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2,4,5-Trifluorophenylacetonitrile

    • Product Name 2,4,5-Trifluorophenylacetonitrile
    • Alias 2,4,5-Trifluorobenzyl cyanide
    • Einecs 244-858-4
    • 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

    456231

    Product Name 2,4,5-Trifluorophenylacetonitrile
    Cas Number 88511-54-0
    Molecular Formula C8H4F3N
    Molecular Weight 171.12
    Appearance White to off-white solid
    Melting Point 41-46°C
    Boiling Point 234-236°C at 760 mmHg
    Density 1.309 g/cm3
    Purity Typically >98%
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Smiles N#CC1=CC(F)=C(F)C=C1F
    Inchi InChI=1S/C8H4F3N/c9-6-2-1-5(4-12)3-7(10)8(6)11/h1-3H,4H2
    Storage Conditions Store at 2-8°C, tightly closed

    As an accredited 2,4,5-Trifluorophenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle, sealed with a red cap, labeled with hazard warnings, containing 25 grams of 2,4,5-Trifluorophenylacetonitrile.
    Shipping 2,4,5-Trifluorophenylacetonitrile is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous chemical, with packaging conforming to international transport regulations. Proper labeling, documentation, and safety information are included to ensure safe handling during shipping and compliance with legal requirements for chemical transport.
    Storage **2,4,5-Trifluorophenylacetonitrile** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Use appropriate safety procedures to prevent inhalation or skin contact, and store in accordance with all local regulations for hazardous chemicals.
    Application of 2,4,5-Trifluorophenylacetonitrile

    Applications of 2,4,5-Trifluorophenylacetonitrile in Industrial Manufacturing

    2,4,5-Trifluorophenylacetonitrile supports high-value transformations in the agrochemical, pharmaceutical, specialty intermediate, and advanced material sectors. We produce this compound to strict purity and batch consistency standards, enabling downstream manufacturers to control processing kinetics, impurity profiles, and regulatory traceability. The following scenarios reflect core industrial segments based on real downstream adoption and end-use product requirements.

    1. Synthesis of Agrochemical Active Ingredients

    Formulators use 2,4,5-Trifluorophenylacetonitrile as a building block in multi-step synthesis of selective herbicides and fungicides, particularly for introducing trifluoromethylated aryl groups that provide stability against UV-induced degradation and metabolic breakdown. It enters as a nitrile precursor for condensation or further functionalization, ultimately controlling the spectrum and duration of field activity in final agrochemical actives. Engineering teams monitor feedstock ratios to optimize Yields and minimize by-products, as strict residue, compositional, and environmental standards drive process control.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (including relevant CIPAC methods)
    • OECD Guidelines for the Testing of Chemicals (Sections 1 & 2)
    • REACH Annex VII & VIII Chemical Safety Assessment
    • ISO 9001 QMS for agrochemical production

    Typical usage ratio

    • 5–20% of molar basis in key reaction steps; adjusted per desired arylation and side-chain modifications

    Downstream process integration

    • Introduced as the main aryl nitrile in intermediate coupling, triggering downstream chlorination or phenoxy substitution
    • Serves as a substrate in transition metal-catalyzed transformations, facilitating functional group installation

    Final product types

    • Trifluorophenyl-based pre-emergent herbicides
    • Selective fungicidal actives for cereal and fruit crops
    • Seed coating protectants

    2. Pharmaceutical Synthesis of Small Molecule Drug Intermediates

    Production groups in the pharmaceutical sector source this nitrile to deliver the trifluorinated aryl segment in several clinical candidate syntheses, especially within anti-viral and anti-tumor lead structures. During pilot and commercial synthesis, chemists rely on its reactivity for nucleophilic addition, reductive amination, or hydrolysis under controlled pH and temperature profiles. Quality teams validate residue removal and track batch genealogy to support regulatory filings and pharmacopoeia compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF General Chapters on Residual Solvents and Impurities
    • European Pharmacopoeia Monograph 2034 (intermediates for small molecules)
    • FDA 21 CFR Part 211 (finished pharmaceuticals)

