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HS Code |
479365 |
| Chemical Name | 2,2,2,4'-Tetrafluoroacetophenone |
| Cas Number | 75628-66-3 |
| Molecular Formula | C8H4F4O |
| Molecular Weight | 192.11 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 102-104°C at 23 mmHg |
| Melting Point | -4°C |
| Density | 1.369 g/cm3 at 25°C |
| Refractive Index | n20/D 1.433 |
| Flash Point | 85°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC(=O)C1=CC=C(C=C1)F |
| Inchi | InChI=1S/C8H4F4O/c1-5(13)6-2-3-7(9)4-8(6)10,11,12 |
As an accredited 2,2,2,4'-Tetrafluoroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tamper-evident cap, chemical-resistant label, hazard symbols, and product details clearly displayed. |
| Shipping | 2,2,2,4'-Tetrafluoroacetophenone is shipped in tightly sealed, chemical-resistant containers to prevent leaks. Store and transport the chemical in cool, dry conditions and away from incompatible materials. All packages must be clearly labeled, adhering to relevant hazardous material regulations. Protective measures are required for handling due to its potential health and environmental hazards. |
| Storage | **2,2,2,4'-Tetrafluoroacetophenone** should be stored in a tightly sealed container, away from moisture, direct sunlight, and incompatible materials such as strong oxidizers or bases. Store in a cool, dry, well-ventilated area, preferably in a designated chemical storage cabinet. Ensure appropriate labeling and keep away from sources of ignition, as well as food and drinking water. |
Applications of 2,2,2,4'-Tetrafluoroacetophenone in Industrial Manufacturing2,2,2,4'-Tetrafluoroacetophenone serves as a specialized fluorinated intermediate across high-value chemical synthesis sectors. We produce this compound to support stringent process requirements in pharmaceuticals, advanced polymer production, agrochemical synthesis, and specialty electronics materials, ensuring reliable supply with strict batch control. 1. Pharmaceutical Intermediate for Antiviral Ingredient SynthesisOur material enters targeted pharmaceutical synthesis, especially in the preparation of fluorinated building blocks for antiviral agents. Its electron-withdrawing fluoro groups enable precise control over substitution reactions, supporting active ingredient frameworks where metabolic stability and decreased enzymatic degradation are required. Downstream pharmaceutical manufacturers introduce it during multistep synthesis, under controlled temperature and pressure to preserve the fluoroketone functionality, with careful validation at each stage to meet global safety and purity regulations. Adjusted molar ratios depend on the desired molecular backbone, with analytical methods ensuring unreacted precursor remains below pharmacopeia-specified thresholds before batch release. Industry compliance standards
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2. Advanced Polymer Monomer for High-Performance FluoropolymersFluorinated acetophenones play a critical role in custom fluoropolymer manufacture. Polymeric processors use our material to introduce well-defined fluoroaromatic units that raise chemical resistance, thermal stability, and dielectric properties in specialty coatings and engineering plastics. The precise purity of this monomer-grade ketone enables tight molecular weight control during solution or emulsion polymerization, necessary for manufacturing films and sheets in semiconductor and aerospace sectors. Supplier-specific technical data and analytical COAs accompany each batch, supporting real-time monitoring in continuous or batch reactors. Industry compliance standards
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3. Agrochemical Intermediate for Selective Herbicide SynthesisAgrochemical producers utilize this tetrafluorinated ketone to build active ingredients with selective weed control profiles. The distinct substitution pattern imparts enhanced metabolic stability and soil persistence in target molecules. Our production specification addresses not only purity but also trace metal and halide content, critical for downstream catalytic coupling steps such as Suzuki or Heck reactions, often performed under anhydrous and oxygen-free environments. Application-specific safety data and batch records ensure compliance with international pesticide registration requirements. Industry compliance standards
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4. Intermediate for High-Temperature Fluoroaromatic Electronic ChemicalsElectronics material manufacturers require stable, highly pure intermediates for synthesizing fluoroaromatic compounds used in high-temperature circuit board and semiconductor fabrication. This tetrafluorinated acetophenone enables tailored aromatic substitution in aryl ether or polyimide ligand synthesis, vital for next-generation dielectric materials. Standard supply includes batch-level analytical validation (GC, NMR, ICP-MS for trace metals) and meets tight impurity and particle size limits to prevent yield loss in sensitive downstream reactions. Industry compliance standards
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Producing specialty fluorinated aromatics stands as the backbone of our daily operations, and among these, 2,2,2,4'-Tetrafluoroacetophenone regularly draws keen attention. Decades spent handling and refining this compound have taught us about its essential role in streamlining the work of end-users who need performance and dependability, not just a commodity. Countless hours of batch production, quality control, and real-world troubleshooting have shaped our understanding of what makes this specific ketone a valuable tool instead of just another molecule floating in the catalog.
