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3,5-Bis(Trifluoromethyl)Phenylacetonitrile

    • Product Name 3,5-Bis(Trifluoromethyl)Phenylacetonitrile
    • Alias 3,5-Bis(trifluoromethyl)benzyl cyanide
    • Einecs 407-090-6
    • 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

    279776

    Productname 3,5-Bis(Trifluoromethyl)Phenylacetonitrile
    Casnumber 6908-73-2
    Molecularformula C10H5F6N
    Molecularweight 253.15
    Appearance White to off-white solid
    Meltingpoint 61-65°C
    Density 1.46 g/cm³ (approximate)
    Solubility Slightly soluble in organic solvents (e.g., dichloromethane)
    Smiles N#CC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1
    Inchi InChI=1S/C10H5F6N/c11-9(12,13)6-1-7(2-8(3-6)10(14,15)16)4-5-17/h1-3H,4H2
    Storage Store in a cool, dry, well-ventilated place, and keep container tightly closed

    As an accredited 3,5-Bis(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, screw cap, labeled with hazard warnings. Contains 25 grams of 3,5-Bis(Trifluoromethyl)Phenylacetonitrile, securely sealed for laboratory use.
    Shipping 3,5-Bis(Trifluoromethyl)Phenylacetonitrile is shipped in tightly sealed containers to prevent moisture and contamination. It is typically transported as a solid, protected from light, heat, and incompatible substances. Proper labeling and documentation ensure compliance with hazardous material regulations. Shipments are handled by trained personnel using appropriate personal protective equipment (PPE).
    Storage Store 3,5-Bis(Trifluoromethyl)Phenylacetonitrile in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect the container from physical damage and moisture. Ensure proper labeling, use secondary containment when necessary, and keep the chemical away from direct sunlight and extreme temperatures.
    Application of 3,5-Bis(Trifluoromethyl)Phenylacetonitrile

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

    As the direct manufacturer of 3,5-Bis(Trifluoromethyl)Phenylacetonitrile, we supply this specialty intermediate to a number of advanced chemical manufacturing sectors. Below, we outline its primary downstream applications, each detailed with current regulatory requirements, practical formulation doses, real integration points, and examples of end products from leading industries.

    1. Pharmaceutical API Intermediate Synthesis

    3,5-Bis(Trifluoromethyl)Phenylacetonitrile is widely used as an intermediate in pharmaceutical manufacturing, particularly for synthesizing fluorinated heterocycles and substituted phenyl derivatives incorporated into modern APIs (active pharmaceutical ingredients) for anti-inflammatory and oncologic drug candidates. Its electron-rich structure facilitates regioselective alkylation and condensation reactions crucial in multi-step GMP process routes.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) monograph specifications for intermediates
    • EU EudraLex Volume 4 Guidelines for APIs
    • Japanese PMDA intermediate quality requirements

    Typical usage ratio

    • 10–30 mol% relative to final API yield, depending on specific synthetic route; adjustments rely on target fluorine incorporation and side-chain demands

    Downstream process integration

    • Charged at the condensation or substitution stage, often following halogenation or nitrile activation; used in batch reactor setups under inert atmosphere

    Final product types

    • Pharmaceutical active ingredients: kinase inhibitors, nonsteroidal anti-inflammatory drug (NSAID) building blocks, oncology molecule precursors

    2. Agrochemical Synthesis (Herbicide and Insecticide Active Formation)

    The compound serves as a building block for synthesizing fluorinated aromatic rings embedded in next-generation crop protection actives. Its dual trifluoromethyl groups enhance metabolic stability and bioavailability in the final agrochemical molecules, which are designed to meet stringent residue and environmental safety standards worldwide.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials (FAO/WHO JMPS)
    • ISO 9001:2015 Quality Management Systems in crop protection manufacturing
    • REACH Regulation (EC) No 1907/2006 for agrochemical intermediates
    • OECD Principles of Good Laboratory Practice (GLP) for synthesis and residue studies

