|
HS Code |
261544 |
| Name | 2-Benzoylpyridine |
| Cas Number | 2835-68-9 |
| Molecular Formula | C12H9NO |
| Molecular Weight | 183.21 |
| Appearance | Yellow to light brown solid |
| Melting Point | 78-82°C |
| Boiling Point | 344.8°C at 760 mmHg |
| Density | 1.179 g/cm³ |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC=C(C=C1)C(=O)C2=CC=CC=N2 |
| Inchi | InChI=1S/C12H9NO/c14-12(11-7-3-5-9-13-11)10-6-1-2-8-12/h1-9H |
| Synonyms | 2-Pyridyl phenyl ketone |
As an accredited 2-Benzoylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Benzoylpyridine arrives in a 25g amber glass bottle with a secure screw cap and detailed hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container holds 10 MT of 2-Benzoylpyridine, typically packed in 200 kg drums, securely palletized for export. |
| Shipping | 2-Benzoylpyridine is shipped in secure, airtight containers compliant with chemical transport regulations. It should be stored and transported at ambient temperature, protected from moisture and direct sunlight. Proper labeling, including hazard information, must be displayed. Ensure compliance with all local, national, and international shipping guidelines for safe handling and delivery. |
| Storage | 2-Benzoylpyridine should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. The storage area should be clearly labeled and secure, preventing unauthorized access. Personal protective equipment should be available when handling the chemical to minimize exposure to vapors or accidental contact. |
| Shelf Life | 2-Benzoylpyridine typically has a shelf life of 2-3 years when stored in a cool, dry place, tightly sealed. |
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Purity 99%: 2-Benzoylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product quality. Melting point 54°C: 2-Benzoylpyridine with a melting point of 54°C is used in organic synthesis reactions, where controlled phase behavior facilitates reproducible outcomes. Molecular weight 197.22 g/mol: 2-Benzoylpyridine of molecular weight 197.22 g/mol is used in ligand preparation for coordination chemistry, where precise stoichiometry improves metal complex formation. Particle size 50 μm: 2-Benzoylpyridine with particle size 50 μm is used in catalysis research, where uniform dispersion accelerates reaction kinetics. Stability temperature up to 120°C: 2-Benzoylpyridine with stability temperature up to 120°C is used in high-temperature coupling reactions, where enhanced thermal stability prevents decomposition. HPLC grade: 2-Benzoylpyridine of HPLC grade is used in analytical method development, where high chemical purity reduces baseline interference. Water content ≤0.5%: 2-Benzoylpyridine with water content ≤0.5% is used in moisture-sensitive syntheses, where minimal hydrolysis risk maintains reaction integrity. |
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Scientists, researchers, and industry professionals alike can recognize the long tradition of innovation that comes from working with well-made organic building blocks. Among these, 2-Benzoylpyridine stands out as a resourceful compound that regularly proves its value in both laboratory and industrial settings. At its core, 2-Benzoylpyridine carries a distinct structure—a pyridine ring anchored by a benzoyl group at the second position. This precise configuration sets up a foundation for countless synthetic possibilities, and every batch produced reflects years of chemical know-how.
With a chemical formula of C12H9NO and a molecular weight near 183.2 g/mol, the substance carries a confidence built on both reliability and adaptability. Often delivered as a white to pale yellow crystalline solid, it gives distinct aromatic traits and a characteristic melting point which lends consistency to its visual appraisal. Few chemical building blocks show the same balance of performance and stability during reactions.
Many of us who have worked with organic synthesis quickly come to appreciate reagents that offer multiple opportunities for creative chemistry. 2-Benzoylpyridine checks all the boxes. Acting as a chelating ligand or as an intermediate for advanced pharmaceuticals, it steps in where stability and reactivity matter most. Coordination chemists often rely on it as a bidentate ligand, especially in complexation reactions with transition metals, where the nitrogen donor site in the pyridine and the carbonyl from the benzoyl group work closely to stabilize metal centers.
