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4'-Methoxy-2,2,2-Trifluoroacetophenone

    • Product Name 4'-Methoxy-2,2,2-Trifluoroacetophenone
    • Alias p-Anisyl Trifluoromethyl Ketone
    • Einecs 241-824-1
    • 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

    429838

    Chemical Name 4'-Methoxy-2,2,2-Trifluoroacetophenone
    Cas Number 402-46-0
    Molecular Formula C9H7F3O2
    Molecular Weight 204.14
    Appearance White to off-white solid
    Melting Point 54-57°C
    Boiling Point 99°C at 12 mmHg
    Density 1.295 g/cm3
    Smiles COC1=CC=C(C=C1)C(=O)C(F)(F)F
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO, ethanol, acetone
    Refractive Index n20/D 1.466

    As an accredited 4'-Methoxy-2,2,2-Trifluoroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle sealed with a screw cap, containing 25 grams of 4'-Methoxy-2,2,2-Trifluoroacetophenone, labeled with safety and product information.
    Shipping 4'-Methoxy-2,2,2-Trifluoroacetophenone is shipped in tightly sealed containers, protected from light and moisture. It should be transported at ambient temperature, following all relevant regulations for handling and shipping chemicals. Ensure accurate labeling, include a safety data sheet (SDS), and comply with local, national, and international shipping requirements for chemicals.
    Storage 4'-Methoxy-2,2,2-Trifluoroacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible substances such as strong oxidizing or reducing agents. Store at room temperature, preferably in a corrosive-resistant, labeled cabinet designated for chemicals. Avoid moisture and prolonged exposure to air.
    Application of 4'-Methoxy-2,2,2-Trifluoroacetophenone

    Applications of 4'-Methoxy-2,2,2-Trifluoroacetophenone in Industrial Manufacturing

    4'-Methoxy-2,2,2-Trifluoroacetophenone serves as a specialty intermediate for advanced synthesis in multiple industrial sectors. The following applications outline detailed integration practices and regulatory considerations within chemical manufacturing, focusing on established downstream markets where this raw material drives innovation and product quality.

    1. Pharmaceutical Intermediate for Aryl Ketone APIs

    Pharmaceutical manufacturers use this compound as a core building block in the synthesis of select aryl ketone-based active pharmaceutical ingredients, especially those requiring electron-withdrawing trifluoromethyl groups to enhance metabolic stability. In the multi-stage production of such APIs, our material typically enters during the early condensation or Friedel–Crafts acylation sequence, allowing precise functionalization under controlled reaction conditions. Our production ensures high lot-to-lot purity, enabling consistent integration with downstream GMP synthesis steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Pharmacopoeias such as USP, EP, and JP (where applicable for the final API)
    • FDA 21 CFR Part 211 for finished pharmaceuticals
    • EU GMP Annex 1

    Typical usage ratio

    • 0.8–1.3 molar equivalents based on the API synthesis batch size, adjusted per stoichiometric requirements in aryl ketone formation

    Downstream process integration

    • Introduced during early-stage condensation or acylation with aromatic scaffolds; followed by purification, crystallization, and API isolation steps

    Final product types

    • Selective serotonin reuptake inhibitors (SSRIs) with trifluoromethyl acetophenone fragments
    • Other central nervous system pharmaceuticals with aromatic trifluoromethyl groups

    2. Synthesis of Specialty Agrochemical Actives

    In the crop protection industry, 4'-Methoxy-2,2,2-Trifluoroacetophenone is employed as a tailored intermediate for herbicide and fungicide actives that require aromatic ketone motifs offering enhanced chemical persistence and selectivity. Downstream processors value its clean incorporation during structural derivatization, often via nucleophilic aromatic substitution and subsequent alkylation. The material supports stringent impurity profiles necessary for large-scale agrochemical technical concentrate production.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for chemical quality management
    • OECD 301 for biodegradability testing (relevant to environmental fate)

    Typical usage ratio

    • 5–15% (w/w) relative to full synthetic route, depending on molecular weight targets and active ingredient class

    Downstream process integration

    • Added during core structural assembly prior to final functionalization and crystallization of technical active

    Final product types

    • Novel herbicidal actives with aryl-trifluoromethyl structures
    • Fungicide intermediates for further formulation into crop protection products

