|
HS Code |
884593 |
| Cas Number | 18368-63-3 |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.22 |
| Iupac Name | 4-methyl-2-phenylpyridine |
| Appearance | White to off-white solid |
| Melting Point | 54-56 °C |
| Boiling Point | 331 °C |
| Density | 1.07 g/cm3 |
| Solubility In Water | Slightly soluble |
| Smiles | CC1=CC=NC(=C1)C2=CC=CC=C2 |
| Inchi | InChI=1S/C12H11N/c1-10-7-8-13-12(9-10)11-5-3-2-4-6-11/h2-9H,1H3 |
| Synonyms | 2-Phenyl-4-methylpyridine |
As an accredited 4-Methyl-2-phenylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap, labeled "4-Methyl-2-phenylpyridine," including hazard and handling information. |
| Container Loading (20′ FCL) | 20′ FCL container loads 4-Methyl-2-phenylpyridine securely, using sealed drums or IBCs, ensuring safe, efficient bulk chemical transport. |
| Shipping | 4-Methyl-2-phenylpyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It typically requires standard handling for organic chemicals, adhering to local, national, and international transport regulations. Appropriate hazard labeling and documentation accompany the shipment to ensure safe transit and compliance with legal requirements. |
| Storage | 4-Methyl-2-phenylpyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Protect from direct sunlight and moisture. Ensure proper labeling and restrict access to trained personnel. Regularly check for leaks or degradation, and follow local regulations for safe storage and handling. |
| Shelf Life | 4-Methyl-2-phenylpyridine typically has a shelf life of 2–3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 4-Methyl-2-phenylpyridine with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal side-product formation. Melting Point 70°C: 4-Methyl-2-phenylpyridine with a melting point of 70°C is used in organic electronics fabrication, where its thermal profile allows precise control during component processing. Molecular Weight 169.23 g/mol: 4-Methyl-2-phenylpyridine with a molecular weight of 169.23 g/mol is used in ligand design for coordination chemistry, where accurate molecular mass enables predictable complex formation. Stability Temperature up to 200°C: 4-Methyl-2-phenylpyridine with stability temperature up to 200°C is used in catalyst precursor preparation, where its resistance to thermal degradation ensures consistent catalytic activity. Particle Size <10 µm: 4-Methyl-2-phenylpyridine with particle size less than 10 µm is used in fine chemical formulation, where uniform dispersion enhances product homogeneity and reaction efficiency. |
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Walking into any organic chemistry lab, you’ll often see shelves lined with reagents, each bottle promising a slightly different result for the work at hand. 4-Methyl-2-phenylpyridine is one of those compounds that sits quietly among them, but anyone who has worked in synthesis or chemical development recognizes its quiet influence. Having spent years troubleshooting synthesis reactions, I’ve come to appreciate just how important a well-made intermediate can be—especially one as dependable as this pyridine derivative.
At its core, 4-Methyl-2-phenylpyridine offers a strong base for a variety of chemical transformations. Its molecular formula, C12H11N, might look simple, yet its utility stretches across a handful of industries, especially pharmaceuticals, material science, and even fine chemicals. The reason for such broad application lies in its structure: a pyridine ring fused with both a methyl and a phenyl group. This combination brings about both stability and a predictable reactivity profile, so you don’t find yourself second-guessing your results or dealing with surprise side reactions.
When you’re scaling up reactions or designing a new functional material, one lesson hits home fast: purity isn’t just a number on a label. I’ve known fellow chemists who faced entire batches going awry due to a trace impurity in an intermediate. With 4-Methyl-2-phenylpyridine, the focus often lands on consistent purity levels, often above 98%. That commitment stems from its role as an intermediate in synthesizing more sensitive products. Any contamination runs the risk of unpredictable outcomes, whether you’re working on an active pharmaceutical ingredient or an advanced catalyst.
Several years back, I remember a run-in with a supplier who cut corners on their process. The product came in off-color, and the subsequent reaction yields took a nosedive. That experience drove home the value of strict quality control. Chemists working at the intersection of research and industry rely on suppliers who back up their product claims with transparent analysis, regular lot testing, and real documentation—no tricks or glossy stock certificates necessary. It’s these hard lessons that push the industry to raise its standards, and 4-Methyl-2-phenylpyridine often sets the bar by demanding nothing less.
This compound doesn’t merely replicate what’s already out there. Its closest relatives include unsubstituted pyridines or those with different ring substituents, each shifting the characteristics of reactivity. Take 4-methylpyridine, for example: you get some of the methyl’s electron-donating quality, but you miss out on the bulk and stability brought by the phenyl group in 4-Methyl-2-phenylpyridine. Add that phenyl ring, and suddenly you find increased lipophilicity and more resilient aromatic stacking—a trait valued in designing functional materials and certain drug candidates.
Choosing between these variants means knowing both your starting chemistry and your end goals. At the bench, I’ve noticed reactions that favor 4-Methyl-2-phenylpyridine in cross-coupling steps, especially where selectivity matters more than brute reactivity. It’s these subtle factors—often only clear in hands-on practice—that separate those who chase the latest catalogue from those who really understand their chemistry.
