|
HS Code |
183369 |
| Chemical Name | 4-Propanolpyridine |
| Cas Number | 5360-94-1 |
| Molecular Formula | C8H11NO |
| Molecular Weight | 137.18 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 233-235 °C |
| Melting Point | -38 °C |
| Density | 1.045 g/cm3 |
| Solubility In Water | Miscible |
| Refractive Index | 1.513 |
| Flash Point | 97 °C |
| Smiles | CCCN1=CC=CC=N1 |
As an accredited 4-Propanolpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 g amber glass bottle labeled "4-Propanolpyridine, ≥98%" with safety information and hazard symbols, tightly sealed to prevent leaks. |
| Container Loading (20′ FCL) | **Container Loading (20′ FCL) for 4-Propanolpyridine:** Typically loaded as 16–19 metric tons in 200L drums, tightly sealed, ensuring safety, stability, and regulatory compliance during transit. |
| Shipping | 4-Propanolpyridine is shipped in securely sealed containers, typically made of high-density polyethylene or glass, to prevent leakage and contamination. Packaging is compliant with chemical safety regulations, labeled with hazard warnings. During transit, it is kept upright, protected from sunlight, extreme temperatures, and incompatible substances to ensure safe delivery. |
| Storage | 4-Propanolpyridine should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers or acids. Keep the container tightly closed and protected from moisture and direct sunlight. Use appropriate chemical storage containers, and clearly label the storage area. Always follow local regulations and safety guidelines for storing organic chemicals. |
| Shelf Life | 4-Propanolpyridine typically has a shelf life of 2 years if stored in a cool, dry place, tightly sealed. |
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Purity 98%: 4-Propanolpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduces purification steps. Molecular weight 123.18 g/mol: 4-Propanolpyridine with molecular weight 123.18 g/mol is used in heterocyclic compound research, where it enables accurate stoichiometric formulations. Boiling point 210°C: 4-Propanolpyridine with a boiling point of 210°C is used in high-temperature organic reactions, where it improves reaction stability and minimizes volatility losses. Stability temperature 180°C: 4-Propanolpyridine with stability up to 180°C is used in catalyst preparation processes, where it maintains structural integrity and enhances catalyst lifetime. Low water content (<0.5%): 4-Propanolpyridine with low water content (<0.5%) is used in moisture-sensitive syntheses, where it prevents side reactions and increases product purity. Density 1.03 g/cm³: 4-Propanolpyridine with density 1.03 g/cm³ is used in formulation of specialty coatings, where it delivers uniform application and consistent performance. Melting point −30°C: 4-Propanolpyridine with melting point −30°C is used in cryogenic chemical reactions, where it enables efficient handling at low temperatures. Assay (GC) ≥99%: 4-Propanolpyridine with assay (GC) ≥99% is used in analytical reference standards, where it ensures precise calibration and reproducible results. |
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4-Propanolpyridine draws the attention of researchers and manufacturers looking for precision and reliability in their chemical processes. Recognized by its structure as a pyridine ring substituted at the fourth position with a propanol group, this compound bridges the world of academic curiosity and practical industry applications. For those who spend any part of their day flipping through catalogs and journals, the structure stands out right away: it is less common than simple pyridines, yet more approachable than a lot of specialty functionalized aromatic compounds. Its charm lies in the way a single hydroxyl group transforms otherwise basic nitrogen heterocycles into something much more interesting.
There’s no shortage of pyridine derivatives in the market. Some are punched up with halogens or alkyl groups and end up primarily as solvents or intermediates. 4-Propanolpyridine shifts gears by bringing in a primary alcohol group, which opens up a toolbox of chemical reactivity that plain pyridines just can’t match. The alcohol handle welcomes a diverse range of downstream chemistry, including etherification, esterification, and even advanced cross-coupling reactions. In the hands of a skilled synthetic chemist, this single tweak translates to a much broader horizon, offering both nucleophilic and electrophilic functionality in a single package. Whenever I see a toolkit that cares for both flexibility and specificity, my ears perk up; it just saves time and cuts steps out of complicated routes.
Specifications tell the real story. Most reputable suppliers offer 4-Propanolpyridine with purities above 98%, making it quite dependable for laboratory synthesis and advanced R&D. The majority of users work with it as a colorless to pale yellow liquid, which helps in handling and measuring—nothing’s worse than trying to scrape every last milligram from a sticky solid bottle, after all. Its molecular formula is C8H11NO, and while the molecular weight checks in around 137.18 g/mol, what matters in daily use is its predictable boiling and melting points, which hover in the ballpark for typical small alcohols with aromatic rings. This means it’s generally easy to distill if needed, and doesn’t come with surprises that might wreck a reaction.