    3. Advanced Fluorinated Aromatic Monomer Precursor for Polymer Synthesis

    Manufacturers of specialty fluorinated polymers utilize this raw material as a key monomeric precursor, particularly for high-performance polymeric coatings and membranes enduring aggressive chemical environments. The compound is introduced during the monomer preparation step, typically through controlled condensation and subsequent polymerization, imparting unique hydrophobic and chemical resistance properties to the end material.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical production
    • RoHS Directive (EU) 2011/65
    • Industrial polymer standards such as ASTM D882 for thin film performance
    • REACH for monomer and polymer registration

    Typical usage ratio

    • 3–10% (mole basis) within specialty monomer pools, scalable per targeted crosslink density and fluorine content in the backbone

    Downstream process integration

    • Employed in monomer synthesis before polymerization via condensation or free radical methods, followed by casting, curing, or extrusion

    Final product types

    • Fluorinated protective coatings for electronics, industrial valves and pipelines
    • Membrane films for filtration in corrosive or high-purity applications

    4. Custom Intermediate for Analytical Reference Standards Synthesis

    Producers of certified analytical reference materials incorporate 4'-Methoxy-2,2,2-Trifluoroacetophenone as a key intermediate during the controlled synthesis of trace-level standard compounds. Due to its well-defined structure and traceability, commercial reference laboratories use it in preparative synthesis workflows demanding ultra-high purity, followed by strict quality control with NMR and MS verification.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • ISO/IEC 17025 lab accreditation for analytical testing
    • Accreditation protocols from organizations such as NIST and Eurachem
    • REACH and CLP Regulation for chemical handling and registration

    Typical usage ratio

    • Varies from milligram to gram scale depending on required batch size of certified standard, with stoichiometric control at <1–5% per synthesis step

    Downstream process integration

    • Applied in precise preparative stages of chemical reference synthesis, followed by multi-mode purification and identity confirmation by spectroscopic techniques

    Final product types

    • Certified analytical reference standards for pharmaceutical, environmental, and food safety laboratories
    • Internal calibration compounds for chromatographic and spectral analysis
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4'-Methoxy-2,2,2-Trifluoroacetophenone: A Reliable Building Block for Modern Organic Synthesis

    Bringing Real-World Experience to Chemical Manufacturing

    Every day, as a chemical manufacturer who works directly on the line, I see requests come in for compounds that hold real value for researchers, pharmaceutical developers, and specialty chemical producers. One compound that has stood out over the years is 4'-Methoxy-2,2,2-Trifluoroacetophenone, also known by its model name through industry shorthand as 4-MeO-TFAcetophenone. Manufacturing this molecule, I have come to appreciate not only its versatility in applications but also the attention to quality and process consistency that brings success to downstream innovations.

    Understanding 4'-Methoxy-2,2,2-Trifluoroacetophenone

    What sets this compound apart lies in its distinct structure: a methoxy group at the para position, together with a strong electron-withdrawing trifluoromethyl carbonyl moiety. This combination shapes its reactivity, solubility, and the subtle ways it interacts in various synthesis steps. In practical terms, we keep a close watch on purity because minor impurities can cause wide swings in yields or entirely change the course of a reaction. Typical lots from our facility consistently exceed 99% purity by HPLC and GC, meeting even stringent requirements set by life sciences and material researchers.

    Practical Functions Across Diverse Fields

    Over years in this field, feedback from clients has shaped our perspective on the real-world uses of 4'-Methoxy-2,2,2-Trifluoroacetophenone. Most commonly, the compound gets deployed as a key intermediate during pharmaceutical synthesis. Medicinal chemists value the electron-rich aromatic ring paired with the highly polar trifluoromethyl ketone, offering a launching point for further functionalization—such as nucleophilic aromatic substitution or enolate chemistry. Some labs have pointed out how it plays a pivotal role in constructing fluorinated building blocks, which influence the metabolic stability and bioavailability of candidate drugs. We’ve supported projects where minor tweaks on the methoxy position allowed lead molecules to move from bench to preclinical stages.

    Outside pharmaceuticals, our customers in agricultural chemistry see value too. Introducing a trifluoromethyl group into candidate molecules alters not just their reactivity, but confers the environmental resistance and potency needed in modern crop protection agents. This kind of feedback has nudged us to maintain a consistent physical profile: pale yellow crystalline solid, with a melting point usually falling in the 38–42°C range. Solubility profiles in dichloromethane, ether, and other common organic solvents have matched published benchmarks in both lab and pilot settings.

