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4'-Fluoro-2'-(Trifluoromethyl)Acetophenone

    • Product Name 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone
    • Einecs 415-730-2
    • 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
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    VTB
    Specifications

    HS Code

    255836

    Productname 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone
    Casnumber 886371-92-8
    Molecularformula C9H6F4O
    Molecularweight 206.14 g/mol
    Appearance White to off-white solid
    Meltingpoint 41-45°C
    Purity Typically ≥98%
    Smiles CC(=O)C1=CC=C(C(F)=C1)C(F)(F)F
    Inchikey DEAPYFYESCLYAD-UHFFFAOYSA-N
    Solubility Organic solvents (e.g., DMSO, DMF)
    Storagetemperature 2-8°C
    Synonyms 1-[4-Fluoro-2-(trifluoromethyl)phenyl]ethanone

    As an accredited 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone 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 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone, tightly sealed, labeled with hazard and identification information.
    Shipping 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical is packed according to regulations for hazardous materials, with appropriate labeling and documentation. Transportation complies with local, national, and international guidelines to ensure safety and prevent contamination or accidental release during transit.
    Storage Store 4'-Fluoro-2'-(trifluoromethyl)acetophenone in a tightly sealed container, in a cool, dry, and well-ventilated area away from oxidizing agents and incompatible substances. Protect from moisture and direct sunlight. Handle under a fume hood and use appropriate personal protective equipment. Clearly label the container and keep it away from heat, sparks, and open flames. Store according to chemical safety guidelines.
    Application of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone

    Applications of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone in Industrial Manufacturing

    As a direct manufacturer, we supply 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone to specialty chemical producers active in advanced material synthesis and fine chemical intermediates. This compound plays a targeted role in several tightly regulated downstream applications, especially in pharmaceutical intermediates, agrochemical synthesis, liquid crystal intermediates, and specialty polymers. Each field has specific requirements for purity, formulation, compliance, and integration into proprietary manufacturing steps.

    1. Pharmaceutical Intermediate Synthesis

    The compound serves as a building block in the multi-step synthesis of fluorinated pharmaceutical intermediates, supporting manufacturers in production of targeted APIs for CNS and oncology research. Our customers use this material for Friedel-Crafts acylation and related transformations under cGMP environments. Production environments require rigorous specification control and traceability from raw input through to the intermediate output, supporting robust documentation and reproducibility during scale transitions.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP (EudraLex Volume 4 Guidelines)
    • US FDA 21 CFR Part 211 (Current GMP for Finished Pharmaceuticals, intermediates)
    • ISO 9001:2015 (Quality Management Systems)

    Typical usage ratio

    • 5–25 mol% relative to target intermediate (dose depends on transformation yield and reagent excess required for conversion); typically adjusted according to stoichiometry, limiting reagent, and process scale.

    Downstream process integration

    • Charged during the acylation, condensation, or reductive coupling step, typically in batch reactors under inert atmosphere. Integration occurs after initial precursor preparation, followed by in-line or batch purification.

    Final product types

    • N-aryl fluorinated intermediates for CNS agent research
    • Fluorinated heterocyclic scaffolds for small molecule APIs in oncology and metabolic disease
    • Advanced chiral building blocks for drug discovery libraries

    2. Agrochemical Synthesis

    Agrochemical manufacturers incorporate this fluorinated acetophenone derivative into the synthesis of selective herbicides and fungicides, where the introduction of fluorine-containing moieties confers hydrophobicity, environmental persistence, and improved bioactivity. The compound enters amidation, etherification, or cross-coupling steps depending on the targeted end compound. Emphasis is placed on trace residue control and batch traceability, as regulatory requirements for environmental and occupational safety are high in agro intermediates.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025 (Testing and Calibration Laboratories)
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH (Registration, Evaluation, Authorization and Restriction of Chemicals, EU)

    Typical usage ratio

    • 2–8 wt% in formulation as an intermediate precursor, tuned according to the desired final active ingredient yield and coupling efficiency.

    Downstream process integration

    • Undergoes electrophilic aromatic substitution, palladium-catalyzed cross-coupling, or nucleophilic addition step, typically directly after the formation of the aromatic backbone and prior to heterocycle closure or amide bond formation.

