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HS Code |
114860 |
| Chemical Name | Alpha-Phenyl-2-Pyridineacetonitrile |
| Cas Number | 28324-98-9 |
| Molecular Formula | C13H10N2 |
| Molecular Weight | 194.23 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 97-99°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | N#CC(c1ccccc1)c2ccccn2 |
| Synonyms | 2-(Phenyl(pyridin-2-yl)methyl)acetonitrile |
| Storage Conditions | Store in a cool, dry place, tightly closed container |
| Hs Code | 292690 |
As an accredited Alpha-Phenyl-2-Pyridineacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle with secure screw cap, labeled "Alpha-Phenyl-2-Pyridineacetonitrile, 25g," hazard symbols, batch number, and storage instructions. |
| Shipping | Alpha-Phenyl-2-Pyridineacetonitrile is shipped in tightly sealed containers, protected from moisture and light. Packages comply with chemical transport regulations, including labeling and documentation. The product is typically shipped as a solid, with cushioning to prevent breakage. Ensure compatibility with other shipped goods, and store at room temperature during transit unless otherwise specified. |
| Storage | Alpha-Phenyl-2-Pyridineacetonitrile should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Keep the chemical in a tightly sealed container, protected from direct sunlight and sources of ignition. Ensure storage is in accordance with local regulations, preferably in a dedicated flammable or chemical storage cabinet. |
Applications of Alpha-Phenyl-2-Pyridineacetonitrile in Industrial ManufacturingAlpha-Phenyl-2-Pyridineacetonitrile serves as a pivotal intermediate in several regulated industrial manufacturing pathways, particularly where precise chemical transformation and controlled purity are critical. Our manufacturing expertise ensures consistent material quality for integration into advanced organic syntheses across select downstream sectors. Below we detail key industrial applications, regulatory parameters, usage specifications, process implementation, and end product categories based on proven market and production data. 1. Pharmaceutical Intermediates for Heterocyclic Compound SynthesisLeading pharmaceutical manufacturers use this compound as an intermediate in the synthesis of heterocyclic agents and active pharmaceutical ingredient (API) precursors, particularly for molecules leveraging the pyridyl and phenyl moieties. The controlled reactivity and high purity levels support integration into multistep synthetic routes, such as cross-coupling and cyclization processes, allowing precision modifications in regulated API workflows. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingKey players in the agrochemical sector deploy this nitrile intermediate during the elaboration of complex pyridyl-based active compounds, improving selectivity in the formation of herbicide and pesticide actives. It is critical in applications where precise substitution on the aromatic or heteroaromatic core impacts final biological action or regulatory residue compliance. Industry compliance standards
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3. Specialty Catalyst Ligand PrecursorResearch and industrial entities producing custom ligand systems for homogeneous catalysis use this compound as a scaffold for tailored N- or C-functionalized pyridine ligands. The robust nitrile moiety supports regioselective transformations necessary for next-generation catalyst development in fine chemical and materials processing sectors. Industry compliance standards
Typical usage ratio
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4. Organic Electronic Material IntermediateProducers of advanced electronic components and organic optoelectronic materials utilize this chemical in the preparation of conjugated heterocyclic monomers. Its structural features enable incorporation into core units required for OLED emitters, charge transport layers, and semiconducting polymers, supporting strict control of impurities and batch repeatability. Industry compliance standards
Typical usage ratio
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Stepping onto the manufacturing floor each day, you quickly spot which chemicals cut through the clutter with both demand and reliability. Alpha-Phenyl-2-Pyridineacetonitrile stands out in that group. This compound, with its pyridine ring joined firmly to a phenyl group through the acetonitrile bridge, shows up in projects where nothing less than robust, well-characterized intermediates will do. Working at the synthesis reactors, you learn quickly that some molecules pull more weight than others when it comes to scaling up and making higher-value targets achievable.
Alpha-Phenyl-2-Pyridineacetonitrile (CAS: 3739-56-2) delivers more than just a mouthful to name. Its structure sets it apart: a rigid aromatic frame aids thermal and chemical stability while the acetonitrile group imparts a vital reactive site for further derivatization. Chemists meet this compound in both pharmaceutical explorations and fine chemical development, mostly because it offers multiple points for modification and holds up under the pressure of process-scale chemistry. We've pushed batch sizes into the multi-kilogram range without noticing loss of purity or integrity—a claim not every intermediate can make.
What it comes down to is reliability. Each molecule of Alpha-Phenyl-2-Pyridineacetonitrile churned out under our roof passes not only classic purity screens but also wider impurity profiling. Our continuous investments in analytical equipment—NMR, GC-MS, HPLC—help us follow even subtle differences from run to run, which in turn narrows variation between lots for customers who rely on predictable supply chains.
