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HS Code |
920896 |
| Name | 3-Ethynylpyridine |
| Cas Number | 536-78-7 |
| Molecular Formula | C7H5N |
| Molecular Weight | 103.12 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 187-188 °C |
| Melting Point | -32 °C |
| Density | 1.047 g/cm3 |
| Flash Point | 68 °C |
| Refractive Index | 1.581 |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Synonyms | 3-Pyridylethylene, m-Ethynylpyridine |
| Inchi | InChI=1S/C7H5N/c1-2-7-4-3-5-8-6-7/h1,3-6H |
| Smiles | C#CC1=CN=CC=C1 |
As an accredited 3-Ethynylpyridine 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 labeled "3-Ethynylpyridine," featuring hazard symbols, safety information, and manufacturer details for laboratory use. |
| Shipping | 3-Ethynylpyridine is shipped as a hazardous material due to its flammability and potential health effects. It must be packaged in tightly sealed containers, cushioned to prevent breakage, and labeled according to regulatory standards. Delivery typically requires ground or specialized carriers in compliance with local, national, and international transport regulations. |
| Storage | 3-Ethynylpyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated place, away from sources of ignition and incompatible substances. Keep it away from heat, open flames, and oxidizing agents. Store under an inert atmosphere if possible to prevent degradation. Ensure proper labeling and use chemical-resistant secondary containment to prevent accidental leaks or spills. |
Applications of 3-Ethynylpyridine in Industrial Manufacturing3-Ethynylpyridine is an advanced pyridine derivative extensively adopted in specialty chemical and pharmaceutical manufacturing. As the original producer, we support global partners in precise application fields where high-purity intermediates, controlled reaction steps, and reproducible integration are critical to final product quality. 1. Active Pharmaceutical Ingredient (API) Intermediate for Antineoplastic AgentsAPI manufacturers incorporate 3-Ethynylpyridine in multi-step syntheses of targeted oncology drug molecules, specifically for constructing pyridine-modified ring systems via Sonogashira couplings and nucleophilic addition. The compound functions as a core-building block where trace impurities or structural isomers directly impact regulatory submissions and final compound safety profiles. Customers adjust input ratios to balance reactivity and impurity control depending on molecule-specific route designs. Industry compliance standards
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2. Agrochemical Active Ingredient Synthesis (Herbicide & Insecticide Intermediates)Agrichemical producers utilize 3-Ethynylpyridine as a critical intermediate in the synthesis of heterocycle-rich actives, integrating the pyridyl-ethynyl motif into complex molecular scaffolds that influence herbicidal or insect-repellent activity. The compound enters acetylenic coupling sequences to functionalize parent molecules for improved field stability and biological selectivity, contributing directly to the differentiated performance in final crop protection agents. Industry compliance standards
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3. Advanced Organic Electronic Materials (OLED and Display Component Synthesis)Manufacturers of organic electroluminescent materials employ 3-Ethynylpyridine to introduce ethynylpyridine moieties into conjugated monomers and polymers for optoelectronic applications, enabling electron transport and emission properties for light-emitting devices. The chemical’s role in precise functional group installation enhances the stability and performance of final OLED stacks used in consumer electronics and high-end display devices, where electronic structure and film purity drive end-use reliability. Industry compliance standards
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4. Specialty Chemical Synthesis for Analytical StandardsProducers of certified analytical standards and reference materials apply 3-Ethynylpyridine for custom synthesis of isotope-labeled pyridine derivatives and acetylenic reference substances. The controlled incorporation of the ethynyl group by quantitative chemists ensures structural precision, trace-level impurity management, and batch traceability, fundamental for standards used in pharmaceutical QC labs, regulatory bodies, and method validation services. Industry compliance standards
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Having worked hands-on in chemical manufacturing for decades, I’ve learned the difference a well-made intermediate can make in a research lab or production plant. 3-Ethynylpyridine offers an unappreciated yet impactful solution for applications in organic synthesis, medicinal chemistry, and materials research. This compound, with the model name 3-ethynylpyridine and CAS number 4606-59-9, stands out due to its reactive ethynyl group attached at the third position of the pyridine ring. In practice, this molecular detail opens a window for forming robust carbon-carbon bonds during cross-coupling or cycloaddition reactions. Many chemists tighten their specifications for purity to protect reaction yields, and that’s a challenge we take seriously during production.
Our team synthesizes 3-Ethynylpyridine to a purity up to 98%, which holds up under GC inspection even when researchers push the limits. We store every lot in amber bottles, under nitrogen, reducing degradation. Handling this material means considering both its intrinsic reactivity and sensitivity. Every batch arrives as a transparent to faintly yellow liquid or pale crystalline solid, thanks to the extra filtration steps and controlled drying at the end of the process. Our own quality control lab has run melting point, NMR, and HPLC purity checks routinely, and we know from returning customers that reliable analytics reduce headaches downstream.
