|
HS Code |
332469 |
| Chemical Name | 3-acetylpyridine |
| Iupac Name | 1-(pyridin-3-yl)ethanone |
| Molecular Formula | C7H7NO |
| Molar Mass | 121.14 g/mol |
| Appearance | Colorless to pale yellow liquid or crystalline solid |
| Melting Point | 53-56 °C |
| Boiling Point | 234-237 °C |
| Density | 1.112 g/cm³ |
| Solubility In Water | Moderate |
| Cas Number | 350-03-8 |
As an accredited 3-acetylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, with secure screw cap and hazard labeling for 3-acetylpyridine, including chemical identifiers and safety warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 3-acetylpyridine: Typically 12–14 metric tons, securely packed in drums or IBCs, ensuring safe, compliant shipping. |
| Shipping | 3-Acetylpyridine is shipped in tightly sealed containers to prevent leaks and contamination. It should be stored and transported in a cool, dry, well-ventilated area, away from incompatible substances and ignition sources. Comply with all local, national, and international regulations for shipping hazardous materials; packing group and UN code may apply. |
| Storage | 3-Acetylpyridine should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as oxidizing agents. Keep it away from direct sunlight and moisture. Use appropriate chemical storage cabinets if available, and ensure the container is properly labeled. Follow all relevant safety and regulatory guidelines for chemical storage. |
| Shelf Life | 3-Acetylpyridine typically has a shelf life of 2-3 years if stored tightly sealed, cool, and protected from light and moisture. |
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Purity 99%: 3-acetylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurity levels. Melting point 56°C: 3-acetylpyridine with melting point 56°C is used in agrochemical formulation, where it facilitates smooth processing and homogeneous mixing. Molecular weight 121.14 g/mol: 3-acetylpyridine with molecular weight 121.14 g/mol is used in fine chemical research, where it provides accurate reactant dosage calculations. Stability temperature 120°C: 3-acetylpyridine with stability temperature 120°C is used in high-temperature organic synthesis, where it maintains compound integrity during reactions. Low moisture content (<0.2%): 3-acetylpyridine with low moisture content (<0.2%) is used in catalyst preparation, where it prevents side reactions and enhances catalyst efficiency. Analysis grade: 3-acetylpyridine of analysis grade is used in analytical laboratories, where it delivers reliable and reproducible chromatographic results. Dense liquid form: 3-acetylpyridine in dense liquid form is used in organic extraction processes, where it improves solvent phase separation and product recovery. |
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Anyone who's spent time in a lab will recognize the sharp tang of pyridine derivatives long before putting a label to the bottle. One of those distinct compounds, 3-acetylpyridine, often goes overlooked in public discussions, but you find it quietly working behind the scenes across a surprising range of scientific efforts. Let's dive into why researchers, chemists, and industry professionals value this chemical and how it stands out from its near relatives.
Chemists look at structural differences to predict how a compound will behave. In the case of 3-acetylpyridine, the acetyl group attaches to the third carbon on the pyridine ring. That location changes the game when you compare it to pyridine itself, or even to its 2- and 4-acetyl isomers. Subtle differences in where that acetyl sits can create noticeable changes in reactivity, solubility, and the way it acts as a building block in synthesis. Structural tweaks matter—a lesson most folks learn the hard way.
In my own experience, reaching for a bottle of 3-acetylpyridine inevitably meant I was aiming for precision. Say you're taking on the challenge of constructing heterocyclic rings or prepping ligands for metal complexes. Using the right isomer ensures predictable yields and cleaner workups, saving you time and headache later. Choosing between 2-, 3-, or 4-acetylpyridine isn’t just a game of spot-the-difference; it’s the deciding factor in reaction control and reproducibility.
For labs, it’s all about purity and reliability. Most suppliers offer 3-acetylpyridine in high-purity grades, commonly 98% or above, because researchers can’t afford to gamble on contaminants that could throw off experimental outcomes. As a crystalline solid, it dissolves well in common solvents like ethanol, ether, or chloroform. You don’t need glitzy packaging or branding here—the biggest model distinction comes down to purity levels and batch-to-batch consistency.
Granular details, like molecular weight and melting point, matter for workflow planning. 3-acetylpyridine clocks in with a molecular formula of C7H7NO and a melting point that typically falls between 54°C and 57°C. Handling and storage are straightforward; protecting the compound from moisture and excessive heat keeps it ready for action. I’ve lost material to leaky containers before, so attention to basics like proper sealing pays off more than anything ‘innovative’ on the shelf.