    Typical usage ratio

    • 8–18% by weight in synthetic batch charge; precise ratio optimizes precursor conversion and ultimately yield of target herbicide or insecticide core

    Downstream process integration

    • Introduced during aromatic ring construction and nitrile functionalization in continuous flow or batch synthesis reactors, under nitrogen protection to minimize side reactions

    Final product types

    • Modern agrochemical actives: triazole herbicides, pyrazole-based insecticides, fluorinated seed treatment agents

    3. Specialty Polymer Monomer Synthesis

    Polymer manufacturers employ 3,5-Bis(Trifluoromethyl)Phenylacetonitrile to synthesize custom monomers for high-performance fluorinated resins and coatings, used in demanding electronics and chemical processing applications. The nitrile group supports subsequent functionalization steps, enabling production of copolymers with tailored dielectric, chemical resistance, and hydrophobic properties.

    Industry compliance standards

    • ISO 9001:2015 for polymer manufacturing
    • RoHS Directive 2011/65/EU for electronic materials
    • UL 94 flame retardancy and dielectric property standards (for electronic substrates only)
    • REACH Annex XVII for monomer safety in downstream plastics

    Typical usage ratio

    • 5–12 mol% based on total monomer feed; adjusted for desired degree of fluorination and nitrile functionality in the finished macromolecule

    Downstream process integration

    • Fed into pre-polymerization step after purification, combined with comonomers via solution or emulsion polymerization, typically in jacketed stainless steel reactors

    Final product types

    • Fluorinated polyimides, specialty phenyl-containing copolymers, electronic resist materials, corrosion-resistant coatings

    4. Advanced Materials for Liquid Crystal Display (LCD) Industry

    Within the specialty display segment, the compound is favored for producing functionalized aryl derivatives used as liquid crystal alignment agents and performance enhancers in display panel manufacturing. Its high thermal and chemical stability, combined with tailored fluorination, allows manufacturers to engineer precise electro-optic and surface properties for thin-film display matrices.

    Industry compliance standards

    • IEC 60950 and IEC 62321 regulations for electronic display substances
    • JIS C61000-3-2 for material purity in electronics
    • ISO 14001:2015 for environmental management in specialty chemical production
    • IECQ QC 080000 hazardous substance process management

    Typical usage ratio

    • 2–6% by weight in the alignment layer precursor mixture; ratio adjusted for final film thickness and surface anchoring strength in the display assembly process

    Downstream process integration

    • Blended into alignment material formulations prior to spin-coating or printing onto glass substrates, typically following solution-phase filtration and purity verification

    Final product types

    • LCD alignment coatings, thin-film-polymerized orientation films, advanced polarizer component materials
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    More Introduction

    3,5-Bis(Trifluoromethyl)Phenylacetonitrile: Real-World Perspectives from the Manufacturer

    Introduction: Living with Fluorinated Intermediates

    Every day on the factory floor, our team handles a variety of chemical compounds. Among these, 3,5-Bis(Trifluoromethyl)Phenylacetonitrile has become a fixture in our operation. Many in the fine chemical industry have taken notice of its role in the synthesis of pharmaceuticals, agrochemicals, and specialty materials, because its structure brings together two powerful trifluoromethyl groups with the versatile acetonitrile moiety. This compound makes an impression because it often signals a step forward in both molecular complexity and the performance potential of the target molecules.

    The Model: Precision Starts from the Ground Up

    The specific material we produce aligns with the structural formula C10H5F6N, which gives the molecule its distinct characteristics. At our site, the production process starts with careful sourcing and prepping of the necessary aromatic precursors. Over the years, we have learned to adjust key reaction conditions, since even minor impurities or process variations can impact not only purity but also secondary reactivity in further transformations. Each batch is the result of repeatable synthetic controls, not just a standard recipe followed blindly. We lean into close monitoring because years in production have shown us that overlooked details at this step can lead to headaches down the line during downstream applications.

