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HS Code |
313129 |
| Productname | 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone |
| Casnumber | 886373-37-9 |
| Molecularformula | C9H6F4O |
| Molecularweight | 206.14 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 87-89°C at 18 mmHg |
| Purity | Typically ≥98% |
| Density | 1.326 g/cm³ |
| Smiles | CC(=O)C1=CC(=CC(=C1)F)C(F)(F)F |
| Inchikey | SBHQERKPTXIMEM-UHFFFAOYSA-N |
As an accredited 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 5 grams; features a tamper-evident screw cap, hazard labels, and chemical identification details clearly printed. |
| Shipping | 3'-Fluoro-5'-(Trifluoromethyl)acetophenone is shipped in tightly sealed containers, protected from light and moisture. The chemical is handled as per standard hazardous material protocols, transported under ambient conditions, and labeled in accordance with international shipping regulations. Ensure proper documentation accompanies each shipment for safe and compliant delivery. |
| Storage | Store 3'-Fluoro-5'-(trifluoromethyl)acetophenone in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from direct sunlight and moisture. Label containers clearly, and handle using appropriate personal protective equipment including gloves and safety eyewear to avoid skin and eye contact. |
Applications of 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone in Industrial ManufacturingAs a specialized manufacturer of 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone, we focus on supplying this key intermediate for well-established downstream sectors. Below are real-world production scenarios where our material provides targeted value through its structural properties, enabling customers to achieve stringent formulation and compliance goals in complex manufacturing systems. 1. Pharmaceutical Intermediates for Advanced API SynthesisChemical producers engaged in small-molecule drug development utilize our material as a fluorinated building block for synthesis of pyridine and benzene-ring containing pharmaceuticals, exploiting its electron-withdrawing features to introduce metabolic stability in core scaffolds. The integration comes during custom route elaboration and amidoxime, ketone, or ether segment synthesis where strict traceability and material pedigree are required to meet submission standards for regulated drug substances. Industry compliance standards
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2. Agrochemical Synthesis for Modern Herbicides and FungicidesTop-tier agrochemical companies adopt our raw material during late-stage functionalization of selective herbicide and fungicide molecules. The unique fluorine substitution on the acetophenone backbone enhances lipophilicity and soil persistence, a key attribute in formulation chemistry for crop protection products. This application requires robust documentation and exact adherence to industry guidance for raw material provenance and batch reproducibility. Industry compliance standards
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3. Specialty Chemicals for Liquid Crystal Display (LCD) MaterialsProducers of advanced materials for display technology use our compound as a structural modulator in the production of liquid crystal intermediates. Its fluorinated functional groups are crucial for precise tuning of dielectric anisotropy and clearing point in nematic and smectic mixtures. The supply chain for this segment is highly scrutinized, requiring meticulous material tracking and cleanroom-compatible standards for batch production intended for high-definition electronics. Industry compliance standards
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4. Advanced Materials for Specialty Polymer SynthesisLeading polymer research and industrial manufacturers leverage our fluorinated acetophenone during copolymerization steps to impart thermal resistance, hydrophobicity, and chemical stability to specialty polymers. The compound’s molecular attributes facilitate inclusion into the mainchain or sidechains via Friedel-Crafts acylation, enhancing the ultimate polymer’s tolerance to environmental and chemical stress for use in precision engineering sectors. Industry compliance standards
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In our labs and production floors, we have seen numerous molecules come and go through early R&D, scale-up, and on to global commerce. Among the many acetophenone derivatives developed and manufactured over the years, 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone stands out, both in synthesis challenge and practical value. For those of us who produce it, this compound represents not only complex molecular engineering but also answers to concrete demands from researchers, pharmaceutical method developers, and advanced material formulators.
Speaking from direct production experience, 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone exhibits qualities not found in its close structural relatives. The addition of both a fluorine atom in the meta position and a trifluoromethyl group in the para position on the acetophenone aromatic ring is not easily achieved through a single-step process. It requires a precise orchestration of fluorination and acylation, followed by careful purification to remove side-products common in competitive systems.
Every batch comes through rigorous in-house gas chromatography and NMR analysis, and no shipment leaves without confirmation of high assay and minimal isomeric contamination. Over time, the best practice protocols developed alongside product evolution; only through repeated production runs and direct feedback from analytical chemists have we been able to tune our process for superior batch consistency.
Our approach to manufacturing this compound started with feedback from medicinal chemists and agrochemical discovery teams. Routine acetophenone or mono-fluoro acetophenone products didn’t provide them with the reactivity or physicochemical profiles needed for next-gen molecular scaffolds. Only once we introduced dual modification—applying fluorine and trifluoromethyl groups at specific positions—did clients report sharper NMR signals, increased oxidative resistance, and improved stability under demanding reaction conditions. These outcomes weren’t only theoretical. We saw, batch after batch, less decomposition in storage, more reliable recovery after cold-chain shipping, and better compatibility with palladium or nickel catalysts in cross-coupling applications.
