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3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile

    • Product Name 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile
    • Alias 3-FLUORO-5-(TRIFLUOROMETHYL)BENZYL CYANIDE
    • Einecs 696-032-1
    • 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

    228866

    Product Name 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile
    Cas Number 886762-23-0
    Molecular Formula C9H5F4N
    Molecular Weight 203.14
    Appearance White to off-white solid
    Purity Typically ≥ 98%
    Smiles N#CC1=CC(=CC(=C1)F)C(F)(F)F
    Inchi InChI=1S/C9H5F4N/c10-7-2-6(4-5-14)1-8(3-7)9(11,12)13/h1-3H,4H2
    Synonyms 2-(3-Fluoro-5-(trifluoromethyl)phenyl)acetonitrile
    Storage Temperature Store at 2-8°C
    Solubility Soluble in organic solvents

    As an accredited 3-Fluoro-5-(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 with tamper-evident cap, labeled with chemical details. Contains 25 grams of 3-Fluoro-5-(trifluoromethyl)phenylacetonitrile.
    Shipping 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile is shipped in sealed, chemical-resistant containers to ensure safety and stability during transit. The package is clearly labeled according to regulatory standards, with documentation for safe handling. Shipping is expedited to minimize transit time and complies with all local and international chemical transportation regulations.
    Storage Store **3-Fluoro-5-(trifluoromethyl)phenylacetonitrile** in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Protect from moisture and direct sunlight. Use appropriate personal protective equipment (PPE) when handling to prevent skin and eye contact. Store in accordance with local regulations.
    Application of 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile

    Applications of 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile in Industrial Manufacturing

    As the original producer of high-purity 3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile, we support the global specialty chemicals sector with core raw materials developed for compliance-driven industries. This compound, characterized by its aromatic fluoro and trifluoromethyl substitutions, functions as a critical building block in synthesis-intensive segments with stringent quality controls and regulatory requirements.

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

    Leading pharmaceutical producers source this aromatic nitrile as a key intermediate in the development of selective central nervous system and oncology APIs, where its unique structure is essential for downstream arylation and functionalization steps. Our material consistently meets the purity profiles required by international pharma regulations, allowing formulators to maintain batch consistency through various hydrogenation, coupling, and alkylation routes en route to advanced heterocycles and final APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) reference standards for intermediate handling
    • U.S. FDA 21 CFR Part 211 for cGMP manufacturing
    • Chinese Pharmacopoeia ChP (for exported pharmaceuticals)

    Typical usage ratio

    • 0.9–1.2 molar equivalents per target API synthesis, adjusted to stoichiometry of coupling step and final API yield optimization; scale-up lots often utilize 1.05 equivalents to excess for yield assurance.

    Downstream process integration

    • Charged in early-stage batch reactors during Grignard or Suzuki coupling as an acetonitrile-bearing nucleophile, with subsequent functionalization or reduction in multi-step synthesis; typically introduced after catalyst pre-activation or base addition for controlled conversion rates.

    Final product types

    • Central nervous system therapeutics (intermediate stage and finished API)
    • Targeted anti-cancer compounds
    • Precursor libraries for small molecule drug discovery
    • Advanced heterocyclic pharmaceutical ingredients

    2. Agrochemical Intermediate for Selective Herbicides

    Our fluorinated phenylacetonitrile is routinely utilized as a specialized intermediate for the synthesis of next-generation herbicidal actives, where precise aromatic substitution enhances selectivity toward broadleaf and grass weed species. Downstream formulators integrate this product into custom nitrile-group insertion processes, which set the foundation for proprietary active molecule design in regulated crop protection.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • ISO 9001:2015 quality management (production and traceability)
    • OECD Principles of Good Laboratory Practice (GLP) for field and residue trials
    • EPA 40 CFR Part 180 for U.S. pesticide residue tolerance

    Typical usage ratio

    • 0.7–1.1 molar equivalents per herbicide synthesis batch, based on the substitution pattern of the target scaffold; adjustment depends on downstream conversion rate and waste minimization targets.