    Typical usage ratio

    • 0.2–2.5 molar equivalents per step, depending on scaffold design and required aryl substitution density

    Downstream process integration

    • Charged in amidation steps during heterocycle construction or side-chain diversification
    • Incorporated prior to hydrogenation or hydrolysis for amino acid derivative synthesis

    Final product types

    • Key intermediates for kinase inhibitors
    • Nucleoside analog precursors
    • Immunomodulatory agent scaffolds

    3. Specialty Chemical Intermediates for Liquid Crystal Materials

    R&D and process teams in electronics materials manufacturing select this raw material for liquid crystal and organic display intermediate formulations where trifluoroaryl moieties are essential for dielectric tuning and molecular orientation. Integration occurs through bond formation generating core mesogenic structures, followed by further purification and polymerization steps. Batch uniformity directly impacts device consistency, defect rates, and optical performance, requiring stringent lot documentation and impurity tracking.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic device components
    • IEC 61340 ESD process control for OLED/LCD manufacturing
    • ISO 14001:2015 for environmental impact of specialty chemicals
    • Customer-specific QMS protocols for high-purity electronic raw materials

    Typical usage ratio

    • 10–30% weight/weight in mesogen intermediate synthesis, fine-tuned for phase transition temperature and viscosity targets

    Downstream process integration

    • Utilized in primary nucleophilic aromatic substitution forming oligomer backbones
    • Directly modified to introduce terminal or lateral groups to adjust optic axis alignment in final materials

    Final product types

    • High-performance liquid crystal display (LCD) intermediates
    • TFT and OLED prepolymer blends
    • Specialty films for touch sensors

    4. Fine Chemicals: Synthesis of Fluorinated Flavor Fragrance Intermediates

    Within fine chemical manufacturing, 2,4,5-Trifluorophenylacetonitrile serves as an advanced arylation handle for the selective introduction of fluorinated motifs in the synthesis of fragrance and flavor compounds. The compound’s use supports the creation of stable, low-odor intermediates that bring specific organoleptic profiles and stability against oxidation in end products. Process engineers control addition timing, solvent choices, and downstream purification to ensure compliance with end-use safety and purity requirements for regulated consumables.

    Industry compliance standards

    • IFRA Standards for Fragrance Material Composition
    • EU Regulation (EC) No 1334/2008 on Flavorings
    • FCC (Food Chemicals Codex) for flavor ingredient purity
    • ISO 22716 Cosmetics GMP, where applicable

    Typical usage ratio

    • 0.05–0.2 molar ratio as precursor for high-impact aromatic note modifiers; rate adjusted by target molecular weight and volatility design

    Downstream process integration

    • Employed in early alkylation or arylation reactions during key flavor or fragrance intermediate synthesis
    • Modified under controlled hydrogenation or oxidation conditions for aldehyde or alcohol derivatives

    Final product types

    • Fluorinated floral toner intermediates
    • Specialty flavor masking ingredient bases
    • Stabilized musky aroma blends
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    Certification & Compliance
    More Introduction

    Introducing 2,4,5-Trifluorophenylacetonitrile: An Operator’s Perspective

    Real-World Demands in an Evolving Industry

    Specialty intermediates have always required consistency and real-world understanding on the shop floor. From the earliest days in fine chemicals to today’s higher regulatory standards, producers face a working environment that rewards reliability and transparency. 2,4,5-Trifluorophenylacetonitrile isn’t just a niche item on a spreadsheet; most downstream partners ask for it because it bridges the gap between structure and reactivity. Through years spent scaling up phenylacetonitrile derivatives, direct feedback from partners and colleagues has set a higher standard for both process and result.

    Each new inquiry draws out different needs: some project managers look for tight impurity controls, others push for solvent compatibility, and most hope to reduce cost while improving project windows. Practical considerations drive these requests. Our team only started producing this compound after seeing repeated interest from process chemists working with fluorinated intermediates—particularly where both electron-withdrawing strength and selective reactivity were crucial.

