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HS Code |
405935 |
| Chemical Name | 2-Cyano-4'-Methylbiphenyl |
| Molecular Formula | C14H11N |
| Molecular Weight | 193.24 g/mol |
| Cas Number | 115373-03-6 |
| Appearance | White to off-white solid |
| Melting Point | 85-89°C |
| Boiling Point | Unknown |
| Solubility | Slightly soluble in organic solvents |
| Smiles | CC1=CC=C(C=C1)C2=CC=CC=C2C#N |
| Density | Unknown |
| Synonyms | 2-Cyano-4'-methyl-1,1'-biphenyl |
| Purity | Typically >98% |
| Storage Conditions | Store at room temperature, keep container tightly closed |
| Refractive Index | Unknown |
| Usage | Laboratory chemical, research purposes |
As an accredited 2-Cyano-4'-Methylbiphenyl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g, sealed with tamper-evident cap. Labeled with chemical name, CAS number, and hazard pictograms for safe handling. |
| Shipping | 2-Cyano-4'-Methylbiphenyl is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. The packaging complies with relevant chemical safety regulations. The chemical is labeled appropriately and handled as a hazardous material, using protective measures during transit to prevent leaks or spills. Suitable for ground or air shipment per applicable guidelines. |
| Storage | 2-Cyano-4'-Methylbiphenyl should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Keep away from sources of ignition and moisture. Properly label the storage area and use secondary containment to prevent spills. Ensure access to safety equipment like eyewash stations and spill kits. |
Applications of 2-Cyano-4'-Methylbiphenyl in Industrial Manufacturing2-Cyano-4'-Methylbiphenyl is a specialty intermediate widely used in multiple value-added industrial sectors. Our production partnerships support formulators and manufacturers in fine chemicals, electronics, and advanced materials, ensuring tailored integration and batch consistency aligned with technical standards relevant to each downstream area. 1. Advanced Liquid Crystal Materials ProductionManufacturers in the display technology sector use this compound as a core intermediate when synthesizing advanced nematic liquid crystal mixtures for thin-film transistor liquid crystal displays (TFT-LCDs). The aromatic core's cyano substitution achieves precise dielectric anisotropy, enhancing switching performance and stability under rigorous conditions. Strict control of purity and isomer ratios throughout multiple condensation and coupling stages ensures batch uniformity for mass-market and high-resolution screens. Industry compliance standards
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2. Pharmaceutical Intermediate Synthesis (Non-API, Structural Building Block)Pharmaceutical companies utilize this compound in multi-stage synthesis protocols for complex aromatic active intermediates. The nitrile group supports regioselective transformations, such as amide or carboxylate conversions, while retaining stability under high-temperature hydrogenation and cyclization conditions. This enables the design of late-stage intermediates with improved yield control for anti-inflammatory and CNS projects. Industry compliance standards
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3. Specialty Fine Chemical ManufacturingProducers of complex fine chemicals employ our material in the synthesis of custom biphenyl derivatives, colorants, and specialty reagents. The methylbiphenyl framework with a cyano anchor enables targeted substitutions and high-yield couplings in controlled batch reactors. This route supports bespoke pigments and functionalized ligands for advanced laboratory and pilot scale applications. Industry compliance standards
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4. Electronic Material Intermediate for OLED SynthesisFabricators in the electronics sector use this compound within organic light emitting diode (OLED) emissive layer and host material synthesis. The rigid biphenyl system with cyano functionality provides controlled electron transport and balanced photophysical response in the OLED stack. During downstream synthesis, it enables development of higher color purity and improved device lifetime for flat panel and flexible displays. Industry compliance standards
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Every batch of 2-Cyano-4'-Methylbiphenyl reflects hard-won experience on the plant floor and in the lab. Manufacturing organonitrile compounds like this particular biphenyl derivative draws on specific expertise in aromatic chemistry. The appeal of 2-Cyano-4'-Methylbiphenyl depends on more than its pale appearance or its raw analytical numbers. What makes this product stand out—based on our direct work with it—is the reliability it brings as an intermediate and as a building block in fine chemicals and advanced material synthesis.
Colleagues in medicinal chemistry notice its utility when the goal is selective functionalization of an aromatic molecule with defined electron-withdrawing character. The cyano group attached at the 2-position on the biphenyl skeleton tunes the molecule’s reactivity profile. Factory teams feel this during multi-step processes, especially in cases where side reactions present a real risk. That methyl group on the 4'-position doesn’t just serve as a minor detail; it shapes both solubility and reactivity, making purification step smoother, and helping reactions run without unnecessary downtime.
