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HS Code |
877045 |
| Chemical Name | 2-(4-Methylphenyl)pyridine |
| Molecular Formula | C12H11N |
| Molecular Weight | 169.22 g/mol |
| Cas Number | 31859-35-7 |
| Appearance | White to pale yellow solid |
| Melting Point | 54-57°C |
| Boiling Point | 314-315°C |
| Density | 1.08 g/cm³ |
| Smiles | CC1=CC=C(C=C1)C2=CC=CC=N2 |
| Inchi | InChI=1S/C12H11N/c1-10-5-7-11(8-6-10)12-3-2-4-9-13-12/h2-9H,1H3 |
As an accredited 2-(4-Methylphenyl)Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with screw cap; white label displays "2-(4-Methylphenyl)Pyridine, 25g", CAS number, and hazard warnings. |
| Shipping | 2-(4-Methylphenyl)pyridine is shipped in tightly sealed containers to prevent contamination and volatilization. It is packaged in accordance with chemical safety regulations, protected from moisture and light, and labeled with hazard warnings. Transport is conducted following local and international guidelines for laboratory chemicals to ensure safe, compliant delivery. |
| Storage | Store 2-(4-Methylphenyl)pyridine in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from strong oxidizing agents and incompatible materials. Ensure proper labeling and restrict access to trained personnel. Follow standard chemical storage protocols and consult the safety data sheet (SDS) for additional precautions. |
Applications of 2-(4-Methylphenyl)Pyridine in Industrial Manufacturing2-(4-Methylphenyl)Pyridine serves as a specialized intermediate in select advanced materials and fine chemicals sectors. Below, we detail authentic industrial downstream applications—strictly aligned with documented use cases—focusing on differentiated compliance, formulation, process, and final product requirements as observed in manufacturing environments. 1. OLED Display Emitting Layer SynthesisManufacturers employ this compound as a ligand precursor in the production of iridium-based phosphorescent emitters, contributing to color tuning for blue and green light emission in OLED display panels. This application leverages its structural role, photophysical properties, and compatibility during complex synthesis, positioned during the precursor feedstock stage to enable final device efficiency improvements at the nanomaterial interface. Industry compliance standards
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2. Heterocyclic Active Pharmaceutical Ingredient IntermediateThis compound acts as a core building block in the multi-step synthesis of pyridine-based active pharmaceutical ingredients, typically for anti-inflammatory and CNS therapeutic agents. Process chemists select the material for its electronic influence on the pyridine ring to achieve selective functionalization and downstream coupling precision during advanced synthesis routes carried out in cGMP-compliant environments. Industry compliance standards
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3. Ligand Precursor for Homogeneous CatalystsChemical and specialty materials manufacturers utilize this molecule as a precursor in synthesizing custom ligands for transition metal complexes, enabling efficient homogeneous catalysis in fine chemical production, including cross-coupling and selective alkylation reactions. Its electronic profile allows tuning of catalytic selectivity and activity, with process engineers overseeing rigorous inclusion protocols for downstream reaction reproducibility. Industry compliance standards
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4. Architectural Building Block for Specialty PigmentsThe compound functions as a heterocyclic precursor for manufacturing high-performance dye molecules—specifically, in the creation of colorants with enhanced photostability for printing ink formulations and security markings. Specialty pigment manufacturers rely on its aromatic-pyridine skeleton to achieve desirable absorption and longevity parameters required for high-end graphic and security material applications. Industry compliance standards
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At the plant, every batch of 2-(4-Methylphenyl)Pyridine tells the story of reliability and focus. Years of refining production have taught us that customers count on consistent purity to unlock the compound’s potential across a range of advanced synthesis projects. It goes by its molecular structure—where the 4-methylphenyl group attaches at the second position of the pyridine ring—and this unique arrangement remains the core reason chemists seek it out. Our work with this compound extends across pharmaceuticals, ligands for catalysis, and specialty materials that underpin research and commercialization.
Our in-house controls set purity well above 98 percent, based on HPLC, while moisture stays below 0.2 percent at time of dispatch, as measured by Karl Fischer titration. Years of troubleshooting have convinced us to sharpen focus on real stability, not just numbers on a spec sheet. In storage, the powder remains free-flowing and easy to weigh because drying protocols and packaging procedures prevent clumping. Particle size sits within a narrow range, minimizing handling hiccups whether material heads to a kilo-lab or full scale reactor. Color typically runs off-white, sometimes faintly yellow if exposed to light above a certain level—a known trait, monitored closely at quality checkpoints.
Processes for aromatic coupling have evolved a lot since the early days. Early on, one-pot methods brought yield headaches, sparking years of small tweaks, from catalyst choice to solvent swaps. Today, each batch proceeds through defined reaction stages, often under an inert atmosphere, before filtration, workup, and a carefully monitored crystallization. Operators track temperature control with digital systems, and purging lines with dry nitrogen keeps oxygen out, protecting every lot from degradation. Every step gets logged and reviewed as part of ongoing process improvement, not just regulatory compliance.
