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2-(Trifluoromethyl)Phenylacetonitrile

    • Product Name 2-(Trifluoromethyl)Phenylacetonitrile
    • Alias 2-(Trifluoromethyl)benzyl cyanide
    • Einecs 252-063-8
    • 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
    VTB
    Specifications

    HS Code

    836713

    Chemical Name 2-(Trifluoromethyl)Phenylacetonitrile
    Cas Number 2774-63-8
    Molecular Formula C9H6F3N
    Molecular Weight 185.15
    Appearance Colorless to pale yellow liquid
    Boiling Point 90-92 °C at 12 mmHg
    Density 1.24 g/cm3
    Refractive Index n20/D 1.496
    Solubility Slightly soluble in water, soluble in organic solvents
    Flash Point 98.6 °C
    Smiles N#CC1=CC=CC=C1C(F)(F)F

    As an accredited 2-(Trifluoromethyl)Phenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-(Trifluoromethyl)Phenylacetonitrile, sealed with a Teflon-lined cap, labeled with hazard warnings.
    Shipping **2-(Trifluoromethyl)Phenylacetonitrile** is shipped in tightly sealed containers, protected from light and moisture. It is transported as a hazardous chemical, following all applicable regulations for handling organic nitriles. Proper labeling, documentation, and spill containment measures are ensured to guarantee the safety of personnel and compliance with local and international shipping guidelines.
    Storage Store **2-(Trifluoromethyl)phenylacetonitrile** in a cool, dry, well-ventilated area, away from heat, ignition sources, and strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers and label clearly. Handle under a fume hood and use gloves and eye protection to prevent direct contact. Follow all local regulations for hazardous chemical storage.
    Application of 2-(Trifluoromethyl)Phenylacetonitrile

    Applications of 2-(Trifluoromethyl)Phenylacetonitrile in Industrial Manufacturing

    As the original producer of 2-(Trifluoromethyl)Phenylacetonitrile, we support multiple advanced chemical industries with a focus on reliable supply chain integration, batch consistency, and regulatory compliance. Below, we describe its principal downstream industrial applications based on real global market requirements and validated industrial practices.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Our material is widely utilized as a key synthetic intermediate in the production of several pharmaceutical APIs, especially in the development of molecules targeting central nervous system disorders and anti-inflammatory agents. Customers implement this compound during the late-stage functionalization of aromatic scaffolds, where the trifluoromethyl motif delivers improved metabolic stability and biological activity. Use within cGMP facilities mandates strict documentation and traceability from raw material intake to the final synthesis of the active ingredient.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for APIs
    • USP-NF (United States Pharmacopeia)
    • European Pharmacopoeia (Ph. Eur.)
    • US FDA 21 CFR Part 211

    Typical usage ratio

    • Ranges from 0.7 to 1.2 molar equivalents per API batch, adjusted by process stoichiometry and reaction yield requirements

    Downstream process integration

    • Used after initial halogenation or alkylation steps; generally enters multi-step organic synthesis through controlled addition to N- or O-nucleophile coupling reactions

    Final product types

    • Neuroleptic agents
    • Non-steroidal anti-inflammatory drugs (NSAIDs)
    • Antihypertensive agents
    • Specialty CNS-targeting small molecules

    2. Agrochemical Intermediate for Herbicide Synthesis

    Manufacturers of advanced herbicides employ this compound as an essential fluorinated aromatic building block to construct active crop protection agents. It contributes improved photostability and selectivity for target plant biochemistry. The raw material enters the agrochemical workflow where strict trace impurity control defines suitability for downstream formulations designed for large-scale agricultural deployment.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH Regulation (EC) No. 1907/2006
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Employed at 0.5 to 1.1 equivalents relative to target actives, with adjustment based on the desired degree of functionalization and downstream yield optimization

    Downstream process integration

    • Added to batch or continuous flow synthesis during the nucleophilic substitution or amide bond-forming steps, following aromatic derivatization of the precursor molecule

    Final product types

    • Pre- and post-emergence herbicides
    • Selective weed control agents
    • Integrated pest management active substances

    3. Specialty Chemical for Liquid Crystal Materials

    Producers of liquid crystal functionalities for display technologies utilize this compound to introduce electron-withdrawing fluorinated aromatic groups, which fine-tune dielectric anisotropy and viscosity in end-use mixture formulations. High chemical purity and defined physical properties are critical due to sensitivity of downstream display applications, where even minor impurities can impact performance. Raw material intake frequently involves real-time analytical verification and full batch reproducibility audits.