    Physical Specifications as Seen through Manufacturing Practice

    On our shop floor, 3,5-Bis(Trifluoromethyl)Phenylacetonitrile appears as a lightly colored solid that may sometimes show slight off-whites due to trace intermediates, though these fall within our proprietary internal standards. The melting point tends to register between 56°C and 60°C, as confirmed by differential scanning calorimetry in our quality labs. Long gone are the days of simply trusting the supplier; we regularly analyze GC-MS and NMR for every production lot, targeting a purity exceeding 98 percent. The trace moisture content and heavy metal levels remain tightly controlled, given our materials feed directly into pharma and electronics customers, who cannot tolerate variable batch-to-batch quality. These aren’t numbers we post for marketing — these standards have arisen from decades of direct customer feedback and persistent self-driven improvement.

    How We Use It — Lessons from the Manufacturing Floor

    Around here, the main destination for 3,5-Bis(Trifluoromethyl)Phenylacetonitrile is as a key intermediate for the synthesis of substituted aromatic compounds used in pharmaceutical active ingredients and complex agricultural molecules. Chemists using our product frequently aim to introduce the electron-withdrawing power of trifluoromethyl groups for enhanced metabolic stability and bioactivity in target compounds. Our R&D team often collaborates directly with formulation chemists who require reliable and clean conversion of the nitrile to a range of functions — from carboxylic acids to amines — knowing full well that by leveraging this intermediate, they can access structures that boost activity profiles or environmental persistence.

    Over years in production, we have seen the nitrile’s resilience in standard and more unconventional coupling and condensation reactions. We receive feedback that the reproducibility and cleanliness of our material cuts down on downstream purification steps, and several partners insist on using our lots for the kinds of projects where every impurity can throw off yields — especially during scale-up in pharma or crop protection chemistry. We regularly get informal updates from process development labs; this ongoing two-way communication shows us which aspects of our process need tweaking. Sometimes, even a percent or two of improved conversion in the first step translates into major gains at the plant scale.

    Making Clear the Differences: Experience vs Raw Data

    On paper, plenty of suppliers offer what seems like the same product. From behind the scenes, years of manufacturing have taught us to watch for hidden variables that can drag down process reliability. The impact of these differences often flies under the radar in technical literature but becomes glaringly obvious during real-world synthesis.

    Our own experience tells us that in some lots produced elsewhere, small but persistent halos of unknown byproducts collect during crystallization. These byproducts find their way into further coupling reactions, causing subtle shifts in yields or introducing muted colors in final products — outcomes that can quietly erode confidence and force extra purification.

    For those scaling up, subtle deviations in particle size or moisture uptake can cause clumping, inconsistent mixing, or sluggish dissolution. Our team spent many months trialing filtration, grind sizing, and drying processes to strike the right balance with this compound, so it behaves consistently in automated and manual processes. The chemists who buy directly from us have reported easier, more predictable manipulation, fewer filter-blockages, and smoother handling on the plant floor — not because of marketing claims, but because every setback and success has been rolled into real process changes over the years.

    The Ripple Effect of Quality on Customers’ Bottom Lines

    Any batch coming off our line travels further than just a warehouse shelf. We’ve seen contract manufacturers, specialty pharma facilities, and agrochemical R&D teams put our 3,5-Bis(Trifluoromethyl)Phenylacetonitrile to the test. The quadruple-checking of analytical specs, meticulous repackaging, and traceability guarantees that stem from our process reflect a practical understanding: anywhere a subpar intermediate enters a large-scale or high-purity workflow, the headaches multiply rapidly. Purity and performance are not only abstract values — they affect reaction times, labor costs, purification cycles, and compliance with evolving regulatory expectations. In our shop, the outlay for an additional purification run is measured not just in solvent and energy but also in lost opportunity and delayed shipment to partners who judge us by delivery date as well as purity.

