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4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One

    • Product Name 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One
    • Alias ETFBO
    • Einecs 'EINECS 211-293-2'
    • 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
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    584384

    Chemical Name 4-Ethoxy-1,1,1-trifluoro-3-buten-2-one
    Cas Number 406-78-0
    Molecular Formula C6H7F3O2
    Molecular Weight 168.11 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 78-80 °C at 14 mmHg
    Density 1.237 g/mL at 25 °C
    Refractive Index n20/D 1.369
    Smiles CCOC(=C)C(=O)C(F)(F)F
    Solubility Slightly soluble in water; soluble in organic solvents
    Flash Point 29 °C (closed cup)

    As an accredited 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed with a PTFE-lined cap, labeled "4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One, 25g, for laboratory use."
    Shipping **Shipping Description:** 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One should be shipped in tightly sealed, corrosion-resistant containers under inert atmosphere. Store and transport in a cool, dry place, away from heat and incompatible materials. Comply with all local, national, and international chemical transportation regulations. Handle as a hazardous material; ensure proper labeling and safety documentation.
    Storage Store **4-Ethoxy-1,1,1-trifluoro-3-buten-2-one** in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep the container tightly closed and protected from moisture and incompatible substances such as strong oxidizers and bases. Use only in a fume hood, and avoid prolonged exposure. Label containers clearly and ensure proper secondary containment to prevent spills.
    Application of 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One

    Applications of 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One in Industrial Manufacturing

    As a specialized manufacturer, we supply 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One to a range of advanced industrial segments. Below, we detail key downstream applications, focusing on unique compliance, ideal incorporation ratios, specific process steps, and the types of finished goods produced in each area.

    1. Pharmaceutical Intermediate for Fluorinated APIs

    Research-based pharmaceutical companies use this compound as a building block in synthesis routes for selective fluorinated active pharmaceutical ingredients (APIs). It introduces CF3 groups into advanced intermediates, which imparts metabolic stability in target molecules. End users implement it in multi-step synthesis under stringent production standards, especially in the development of next-generation antivirals and CNS drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 Current Good Manufacturing Practice for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) monographs related to intermediates
    • REACH Registration for downstream pharmaceutical chemical handling

    Typical usage ratio

    • Applied at 1–8 mol% with respect to the key nucleophilic substrate, depending on desired fluorine incorporation and batch scale

    Downstream process integration

    • Added during the alkylation step post-protection of functional groups; used under controlled temperature in reagent-grade solvents

    Final product types

    • Fluorinated pharmaceutical intermediates
    • Selective serotonin reuptake inhibitor (SSRI) precursors
    • Potent CNS drug candidates
    • Lead compounds for small-molecule therapeutics

    2. Agrochemical Synthesis: Crop Protection Actives

    Major agrochemical companies source this raw material for the synthesis of novel trifluoromethylated herbicides and fungicides. Its reactive alkenone structure aids in constructing highly stable active moieties that exhibit enhanced resistance to biodegradation in field conditions. The compound enters the synthesis chain in pre-formulation, contributing to higher crop yield protection products.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration of Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • European Union Regulation (EC) No 1107/2009 for Plant Protection Products
    • China GB / T 27741 Testing for Agricultural Chemicals

    Typical usage ratio

    • Employed at 2–15% w/w based on target molecule design; adjusted per structure–activity relationship screening

    Downstream process integration

    • Introduced at the key keto-enol cyclization stage in batch or continuous-flow reactors following catalyst addition

    Final product types

    • Pre-emergent herbicide intermediates
    • Trifluoroalkylated fungicidal actives
    • Seed treatment agent precursors
    • Crop-specific formulation components

    3. Specialty Polymer & Coating Modifier

    Manufacturers of high-performance polymers and industrial coatings utilize this molecule as a specialty modifier to impart fluorinated character and enhance surface properties such as low surface energy and chemical resistance. It acts as a co-monomer or chain-terminator in the synthesis of fluorinated acrylics and resins, which are then compounded into advanced coatings for electronics, aerospace, and automotive components.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for polymer manufacturing
    • RoHS Restriction of Hazardous Substances Directive
    • REACH Annex XVII (for polymers and coatings)
    • ASTM D6083 for coating performance testing