    Downstream process integration

    • Dosed into reaction vessels during acylation or cyanation steps, often under controlled temperatures with acid/base catalysts for regioselective introduction onto the aromatic ring; included during intermediate quenching to ensure full conversion before work-up.

    Final product types

    • Selective post-emergence herbicidal actives
    • Novel pre-mix intermediates for broad-spectrum weed control formulations
    • Enabling scaffolds for patent-protected agrochemical APIs
    • Intermediate forms for combination crop protection cocktails

    3. Advanced Material Monomer Sourcing for Specialty Polymers

    The compound is specified by downstream specialty polymer manufacturers as a niche monomer or chain-end modifier in the synthesis of fluoroaromatic polymers where aromatic nitrile groups introduce enhanced chemical resistance, thermal stability, and dielectric performance. Our customers incorporate this material directly during polymerization or as a functional group donor to tailor final polymer attributes for demanding electronic and industrial film applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 registration for high-molecular-weight intermediates
    • RoHS 2 Directive 2011/65/EU for electronic component polymers
    • ISO 9001:2015 for production consistency and documentation
    • UL 94 flammability standard (for electrical insulation end-use)

    Typical usage ratio

    • 0.2–0.6 parts by weight per 100 parts polymer resin, depending on backbone substitution level and cross-linking requirements in specialty film and fiber grades; selection based on end-use electrical or thermal resistance targets.

    Downstream process integration

    • Fed during step-growth or chain polymerization stages as an end-capper or branching agent; introduced with co-monomers and initiators under inert atmosphere to control molecular weight and incorporate functional fluoroaromatic segments.

    Final product types

    • High-performance specialty films for electronic devices
    • Engineered coatings for printed circuit boards
    • Dielectric engineering plastics for connectors and insulators
    • Heat-resistant polymer fibers for industrial filtration

    4. Fine Chemical Intermediate for Liquid Crystal and OLED Materials

    Major display technology manufacturers require this structure-specific nitrile for synthesizing advanced liquid crystal (LC) and OLED intermediates, where the fluorinated aromatic core imparts desired mesogenic properties and electronic tuning. The material enters controlled processes to assemble core fluorinated backbones that underpin performance characteristics in commercial flat-panel displays and lighting applications.

    Industry compliance standards

    • IEC 61249-2-41 for low-halogen materials in electronics
    • ISO 14001 for environmental management during fine chemical production
    • China RoHS standards for electronic materials
    • Supplier qualification per customer-specific quality control protocols

    Typical usage ratio

    • 0.8–1.0 molar equivalents per core LC or OLED precursor synthesis, fine-tuned based on the assembly route and the targeted final property of the liquid crystal host or emitter; excess may be used for yield optimization in pilot batches.

    Downstream process integration

    • Integrated at the aromatic core assembly stage of LC/OLED intermediate synthesis through coupling or condensation reactions; addition monitored via HPLC to ensure precise substitution level and mitigate color impurity formation in electronic-grade batches.

    Final product types

    • High-purity liquid crystal intermediates for LCD panels
    • OLED emitter and host precursors for display and lighting modules
    • Advanced fluorinated compounds for high-contrast optical applications
    • Intermediates for low-dielectric constant electronic components
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    Certification & Compliance
    More Introduction

    3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile: Bridging Challenges in Fine Chemical Synthesis

    Integrating Science and Real-World Manufacturing Experience

    3-Fluoro-5-(Trifluoromethyl)Phenylacetonitrile (Model: FTFPAN-99) stands out at our plant for its stable profile and sharp reactivity. Since we work daily with aromatic nitriles, we’ve tracked how subtle changes in ring substitution patterns build up or take away utility for our customers. This molecule, bearing both fluoro and trifluoromethyl signatures on a phenylacetonitrile backbone, has prompted synthetic chemists to pursue transformations not easily accessible with simpler nitriles.

