|
HS Code |
585213 |
| Iupac Name | 4-phenylpyridine |
| Cas Number | 1008-89-5 |
| Molecular Formula | C11H9N |
| Molar Mass | 155.20 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 132-134 °C |
| Boiling Point | 320 °C |
| Density | 1.11 g/cm3 |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC=C(C=C1)C2=CC=NC=C2 |
| Inchi | InChI=1S/C11H9N/c1-2-6-10(7-3-1)11-4-8-12-9-5-11/h1-9H |
| Pubchem Cid | 13576 |
As an accredited 4-Phenylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A clear glass bottle labeled "4-Phenylpyridine, 99%," containing 100 grams, sealed with a blue screw cap and safety warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Phenylpyridine: 14–16 metric tons securely packed in 200 kg drums per 20-foot full container load. |
| Shipping | 4-Phenylpyridine is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Packaging complies with international regulations for hazardous chemicals. During transit, it’s labeled according to relevant safety standards, and handling instructions are provided to ensure safe transportation. Only authorized personnel should manage the shipping process. |
| Storage | 4-Phenylpyridine should be stored in a tightly closed container, placed in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers. Keep away from sources of ignition. Store at room temperature and protect from moisture. Proper labeling and secondary containment are recommended to prevent accidental release or contamination. |
| Shelf Life | 4-Phenylpyridine has a shelf life of at least 2 years when stored in a cool, dry, and tightly sealed container. |
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Purity 99%: 4-Phenylpyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting point 143°C: 4-Phenylpyridine with a melting point of 143°C is used in organic electronic material manufacturing, where it provides thermal stability during processing. Molecular weight 169.22 g/mol: 4-Phenylpyridine with molecular weight 169.22 g/mol is used in catalyst ligand preparation, where it enables precise stoichiometric calculations. Stability temperature up to 200°C: 4-Phenylpyridine with stability temperature up to 200°C is used in high-temperature reaction processes, where it maintains chemical integrity under thermal stress. Particle size <50 μm: 4-Phenylpyridine with particle size below 50 μm is used in fine chemical formulation, where it promotes homogeneous mixing and reaction kinetics. Water content <0.1%: 4-Phenylpyridine with water content below 0.1% is used in moisture-sensitive reactions, where it minimizes unwanted hydrolysis and side reactions. UV absorbance 254 nm: 4-Phenylpyridine characterized by UV absorbance at 254 nm is used in analytical reference standards, where it facilitates accurate HPLC quantification. Chromatographic purity 99.5%: 4-Phenylpyridine with chromatographic purity of 99.5% is used in API synthesis, where it guarantees absence of critical impurities. Density 1.08 g/cm³: 4-Phenylpyridine with density 1.08 g/cm³ is used in reaction mass balancing, where it supports accurate volumetric dosing. Assay (HPLC) ≥99%: 4-Phenylpyridine meeting assay (HPLC) ≥99% is used in medicinal chemistry research, where it ensures reproducibility and reliability of bioactive compounds. |
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Drawing from my years spent in both academic and commercial laboratories, certain chemicals often become mainstays not because they are flashy, but because they reliably bridge gaps in complex syntheses. 4-Phenylpyridine has found itself in that category for a good reason. Chemists seek molecules that provide stable scaffolding, and this compound, with its simple yet sturdy pyridine ring fused to a phenyl group, helps unlock new molecular spaces. It serves as a versatile intermediate, not just in research but in the toolkit of process chemists where reproducibility and reliability make a tangible difference on a daily basis.
4-Phenylpyridine contains a pyridine structure substituted at the para position with a phenyl group. The simplicity of the naming belies the practical importance. The rigid aromatic core, combined with a nitrogen atom, presents a unique combination of electron-rich and electron-withdrawing regions. The result is a molecule that slips into a variety of reaction schemes where tuning of electronic properties matters. For example, coupling reactions benefit from its ability to stabilize transition metal complexes, and it can act as a building block for ligands in asymmetric catalysis—a crucial aspect in pharmaceuticals and materials science.
In day-to-day laboratory work, 4-Phenylpyridine stands out because it brings a welcome stability. I remember first handling it during a cross-coupling run—its solid, crystalline powder handled more like a sugar than a reactive hazard. No strange odors, no sudden discoloration, and most importantly, no finicky storage requirements. Colleagues working on the development of new OLED materials noted its reliability in forming clean, well-defined products, even under less-than-ideal conditions.
Unlike reagents that degrade rapidly in air or pick up water from the humidity, 4-Phenylpyridine sits comfortably on the shelf. I came to appreciate this after too many afternoons were lost to weighing sticky powders or re-drying unreliable stock. There’s a peace of mind that comes with reagents you can count on to behave the same whether it’s the first scoop from a fresh bottle or near the end of a project.