    Insights From Direct Manufacturing Experience

    Our plant operators have worked with a wide array of acetophenones and trifluoromethyl ketones, so we see firsthand how 4'-Methoxy-2,2,2-Trifluoroacetophenone stacks up against similar products. The introduction of the trifluoromethyl group into the acetophenone backbone changes everything about reactivity—sometimes requiring new purification steps or adjustments to parameters. We maintain strict process controls to avoid over-halogenation or side-product formation, both of which can haunt high-precision chemistry, especially for customers scaling up reactions.

    Compared to plain acetophenone or non-fluorinated para-methoxyacetophenone, this compound resists oxidation more robustly and shows a markedly different profile during aromatic halogenation or nitration. Clients working on combinatorial libraries in fluorinated drug discovery programs have shared that, with this building block, they see much lower rates of unwanted side-product formation due to the electron withdrawal imparted by the trifluoromethyl group. This is no abstract claim, but something that shows up in chromatograms and batch records. In our facility, we actively monitor for isomeric contaminants and variable moisture content, which can undo a chemist’s hard work in a single step.

    Safety, Handling, and Downstream Impacts

    Years of batch production reveal little quirks about this molecule. Its relatively low melting point can catch some off-guard, especially when transferring during warmer seasons or in a facility that’s been sunlit. We recommend cool, dry storage based on our own operational experience. Handling powders of this type requires proper ventilation and standard PPE; our team uses localized exhaust where the compound is weighed and transferred to avoid inhalation of fine particulates.

    Incidents from the past have taught us the importance of clear labeling and robust segregation from strong oxidizing agents or incompatible solvents such as concentrated acids. This practice doesn’t just keep lines running smoothly—it also prevents disruptions to research timelines or process scale-ups on the client side. Our QHSE teams run annual risk assessments specific to both the product itself and the waste streams generated, ensuring full compliance with both regional and international regulatory expectations.

    Navigating the Supply Ecosystem

    Some buyers might ask why to source 4'-Methoxy-2,2,2-Trifluoroacetophenone directly from a manufacturer rather than a reseller or stockist. From the production line, I can say the answer boils down to process continuity and direct accountability. When you deal with us, you’re tapping into years of process data that allows us to tweak batch profiles, react quickly to specification changes, and troubleshoot collaboratively if an anomaly crops up during your application. Distributors serve a role in the chain but, having worked with every raw material and handled purification steps ourselves, we can answer questions about process impurities or alternative synthetic access routes.

    We’ve set up in-house analytical labs based on direct feedback—sometimes at the urging of customers who needed an unexpected impurity pool analyzed or an NMR confirmed on short notice. These direct interactions shape the quality standards we hold and help to ensure each outgoing lot not only matches previously supplied product but also aligns with the evolving needs of the industries using it.

    Distinctive Qualities Compared to Related Compounds

    From a manufacturability standpoint, adding a trifluoromethyl group to any organic backbone introduces fresh challenges. Routine acetophenones, like 4'-methoxyacetophenone, lack this functional group, and so their synthesis often proceeds with fewer steps and a gentler set of conditions; their boiling and melting points are higher, and their environmental persistence can be lower. In contrast, 4'-Methoxy-2,2,2-Trifluoroacetophenone sits at the intersection of increased hydrophobicity and elevated electron-withdrawing influence, which radically reshapes how it behaves during further synthetic manipulation.

    We see clear evidence of this in the field. Teams working on electron-rich systems (like some natural product syntheses) have told us that trifluoromethyl ketones such as this, compared to their plain cousins, deliver selectivity not easily achieved by aromatic methyl ketones or simple propenones. The increased reactivity toward certain nucleophiles makes a world of difference during cascade reactions, especially in the precise assembly of polyfunctionalized scaffolds. The fluorine atoms play another significant role: they improve metabolic resistance in both pharma and agrochemical final products. We’ve collaborated with labs who confirmed, by analytical follow-up, that the inclusion of this fragment extended half-lives and altered metabolic degradation pathways in ways non-fluorinated analogs simply don’t match.

    Responsiveness and Process Documentation

    Direct manufacturing brings responsibilities that go beyond just synthesizing and packing a chemical. Customers often need supporting documentation: not only a certificate of analysis, but data from spectral libraries, trace impurity analysis, and—where relevant—full batch production records. Over the years, I’ve learned that being able to provide such support builds lasting relationships and minimizes the guesswork during transfer from lab to plant.

    For teams working under tight regulatory frameworks, this compound’s known analytical fingerprint (measured by NMR, FTIR, and mass spectrometry in our lab) streamlines both process validation and downstream QC. We log every deviation, every equipment calibration, and monitor environmental factors that could influence key product parameters (appearance, purity, solubility). In this way, we ensure every drum or bottle sent out represents what we’ve promised—and what our customers have tested and validated on their side.

