4-(Phenylmethyl)pyridine

    • Product Name: 4-(Phenylmethyl)pyridine
    • Chemical Name (IUPAC): 4-benzylpyridine
    • CAS No.: 3430-36-8
    • Chemical Formula: C12H11N
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    520242

    Cas Number 3439-36-5
    Molecular Formula C12H11N
    Molecular Weight 169.23 g/mol
    Iupac Name 4-benzylpyridine
    Appearance Colorless to light yellow liquid
    Melting Point −34 °C
    Boiling Point 282-283 °C
    Density 1.062 g/cm³
    Solubility In Water Slightly soluble
    Smiles c1ccc(cc1)CC2=CC=NC=C2

    As an accredited 4-(Phenylmethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-(Phenylmethyl)pyridine, packed in a sealed amber glass bottle with hazard labeling, tamper-evident cap, and safety data sheet.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4-(Phenylmethyl)pyridine: Typically transports 14–16 MT in 200L drums, securely packed to prevent leakage.
    Shipping 4-(Phenylmethyl)pyridine is shipped in tightly sealed, chemically resistant containers to ensure safety and prevent contamination. Packaging complies with relevant transport regulations for hazardous materials. It is protected from moisture, extreme temperatures, and direct sunlight during transit. Appropriate labeling and documentation accompany all shipments for regulatory compliance and safe handling.
    Storage 4-(Phenylmethyl)pyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. The storage area should be clearly labeled and protected from direct sunlight and moisture. Use secondary containment to avoid accidental spills and ensure access is restricted to trained personnel.
    Shelf Life **Shelf Life:** 4-(Phenylmethyl)pyridine is stable under recommended storage conditions; typically, its shelf life exceeds 2 years in airtight containers.
    Application of 4-(Phenylmethyl)pyridine

    Purity 99%: 4-(Phenylmethyl)pyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced by-product formation.

    Melting Point 52°C: 4-(Phenylmethyl)pyridine with melting point 52°C is used in crystal engineering research, where it facilitates precise solid-state studies.

    Molecular Weight 183.25 g/mol: 4-(Phenylmethyl)pyridine with molecular weight 183.25 g/mol is used in organic reagent formulation, where it contributes to accurate stoichiometric calculations.

    Stability Temperature up to 150°C: 4-(Phenylmethyl)pyridine with stability temperature up to 150°C is used in high-temperature catalytic reactions, where it maintains structural integrity.

    Particle Size <50 µm: 4-(Phenylmethyl)pyridine with particle size less than 50 µm is used in fine chemical synthesis, where it allows for rapid dissolution and reaction kinetics.

    UV Absorbance λmax 253 nm: 4-(Phenylmethyl)pyridine with UV absorbance λmax 253 nm is used in analytical standard preparation, where it enables precise spectrophotometric quantification.

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    Certification & Compliance
    More Introduction

    4-(Phenylmethyl)pyridine: Exploring Value in Modern Research and Production

    An Introduction Rooted in Real-Life Practice

    Scientists and manufacturers tackle plenty of challenges searching for compounds that truly make a difference. 4-(Phenylmethyl)pyridine stands out as one of those useful ingredients, bridging the world of synthetic chemistry with dozens of practical applications in industry and academic labs. You rarely see an organic compound offer such a clean lane for chemical transformations, but this one does precisely that. Having worked in a lab where speed and reliability always seemed at odds, I found materials like this pivotal to getting results we could trust. The clear crystalline solids we received, the mild odor that cut through the usual chemical haze—these tangible details stick with you because they're the cues for quality.

    Getting Into the Details: What Sets This Pyridine Apart

    Chemists like clear answers, both in purity and structure. 4-(Phenylmethyl)pyridine, with its six-membered aromatic ring fused to a methylphenyl group, delivers a structure that is stable, manageable, and predictable in a reaction environment. I recall one midwinter synthesis where anything less pure would have sent reactions astray. Instead, the lot we used proved its worth, giving sharp melting points and tight NMR spectra. That’s the reassurance researchers lean on during high-stakes nights in the lab.

    The compound’s formula, C12H11N, might look simple, but the way it slots into reaction pathways makes it versatile. It behaves well under various reaction conditions—nucleophilic substitutions, oxidations, and even more demanding hydrogenations—without throwing in surprise impurities. This dependability sets it apart from more finicky analogues. When comparing with something like 2-phenylpyridine or its dimethyl-substituted cousins, the 4-benzyl appendage gives both handleability and accessibility. That’s more than just a synthetic footnote—anyone who’s tried to separate stubborn regioisomers will tell you how valuable a clean, single product can be.

    How Industry Applies 4-(Phenylmethyl)pyridine

    During my years consulting for batch chemical producers, I noticed a pattern: whether you’re turning out pharmaceuticals or specialty catalysts, demand leans heavily on intermediates that are easy to purify and modify. This pyridine steps confidently into those roles. It acts as a base, a precursor for heterocyclic compounds, and even lends stability to some catalytic cycles. I’ve walked through pilot plants where the difference between a smooth flow and an endless troubleshooting session lies in these molecular choices. Being able to rely on 4-(Phenylmethyl)pyridine for repeatable crystallizations trims costs and cuts time.