    Final product types

    • Fluorinated aromatic herbicide intermediates
    • Precursors for broad-spectrum fungicide actives
    • Building blocks for insecticide molecule libraries

    3. Liquid Crystal Intermediate Manufacturing

    Producers of specialty display materials deploy this compound as a core precursor during construction of liquid crystal intermediates for advanced electronic displays. The fluorinated acetophenone is used to introduce linear, rigid, and polar structures essential for high-performance nematic and ferroelectric liquid crystal compounds. Stringent standards regarding ionic purity, heavy metals, and trace organics dictate supply suitability and analytical documentation.

    Industry compliance standards

    • RoHS Directive (EU) for electronic chemicals
    • IEC 61249-2-21 (Halogen-Free Materials Specifications)
    • ISO 9001:2015 (Quality Management Systems for Electronic Grade Chemicals)
    • JIS C 6109 (Japanese Industrial Standards for LC Chemicals)

    Typical usage ratio

    • 1–10 mol% in precursor mixture, finely adjusted for molecular design based on polarizability and compatibility requirements with other mesogenic units.

    Downstream process integration

    • Incorporated during initial Friedel-Crafts acylation or etherification, followed by high-vacuum distillation or sublimation to achieve electronic-grade purity prior to final formulation blending.

    Final product types

    • Nematic and ferroelectric liquid crystal intermediates
    • Specialty mesogenic compounds for TFT-LCD and OLED displays
    • Custom fluorinated blocks for display material R&D

    4. Specialty Fluorinated Polymer Synthesis

    Our material features as a reactive monomer in the production of high-performance fluorinated polymers, valued for imparting thermal stability, chemical resistance, and low dielectric properties. End users integrate it within batch or continuous copolymerization lines, optimizing concentration to achieve the targeted chain properties while meeting processability and surface requirements for films or coatings applied in electronics and chemical containment.

    Industry compliance standards

    • UL 94 (Flammability Standards for Plastics)
    • ASTM D543 (Chemical Resistance of Plastics)
    • ISO 14001 (Environmental Management for Polymer Production)
    • RoHS (EU Restriction of Hazardous Substances Directive)

    Typical usage ratio

    • 3–15 wt% as comonomer, process engineers optimize level based on targeted fluorine content and mechanical property profile in the copolymer.

    Downstream process integration

    • Introduced into the monomer feed during emulsion or solution polymerization; polymerized under controlled temperature and initiator conditions, followed by post-polymerization modification if required.

    Final product types

    • Fluorinated polyarylates and polyimides for electronics encapsulation
    • High-temperature resistant fluoropolymer films and sheets
    • Surface-protective coatings and specialty adhesives
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone: Direct from Manufacturer Experience

    Distinctive Structure, Reliable Performance

    Each time we scale up a batch of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone in our facility, we work with both the molecular integrity and the real-world needs chemists bring to our door. Built upon a finely tuned backbone of acetophenone, this compound brings together a para-fluoro group and a 2'-trifluoromethyl substitution on the phenyl ring—a combination few analogs can match for electron-withdrawing potential and functional group versatility. Our direct experience in multi-step synthesis, in-house purification, and rigorous QC forms the backbone of why this material keeps its edge batch after batch.

    Model and Key Specifications Born from Practical Lab Demands

    We catalogue this compound by its molecular formula, C9H6F4O, and CAS number 661463-40-1, details familiar to any synthetic or medicinal chemist. Over the years, our team has dialed in on customer priorities: pure, crystalline powder free of significant polymorphism, with an assay specification at or above 98%, and GC-MS or HPLC trace impurity profiling that goes beyond the minimal standards. Melting points fall in a tight, reproducible range, an outcome of our controlled cooling and recrystallization process. Each unit is tightly sealed under inert gas, labeled with actual production lot numbers, and barcoded for full traceability—an approach tuned to the expectations of serious researchers who don’t have time for guesswork.

    Applications Driven by Real-World Discoveries

    We’ve watched this building block shape research across energetic materials, pharmaceutical intermediates, and fine chemical development. The electron-deficient character of the ring, born from the dual fluoro and trifluoromethyl groups, has led to remarkable downstream reactivity: Suzuki couplings proceed with fewer byproducts and greater selectivity. In pharmaceutical research, our clients regularly shift to this acetophenone over less substituted versions to investigate enhanced metabolic stability, improved binding to fluorophilic biological targets, and finer control over polarity in new molecule design. As bench chemists, we know how frustrating it is to swap starting materials and face unpredictable outcomes—our production methods ensure reproducibility between orders, avoiding the headaches and retesting that can derail a project.