    Industry compliance standards

    • IEC 60417 for Display Component Substances
    • RoHS Directive 2011/65/EU
    • ISO 14001:2015 Environmental Management
    • Chinese National Standard GB/T 5211 for Fine Chemicals

    Typical usage ratio

    • Formulation typically requires 0.3–0.9% by weight in nematic LC mixtures, with optimization depending on target optical and electrochemical properties

    Downstream process integration

    • Batch addition to precursor mixture prior to polycondensation, or as a component in the final tweaking stage to reach desired phase transition parameters

    Final product types

    • TFT-LCD panel fluid crystals
    • OLED pre-mixture chemical blends
    • Advanced sensor read-out media

    4. Intermediate for Advanced Organic Dye and Pigment Synthesis

    Producers of high-performance dyes and specialty pigments use this compound to introduce trifluoromethylphenyl units that enhance color fastness and chemical stability under UV exposure. Its implementation supports synthesis of pigments for plastics, inks, and technical textiles that require high resistance to fading, chemical corrosion, or aggressive cleaning agents. Controlled addition and monitoring of impurity levels ensure compatibility with eco-label certification and regulated end-user industries.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of Certain Elements)
    • Oeko-Tex Standard 100 for Textile Chemical Inputs
    • EU REACH Regulation for Colorants
    • ISO 9001:2015 for Production Consistency

    Typical usage ratio

    • Incorporated at 1–5% by total reactant mass, typically chosen based on chromophore target and pigment matrix composition

    Downstream process integration

    • Added to condensation or azo-coupling step after foundation scaffold construction, serving as a core functionalization agent

    Final product types

    • Technical textile dyes
    • UV-stable plastic colorants
    • Specialty printing inks and coatings
    • Resistant industrial pigments for automotive and electronics plastics
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    Certification & Compliance
    More Introduction

    2-(Trifluoromethyl)Phenylacetonitrile: More Than a Starting Material

    Our Approach to Synthesis

    Manufacturing 2-(Trifluoromethyl)phenylacetonitrile isn’t about the routine mixing of ingredients or scaling up a generic protocol. We pay attention to the details that matter, improving purity and consistency batch after batch. Over years spent with this molecule, the process has taught us that controlling reaction temperatures, choosing the right solvents, and selecting stable reagents beat rote repetition. Each small adjustment results in a cleaner product, greater yield, and less waste, all of which feed directly into downstream reliability for our customers—be they engaged in discovery chemistry or scaling up agrochemical intermediates. Our process favors a route that keeps byproducts in check, not because regulations dictate, but out of pride in what leaves our factory gates.

    The Product: What Sets it Apart

    The 2-(trifluoromethyl) group introduces a distinct reactivity that shapes its utility. Chemists look to this acetonitrile for reliable cyanomethylation of aromatic scaffolds. Other nitriles often fall short where this compound excels, as the electron-withdrawing CF₃ pulls the aromatic system into a sweet spot: neither too reactive nor too sluggish. From our hands-on work supporting custom synthesis teams and formulations groups, we’d argue the biggest value-add comes from the balance between functional group tolerance and predictable transformation in alkylation, reduction, or Grignard-type reactions.

    Specifications That Make a Difference

    Our product routinely reaches 99% minimum purity by GC assay. For most uses in pharmaceutical research or API intermediates, this level supports direct conversion without elaborate pre-cleaning. Residual solvents remain tightly controlled—our drying protocols and distillation steps cut the odd peaks that interfere with analytical work or scale-up. Moisture finds no friend here, and we equip every shipment with low-volume packaging for those aiming to run small-scale reactions where exposure matters. We oversee the quality at every step, not least because the presence of unreacted starting material, isomers, or trace acidic contaminants can derail sensitive transformations, something every chemist learns to respect.