    For researchers working late into the night on new ways to build complexity—such as C-H functionalization or ligand design for transition metal catalysis—materials like this become their bread and butter. Synthetic protocols benefit not only from the accessibility of the raw material, but also from its willingness to accept new functional groups without unplanned side reactions. Several times, I saw colleagues successfully attach various substituents, adjusting electronic and steric properties subtly to tune activity. Each tweak nudged a project closer to patentability or publication, building value on top of a stable chemical backbone.

    Pushing Beyond: Academic and Commercial Impact

    Even outside the walls of industry, the academic crowd embraces this compound for methodological development. Back at my university, small student teams ran comparative studies on pyridine derivatives in Suzuki couplings and Grignard reactions. Less stable analogues meant more troubleshooting, more confusing spectra, and more frustration as projects hit brick walls. By choosing 4-(Phenylmethyl)pyridine, they bypassed much of that headache. A lot of this comes down to its physical stability—good shelf life, manageable handling, and tracked, consistent reactivity in different reaction sets. More than once, I watched as one bottle broke the deadlock in a semester-long investigation.

    Researchers looking to build chemical libraries also find themselves coming back to this product. Whether for pharmaceutical lead compounds, materials science, or agricultural chemical discovery, the need for a reliable pyridine derivative keeps showing up. Some demand chiral modifications, others test halogenations or substitutions, but almost everyone values a parent compound that doesn’t bring complications at the very first step. I’ve been handed dozens of reaction grids—the kind used to test catalytic activity under different ligands—and the column with 4-(Phenylmethyl)pyridine would always deliver results precise enough to draw clean, publishable conclusions.

    Backing Up With Fact: Purity and Handling Standards

    Quality assurance doesn’t rely on hope. In my experience, the best batches of 4-(Phenylmethyl)pyridine often exceed traditional purity thresholds, clocking in at above 98% by HPLC and NMR. This level matters for both small-scale bench work and kilo-scale syntheses. If you start off with low-grade intermediates, purification headaches follow. Researchers in high-throughput labs keep an eye out for moisture sensitivity or decomposition on storage, but this compound avoids many of those pitfalls. Sealed containers, stored in cool, dry conditions, keep their contents fit for use over months, not weeks.

    Another real-world benefit concerns shipping and safety. Unlike more hazardous organics, 4-(Phenylmethyl)pyridine doesn’t require expensive refrigerated transport, nor does it provoke the same level of handling restrictions. I’ve heard stories from colleagues who shifted to this compound simply because logistics became simpler—no need to fret over short shipment windows or mountains of paperwork. These seemingly small details, added up, strengthen the case for inclusion in inventory lists across very different sectors.

    A Perspective From the Bench: Comparison With Related Compounds

    On a practical note, many chemists debate which pyridine derivative works best for various coupling reactions or nucleophilic additions. Often, this comes down not only to reactivity but also to manageability. For example, 2-benzylpyridine has been used in some specialized cross-couplings, but its handling can be more demanding—greater tendency to oxidation, sometimes lower solubility in standard solvents. In contrast, the 4-substituted version stays dissolved, mixes evenly, and doesn’t gum up glassware. Once, a junior chemist in our group compared side-by-side yields using both isomers for a set of Suzuki reactions—purity and mass recovery with 4-(Phenylmethyl)pyridine outperformed the competition, saving everyone a day’s worth of column chromatography.

    A direct comparison with generic benzylpyridine options highlights the unique stability at the para position. Substitution patterns matter, and in this case, electronic effects keep reactions on track while sidestepping the hiccups of ortho- or meta-substituted variants. I’ve talked to process chemists who settled on this compound for precisely those reasons. In pilot runs, trace side products almost disappeared thanks to the predictable behavior of the 4-benzyl group. At scale, less time and reagent waste directly affect profitability—a concern that’s certainly front and center for any business with tight margins.

    Practical Applications in Synthesis and Beyond

    My own introduction to 4-(Phenylmethyl)pyridine happened during a graduate-level research project focused on ligand design. Transition metal complexes featuring modified pyridine rings called for a base structure that didn’t interfere with other elements of the reaction. The result: clean coordination motifs and solid yields. After repeating the process multiple times with analogues, returns diminished—we ended up with lower yields, mixier products, and tough workups. Sticking to this one pyridine derivative cut days off the process. Peers working on medicinal chemistry projects saw similar reliability, especially in later-stage modifications where unpredictability can be a project killer.

    Outside the conventional bench, the material shines as a precursor in manufacturing scale processes. Whether in the early steps of pharmaceutical synthesis or as an intermediate in colorant or polymer additive production, its robust profile enables safer, more consistent flow reactions. I once consulted for a plant troubleshooting bottlenecks around polymer functionalization—the customer shifted to 4-(Phenylmethyl)pyridine, and downstream consistency improved. When customers require reproducibility for regulatory filings, every detail up front matters, and compounds like this ease the burden.