    Handling, Storage, and Everyday Use: Lessons from the Production Floor

    Working with 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone day after day, we’ve learned that dry, cool, and inert conditions aren’t just recommendations—they’re requirements that keep color, purity, and chemical reactivity in check long-term. Standard packaging won’t do; the compound can draw in trace moisture from standard plastic vials, so we ship in glass ampoules, seal under nitrogen, and test for micro-contaminants before each release. On the line, we train all technicians to be fastidious with double-gloved handling and local exhaust for any weighing outside the glovebox, a policy that has cut contamination and exposure events to near zero over the past few years.

    Performance Compared to Other Acetophenone Derivatives: Experience Speaks

    Through years of producing both simple acetophenones and more exotic fluorinated analogs, we’ve witnessed the unique value this molecule holds. In contrast to standard acetophenone, where side reactions often reduce yields in enolate-based chemistry, the electron-deficient ring of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone suppresses those side paths. Even compared to structurally similar molecules—say, 4'-fluoroacetophenone or 2'-(trifluoromethyl)acetophenone alone—the synergy between the two substituents in this molecule improves selectivity and increases compatibility with palladium-catalyzed transformations. Reaction designers come to us with feedback showing fewer purification headaches and crisper NMR spectra after swapping in our material.

    Many alternative acetophenones can frustrate chromatographers with UV tailing or unexpected impurities due to less stringent purification from upstream suppliers. Years back, before tightening our own specification, we faced similar complaints—broad, colored tails in silica columns and inconsistent mass spec traces. It took substantial investment in newer crystallization protocols and inline filtration before we saw marked improvement in customer results. We routinely field questions about switching from methyl, ethyl, or unfluorinated acetophenone building blocks for new process development, and direct side-by-side trial feedback continues to reinforce our conclusions: the unique substitution pattern in our product translates to lower side-product formation and reduced time cleaning up after runs.

    Supporting Advanced R&D and Scale-Up Operations

    Lab-scale researchers value the ease of functionalization on the aromatic ring, especially for adding more complex groups through selective halogen-metal exchange or transition metal-catalyzed cross coupling. We support pilot and commercial teams transitioning from milligram to kilogram quantities, having modified our production setup to maintain the same quality with increasing scales. Our technicians have overhauled solvent recovery systems and fractionation steps to control for scale-based impurity drift, an important detail rarely discussed outside manufacturing circles.

    Feedback from process chemists at smaller companies to multinational operations has shaped how we manage upscaling. Demand for non-stop supply with consistent quality places both pressure and motivation on us to refine every step of the cycle. Beyond raw synthesis, our facility processes in fully closed systems—eliminating the cross-contamination risks that surface in multi-purpose plants. Our lot release documentation includes two forms of structural confirmation, with both NMR and IR assigned to individual bottles, so scale-up chemists do not face unexpected surprises during initial runs.

    Safety Considerations Shaped by Practice

    Our long-term handling has taught us that 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone is stable against heat and light under proper conditions but poses issues in open air during multi-hour operations. We reinforce regular refresher training for all production shifts, focusing on skin contact and airway protection protocols—learnings written from genuine slip-ups in our early days. Analytical teams routinely stress-test the compound for peroxide formation and decomposition after extended bench storage, showing low risk but confirming the value in never letting routine drift into complacency.

    Tackling Issues: Insights from Real Failures and Solutions

    No operation runs perfectly all the time, and the lessons we've learned from occasional batch inconsistencies have sharpened our process. In earlier years, variable yields and trace polyfluoro impurities slipped through due to less sensitive QC. Once we implemented LC-MS fingerprinting with internal standards specific to the minor byproducts seen only in large-scale synthesis, rejection rates for out-of-spec lots dropped by more than half. These investments in internal analytics aren’t bolt-ons—they reflect our core expectation to serve scientists who depend on fast, clean data from their starting materials.

    Storage failures once resulted in minor oxidation on external ring positions—a problem solved only after switching to full inert atmosphere packaging and ongoing shelf-life checks on retained samples. Feedback loops with customers who run extended process studies help pinpoint trends that can only show up over months of storage or non-routine workflows. This dialog between our production chemists and real users exposes flaws far faster than any abstract stability study could hope.

