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2',3',4',5'-Tetrafluoroacetophenone

    • Product Name 2',3',4',5'-Tetrafluoroacetophenone
    • Einecs 247-422-2
    • 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
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    Specifications

    HS Code

    528998

    Chemical Name 2',3',4',5'-Tetrafluoroacetophenone
    Molecular Formula C8H4F4O
    Molecular Weight 192.11 g/mol
    Cas Number 946-26-5
    Appearance Colorless to pale yellow liquid
    Boiling Point 135-137 °C (at 20 mmHg)
    Density 1.383 g/cm³
    Pubchem Cid 76148
    Smiles CC(=O)C1=CC(=C(C(=C1F)F)F)F
    Inchi InChI=1S/C8H4F4O/c1-4(13)5-2-6(9)8(11)7(10)3-512/h2-3H,1H3
    Solubility Slightly soluble in water, soluble in most organic solvents

    As an accredited 2',3',4',5'-Tetrafluoroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 2',3',4',5'-Tetrafluoroacetophenone is supplied in a tightly-sealed amber glass bottle with hazard labeling.
    Shipping 2',3',4',5'-Tetrafluoroacetophenone is shipped in sealed, chemical-resistant containers, protected from moisture and light. Packaging complies with all regulations for hazardous materials. Proper labeling and documentation are included to ensure safe handling during transport. Shipment is via trusted carriers, with temperature control and secondary containment as needed for stability and safety.
    Storage 2',3',4',5'-Tetrafluoroacetophenone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from moisture and direct sunlight. Use appropriate chemical storage shelving and ensure containers are clearly labeled. Follow all safety and handling regulations as outlined in the chemical’s safety data sheet (SDS).
    Application of 2',3',4',5'-Tetrafluoroacetophenone

    Applications of 2',3',4',5'-Tetrafluoroacetophenone in Industrial Manufacturing

    As a direct manufacturer, we deliver high-purity 2',3',4',5'-Tetrafluoroacetophenone exclusively for advanced markets where its distinct chemical profile enables value-added performance in demanding downstream environments. Below, we summarize four industrial segments where our material consistently supports customer production lines, offering unique technical advantages based on real-world application experience.

    1. Specialty Agrochemical Synthesis

    Within modern agricultural chemistry, tetrafluoroacetophenone derivatives serve as essential intermediates for selective herbicide and fungicide actives due to their electrophilic aromatic substitution reactivity. Our product enters stage-gate synthesis routes to introduce multi-fluorinated motifs critical for crop protection product registration and patentability. Material qualification always involves multi-batch traceability, and agrochemical customers frequently request application-tailored supply chain documentation for field performance validation.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 (EU agrochemicals)
    • US EPA Pesticide Assessment Guidelines
    • China GB 2763 Maximum Residue Limits
    • ISO 9001:2015 for batch and lot traceability

    Typical usage ratio

    • 0.5%–3.5% of total precursor batch mass for final active synthesis; actual ratio adjusts based on desired activity profile and downstream coupling step requirements

    Downstream process integration

    • Added during phased substitution or acylation reactions after initial core framework assembly, under controlled temperature and pressure; often used in parallel reactor configurations for high-throughput screening

    Final product types

    • Triazole herbicide intermediates
    • Fluorinated strobilurin fungicides
    • Active ingredient concentrates for seed treatment
    • Regulated pesticide formulation blends

    2. Pharmaceutical Intermediate Manufacturing

    This material is routinely specified as a key fluorinated building block for chemoselective functionalization in the assembly of API candidates, especially for CNS and oncology actives where metabolic stability and lipophilicity require precise fluorine incorporation. Process chemists often introduce it in the late-stage synthesis to secure patent space and optimize analytic signature for regulatory submissions. Our batch records support direct traceability to assist in GMP submissions and audit procedures.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guide for APIs
    • United States Pharmacopeia (USP) General Chapter <823>
    • European Pharmacopoeia 11.0 Section 5.10 on impurities
    • FDA DMF II and III guidance for intermediates

    Typical usage ratio

    • 0.2–1.2 equivalents relative to the core reaction substrate (by molar consideration); ratio is fine-tuned based on specific target molecule pathway and safety margin calculations

    Downstream process integration

    • Charged to the reactor at the penultimate step during advanced fluorination, either in batch or continuous processing, followed by rapid quench to preserve product quality; typically integrated in cGMP suites with dedicated containment

    Final product types

    • CNS-active pharmaceutical intermediates
    • Pyridine-based fluorinated compounds for oncology
    • Lead candidates for pharmaceutical contract research
    • Regulatory reference standards (intermediate grade)

    3. Electronic Materials for Organic Synthesis

    Electronic device fabrication increasingly specifies highly fluorinated aromatic compounds as performance precursors for designing new organic semiconductors, photoresist agents, and OLED emitters. Our product integrates into the synthesis of arylated monomers where low impurity profiles and fluorine position specificity are mandatory for device-grade polymerization. Detailed impurity analysis and tight process controls make our offering suited to electronics supply chains with stringent quality requirements.