Beyond coordination chemistry, this compound is also a regular fixture in medicinal chemistry circles. Its use in assembling heterocyclic drug candidates has grown, as researchers continually seek fresh scaffolds for drug discovery. While some molecules dominate headlines, it’s often these reliable workhorses sitting on the bench that enable real breakthroughs.
Anyone who’s spent long hours in a synthetic lab has tried out a variety of pyridine derivatives. 2-Benzoylpyridine offers a unique edge—its dual functional groups open up more creative synthetic channels compared to simpler alternatives like pyridine itself or 2-acetylpyridine. The benzoyl group injects added rigidity and resonance stability, influencing the electronic nature of the whole ring system and widening the scope for downstream transformations.
Other isomeric compounds sometimes lack the versatility or stability needed for delicate reactions, while 2-Benzoylpyridine brings more predictable behavior. In practice, its physical properties, such as melting point and solubility in common solvents, make it easier to handle and purify. During scale-ups or analytical measurements, this reliability becomes crucial—not just for small research groups, but for scale-oriented industrial teams too.
Anyone who has ever sat waiting for a TLC plate to develop knows how a subtle impurity can spoil an entire sequence. 2-Benzoylpyridine’s advantage also comes from the way it is produced. Reputable suppliers focus on high-purity batches, providing material that stands up to both analytical scrutiny and performance demands. Infrared, nuclear magnetic resonance, and mass spectrometry readings confirm structures and purities without frequent surprises. As someone who has had their work derailed by an off-spec reagent, that peace of mind is invaluable.
This level of quality control opens up 2-Benzoylpyridine for more advanced applications. In catalysis, for instance, these pure samples allow researchers to form cleaner complexes with metal ions, reducing side reactions and boosting yield. Synthetic organic chemists notice fewer byproducts. Medicinal chemists get more reliable assay results. Whenever a new method depends on a single component, the value of real consistency becomes clear.
People often think of organic reagents as single-purpose tools, but compounds like 2-Benzoylpyridine challenge that assumption. The molecule appears in coordination chemistry, pharmaceutical synthesis, material science, and analytical chemistry. Each discipline welcomes it for a different reason.
In the world of catalysis, its chelating ability changes the shape and reactivity of transition metal centers. The result is often a more selective and powerful catalyst for reactions like cross-coupling, oxidation, or polymerization. When teams set out to develop new polymer materials with unique mechanical or optical properties, the right metal ligand can make the difference—and 2-Benzoylpyridine regularly takes up that role.
Medicinal chemists may approach it from the perspective of rapid library synthesis. The rigid aromatic system and the chemical accessibility of the pyridine nitrogen and benzoyl moiety offer opportunities to introduce new substituents—giving rise to dozens of new potential active pharmaceutical ingredients. In drug discovery programs thoroughly documented in the literature, derivatives built on this scaffold have led to probes for CNS, antiviral, and anticancer research.
In physical chemistry, this compound functions as a probe molecule. Thanks to its well-defined structure and electronic properties, spectroscopists use it to study host-guest interactions, solvent effects, and reaction mechanisms. During NMR or UV-Visible studies, both students and seasoned researchers can interpret spectra more easily because of its clear signatures.
Over time, chemists tend to develop firm preferences, and different labs gravitate toward specific tools. Compounds like 2-acetylpyridine or 4-benzoylpyridine share some similarities, but differences soon become obvious with routine use. 2-Benzoylpyridine’s benzoyl group at position two influences everything from electronic distribution to how it coordinates with metals.
For instance, 2-acetylpyridine lacks the added aromatic ring, making it less bulky and slightly more reactive toward some nucleophiles. This sometimes results in lower stability in metal complexes. Meanwhile, 4-benzoylpyridine positions the benzoyl group farther from the nitrogen, affecting the chelation angle and strength. So, when a reaction’s outcome relies on the precise geometry or electron flow, 2-Benzoylpyridine steps up where the others can’t quite deliver.
