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1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One

    • Product Name 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One
    • Alias 4-(Trifluoromethyl)chalcone
    • Einecs 694-020-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    661608

    Iupac Name 1-[3-(Trifluoromethyl)phenyl]but-1-en-3-one
    Molecular Formula C11H9F3O
    Molecular Weight 214.18 g/mol
    Cas Number 160437-23-0
    Appearance Yellow to orange liquid
    Boiling Point 257-259 °C
    Density 1.198 g/cm³
    Solubility Soluble in organic solvents like DMSO and ethanol
    Smiles CC(=O)C=CC1=CC(=CC=C1)C(F)(F)F
    Inchi InChI=1S/C11H9F3O/c1-8(15)6-7-9-3-2-4-10(5-9)11(12,13)14/h2-7H,1H2
    Refractive Index 1.513 (predicted)
    Flash Point 109 °C
    Pubchem Cid 12829033

    As an accredited 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, screw cap; labeled with chemical name, hazard warnings, and batch number; securely sealed for transport.
    Shipping 1-[3-(Trifluoromethyl)Phenyl]but-1-en-3-one is securely packaged in sealed, chemical-resistant containers compliant with safety regulations. The shipment includes appropriate labeling and documentation detailing hazard information. Temperature and handling instructions are provided as needed to ensure product stability and integrity during transportation. All shipments comply with international and local chemical shipping standards.
    Storage Store **1-[3-(Trifluoromethyl)phenyl]but-1-en-3-one** in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, strong oxidizers, acids, and bases. Always use appropriate chemical safety protocols, including gloves and goggles, when handling to prevent exposure or contamination. Store according to local regulations for hazardous chemicals.
    Application of 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One

    Applications of 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we supply 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One for advanced production in core chemical sectors. Below we detail primary downstream applications, specific incorporation practices, sector regulations, formulation ratios, and targeted end products, based on current industry adoption.

    1. Pharmaceutical Intermediate for API Synthesis

    Leading pharmaceutical clients utilize this compound as a building block in the synthesis of active pharmaceutical ingredients (APIs), particularly for anti-inflammatory and central nervous system drugs. Our material enters during early-stage condensation or coupling reactions, integrating precise trifluoromethyl functionality to enhance product bioactivity. Customers follow strict GMP controls at every process stage, from reagent qualification through to intermediate isolation and purification. Formulation specialists adjust input ratios based on the molecular yield of target compounds and impurity profile management for regulatory compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monographs for Intermediates
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) for pharmaceutical intermediate quality

    Typical usage ratio

    • Input at 0.5–1.5 molar equivalents, adjusted per target API synthetic route
    • Standard addition based on step yield optimization and impurity minimization

    Downstream process integration

    • Introduced during initial carbon–carbon coupling or Friedel–Crafts alkylation sequences
    • Reaction performed in controlled, closed reactor systems with in-process monitoring
    • Intermediate isolated after key transformation and purified for API assembly

    Final product types

    • Anti-inflammatory drug substances
    • CNS modulators
    • Other specialty APIs bearing trifluoromethyl aryl subunits

    2. Agrochemical Intermediate for Herbicide and Fungicide Formulation

    Major agrochemical producers select this raw material for use in synthesizing new-generation herbicides and fungicides. Its unique aromatic trifluoromethyl moiety imparts resistance to environmental degradation and increases bioavailability for field application products. Industrial batch processes require tightly controlled stoichiometric calculations, with ratios varying based on crop target compound pathways and desired molecular persistence in soil. Process engineers introduce this intermediate through nucleophilic addition or condensation steps, with downstream formulation adjusted seasonally for different active agent derivatives.