    Where We See it Used

    Talk to a handful of process chemists and the story stays surprisingly consistent: 2-(Trifluoromethyl)phenylacetonitrile often gets pulled into developing next-gen agrochemicals, pharmaceuticals, and high-performance materials. Unlike plain phenylacetonitrile, the trifluoromethyl group confers metabolic stability, lipophilicity, and unique binding properties. This underpins a lot of recent patent activity and keeps raw material demand high. At our facility, requests start with scale-up feasibility, but quickly pivot to regulatory questions, analytical validation, and batch-to-batch consistency. Our operators and QC analysts don’t just know the smell of the product—most can rattle off the subtle changes in crystal habit or color that show up when process parameters shift.

    Comparing to Alternatives

    Standard benzyl cyanides lack the trifluoromethyl punch. They might suit some baseline syntheses, yet the wealth of pharmaceutical programs demanding fluorinated building blocks renders them less relevant in industrial settings and academic labs pushing the envelope in medicinal chemistry. Other fluorinated nitriles do circulate, but not with the pattern of selectivity and reactivity that makes 2-(Trifluoromethyl)phenylacetonitrile a staple in SAR studies. Bulk buyers have asked if we’ll make the para-substituted variant or tri-substituted versions. These might work in narrow applications, but when it comes to synthetic flexibility and predictable downstream behaviors, the ortho-trifluoromethyl still leads the pack.

    Dealing With Supply Pressures

    Recent years haven’t been easy for global chemical supply chains, particularly for niche building blocks with tight tolerances like this one. We watched as disruptions in fluorinating agents and upstream intermediate prices rippled through the market. While some speculators offer off-spec material at tempting rates, we’ve found this practice undermines genuine innovation. We’ve held to our standards, sourcing precursors from vetted partners and steering clear of recycled or dubious lots. Our staff occasionally spend long nights requalifying raw material sources—an experience, not a choice—and the difference turns up in the downstream performance of our acetonitrile. Put simply, unreliable feedstock creates batch failures and delayed research, eroding confidence from project teams and regulatory reviewers alike. Real-world performance guides our sourcing, not spreadsheets or procurement convenience.

    Attention to Handling and Safety

    Direct experience teaches a deep respect for both the potency and hazards of organic nitriles, especially ones carrying reactive functional groups like trifluoromethyl. Our technicians adopt rigorous controls during synthesis and packaging, including multiple containment checks and vapor mitigation strategies that prevent fugitive emissions. We supply high-integrity containers suited for air- or moisture-sensitive shipments and believe in full transparency on stability, degradation products, and handling tips that go beyond the MSDS. End users have told us our consistency in this area saves time on unnecessary repurification and researchers avoid unexpected side reactions or yield losses.

    Continuous Improvement

    Our roots in custom manufacturing led us to treat every recurring batch as both a validation and a fresh opportunity to rethink parameters. Improving product crystallinity, optimizing yield, reducing impurities below the threshold of analytical detection—these aren’t abstract goals. They mark our ongoing efforts, spurred by customer feedback and by setbacks overcome on the plant floor. Last year, for example, a minor change in filtering media reduced carry-over of microimpurities, allowing several pharma partners to simplify their work-up procedures. We’ve learned that a single small tweak, born from watching an operator resolve a pressure drop in filtration, can reverberate through the entire production cycle and ultimately improve reliability for everyone downstream.

    Sustainability

    Producing fluorinated intermediates carries environmental responsibilities not easily dismissed with compliance checkmarks. Our commitment starts with process design—reducing solvent consumption and maximizing reagent economy whenever possible. Process residuals are regularly analyzed and managed in accordance with regional and international standards, but our ambitions run deeper. We invest in solvent recovery systems and energy efficiency upgrades, auditing every step for waste minimization and emission control. Customers in pharmaceutical supply chains operate under intense regulatory scrutiny, so any upstream supplier slack risks project delays or regulatory hurdles. Reliable, responsible operations underpin trust—our partners have come to expect regular audits and open plant tours, proof we treat stewardship and transparency as integral, not afterthoughts.

    Adaptability to Reactor Scale

    One common misconception is that a product made smoothly at kilogram scale will behave predictably at pilot or production scale. In our experience, 2-(Trifluoromethyl)phenylacetonitrile can exhibit subtle shifts: agglomeration in crystallization, color change with trace metal contamination, or stratification upon storage. We’ve invested heavily in scale-down simulation bays, where we recreate customer environments to preempt scale-up surprises. This close alignment means our process engineers can warn about exothermic events, filtration bottlenecks, or reaction time changes before customers encounter them. Our willingness to simulate these subtle shifts results in fewer delays, less scrapped product, and faster route validation.