Ask ten chemists what they’re doing with a bottle of 4-Propanolpyridine and you'll rarely get the same answer twice. In my own lab days, it turned up as a low-profile hero, linking up as a building block for more complex heterocycles or sliding into position as a ligand in catalysis. The alcohol group loves forming esters, so it fits right into synthetic pathways for drugs, agrochemicals, and specialty materials. One of the neatest aspects—at least for those looking to scale—is how it reacts cleanly under standard organic conditions. No exotic reagents needed. Even under milder approaches like enzymatic transformations, it behaves predictably, which means less troubleshooting and more productivity.
Stacking up 4-Propanolpyridine against its relatives quickly highlights why it’s more than just another entry in the catalog. Compared to plain pyridine, the alcohol group is the star. It sets the molecule apart by offering better solubility in various solvents and by unlocking a set of reactions that simple alkyl pyridines can’t touch. Even among other substituted pyridines, the position of the propanol group matters. While derivatives substituted at the 2- and 3- positions already exist, only the 4-position arrangement consistently minimizes steric clashes in many reactions, leading to fewer side reactions and cleaner product profiles.
Anyone who’s spent much time studying advanced pharmaceuticals knows pyridine rings pop up everywhere. Slipping an alcohol onto the 4-position grants medicinal chemists a new route to introduce polarity and hydrogen bonding—two features often correlated with improved biological activity and solubility. Across dozens of patent filings, you can spot this motif being leveraged for everything from kinase inhibitors to antifungals. In materials science, the primary alcohol lets it serve as a starting node in polymer synthesis or as a cross-linking agent in specialty resins. My own colleagues have explored its use in creating responsive materials that switch characteristics depending on environment, thanks to the subtle reactivity of that hydroxyl group.
Anyone who’s spent an evening cleaning up after a leaky bottle knows the importance of storing and handling chemicals with respect. 4-Propanolpyridine earns some points here: its volatility sits low enough to avoid rapid losses, yet doesn’t linger with heavy, noxious fumes. While standard precautions still apply—avoid inhaling vapors, guard skin and eyes—routine lab gear and standard chemical hygiene have proved sufficient in my experience. A well-kept bottle, sealed tightly and housed away from acids or oxidizers, generally lasts its shelf-life without surprises.
Chemical manufacturing faces mounting pressure to reduce environmental impact, so sourcing and using compounds like 4-Propanolpyridine responsibly makes sense both for conscience and compliance. Many producers have shifted to greener synthetic methods, cutting out halogenated waste streams and using recyclable solvents wherever practical. For end users, disposal routes align with those established for similar nitrogen heterocycles; following local waste regulations remains the best bet. Whenever possible, unreacted quantities can be recovered and repurposed, limiting unnecessary waste. In cases where large-scale processes are involved, more labs are moving toward closed-loop systems that capture and recycle vapors, trimming down emissions and operational costs at the same time.
Students and experienced chemists alike benefit from tools that balance versatility and reliability. 4-Propanolpyridine slots into this space effectively, serving as an intermediate in multi-stage syntheses. Early-stage research programs look for compounds that can be easily modified; a functional alcohol on the pyridine ring means derivatization routes multiply instantly. In my academic circles, I’ve seen it show up in everything from constructing rigid frameworks for supramolecular chemistry to acting as a handle for attaching reporter groups in analytical assays. The pattern is clear: compounds that offer multiple points of reactivity open more experimental possibilities.
Bench-scale work rarely prepares anyone for the headaches of pilot plant scale-up, where every dollar and every hour matter more. 4-Propanolpyridine’s stability under a range of conditions eases this transition. Processes designed on the gram scale tend to scale predictably; thermal stability means fewer upsets, and controlled reactivity allows for precise conversions without running through buckets of scavengers or quenchers. Having spent long nights troubleshooting sticky intermediates, I value that predictability. Projects typically move faster, and batch-to-batch reproducibility climbs. This translates to reduced cost overruns and happier clients, whether the deliverable is a library of novel molecules or a standard industrial intermediate.
Quality assurance is only as good as the input materials. Any manufacturer who’s battled with mysterious impurities knows how critical this is. High-purity 4-Propanolpyridine means reactions start on the right foot—nobody wants to chase down unknown peaks in their chromatogram for days on end. As more organizations move toward in-house QA, reliability in sourcing has become a major asset. Over several projects, I’ve noticed how skewed results can become if small differences creep in; even minuscule variations in alcohol content or oxidative profiles can throw off downstream steps, especially in pharmaceutical settings. The demand for certificates of analysis and batch-specific data reflects a wider industry expectation: quality has to be proven, not just claimed.