If you walk through a pharmaceutical pilot plant or a research center, you’ll find bottles and drums of chemicals competing for shelf space, so every selection needs a purpose. 3-Ethynylpyridine brings the ethynyl function to an aromatic nitrogen ring scaffold, preparing the ground for introducing functional diversity. This versatility means a synthetic chemist can use it in complex molecule assembly or as a fragment for conjugation. Traditional alkynes often face problems when researchers want to append them to heterocyclic components; this molecule solves that by offering compatibility with reactions such as Sonogashira and other palladium-catalyzed couplings. Over years, we have worked with teams scaling up reactions from a single gram to multi-kilogram batches, and the efficiency of this compound during scale-up has been consistent. Delays from incomplete reactions or troublesome impurities can cost days, so our colleagues depend on material that behaves predictably batch after batch.
Within our facility, reliability goes beyond a purity figure on a certificate. When prepping 3-Ethynylpyridine, we track oxygen levels, temperature, and moisture exposure in real time. Outgassing the product vessel during bottling reduces side reactions that could introduce unwanted byproducts. These steps might look excessive, but downstream they mean fewer purification headaches for our customers. Our own R&D teams use the same lots for their catalyst screening programs—the feedback loop between our manufacturing and internal research helps fortify improvements in each run, whether changes relate to yield improvement, byproduct minimization, or storage stability.
I’ve seen new entrants on the market, such as 2-ethynylpyridine or 4-ethynylpyridine, each with structural differences that produce measurable changes in behavior. For example, the position of the ethynyl group on the ring affects both electron density and accessibility, which can dictate outcomes in C-H activation or regioselective reactions. 3-Ethynylpyridine helps chemists bypass some selectivity issues seen with the 2- or 4-analogs, particularly during direct arylation or metal-catalyzed coupling. In one customer’s route to a nitrogen-containing pharmaceutical intermediate, switching from 2-ethynylpyridine to our 3-position product increased regioselectivity, cutting down on time spent in column chromatography and simplifying purification of the end product.
From a handling perspective, 3-ethynylpyridine is less volatile and less odorous than many of its close relatives. It has a less intense aromatic odor, which not only improves lab comfort but also simplifies fume management in scale-up settings. This isn’t a top-line feature you’ll find listed in brochures, but anyone in the field knows that practical differences like this influence productivity more than abstract claims. I recall a client working on multi-gram scale macrocyclizations—a reaction that suffered yield drops due to side reactions caused by moisture-sensitive intermediates. After changing suppliers, they found that our 3-ethynylpyridine's packaging integrity preserved product quality from first opening to the end of the run. This knowledge has helped us reinforce our own traceability and packing standards across the board.
It’s tempting to look for easy wins by sourcing intermediates through traders or aggregators, but the problems with inconsistency and trace contaminants always surface at the worst moments. Our manufacturing practice addresses these issues head-on. Every run is documented from raw material sourcing through final drumming. Our technicians keep detailed records of each precursor batch, reaction time, and critical parameters. This attention to detail supports tight batch control, so that customers can expect consistent melting point range, purity, and physical appearance every single order. In our own trials, we’ve re-ran reactions using archived material from twelve months prior and found little difference in performance, something we attribute to both our synthesis and post-synthetic handling protocols.
As the market for advanced intermediates expands, the temptation grows to cut corners, but our customers—many of whom develop life-saving drugs or high-performance materials—count on reliable, reproducible results. If a single batch contains unexpected levels of metallic or organic contamination, entire development timelines might slow or derail. We’ve seen more than a few projects hit setbacks this way, and we invest heavily in batch analytics so those frustrations don’t start with material from our plant. Each time incoming feedback highlights a specific pain point, our process engineers dig into the root causes, running trial batches and tweaking our purification train or storage methods as needed. Quality in the bottle is built hour by hour on the production line, not just checked at the end.
Academic research and industrial innovation depend on the reagents that allow teams to move quickly and with confidence. 3-Ethynylpyridine continues to earn its role in synthesis routes that build novel and patentable compounds. Whether the goal is to create complex heterocyclic scaffolds or linkers for modern medicinal chemistry projects, the reliability of the precursor sets the tone for the whole workflow. The relationship between compound purity and research efficiency plays out in meetings with our technical contacts, who often request custom documentation or share their specific downstream requirements. In more than one instance, we’ve been asked to provide a customized lot with impurities characterized by LC-MS or to deliver a convincing stability study. Long-term business comes from collaboration, and chemists from growing biotech firms return to us because we remember their preferences and adapt to specialized process flows.
One memorable case involved a customer facing precipitation and filtration issues due to inconsistent alkyne-pyridine intermediates. They brought us their synthesis route and we worked through their bottlenecks, tightening distillation and crystallization parameters during pilot runs. A clear batch and easier filtration followed, smoothing their next development phase. Over the years, this sort of partnership mentality has encouraged us to keep technical communication channels open. Every time a customer shares reaction data tied to our product, we treat it as a learning opportunity for future batches.
The world of fine chemicals grows more complex by the year. Regulatory compliance is not just paperwork for us; it’s the backbone of cross-border trust, especially for customers in Europe, Japan, and North America who face audits and inquiries on every ingredient. We invest carefully in data integrity for our analytical documentation—archiving retention times, instrument certificates, and chromatograms. Years ago, a client’s legal team requested full traceability and documentation for the origin and intermediates used in synthesizing 3-ethynylpyridine for an IND submission. We walked them through our records, demonstrating origin claims and supporting every point with certified reports. That investment didn’t just help one client clear a hurdle; it set our approach to record-keeping for every subsequent order.
