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2,5-Bis(Trifluoromethyl)Benzonitrile

    • Product Name 2,5-Bis(Trifluoromethyl)Benzonitrile
    • Alias 2,5-Bis(trifluoromethyl)benzonitrile; 2,5-Bis(trifluoromethyl)cyanobenzene; 2,5-DCBTF
    • Einecs 249-930-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    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 & Storage
    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.
    Application of 2,5-Bis(Trifluoromethyl)Benzonitrile

    Applications of 2,5-Bis(Trifluoromethyl)Benzonitrile in Industrial Manufacturing

    As 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 Synthesis

    This 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

    • Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH, EU)
    • US EPA Pesticide Registration requirements (40 CFR Part 158)
    • Chinese National Standard GB 2763 for Maximum Residue Limits in Food
    • ISO 9001:2015 Quality Management System (for traceability in supply chains)

    Typical usage ratio

    • 15–35% relative to total active ingredient precursors, adjusted based on molecular design and yield optimization

    Downstream process integration

    • Introduced at the initial halogenation or metal-catalyzed coupling step
    • Flows into subsequent reduction, cyclization, or amination stages for AI formation
    • QC checkpoint for purity and water content prior to downstream usage
    • Waste minimization procedures implemented for spent solvents containing trifluoromethyl fragments

    Final product types

    • Pyridine-based herbicides (e.g., selective broadleaf weed herbicides)
    • Phenylpyrrole fungicides
    • Insecticidal intermediates
    • Pre-emergent soil treatment actives

    2. Pharmaceutical Intermediate for Aromatic Fluorination

    Downstream 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapters <232> and <233> (Elemental Impurities)
    • EDQM guidelines for APIs used in EU medicinal products
    • Chemical Registration and Pharmacopoeial Monograph Listing (where applicable)

    Typical usage ratio

    • 20–45% within the specific reaction sequence, based on desired substitution pattern; adjusted for stoichiometric excess if used in coupling reactions

    Downstream process integration

    • Direct reagent in Suzuki, Buchwald–Hartwig, or copper-catalyzed couplings
    • Feeds into hydrogenation, hydrolysis, or condensation following aromatic substitution
    • Subjected to in-process testing for residual CN functionality and trace organic volatiles
    • Integrated quality release with full batch documentation for regulatory submissions

    Final product types

    • CNS-active pharmaceutical intermediates
    • Trifluoromethylated drug candidates in oncology and anti-inflammatory pipeline
    • Lead compounds for small molecule screening
    • Impurity reference standards and metabolite synthesis

    3. High-Performance Electronic Material Precursor

    In 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

    • RoHS (Restriction of Hazardous Substances Directive, EU)
    • IEC 61249-2-21 (Halogen-Free electronic base material standard)
    • ISO 14001 Environmental Management System
    • IECQ QC 080000 (Hazardous Substance Process Management)

    Typical usage ratio

    • Typically 5–12 mol% as a starting monomer, adjusted based on device target properties and co-monomer ratios

    Downstream process integration

    • Enters condensation or functionalization step for monomer synthesis
    • Feeds into polymerization reactors for specialty polyimides or aromatic polyethers
    • QC for ionic residue and fluorine analysis at the solution and thin film stage
    • Managed in solvent flows to minimize cross-contamination in cleanroom environments

    Final product types

    • Liquid crystal display (LCD) monomer units
    • Organic thin-film transistor (OTFT) precursors
    • Fluorinated high-frequency PCB materials
    • Specialty insulating films for flexible circuits

    4. Specialty Polymer and Resin Modifier

    Advanced 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

    • ASTM D6847 Standard for Fluorinated Polymer Properties
    • FDA 21 CFR 177.1520 (for indirect food-contact resin rules, where applicable)
    • UL 94 Flammability Rating for Plastics
    • REACH SVHC requirements for monomer content disclosures

    Typical usage ratio

    • 0.5–8 wt% as a copolymerization component, customized according to final polymer requirements and compatibility

    Downstream process integration

    • Added to prepolymer reactor prior to chain initiation
    • Participates in batch or continuous polymerization for specialty copolymers
    • In-process monomer recovery and waste stream treatment
    • QC on conversion rate and residual monomer prior to final product extrusion or casting

    Final product types

    • Fluorinated filtration membranes
    • High-durability coatings for chemical process equipment
    • Specialty adhesives for electronics and aerospace
    • Resistant elastomer blends for pump and seal applications
    Free Quote

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    Certification & Compliance
    More Introduction

    2,5-Bis(Trifluoromethyl)Benzonitrile: An Insider’s Perspective from the Lab Floor

    Introducing Our Approach to Advanced Fluorinated Aromatics

    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.

    Understanding the Product’s Core Attributes

    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.

    Production Insights: Consistency Backed By Hard Data

    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.

    Why Chemists Request This Compound by Name

    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.

    Real-World Applications as Seen in Our Customers’ Pipelines

    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.

    What Sets Our 2,5-Bis(Trifluoromethyl)Benzonitrile Apart

    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.

    Differences from Related Benzonitriles

    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.

    Navigating Regulatory Expectations and Quality Trends

    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.

    Challenges in Ongoing Production

    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.

    Supporting Researchers: Beyond Just a Product

    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.

    Perspective on Supply, Demand Shifts, and Future Outlook

    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.

    Commitment to Progress: The Practical Science Behind Every Batch

    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.