3-acetylpyridine pulls its weight in a host of reactions. From the outset, it lends itself to organic synthesis, making life easier for anyone aiming to build up more complex molecules. You’ll see it featured in the creation of pharmaceuticals, flavoring agents, and agrochemicals. The nitty-gritty of why it’s often chosen over similar compounds boils down to how it can act as both a nucleophile and an electrophile—giving synthetic chemists options in multistep reactions.
One of my mentors used to call it ‘the silent partner’ in vitamin B6 synthesis. Without it, scaling up the industrial route to pyridoxine production wouldn’t be so smooth. In biochemistry, those pyridine rings echo through countless essential processes. Having a reliable source of 3-acetylpyridine helps bridge basic research to applied product development, especially as demand for better vitamins and efficient crop protectants grows worldwide.
For those who work in research, especially in pharmaceutical discovery, 3-acetylpyridine’s versatility can open up new pathways to active ingredients. Unlike its close cousins, its third-position acetyl tweak allows for downstream modifications that can translate to selectivity in drug targeting. It’s these differences—often invisible to the untrained eye—that transform a simple chemical into a foundation for health innovation.
Let’s not ignore what sets this compound apart from its siblings. You’ll encounter 2-acetylpyridine and 4-acetylpyridine in similar circles, but each one brings a distinct flavor. Having handled all three, I can say that substitution at the 2-position tends to feel bumpier, with more side products cropping up during synthesis. Going with the 3-position leads to more straightforward reactions, cleaner profiles, and fewer rogue trace impurities. That means less time recalibrating and more time focusing on results.
Pricing trends reflect this, too. Because 3-acetylpyridine offers the right mix of reactivity and reliability, suppliers see steady demand and tend to invest more in refining their production, rather than banking on bulk sales alone. For a working scientist, investing in a slightly more expensive but purer standard pays off in fewer failed assays and greater confidence in reproducibility. There’s a reason some labs stay loyal to it, despite the lure of cheaper alternatives.
I remember running side-by-side syntheses in graduate school, swapping out each isomer. Invariably, the reactions using 3-acetylpyridine ran cleaner, required less post-reaction purification, and produced fewer byproducts. It meant I could actually make the deadline instead of spending extra hours with a rotary evaporator. These small differences compound into real competitive advantages over the course of a research project or a production line.
Don’t expect 3-acetylpyridine to grab headlines, but look closely at the research that drives innovation in antibiotics, anti-cancer compounds, and flavors. A compound like this, with well-understood reactivity, brings a level of reliability to synthetic protocols that less-characterized chemicals just don’t offer. Many scientists feel more confident optimizing reactions when their core materials hold no surprises.
In the food and flavor industry, the need for authenticity and safety in flavor production has increased. Regulatory agencies continue to watch for anything that could introduce risk, so manufacturers rely on high-quality intermediates. 3-acetylpyridine finds use in nuanced formulations, especially in creating aroma compounds and mimicking natural flavors where sourcing direct extracts would prove too expensive or inconsistent.
Patents in pharmaceutical chemistry often cite specific acetylpyridine isomers in synthetic routes. Pros working on proprietary molecules can’t just swap in a different isomer for convenience—the structure-activity relationship depends on better predictability, which 3-acetylpyridine handles well. Consistency in key building blocks gives drug developers more control over purity, potency, and the pathway from bench to clinical study.
Chemistry evolves in step with public scrutiny and tighter regulations. Sourcing 3-acetylpyridine now means working with suppliers who can guarantee repeatable purity and transparency in their operations. I’ve learned to look for well-documented supply chains and avoid bargain-basement imports that don’t stand up to analytical scrutiny. Product recalls and regulatory headaches aren’t worth the risk of unknowns.
Environmental impact often comes into play as labs aim for safer and greener processes. The rising interest in sustainable manufacturing methods is pushing chemical suppliers to improve the energy efficiency and waste profile of their production lines. Responsible use of 3-acetylpyridine includes attention to safe handling, reduction of organic solvent waste, and efforts to reclaim unused material. The push for greener synthesis isn’t just theoretical—saving money on disposal and reducing exposure risks helps the bottom line.
Over the past decade, major producers have tightened protocols on everything from precursor sourcing to emission controls. Fewer accidents and reduced waste streams translate into both financial savings and a cleaner record for regulatory compliance. Labs and factories see reputational benefits from communicating their use of responsibly produced chemicals—something clients and funding bodies increasingly value.
Dealing with 3-acetylpyridine rewards caution and respect. This is no everyday grocery item, and its distinctive odor alone offers a constant reminder to maintain good ventilation. Although less volatile than base pyridine, exposure to concentrated vapors can quickly become uncomfortable. From experience, the difference between a headache-free day and a wobbly afternoon lies in the care taken with both personal protective gear and bench practice.
