has become more intense as labs strive to do more with fewer resources. 2-Benzylpyridine remains a mainstay for those looking to build complex molecules from stable, proven blocks.
Efforts to develop greener, safer production methods will likely continue, offering new routes forward that don’t sacrifice quality or performance. In practice, these improvements take time to scale up, calling for close collaboration across industry and academia.
Lessons gathered over decades—about the importance of purity, the pitfalls of hasty storage, the benefits of open knowledge sharing—will carry into future generations of chemists. The humble bottle of 2-Benzylpyridine sitting on a dusty shelf serves as a quiet reminder of both the progress already made and the work still ahead.