    Industry compliance standards

    • FAO/WHO specifications for pesticide intermediates
    • REACH (EU) Regulation (EC) No 1907/2006
    • US EPA 40 CFR Part 158 data requirements for pesticide registration
    • ISO 9001:2015 Quality Management for agrochemical manufacturing

    Typical usage ratio

    • Applied at 0.3–1.0 molar equivalents depending on downstream active ingredient synthesis
    • Adjusted in lab-scale studies to maximize active agent yield and environmental stability

    Downstream process integration

    • Charged into sealed agitated reactors during early heterocycle formation or Michael addition reactions
    • Monitored by on-line HPLC or GC analysis for conversion and by-product control
    • Isolated product transferred to blending for formulation of technical-grade agrochemicals

    Final product types

    • Pre-emergent and post-emergent herbicides
    • Systemic field fungicides
    • Seed treatment actives with enhanced weather resistance

    3. Specialty Chemical Synthesis for Electronic Materials

    Electronics manufacturers depend on high-purity precursors to fabricate advanced organic semiconductors and display materials. This compound’s electron-withdrawing trifluoromethyl group enables synthesis of aryl ketone monomers used in low-dielectric constant polymers, crucial for high-speed data circuits and flexible display films. Operators integrate our material via precision-controlled condensation with high-resolution monitoring for microelectronic performance requisites, maintaining sub-ppm residual metal content throughout the process.

    Industry compliance standards

    • IPC-4101B laminate specification for base electronic materials
    • JEDEC JESD990 Certificate for organic substrate inputs
    • RoHS Directive 2011/65/EU (lead and cadmium content requirements)
    • Cleanroom manufacturing protocols ISO 14644-1

    Typical usage ratio

    • Input at 0.2–0.8 molar equivalents in polymer backbone synthesis
    • Adjusted depending on targeted dielectric properties or thermal stability

    Downstream process integration

    • Added directly into anhydrous solvent systems under inert atmosphere protection
    • Process parameters include extended reaction times and controlled polymerization
    • Finalized monomers isolated and purified before resin formation

    Final product types

    • High-performance printed circuit board (PCB) laminates
    • Organic light-emitting diode (OLED) display layers
    • Low-k dielectrics for microchip insulation

    4. Fine Chemical Intermediate in Fragrance and Flavor Synthesis

    Flavors and fragrance firms incorporate this aromatic ketone derivative to synthesize novel scent and taste molecules. Its trifluoromethyl group imparts volatility and unique organoleptic properties essential for designer fruity and citrus notes, especially in high-end perfumes and specialty food flavorings. Compounders optimize input quantities based on gas chromatographic profiles and sensory evaluation, maintaining compliance with regional additive legislations and ensuring batch-to-batch identity.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • US FEMA GRAS (generally recognized as safe) guidelines
    • EU Regulation (EC) No 1334/2008 on flavorings
    • Kosher and Halal material certification (for global export)

    Typical usage ratio

    • Formulated at concentrations ranging from 0.05% to 0.3% in fragrance compositions
    • Distribution based on target formulation intensity and regulatory maxima per region

    Downstream process integration

    • Blended by perfumers during top-note composition adjustment
    • Processed at low temperatures to control evaporation loss
    • Subjected to panel testing and analytical verification

    Final product types

    • Luxury perfumes with citrus and green notes
    • Specialty beverage flavor concentrates
    • Citrus and berry-scented cleaning agents
    Free Quote

    Competitive 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One: Insights from a Chemical Producer

    Understanding the Demand for 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One

    Every year, as the chemical industry moves forward, we keep seeing stronger interest in specialized building blocks. 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One stands out in the crowded field of trifluoromethyl aromatics. Clients come to us directly for this compound, not just because of its fluorinated motif, but because the molecule’s design answers a specific need in fine chemical synthesis. Feedback over the years has made clear that reliable access to this intermediate makes a real difference for research teams and production chemists working in pharmaceuticals and advanced materials.

    Molecular Format and Consistency

    Our facility produces 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One by focusing on yield, purity, and consistency. The core structure — a trifluoromethyl-substituted phenyl ring linked to an enone — isn’t just a showcase of synthetic knowhow. As veterans in production, we’ve experienced the hurdles of scale-up with this molecule. Few chemicals challenge purification systems quite like it, especially when customers require less than 0.5% impurity content. We achieve this by tailoring every part of the process, from selection of reagents to precise control of reaction temperature and isolation steps.