    Product Properties: Delivering Consistency with Purity

    Reproducibility takes priority in our laboratory and manufacturing lines. Our standard lots achieve GC purity above 99 percent. The light, nearly colorless solid powder is kept dry in sealed drums, as aromatic nitriles absorb moisture over time. We test each batch for moisture content below 0.2 percent, using coulometric Karl Fischer titration. The melting point we routinely get ranges from 52 to 55°C, in agreement with our NMR and HPLC validation data. Many off-the-shelf analogues lack this combination of high purity and tight analytical specification, especially in regions where cold-chain logistics or storage conditions waver.

    Scalability: From Kilo Lab to Multi-Ton Production

    Laboratories can afford to overlook supply bottlenecks on gram-scale synthesis, but kilo-labs and pilot plants see material loss and delays firsthand. We scaled up FTFPAN-99 using a solvent-free condensation method and follow with column purification and careful vacuum drying. This approach minimizes side-products which show up through extended aromatic fluorination or nitrile group hydrolysis, both of which create tricky separations downstream. Every year, requests arrive for batch lots exceeding several hundred kilograms, often with special handling needs. Our blending line and nitrogen-flushed packaging address contamination and degradation risks, especially in warm or humid conditions.

    Application Context: Where This Intermediate Matters

    Markets for complex fluorinated intermediates expand as new agrochemical scaffolds and drug candidates emerge. Fluoroaromatics, especially those with both electron-withdrawing fluoro and trifluoromethyl groups, give medicinal chemists and process engineers ways to modulate metabolic profiles, lipophilicity, and binding affinity. Our FTFPAN-99 supplies major R&D efforts aiming at pest-resistant crop chemicals, CNS drug candidates, and high-performance liquid crystal monomers.

    Compared to plain phenylacetonitrile or those carrying just one ring substitution, the dual presence of fluorine and trifluoromethyl alters the compound’s electron density, shifting typical reaction rates and selectivities. Nucleophilic additions display higher regioselectivity, and reduction steps progress with fewer byproducts, observed during our in-house ketone and amine synthesis trials. These differences, though subtle on paper, play out as clear cost and time advantages for downstream chemists dealing with complex multi-step syntheses.

    Reliability: Trusted Data, Repeatable Results

    R&D teams value batch-to-batch performance, not only catalog promises. Our documented characterization runs include proton and carbon-13 NMR, confirming signature peaks unique to the compound’s substitution pattern. 19F NMR shows two distinct signals, matching the expected chemical environments. Analytical HPLC traces hold impurity peaks below 0.5 percent. Mass spectrometry cross-validates the molecular ion at m/z 211, ensuring no confusion with positional or constitutional isomers, which often arise as side-products in smaller, less controlled setups. Unlike third-party trading houses, our laboratory stays accountable for each finished drum, year after year, through a complete supply chain link.

    Why Purity and Authenticity Set Us Apart

    Impurity issues cost chemists precious weeks and force repeat syntheses. During one customer’s campaign for a trifluoromethyl ketone, imported material from another source led to persistent side-reactions — eventually traced to an isomeric contaminant at just 2 percent frequency. Their project timeline suffered. We’ve focused on continuous improvement by updating our purification sequence, adding a high-efficiency silica gel column and screening for trace amine and aldehyde impurities.

    The benefit for downstream producers is measurable. Intermediates from our lines show reliable reactivity whether entering Suzuki couplings, reductions, or methylene protection-deprotection cycles. Superficially, specifications from various suppliers might sound similar — but synthetic practicality and low impurity content separate workable material from reagents that undermine a campaign. Our technical support team has witnessed cases where a switch to our FTFPAN-99 halved the time needed for final product isolation, especially in the preparation of UV-absorbing fluorocarbon oligomers.