Synthetic and analytical chemists both look for the same things in a working material: purity, consistent physical form, and performance that matches what’s on the label. 4-Phenylpyridine usually meets these expectations, with purity levels reaching above 98% from reputable suppliers. It often appears as fine off-white crystals or powders, melting between 137 and 140 degrees Celsius. I tend to check the melting point routinely as it offers a quick confirmatory check for identity and quality beyond certificate promises.
Comparing 4-Phenylpyridine to other benzene-heterocycle hybrids helps clarify why synthetic chemists come back to it. Take pyridine itself—it’s more volatile, with a distinct fishy odor, and doesn’t offer the same extended aromatic system. 4-Phenylpyridine adds bulk and changes the electronic profile, opening different possibilities in catalysis and materials chemistry. Other phenylpyridines, like the 2- isomer, interact with metals and reagents differently due to their geometry. For example, the 2- variant tends to coordinate more strongly to metal centers, which can restrict options in catalysis. With the para-substituted variation of 4-Phenylpyridine, the less pronounced chelating ability can sometimes be an advantage by allowing greater freedom for the metal center, tailoring reactivity in ligand design.
4-Phenylpyridine sets itself apart by hitting a sweet spot: it brings enough chemical flexibility to be valuable in large-scale couplings, yet remains simple enough to avoid side-reaction headaches. In projects focused on bulk electronic materials, I’ve repeatedly seen 4-Phenylpyridine substituted in place of more expensive or sensitive analogs with little need for protocol change, leading to significant cost savings without loss of yield or product purity.
Applications drive chemical sales, not glossy brochures. In pharmaceutical routes, 4-Phenylpyridine participates as a ligand or reactant, especially in palladium-catalyzed cross-coupling. Reproducibility became a buzzword in the mid-2010s research push, but it’s always been vital in my experience—especially in combinatorial libraries, where hundreds of experiments run in parallel. A reagent that forms strong, clean bonds and releases them at the right moment proves invaluable.
I have seen teams using 4-Phenylpyridine to develop new dye architectures and light-emitting molecules. Its ability to bridge organic electronics and coordination chemistry means it turns up frequently in progress reports and patent applications. Its solid-state properties, from thermal stability to electron affinity, keep it relevant in current development cycles for OLED and photovoltaic research. Unlike compounds that require careful staging and slow addition protocols, 4-Phenylpyridine goes directly into batch processing without the need for elaborate pre-activation or protection steps.
Researchers in medicinal chemistry value efficiency but also demand purity and predictable behavior. I recall the shift in a collaborative project from a halogenated aromatic to 4-Phenylpyridine as a core structure. The move improved not only yields but also reduced by-product profiles, simplifying purifications and cutting days off timelines. In tight regulatory environments, the benefit of less complicated purification procedures resonates from the early stages of candidate selection to the scale-ups required for clinical production.
Choosing among available batches and suppliers requires careful evaluation, especially as research funding tightens and laboratories seek more value for money. Chemists find that sources providing rigorous spectral data and traceability engender trust. I always prefer those that publish detailed NMR, GC-MS, and elemental analysis data, since reproducibility starts with chemical certainty. My own best results have come from batches whose data met or exceeded industry certification standards—subtle impurities can skew yields and reaction outcomes, making up-front diligence essential.
Grain size, moisture content, and purity only tell part of the story. True differentiation comes from experience with both product and supplier: technical support that can answer tough questions, quick fulfillment in emergencies, and transparent batch variation data. Previously, I encountered supply interruptions that forced substitution with “just as good” analogs, but found they never quite matched the performance profiles—stresses on reactivity, handling, and downstream product quality confirmed that not all 4-Phenylpyridines function identically.
Interest in sustainable sourcing grows stronger each year. Younger scientists entering the field consistently ask about feedstock origin and the environmental impact of chemical manufacture. 4-Phenylpyridine, by design and production, traces its lineage to both petrochemical and emerging biobased approaches. Responsible producers share information on waste minimization and alternatives to hazardous solvents used during synthesis.
My own experience reviewing supplier ESG (Environmental, Social, and Governance) reports has shown that the best outcomes arise when buyers push for disclosure about environmental footprints and labor practices along the entire supply chain. Forward-thinking vendors have begun implementing green chemistry principles in synthesis of standard organics, from process water recycling to carbon emissions tracking. Clear product documentation and transparent reporting encourage informed decisions when choosing regular sources for 4-Phenylpyridine.
Chemical availability and supply volatility challenge researchers worldwide. When a preferred reagent like 4-Phenylpyridine becomes hard to source, timelines stretch and costs rise unpredictably. Open communication with suppliers can help build reliable stock strategies—diversifying sources, maintaining safety stock, and partnering with distributors who alert clients early to potential shortages smooth project cycles.