    Through years of direct handling, we’ve confirmed that optical clarity, uniform color, and stable melting points matter. Customers expect a product that’s reliable not just in its specifications, but in the experience of working with it on the bench. Our material meets or exceeds the required spectroscopic and chromatographic benchmarks. We routinely validate every batch using NMR, mass spectrometry, and GC, comparing results to our own in-house standards, not just generic data sheet numbers.

    Key Role in Synthesis Pathways

    Industry researchers choose 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One during route scouting for new chemical entities and API intermediates. The compound’s unique combination of reactivity and stability allows for straightforward engagement in both electrophilic and nucleophilic chemistry. Chemists use it in medicinal chemistry libraries because the trifluoromethyl group often tweaks bioactivity, changing metabolic profiles and improving target affinity.

    Several research groups report that this enone serves as an entry point into more complex heterocycles. From our vantage point in manufacturing, we see the end use expanding, particularly in the design of fluorinated ligands and catalyst precursors. Its handling characteristics — a manageable solid, not prone to hazardous dust — lower the safety barrier for both kilo-lab and pilot plant production.

    Why Source Directly from a Manufacturer?

    Unlike distributors or third parties, we don’t import or relabel; we take personal responsibility from reaction to packaging. Any deviation in melting point, hue, or moisture content flags for us long before it ever ships. Clients often talk about variability encountered with intermediaries and how it adds delays to project timelines. By owning every step, we control for even subtle batch-to-batch variation, responding in real time to customer feedback on handling, yield, and process performance.

    Those who use 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One for sensitive work — such as preparing drug candidates intended for preclinical tests — rely on source transparency. If your synthetic route hits a bottleneck or analytic results suggest an impurity pathway, we give direct answers because we’ve seen it in our tanks and columns. Traceability matters, especially when scaling from milligrams to kilograms or when regulations tighten around process validation and documentation.

    Practical Differences from Similar Products

    Not all trifluoromethyl phenyl ketones act the same. Our years of process feedback demonstrate clear differences. Substituent position on the phenyl ring greatly influences both reactivity and downstream compatibility. The meta-trifluoromethyl placement on our product balances electronic effects — making it more reactive in conjugate additions than certain para-substituted counterparts, without the instability or byproduct formation seen in ortho-analogs.

    We've seen R&D groups test multiple positional isomers, documenting higher yields and less unwanted side-reactions with the meta variant, especially in microwave or flow chemistry conditions. The butenone structure grants added versatility. Where a simple aryl methyl ketone limits coupling reactions, this enone opens further options through Michael additions, aldol-type reactivity, and cyclization strategies.

    We also see a trend among process chemists moving from chlorinated aryl ketones to fluoroalkyl variants like this one, influenced by both regulatory and performance considerations. Chlorinated residues sometimes trigger extra waste handling, while trifluoromethyl groups rarely pose those same disposal issues.

    Handling, Shipping, and Storage Experience

    Over the last decade, best practices for packing, labeling, and storing specialty ketones have evolved sharply. Our approach draws on first-hand knowledge of transport across multiple climate zones — from humid port cities to dry inlands. Each batch of 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One undergoes inspection prior to drum or vial filling, not just for technical parameters but for crystalline integrity and lump formation. We select containers and liners to minimize exposure to light, moisture, or reactive air.

    Smart logistics make a difference, too. Delays on docks, especially in summer, can impair shelf life or cause caking. By controlling dispatch and warehousing, we provide accurate timelines and keep product stability intact. User feedback often points to the value of getting material directly from a producer who understands transit risks, not just a shipper who fills a tracking label.

    We’ve tackled the questions of product auditability and documentation demanded for both GLP and GMP environments. Documentation follows each lot, and we work with research buyers to provide necessary analytical and regulatory background, avoiding roadblocks down the line.

    Quality, Compliance, and Analytical Transparency

    Features like low impurity content, narrow melting range, and distinct spectral signatures matter most in regulated synthesis. Our quality assurance workflow comes from decades of experience, not template documents. Each lot comes with a full analytical set. Rather than hiding behind generic certificates, we interpret and discuss the actual spectra. If a project’s progress depends on following specific impurity peaks or tailing, our chemists communicate directly to resolve method variations or explore unusual process results.