Direct manufacturers like us spend time controlling for trace metals, as even minor contamination can interfere with downstream synthesis. Through hands-on process improvement, we established a routine of multiple recrystallizations and customized purification. This isn’t just for meeting spec sheets. High-end downstream users gave clear direction: product clean enough to not adulterate their own test results, but robust enough to handle atmospheric moisture for short periods outside inert conditions.
The broadest use we’ve witnessed involves its role as an intermediate in pharmaceutical research pipelines. The combination of electron-withdrawing fluoro and trifluoromethyl groups enables molecular designs that resist metabolic breakdown, a challenge in modern medicinal chemistry. Nearly every month, we field requests from teams running parallel syntheses with dozens of substituted aromatic ketones, and those who’ve made the switch to our dual-substituted variant note shorter purification timelines and higher yields after functionalization. In direct feedback, process improvement groups from pharma clients point out reduced impurity profiles and reduced loss in their catalytic cycles.
Agrochemical labs have adopted this compound within active ingredient design. Here, fluorinated aromatics are prized for selective biological activity and reduced off-target toxicity. The specific configuration of 3'-Fluoro and 5'-(Trifluoromethyl) substitution unlocks pathways to molecules not accessible by more common halogenated acetophenones. We have shipped to research teams who focus exclusively on crop protection molecules, where each fluorine atom placement can mean breakthrough selectivity or regulatory success. Because our entire production operation is streamlined for small to medium-size batch control, we frequently turn around custom orders for structure-activity-relationship (SAR) libraries, supporting rapid innovation at the preparative gram and kilogram scales.
From a manufacturing standpoint, standard acetophenones, those with little or no fluorination, offer ease in both synthesis and handling. Their reactivity and behavior have been charted for decades. Introducing a trifluoromethyl group changes several important process variables—boiling point, polarity, and, more notably, sensitivity to strongly basic or nucleophilic reaction conditions. Adding a third-position fluorine compounds these changes, requiring specially lined reactors and scrupulous exclusion of certain solvents to prevent unwanted side reactions.
On the floor, we’ve seen the difference play out in everything from raw material logistics to the practical shelf stability of finished product. Mono-fluorinated analogs can exhibit decent stability, but dual-substituted 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone delivers lengthened storage horizons. Batches retain purity longer, even under less-than-ideal conditions. In comparative runs, single-fluorinated products often require additional stabilization steps or storage below ambient temperature. With our compound, customers can expect reliable quality performance in ambient warehouse environments, which supports cost control throughout the supply chain.
Direct production of this compound brings a set of real-world challenges not present with less heavily fluorinated analogs. Our operators work with specialty distillation rigs, specifically designed for handling low-flash-point, high-volatility molecular intermediates. It took hands-on fine-tuning to identify purification workflows that wouldn’t leave residues or risk cross-contamination, especially when switching between halogenated product batches.
Reactor loading, solvent selection, temperature ramp profiles—each step must account for the exothermicity introduced by dual activation of the aromatic ring. Early synthesis campaigns had their share of failed runs, but as a direct producer, troubleshooting meant literally standing over vessels, monitoring for phase separation, and knowing any slip in temperature control could cost both time and substantial raw material. Each time a run succeeded, that experience turned into operational protocols—stable enough now to routinely achieve high-purity batches.
Our direct customers, particularly those running multi-step syntheses for clinical candidates or specialty agrochemicals, expect their aromatic ketone building blocks to integrate with minimal customization. With standard acetophenones, secondary reactions or side-chain oxidations often crop up. With 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone, downstream transformations tend to proceed with fewer byproducts, based on consistent NMR and MS verification performed on site.
Repeated customer experience has shown time saved at the purification stage. Instead of column after column, many labs move quickly to the next step. In our own pilot reactions, Suzuki couplings and Buchwald-Hartwig aminations run clean with standard opposing partners, supporting the reliability claims reported from our customers.
Achieving genuine batch-to-batch consistency has become a bit of an obsession among our shift leads and chemists. The complexity of this molecule heightens the risk of minor isomer formation or trace byproduct persistence, particularly if equipment isn’t perfectly prepped between runs. Over years of actual manufacturing, we’ve identified and fixed the sources of inconsistency—be it from raw material supplier changes or seasonal humidity shifts in the plant. We inspect each shipment with high-sensitivity analytical methods inside our own labs before approving release.
Direct users, especially those scaling up to pilot-scale or preparing regulatory dossiers, value full confidence in chemical purity. Open access to our analytical data, and ongoing willingness to field technical inquiries, have encouraged collaborative relationships. Real feedback makes a difference—from techniques for solvent switch to tweaks for catalytic system preparation—informing both our own process and customer success.
