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HS Code |
874627 |
| Chemical Name | 2,5-Bis(Trifluoromethyl)Benzonitrile |
| Cas Number | 328-71-0 |
| Molecular Formula | C9H3F6N |
| Molecular Weight | 241.12 |
| Appearance | White to off-white solid |
| Melting Point | 53-57°C |
| Boiling Point | 162-164°C (at 13 mmHg) |
| Density | 1.48 g/cm3 |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, acetone) |
| Purity | Typically ≥98% |
| Smiles | N#CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 |
| Inchi | InChI=1S/C9H3F6N/c10-8(11,12)6-1-2-7(9(13,14)15)5(3-6)4-16/h1-3H |
| Synonyms | 2,5-Bis(trifluoromethyl)benzonitrile |
| Storage Conditions | Store at room temperature, tightly sealed, away from light |
As an accredited 2,5-Bis(Trifluoromethyl)Benzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g of 2,5-Bis(Trifluoromethyl)Benzonitrile is packaged in a sealed amber glass bottle with tamper-evident cap. |
| Shipping | 2,5-Bis(Trifluoromethyl)Benzonitrile is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported as a solid under cool, dry, and well-ventilated conditions. Handle with care, following all relevant hazardous chemical shipping regulations. Packaging complies with international safety standards for chemical transport. |
| Storage | 2,5-Bis(Trifluoromethyl)Benzonitrile should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Handle under an inert atmosphere if possible, and avoid prolonged exposure to air. Store according to local regulations for hazardous chemicals. |
Applications of 2,5-Bis(Trifluoromethyl)Benzonitrile in Industrial ManufacturingAs a direct manufacturer of 2,5-Bis(Trifluoromethyl)Benzonitrile, we enable high-value downstream synthesis for competitive industrial sectors requiring selective fluorination. Our quality control processes, integrated production lines, and compliance systems meet the stringent requirements of global end users in specialty chemicals and advanced materials manufacturing. 1. Agrochemical Intermediate SynthesisThis compound serves as a crucial building block in the synthesis of advanced herbicide and insecticide active ingredients, especially for introducing trifluoromethyl and benzonitrile moieties. Agrochemical manufacturers incorporate it into pyridine and phenylpyrrole skeletons after nucleophilic aromatic substitution or condensation steps. The presence of robust electron-withdrawing groups enhances metabolic stability in field conditions, ensuring residual activity in challenging agricultural applications while supporting efficient synthetic routes established in recent generations of crop protection molecules. Industry compliance standards
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2. Pharmaceutical Intermediate for Aromatic FluorinationDownstream pharmaceutical manufacturers use this material to access pharmacologically active scaffolds bearing electron-deficient aromatic rings. It acts as a precursor in the synthesis of CNS drug molecular backbones, utilizing transition metal-catalyzed cross-couplings and nucleophilic substitutions. By installing metabolic blocking groups using this raw material, formulators achieve increased bioavailability and improved pharmacokinetics for late-stage clinical candidates and APIs. Industry compliance standards
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3. High-Performance Electronic Material PrecursorIn the electronics sector, this compound functions as a fluorinated aromatic precursor for the manufacture of advanced organic electronic materials such as liquid crystal monomers and thin-film transistor precursors. Its use enables enhanced dielectric properties and moisture stability, especially in heat-resistant polymers and high-purity films. Manufacturers seek consistent fluorine content and low ionic impurity levels in every batch to ensure downstream device reliability. Our material supports strict process integration for global display module lines. Industry compliance standards
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4. Specialty Polymer and Resin ModifierAdvanced resin compounding operations use this material for introducing unique trifluoromethyl and cyano functionalities into specialty polymers. The compound provides increased chemical resistance, thermal stability, and surface energy control—especially in resins designed for filtration membranes, fluorinated elastomers, and engineering plastics. Its controlled reactivity suits downstream copolymerization or post-polymer modification without typical side reactions, allowing precise molecular weight control and performance tailoring. Industry compliance standards
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In chemical manufacturing, precision isn’t a buzzword. It’s the only path to a compound that consistently meets a customer’s intent, and that’s where 2,5-Bis(Trifluoromethyl)Benzonitrile comes into play. Looking over decades of bench work, we’ve advanced a synthesis that consistently furnishes high-purity material, batch after batch. This compound, known for the strong electron-withdrawing character of those two trifluoromethyl groups and the versatile nitrile functionality, brings a unique set of properties to research benches and industrial reactors alike.
