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4'-(Trifluoromethyl)Propiophenone

    • Product Name 4'-(Trifluoromethyl)Propiophenone
    • Einecs 241-229-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    936638

    Chemical Name 4'-(Trifluoromethyl)Propiophenone
    Cas Number 348-67-4
    Molecular Formula C10H9F3O
    Molecular Weight 202.18 g/mol
    Appearance Colorless to pale yellow liquid
    Melting Point 13-15 °C
    Boiling Point 106-107 °C at 15 mmHg
    Density 1.206 g/cm³ at 25 °C
    Solubility Insoluble in water; soluble in organic solvents
    Refractive Index n20/D 1.482
    Purity Typically ≥98%
    Smiles CCC(=O)C1=CC=C(C=C1)C(F)(F)F

    As an accredited 4'-(Trifluoromethyl)Propiophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with a secure, screw cap; white label displaying "4'-(Trifluoromethyl)Propiophenone, 100g," chemical formula, and hazard symbols.
    Shipping 4'-(Trifluoromethyl)Propiophenone is shipped in tightly sealed, chemical-resistant containers to prevent leakage and contamination. It is transported as per regulations for hazardous chemicals, typically under ambient conditions, with appropriate labeling for safety. Ensure the package is handled by trained personnel and kept away from incompatible substances during transit.
    Storage 4'-(Trifluoromethyl)Propiophenone should be stored in a tightly sealed container, away from direct sunlight, heat sources, and moisture. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet. Avoid storing near incompatible substances such as strong oxidizers or acids. Ensure appropriate labeling and access only to trained personnel.
    Application of 4'-(Trifluoromethyl)Propiophenone

    Applications of 4'-(Trifluoromethyl)Propiophenone in Industrial Manufacturing

    As an established manufacturer of 4'-(Trifluoromethyl)Propiophenone, we supply this high-purity intermediate to global industrial partners operating in sectors with stringent quality control and regulatory requirements. Outlined below are the core application scenarios implemented by downstream processors and end-product manufacturers. Each segment details compliance benchmarks, formula reference ratios, workflow integration points, and the produced goods associated with each industrial use.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    This fluorinated ketone serves as a critical intermediate for the API synthesis of specialty pharmaceuticals, particularly CNS-active compounds and targeted analgesics. Process chemistry teams often exploit its electron-withdrawing group to drive regioselective functionalization in multi-step syntheses, catering to advanced drug molecule development pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF & EP monograph compliance for intermediate traceability
    • FDA 21 CFR Part 211 (cGMP for finished pharmaceuticals)
    • ISO 9001:2015 for quality management in raw material processing

    Typical usage ratio

    • 0.7-1.2 molar equivalents as an advanced intermediate, adjusted based on targeted API structural requirements and yield optimization after route scouting

    Downstream process integration

    • Introduced during Grignard or Friedel-Crafts acylation stages, followed by reductive amination or coupling to other heterocyclic intermediates
    • Monitored by HPLC or LC-MS for process control to meet regulatory batch release criteria

    Final product types

    • Central nervous system agents (e.g. antidepressants, anticonvulsants)
    • Custom analgesic agents
    • Precursor intermediates for contract manufacturing organizations (CDMO) pipelines

    2. Agricultural Chemical Intermediate (Herbicide and Fungicide Synthesis)

    Formulators in agrochemicals use this aromatic ketone as a building block to introduce trifluoromethylated functionality into selective herbicides and crop protection agents. Product development chemists value its stability and reactivity in complex ring closure reactions and its compliance with global residue standards for field applications.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius for pesticide residue limits
    • China GB 2763 Maximum Residue Limits for Pesticides in Food
    • US EPA Pesticide Registration Review protocols
    • ISO 9001:2015 and ISO 14001:2015 Environmental Management

    Typical usage ratio

    • 5–15% by weight in key synthesis steps, adjusted based on crop selectivity and intended active moiety concentration following efficacy tests and regulatory submissions

    Downstream process integration

    • Fed into nucleophilic aromatic substitution or cyclization steps to generate fluorinated aromatic backbones
    • Reactive intermediates purified and formulated with approved adjuvants prior to granulation or concentrate blending

    Final product types

    • Pre-emergent herbicide technical concentrates
    • Fungicidal active ingredient intermediates
    • Bulk active ingredients for agrochemical finished formulation

    3. Specialty Fine Chemical Synthesis for Electronic Materials

    Manufacturers in the electronics sector utilize this compound for the synthesis of precise molecular blocks in high-performance liquid crystals and advanced photoresist systems. The trifluoromethyl group imparts enhanced dielectric properties and thermal resistance demanded by OEMs in display and semiconductor applications.