Companies using typical benzyl cyanides or plain pyridines bump into limits early: unwanted byproducts, sluggish reactivity, or even outright decomposition when solvents or temperature push too hard. With Alpha-Phenyl-2-Pyridineacetonitrile, synthetic routes broaden, bringing the benefit of that pyridine ring’s electron-rich character. For instance, in the preparation of heterocyclic structures destined for medicinal chemistry, the extra phenyl group delivers steric and electronic flexibility. That translates to designers introducing unique pharmacophores unavailable from simpler nitriles.
Over the years, collaborating with med-chem teams, agrochemical designers, and dye manufacturers, we watched plenty of efforts miss a beat when a standard arylacetonitrile lacked performance. Alpha-Phenyl-2-Pyridineacetonitrile brings necessary upgrades—both in stability for storage and versatility for downstream processing. As a manufacturer, it’s striking how little waste and off-spec material results compared with more common building blocks.
Building consistent supply starts in our labs, extends through kilo labs, and ends in the main reactors. A lot hinges on tight temperature control, dry solvents, and real-time monitoring for byproduct development. One thing we learned from scaling Alpha-Phenyl-2-Pyridineacetonitrile: exposure to air and moisture during crystallization makes a real impact on appearance and filtration properties, so we keep things inert and controlled right through to packaging. Even particle size can change handling—finer material tends to cause less dusting, but coarser grades speed up filtration. Customizing to what end-users find workable often comes down to working side by side with production chemists in the field.
Bad batches make a splash—delayed plant schedules, off-spec downstream material, or even lost customer trust. We maintain a dedicated feedback loop from dispatch to customer dock. Once, a pharma customer observed subtle differences in melting point, which set our quality team digging into trace amines in incoming raw materials. Addressing that narrowed variation until the melting range locked within a single degree. Dialing into those differences is where knowledge gained on the plant floor outpaces what textbooks provide.
Alpha-Phenyl-2-Pyridineacetonitrile finds its strongest footing in advanced chemical research and tool molecule creation. Where complexity in target molecules grows, so does the need for well-characterized, reliably reactive intermediates. Medicinal chemists appreciate that both the pyridine and phenyl rings can participate in further transformations—cross-coupling, hydrogenation, or additions to introduce functional groups. Compared to plainer acetonitriles, this molecule opens reaction maps across multiple branches, helping synthesize libraries and targeted compounds for testing.
Performance in applications such as agrochemistry marks an important difference. Here, the molecule tends to stand up during the harsher processing steps typical for bulk crop protectant manufacturing. Customers comment on how color-holding properties in dye synthesis get a bump from starting with this intermediate versus basic aliphatic nitriles. Some of these differences boil down to batch-to-batch purity and the minimal presence of related pyridine impurities—or the lack of aggressive, unpleasant odors sometimes lurking in less-refined chemical lots.
We’ve worked with enough nitrile intermediates over decades to know just how much headache less robust molecules cause. Those based on simple benzyl cyanides suffer from reactivity too easily deflected by nucleophilic attack at weak spots, or from the tendency to hydrolyze under even moderate aqueous conditions. Alpha-Phenyl-2-Pyridineacetonitrile’s aromatic system stabilizes it against these mishaps. The extra structural complexity adds cost to synthesis, but our process gains from high yield and low waste offset that over the production campaign.
Regulatory teams often ask for impurity profiles and trace metal content, since downstream biological testing doesn’t tolerate contamination. Over the past few years, we’ve refined purification steps based on feedback from those sectors. A few customers, earlier satisfied with commercial-grade material, switched to our pharmaceutical standard after reporting improved crystallization and filterability, especially in reactions where trace amines or metals wreck endpoints.
Direct hands-on time with process batches reveals differences no specification sheet uncovers. In one instance, a trial replacing Alpha-Phenyl-2-Pyridineacetonitrile with 2-benzylpyridine nitrile resulted in sluggish coupling and unexpected tarry byproducts. Chemical intuition pushed us back to our product, restoring cleanliness to the conversion and improving isolation yield by nearly 15%. This illustrates the difference robust chemical manufacturing makes to lab and production outcomes.
Decades of scaling organic nitrile production have taught us to respect their hazards—not just on paper, but in the daily handling, ambient ventilation, and clean-out procedures each campaign demands. Alpha-Phenyl-2-Pyridineacetonitrile behaves better than many volatile nitriles, with manageable vapor pressure and low tendency for off-gassing under standard operating temperatures. Still, our crews keep air monitoring tight, especially during solvent stripping and packaging.
We participate in local environmental audits and carry out all effluent treatment in-house. Alpha-Phenyl-2-Pyridineacetonitrile’s limited water solubility covers some risk, yet we know even trace emissions can collect in solvent recovery units. Attention to these small details—closed transfers, spill-prep plans, and regular crew training—keeps incidents rare. One year, after fielding a concern from regulatory compliance about acrylonitrile traces in discharge, we revamped stripping columns and began routine GC checks, finding leaks early and improving outcomes for both our neighbors and plant team.