Each molecule of 2,5-Bis(Trifluoromethyl)Benzonitrile (CAS: 328-75-6) bears two CF3 groups anchored at the 2 and 5 positions on the aromatic ring, not just as a structural choice, but as a path to function and selectivity in downstream transformations. The para relationship between the nitrile and trifluoromethyl groups makes this compound more than a sum of its parts; in the lab, it means chemists count on specific reactivity, thermal stability, and effect on adjacent functional groups. Our product typically arrives crystalline, off-white, with minimal impurity profile, a melting range users can trust, and packed under inert atmosphere to fend off hydrolysis.
Our facility operates under real-world conditions—temperature, pressure, and stoichiometry aren’t just lines in a protocol, they are realities faced every batch. Ensuring product integrity for this compound, we control all incoming fluorinating agents and deploy chromatography that’s more than just a checkpoint—it becomes a record of the efforts put into controlling every stage. GC-MS and 19F-NMR are central here; spectral clarity isn’t just marketing talk, but a guarantee we make to customers who depend on accuracy and reproducibility. Every kilo of 2,5-Bis(Trifluoromethyl)Benzonitrile we ship comes with the confidence it will react as described in the literature, not just in theory but in your actual glassware.
The demand for 2,5-Bis(Trifluoromethyl)Benzonitrile doesn’t come from hype. It’s earned by performance in real-world reactions where it behaves as a rugged intermediate and building block. Medicinal chemistry pushes the envelope with new targets, and this nitrile changes solubility profiles and brings metabolic stability to candidate molecules. Agrochemical developers rely on it for introducing fluoroaromatic motifs, which often translate into robust bioactivity in the field. Specialty polymer chemists count on it for tailored substitution in high-performance materials. Each discipline pulls at the same thread: they don’t want to revisit starting material headaches, they want the freedom to innovate at the next synthetic step.
Customers have taken this compound into lead series for pharmaceuticals, where fluorine’s unique interaction with biological targets can tip the scales toward viability. In heterocyclic syntheses, it finds use as a precursor for constructing fluorinated azaaromatics and elaborate ligands. On the agricultural side, crop protection research uses it to build triazine and pyrimidine motifs that withstand degradation, extending field lifespans and improving yield protection. Its role in performance polymers shouldn’t be understated either; those same electron-withdrawing groups increase weather resistance and lower the friction coefficients of specialty coatings. Rather than chasing applications out of fashion, we see lasting trends: fluorination as a strategy remains steadily in demand across sectors.
Nobody builds trust on specs alone. Lab conversations often focus on trace impurities—minute byproducts that, left unchecked, will interfere with catalysis or biological screens. Drawing from our in-house monitoring data, impurities consistently fall below 0.2%, so researchers avoid the pain of mysterious peaks in their NMR or problematic side reactions. We hear from customers who previously used bulk-sourced material, and their switch to our more tightly controlled batches often matches a reduction in troubleshooting, not just in yield but in reliability over dozens of syntheses. This translates to fewer wasted resources—no need for repeated purifications, no stalls mid-project waiting for a new supply.
The choice of solvent systems and drying conditions matter as well. We use strictly anhydrous solvents during synthesis and handle material in atmospheres free of moisture, simply because the product’s longevity and purity demand it. Handling fluorinated aromatics can challenge even experienced operators, since trace metals and adventitious impurities risk catalyzing unplanned side reactions. Because we control packaging and logistics with the same attitude we bring to synthesis, deliveries stay stable, and our clients avoid synthetic setbacks due to bottles arriving degraded or contaminated.
Comparisons often arise between this compound and its non-fluorinated or mono-substituted analogs. Substituting one or both hydrogens with trifluoromethyl fundamentally alters reactivity. Nucleophilic aromatic substitution proceeds under milder or more selective conditions, and the resulting products frequently display greater metabolic resilience. We’ve run the side-by-side tests: products lacking the symmetrical CF3 pattern can fail to deliver the same degree of bioactivity or process robustness, especially in late-stage functionalization.
Try using a mono-trifluoromethylbenzonitrile under Suzuki-Miyaura cross-coupling and watch the difference in catalyst turnover—the difluorinated variant runs cleaner, produces fewer side products, and tolerates a wider set of conditions. These aren’t just literature observations, but outcomes measured over dozens of actual process runs. Our chemists routinely consult with customers unsure about structural requirements, and based on this ground-level insight, 2,5-Bis(Trifluoromethyl)Benzonitrile often emerges as the better fit for current regulatory demands, especially in formulations that must pass stringent stability testing.
