|
HS Code |
690402 |
| Cas Number | 1126-20-9 |
| Molecular Formula | C9H13N |
| Molar Mass | 135.21 g/mol |
| Iupac Name | 3-butylpyridine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 207-210°C |
| Melting Point | -58°C |
| Density | 0.917 g/cm³ |
| Refractive Index | 1.507 |
| Flash Point | 88°C |
| Solubility In Water | Insoluble |
| Purity | Typically ≥ 98% |
| Smell | Aromatic, pyridine-like odor |
As an accredited 3-n-Butylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-n-Butylpyridine, 100 mL: Supplied in a sealed, amber glass bottle with secure screw cap and clear hazard labeling for safe laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-n-Butylpyridine: Typically packed in 200L drums, total capacity about 16–18 metric tons per container. |
| Shipping | 3-n-Butylpyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified under UN1993, Flammable liquid, requiring transport in accordance with regulations for hazardous chemicals. Appropriate hazard labeling and documentation must accompany the shipment to ensure safe handling and compliance with safety standards. |
| Storage | 3-n-Butylpyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure storage temperature is controlled, ideally at room temperature. Use appropriate chemical storage cabinets and label containers clearly to prevent accidental misuse or contamination. |
| Shelf Life | **Shelf Life of 3-n-Butylpyridine:** Typically stable for 2 years when stored in a cool, dry, tightly sealed container, away from light and moisture. |
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Purity 99%: 3-n-Butylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal byproduct formation. Density 0.90 g/cm³: 3-n-Butylpyridine with a density of 0.90 g/cm³ is used in catalyst system formulations, where precise blending improves reaction yield. Boiling Point 201°C: 3-n-Butylpyridine with a boiling point of 201°C is used in organic solvent extraction, where thermal stability allows for efficient solvent recovery. Molecular Weight 149.23 g/mol: 3-n-Butylpyridine with a molecular weight of 149.23 g/mol is used in heterocyclic compound manufacturing, where accurate dosing optimizes target compound synthesis. Stability Temperature up to 120°C: 3-n-Butylpyridine with stability temperature up to 120°C is used in high-temperature resin production, where it maintains chemical integrity during processing. Water Content ≤0.1%: 3-n-Butylpyridine with water content ≤0.1% is used in electronic chemical applications, where low moisture prevents corrosion and degradation. Refractive Index 1.494: 3-n-Butylpyridine with a refractive index of 1.494 is used in optical material development, where consistent optical properties enhance product performance. Melting Point -50°C: 3-n-Butylpyridine with a melting point of -50°C is used in low-temperature reaction media, where liquid-phase stability at subzero temperatures is required. |
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There is a reason chemists and manufacturers keep returning to 3-n-Butylpyridine. This compound might not shout for attention in a lineup of pyridines, yet it stands out on the lab bench and in industrial applications for simple, practical reasons. Not every chemical carries unique benefits that justify its place on a purchasing list. With 3-n-Butylpyridine, the difference is obvious to those who know what matters: consistent quality, reliable performance, and practical versatility.
In my years working with specialty chemicals, what sets a product apart goes beyond a mere list of numbers. Still, for those who like to check the basics, most 3-n-Butylpyridine products come as a clear, colorless-to-pale yellow liquid with a distinctive, somewhat fishy odor—no surprise to those familiar with pyridine derivatives. Boiling point generally hovers around 202-204°C, with a density near 0.92 g/cm³. Solubility varies: water won’t see much action, while organic solvents blend without issue. Purity typically exceeds 98 percent, offering security for those who need consistency across runs or batches.
Labs and factories alike see similar benefits. The chemical stability means that it rarely gets fussy in storage or handling, and I can recall only rare occasions when issues with decomposition cropped up, even in less-than-ideal storage conditions. That reliability takes precedence for anyone managing large inventories, where reactivity or degradation spell financial and logistical headaches.
