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HS Code |
490794 |
| Cas Number | 1445-07-4 |
| Molecular Formula | C8H6N2 |
| Molar Mass | 130.15 g/mol |
| Iupac Name | 2-(pyridin-3-yl)acetonitrile |
| Appearance | White to off-white crystalline powder |
| Melting Point | 50-54°C |
| Boiling Point | 286-288°C |
| Density | 1.13 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 129°C |
As an accredited 3-Pyridylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g package of 3-Pyridylacetonitrile comes in a sealed amber glass bottle with a printed chemical label and hazard symbols. |
| Shipping | 3-Pyridylacetonitrile is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and must be handled according to relevant transportation regulations, including proper labeling and documentation. Shipping is typically via ground or air freight, depending on urgency and destination requirements. |
| Storage | 3-Pyridylacetonitrile 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 oxidizing agents. The storage area should be protected from moisture and direct sunlight. Ensure appropriate chemical labeling and secure the container to prevent leakage or accidental exposure. Use appropriate personal protective equipment when handling. |
Applications of 3-Pyridylacetonitrile in Industrial ManufacturingAs a direct manufacturer, we supply 3-Pyridylacetonitrile to multiple advanced industries where its unique molecular structure enables key transformations in specialty synthesis. Below, we detail distinct real-world applications, industry compliance, processing parameters, and resulting high-value finished products. 1. Pharmaceutical Intermediate for Nicotinic Acid Derivatives3-Pyridylacetonitrile acts as an essential precursor in the multi-step synthesis of selective nicotinic acid-based drug molecules. During pharmaceutical production, this intermediate couples into pyridine-based scaffolds under regulated conditions, enabling downstream elaboration through oxidation, alkylation, or amidation. Pharmaceutical processors closely control impurity profiles and traceability through ICH Q7-compliant batch records. The material enters synthesis at the nitrile input stage, where stringent in-process controls track residual solvents and reagent ratios. Finished drugs from this route include cardiovascular therapies and CNS agents with defined pyridine architectures. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Agrochemical Synthesis for Pyridine-based HerbicidesThe compound serves as a vital intermediate in producing pyridine ring-containing agrochemicals, particularly pre-emergent and post-emergent herbicides. In agrochemical plants, 3-Pyridylacetonitrile undergoes custom catalytic reactions yielding specific alkylated or carboxylated derivatives used in field crop protection. Compliance with global agricultural chemical registration dictates detailed record-keeping, impurity control, and alignment with FAO and OECD purity guidelines. The raw material typically enters as a core substrate in the condensation or amination stage prior to formulation of active herbicide agents. End users formulate directly into granules or suspension concentrates for use in multiple geographies. Industry compliance standards
Typical usage ratio
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3. Specialty Chemical Intermediate for Functional Dye ManufacturingIndustries producing high-performance dyes for textiles, plastics, and electronic displays use 3-Pyridylacetonitrile as a key nitrogen-rich building block. Its introduction enables controlled integration of pyridine units for improved photostability and colorfastness. Dye manufacturers must adhere to textile safety directives, RSLs, and electronic industry quality guides, ensuring trace removal of free nitriles and side byproducts. The chemical enters at the amination or cyclization stage in multi-component synthesis, immediately before final diazotization or metal-complexation. Downstream processors transform these intermediates into colorants for finished goods across diverse product lines. Industry compliance standards
Typical usage ratio
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4. Intermediate for Advanced Material Polymerization CatalystsProducers of specialty catalysts for polymer manufacturing frequently incorporate 3-Pyridylacetonitrile when engineering ligand frameworks for catalyst complexes. Applied within transition metal-catalyzed polymerization, these ligands modify selectivity, molecular weight distribution, and activation rates for technical plastics and elastomers. Compliance demands tight adherence to ISO catalyst production norms and trace element controls for downstream FDA or EU food contact safety. Chemists add the raw material at the ligand synthesis or complexation stage prior to metalation. The resulting catalysts serve in various high-consistency polymer productions. Industry compliance standards
Typical usage ratio
Downstream process integration
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After years in chemical manufacturing, we have watched the importance of pyridine derivatives grow across several industries. Among these, 3-pyridylacetonitrile has come to stand out as a core intermediate for many different synthetic routes. With the CAS number 5445-17-0 and molecular formula C7H6N2, this compound appears in high demand across pharmaceutical research, agrochemical development, dye production, and even specialty materials. It brings a unique combination of reactivity and selectivity, opening access to a wide array of downstream molecules that would be much harder to build from scratch.