Modern laboratories have rapidly embraced automated synthesis and high-throughput screening. 4-Propanolpyridine fits in neatly because its liquid state allows for easy dispensing using modern robotics, reducing downtime and material loss. As instrument platforms grow more sophisticated, having input chemicals in well-defined, manageable forms reduces operational headaches. At several facilities, I’ve seen standardized workflows that integrate liquid handling of 4-Propanolpyridine into parallel synthesis platforms, feeding into streamlined analytical pipelines. This compatibility supports faster cycles from ideation to result without interrupting the broader flow of discovery.
With stricter regulations and evolving global supply chains, buyers keep a closer eye on origin, documentation, and transport. 4-Propanolpyridine, classified among relatively low-toxicity specialty chemicals, generally travels without the heavy restrictions placed on some pyridine derivatives. Still, country-specific import and shipping requirements do come into play. The advantage of working with compounds that straddle the line between commodity and specialty status is the flexibility it brings. Reliable sourcing matters; interruptions caused by customs snafus or sudden shortages can throw project timelines far off track. Through the years, building relationships with reputable suppliers, staying on top of documentation, and keeping modest buffer stocks have all paid off in project continuity.
The search for cost savings never takes a holiday. In sourcing intermediates like 4-Propanolpyridine, price considerations meet head-on with quality demands. Overly aggressive bargain hunting often leads to problems down the road, as off-spec materials creep in through unvetted channels. My approach boils down to trust but verify—a reliable supplier willing to back up batches with documentation and transparency consistently outperforms discount brokers. Sourcing at scale does drive economies, though, so periodic re-negotiation, long-term contracts, or collaborative partnerships with producers often help keep margins healthy. More than once, direct conversations with manufacturers have revealed room for customization on packaging or batch sizes, further optimizing procurement flows for specific operations.
Chemical innovation often collides with practical bottlenecks. Those looking to bring new derivatives of 4-Propanolpyridine to market quickly encounter both classic and emerging hurdles: regulatory navigation, purification at scale, and making the business case for unique functional benefits. Once a clear synthetic or utility advantage emerges—be it in higher selectivity or a better safety profile—interest typically grows. Success stories have cropped up in catalysis, ligands for asymmetric synthesis, and precursor routes for advanced pharmaceuticals. In each, the alcohol function doesn’t just participate; it often makes all the difference by omitting the need for more cumbersome protecting group strategies or offering access to functional handles previously out of reach.
The future for 4-Propanolpyridine seems to grow as new fields of chemistry open doors for functionalized nitrogen heterocycles. Continued efforts in green chemistry may drive new methods for both its synthesis and downstream derivatization, particularly as researchers develop mild, energy-efficient catalytic approaches. With artificial intelligence and machine learning taking stronger roles in predicting reactivity and optimizing synthetic routes, the available data sets benefit enormously from compounds with both aromatic and polar functional groups, like those found in 4-Propanolpyridine. I expect to see more tailored explorations of its uses as both a ligand and a reactive intermediate in the coming years, particularly as more efficient and lower-impact pathways become available.
Even experienced chemists benefit from periodic refreshers and updated literature on specialty intermediates like 4-Propanolpyridine. Training programs that couple hands-on safety with real examples—successful syntheses, efficient downstream transformations—make all the difference. In my own teaching, walking through the practical advantages of alcohol-functionalized heterocycles helps bridge the gap for students moving from textbook learning to real-world application. Manufacturer and supplier webinars, updated technical bulletins, and in-house seminars all provide value by translating what can often seem like abstract molecular structure into direct experimental benefit.
The chemical industry thrives on connectivity and rapid information sharing. Staying in touch with peer-reviewed research, patent literature, and industry trade news helps researchers and buyers spot new trends for compounds like 4-Propanolpyridine. Professional networking—whether at conferences, virtual symposia, or in online forums—often uncovers new suppliers, advances in green chemistry, or previously overlooked applications. I’ve gained some of my best process insights through after-hours discussions with colleagues who faced similar synthetic puzzles. The repeated lesson: few challenges remain unsolved when knowledge flows without bottlenecks.
As laboratories look for reliable, versatile intermediates, 4-Propanolpyridine presents an example of how small molecular changes produce disproportionate benefits. Its balanced structure, pairing aromatic backbone with a functional alcohol, appeals to both theorists and practical chemists aiming for new advances. Whether in small-batch pharma, pilot-scale materials synthesis, or high-throughput discovery, its straightforward performance, high purity, and compatibility with evolving techniques fill a real need. Chemical supply continues to evolve rapidly, and those equipped with adaptable, well-characterized intermediates are better positioned to innovate, solve problems, and keep moving science forward.