    Industry compliance standards

    • IEC 62474 Material Composition Declaration for the Electrical and Electronic Industry
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • Internal customer QC protocols for particle and ionic purity

    Typical usage ratio

    • 0.2–2.5% by formulation weight, with adjustment according to dielectric constant targets and fabrication process compatibility

    Downstream process integration

    • Introduced as a precursor during the synthesis of alignment layers and mesogen precursors for LC panels, or as an additive in positive/negative photoresist resins for photolithography
    • Processed under strictly controlled temperature and solvent environments to prevent contamination in cleanroom settings

    Final product types

    • Advanced liquid crystal materials for FPD (Flat Panel Display)
    • Photoresist compounds for printed circuit board manufacturing
    • Functionalized additives for dielectric layer coatings

    4. Intermediate for Fragrance and Aroma Chemical Production

    Flavor and fragrance houses leverage this specialty ketone as a structural precursor in the synthesis of high-end aroma molecules, especially for creation of musky, fresh, or green fragrance notes where trifluoromethyl substitution amplifies volatility and sensory profile stability in finished blends.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for ethical and safe use of fragrance materials
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation) for fragrance ingredient notification
    • FDA 21 CFR 172.515 (Synthetic flavoring substances and adjuvants)
    • Allergen labeling per European Directive 2003/15/EC

    Typical usage ratio

    • 0.05–1.0% in synthetic aroma concentrate production, established based on olfactometric panel evaluations and final application (fine fragrance vs. industrial scent components)

    Downstream process integration

    • Reacted in sequential aldol condensations or reductions to yield high-value aroma intermediates
    • Blended in anhydrous conditions to avoid off-notes and maintain purity for fragrance compounding

    Final product types

    • Specialty fragrance molecules for fine perfumes
    • Aroma ingredients for personal care and home care fragrances
    • Olfactory building blocks for F&F houses

    5. Intermediate for Industrial Polymer Modifier Synthesis

    Producers of high-spec polymers incorporate this compound as an intermediate during the introduction of fluorinated side chains into specialty polymers used for coatings, adhesives, and high-performance elastomers. Its structural features enhance weatherability, surface energy reduction, and chemical inertness of final polymer products.

    Industry compliance standards

    • ISO 9001:2015 for consistent product quality
    • REACH Regulation (EC) No 1907/2006 for polymer and monomer registration
    • ASTM D5630 standard for fluorinated polymer residue analysis
    • MISRA QAS guidelines for manufacturing traceability in polymer supply

    Typical usage ratio

    • 0.5–3% by mass in functional monomer precursor synthesis; optimized through pilot production trials to match performance specifications of customer polymers

    Downstream process integration

    • Fed into single-step or staged fluorination polymerization prior to extrusion or solvent casting
    • Technology transfer batches accompanied by scaling protocols to minimize batch-to-batch variation

    Final product types

    • Specialty fluorinated copolymers for architectural coatings
    • Hydrophobic surface coating resins
    • Performance elastomers in automotive and electronics
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    Certification & Compliance
    More Introduction

    4'-(Trifluoromethyl)Propiophenone: A Manufacturer’s Perspective

    From Our Reactor to Your Lab: An Honest Introduction

    Working with chemicals every day, you start to recognize how a molecule like 4'-(Trifluoromethyl)Propiophenone finds its way into the hands of researchers, pharmaceutical chemists, and material innovators around the world. We don’t trade it on a concept—we manufacture it from the ground up, monitor every batch, and are fully involved at every stage from raw material choice through to the last purification pass. That involvement means we know the quirks and character of this compound and appreciate the roles it plays and the needs it fills.

    What Makes This Ketone Unique

    You might see many aromatic ketones in catalogs. The addition of a trifluoromethyl group at the para position gives 4'-(Trifluoromethyl)Propiophenone a unique profile that can't be matched by its non-fluorinated or meta-substituted siblings. That CF3 group draws attention in chemistry for more than just its rugged stability. It modifies electronegativity, influences reaction outcomes, and feeds directly into specific transformation pathways. These aren’t just small details on paper—they steer whole synthetic campaigns in pharma, agrochemical, and pigment manufacturing.

    The real-life effect: downstream groups, especially in medicinal chemistry, lean on trifluoromethyl motives to influence bioavailability and metabolic stability of molecules. The difference between a phenyl and a para-trifluoromethylphenyl ring in a candidate molecule can decide who passes preclinical hurdles and who ends up a dead end in a folder. We’ve heard customers explain how the ketone backbone on this compound works as a stepping stone, introducing that fluorinated character early in the pathway without needing late-stage specialty fluorination steps.

    Why Find 4'-(Trifluoromethyl)Propiophenone From a Manufacturer?