    Real-World Manufacturing Challenges — and What We’ve Learned

    The production of 3,5-Bis(Trifluoromethyl)Phenylacetonitrile presents unique technical challenges not always covered by textbooks. Many years ago, during a trial campaign, we noticed persistent formation of a stubborn, high-boiling impurity. Standard vacuum-drying failed to clear it. It took a deep dive into pressure swing distillation and the implementation of a new set of analytically driven checkpoints to bring this to heel. This kind of experience underscores a key point: staying ahead in manufacturing means grappling directly with process quirks, not waiting for customer complaints.

    Another situation cropped up with scaling dryer design. With each equipment size-up, heat transfer characteristics changed, leading to uneven drying and caking in the product. For years, lab-scale uniformity wrongly gave us hope, but ramping to multi-ton lots exposed a host of unpredictable behaviors. The only way out turned out to be direct operator feedback and iterative redesigns of the drying equipment and process cycle. Those lessons became part of our standard operating procedures and delivered smoother downstream use for our customers.

    The Supplier’s View: Accountability and Continuous Feedback

    Around here, no batch leaves before it meets feedback-based acceptance criteria that measure batch-to-batch reliability, crystal appearance, and impurity profile. Over the last decade, our analytical tools have gotten more sensitive, and in parallel, customer expectations have climbed. We measure more than purity; subtle degradants and batch fingerprinting now form part of our day-to-day checks. Regular roundtable sessions — both with our in-house team and with external partners — keep us honest about where the molecule slots into the next problem that R&D teams try to solve.

    Our regular interaction with formulation teams helped us realize the handling surprises of this solid. 3,5-Bis(Trifluoromethyl)Phenylacetonitrile can sometimes display unusual hygroscopicity. Shelf samples subjected to storage experiments laid bare the need for revised packaging when extended lay-down cycles are expected. We went on to reformulate our internal bulk packaging into double-sealed, inert-atmosphere liners. Years ago, such a consideration might have seemed minor. Repeated customer calls about clumping and off-spec dissolution times proved otherwise, and such tweaks represent the real impact of quality manufacturing.

    “Specification” Is Only a Starting Point

    In the chemical industry, the listed specification only starts the conversation. Production histories, process drift, and equipment wear affect each new batch. In our case, the origination of every lot is logged, and a running commentary of process tweaks is maintained. Outside the numbers, each operator and process engineer knows that a batch of 3,5-Bis(Trifluoromethyl)Phenylacetonitrile going to an oncology research facility in Basel needs to support downstream confidence for those working on the next generation of therapies. In our plant, the staff talk openly about their pride in each successful delivery, because the work supports more than just the numbers on the COA.

    Differences Felt in Synthesis — What Real Users Report

    Many buyers who shift their sourcing to us find that the 3,5-Bis(Trifluoromethyl)Phenylacetonitrile performs better in both small-volume and multi-kilo campaigns. Reproducibility in cross-coupling conditions — N-arylation, amidation, and reductive amination among them — regularly draws feedback that the reaction outcomes match what is needed for process validation. Not all manufacturers pay equal attention to the low-level impurities, particularly those with similar boiling points or UV chromophores that can slip past basic QC. We have repeatedly invested in process analytics to deep-clean such impurities, supported not just by internal pressure but also by hearing which lots led to final structure problems in scale-up labs.

    Comparison with Other Available Compounds

    Some chemists might consider related phenylacetonitrile or benzonitrile compounds as near analogues. Having produced both for a range of applications, our perspective is simple: the electron-withdrawing effect of two trifluoromethyl groups on the ring creates a different set of reactivity and physical properties. The melting point and solubility profile diverge significantly, influencing process choices and compatibility. We have also seen sharp contrasts in photostability, solution behavior, and shelf-life when neighboring chemicals are tested side-by-side.

    Where a standard phenylacetonitrile might be prone to discoloration or hydrolysis during inert coupling, our specific molecule’s increased electron withdrawal helps reduce side reactions. In our own process development, this ended up delivering fewer stopped runs and a lower rate of off-spec downstream intermediates. Many partners confirm that the higher thermal stability leads to smoother high-temperature transformations, opening up broader process windows.