Researchers have shared direct feedback over the years—good product means fewer repeats, stronger signals in NMR and LC-MS, better yields when moving to next steps. That feedback shapes our attention to trace impurity profiles, especially since certain byproducts—like traces of methylbiphenyl or incompletely halogenated precursors—can seriously trouble a downstream Suzuki coupling or hinder palladium complexation. We screen for these at levels below 0.1 percent. That discipline came from troubleshooting customer syntheses, not just following V-signed certificates.
2-(4-Methylphenyl)Pyridine often does its work as a building block in preparation of pharmaceutical intermediates. Synthetic chemists lean on its stability under standard base and acid conditions, which means it doesn’t degrade or polymerize in multi-step processes. In catalysis, demand remains steady for its use in designing ligands—an area where minor structural changes can swing activity and selectivity up or down. Its aromaticity and electron distribution give it a distinct profile, and organometallic teams have used it in novel cyclometalated complexes for OLED research and cross-coupling catalyst libraries.
Sometimes a researcher asks if they really need 2-(4-Methylphenyl)Pyridine or if another substituted pyridine could serve. We’ve run head-to-head trials with analogues—4-methyl vs. 3-methyl, methylphenyl vs. phenyl, and the results are never interchangeable. Position and substitution actually change reactivity: the 4-methyl increases electron-donating power, and the 2-position on the pyridine dictates how it coordinates to metals or conjugates in coupling reactions. If you swap structures, reaction rates change, side-products pop up, and in downstream analysis, yields rarely match initial projections.
One of the biggest shifts came when biopharma customers started pushing for tighter analytical results. Instrument calibration grew sharper, auditors made surprise stops, and operators had to keep meticulous logs of every step. In the old days, an extra wash or longer drying seemed minor; now, every tweak translates to verifiable results on the certificate of analysis. That rigor paid off long-term, helping our batches deliver reproducible performance not only in R&D but also in final product manufacturing.
Shipping standards matter too. We never ship in drums that held oxidizing agents, and each lot flows into high-barrier packaging that blocks light and moisture. Blow-molded HDPE jars inside aluminum-lined boxes became standard, based on a handful of customer complaints about caked powders a decade ago. All those packaging upgrades came from real lessons on the shop floor, not theory or sales promises.
Some users have asked how well 2-(4-Methylphenyl)Pyridine holds up to extended storage. Each lot survives accelerated aging tests: heating samples at 40°C for weeks while monitoring for discoloration or formation of tars. In our own stores, sealed containers show no degradation for over three years, as long as temperature stays below 30°C and direct sunlight stays away. That durability helps, since research timelines often stretch out or pivot midway.
Powdered products will always bring some dust, but formula tweaks since 2016 yielded a granularity that minimizes airborne load. That’s been a big win for users in kilo-labs with shared bench hoods. Our technical support often fields questions on solubility in polar aprotic solvents or whether flash chromatography gives acceptable separation. For this compound, it dissolves efficiently in DMSO, DMF, and ethyl acetate, though crystallization from hexane gives higher purity in most rework cases.
As a manufacturer, seeing the full batch cycle—raw materials in, material out, feedback looping back in—has taught us what separates strong compounds from the also-rans. Some products move well with just a decent purity and a tidy appearance. For 2-(4-Methylphenyl)Pyridine, repeat buying happens only if downstream results stay consistent. Our experience has shown that tiny details—like holding batch temperature steady within a half degree at condensation, or checking residual solvent not just at dispatch but also after transit—are what keep complaints low and repeat business high.
Other suppliers may offer this compound with a more relaxed impurity profile aimed at non-critical uses, but we have seen how that leads to trouble. In catalysis work, even subtle byproducts that pass general tests can wreck a ligand’s coordination or slow down an otherwise robust transformation. Partners in green chemistry projects want proof that feedstock sources follow good manufacturing practice and traceability. That’s why tracking each step, batch coding, and even video documentation during packaging helps us back up each shipment with hard evidence.
Every so often, a project throws a curveball—an academic team struggling to get a metal complex to crystallize, or a contract researcher unable to remove a trace of pigment from their final product. Over time, this has led to pushing our detection limits lower for iron, copper, and halide residues. Academic partners in one catalysis consortium gave direct feedback: side-by-side work with our material and a competitor’s showed sharper NMR signals, higher isolated yields, and less post-reaction processing. This kind of feedback beats any spec sheet for real-world validation.