Chemists approach 2,2,2,4'-Tetrafluoroacetophenone for its unique blend of properties that can’t be duplicated easily by other acetophenones. This molecule, simply put, features a trifluoromethyl group at the 2-position and another fluorine at the para position of the aromatic ring. We prioritize consistent molecular structure and purity, since even minor process deviations affect downstream reactions for advanced pharmaceutical, agrochemical, and specialty polymer applications.
Handling the synthesis and crystallization year after year leaves us hyper-aware of the nitty-gritty realities: you get a crystalline solid that dissolves in most organic solvents, but the volatility is markedly lower than many mono-substituted fluoro analogs. It stands up to higher-temperature workups. In practice, that means it survives demanding synthetic transformations, minimizing losses without risking unwanted side reactions from breakdown or uncontrolled volatility.
On the shop floor, specifications go beyond numbers in a certificate. 2,2,2,4'-Tetrafluoroacetophenone typically boasts a purity above 98 percent—anything less prompts us to revisit our process controls. We keep residual solvents, heavy metals, and isomeric byproducts low. Moisture can be a subtle enemy; a hydrative impurity drags down crystallization, forces redrying, and compromises reactivity in coupling steps or nucleophilic aromatic substitutions. Our best runs keep water below 0.05%, using dedicated dryers and tight packaging protocols, because every shortcut here leads to headaches at the bench and lost yield for users.
Physical checks run in parallel with instrument analysis. The melting point shouldn’t waver beyond half a degree from the established range. A sight test, an honest sniff, and even tactile checks remain routine in our process. Subtle yellowing or off-odors point to the presence of trace oxidized byproducts that can ruin downstream applications. These might not show on routine chromatography, but years of handling teach detection beyond instruments alone.
Day-in, day-out, 2,2,2,4'-Tetrafluoroacetophenone goes to labs and plants that look for more than a catalog entry—they seek reliability and performance. In pharmaceutical R&D, chemists introduce this group to achieve electron-withdrawing effects on aromatic rings, tuning the reactivity of intermediates and metabolic profiles of final molecules. Formulators find that its multi-fluorinated structure delivers both steric resistance against biodegradation and enhanced pharmacophore potential—attributes that single-fluorinated or unfluorinated acetophenones don’t replicate.
Agrochemical producers look for the same electron-withdrawing nature to boost stability and selectivity of crop protection agents. We’ve worked directly with customers modifying herbicide backbones, where a single misplacement of a fluorine atom changed an inert building block into a superior bioactive. Our batch-to-batch records and application notes track which conditions deliver optimal conversions—even subtle process tweaks like solvent swap or catalyst concentration can push a yield from eighty to ninety percent or more.
Polymer researchers come to us for customizations. The extra fluorines on the aromatic ring open routes for building monomers that resist temperature, oxidation, and corrosive conditions—a fact that reflects in high-performance films, membranes, and specialty coatings. These end-users demand unwavering purity and reproducibility, as any batch variation ripples into hours or even weeks of lost productivity.
Among all the acetophenones, this molecule stands apart thanks to the combination and position of its fluorine atoms. We’ve worked with the full range—plain acetophenone, mono-fluoro, or trifluoromethyl variants. Most clients who start with basic acetophenone or 4'-fluoroacetophenone soon realize they hit a limit on what those simpler molecules can do in terms of ring activation and stability. By comparison, 2,2,2,4'-Tetrafluoroacetophenone offers an ideal profile: the trifluoromethyl group at the alpha carbon exerts a strong electron-withdrawing effect, dramatically impacting both chemical reactivity and metabolic fate in complex molecules.
Mono-fluoro and even difluoroacetophenones rarely provide the same combination of steric bulk and electron control. Our test data—and direct user feedback after pilot runs—show that substitution patterns fundamentally alter reaction sites and yields. The extra fluorine at the para position further tunes reactivity, which leads to greater selectivity in synthesis, reduced byproducts, and a better safety profile, especially where impurities in pharmaceutical actives could raise regulatory concerns.
We do see interest in alternatives driven by cost pressures. Sometimes clients turn to less heavily fluorinated analogs, only to return after seeing drop-offs in product performance or regulatory difficulties due to undesired byproducts. Narrowing source materials or modifying process conditions can’t always bridge these gaps. In fact, cutting the number of fluorine atoms from four down to three or two too often forces trade-offs on stability, resistance to biodegradation, or hydrophobicity that downstream customers aren’t willing to accept.
Consistently producing this molecule isn’t as simple as hitting a recipe and letting automation run its course. Small changes in raw material batches—subtleties hidden in trifluoroacetyl chloride or para-fluoroacetophenone precursors—can shift the impurity profile and crystallization characteristics. Over the years, we invested in in-line monitoring and operator training, but we’ve also learned that even the best controls won’t compensate for low-quality inputs. Maintaining trusted supplier relationships and running incoming check batches remain permanent parts of our workflow.