Our 2-Cyano-4'-Methylbiphenyl falls under CAS number 14403-04-6. Synthesizing this product at scale means more than shifting glassware methods to steel reactors. The process must deliver tight control over every parameter, especially since trace by-products from incomplete nitrile formation or uncontrolled methylation quickly reveal themselves in downstream reactions. For actual practitioners, purity figures by HPLC or GC are not just a marketing claim; a purity above 98% often means hitting product targets and passing QA on the first attempt.
Operators check melting range, color, residue, and solvent profile by strict internal standards. Researchers in the field rely on those details to ensure their own synthetic schemes don’t grind to a halt over solubility or unknown contaminants. Over the years, we have optimized crystallization and filtration steps to keep color and residual solvents at levels where users don’t have to pause work for extra clean-ups or column purifications. Suppliers not operating their own reactors rarely know which bottlenecks or shortcuts can lead to headaches during scale-up or transfer into regulated environments.
Customers often ask about the rationale behind selecting this compound over similar biphenyl nitriles or methylated analogues. Medicinal chemistry teams tend to choose 2-Cyano-4'-Methylbiphenyl to explore SAR (structure-activity relationships) where electron density and position matter. The cyano group on the proximal ring affects both metabolic stability in vivo and binding affinity in vitro. Those running pilot plants for custom materials (such as advanced polymers or heterocycles) also look for the accessibility of the cyano group to downstream transformation. We’ve noticed most success stories from clients stem from cases where molecule’s substitution pattern allows for specific cross-coupling or nucleophilic displacement reactions.
From a manufacturing perspective, switching to a different regioisomer or removing the methyl group often disrupts not just synthetic yield, but also changes the behavior during scale-up. QA teams doing analytical runs find that the methyl group helps avoid overlaps with potential impurities commonly produced in related processes. For those preparing reference or working standards, this saves both time and solvent.
We never treat aromatic nitriles lightly. Moisture, light, and heat all pose real threats when storing and moving bulk quantities. 2-Cyano-4'-Methylbiphenyl enters our warehouse in tightly sealed, nitrogen-flushed containers even if the batch spends only a few days before shipment. Over the years, we have seen the difference between proper storage and careless exposure: off-odors, discoloration, and, in rare cases, gradual decomposition. These issues reflect in our complaint logs and inform our procedures. End users often thank us for sending a product that doesn’t clog filters or show yellowing, which originates from painstaking sample handling—steps that seem minor until they ruin a multi-kilogram batch downstream.
Feedback from regular users influenced our switch to smaller, ergonomically designed drum liners for easier handling in confined production rooms. This is not about flashy packaging, but about preventing fine powders from sticking or dispersing into the air—an issue that can lead to both safety and yield concerns in a busy plant.
Comparisons help clarify why our 2-Cyano-4'-Methylbiphenyl keeps finding new customers. Those familiar with 4'-Methylbiphenyl or simple biphenyls lacking a cyano group rarely achieve the same combination of reactivity and physical form. The cyano group tunes the electronic properties of the biphenyl core, which has knock-on effects for reactivity with palladium-catalyzed couplings or as a precursor in stepwise syntheses aimed at introducing more complex heteroatoms.
Operators working in quality control will vouch for how our optimized synthesis yields a product nearly free of bis-cyano or mono-methyl impurities—compounds that can behave unpredictably in both biological and polymerization reactions. Others in the field may cut corners on purification or process timing, generating inconsistent lots that fail on chromatographic checks. Our batch records show that a few extra hours of post-reaction cooling or double-filtration make all the difference for end users aiming for a smooth process.
Most 2-Cyano-4'-Methylbiphenyl leaves our plant headed for labs and plants involved in active pharmaceutical ingredient development and specialty materials. Modern drug discovery efforts often focus on aromatic fragments with distinctive polar groups, and our product plays a key role as an intermediate in these fragment-based drug design programs. Feedback from medicinal chemists highlights reliable yields after cross-coupling, ease of scale-up from milligram synthesis to several hundred-gram lots, and minimal issues from residual metal catalysts—outcomes that reflect deliberate design of our crystallization and washing steps.
In electronic material industries, this molecule serves as a stepping stone toward liquid crystal materials and specialty resins. Our partners developing advanced displays or functional polymers count on the methyl-cyano profile to control optical and electronic properties with a precision not offered by plain biphenyls. One customer integrated it into pilot lines for OLED materials; their experience highlighted both the robust thermal stability and the consistent melting range—both features that come not by chance but by careful adherence to procedural details during drying and final packaging.
Scaling up isn’t just a matter of running the same sequence on bigger equipment. Batch-to-batch consistency presents a genuine challenge for aromatic nitriles with multiple substituents. We have found that minor process tweaks—timing of base addition, agitation rate, the sequence of reagent introduction—can cause bigger swings in API precursors than those working on milligram scales might expect. Years of batch record reviews taught us to tune each stage for high-purity output, and frequent calibration of analytical tools keeps compliance tight.