    Handling, Storage, and Shelf-Life: The Real-World Context

    Field chemistry isn’t kind to compounds that degrade under average warehouse or transport conditions. Our compound stores well at room temperature under nitrogen and survives several months with negligible change in purity or melting point, provided exposure to ambient humidity is minimized. Grain size is managed during crystallization, so the product pours freely and resists clumping. Customers in regions with frequent temperature swings report no caking or oxidative decomposition, issues that plagued earlier generations of nitrile intermediates. Some analogues, especially difluoro or mono-trifluoromethyl derivatives, show color change within weeks when not protected from light or moisture; FTFPAN-99 holds up much better under equivalent conditions.

    Efficiency Gains for Process Development

    Working as chemical manufacturers for over a decade, we’ve shared direct feedback channels with synthesis labs developing both commercial and research target molecules. During one collaboration aiming at CNS-active heteroaryls, switching to this fluorinated phenylacetonitrile increased overall yield by 12 percent and cut post-reaction purification time in half. Our in-process QC flagged no issues along the way, confirming trace-level impurities under control. These gains often go unnoticed by those who never see the difficulties of scaling up, but process chemists looking to minimize waste and maximize consistency see the value immediately.

    Chasing after nominal yield increases sometimes betrays bigger wins waiting in unassuming details: reaction reproducibility, manageable workups, and stability under standard lab storage.

    Distinctives vs Promotional Lookalikes

    Markets today overflow with third-party resellers pushing nearly identical catalogs. But trying to cut corners on source material usually brings setbacks. Our own trial batches of externally sourced “equivalent” phenylacetonitriles found multiple failures: off-spec melting points, unwanted by-products, unpredictable solubility. In more than one case, reaction profiles changed mid-way through campaigns. For pharmaceutical trials or advanced materials, inconsistency raises direct risks — regulatory documentation gets derailed, material needs repurposing, operations slow as critical path studies must restart.

    With FTFPAN-99, impurities arising from incomplete fluorination or cyclization are under our analytical limits, and the supply always traces back to a full batch record. By taking responsibility for both synthesis and purification, we provide technical data packages and shipment samples backed by real laboratory records and full traceability.

    Addressing Key Challenges: Toward Solution-Driven Partnerships

    Chemists navigating new reaction territory lean on reliable, transparent suppliers. Every batch of FTFPAN-99 carries full trace data, but the conversation doesn’t end at a certificate. Demand for customized particle size, bulk packaging, or express shipment routes has become routine in our shop. Customers developing new ligands or fluorinated materials may request pre-shipment stability studies, or ask that samples undergo repeat HPLC or moisture checks after international transit.

    Through regular two-way technical exchanges, both sides adapt to shifting ground: changes in environmental regulations, updated synthetic targets, unpredictable logistics. Most importantly, advice flows both ways. More than once, a customer flagged a subtle color or odor change ahead of time, prompting an internal process review that boosted long-term batch consistency for all clients.

    Balancing Innovation and Regulation

    Preparing advanced intermediates today means managing a sea of compliance paperwork, transport regulations, and customer audits. We anticipated REACH and TSCA updates and built our batch documentation and safety protocols accordingly. We exclude persistent solvents and denied fluorochemicals at the raw material stage, double-checking every supply for new restrictions or regional transport embargoes.

    We provide not only the compound but also rigorous safety, transport, and waste protocol support for every order. Labs in Europe and the Americas receive shipments with regulatory compliance documentation, supported by up-to-date analytical data. When creative synthesis or rapid project pivots call for new tests, we treat them as shared technical challenges.

    Product Versatility in Applied Chemistry

    Across four continents, FTFPAN-99 finds a home in medicinal, agricultural, and advanced materials synthesis. Recently, its use expanded into exploratory routes for perfluorinated polymers, thanks to the unique combination of hydrophobicity and polarity. In the preparation of aryl ketones, chemists have drawn on its predictable reactivity and manageable workup protocols to scale up reactions without special drybox equipment. The electron-deficient aromatic ring resists oxidative dimerization and side-ring substitution, compared to similar mono-substituted phenylacetonitriles or aryl nitriles.