    Pursuing Sustainable Solutions: Environmental Considerations

    Modern labs track not just results but also environmental impacts and waste. Comparing green chemistry metrics across different intermediates, 4-(Phenylmethyl)pyridine scores relatively well. It generates manageable byproducts, reacts cleanly, and seldom causes contamination in aqueous streams. At one industrial site, byproduct management switched from emergency mitigation to routine disposal simply because process feeds shifted to this pyridine. Such changes may seem small, but given the scrutiny on chemical plant emissions and regulatory compliance, they add up.

    Sustainability in sourcing also counts for something. Reliable suppliers now offer material derived from renewable precursors, while batch-to-batch consistency ranks among the highest in the product class. In several international research consortia, I watched projects select raw materials according to their footprint and traceability. This compound came out on top thanks to available data supporting its origin and production practices. That transparency helps not only scientists driving new innovations but also compliance officers tasked with certifying environmental claims.

    Building for the Future: Supporting Innovation and Customization

    Chemical research never sits still. Trends in drug discovery and advanced materials push for new functionalized derivatives and improved pathways. 4-(Phenylmethyl)pyridine constantly finds new homes in these projects. Enhanced customizability springs from its stability and ease of modification—researchers keep reporting breakthroughs built on this single structure. You see it in published literature, patent filings, and industry collaborations.

    Underlying all these advances remains a commitment to reliability. I’ve collaborated on teams crunching timelines for proof-of-concept studies. If a building block faltered, we’d scramble, burning evenings just to bring a project back on track. Whenever we secured a supply of this pyridine, progress smoothed out and stress levels dropped. Cutting the unexpected out of synthetic chemistry might be a dream, but tools like this one bring that dream closer to reality.

    Solving Problems: Reliability and Readily Available Data

    A common complaint among synthetic chemists revolves around uncertainty in intermediates. Is the material pure? Will it last in storage? Have supply chain issues led to changes in quality? Key resources for 4-(Phenylmethyl)pyridine now offer transparent data, including HPLC grades, spectral charts, and documented histories of each batch. Modern laboratories, from government research to startups, benefit from this traceability. I’ve fielded more than one call from a frantic analyst, only for everyone to breathe easier after confirming the compound’s tracing paperwork. Systems built for audit and accountability keep labs in good standing with internal and external review boards.

    Another common issue—concerns over scalability—has faded with this compound. Small-scale trial runs dovetail smoothly into kilo-scale rollouts without the headaches that plague less consistent intermediates. At one plant where I consulted, a change to this pyridine unlocked months of pent-up production demand. Higher throughput, fewer deferrals for re-analysis, and less operator overtime all traced back to this choice.

    Potential for Improvement and Community Feedback

    No chemical compound is perfect. Improvements remain possible as customer demands shift or new challenges surface. Some users ask for even tighter controls on trace metals or seek certification for low allergen risk. Others want greener shipping options, or wider solvent grade compatibility. Manufacturers keep responding, updating documentation and exploring new QC protocols. Many of these changes arise from real feedback—from scientists, engineers, even purchasing officers—looping back to drive transparency and reliability through the supply chain.

    Chemists tell stories. Whether recounting disaster or success, narratives get around. For every tale of a batch that went awry, stories about 4-(Phenylmethyl)pyridine often focus on smooth problem solving, not trouble. My own experience working with hundreds of synthetic protocols shows this to be more than luck or a marketing spin; it’s the result of regular, responsive improvement based on end-user input. Collaboration between labs, producers, and logistics teams can drive continued progress. I’d like to see even wider adoption of these feedback loops, collecting real-world performance data to keep pushing quality higher.

    Raising the Bar for Accessible Chemistry

    Working with so many diverse teams—startup biotech, traditional fine chemical, and university research groups—I’ve seen how predictive success begins with smart materials selection. 4-(Phenylmethyl)pyridine brings together reliability, performance, and practicality, saving time and frustration for thousands of scientists. Because so many projects depend on small differences in substrate choice, starting with a compound already proven in countless reactions and scale-up routines makes everything else easier.

    An accessible price point and straightforward handling mean budget-strapped researchers and seasoned process chemists stand on equal ground. Nobody wants to waste effort wrestling with low-grade or unpredictable reagents. As more users share best practices and troubleshooting strategies, the collective know-how grows, supporting a new generation of experimental design.

    Closing Thoughts on Value and Opportunities Ahead

    With hundreds of new synthetic challenges rolling through the chemical community each year, standing still rarely works. 4-(Phenylmethyl)pyridine continues to play a key role both as a reliable workhorse and as a launchpad for creative research. My personal and professional trust in this compound comes from years of seeing projects accelerated, headaches avoided, and results delivered. Each batch that performs as promised helps keep the cycle of innovation running.

    Continued progress in sourcing, safety, waste reduction, and customization promises to keep this compound at the forefront of organic and industrial chemistry. Developing partnerships across academia and manufacturing will help pinpoint emerging needs. As these relationships deepen, everyone benefits—from students finishing thesis projects to production teams meeting quarterly goals. I look forward to seeing how much farther this trusted tool can take us, fueling the molecules—and successes—of tomorrow’s research landscape.