The chemical marketplace moves fast, but regulatory frameworks persist—compliance with REACH, SDS transparency, and tracking of batch traceability all enter into the conversation with sophisticated customers. We don’t see these expectations as external constraints, but as necessary features of responsible production. Our audit records follow every shipment as a matter of course, and customers gain confidence that their supply chain won’t unravel on account of shifting rules or unreported changes in formulation. That focus on traceability has a practical dimension: customers have come back years later, needing to retrace results to a specific batch, and we’ve been able to help, because recordkeeping isn’t an afterthought.
Sustainability, from raw materials to process waste, has become increasingly important. While working with fluorinated aromatics presents unique disposal and health considerations, our protocols minimize emissions and carefully manage effluent streams through on-site treatment and abatement. Our strategy favors lifecycle thinking, not just single-cycle output, so that each project stays aligned with evolving external scrutiny on environmental impact. Employees undergo periodic training—not as a box-checking exercise, but because one slip in handling can mean a loss of a high-value batch or, worse, a safety incident.
Scaling up a bench-scale reaction for 2,5-Bis(Trifluoromethyl)Benzonitrile involves more than just multiplying reagent quantities. Each transition to a larger vessel exposes subtle dynamics—heat transfer, mixing efficiency, and material compatibility—that the original literature often glosses over. We’ve encountered hurdles: exotherms that required revised cooling protocols; unexpected aggregation leading to filtration headaches. Overcoming those taught us that small impurities become substantial at scale. The biggest difference between lab and plant doesn’t rest in fancy equipment; it shows up in the attitude towards troubleshooting and proactive maintenance.
Quality control often reveals that trace solvents or unanticipated byproducts can sneak through unless monitored aggressively. Chromatograms from early days showed ghost peaks, some resulting from supplier-to-supplier batch variability. We shifted raw material vendors—sometimes more than once—to keep impurity fingerprints in check. This experience underscores a straightforward lesson: there’s rarely a final, fixed recipe for consistently pure 2,5-Bis(Trifluoromethyl)Benzonitrile. It’s about iteration, testing, and constant feedback from both data and the end users that depend on our efforts.
Chemists don’t just want a bottle and a data sheet. The real need is advice refined through hundreds of runs and accurate interpretation of NMR data or LC-MS results. Our team spends plenty of time answering technical queries and troubleshooting odd reaction outcomes for customers—because we have seen those same issues on our own systems. Bonding with researchers over shared challenges makes the product more than just a commodity. Problems like slow dissolution, sensitivity to moisture, or side reactions aren’t mysteries; they’re learning moments that feed into the next generation of synthesis and purification strategies.
Feedback from the field—the actual bench scientists and plant chemists—shapes continuous adjustments. One customer found odd discoloration in an aromatic substitution protocol. Through collaborative investigation, we traced the problem to shipping temperature spikes, prompting a change in our logistics approach and improved insulation for long-haul shipments. These stories aren’t accolades; they’re just examples of daily learning that shapes reliability into every bottle and drum that leaves our gate.
Trends in demand for highly fluorinated benzonitriles stem from several forces. The pharmaceutical sector, constantly iterating through fluorinated scaffolds in new leads, hasn’t shown signs of stepping back from these motifs. As regulatory scrutiny on impurities and process emissions rises, suppliers who can produce rigorously pure intermediates gain ground, while bulk traders focused solely on volume have begun to lose favor. Customers expect not only a kilogram at the right price, but assurance on provenance, purity, and traceability.
Our investment in process analytics, and the know-how to interpret and act on that data, sits behind every order. Customers facing tighter project timelines and cost pressures look for compounds that keep projects moving, not hung up in purification. We notice increased frequency of repeat orders from customers who, after sampling from different suppliers, realize that not all fluorinated benzonitriles are equal. Achieving this reputation means investment in people and analytical tools, powered by a deep respect for what can—and sometimes does—go wrong in chemical manufacturing.
In every kilo of 2,5-Bis(Trifluoromethyl)Benzonitrile produced here, there are lessons baked in from past syntheses—successes and failures, large-scale mishaps and small, incremental improvements. No specification sheet or marketing claim captures the full reality. There’s pride not just in the purity or the NMR profile, but in feedback from end users who report higher yields, fewer purification headaches, and real project progress as a result. These outcomes are built on mutual respect: between those synthesizing the compound and those turning it into life-saving drugs, crop protectants, or new functional materials.
We continue to push on process safety, environmental safeguards, and analytical rigor, because the real value of a specialty chemical never lies in inventory or catalog entries. The value emerges from reliability under real-world pressures—scientific, regulatory, or logistical. As new applications for fluorinated aromatics arise, we stand ready to adapt with them. This ongoing dialogue, built on technical knowledge, long memory, and honest feedback, is the foundation for producing 2,5-Bis(Trifluoromethyl)Benzonitrile at a standard researchers and industry partners trust, season after season.