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2,2,2,4'-Tetrafluoroacetophenone

    • Product Name 2,2,2,4'-Tetrafluoroacetophenone
    • Einecs 216-102-0
    • 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

    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 & Storage
    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.
    Application of 2,2,2,4'-Tetrafluoroacetophenone

    Applications of 2,2,2,4'-Tetrafluoroacetophenone in Industrial Manufacturing

    2,2,2,4'-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 Synthesis

    Our 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

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US Pharmacopoeia (USP) monographs (for intermediates and residual solvents)
    • European Pharmacopoeia (Ph. Eur.) and Japanese Pharmacopoeia (JP) relevant APIs
    • FDA 21 CFR Part 210/211 regarding process validation and cleanliness

    Typical usage ratio

    • 0.2–1.5 equivalents per step, adjusted based on target molecule design
    • Fine-tuned via in-process QC to ensure <0.05% unreacted intermediate in final API

    Downstream process integration

    • Engaged post-condensation/aromatic substitution steps using anhydrous and inert conditions
    • Introduced after core scaffold assembly for selective fluorination reactions
    • Material tracked in process documentation as a designated hazardous intermediate

    Final product types

    • Nucleoside analog antivirals
    • Fluorinated kinase inhibitors
    • Antitumor small molecules with higher first pass stability
    • Diagnostic imaging agents containing fluoro-aromatic moieties

    2. Advanced Polymer Monomer for High-Performance Fluoropolymers

    Fluorinated 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

    • ISO 9001:2015 Quality Management System for material traceability
    • REACH (EC 1907/2006) registration for polymer starting materials
    • ASTM D4065-12 for polymer thermal analysis
    • RoHS Directive 2011/65/EU for electronic materials (if applicable)

    Typical usage ratio

    • 5–15 mol% comonomer relative to main monomer, depending on desired fluorine content
    • Batch-to-batch adjustments based on DSC/SEC molecular weight outcomes

    Downstream process integration

    • Dosed as a co-monomer during initial charge of polymerization reactors
    • Pre-dispersed in solvent or emulsifier prior to polymer chain initiation
    • Monitored with in-line FTIR or GC for consistent incorporation

    Final product types

    • High-frequency PCB dielectric films
    • Fluorinated coatings for specialty optics
    • Chemical-resistant process tubing
    • Microporous membranes for fuel cells

    3. Agrochemical Intermediate for Selective Herbicide Synthesis

    Agrochemical 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

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No. 1107/2009 for active substance approval
    • US EPA 40 CFR Part 180 (tolerance and impurity criteria)
    • OECD Guidelines for Testing of Chemicals (batch analysis and stability)

    Typical usage ratio

    • 0.5–1.3 equivalents per active ingredient synthesis, defined by pathway selectivity
    • Optimized after pilot-scale trials and environmental impact reviews

    Downstream process integration

    • Added to key C–C or C–N coupling steps for arylation
    • Sequenced prior to ring-closing or further functional group modification
    • Reacted in moisture-controlled vessels to avoid hydrolysis side reactions

    Final product types

    • Fluorinated urea-based selective herbicides
    • Pyridine- or triazine-derived crop protection agents
    • Preparations for grass and broadleaf weed resistance management

    4. Intermediate for High-Temperature Fluoroaromatic Electronic Chemicals

    Electronics 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

    • IEC 61249-2-7 for base materials used in electronics
    • IPC-4101 for laminate and prepreg material specifications
    • RoHS and REACH compliance (low heavy metal and halogen content)
    • In-house QA protocols for microelectronic grade chemicals

    Typical usage ratio

    • 3–12 wt% relative to polyimide or aryl ether precursor charges
    • Adjusted for property targets such as Tg, dielectric loss, and thermal expansion coefficient

    Downstream process integration

    • Fed into etherification or condensation steps under high-purity, oxygen-free conditions
    • Processed with automated DCS batch controls for continuous electronic chemical output
    • Monitored by HPLC and microanalytical QC throughout the process

    Final product types

    • High-leading flexible circuit substrates
    • High-frequency (GHz-range) dielectric thin films
    • Semiconductor grade insulating coatings
    • Low-loss PCB laminates for telecom equipment
    Free Quote

    Competitive 2,2,2,4'-Tetrafluoroacetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,2,2,4'-Tetrafluoroacetophenone: Insights From the Manufacturer’s Floor

    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.

    The Substance: Practical Considerations and Properties

    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.

    Specifications We Pay Attention To

    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.

    Usage: Real-World Contexts and End Results

    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.

    How It Stacks Up: Comparing to Related Acetophenones

    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.

    Bottlenecks, Process Realities, and Solution Paths

    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.

    Supporting End Users: The Human Element

    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, Sourcing, and Intellectual Property Pressures

    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.

    Quality Culture and Continuous Improvement

    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.

    Navigating the Future: Emerging Trends and Manufacturing Priorities

    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.

    Conclusion: Manufacturer’s Commitment to Real-World Outcomes

    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.