    Typical usage ratio

    • 0.2–3.5% by mass in polymerization feedstocks, with concentration tailored to end-use coating specifications

    Downstream process integration

    • Charged at the pre-polymerization stage during reaction with acrylic or methacrylic monomers under controlled radical or cationic initiation

    Final product types

    • Fluorinated acrylic resins
    • Low-energy protective coatings
    • Anti-fingerprint display overlays
    • Weather-resistant automotive clearcoats

    4. Electronic Chemical Intermediate (Semiconductor Industry)

    In the manufacture of advanced microelectronic materials, this compound functions as an intermediate in formulation of photoresists, etching agents, and dielectrics. The introduction of trifluoro groups improves performance in high-frequency environments and increases plasma resistance for next-generation semiconductor fabrication.

    Industry compliance standards

    • SEMI S2 Environmental, Health, and Safety Guideline for Semiconductor Manufacturing Equipment
    • ISO/TS 16949 for automotive electronics chemical quality
    • Taiwan EPA Toxic Chemical Substance Control Act for semiconductor chemicals
    • IPC-4101 for base materials in printed circuit boards (PCB)

    Typical usage ratio

    • Ranged between 0.5–6% in formulation, modulated according to lithography type and pattern resolution requirements

    Downstream process integration

    • Blended with base resin and photoacid generators during photoresist compounding prior to spin-coating and curing

    Final product types

    • Advanced photoresist solutions for photolithography
    • Dielectric precursor materials
    • Etching-resistant coatings
    • Micro-patterned chemical works for advanced node devices

    5. Fine Chemical Intermediate: Flavor and Aroma Ingredient Synthesis

    Key flavor and fragrance houses procure this compound for selective fluorination in synthesis of aroma ingredients. It plays a role as a reactive synthon to introduce trifluoromethyl functionalities, increasing molecular volatility and olfactory properties in high-end perfumery and specialty flavors.

    Industry compliance standards

    • IFRA International Fragrance Association Standards
    • US FDA 21 CFR 172.515 for synthetic flavoring substances
    • European Regulation (EC) No 1334/2008 on Flavourings
    • FEMA GRAS (Generally Recognized as Safe) listing for safe use in food

    Typical usage ratio

    • Used at 0.1–2% in reaction batch depending on the required aromatic note and safety assessments

    Downstream process integration

    • Dosed during esterification or acylation of alcohol substrates under inert gas at controlled pressures

    Final product types

    • Fluorinated aromatic esters
    • High-purity flavor enhancers
    • Intermediate bases for perfumery houses
    • Complex aroma ingredient blends
    Free Quote

    Competitive 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One: A Direct Manufacturer's Perspective

    The Place of 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One in Modern Chemistry

    Over the years, we have worked with a variety of specialized fluorinated molecules, but few offer the same versatility and reactivity as 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One. While it may not be a household name, this compound has carved a solid place on laboratory benches and production floors wherever efficient fluorinated building blocks hold value. We see requests for this material from both research chemists and full-scale production managers, and each conversation reveals new application angles—reinforcing its growing importance in the landscape of organic synthesis.

    Our facility keeps a close connection with processes that demand high-purity and consistent fluorinated reagents. In our experience, subtle differences in molecular architecture, such as the substitution of an ethoxy group for a more common alkoxy variant, or the strategic placement of a trifluoromethyl group, can determine whether a process sails smoothly or stalls in the pilot phase. 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One stands out among its peers for these reasons. Chemists regularly gravitate to this compound not because of marketing but because it works—whether in exploration or established production trails.