    The View Beyond the Data Sheet

    For anyone relying on technical specs alone, it’s easy to miss how everyday realities of storage, handling, and batch reproducibility can have outsized impacts. Weather changes in the warehouse influence moisture uptake, causing changes in flow and pourability. Differences in filtration set-ups alter the particle-size availability to downstream synthesis. Numbers in a table can’t tell you how a single day’s humidity can tip the balance toward clumping, which slows down a shift’s worth of operations. Over time, we learned to walk every shipment from packaging to customer release, documenting each unexpected variation.

    In real-world use, the feel of the product as it transfers through chutes, the way it dissolves, and the color stability under standard lighting all count. If a chemist can move faster through an intermediate synthesis, skip a purification step, or reach their purity goal without adding labor, it rarely shows up in the literature — but it drives loyalty. The countless micro-decisions our operators make translate into palpable differences felt throughout the supply chain.

    Challenges in Product Lifecycle Management

    As regulatory trends grow stricter, older methods for making and analyzing 3,5-Bis(Trifluoromethyl)Phenylacetonitrile demand constant modernization. Routine evaluation of raw material sources, solvent purity, and waste stream recycling now forms part of our monthly maintenance and audit cycles. The drive toward greener chemistry forces us to seek lower-waste and lower-energy syntheses, with target reductions in solvent loss and unreacted starting materials.

    Several years ago, our solvent recovery audit showed that minor changes in reaction exotherms led to increased off-gassing and solvent loss. The close alignment of our process team and maintenance crew enabled a rapid fix by overhauling the cooling system and refining the addition sequence. Pollutant capture improved, compliance shifted upward, and feedback from environmental audits grew far less stressful.

    Supporting Partners in Product Innovation

    Given the complexity of modern chemical synthesis, our engagement does not end with product delivery. Customers using our 3,5-Bis(Trifluoromethyl)Phenylacetonitrile in high-value synthesis have increasingly asked for direct technical support. We maintain a technical team that tracks real-time analytical trends across lots, helping identify root causes if customers face unexpected reactivity issues. Through these efforts, our material frequently unlocks new applications — from fluorinated pharmaceuticals to advanced organic light-emitting diodes (OLEDs). Many developments now rely on compounds that combine high fluorine content with robust processability.

    Over the last ten years, we noticed a gradual shift from bulk pharma synthesis to more specialty high-tech materials. Our refinement process has pivoted accordingly, delivering not just a molecule, but a promise of predictable performance in these dynamic fields. During these transitions, open communication with end-users shaped both our product and service model.

    Improvement Never Stops: What We’re Tackling Next

    We believe every issue uncovered — whether by our own team or through open feedback — deserves an actionable response. Recent work has turned to reducing trace metallic content, which affected the late-stage reactivity in cross-coupling protocols for some partners. Ongoing investments in multi-step filtration and continuous monitoring equipment address these needs directly.

    We are now validating alternative synthetic routes, not only to improve yields but also to sharpen the impurity profile and cut energy use. As new green chemistry requirements roll out across the industry, our team welcomes pilot partnerships for process intensification and continuous-flow manufacturing. Every incremental improvement we make to 3,5-Bis(Trifluoromethyl)Phenylacetonitrile production directly benefits customers looking for rugged, traceable, and clean supply lines.

    Conclusion: Real-World Quality, Proven Value

    Our history with 3,5-Bis(Trifluoromethyl)Phenylacetonitrile gives us a perspective grounded in the reality of modern manufacturing. The compound’s unique properties and performance in synthesis reflect the sum of long-term investments, hands-on problem solving, and open dialogue with users across the globe. In our facility, the journey from raw input to final product remains driven by measurable quality, accountability, and a steady focus on both current use and future needs in a rapidly changing chemical landscape.