Beyond its obvious place in synthesis, 4-Methyl-2-phenylpyridine has shown up in less expected places. I’ve watched researchers lean on this compound in the search for new ligands and chiral auxiliaries. Its unique structural features open doors for creating more complex molecules, and the pathway it provides is often smoother compared to less substituted analogues. In my own work, I’ve seen it serve both as a backbone for more elaborate heterocycles and as a stepping stone in building up libraries of candidate drugs.
Production of specialty materials sometimes calls for exactly the blend of electronic and steric effects that this compound provides. In those cases, the methyl group gives you a slight boost in electron density, while the phenyl group lends both rigidity and a handle for further modification. Few other pyridine analogues give you quite the same balance. The upshot is an intermediate that stays flexible enough for modification but robust enough to endure harsh reaction conditions.
Keeping a jar of this compound on the shelf isn’t complicated, but certain habits will prolong its shelf life and preserve that all-important purity. Store it sealed tightly, away from sources of moisture, and shielded from extreme heat. I’ve seen colleagues disadvantaged by not paying attention to the basics and ending up with discolored, degraded product. That kind of mishap can undo days of careful work. Stable compounds are worth little if they go bad in substandard storage, so time spent labeling and organizing pays its way many times over.
Once you’ve spent enough time running reactions, you develop a nose for which intermediates play well with others and which ones need hand-holding. 4-Methyl-2-phenylpyridine occupies a sweet spot. It dissolves well in most common organic solvents and stands up to a variety of reaction conditions, including elevated temperatures and either acidic or basic settings. You don’t get the volatility issues that some pyridines bring, nor do you have to fight crystallization problems that stall reactions.
Experimenting with this compound, I’ve found its stability under both oxidative and reductive conditions to be a big advantage. In multi-step synthesis, especially when each intermediate is precious, knowing that your compound won’t degrade makes planning far less stressful.
Green chemistry principles have shifted the conversation around chemical sourcing and production. Labs and companies now favor suppliers who minimize waste and use renewable practices. In the case of 4-Methyl-2-phenylpyridine, more manufacturers announce environmentally conscious synthesis routes, reducing hazardous byproducts and limiting energy use during production. Having worked on procurement teams before, I know the value of a paper trail and environmental disclosures. Verified supply chains help prevent contamination and environmental oversight, reducing the risk of finding your lab in a regulatory bind.
Some vendors offer this compound using alternative synthetic routes that cut down on heavy metals or excess reagents. While these products sometimes carry a higher price tag, responsible buyers consider the broader impact. Wasted solvent or contaminated byproducts don’t just disappear—they can create headaches down the line, for both waste treatment and the planet.
The growth of demand for high-purity chemicals also means some producers adopt closed-loop systems and recycle solvents. As someone with a few horror stories about poor-quality imports, I always check for supplier transparency, detailed batch records, and clear environmental commitments. In today’s climate, these aren’t just side notes—they directly impact your safety, the environment, and the integrity of your results.
Handling specialty chemicals, even stable ones, requires respect for the risks they carry. 4-Methyl-2-phenylpyridine isn’t notorious for acute toxicity, but working with any pyridine derivative means taking precautions. Gloves, eye protection, and fume hoods are part of every well-run lab. I’ve seen corners cut on basic protection, and the consequences range from stained hands to more serious incidents. Using basic precautions pays off not just in personal safety, but in preventing contamination of results.
One practical piece of advice: keep separate disposal protocols for nitrogen-containing organics. That way, you avoid surprise reactions in waste streams, which can cause unwanted off-gassing or safety incidents. Even routine chemicals demand respect, and building the habit of safety means you’re less likely to make the kind of mistake that lingers for days.
Transitioning a reaction from the academic bench to industrial scale isn’t as simple as pouring in more solvent. With 4-Methyl-2-phenylpyridine, reproducibility, access to larger volumes, and purity standards become make-or-break issues. My work teaching scale-up chemistry taught me that guessing at impurity levels, solvent compatibility, or batch consistency only sets projects up for failure.
Manufacturers offering kilo-scale quantities know bench-top synthesis is just the start; what matters most is keeping product quality rock solid as batches increase. At scale, costs, waste management, and logistics come to the front. Every unnecessary side reaction or impurity introduces inefficiency and regulatory headaches. Choosing a compound with a strong track record—like 4-Methyl-2-phenylpyridine—saves far more than it costs.
Recent years have seen this molecule featured in publications exploring new catalysts, organic electronics, and advanced pharmaceuticals. This isn’t just random; the balance of electron-rich methyl and aromatic phenyl groups produces intriguing coordination chemistry and adaptable scaffolds. Grant proposals in these areas frequently call out its effectiveness, especially for creating new ligands that can tune metals for precise catalysis.
Modern pharmaceutical research keeps searching for scaffolds with fine control over solubility, bioavailability, and metabolic stability. The combination of the methyl and phenyl groups often enables researchers to adjust the molecule for more selective targeting. From experience, I can say that subtle electronic variations sometimes make the difference between a hit and a miss in drug screening assays.