    Understanding the Structure and Its Significance

    This molecule carries an alluring combination—a reactive enone, the powerful electron-withdrawing effect of three fluorines, and the solubilizing influence of an ethoxy group. Our synthesis team often discusses how each piece impacts reactivity and product stability. The trifluoromethyl group, positioned on the terminal carbon, dramatically boosts the electrophilicity of the carbonyl, making nucleophilic addition more selective and efficient. The butenone backbone, meanwhile, delivers accessible sites for further elaboration. By modifying the ethoxy side, we notice changes in solubility and process handling, a detail appreciated by experienced operators moving from bench to pilot reactor.

    We have compared direct cousins of this molecule—4-alkoxy-3-buten-2-ones lacking fluorination, or trifluoromethylated ketones without the unsaturated tail. The contrasts often turn up in yield, reaction times, and by-product formation. With 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One in the mix, couplings tend to proceed with sharper conversions, and purification steps become less challenging. That saves valuable hours for both researchers and plant operators—something often overlooked until project timelines start to tighten.

    Specification and Consistency: Manufacturer’s Commitment

    The journey of this compound from raw fluorinated feedstocks to high-purity product involves tight process control. Manufacturing teams rely on robust methods not only for synthesis but also for purification. Each batch, we draw upon years of process data to maintain tight specification ranges—color, physical state, GC and NMR profiles, and controlled moisture levels. End-users tell us that material consistency has become a distinguishing feature. Variations in purity or moisture content can impact downstream processes, particularly where sensitive organometallic catalysts or high-precision reaction conditions are in play. Our ongoing dialogue with users has driven us to maintain specifications suited to advanced organic synthesis and material science research, where reproducibility cannot be left to chance.

    The colorless to pale yellow transparent liquid we deliver reflects the care taken to avoid polymerization or decomposition during storage. Handling fluorinated molecules often brings unique challenges in containment, waste management, and stability. Over years of production, our team has refined protocols from solvent washes down to the right grade of glassware to minimize contamination traces. While we meet standard specifications as a baseline, we collaborate with partners pushing boundaries in custom applications or process scale-ups, offering tailored lots when standard grades are not enough. This might involve tighter purity windows, special packaging, or on-demand batch sizes. Real-world manufacturing experience tells us that these details make the difference between frustrating reruns and streamlined syntheses.

    Practical Applications: Lessons from the Laboratory and Production Plant

    This compound features often in pharmaceutical research projects. Researchers tell us the unique blend of electrophilicity and modifiable side chain helps them construct fluorinated intermediates that mimic drug-like properties—membrane permeability, metabolic stability, and binding selectivity. The presence of both a reactive enone group and a trifluoromethyl moiety simplifies the journey to complex molecular targets. Medicinal chemistry teams use the compound as a stepping stone for fragment elaboration, introduction of chirality, or installation of stable bioisosteres. Access to a reliable source with predictable batch quality gives our partners confidence during process transfer and scale-up, areas when surprises can carry real cost consequences.

    Away from pharmaceuticals, the material appears in advanced agrochemical synthesis, specialty polymers, and fine chemical intermediates. Process chemists in crop science mention the trifluoromethylated backbone, coupled with the reactive enone, as a tool for crafting new herbicides or fungicides with enhanced bioavailability. The molecule’s reactive character lets them install functional groups not easily achieved with non-fluorinated analogs. Our experience handling ton-scale lots of similar fluorinated ketones tells us that containment, waste stream management, and process safety all demand close attention—something that research-scale users may not encounter until they attempt plant trials. These operational details explain why buyers from new sectors often consult our manufacturing engineers before ordering bulk volume.

    Comparison with Alternative Fluorinated Intermediates

    Over the years, the market has seen surges of interest in various fluorinated synthons. Trifluoromethyl ketones, vinyl fluorides, and perfluorinated alcohols each have design appeal. We have offered catalogs with several, and in working with clients, the nuanced differences between 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One and its cousins become clear. Some chemists try trifluoroacetyl derivatives first, hoping for similar reactivity—but the lack of the enone’s unsaturation can mean sluggish addition reactions, poor selectivity, or increased by-products. Simple trifluoroacetic esters often hydrolyze too readily, raising isolation headaches or requiring excess drying.