Most chemists first bump into 3-n-Butylpyridine in organic synthesis. Its reputation as a versatile intermediate stems from the way it enables selective alkylation or forms stable complexes. I have seen it used effectively in the synthesis of advanced pharmaceutical ingredients and specialized catalysts, where the butyl group’s presence tweaks the reactivity of the pyridine ring in ways that open up new synthetic routes. Anyone troubleshooting a sticky pathway knows the relief that comes when an intermediate delivers results cleanly.
Beyond pharmaceuticals, 3-n-Butylpyridine finds its way into liquid crystals and advanced materials. Display manufacturers, for example, turn to such compounds not because they're trendy, but because they respond reliably to voltage and light, translating directly to sharper images or more efficient energy consumption. Electrochemistry also draws heavily from this molecule as an additive or solvent, especially in the development of redox flow batteries and ionic liquids. The stable electron density around the nitrogen atom, influenced by the n-butyl group, gives it a unique edge in these applied sciences.
I often think about the time a team struggled with sluggish reactivity in a step requiring selective nitrogen coordination. Switching to 3-n-Butylpyridine moved the project ahead—sometimes the right choice isn't the most obvious, but the one that simply works in the real world. This practicality plays out across industries. Agricultural research, which sometimes calls for subtle shifts in molecular structure to target specific pests or encourage growth, finds an ally in this compound. Its selectivity and adaptability offer solutions that plain pyridine or shorter-chain relatives tend not to deliver.
Anyone comparing pyridines by chain length, branching, or aromatic behavior knows they don't act the same. 3-n-Butylpyridine stands apart mainly because the n-butyl group attached at the 3-position nudges both physical and chemical properties. If you line up the lower-chain analogs—say, methyl or ethyl substitution—a chemist notes shifts in boiling point, solubility, even odor. What often matters more, though, is the subtle way this butyl group influences reactivity.
In catalysis, for instance, the extra carbon chain can provide both steric protection and increased electron-donating ability, compared to its shorter siblings. This alteration doesn't just show up in theory but translates to processes that simply run better—higher yields, greater selectivity, or easier purification at scale. Those small molecular tweaks provide the control needed for advanced synthesis, especially as molecular complexity grows. I’ve seen my share of disappointing results when using more common pyridines, only to see improvements by switching to this model.
Some researchers argue about two- or four-position substitution; in practice, the three-position n-butyl chain strikes a balance between manageable reactivity and tangible benefits to product performance. The longer chain avoids the volatility and handling issues common with lighter pyridine analogs. It also makes 3-n-Butylpyridine easier to separate and purify in downstream industrial processes, a non-trivial concern for anyone managing scale-up or regulatory compliance.
There are aromatic amines and N-heterocyclic solvents that seem interchangeable at first glance, but direct experience shows this isn’t the case. Take extraction protocols, for instance: 3-n-Butylpyridine sometimes solubilizes target molecules that stump simpler pyridines, especially when dealing with hydrophobic compounds. This small edge translates into savings in time or purification steps down the line.
I have often had to convince others—sometimes even procurement teams—that the difference between an adequate intermediate and a superior one comes down to qualities you only appreciate over a series of projects. Nobody notices high purity until a batch fails, or consistent stability until a year-old bottle still does its job. 3-n-Butylpyridine offers this peace of mind, and that means something on any production floor or research bench.
From a safety perspective, any pyridine should be handled with care for both toxicological and environmental reasons. Here the bulkier butyl group does not eliminate risk, but many users attest to the more manageable vapor pressure and odor compared to the “classic” pyridine, which can quickly permeate lab spaces and draw complaints. Waste management improves, too, as lower volatility means less concern about airborne contamination.
Sourcing can make or break a decision. With many specialty pyridines, reliability and transparency from the supplier remain crucial. Consistent, repeatable chromatographic verification, and in-house testimony from countless routine tests, go a lot further in reassuring quality than a data sheet alone ever could. Reputable manufacturers will confirm that material purity runs consistently above advertised, and impurities remain just as low after several months in proper storage. Anecdotes carry weight here; one well-known glass manufacturer found that using lower-purity analogs produced streaks in their specialty coatings—an issue resolved after switching to high-purity 3-n-Butylpyridine.