Another area of focus has been organic electronics, where stable aromatic compounds with tunable properties form the basis of new materials. Those working at the junction of chemistry and materials science often prefer intermediates like 4-Methyl-2-phenylpyridine for their tailorability. Having spent time collaborating on new conductive polymers, I’ve seen first-hand how small changes in core structure can multiply the range and reliability of final products.
Cutting my teeth on pyridine chemistry came with plenty of surprises. Each substitution pattern changes the entire game—miss a detail, and your expected yield drops, or your side reactions become a new main event. With 4-Methyl-2-phenylpyridine, regular use reveals a manageable learning curve. Begin by understanding its role in your reaction pathway. Its balance of electron-rich and bulky substituents tends to reduce unwanted side reactions and sharpens product selectivity. This keeps reaction troubleshooting to a minimum and lets you spend more time refining outcomes rather than putting out fires.
Relying on real-world feedback from colleagues makes a difference, too. Reading through online forums, peer-reviewed articles, or direct communication with other researchers often brings out the little tricks that make a reaction succeed. From solvent choices to reaction timing, sharing practical knowledge beats memorizing product manuals every time.
No compound solves every synthetic problem. 4-Methyl-2-phenylpyridine offers stability and selectivity, but in more nucleophilic or radical conditions, other intermediates may bring better performance. There’s also the question of cost; specialty pyridine derivatives rarely come cheap, especially at high purity or small scale.
Facing tight project budgets, I’ve seen teams weigh the upfront price versus time saved in troubleshooting and failed runs. Often, choosing reliability yields smaller long-term costs. It’s also important to check that your chosen intermediate doesn’t create bottlenecks elsewhere—like challenging purification steps, regulatory hurdles, or raw material shortages. Keeping careful track of how your selected materials perform in practice, rather than relying solely on supplier claims, will prevent painful late-stage surprises.
Advances in organic synthesis demonstrate that seemingly minor shifts in structure translate into major performance leaps. As academic groups and private companies push the boundaries of catalyst and pharmaceutical design, the demand for compounds like 4-Methyl-2-phenylpyridine isn’t fading. Instead, new uses keep emerging. Some research groups focus on C-H activation, others on asymmetric catalysis, and there’s always a buzz around next-generation OLED material pathways.
Having attended international conferences and worked alongside researchers from Asia, Europe, and the Americas, I’ve noticed a universal reliance on reliable intermediates. No matter the final application, those doing the heavy lifting behind the scenes keep coming back to compounds with proven track records and adaptable chemical profiles.
Anecdotes from the field show this compound bridging traditional and emerging technologies. In the world of materials science, the demand for stable, modifiable heterocycles mirrors the continued interest from pharmaceutical developers who need both selectivity and process-friendly characteristics. The compound you choose can shape the efficiency, safety, and success of your entire project.
The days of picking random catalogue compounds without research are over. Professionals and academics now recognize that sourcing decisions echo far beyond the immediate project. Social platforms, scholarly literature, and direct peer-to-peer advice all play a role in ensuring that the product you open today will work the same way a year from now. Sharing lessons—both successes and mistakes—helps advance the whole community. I’ve benefitted from learning about practical setbacks, such as solubility surprises or unexplained impurities, long before they reached my own bench.
Educated buyers ask questions and demand transparency. Does the vendor provide up-to-date analysis of every lot? Are there environmental reports, and does the company publish them? Do the supplier’s claims stand up to repeat testing? Sometimes these questions slow down procurement, but the payoff shows in smoother workflow, safer operations, and better research.
Real progress comes from facing up to recurring bottlenecks. For 4-Methyl-2-phenylpyridine, consistent supply and clear documentation remain the two biggest hurdles for both researchers and commercial teams. A lab stumbling over an unpredictable intermediate sees wasted months and budgets eaten up by trouble-shooting. Better supplier partnerships—founded on clear standards, robust batch validation, and straightforward communication—can wipe out those delays. I’ve worked with teams that dedicated time up front to supplier vetting and found that process failures dropped, yields went up, and the grind of tedious troubleshooting became rare.
There’s an opportunity, too, for more user-driven review sharing across the scientific community. Less reliance on filtered product sheets and more attention to real, practical feedback would help steer future buyers away from low-quality sources. As open-science continues to take root, an honest exchange of experience will help keep standards high.
Every lab or project faces choices that ripple through both workflow and results. Choosing the right intermediate—one as robust and adaptable as 4-Methyl-2-phenylpyridine—can pay off in smoother scale-up, reproducible results, and fewer last-minute headaches. It isn’t the only option for every reaction, but for those who appreciate its balance of structure, stability, and proven performance, this compound remains a favored tool. Experience shows that the right choice on the small stuff often decides the outcome of the big stuff in chemical work.
Looking ahead, the value of information and accountability in chemical sourcing—whether it’s posted in a forum, published in a peer review, or traded over lunch at a conference—can shape better science. For those shaping new molecules and new materials, a dependable intermediate does more than fill a reagent shelf; it anchors productive research, safer labs, and more innovative outcomes.