    Comparatively, 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One offers a middle ground between reactivity and stability. The combination of the ethoxy group and the conjugated enone chain maintains solubility in common polar and low-polarity solvents, aiding both small-scale screening and scale-up into multi-liter reactors. Many companies have tried to adapt earlier-generation trifluoromethyl intermediates to modern high-throughput settings, only to hit barriers with volatility, odor, or environmental loading in waste streams. Our process development teams understand these headaches firsthand and are ready to share protocols or options that reduce these risks in end-user settings.

    Supply Chain and Regulatory Notes from the Factory Floor

    Chemical manufacturing hinges on the reliable flow of raw materials and components. Our procurement team has weathered fluorinated feedstock shortages, fluctuations in specialty solvent prices, and logistics bottlenecks across continents. Suppliers come and go, but our ethos revolves around contingency planning and robust relationships with primary producers of key fluorinated building blocks. Because we produce 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One in-house, feedback loops between R&D, QC, and production happen in real time. Our process teams catch variations or impurities in early synthesis steps before bottles hit the warehouse—a layer of quality control that resellers and brokers struggle to match.

    On regulatory fronts, our team stays attuned to evolving rules around fluorinated organics. Some markets tighten import requirements, demand detailed traceability, or impose new emission controls. Over the last decade, these rules increasingly focus on both worker safety and environmental stewardship, compelling manufacturers like us to continuously improve containment, monitoring, and documentation practices. The direct feedback from both downstream partners and our own production team feeds into upgrades aimed at keeping ahead of regulations instead of scrambling to adapt.

    Sustainable Manufacturing and Environmental Footprint

    Handling fluorinated organics often means environmental risk looms larger than with basic hydrocarbons. Solvent recovery, air emissions, and wastewater—all draw critical attention. From the earliest days, our team prioritized molecular-level stewardship, aiming to minimize vent losses and recycle solvents wherever feasible. As demand for molecules such as 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One grows, sustainable practices have shifted from “nice-to-have” to operational imperatives. Our engineers monitor each production run for opportunities to recover by-products, reuse catalyst beds, and reduce the tonnage of disposal waste per kilogram delivered.

    Feedback from global partners has underscored the shift. End-clients now include not just R&D teams but also sustainability officers, compliance auditors, and board-level executives—each wanting clear documentation and credible commitments. Drawing on our own metrics, we continue to invest in emissions controls and process efficiency. This means the 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One we ship today comes with a lighter footprint than its predecessors, an outcome that keeps our team motivated and drives technical innovation on the shop floor.

    Process Improvement: What Decades of Experience Teach

    Our expertise in making this molecule did not come overnight. Every batch, each feedback loop, revealed tweaks that deliver tangible gains. Early runs showed us the impact of trace metal catalysis, glass surface passivation, and staged solvent addition. These lessons emerged only because we operate full-stack from bench to drum—R&D chemists, process engineers, and QA specialists all within shouting distance of each other. The result: tighter controls, less waste, and repeatable purity benchmarks.

    Process improvement never hits pause. As our customers experiment with greener alternatives to traditional coupling agents, or push for lower-waste workup routines, we listen and adapt. One example came from a customer in the electronics sector who prompted us to phase out a marginal solvent in favor of a recyclable alternative. On review, our cost and yield improved. Insights like these accumulate not from manuals, but from direct engagement with users driving new applications. Open channels between the plant and real-world adopters turn “complicated” into “doable.” We consider this dialogue one of the greatest assets any true manufacturer can wield.

    Supporting Innovation: Roles in Deep Science and Real-World Production

    Supply of a molecule like 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One is more than ticking boxes on a spec sheet. We provide technical support that spans scale, from milligrams for synthetic exploration to drums for pilot or technical production. In the pharmaceutical sector, the molecule often serves as a backbone for SAR (structure–activity relationship) studies. The reliable performance we build into each batch means fewer dead-ends, more actionable data, and closer collaboration between supplier and solver. Our technical team fields direct queries—mechanistic insight, prep hints, and pilot plant troubleshooting.