    Manufacturing this ketone at scale isn’t as forgiving as bulk commodity chemicals. Our process anchors on reliable starting material supply, finely tuned reaction controls, and post-synthesis handling shaped over years of practice. The trifluoromethyl group isn’t prone to contamination, but any mishandling—particularly in the aromatic ring—can shift byproducts into the mix, especially regioisomers. We focus on chromatographic and spectroscopic analyses at every checkpoint. NMR, GC-MS, and HPLC profiles show what pharmacists and analysts need, not what looks good on a spreadsheet.

    Some traders claim equivalent grades, but you see what you get after just a few purification attempts in the lab. With our material, you open the bottle and don’t contend with variable color, persistent odors, or a spread of boiling points. You can focus on your synthesis rather than chasing ghosts introduced from an unclear supply chain.

    Where Our Manufacturing Choices Shape the Product

    Our setup relies on stainless vessels with controlled atmosphere, as water and acid traces can trigger side reactions with sensitive trifluoromethyl aromatics. The reaction sequence moves swiftly, and we design it to optimize yield without raising impurity profiles. Each lot cycles through in-house distillation and gets rechecked against twin standards. Many competing suppliers might send off samples without extra attention to micro impurities; we’ve seen how those cause headaches later—unexpected spots on TLC or drifting peaks in LC.

    Over years of production, we’ve switched between several fluorinated precursors and mapped every effect on end-product stability. One of the underrated skills here is watching how each tweak at scale impacts not only purity, but reproducibility. This consistency makes workflow easier in downstream labs. Repeat runs across years deliver the same spectral fingerprint, allowing research chemists to trust each bottle—today, next month, next year.

    What Sets 4'-(Trifluoromethyl)Propiophenone Apart from Other Aromatic Ketones

    While many aromatic ketones serve as templates for elaborate syntheses, the para-trifluoromethyl feature twists both reactivity and properties toward specialty use. Benzophenone, propiophenone, or acetophenone derivatives won’t show the same polarity, acidity, or compatibility profiles under identical reaction conditions. You may find commercial grades of simpler analogs for less, but the moment your pathway requires that trifluoromethyl punch—higher metabolic robustness, sharpened reactivity—you’re in a different class.

    We’ve seen this compound used as an intermediate for introducing CF3 on larger scaffolds, for serving as a reference material in analytical chains, and as feedstock in custom ligand preparation. Its clean response in GC, resilience in chromatography, and manageable volatility make it both a practical and strategic choice, especially where uncontrolled impurities in analogs introduce roadblocks.

    Uses That Drive Demand—Real-World Applications

    Among our clientele, the leading attraction to 4'-(Trifluoromethyl)Propiophenone is its ready role in pharma R&D. Big and small companies alike rely on it for constructing next-gen active pharmaceutical ingredients. The trifluoromethyl substituent is more than a badge of structural innovation; it’s a time-tested way to drive optimum lipophilicity and block metabolic degradation.

    The story isn’t just the science though. Practical demand comes from the need to avoid tricky late-stage trifluoromethylations, which often mean harsher conditions, poor yield, or toxic reagents. Building the fluorine motif in early with this ketone simplifies synthesis and risk management. In crop protection, similar logic holds—the molecular robustness and polar nature open pathways to more effective agrochemicals that land where intended and hold up against environmental stress.

    The pigment and specialty polymer industries also plant regular orders. The electron-withdrawing capability of the CF3 group influences chromophore behavior, thermal properties, and end-use stability. Compound libraries—screened for everything from OLED applications to new battery membranes—tap this ketone as a foundational block.

    Specification and Quality Experience

    One of our ground rules is never to generalize about quality. Instead, we offer an experience shaped by thousands of production hours and dozens of QA steps. Our 4'-(Trifluoromethyl)Propiophenone typically arrives as a pale yellow, nearly colorless oil, free from particulates and discoloration. That near-colorless appearance is the best first sign of clean manufacture. Next comes the smell—should be faint, never sharp or sweet. You won’t find tails of aldehydes or other process residues lingering when you use our product.

    Typical purities come in at over 99% by HPLC, and water content stays well below 0.1%. Customers report consistency in melting and boiling range, confirming the absence of significant impurity load. Spectral confirmations mean no hidden co-distilled byproducts—every bottle matches the CAS specification for this product, with certificates describing impurities above 0.05%. Each shipment includes full traceability: from raw material supplier, batch processing dates, storage times, and in-house analytical graphs.

    We don’t hide behind broad standard ranges; we report every deviation and never blend off-spec product into lots. Over the years, our approach reduced customer complaints, sped up onboarding in new customer projects, and improved reliability for scale-up labs.

    Customer Stories and Direct Feedback

    Feedback from medicinal chemists is direct and to the point. Experienced labs prefer our material because it outperforms resold lots that have vague provenance. Experienced researchers spot oddities in crystallizations and chromatography long before paperwork comes their way. Word travels—when a product just works, buying decisions become automatic.