These lessons became vital during global supply shocks, where even basic research could stall for weeks over a missing intermediate. Strong supplier relationships, along with a habit of reviewing multiple lot numbers and production dates, mean fewer surprises. I’ve met chemists who keep their favorite sources on speed dial—such is the need for reliability and responsiveness in synthetic work.
Another longstanding challenge involves counterfeit or off-specification chemicals entering the market. Dedicated quality control makes a critical difference. Rigorous in-house or third-party validation supplements the sometimes optimistic claims from unknown labels. Across my career, small investments in routine NMR or melting point checks paid back in saved time and avoided ruined experiments.
Reliable data support good decisions. Chemists and engineers often publish reaction procedures involving 4-Phenylpyridine with explicit details about batch numbers, supplier, and purity. This attention to transparency allows others to replicate findings, troubleshoot issues, and improve upon published work. I have seen projects rescued by cross-referencing published data and realizing an obscure impurity explained a puzzling result.
Open sharing of both successful and failed uses of 4-Phenylpyridine, through preprints, supplementary files, and candid technical forums, fosters a healthy research culture. Broad access to technical bulletins and honest supplier communication empowers users to spot problems before they escalate—a practice increasingly valued in both academia and industry.
The jump from small-scale lab work to real-world application can feel immense, but certain molecules earn their place as reliable platforms. Materials scientists have pressed 4-Phenylpyridine into service as both a component and a structural motif in emerging ligands, dendritic architectures, and tunable supramolecular assemblies. It provides rigidity without excessive bulk, so developers in OLED and organic semiconductors deploy it to fine-tune photophysical properties.
This flexibility stands in contrast to benzothiazole or carbazole derivatives, which offer niche advantages but sometimes border on the unwieldy. The moderate molecular weight and clean handling make 4-Phenylpyridine a natural choice for scale-up—one I regularly recommend when training new hires tasked with bridging synthesis and engineering. Projects aiming to translate from bench to commercial production look for candidates that act predictably across thousands of batches, and 4-Phenylpyridine delivers that reassurance.
Quality assurance in chemical manufacturing marks the difference between a research curiosity and a trusted staple. Tight control of synthetic routes, proper isolation steps, and comprehensive analytical testing define a respected source. I once followed the journey of a shipment from initial synthesis to final packaging, discovering that each transfer risked introducing impurities or moisture—consistent training and clear standard operating procedures reduced these risks.
End users on the lab floor value traceable data: HPLC chromatograms, NMR spectra, and clear expiration timelines support confidence in each batch. Sometimes it is the attention to seemingly minor details—screw caps sealed with PTFE liners, inert gas purging before shipment, or transparent lot histories—that offers peace of mind to those running sensitive reactions.
I’ve used 4-Phenylpyridine as an example in teaching students the nuances of aromatic chemistry and ligand formation. Its chemical structure illustrates resonance effects, substitution patterns, and their influence on reactivity. Discussing it bridges theory and practice, helping newcomers grasp the interplay of molecular electronics and real-world function.
Best practices stress thoughtful storage—keeping it dry, away from corrosive atmospheres, and protected from extended exposure to strong light. Packaging often includes amber vials or protective barriers to prevent degradation, and simple labeling ensures year-to-year consistency. From high school educators to pharmaceutical manufacturing managers, clear protocols keep this compound a reliable performer.
In group settings, sharing experiences about handling quirks or challenging reactions helps flatten the learning curve for junior staff. Veteran chemists pass on lessons about avoiding contamination from scoopulas or recognizing subtle changes in texture—a slightly clumped powder might indicate moisture ingress, prompting a fresh sample and quick analytical check.
No chemical tool is without limitations, and forward progress means recognizing these honestly. While 4-Phenylpyridine generally resists oxidation and hydrolysis, some synthetic pathways still generate by-products that complicate downstream processing. Improved purification protocols, continuous process monitoring, and exploration of new derivatization strategies all help extend its utility.
Efforts to minimize solvent use or transition to greener alternatives during its manufacture find growing acceptance in institutions committed to sustainable practices. Input from end users drives suppliers to redesign processes, capturing waste heat or recycling intermediates to lower environmental burdens. This feedback loop benefits everyone using 4-Phenylpyridine, from individual researchers to global manufacturers.
As chemists, we select tools based on a blend of technical needs, past experience, and evolving project demands. 4-Phenylpyridine consistently earns a place due to its dependable physical profile, chemical resilience, and ability to advance both research and industrial goals. Its track record, supported by transparent data and supplier accountability, continues to inspire trust across a wide range of applications.
The future of chemical sourcing leans heavily on openness—clear documentation, accessible quality metrics, honest discussion of strengths and weaknesses. For those seeking a balance between performance, cost, and safety, 4-Phenylpyridine presents an enduring example of practical chemistry that thrives at the intersection of tradition and innovation.