Customers often try products from different sources before returning to ours after discovering yield losses, unexpected side reactions, or issues meeting regulatory documentation needs. We focus on controlling every variable, from raw material sourcing to final filtration, because many stakeholders depend on not having to repeat months of synthesis work on account of starting material variability.
Regulatory expectations and audits rarely leave much margin for error. Our clients appreciate full batch traceability, not just for peace of mind in end use, but for their own internal compliance. Documentation packages include not only certificates of analysis but method validation and impurity profiles derived from our in-house protocols. We've seen an uptick in clients requesting these details as new guidelines emerge on trace contaminants and downstream risk assessment.
For those in larger organizations, the clean supply chain and rapid certificate turnaround translate to fewer delays in both R&D projects and production runs. Over time, consistent performance and transparent data build trust that goes beyond any single purchase order.
Manufacturing specialty biphenyl compounds like 2-Cyano-4'-Methylbiphenyl brings safety and environmental responsibilities. Our process engineers weigh not only yield and purity but solvent recovery and exposure minimization. Aromatic nitriles require careful handling, yet the environmental profile of our process has improved steadily as we've swapped hazardous intermediates for greener options and invested in better emission controls.
Routine team training targets the practical hazards of volatile organics. Real-life incidents—minor leaks, unexpected exotherms, or logistical delays—have all contributed to a culture that catches risks before they escalate. Local environmental permits require disclosure of even minor waste streams. Direct experience with authorities shapes our protocols for containment and waste minimization. Workers know the importance of those principles, because safer jobs mean fewer disruptions and more pride in the plant’s reputation.
Rarely does product improvement stem from brainstorming in conference rooms. Most of our process and product pipeline advances start with questions about solubility, workup, or analytical clarity from customers hitting real-world snags. We take these reports seriously and back track through lab notebooks and plant logs, identifying process conditions that might affect future batches. This dialogue has given rise to more robust production protocols and even improved scale-down validation for users working in resource-limited labs.
Occasional batch failures drive continuous skill development. A few years ago, we traced an off-spec impurity to vendor material drift that analytical screening had missed. This led to an overhaul of supplier approval procedures and buildout of new backup test methods using both HPLC and NMR. Improvements like these reach all customers—not just the ones who flagged the initial issue.
No organization operates perfectly. Instead of waiting for audits or customer complaints, we run internal reviews after every significant batch. Key process parameters—pH, temperature, agitation—get logged and checked to flag deviations early. Years spent in plant and lab settings show that hands-on attention pays dividends in both quality and repeat business.
Partnerships with academic and industrial collaborators have given insight into the full range of 2-Cyano-4'-Methylbiphenyl’s molecular utility and process bottlenecks. By sharing non-proprietary methods and impurity data, researchers gain confidence, and we receive candid feedback not often found in conventional sales exchanges. In return, we draw lessons for both scale-up and early-stage research, bridging the knowledge gap between R&D and full-scale operation.
Demand for high-purity aromatic building blocks continues to grow. Over the last decade, we've noticed end users becoming more discerning—expecting not just basic compliance but proactive support on documentation, risk assessment, and application-specific advice. New regulations and heightened scrutiny from both customers and authorities drive us to maintain a genuine quality culture.
More specialty manufacturers bring new entrants every year, but few control every step from synthesis to final packout. Those working in high-throughput next-gen applications—OLEDs, advanced pharmaceuticals, and specialty electronics—want their key intermediates from experienced teams that know every subtle variation impacts final outcome. Reputational risks and actual project timelines depend on this expertise.
Years of making and shipping organonitriles have shown us the weight of sustainability pressures on manufacturing. By investing in solvent recovery, optimizing reagent use, and working toward minimization of hazardous intermediates, we improve not just the bottom line but our ability to serve clients facing their own environmental stewardship challenges. Many new projects come with requests for environmental impact statements and traceability data, which we've built into routine production and reporting.
Safety experts and process chemists meet regularly to review process design, worker feedback, and new green technology developments. This dialogue promotes a real shift in how we approach both routine and custom production—the kind of attitude that leads to safer, more sustainable, and more reliable manufacturing outcomes for everyone in the supply chain.
Crafting 2-Cyano-4'-Methylbiphenyl at commercial scale pulls together expertise in chemistry, logistics, and compliance. The subtle differences between aromatic derivatives influence everything from reactivity to process safety. By sticking close to the plant floor, monitoring every batch with rigorous attention, and learning from both customers and past mistakes, we aim to deliver a product that meets both the practical and regulatory realities of the modern chemical industry. In this business, every detail counts, and genuine knowledge gained from hands-on experience makes all the difference for end users worldwide.