Of course, no chemical comes without challenges. Toxicity stands among the leading concerns, and no one should ignore risk mitigation. My own policy: treat all pyridines as capable of causing harm, and employ gloves, glasses, and fume hoods, no matter the situation. Environmental regulations around disposal and emissions keep tightening, so investing in safer containment and recovery methods pays for itself over time.
Supply chain volatility has recently highlighted the importance of supplier diversity. Disruptions do not discriminate based on molecular structure. For those relying heavily on 3-n-Butylpyridine, maintaining relationships with multiple vetted providers minimizes delays. Setting up reliable analytical methods in-house—such as consistent GC or NMR analysis—also guards against unwanted surprises when dealing with bulk shipments. I have always found that investing upfront in analytical equipment leads to fewer headaches in the long-term, particularly when regulatory agencies conduct audits or request records.
Handling and waste present another set of issues, especially in countries with stringent chemical control laws. Establishing clear protocols for spill management and containment isn’t just about compliance; it keeps teams safe and minimizes environmental impact. Continuous staff training helps reinforce good handling habits and can keep companies ahead of both accidents and fines.
On a technical level, reactivity sometimes introduces challenges, especially for those working with sensitive substrates or designing large-scale syntheses. Careful test runs help minimize surprises, and incremental scaling gives production teams the data they need to prevent costly missteps. Troubleshooting with 3-n-Butylpyridine generally takes less time than with some of its more temperamental peers, but professional caution and careful monitoring remain non-negotiable.
There’s been a steady increase in demand for pyridine derivatives as emerging industries look for specialized intermediates. Clean energy, digital display technology, and advanced pharmaceutical synthesis depend on flexible building blocks capable of adapting to new requirements. While I remember a time when the options for pyridine derivatives were limited, and most professionals made do with whatever stock happened to be on hand, the field has evolved. Now, end-users expect tighter control over molecular structure, purity, and consistency.
Producers of 3-n-Butylpyridine who invest in advanced purification steps or more robust quality control processes help set themselves apart, but this only matters if their products meet real-world needs on the ground. From my vantage point, users respect honest, transparent reporting of side products, degradation pathways, and shipment traceability more than just an impressive guarantee on a website. Building trust requires commitment from both supplier and user—direct feedback loops, batch records, and support with unusual application questions set leaders apart from the pack.
Looking ahead, evolving fields like microelectronics and medical imaging will only increase their demand for specialty pyridines. As research pushes into more complex areas—whether that means highly functionalized bioactive molecules or multi-phase display layers—3-n-Butylpyridine has positioned itself as the kind of backbone that makes innovation possible. Each time a newly developed synthesis leverages the subtle electron-donating properties of this molecule, or a display layer formulation achieves improved stability, it reminds me why investing in dependable chemical building blocks matters for industry progress.
At the end of the day, real impact comes from understanding chemical structure and performance together—in practice, in the pilot plant, and under regulatory scrutiny. 3-n-Butylpyridine offers a unique mix of practical reactivity, reliable availability, and a well-understood safety profile. The experiences of those who have solved practical problems with its help, or saved projects by switching to a purer, more reliable source, carry more weight than any abstract claims.
From my own career and from speaking with colleagues, I see the trend: those who take a little extra time to weigh the impact of molecular structure on overall workflow, waste, yield, and safety always come out ahead. This approach doesn’t only deliver technical success—it also helps control costs, maintain compliance, and keep teams working safely and efficiently in the long run.
So, if you’re considering 3-n-Butylpyridine for your next project—whether it’s for organic synthesis, materials production, or process optimization—it’s worth recognizing both its strengths and its limits. The best outcomes always follow from practical knowledge built over time, an honest assessment of needs, and a commitment to safety and reliability at every step.