    In polymers and advanced materials, the molecule’s unique substitution permits label-free tracking in analytical scenarios—NMR, MS, or real-time reaction monitoring. Downstream, the result often materializes as performance polymers with tailored fluorine loading or organofluorine tags for next-generation analytics. Researchers have approached us with unique coupling requirements, sometimes outside the classic reaction playbook. In these cases, close process dialogue, real-time analytical feedback, and on-demand pilot batches keep cutting-edge work from becoming stranded between theory and reality.

    What Sets Direct Manufacturing Apart from Third-Party Channels

    Experience shows that source matters, particularly in complex fields like fluorinated fine chemicals. Material bought “off the shelf” from resellers or brokers often traces back to uncertain hands. Price may look tempting; quality often dips just when consistency matters most. We have encountered these pitfalls ourselves during early years sourcing specialty solvents—a poor lot costs more in lost time, excessive purification, or failed reactions than any upfront invoice. Manufacturing the product in-house means stability, direct control, and answers when the unexpected appears.

    End-users frequently share stories of “mystery” products turning up—vague provenance, unverified certificates, or lots with subtle color and odor differences. Even small deviations can introduce headaches downstream. We pride ourselves on a transparent manufacturing history. Each lot passes through physical, chemical, and spectral checks. Technicians tap into both instrument data and years of “sense” for tiny off-spec issues—something hard to teach, but easy to spot once experience accumulates. Clients return not out of habit, but because their projects depend on reliability at every run.

    Quality Assurance, Packaging, and Logistic Care

    Each container leaves our factories only after triple-checks. Fulfillment teams rely on their own checklists developed over years of shipping global orders—inspect for seal integrity, contamination, labeling accuracy. Packaging selection grows out of knowledge of how fluorinated ketones interact with seals, liners, and containers over time. Shipments reach the client with supporting documentation—this practice, driven by custom and necessity, simplifies regulatory review and unlocks doors when project cycles run tight.

    Clients working at the edge of sensitivity—living-cell screens, catalysis, or electronics—often return with notes on packaging or storage quirks. We welcome this feedback and use it to nudge continuous improvement, whether through new drum liners or revised label protocols. Real-world logistics rarely run seamlessly, and long distances or adverse climates bring surprises. Years of adaptation let us spot issues before they reach the customer—a quiet confidence that comes only from direct manufacturer’s care.

    The Human Element: Teamwork and Knowledge Transfer

    Behind every bottle stands a team—from Ph.D. chemists who designed the first gram-scale runs to the operators monitoring reactors night and day. Manufacturing, at its core, is a human-driven art as much as science. New hires learn why we baby certain pumps, triple-pass filter at critical steps, and maintain redundant batch logs. The knowledge transfer within our shop runs vertically—never locked in manuals, but passed from one story to another, often over hot coffee at shift change. Every successful batch reflects personal accountability—an invisible insurance policy for the customer searching for absolute certainty in a specialty compound.

    We invest actively in upskilling, from advanced analytical methods to plant safety. Auditor feedback, customer site trials, and regulatory reviews all shape our process—from glassware standards in the lab to satellite-enabled shipment tracking. Families, teams, and whole communities build brands through these daily acts, not slogans. That sense of hands-on engagement remains our main defense against error, drift, or complacency.

    Looking Ahead: Challenges, Opportunities, and the Next Generation

    The world’s appetite for new synthetic intermediates—especially multifunctional, fluorinated building blocks—will only grow in the years to come. As researchers in medicine, agriculture, and electronics push further, they count on robust supply chains and reliable partners. 4-Ethoxy-1,1,1-Trifluoro-3-Buten-2-One stands as a marker on this journey, a testament to what experience, investment, and real human collaboration can produce.

    Our teams remain deeply committed to sharing knowledge, keeping communication swift, and maintaining the highest standards. From scale-up to global logistics, regulatory review to process troubleshooting, we deliver not simply product, but the earned assurance that comes from long practice. We see each client as a permanent partner. For us, this compound is not just a line-item, but a bridge between lab promise and real-world delivery—a story written daily through careful craft, dialogue, and shared ambition.