Our staff have handled and produced batches of 3-pyridylacetonitrile ranging from a few kilograms for research customers to tons for established factories. Chemists often require a reliable, well-characterized product that gives predictable results in both pilot and full production. They look for clear NMR spectra, consistent GC purity, and stable performance through long synthesis cycles. The material’s appealing feature lies in the way it behaves during alkylation, condensation, or coupling reactions, especially where controlled addition to the pyridine ring can radically change synthesis outcomes.
3-pyridylacetonitrile displays as a white to pale yellow crystalline substance when manufactured under careful conditions. Our current production model focuses on high-purity batches, with specification targets aligned to 99 percent minimum by GC or HPLC, barring the odd trace impurity. We maintain moisture and residual solvent at low levels, because downstream chemistry often reacts badly to contamination. The product shows a melting point close to 60-63°C, with batch-to-batch consistency providing smooth processing in scale-up.
Handling this intermediate calls for basic chemical hygiene: gloves, goggles, lab coats, and exhaust ventilation tackle most routine tasks. Drying, storage, and packaging use air-tight containers to keep product free from water and dust. Our process skips the use of strong acids in final steps, reducing salt residues. Chemists working on pilot plants tell us they want easy transfer between reactors, so we granulate or powder the product with careful particle size control. This supports even feeding and fast dissolution in the organic solvents routinely used.
Much of our 3-pyridylacetonitrile output heads into pharmaceutical synthesis lines. Medicinal chemistry depends on predictable building blocks, and this one gives access to a host of pharmacophores by straightforward transformations. Customers have fed it into bases for antihypertensive compounds, antifungal agents, and interesting kinase inhibitor scaffolds. They favor this intermediate for its ability to accept further substitution at the methylene and pyridine sites, producing structural motifs that are hard to fashion from other starting points.
Outside drug research, plant protection scientists count on this same intermediate to build modern pesticide candidates. Complex heterocycles needed for selectivity and environmental persistence often depend on functionalizing the nitrogen of the pyridine ring. Further cyanation or amination of the acetonitrile group has led to high-value products showing reliable bioactivity. Here, clean starting material avoids nasty surprises in regulatory testing stages, where impurities and byproducts spell trouble for product registration.
Dye development groups have come to rely on the reproducibility of 3-pyridylacetonitrile. They often use the material as a cornerstone for specialty pigments and functional colorants. In some electronic displays, derivatives can tweak wavelength emission bands, impacting hue, brightness, and UV stability.
For manufacturers, consistency is not just good for paperwork; it keeps entire synthesis chains on time and budget. We carry out most steps of the process on-site, including the purification and quality control. Partners who rely on their material suppliers for routine as well as one-off runs know what it means when a cubic meter of solvent carries off-spec residue. Control over every stage, from raw material sourcing to final storage, keeps dust and moisture at bay; it also limits exposure to unexpected delays or costly reprocessing jobs.
We have learned that not all 3-pyridylacetonitrile on the market is equal. Impurities coming from incomplete reaction or poor solvent removal cripple later steps. By keeping batch analytics open to our customers, we offer transparency and the chance to spot issues before they become expensive failures in pilot or production scale. Technicians often check by GC-MS, NMR, or simple HPLC runs, comparing every lot with those used in previous campaigns to verify both purity and the absence of unusual peaks.