    Compliance expectations keep rising, and we stay ahead by engaging with both industry standards and regulatory updates. We adjust our methods based on customer input from pharmaceutical, agricultural, and specialty materials sectors. Years ago, a surge in demand for higher fluorocarbon purity led us to replace several upstream reagents, lowering levels of residual heavy metals and halide traces.

    Environmental and Process Safety Perspective

    Unlike traditional halogenated intermediates, 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One aligns better with design-for-safety practices. Its structural stability means no unexpected gas release during storage or handling, reducing risks in both production and end use. By working closely with our in-house environmental specialists, we minimize solvent and reagent waste while maximizing recovery for both energy and cost reasons.

    Customers often ask about the end-of-life fate for fluorinated molecules. Through collaboration with downstream users, we have participated in method development for safer waste treatment. Neutralization or incineration protocols get tested directly on our spent solutions before we make any disposal recommendations.

    Fluorine chemistry carries a reputation for persistence, but measured handling and robust process design greatly mitigate environmental risks. Our own waste minimization steps have cut hazardous solvent consumption for this product by more than half since 2015.

    Process Innovation and Future Development

    Time spent on the production floor shows that process innovation never stops. Our team continues to improve throughput and yields. We invest heavily in staff development, giving chemists a real stake in designing safer, cleaner synthetic routes. Automation, real-time monitoring, and inline analytics now guide every batch of 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One through the process. The result is fewer failed runs and better reproducibility for our clients.

    R&D programs led to significant reduction in byproduct formation, not just by optimizing conditions, but by redesigning the entire synthetic route where possible. Pilot plant feedback became part of our continuous improvement culture, allowing incremental adjustments before rolling out changes to full-scale production.

    Over the years, collaborative development with end users led to improved physical forms — whether more free-flowing crystalline grades or solvent-wet cakes for easier incorporation into continuous processes. We modify drying or granulation approaches based on insights from those actually using the material, not just lab-scale curiosity.

    Customer Experiences and Industry Applications

    Feedback flows both ways with this intermediate. In one instance, a pharmaceutical team reported unusually high conversion during C–C bond formation, linking back to the particular crystalline habit of the batch they received. Continuous dialogue means process tweaks can translate directly to better outcomes downstream. We analyze such trends and feed them back into process control protocols.

    Aside from small-molecule pharmaceuticals, this molecule finds frequent use in crop protection candidates and advanced material design. The structure’s robustness often translates to greater shelf lives for precursors, which matters when materials sit in storage awaiting regulatory approval.

    Our vantage at the point of manufacture lets us recognize recurring technical questions early, sharing successful workarounds or optimized workup procedures with users tackling the same challenges.

    Honest Dialogue and Technical Support

    Chemical producers have a responsibility beyond shipping barrels or bottles. We offer hands-on support during both method development and scale-up. Years spent navigating the ups-and-downs of production taught us never to overpromise or undersell technical difficulty. If a challenge arises with robust workup, unexpected product profile, or process integration, customers can reach a chemist from our team who has spent real time with this molecule, not a generic support desk. Most of the reliability we deliver comes from knowing exactly how the product behaves, not just from a data sheet but from experience drawn from every batch we've run.

    Looking Ahead

    Seeing customer projects blossom from initial R&D to commercialization motivates continuous investment in both capability and consistency. Applications for 1-[3-(Trifluoromethyl)Phenyl]But-1-En-3-One keep growing, sometimes along lines we never predicted. We remain committed to supporting scientific progress by delivering the product as chemists ourselves would want to receive it — well-characterized, well-supported, and honestly described.

    We invite researchers and formulators to engage directly with the manufacturing process. Not only does this open the door to rapid troubleshooting, but it strengthens trust and long-term collaboration. Together, these connections yield both immediate process solutions and help set the standard for reliability in specialty chemical supply.