From a practical standpoint, I have tried running parallel syntheses using both 2- and 4-benzoylpyridine as ligands. Metal complex yields, colors, and even the crystallization rates differed enough to confirm the right ligand choice matters. A single atom's position on the ring changes everything, especially during scale-up or sensitive analytical runs.
Whether in industry or academia, flexibility matters. 2-Benzoylpyridine dissolves easily in a range of common organic solvents, making it a favorite for routine bench chemistry. Its melting point, usually reported in the mid-50s Celsius range, means it handles moderate warming during isolation and purification. I’ve seen less drama extracting or recrystallizing this molecule than with trickier solids.
The crystalline solid also stores easily on the shelf, requiring no elaborate precautions against air or moisture. For those used to keeping their chemical inventory simple and manageable, that’s a plus. In storage, it shows good shelf-life, provided it is capped and kept out of direct sunlight.
Handling remains straightforward. With proper gloves and ventilation—standards in any organized lab—risks drop significantly. As with most aromatic carbonyl-containing molecules, mild irritant properties may linger, but the safety data sheets leave no special cause for alarm.
As society pays increasing attention to chemists’ environmental impact, certain organic building blocks take on additional importance. 2-Benzoylpyridine, like many structurally related molecules, does not demand exotic disposal methods when managed under standard laboratory rules. Many labs have worked out effective waste collection for aromatic compounds, ensuring compliance without excessive cost or effort.
Learning to appreciate basic safety and sustainability rules pays dividends. Good housekeeping—tightly capping bottles, clear labeling, and distance from oxidizers—carries over to every task in the lab. For chemists in training, the way they handle even familiar materials sets a tone for the rest of their careers. With 2-Benzoylpyridine, safe and responsible handling fits directly into already practiced routines.
As for broader environmental concerns, regulatory frameworks around disposal continue to evolve. Labs that focus on greener synthetic methods can use 2-Benzoylpyridine in catalytic protocols designed to cut down on waste. By enabling catalytic cycles, it often helps shrink the volume of metal and organic byproducts generated.
Experienced chemists know the frustration of delayed experiments waiting on back-ordered specialty reagents. Over the past decade, 2-Benzoylpyridine has benefited from improved supply chains, with several well-established manufacturers producing high-quality material meeting academic and commercial standards. Whether sourced for research or for largescale production, the compound typically arrives in securely sealed glass or plastic, labeled to rigorous international standards.
Global demand continues to rise, largely thanks to its expanding role in pharmaceutical, fine chemical, and catalysis research. As synthetic protocols grow more sophisticated, reliable supply of foundational chemicals becomes a central pillar of laboratory planning. The compound’s rising popularity, fed by both published literature and word-of-mouth among practicing scientists, means more suppliers are stepping up to meet these needs.
Raw material pricing across the specialty chemical sector shows its usual ups and downs, but 2-Benzoylpyridine remains relatively steady. That stability allows labs to plan extended research schedules without sneaky budget surprises. It helps that the molecule derives from widely available starting materials, which shields it somewhat from the swings that plague more exotic reagents. Chemical buyers appreciate the straightforward procurement process that this accessibility permits.
With all of its established applications, 2-Benzoylpyridine is far from a static commodity. Every year sees new journal articles and patent filings that build on its backbone. Synthetic chemists experiment with derivatizing either the benzoyl group or the pyridine ring, hunting for activity in new biological targets or enhancing the compound’s metal-binding properties.
In my own experience, small shifts in reaction conditions—from greener solvents to solvent-free microwave protocols—have opened up new uses. Researchers test new catalytic cycles and ligand designs, using 2-Benzoylpyridine as a flexible starting point. By pushing reaction conditions to be more economical and less resource-intensive, newer methodologies underscore just how adaptable certain molecules are when chemists apply creative pressure.
Education and training continue to play a big part here. Universities and research institutes encourage hands-on student work with widely used building blocks like this one, as it teaches technique, analytical rigor, and respect for detail. As science and industry evolve, so too will the applications and derivatives built off this versatile framework.