    This isn’t just about chemistry happening on paper. More often than not, successful batch outcomes depend on a memory for how operations actually work at scale. We’ve trialed and errored the finer points: the choice of fluoride source, clean phase-separation, water workups, quench timing, and minimizing byproduct formation. Our operations crew knows there’s more at stake than yield percentages. They’ve dealt with tank blockages, repetitive filtration runs, and even persistent odor that can cling despite engineering controls. By refusing to treat these headaches as simple line items, our team keeps learning what genuine reliability looks like for high-purity fluorinated nitriles.

    What Makes 2,4,5-Trifluorophenylacetonitrile Different

    Anyone who has worked with phenylacetonitrile analogues sees the influence of fluorination immediately: not just in how cleanly substitution proceeds, but how each pattern shifts melting points, density, and even bulk handling feel. The 2,4,5-trifluoro pattern proves popular for a reason. One fluorine often means just a small tweak in reactivity, but two or three can reshape the entire landscape—altering solubility, acidity of the methylene, and the temperature required in condensation steps.

    We’ve run head-to-head comparisons with related intermediates—2,4-difluorophenylacetonitrile for pharmaceutical intermediates, or 3,5-difluorophenylacetonitrile for specialty polymers. With the 2,4,5-trifluoro isomer, there’s a sharper electron-withdrawing effect, making the nitrile group even more responsive in nucleophilic substitutions. It’s a detail that seems trivial until you watch a process that’s been sluggish suddenly kick into gear with increased selectivity, cutting down the cleanup steps downstream.

    Others may market this compound as a mere tweak on the classic phenylacetonitrile core. People in production know that switching from 2,4-difluoro to 2,4,5-trifluoro can change solubility profiles just enough to reduce solvent swaps. The powder itself behaves differently in drum handling: less hygroscopic, finer flow, less caking after months in storage. Anyone responsible for weekly inventory rotation notices which lots remain stable, which form clumps when humidity spikes, and which draw more maintenance attention.

    Specifications that Matter—And the Reason Behind Them

    Different applications call for tailored ranges, but most process teams request 2,4,5-Trifluorophenylacetonitrile with a purity of 98 percent or higher, typically via GC. Product from a standard run appears as an off-white to pale yellow crystalline powder. Bulk density falls within a working range optimal for both automated feeders and manual scoops, allowing smooth transfer into reactors. Moisture content runs low if stored in airtight containers, with our in-house limit not just driven by a figure, but by lessons learned when off-spec moisture created side-reactions in partner campaigns.

    Boiling points and melting points matter most in thermal processing or distillation; many of our partners demand a melting point between 50-55°C, offering flexibility in both shipping logistics and low-temperature handling. It’s not just chemistry statistics—it’s about simplifying day-to-day reality in the warehouse and on the truck dock as loads move between climate zones. Those who scale up rarely ignore the impact of a five-degree swing when planning process windows or downstream handling.

    Some buyers have asked about trace fluoride or halide content, residual starting material, and byproduct quantification. We track these because every bit of experience—from clogged columns to sticky residues—points to the unavoidable conclusion: what the spec sheet demands today will become the safety margin for an unexpectedly complex project tomorrow. Nobody wants a smooth synthesis to be derailed by off-the-chart impurities, especially when time is running out before an audit or a regulatory milestone.

    Usage in the Real World—Recent Insights

    Those who’ve watched the evolution of fluorinated intermediates over the last decade recognize a familiar pattern. Just as trifluoromethylation took off in the agrochemical industry, pharmaceutical intermediates have embraced selective fluorination for both metabolic stability and potency. 2,4,5-Trifluorophenylacetonitrile appears in libraries targeting kinase inhibitors, CNS agents, antiviral scaffolds, and even more exotic applications like OLED ligands. It fills a sweet spot: strong electron withdrawal, room for further modification, and the reliability of a straightforward nitrile group.

    Process chemists from small biotechs to multinationals have shared case studies with us—achieving increased coupling efficiency, reduced need for protecting groups, and even higher selectivity in Grignard reactions. There’s satisfaction knowing the material you batch helps another team make a tough process go from research purity to pilot scale with fewer surprises.