Standard safety steps apply: gloves, goggles, and a well-maintained fume hood. Smart labs pair careful handling with training refreshers and up-to-date spill kits. Accidents rarely come from the chemical itself; they stem from rushed routines or overlooked protocols. I recall one incident where a new team member underestimated the compound’s spill potential, leading to an evacuation and a mountain of paperwork. Polished habits cut those risks down to almost zero.
Safe disposal runs parallel with smart use. Collecting residues and spending the time on proper neutralization—rather than cutting corners—protects both people and the local watershed. It’s not only about compliance but about respecting your fellow researchers and neighbors. Sharing this responsibility gets easier as labs swap tips and strategies that really work rather than just parroting what’s in the manual.
No chemical escapes scrutiny. For 3-acetylpyridine, supply instability and global demand spikes sometimes create headaches for project timelines. Labs juggling tight deadlines can get caught out by sudden stockouts or unexpected import restrictions. Building buffers in inventory and maintaining good relationships with trusted suppliers lessens the chance of work disruptions. I’ve found that collective purchasing agreements or consortia-style buying arrangements can further reduce risk and negotiate better terms.
Quality drift between lots from lower-grade suppliers remains a thorny issue. Analytical testing—routine in high-stakes operations—can catch small problems before they damage whole batches or invalidate expensive experiments. For smaller outfits that can’t afford state-of-the-art instrumentation, cooperation with partner labs or third-party testing facilities pays dividends. Skipping this step causes more heartbreak than any initial cost savings justify.
The push toward sustainable chemistry puts pressure on to develop new routes to 3-acetylpyridine that generate less waste and use less energy. Researchers who experiment with biocatalytic methods or more efficient synthetic pathways may soon notice better yields with smaller environmental footprints. As public and investor attention sharpens on sustainability reports, progress in green chemistry stands to move faster than ever. Cross-industry sharing of successes and failures in alternative production routes will likely shorten the learning curve for everybody involved.
In the world where research meets commerce, transparency matters. Mislabeling, counterfeits, or poor traceability can all undermine the trust that labs and manufacturers build over many years. I’ve seen collaborations run aground because a critical 3-acetylpyridine batch failed to meet promised specs, resulting in wasted funds and lost time on crucial projects.
Building better supply chains calls for a willingness to invest in documentation, traceability, and external verification. More suppliers now provide certificates of analysis, trackable lot numbers, and digital audit trails. Steering clear of any source that won’t stand by these practices makes sense, especially for organizations driven by compliance or ethical guidelines. Real progress comes when researchers ask hard questions of their suppliers and support best practices industry-wide instead of chasing short-term price breaks.
Facing up to the realities of a competitive market helps everyone. Those seasoned in procurement know that real value comes from product support and accountability more than sticker price. Longstanding supplier relationships, built on clear communication and mutual respect, often pay off during market shocks or regulatory changes. As new players enter the market, their willingness to match or exceed these standards will shape the next generation of chemical suppliers.
No scientist works in a vacuum. Whether you’re a postdoc following established protocols or a process engineer boosting batch throughput, the collective wisdom around best practices with 3-acetylpyridine grows every year. Conference talks, journal papers, and candid hallway exchanges all feed a body of knowledge that lowers barriers for those coming next.
I’ve learned half of what I know about handling and troubleshooting chemical reactions not just from textbooks, but from patient colleagues willing to share their failures and successes. The global community benefits when professionals document what actually happens on the bench—how unexpected humidity, for example, can impact crystallization, or why a certain purification step eliminates hours of rework down the line.
As digital platforms connect researchers and engineers more rapidly than ever, expect the speed of know-how transfer to keep increasing. Sharing protocols, batches, and case studies of 3-acetylpyridine use will keep raising the standard for reliable, safe, and creative science. The more we document and share, the less each new generation has to reinvent the wheel.
At its core, 3-acetylpyridine stands as a quiet success story in the world of laboratory chemicals. Its well-charted properties, suitability for multiple applications, and trustworthy performance make it a fixture in chemistry labs everywhere. From simple undergraduate experiments to sophisticated industry-scale synthesis, its distinct structure and predictable reactivity deliver a combination that few alternatives can match.
Looking forward, the challenge remains clear. Balancing the demand for effectiveness, ethical sourcing, and sustainable production will keep pushing the industry forward. Lab veterans and newcomers alike will keep choosing tools and reagents that not only get the job done, but also stand up to the values of safety, transparency, and respect for both people and the planet. 3-acetylpyridine, by virtue of its proven track record, looks set to stay in the lineup for years to come.