Engaged every day in the synthesis and packaging of this compound, safety goes beyond basic labeling. We have invested in on-site engineering controls—local ventilation, active carbon filtration, and monitored temperature controls during both reaction and storage phases. Worker training doesn’t just check compliance boxes. Employees learn firsthand to recognize subtle signs of decomposition risk and manage exothermic events before they develop.
Shipping teams prepare batches under inert gas, seal samples for transit, and time deliveries to minimize exposure to fluctuating environmental conditions. A practical understanding of the product’s behavior—its volatility, limited moisture sensitivity, and tendency to form fine crystalline dust—feeds directly into our production SOPs and training. Customers appreciate receiving product that is in prime condition, supported by a team ready to address hands-on questions about safe handling and storage, informed by our own operational experience.
Years of manufacture taught us that specialty fluorinated aromatics demand thoughtful waste management. Our process improvements now include solvent recovery, on-site treatment for fluoride-containing effluents, and partnerships with certified hazardous waste handlers. The structure of this compound means it can resist breakdown in standard biological treatment systems, so we take active roles in cradle-to-grave chemical tracking and advocate for end-users to follow best disposal practices.
Reducing green-house gas emissions from unnecessary energy input, and reusing purification solvents wherever purity allows, lets us keep costs in check while lessening downstream impact. We collaborate with raw material suppliers with demonstrated environmental compliance histories, since sourcing affects the entire life cycle. Beyond daily production, we are committed to sharing technical details supporting safe use and responsible end-of-life handling, making real-world sustainability progress a team goal.
Delivering a molecule like 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone at consistent scales requires attention to detail at every production stage. Managing our own inventory of precursor chemicals, staying ahead of global market swings, and planning manufacturing windows for surge periods driven by research cycles all form part of our operational rhythm.
As a manufacturer, we see patterns develop: every time a major pharmaceutical program advances or a new patent publishes, demand surges. We respond by blending just-in-time production principles with strategic raw material stocking. Holding direct relationships with our suppliers keeps our process flexible; experience has shown us which upstream chemicals become pinch points and which ones can swing lead times by weeks. We continue adapting production schedules, leveraging our batch history database to smooth out peaks and troughs, So that our clients hardly ever face delays or shortfalls.
Our product makes a difference to teams running ambitious chemical syntheses that traditional building blocks can’t address. Our presence in countless collaborative projects—where first-pass results led to novel analogs, eventual publications, and sometimes new proprietary product lines—gives us a unique perspective beyond what any raw market data could show. Whether it's as a reactant in a challenging multi-step route to an active pharmaceutical ingredient, or as a scaffold for proprietary agrochemical agents, our expertise fuels more than simple molecule supply.
Researchers push boundaries by reaching for challenging substituents, and our hands-on work with this unique acetophenone lets us keep pace with them. Every time a new request comes in for a tailored impurity profile, or feedback highlights a subtle improvement, we look to integrate that learning back into our process. The value of working directly with synthesizers—not just selling to managers—shows up in the nuanced technical support we offer, the openness to customization, and the communal sense of moving the field forward, one batch at a time.
Only by making this product ourselves—from the start of synthesis to final packaging—do we retain the practical know-how and flexibility that trading intermediaries miss. We know the quirks of each production run, right down to which raw material supplier's batch led to a slightly different color or melting profile. We aren't confined by reseller rules or rigid minimum run requirements, so custom projects or last-minute adjustments receive thoughtful, experience-based attention.
Direct accountability to our clients means every complaint or request filters directly back into work on the floor. Some of our best innovations have come from first-hand communications with bench chemists running exploratory syntheses or process teams scaling up gram quantities for regulatory submission. The relationships built through honesty, responsiveness, and technical depth let us continuously refine both product and process, avoiding the generic, less consistent results encountered with less involved suppliers.
Our work creating 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone comes from day-in, day-out engagement with both matter and method. No batch is routine. New scientific literature, regulatory changes, and shifting end-market requirements demand our attention and willingness to improve. We provide traceable lot histories, all supporting analytical data, and open lines for technical dialogue, serving not just as suppliers but as genuine partners in the creative process of modern chemistry.
We recognize leading researchers value suppliers who can adapt to project feedback, offer practical improvements, and understand the granularity of each application’s requirements. Our progressive process improvements, safety protocols, and environmental safeguards come from a conviction: by staying close to both molecule and market, we drive both security of supply and the evolution of applied science.
Each time a shipment of 3'-Fluoro-5'-(Trifluoromethyl)Acetophenone leaves our production facility, it does so backed up by the work, skill and direct ownership that only genuine manufacturers can claim. Every learning—technical, operational, procedural—filters through to the next batch, making the difference in the day-to-day progress of science and industry. This hands-on continuity, from raw material to application, sets our product apart from those sourced at arm’s length and enables us to respond meaningfully to the growing demands of chemists at the frontier of research and application.