    Fluorinated acetonitriles also see use in specialty electronics materials, where the stability of the aryl-fluorine pattern brings on thermal robustness not found in simpler analogues. Anyone in OLED precursor synthesis or liquid crystal research can appreciate the options opened up by more aggressive electron withdrawal paired with manageable reactivity. Robustness against oxidative degradation and the ability to fine-tune LUMO energies give design teams more freedom.

    Common Production Issues and Real Solutions

    Manufacturing this compound at large scale isn’t an academic exercise. The production line needs close monitoring; venting of hydrogen fluoride and other byproducts demands effective absorption systems. Through hands-on iteration, exhaust traps and scrubbing columns got re-designed several times over to handle unexpectedly high outputs during certain reaction profiles. Rubber seals and gasket materials need regular checks and a willingness to swap out for PTFE or perfluorinated alternatives if degradation creeps up.

    In the early years, lab-scale operations failed to fully prepare us for issues of crystallization and filtration during the isolation of the trifluoroacetonitrile. At 5 kg or less per batch, you can get away with slower gradations in solvent ratios, but as production climbed, delays mounted and operators found themselves cleaning out filter cloths with increasing regularity. Adjusting agitation rates, optimizing filtration stepwise through pressure control, and evaluating both batch and continuous modes in real time led to genuine improvements—not theoretical yield boosts, but smoother operator shifts and reduced downtime.

    Storage and shipping also play their part. We learned the hard way that drum liners become brittle after extended UV exposure when filled with highly fluorinated material. Adopting opaque, UV-resistant packaging led not just to lower wastage but to fewer customer complaints about discolored or off-texture shipments. Maintaining proper desiccant levels and monitoring units for trace condensation has cut down on both caking and shelf-life questions.

    Environmental and Safety Considerations Grounded in Experience

    The industry faces no shortage of regulatory updates around halogenated intermediates. Operators must weigh efforts to reduce fugitive emissions and comply with both local and international waste standards. Our facility switched over to closed-loop capture and neutralization protocols for fluorinated waste streams after seeing above-average corrosion rates in standard waste holding systems. Investment in dedicated alloy systems—beyond code minimums—started as a precaution and has proven itself each audit cycle. Colleagues who’ve faced regulatory scrutiny or pushback on untreated halide waste know that shortcuts always come back in the form of downtime, equipment repair, or lost permits.

    Handling risks receive daily attention from both management and floor-level personnel. Operators, from new hires to veterans, train and re-train on PPE selection, HF neutralization, and clean-room loading to minimize both acute and long-term exposure. We all share a collective memory of close calls; there’s no room for complacency even on days when everything goes smoothly. Having been on teams where near-misses prompted systemic safety overhauls, there’s a commitment here to continual review of safety protocols—not just what’s written, but what actually gets practiced each shift.

    Waste management isn’t just a paperwork checklist. Our team tracks every lot for full traceability, working with both internal environmental staff and third-party specialists to ensure all effluent meets—or exceeds—local discharge criteria. Shared experience with regulatory reviews keeps everyone on their toes; quality reports and environmental logs are treated as working documents, not box-ticking exercises.

    Integrating Feedback into Real Product Improvements

    No product emerges fully formed from its catalog entry. 2,4,5-Trifluorophenylacetonitrile batches from a decade ago differ in ways big and small from today’s stock—less due to regulatory pressure, more due to direct feedback from partners. End users in both pharma and electronics gave early guidance on key changes: minimizing residual halide traces, optimizing particle sizing for better suspension, and tightening moisture control during packaging.

    There were challenges, from inconsistent lot coloration to variable solubility profiles, which couldn’t be understood until consistent partner feedback came in from those scaling up in full-size reactors. Adjustments to purification methods—switching from single-solvent to phased precipitation, for example—came about after watching how residue affected yield at scale, not just in a flask. No one sees granular improvements until someone is brave enough to report what went wrong in the real world.

    Process logs and plant walkarounds tell the rest of the story. Operations teams track the number of filter changes, reports of excess static buildup in powder handling, and trends in particle size over the course of a production run. Whenever the same issue surfaces in three or more unrelated campaigns, it triggers a review—sparking interventions that might seem minor but which add up to a less-disrupted daily operation.