Through direct feedback, many users point toward ease of purification and stability as the two major factors boosting productivity with this intermediate. We avoid strong oxidants and aggressive decontaminants during synthesis. This protects the methylene bridge and cuts down on oxidation byproducts, simplifying downstream hydrogenation, halogenation, or other transformations. Chemists gain a cleaner baseline in chromatograms, which cuts the time and solvent needed for product clean-up.
Many buyers approach us after working with reseller or distributor-sourced products. Often, they report trouble with unpredictable crystallization, color changes during storage, or excessive sulfur-based odor, all pointing to uncontrolled production and storage conditions. By maintaining clear temperature and humidity controls throughout manufacture and warehousing, we keep the product tightly within its specification from batch release until delivery.
Handling and shipping practices also matter. Some international supplies arrive as sticky lumps, especially during warm weather. Our shipping protocols include thermally insulated packaging and silica gel pouches, even for small-volume research samples. Potential buyers notice the difference almost at once after switching suppliers: powders flow more smoothly from drums or bottles, and the smell of contamination will be much reduced.
Chemists often ask about the distinctions among pyridylacetonitriles. The 3-pyridyl (meta) derivative shows a unique pattern of reactivity unknown to 2-pyridyl or 4-pyridyl analogues. Its side-chain sits off the nitrogen atom by a position that supports smoother condensation with carbonyl or carboxyl reactants. This unlocks streamlined access to complex heterocycles and more selective activation under mild conditions.
By contrast, the 2-pyridylacetonitrile, with its nitrile group immediately next to the nitrogen, introduces extra steric and electronic constraints. This often limits reaction partners or introduces side reactions that call for more labor-intensive purification. The 4-pyridylacetonitrile offers good results in some syntheses but falls short when the meta position’s ortho/para selectivity is absolutely required for target molecule architecture. Feedback from larger production clients favors the 3-position intermediate for cost savings, higher yields, and more flexibility in adapting to evolving project demands.
Compare this to classic cyanomethylated benzenes. A simple phenylacetonitrile does not allow the same breadth of transformations, as the nitrogen in the pyridine ring brings activation sites that benefit further synthetic elaboration. Researchers seeking to build diversity into compound libraries use the 3-pyridylacetonitrile advantage to speed up candidate screening and cut overall throughput time.
Application success often depends on more than just a stated GC purity. We work with customers to define additional specification points that match anticipated applications—down to ppm-level impurities, heavy metal content, particle size distribution, and even color. Staff in our QA/QC labs regularly run batch comparisons over months, storing samples from previous runs for routine benchmarking. This builds a dataset for each customer that helps track trends and anticipate any drift in process control.
Where pharmaceutical routes are involved, our technicians tailor cleaning and grinding to eliminate cross-contamination and ensure traceability. Permanent documentation for each lot follows Good Manufacturing Practices where requested, though we continue to serve customers without strict GMP needs as well. We recognize that trust builds over small details: transparent COAs, open access to chromatography data, and fast response times for technical questions build lasting business relationships. Collaborative problem-solving often reveals ways to shrink cost, reduce waste, or streamline post-production handling.
Over the years, we have learned that not all downstream synthesis challenges can be predicted at the start of a project. Sometimes, an unexpected contaminant blocks an important reaction. Sometimes, instability during storage triggers color changes or a falloff in yield. By keeping post-manufacture testing at the forefront, we can anticipate how our product interacts with solvents or reactants used by customers.
Some users experience challenges with moisture uptake during extended storage. We recommend and support rigorous drying protocols at our end, employ molecular sieves, and vacuum-seal high-value batches. For high-sensitivity synthesis, our team can deliver product in custom packaging, minimizing opportunity for water or oxygen ingress. We adapt particle size and form—powder or granule—based on partners’ needs to optimize solubility and transfer rates.