    Comparing this intermediate to related compounds such as 4-fluoro-phenylacetonitrile or 3-trifluoromethyl derivatives spotlights important contrasts. The dual substitution pattern on FTFPAN-99 balances reactivity and stability: trifluoromethyl provides extra lipophilicity and steric bulk, while the ring fluorine tunes the site selectivity for nucleophilic additions and palladium-catalyzed couplings. Many of our regular customers run head-to-head trials of multiple intermediates, tallying up cycle times, final yields, and ease of isolation. Over dozens of feedback notes, they describe more robust end-to-end syntheses when working with FTFPAN-99, especially when impurity profiles threaten delicate downstream steps like scale-up hydrogenations or halogenation.

    Differences from Comparable Products in Practice

    Speaking as a chemical producer, not just a marketer, we know on-paper equivalence seldom translates to usable end results. Generic phenylacetonitrile may check the price box, but with only a single ring substitution, customers routinely report side-reactions, product discoloration, and batch variability. Crafting FTFPAN-99 to GC purity above 99 percent, with tightly controlled moisture, meets demand for those developing high-barrier products where impurities become catalyst poisons or block critical analytical thresholds.

    Recent experience in API intermediate supply highlights this difference: clients reporting higher isomer content in generic grades saw significant challenges during FDA validation, with repeat purification cycles and analytical headaches. Engineers running high-throughput array synthesis for pesticide analogues needed reliable, replicable outcomes — our FTFPAN-99 scored consistently higher on reproducibility and allowed for tighter process windows, reducing rework and waste by more than 20 percent.

    For chemists needing to downstream to advanced fluorinated ketones, aryl amines, or cyclized building blocks, the molecular signature of FTFPAN-99 avoids common pitfalls seen with less substituted or poorly characterized nitrile intermediates.

    Two-Way Collaboration: Turning Experience into Progress

    Every kilo or ton of FTFPAN-99 we produce represents the outcome of evolving technical insight, hard-won process optimization, and feedback from dozens of real synthesis labs. We refine not by automated rule, but by supporting those who work with our product at bench-level and on plant scales. Data from NMR, GC, and HPLC comes not only as paperwork, but as direct assurance—this batch will behave as expected in any reaction, whether the goal lies in novel heterocycle construction, fine-tuning a pharmacokinetic profile, or stepping into next-generation electronic materials.

    Tailored Support Beyond the Drum

    Manufacturing advanced fluorinated intermediates isn’t about filling inventory or chasing lowest cost per kilo. We shape product lines based on realistic customer constraints, tight delivery windows, and emerging reaction methodologies. Market feedback drives us to adapt — new solvent-free packaging, smaller lot sizes to suit fast-moving R&D teams, technical documentation clear enough to support regulatory submissions on both sides of the Atlantic.

    Working with FTFPAN-99 gives customers the confidence to plan long-term projects without worrying about interruptions or material drift. Our support covers troubleshooting synthetic setbacks, sharing technical advances, and taking responsibility for every unit shipped from our plant.

    Looking Ahead: Meeting Tomorrow’s Synthetic Demands

    Advanced materials, crop protection molecules, and pharmaceuticals all benefit from robust access to high-purity fluorinated intermediates. As global regulations tighten and alternative synthetic routes emerge, long-term supply chains and continued process innovation matter more than ever. By keeping attention fixed on reliability, transparency, and technical problem-solving, FTFPAN-99 continues to see wide application as a critical building block.

    As a manufacturing partner, we look forward to bringing this and other advanced aromatic nitriles to synthesis labs worldwide, solving challenges collaboratively and maintaining standards that keep your projects moving forward.