Years ago, a pharmaceutical customer pointed out that a faint impurity co-eluted in their HPLC check. We worked with them, adjusting one wash process and switching a filtration aid. Subsequent lots dropped that impurity below their detection threshold. These adjustments take time, but direct collaboration often uncovers improvement that standard test protocols might miss.
What sets 2-(4-Methylphenyl)Pyridine apart often comes down to fit in complex syntheses. In building transition metal catalysts, the arrangement of substituents affects not just reactivity, but also color, solubility, and thermal stability. Research groups building OLED materials find that purity shifts optical behavior in meaningful ways. Their spectra narrow; device efficiency increases; lab techs spend less time troubleshooting off-target emission or non-uniform films. Little details—clear melting point, single-peak NMR, or successful recrystallization cycles—let process chemists and graduate students move faster and with more confidence.
From a practical standpoint, this compound’s clean reaction profile means waste streams carry fewer byproducts, translating to easier downstream workup. Synthetic procedures for coupling, especially Suzuki or Buchwald-Hartwig routes, benefit because unreacted starting material runs cleanly and doesn’t gunk up purification columns.
Factory support extends beyond shipping product. We compare data with clients, sharing batch-by-batch spectra, discussing potential sources of trace impurities, and sometimes reworking a lot to meet a project’s critical threshold. For those working in patent-driven environments, documentation and raw data files move with the shipment, allowing chemists to publish or file IP with full confidence in traceability. Our own plant holds sample archives as backup, letting users request a recheck even years later.
We have noticed that industry partners in high-value synthesis rarely accept “close enough”—an attitude that’s encouraged higher scrutiny over standard methods. Realistically, many end-users check for data reproducibility after long-term storage or after transfers between facilities. Our own stability checks echo this—confirming that color, purity, and reactivity persist after months on the shelf or even after intercontinental shipping.
Whether an order covers a hundred grams for a pilot study or dozens of kilos for a production campaign, keeping every lot aligned with the last one means fewer headaches for everyone. We build in buffer stock and document every lot’s property set, so that quickly resupplying a customer on an accelerated timeline never risks a drop in performance. This kind of practical reliability helped us build trusted relationships with research labs, pharma start-ups, and even those scaling toward industrial manufacture of active ingredients.
To this day, most repeat customers come back not just for a product but for confidence in what it delivers throughout long and expensive projects. The ability to call the factory and get technical answers about handling, shelf life, or impurity questions—without being bounced around to third parties—has turned many of our early one-off orders into ongoing partnerships. Our plant staff knows that one uncertain bottle can undo years of trust, so quality sits at the top of every batch’s priorities.
As regulatory demands tighten worldwide, we see ongoing pressure for ever-better traceability, sustainability, and documentation. Responding early, we’ve audited raw materials and increased screening for regulated substances. The team keeps an eye on solvent recycling and energy usage, aiming to stay ahead of environmental requirements before they become mandatory. Periodically, we participate in inter-laboratory comparison studies to ensure our product data matches best-in-class standards globally—not just regionally.
Technical advances in spectroscopy and chromatography over the past decade give deeper views into the compound’s profile than older UV or melting point checks. We continually upgrade instrumentation, and every shift in protocol gets tested in parallel to make sure results remain comparable batch to batch.
Those new to synthetic pathways might ask if 2-(4-Methylphenyl)Pyridine could be swapped with related molecules on the shelf. Through direct observation in the field, we’ve seen that even small changes—like moving the methyl group to the ortho or meta position, or using non-methylated phenylpyridines—always bring trade-offs. Reactivity drops, yield falls, catalytic activity shifts. Spectra reveal minor differences that translate to downstream bottlenecks for teams pushing timelines. We have also seen that some analogues may carry lower costs but introduce higher solvent needs, longer purification times, or form persistent side-products. The choice to use the right compound pays off many times over at the end of a project, not just when crunching starting material costs at the outset.
Our production notes track all such comparisons. For each new variant, pilots run in lab reactors, checking not just for lab-bench success but also for cleaning and recycling outcomes. Feedback proceeds both directions: if internal teams uncover a problem or an improvement, it finds its way into the next production batch. Years of applying this closed feedback loop have shown that there’s no substitute for continuous communication between production, quality, and real-world users.
Manufacturing 2-(4-Methylphenyl)Pyridine is not just about meeting published standards; it’s about continuous improvement driven by evidence from the lab, the plant, and the end-user. Each batch is a composite of hard-won lessons, real collaboration with the scientific community, and the insistence that every gram shipped actually performs in the projects that matter most to our customers. The people running the reactors and analyzing the outputs at the plant see every return customer and positive report as confirmation that attention to detail delivers real progress in chemical innovation.
By focusing on practical outcomes, open communication, and technical rigor, we see our role not just as suppliers, but as partners in innovation that enable discoveries to move from bench to production, with the confidence that comes from real experience and a commitment to doing things right.