A lot of what we’ve picked up about Alpha-Phenyl-2-Pyridineacetonitrile comes out of collaboration—not just static research or customer orders. Early in our scale-up work, custom requests came in from medicinal chemistry partners exploring kinase inhibitors. Some wanted clean lots; others pushed for isotopic labeling. Each modification called for in-house reruns, samples pulled at different reaction stages, or new downstream purification tweaks. Those open lines help both supplier and customer adapt—great ideas often show up unexpectedly during these partnerships.
Down the line, innovations in continuous flow manufacturing promise more consistent product when ramping up volumes. We built trial runs on modular flow reactors, matching time-at-temperature and mixing that’s rarely possible in kettle reactors. Tracking Alpha-Phenyl-2-Pyridineacetonitrile’s behavior through these systems, we see improvements in yield and lot reproducibility. Crystallization protocols adapted in-line, reducing batch variation further. These investments flow back into better product for industrial synthesis and emerging research fields.
The reality of chemical manufacturing isn’t just about hitting weight or purity targets. Our relationships with downstream users, regulatory bodies, and local community hinge on open records and well-documented processes. Customers expect not only product but also the confidence that technical support, supply continuity, and environmental responsibility are built in.
Our technical team hosts quarterly calls sharing method tweaks, common troubleshooting for Alpha-Phenyl-2-Pyridineacetonitrile, and feedback from end-use syntheses. We find that readiness to share—not just numbers but lessons from real manufacturing challenges—brings practical value. One large partnership in Europe needed quick action on a batch delayed during shipping due to port strikes. Our team reworked production priority, moved finished inventory by alternate route, and minimized downtime for a major pharmaceutical pilot plant. Experience in logistics, just as much as chemistry, keeps those projects moving forward.
Alpha-Phenyl-2-Pyridineacetonitrile finds favor with regulatory compliance teams because our continuous investment in documentation and traceability answers tough questions. We regularly pull retain samples, maintain multiyear batch records, and submit representative lots for external testing upon request. Preparation for regulatory submissions means assembling analytical dossiers—chromatography, mass spectrometry, melting range, residual solvent levels, and suspected impurities.
Customers working toward clinical stages cite that clean reporting smooths regulatory audits. Transparency in data presentation pays off in fewer questions or product quarantine incidents. Knowledge gained from the manufacturing line—how change in supplier, analytic method, or drying protocol influences residuals—feeds directly into what customers see on paperwork and in the drum.
Producing Alpha-Phenyl-2-Pyridineacetonitrile in volumes that matter to customers means meeting the pressure of timely delivery, cost control, and evolving international standards. Supply concerns about key reagents, changes in solvent markets, or even geopolitics impact daily batch planning. Our response involves securing alternative suppliers and qualifying incoming raw materials before scale-up, which minimizes risk of disruption.
Chemistry itself brings challenges. For example, a once-minor side reaction resulting in a trace quinoline impurity became troublesome as we scaled above a certain batch size. Adaptation in reactor design and in-process monitoring curbed formation quickly, preventing off-spec batches before reaching customers. One key lesson: keeping analytical staff, process engineers, and warehouse teams communicating closes gaps before they threaten product quality.
Waste reduction stands at the front of ongoing efforts. Even with a relatively clean process, solvent recovery and spent carbon disposal demand steady attention. We keep a running audit identifying redundant steps or energy usage, add heat recovery loops where possible, and monitor distillation tails for optimized recycling. These efforts, though sometimes incremental, feed long-term stability for both budget and environment.
The upward trend in demand for specialized intermediates puts compounds like Alpha-Phenyl-2-Pyridineacetonitrile in sharp focus. Each customer project—whether pharmaceutical, pigment, or agrochemical—asks more from its building blocks: higher levels of purity, batch-to-batch sameness, and greater technical documentation. Meeting those needs head-on, rooted in the chemical craft and process know-how built through daily manufacturing, lets us support everything from pilot programs to commercial production.
We see the field growing as molecular design pushes for greater complexity in lower quantities, rather than massive single-product campaigns. Flexibility in manufacturing, ongoing staff training, and close partnerships with application chemists make this possible—not just tanks and pipes, but shared expertise moving innovation from the bench to the loading bay.
Alpha-Phenyl-2-Pyridineacetonitrile continues to demonstrate its value in settings ranging from exploratory labs to high-volume bulk shipments. Its performance under stress, range of downstream possibilities, and our ability to scale without performance drop-off keep it in demand. Our commitment at the factory level, sharpening methods and developing solutions side by side with customers, turns a chemical into a partner for creative synthesis.
Experience in manufacturing Alpha-Phenyl-2-Pyridineacetonitrile shapes every facet of our offering: from the upstream selection of raw materials to the careful monitoring of every tank, filter, and drum leaving our plant. Years spent navigating challenges in synthesis, scale-up, and logistics reinforce that chemical manufacturing thrives on knowledge, teamwork, and attention to small details. Whether helping a project cross the finish line or troubleshooting an unexpected plant issue, the on-the-ground perspective brings clarity to every batch produced.