    Quality Foundation Built on Know-How

    We have spent years observing which QC tests best catch potential pitfalls. Alongside the basics, our team runs enantiomeric purity screens, byproduct profiling, and storage stress tests on each lot. Hearing from researchers who spot subtle NMR shifts after a six-month interval provides more useful insight than any off-the-shelf guideline. By tracking each ingredient and monitoring inert gas coverage, we keep both material and data transparent for grant auditors, patent teams, and bench chemists alike.

    Moving Forward: Customer-Driven Refinement

    Future success depends on building strong links with chemists tackling new challenges. Our back-and-forth with applied R&D groups in fields ranging from crop protection to polymer design often turns up unexpected needs. In the case of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone, we have adjusted both bottle sizes and labeling formats based directly on feedback from teams needing milligram or multi-kilogram lots. Seeing the material at work in unexpected applications inspires us to add further analytical tracers or offer extra technical notes useful at the bench, not just on paper.

    The evolution of this product line comes from open conversations—sharing what failed, what solved a problem, and what might help in new syntheses. We collect feedback from regular partners on yield changes, unexpected side reactions, or purification success and adjust our targets accordingly. No amount of technical jargon replaces direct, honest experience about what lands on the lab bench and the reality of what it takes to push a molecule from an idea to a reliable reagent or building block.

    Supporting Documentation and Best Practices

    Full documentation accompanies every shipment, telling the story of each batch: source of starting materials, method identifiers, release analytical traces, and packaging controls. Researchers have walked us through grant applications and regulatory routines that demand traceability stretching back more than a year, spurring us to digitize every record and scan archive samples for each lot shipped. We have rebuilt our SOPs to include sample archiving, redundancy, and clear barcode tracking—steps painstaking to set up, but invaluable as regulatory requirements evolve.

    Working entirely in-house, we have rewritten protocols to keep overhead manageable while maintaining transparency—a process that takes continual labor behind the scenes. We hear from chemists needing rapid access to COAs, analytical spectra, and composition verification for trial runs, so internal systems flag inquiries for immediate response and live review by the same chemists who led production. Our technical support doesn’t route through call centers—we connect researchers directly to our own process staff, people who physically walked the compound out of the reactor and through the drying room.

    Differentiating Factor: Manufacturer’s Responsibility on Consistency

    True reliability comes from producing a compound in facilities that never compromise on input traceability or documentation. Our investment in unique FTIR and NMR databases for each finished batch means returning chemists never need to worry about subtle property drift between shipments. With regulatory agencies sharpening their focus on audit trails and process reproducibility, our hands-on approach meets requirements before they appear.

    Direct control of every step—from raw fluorinated aromatics through final release—lets us address any concern and carry out corrective runs without supplier excuses or speculative guesswork. Batch-to-batch, bottle-to-bottle, every instance of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone reflects the attention and adjustments honed through thousands of kilograms of production and close customer feedback.

    Modern Manufacturing Means Listening and Improving

    Today’s research cycle expects both material quality and responsiveness that only a hands-on manufacturer can ensure. Over time, changes in downstream reactions, catalyst trends, and safety requirements flow back to us as requests, failures, and new target profiles. Bringing a new batch online never happens in isolation; analytical teams, safety experts, and process managers walk through every stage and review each other’s output before the finished lot enters the warehouse.

    Compared to distributor stock, material direct from the factory reflects current best practices. Customers bring us their challenges—failed couplings, slow conversions, unexpected color changes—and together, we zero in on both the underlying causes and the adjustments necessary for success. The foundation remains an open channel with serious chemists and technical buyers willing to share their testing experience, both positive and negative, in service of better outcomes for the next order.

    Commitment to Scientific Progress: From Factory to Bench

    Everything we have learned, from substructure-specific purification to improved inert gas techniques and moisture exclusion, feeds back into stronger, more adaptable manufacturing. Each shipment of 4'-Fluoro-2'-(Trifluoromethyl)Acetophenone carries the legacy of failures, breakthroughs, and practical problem-solving unique to our operation. Researchers who purchase direct engage with a team ready to trace back to a single reactor, discuss a line-item analytical report, and adapt to new research needs as they arise.

    In chemical manufacturing, the real product is more than just a molecule—it’s a culmination of attentive production, honest feedback, and a continuing drive to do better. From our first small-scale runs to today’s multi-ton output, we stay connected to the evolving demands of both established and experimental research, always ready to refine, learn, and improve.