    There’s also practical feedback from custom synthesis partners. They want predictable reaction outcomes, not shifting yield curves or odd GC tails. Our 4'-(Trifluoromethyl)Propiophenone delivers those results, helping projects meet tight deadlines and freeing up staff time to focus on innovation rather than troubleshooting unexpected chemical behavior.

    Academic labs value transparency—we publish relevant test data and explain the steps we take for repeatability and purity. Students learn with clean, dependable reagents, not with mixtures that muddy their fundamentals.

    Challenges in Manufacturing and How We Address Them

    Managing fluorous chemistry creates challenges that come from the very properties customers cherish. Trifluoromethyl aromatics demand careful material handling, lower temperatures, and cleaner glassware than non-fluorinated phenyl ketones. We took hits on yield in early years due to small side reactions, often oxidative dimerization or hydrolysis. Tracking down the process changes that cleared up those issues took months, but the outcome benefited everyone: purer product, higher recovery, less waste.

    Another ongoing task is protecting material during storage and shipment. Many aromatic ketones drift toward color formation over time if they see too much heat or light. We avoid this through light-protective packaging, nitrogen blanketing, and as rapid a shipment cycle as customer timelines allow. Every year brings new questions from users as regulations evolve. Our internal database tracks every lot for quality reference, so we can field precise answers on purity or trace byproducts without delay.

    We also saw that control of environmental emissions matters, not just indoors but for surrounding communities. Our process cuts down on vent loss and recycles solvents. Improvements here translated into cleaner workspaces, better yields, safer handling, and a smaller footprint—issues that matter to everyone who works with or around high-energy organofluorine compounds.

    On Competing Products and Industry Pressure

    Some competitors focus on pricing alone. We took a different track, betting that premium purity and detailed documentation mean more to researchers than ever-cheaper deals. Bulk buyers in large industry groups tested low-cost product lines from elsewhere, only to return when yield and reproducibility flagged. Procurement officers tell us that, in the end, it’s the long-term reliability and documentation that keeps supply chains moving, not just rock-bottom prices.

    We stand ready to answer growing demand, as requests for trifluoromethylated scaffolds rise across sectors. Scale presents its own set of problems. As volume climbs, so does the challenge of keeping every drum consistent. Investments in instrumentation, staff training, and process documentation make the margin of error smaller and the output more reliable. Customers tracking sustainability increasingly ask us about solvent recycling rates and energy consumption. We track and publish those numbers for every lot, so users track their own environmental footprints with confidence.

    Future Directions and Continuous Improvement

    The next years will see wider adoption of trifluoromethylated intermediates like this in biopharma, advanced materials, and electronics. To meet higher standards, we’ve already upgraded several production lines, automated more data capture, and brought in analytical improvements that boost confidence in every deliverable. We listen to customer requests, whether they’re pushing for even lower impurity thresholds or more detailed spectra on every batch. Sometimes that means retooling an entire step to address subtle chemical quirks.

    We’re also working with academic collaborators and industrial chemists to understand emerging regulatory requirements. Several countries are tightening rules on organofluorine content in waste, and downstream users rely on our transparency for reporting and compliance. We don’t just watch from the sidelines; we tune our process, innovate for greener chemistry, and share best practices in solvent recovery and waste handling.

    Building Trust—Our Commitment to EEAT Principles

    Everything we do as a manufacturer connects to a living body of evidence, expertise, and trust. We operate from the principle that every batch stands as a statement of our reputation. Our in-house team has decades of direct experience in organofluorine chemistry and commercial-scale operations. Every member of our process and QA staff can walk through the journey from raw material to finished product and answer questions from buyers, chemists, and auditors alike.

    We publish analytical data that meets or exceeds global standards, back it up with operator notes, and link every lot to its full production history. If customers spot irregularities or have questions, we supply reference graphs, process rationales, and set up direct technical calls with our team. We track error rates, non-conformance cases, and continuously review protocols to push quality higher.

    Nothing about chemical supply is routine—unforeseen issues appear, and we solve them through hands-on expertise, established processes, and clear communication. As a manufacturer, we make 4'-(Trifluoromethyl)Propiophenone not just a chemical on a shelf, but a living example of reliability, openness, and continuous technical engagement.

    Pioneering New Possibilities

    Our perspective as manufacturers gives us a front-row seat to where innovation leads. Every trend—stronger medicines, more efficient catalysts, better environmental sensors—brings new calls for trifluoromethyl chemistry. We step up not just as suppliers, but as partners who offer molecules with integrity, rigor, and a readily available story of how they came to be. For those who see beyond a line of code or a catalog entry, our 4'-(Trifluoromethyl)Propiophenone stands as a building block with real manufacturing muscle and the kind of careful expertise you count on to keep your science advancing.