As regulations tighten, we see growing interest from end-users around residual solvents, heavy metals, and other trace contaminants. We answer this demand by publishing detailed specifics and, on request, providing compliance-focused analysis for every newly released batch. Many academic and commercial researchers lose time validating questionable material, re-checking purity just to avoid setbacks. To address this, we tie our batch release criteria directly to end-user feedback, revisiting thresholds or updating analytical methods as industry guidelines change. Documenting and sharing this transparency increases user confidence and builds repeat business relationships.
No certificate or analytical report can fill the gaps left by poor service or missed technical expectations. The most rewarding collaborations come from treating customers as fellow chemists, not just buyers. Our in-house process scientists have encountered most of the challenges users raise. If a batch undergoes unexpected color changes or precipitates on standing, we rerun QA and support investigation, sometimes sending out a new lot at our expense. We learned the hard way that meeting specs isn’t enough if the product doesn’t perform as expected in specific downstream reactions. By running side-by-side syntheses with every new release, we replicate common reaction conditions our customers use, catching issues early rather than waiting for a report from the field.
Sometimes, the substance’s true value only becomes clear in dialogue with customers. A synthetic route that seems routine during our planning stages might reveal new instability pathways or incompatibilities with certain solvents or catalysts. We memorialize these experiences, continually refining the guidance and technical support documents we provide. Through trade shows and site visits, we collect real-world stories that push us to improve how we manufacture, package, and distribute this and other fine chemicals. This direct feedback loop sets manufacturing apart from the brokerage side of the industry, as it forces honest self-assessment and continuous technical growth.
Not every trend shapes the future of chemical intermediates in the same way. Over the past decade, trends in greener synthesis, coupled with automation and catalyst innovation, have redefined the role of compounds such as 3-ethynylpyridine in modern chemistry labs. Interest in C–H activation has driven demand beyond traditional cross-coupling runs, as medicinal chemists search for less wasteful and more direct routes to functionalized building blocks. In response, our R&D division has piloted new routes for producing 3-ethynylpyridine with fewer hazardous byproducts and less solvent usage, attempting to maintain economic feasibility while reducing environmental impact. We’ve adjusted purification steps to allow for easier solvent recycling and implemented new distillation practices to collect and segregate waste streams for responsible disposal.
These improvements are not one-time achievements but ongoing commitments. As new catalyst systems emerge and customers request new analytical panels—testing for lower levels of unknown byproducts or new solvent mixtures—we iterate on both our process and our documentation practices. Early engagement with downstream users uncovers not only new opportunities but also new hazards, pushing us to consider alternate synthesis and handling methods that address both current and anticipated needs. The connection between these upstream adjustments and final product advantages appears in stronger customer relationships and lasting confidence in the batches we send out.
The debate over volume pricing versus premium quality continues in the industry. Cost pressures increase as larger international traders and aggregators undercut by a few percent. The lesson learned through conversations with purchasing managers and bench chemists is that cost savings fade quickly if quality or consistency slip. We maintain close communication with logistics partners and production crews to watch over every step that can influence the final batch—whether temperature spikes during overseas shipping or local handling in the warehouse.
We often remind our partners that a low up-front price cannot make up for lost time, wasted resources, or delayed product launches caused by failed runs. Years of troubleshooting projects with our customers convinced us that dependable quality from the source offers value that goes far beyond the initial invoice. Keeping product knowledge, manufacturing, and quality management under a single roof gives us better control and helps deliver more than just a reagent—it offers reliability during scaling and development, which is the true differentiator as projects grow from milligrams to multiple kilos.
The field of specialty pyridine derivatives continues to evolve as medicine, materials science, and advanced catalyst design expand the landscape of modern chemistry. We pay close attention to the literature and conversations at scientific meetings, taking note as new strategies and catalytic systems emerge. In our own work, we regularly test 3-ethynylpyridine in pilot-scale projects aimed at discovering cleaner, more robust routes to functionalized heterocycles or advanced ligands. Sometimes, fresh uses for this compound show up in surprising fields, such as sensor design or photonics, where the interplay between structure and reactivity drives new applications.
By supporting not only the raw chemical needs but also the project-specific technical requirements of researchers, we aim to strengthen the foundations that allow for innovation and success downstream. We keep the focus on honest production—delivering a product we would want to use ourselves—and opening channels for technical engagement, ensuring the next generation of scientists and engineers receives support from chemical suppliers deeply invested in both process and progress.
From the perspective of hands-on chemical manufacturing, 3-ethynylpyridine represents more than just a name or a CAS number on a specification sheet. Every batch we produce passes through, and is lifted by, the cumulative experience of our technical staff, process engineers, and research collaborators. We believe dependable intermediates sit at the core of successful chemical transformations and are proud to play a role, however quiet, in fueling both scientific advancement and industrial progress.