Feedback from customers also shapes our continuous improvement projects. When a regular client faced sluggish dissolution in large-volume soda-ash based reactors, we adjusted grinding mill settings, identifying a distribution sweet spot that solved both flow and solution-rate issues. Where shipment delays exposed some lots to temperature fluctuations, we invested in better climate-controlled logistics.
We recognize the increasing expectations buyers place on chemical manufacturers regarding environmental stewardship. The production of 3-pyridylacetonitrile traditionally relied on steps using halogenated reagents and solvents. These steps pose risk both in emissions and waste handling. In our practice, we have moved toward greener alternatives—where process chemistry allows—substituting less hazardous reagents, recycling solvents, and improving capture of volatile compounds.
Integrated closed-loop solvent recovery now handles much of the organic effluent from final crystallization. Distillation and purification columns ensure that the same volume can be reused in future campaigns, cutting direct costs and lowering factory impact. Wastewater is monitored and treated above standard compliance levels. Staff actively seek alternative protocols published in recent literature, with the goal of lowering the ecological footprint while keeping product consistent and cost-competitive.
Pricing for 3-pyridylacetonitrile reflects raw material cost swings, process complexity, and customer volume. While bulk prices can trend downward as capacity expands, specialty lot production, for example low-impurity or custom particle size, tends to hold a premium. We have built multiple production lines to address both routine demand and peaks caused by seasonal or regulatory-driven surges. By maintaining inventory buffers, we can respond to research-scale and industrial-scale orders without undue delay.
Some markets wake up to new demand when a major pharmaceutical or agrochemical patents a new route incorporating the molecule. We track patent databases and adjust procurement to anticipate these shifts, which protects users against back-orders or hikes unrelated to true scarcity. Direct relationships with several upstream suppliers help weather shocks in global supply chains. By controlling our own production scheduling and raw material preparation, we stave off surprises filtering through the industry and limiting options for buyers.
Our business model always pivots away from short-term, transaction-based selling toward partnership. Regular dialogue with users keeps our 3-pyridylacetonitrile relevant and tuned for real-world process requirements. We invite discussion not only on immediate needs, but on long-term improvements that benefit everyone: expanded scale, simplified purification, or shifts toward safer process chemistry.
Researchers preparing patent-registration batches work directly with our technical staff to secure detailed batch records, custom forms, or even process documentation supporting regulatory filings. Production engineers focused on cost-down targets count on fast, stable deliveries and product consistency that smooths workflows. Communication around issues, from dissolution to purity, translates into tangible factory-floor results.
Collaboration does not end at shipment. Many partners return for later projects, asking about process upgrades, greener alternatives, or joint exploration of alternative synthetic strategies. Our team draws on years of hands-on experience, academic exchange, and constant process monitoring to suggest options or troubleshoot together.
Pyridine chemistry evolves every year as researchers demand cleaner, smarter, and more versatile building blocks. Investment in new reactor technology allows for more precise thermal control, reduced impurity formation, and better energy management. Our facility plans to expand into continuous processing methods, which promise tighter impurity profiles, faster scale-up, and more reliable delivery on larger orders.
Ongoing R&D keeps our process ahead of stricter regulatory requirements. As limits tighten in pharma and agro applications, we apply predictive analytics on impurity formation and try out new process controls that can spot potential issues before they impact a batch. Input from customers shapes these upgrades, as their experience with evolving targets, new assay requirements, and novel compound classes feeds back into process chemistry.
Through decades of production and supply, we have seen that the best business comes from chemicals that behave predictably, stay in specification, and support a user’s innovation goals. 3-pyridylacetonitrile, produced under controlled, transparent, and responsive conditions, provides chemists in many fields with a foundation for efficient synthesis and novel discovery. Our attention to every step, from raw material through formulation to delivery, ensures users receive more than just a product—they gain a trusted platform for their own success. The knowledge we gain from real-world feedback builds a continuous loop of improvement, keeping both our processes and partners growing together.