    Supporting Sustainable Synthesis Practices

    A factor we take seriously as a producer is reducing the environmental impact, both in upstream sourcing and downstream processing of specialty chemicals. Over time, green chemistry principles have entered our product offering, affecting both the solvents we choose and the waste streams we generate. In synthesizing 4'-Methoxy-2,2,2-Trifluoroacetophenone, we’ve developed catalytic pathways that minimize halogen waste and avoid problematic byproducts. Process improvements, such as solvent recycling, have cut chemical consumption in repeated runs, which translates to a leaner footprint. Input from process engineers and plant chemists has enabled real advances—whether in adjusting the recrystallization steps to limit solvent use or deploying more efficient in-line analytical controls.

    It’s worth sharing that real gains in sustainability come not just from citing eco-friendly buzzwords, but by iteratively refining what works. We learn from each batch, each customer outcome, and each regulatory update. Integration of analytical feedback from our customers worldwide feeds directly into process upgrades, ensuring that the product offered aligns with both technical performance standards and the ethical priorities shaping today’s chemical landscape.

    The Role of Quality and Reliability

    Clients who reach out to a true manufacturer, rather than taking a chance with a nameless commodity supplier, are often seeking confidence: that their experiment, pilot plant, or manufacturing run can rely on batch-to-batch consistency. In our facility, we’ve made a point to run parallel quality checks—comparing current output against retention samples and long-term archives. This approach picks up a trend or drift before it ever becomes a customer’s issue. Over the years, several buyers have inquired about aging profiles and the emergence of secondary spots over time. Our stability studies, conducted under both ambient and stress-testing conditions, provide real assurance of product integrity throughout its shelf life.

    We take corrections seriously. Occasional issues, such as off-coloration or atypical impurity spikes, move directly to our process improvement logs. Root cause analysis, whether from raw material variability or reaction parameter changes, gets documented and resolved with follow-up validation. The result is that our customers rarely face an unexplained deviation—and, if they ever do, we work side-by-side to identify and solve the issue before time or material is lost.

    Challenges and Opportunities Ahead

    In the evolving world of specialty chemicals, nothing remains stagnant. Sourcing of high-purity trifluoroacetic anhydride, flavor of regulatory changes in reagent purchasing, fluctuations in energy costs—any of these can push a producer to rethink upstream processes. Our team continually reviews global regulatory updates, emerging green synthetic routes, and customer performance feedback. Where needed, we’ve partnered with academic groups to develop next-generation synthetic variants or troubleshooting uncommon byproducts.

    End users’ needs have changed significantly over the last decade. Today, purity alone rarely seals a deal. Researchers want full transparency, access to batch-level documentation, and confidence in the physical profile from drum to drum. Our continuous feedback loop with customers and in-house analytical teams means we’re rarely caught by surprise when a new challenge emerges.

    Continuous Improvement—Rooted in Practice

    Routine in-process controls set apart robust production sites from those aspiring simply to move product. Measurements of melting range, spectral analysis, and performance benchmarks against trusted standards all get logged here—a discipline embedded in every shift. Customer requests have sometimes pointed us toward unique application spaces: a flavor and fragrance group tracing subtle notes in reaction output, or a material science team searching for novel dielectric behavior in fluorinated aromatic systems. Each case directs slight process optimizations—maybe a double wash here, a longer drying step there—to deliver the targeted outcome.

    Being close to the manufacturing reality exposes the human side behind scientific precision. We’ve seen the difference a single unexpected peak in a chromatogram can make to someone’s thesis work, or how a short delay in delivery affects multi-million-dollar pilot plants. Solving these challenges as a producer means keeping the lines of communication open, documenting every relevant detail, and backing up claims with more than just paperwork. Reliability, both in the lab and in the field, comes from manufacturing practices you can trust.

    Looking Forward

    Every drum of 4'-Methoxy-2,2,2-Trifluoroacetophenone coming off our line reflects decades of experience, commitment to robust process chemistry, and, above all, partnership with real users shaping the future of applied chemistry. Our work does not end when the compound leaves the facility. Feedback, troubleshooting, and continuous technical dialogue drive every improvement and standard we adopt. Those seeking a dependable source for this unique fluorinated acetophenone can know that each batch delivered is the direct result of countless cycles of learning, refinement, and unwavering dedication from a true manufacturer invested in both performance and progress.