Environmental controls matter. 2,2,2,4'-Tetrafluoroacetophenone doesn’t volatilize as readily as some analogs, yet we capture every fume and minimize fugitive emissions. The heavier molecular weight and strong C–F bonds reduce the risk of accidental loss to air, but that shouldn’t breed complacency. Regular scrubber maintenance and VOC monitoring form a daily discipline, not just a regulatory checkbox.
Waste management challenges often arise due to residual organofluorine byproducts. Regulatory pressure on per- and polyfluoroalkyl substances (PFAS) keeps rising. Our plant routes every liquid or solid stream for detailed analysis, using activated carbon and advanced oxidation to treat process water and cut persistent waste at the source—an expensive, but necessary investment to continue responsible production.
Batch tracking is no minor formality. Each run gets logged, with records updated for reaction temperatures, solvent swaps, and real-world modifications asked for by chemists and plant managers working at the edge of novel synthesis. Documenting these minute details isn’t about bureaucracy, but about troubleshooting unexpected results a year or more down the line. Quality doesn’t happen by accident; it results from documenting successes and failures, and sharing those lessons directly with customers when challenges appear at their end.
Unlike off-the-shelf commodities, specialty ketones like this require ongoing support and adaptation. We’ve walked customers through downstream purifications, even when their specs seemed unachievable at first glance. Sometimes, a small change in crystallization or drying turns a process headache into an efficient routine. Chemistry on paper rarely matches real-world scaling—ballooning up from grams to kilos shifts impurity profiles and requires hands-on experience to manage new challenges. Our technical team spends time not just recommending textbook adjustments, but sharing which solution approaches helped us realize better outcomes on the shop floor.
Years of practical questions from users create a living knowledge base. We keep track of which synthetic protocols play well with our product, what solvent sequences avoid caking or fouling, and how storage container material impacts batch lifespan. Users sometimes ask us about long-term stability or compatibility with reactive organometallics. Our own lab notes, built on thousands of pilot and production runs, prove essential in providing concrete advice, rather than generic suggestions. These lived details distinguish us from sellers lacking manufacturing roots.
Pricing inevitably swings in step with global fluorochemical raw material shifts. Major swings in fluorspar or HF costs ripple down to precursors and ultimately shape end-user budgeting. We keep stores of primary reagents, but price volatility can force sudden production pauses or surges. Unlike third-party traders, direct manufacturers deal with these shocks by re-aligning schedules and informing regular buyers in advance, building a relationship of trust and transparency over simple price negotiation.
Intellectual property adds its own wrinkles. Sometimes researchers work on patented intermediates or seek exclusive access to certain fluorinated scaffolds. We vet every request for proprietary restrictions, balancing open supply with respect for innovation boundaries. Our product history and established plant capacity lend confidence that customers can scale without running afoul of unseen legal risks or running short of supply due to a mismanaged chain.
From the earliest days in small production rooms to purpose-built reactors, our culture emphasizes not simply repeating what worked last year, but chasing opportunities for improvement. Each new synthesis challenge translates into plant trial revisions, real-time analytics, and open channels between our R&D and operations teams. The landscape for fluorinated acetophenones keeps evolving—tighter regulations, rising quality standards, and downstream demand for lower metal content or trace residuals push us to adapt.
We learn a great deal from customer feedback: a string of unexpected byproducts, changes in melting point, or sluggish reaction rates trigger an internal review. There’s no substitute for hands-on sampling, speed tests, and binary solvent washdowns when new anomalies appear. Our reputation rides on consistency, and direct accountability flows from every operator, shift supervisor, and lab tech whose fingerprints appear on every lot out the door.
New application arenas present both promise and pressure, as researchers experiment with fluorinated acetophenones in advanced materials, pharmaceuticals, and energy technologies. Each field brings unique demands from trace-purity to controlled particle size. Close partnerships with formulators or innovators let us pre-empt problems instead of reacting to failures or recalls.
In response to evolving environmental regulations targeting halogenated organics, we proactively explore lower-impact synthetic routes, solvent recovery, and lifecycle analysis of all inputs and byproducts. Trust builds slowly, batch by batch. Technical transparency and the ability to answer hard questions draw respected customers who need more than what trading houses can provide.
Manufacturing 2,2,2,4'-Tetrafluoroacetophenone goes beyond delivering a molecule by CAS number and purity grade. Each batch links us to researchers who rely on seamless chemistry and robust regulatory backing in their daily work. We treat this responsibility as more than a job—it’s a testament to decades of learning, troubleshooting, and partnership. Challenges keep evolving, but practical experience keeps us grounded on what delivers success—not just in theory, but in the realities faced on research benches and manufacturing lines around the world.