    Comparing Across the Market: Why Reliable Sourcing Matters

    Conversations with colleagues always drift to sourcing quality and consistency, especially in the fluorinated intermediates niche. There’s plenty of supply on the global market, but price alone never tells the whole story. Materials that look similar on a COA can behave unpredictably in process settings. Teams who once tried lower-cost sources often share stories of hidden costs—subtle impurity spikes, variable melting points, and unpredictable reaction progress.

    Channel experience also counts. Having managed both import and export shipments for years, our operations crew has learned the real difference between well-packed, high-purity stock and commoditized intermediates that only look the part. Operators expect shipments to hold up across climates, modes of transit, and timing delays. Experienced buyers lift drums, perform a test scoop, and check for critical warning signs—including texture, color, and the familiar but hard-to-define “feel” of consistency year over year.

    Direct relationships with process chemists and researchers cement our approach to ongoing improvement. Many of our larger accounts started with a trial batch—sometimes even a small lot produced by overnight shift teams willing to test a workaround to a persistent bottleneck. These partnerships outlast short-term pricing spikes and have shaped repeat business more than any glossy marketing brochure ever could.

    Continuous Innovation in a Demanding Field

    It’s easy to forget that specialty chemicals don’t stand still. Fluorinated intermediates in particular face growing scrutiny from both regulators and end users alike. With 2,4,5-Trifluorophenylacetonitrile, staying ahead means more than meeting today’s requirements. We invest in better environmental controls, closed-loop systems, and process analytics—not because a regulation demands it, but because hard-won experience shows these changes actually pay off. The need for raw material traceability goes beyond compliance; it means being able to track down and correct the exact batch condition that led to success or failure in our partners’ downstream chemistry.

    Operational feedback doesn’t just reshape batch run protocols. It informs the way we approach investment in plant upgrades, motivates better staff training, and drives the focus on raw material audits. For example, implementing real-time analytics for impurity detection didn’t just stem from regulatory trends—it directly responded to partner labs seeking quicker troubleshooting and better batch reproducibility.

    Daily routines on the plant floor rarely make headlines, but they shape whether a product like 2,4,5-Trifluorophenylacetonitrile meets the trust placed in it. Whether dealing with a surprise solvent shortage or a last-minute change in project priority, the knowledge accumulated by operators, engineers, and quality control teams shapes everything about the product as received by real project teams in pharma, electronics, and beyond.

    Sharing Knowledge for Better Industry-Wide Practices

    We’ve placed a premium on open sharing within the limitations of proprietary process details. Senior staff regularly contribute insight to industry consortia, swapping non-confidential details about pitfalls, innovations, and even failed attempts at improving crystallization or reducing solvent demand. This habit of transparency has gained traction as peers recognize there’s real value in admitting setbacks and building on collective knowledge.

    Our dialogue with partners, competitors, and neutral experts acts as a form of risk mitigation—identifying early warning signs before they escalate into unmanageable problems. The willingness to share issues—like unexpected exotherm profiles, agglomeration during drum storage, or subtle impurity co-elution—creates a feedback loop that benefits not just one manufacturer, but the entire supply chain, right down to the research teams building new molecules.

    Looking Forward: Meeting New Challenges

    The pathway from plant to application keeps changing. Use patterns for 2,4,5-Trifluorophenylacetonitrile now extend into advanced materials, specialty surfactants, crop protection R&D, and increasingly into green chemistry initiatives. With each sector comes new specification demands, unique logistical hurdles, and evolving regulatory oversight. Our long-haul success will rest on how well we listen, adapt, admit mistakes, and put hands-on experience into daily practice.

    Each new project request reminds us that the product isn’t just a database entry. It represents the combined effort, muscle memory, and know-how of everyone on the production and quality team. Scientific rigor, day-to-day repetition, and collective wisdom ensure that 2,4,5-Trifluorophenylacetonitrile remains a trusted partner for teams aiming higher in pharmaceuticals, electronics, and beyond.

    Ethical production demands daily vigilance against complacency—both in environmental stewardship and in delivering quality our counterparts can trust. This is what keeps us attentive not just to the current cycle, but to every detail that shapes the next advance in specialty intermediates.