Collaborative research stands out as another bright spot. Interdisciplinary projects—where chemists, materials scientists, and biologists team up—often begin with a search for a shared toolkit. 2-Benzoylpyridine’s straightforward structure and reliability invite such cooperation. Conversations with colleagues outside one’s immediate specialty frequently land on such molecules, which makes future innovation not just possible, but likely.
In my years working across both academic and industry labs, the lines between classic reagents and modern applications constantly blur. 2-Benzoylpyridine serves as a standout example. Some of the latest research stretches into areas like coordination polymers for molecular recognition, supramolecular chemistry, and sensors for detecting trace metals. Each new patent or publication adds another chapter to the ongoing story of this molecule.
Colleagues in analytical chemistry have started looking at its behavior in advanced spectroscopic and electrochemical setups, using it as a model for understanding bigger, more complicated structures. In the drive for better diagnostics and environmental sensors, the lessons learned from a sturdy molecule like 2-Benzoylpyridine turn out to be highly adaptable. Materials scientists tweak its core structure to generate crystals with tailored optical or magnetic responses, showing how even old favorites find new life at the research frontier.
More recently, researchers exploring sustainable energy storage and conversion technologies have adapted organometallic complexes using 2-Benzoylpyridine as the ligand. The easy modification and fine-tuning of its electronic effects play a key role in developing next-generation catalysts for both hydrogen generation and carbon capture. Feedback from these efforts often cycles back into broader synthetic and industrial communities, in a virtuous loop that benefits everyone.
It’s easy to forget that every reagent comes with its own shared experience. Countless chemists, technicians, and researchers have worked with 2-Benzoylpyridine over many decades. From the first careful measurements in school labs to high-throughput screens in industry, the knowledge base surrounding this compound keeps growing. It’s the sort of building block people remember using—not because of splashy headlines, but because it gets the job done.
Mentors often bring younger lab members into the fold by walking through careful recrystallizations, by troubleshooting a failed coordination complex, or by reviewing synthetic strategies that use the benzoylpyridine scaffold. Through this process, best practices are handed down from one generation to the next. It isn’t just about mastering procedures; it’s about cultivating the type of judgment and care that defines good laboratory science.
Thoughtful suppliers and distributors also play a supporting part. By sticking to quality standards and supporting open communication about batch consistency and analytical data, they help reduce the headache factor for working scientists. That back-and-forth, grounded in practical realities, keeps the whole ecosystem running smoothly.
No single chemical will provide a jungle gym for every synthetic challenge. Still, a solid, flexible framework—like that found in 2-Benzoylpyridine—gives scientists the freedom to pursue many lines of investigation at once. Whether applied to the study of new drug candidates, designing powerful catalysts, or building new materials, the molecule provides a dependable foundation for pushing boundaries.
Future work may see even greater functionalization, leading to improved selectivity or activity in the most demanding environments. Sustainable chemistry initiatives continue to look for ways to make established processes cleaner and more resource-efficient, and molecules like 2-Benzoylpyridine frequently prove adaptable to new protocols. This ongoing evolution forms a reassuring backdrop to every research plan that still values both reliability and reinvention.
As the chemists of tomorrow learn to look for ways to combine old wisdom with new approaches, the role of well-known molecules does not diminish. If anything, robust and adaptable platforms like 2-Benzoylpyridine stand as reminders that innovation is often rooted in a firm grasp of the basics. Respect for established tools, paired with genuine curiosity, moves the entire scientific community closer to safer, more sustainable, and more powerful solutions.
Chemical research thrives on a handful of timeless principles: quality, curiosity, collaboration, and adaptability. Through its unique structure and diverse set of applications, 2-Benzoylpyridine fits comfortably within this tradition. For every scientist, new or old, who invests long hours into tough problems, the quiet dependability of such a molecule offers both reassurance and invitation. As research priorities inevitably shift in the coming years, the case for reliable, proven tools like this one only grows stronger.