    Feedback Loops and Collaboration

    Dialogue with end users has shaped our product as much as internal process development. We solicit and act on input from bench chemists and plant engineers facing unexpected bottlenecks. Whether it’s a preferred particle size for solid transfer or advice on co-solvent selection, these insights translate into tweaks that improve experience for all customers. A memorable collaboration with a multinational pharmaceutical company drove us to modify the drying regime, halving residual acetonitrile content and directly improving product performance in their hydrogenation step. These real-world exchanges keep us grounded and our focus fixed on measurable, actionable improvements.

    Regulatory Landscape and Transparency

    We don’t merely follow regulatory updates; we anticipate them. Tracking developments in global chemical registration—whether for REACH, TSCA, or other regional demands—became routine for our regulatory team. We keep product traceability strong, batch records complete and ready for inspection. This lets downstream partners more efficiently file their own compliance reports, an outcome we value as highly as any technical feat in synthesis. From impurity profiles to packaging changes, transparency forms the foundation for confidence and continuity through audit cycles, tech transfers, and regulatory submissions.

    Craftsmanship: Where Details Matter

    Each bottled shipment reflects a composite skill set, built on decades of collective trade experience. Our technicians don’t take shortcuts, whether managing exotherms, policing raw material inventory, or hand-labeling hazardous material shipments. These sustained habits result in low impurity levels and stable supply over repeated contracts—outcomes appreciated by partners whose own product quality and regulatory compliance depend on secure sources of specialty intermediates.

    Product Lifespan and Storage

    Storage forms a key piece of the product equation. We’ve seen 2-(Trifluoromethyl)phenylacetonitrile maintain its analytical profile under cool, dry conditions for more than a year, but exposure to acidic vapors or unintentional mixing with strong oxidizers can prompt slow decomposition or color changes. By sharing these observations openly, users avoid the needless frustration of finding out mid-process that small deviations risk yield drops or increased solidification. Our packaging format reflects field experience—smaller, lightproof containers suit short-turnaround synthesis, while bulk drums have additional liner protections.

    Quality Assurance as a Lived Value

    Routine batch sampling, GC and NMR verification, and real replications—not just paper QA—anchor our approach. Chemists from customer organizations sometimes visit to watch a batch run, and we encourage it. Trust builds not with slogans, but with open doors and real conversations about process, controls, and outcomes. Auditors walk the plant, remarking on documentation, safety barriers, and the full paper trail back to raw materials. We treat these reviews as learning opportunities, not adversarial events.

    Market Trends and Future Uses

    Research pipelines increasingly aim at fluorinated aromatic intermediates, as their metabolic and physicochemical properties underpin advances in pharmaceuticals, crop protection, and advanced materials. Our participation in these conversations, through consortia and technical conferences, means that we see not just current, but next-generation use cases as they emerge. This visibility enables us to tweak process scale, refine analytical purity, or add application-specific documentation well before formal requests come through.

    Customer Successes and Product Impact

    We care about downstream successes of our partners. More than one client has let us know that switching to our 2-(Trifluoromethyl)phenylacetonitrile improved both campaign consistency and regulatory submission timelines. These stories flow both ways: learning about the hurdles end users face helps us refine what matters in a production setting, whether the focus is on meeting new impurity limits, tighter packaging requirements, or supporting green chemistry upgrades. The best endorsements come as repeat orders and referrals, not from awards or certification logos.

    Challenges and Ongoing Solutions

    Nothing about handling trifluorinated acetonitriles is trivial. We confront supply volatility, rising scrutiny on waste management, and shifting timelines from regulatory bodies. Our response stays focused: ongoing investment in staff training, process engineering, and real-time analytics. Each improvement cycle tightens our process, keeps material moving smoothly, and reduces risk for everyone linked to the supply chain.

    Trusted by Those Who Know

    Word of mouth from chemists and process engineers has done more to shape our reputation than marketing budgets or website traffic. We take this seriously. Satisfaction among experienced buyers translates into more feedback, more opportunities for improvement, and a steady pulse on real-world trends and requirements. This is why every kilogram matters—and why 2-(Trifluoromethyl)phenylacetonitrile, as made here, stands apart among aromatic nitriles.