    Industry compliance standards

    • JEITA ET-7304 (Japan Electronics and Information Technology Industries Association)
    • IEC 61249-2-21 for halogen content in base materials
    • RoHS 3 Directive (EU Restriction of Hazardous Substances)
    • ISO/TS 16949 for automotive electronics materials

    Typical usage ratio

    • 1–5 mol% of total monomer charge, with adaptation based on desired charge carrier mobility and post-polymerization performance in end device

    Downstream process integration

    • Introduced during aryl electrophilic coupling, followed by polymerization under rigorously controlled, humidity-free conditions; often supported by in-line purity monitoring and critical reagents tracking

    Final product types

    • Photolithography photoresists
    • OLED blue/green emitter monomers
    • Fluorinated polymer semiconductor films
    • Electronic sensor substrates

    4. Advanced Coatings and Surface Modification

    The material exhibits a strong track record in the custom synthesis of fluorinated surface modifiers and crosslinkers for high-durability industrial coatings. When converted into downstream agents, these intermediates boost chemical resistance and extend maintenance intervals for specialty applications, including anti-graffiti coatings and electronic device encapsulants. We follow strict in-process analytics to ensure batch uniformity and compliance for end-use within regulated coating systems.

    Industry compliance standards

    • ASTM D6904 for resistance to environmental degradation
    • ISO 12944-6 for protective paints and coatings
    • REACH SVHC restrictions on coating additives
    • EN 13523-10 wet abrasion standards

    Typical usage ratio

    • Typically 0.8%–2.5% by total mass of the modifier precursor batch; ratios are determined by desired crosslinking density and target film thickness in application

    Downstream process integration

    • Utilized during the synthesis of reactive oligomers prior to blend mixing and film casting; functionalized by manufacturers using controlled hydrolysis or aminolysis to enhance surface performance attributes

    Final product types

    • High-durability anti-graffiti coatings
    • UV-cured electronic encapsulants
    • Chemical-resistant fluorinated adhesives
    • Protective top-coat agents for industrial equipment
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    Competitive 2',3',4',5'-Tetrafluoroacetophenone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2',3',4',5'-Tetrafluoroacetophenone: A Practical Perspective on a Specialized Building Block

    What Sets 2',3',4',5'-Tetrafluoroacetophenone Apart

    Within our chemical manufacturing floors, some molecules demand a reputation for problem solving, precision, and reliability. 2',3',4',5'-Tetrafluoroacetophenone holds a respected spot in that lineup. We see it requested by chemists developing pharmaceuticals, electronics, and specialty materials for its unique pattern of fluorine substitution. Four adjacent fluorine atoms on the aromatic ring transform ordinary acetophenone into something powerful and versatile.

    Over years of batch production, our experience with this molecule points to its rare blend of stability and reactivity. While monofluorinated or difluorinated acetophenones appear in some catalogs, this tetrafluoro is a step apart. Substituting hydrogens with fluorine directly impacts electron density, metabolic stability, and reaction outcomes. In our reactors, the challenge isn’t just halogenation but ensuring every molecule matches the substitution pattern. Impurities or isomers in this compound risk ruining an end application—especially in pharmaceutical intermediates, OLEDs, or advanced polymers.

    Product Consistency and Purity: Hard Lessons from the Factory Floor

    During production, crude product often retains not just unreacted starting materials but a mix of regioisomers. Other suppliers sometimes accept trace quantities of ortho or meta isomers. In our process, those levels don’t pass. Each batch follows routine GC-MS analysis and NMR screening to rule out creeping impurities that might clog a synthetic sequence or alter a physical property in devices. Over time, customers have recounted how a few tenths of a percent of a mispositioned fluorine atom can derail an entire project. We have learned that absolute purity and controlled environment synthesis protect both our reputation and the customer's product pipeline.

    This molecule, C8H4F4O, comes as a colorless liquid out of the still. Careful vacuum distillation cleans it up, but several rounds of purification may follow, depending on the end-user need. We've found moisture control crucial through the whole process, as fluoride ion traces or acid byproducts damage downstream applications—particularly during pharmaceutical fragment formation.

    Why Fluorine Patterning Matters in Synthesis

    Fluorination is never a shortcut. Anyone who’s run aromatic halogenation at scale recognizes the value of precise substitution. Fluorines at the 2', 3', 4', and 5' positions alter both physicochemical and biological activity. We routinely hear from medicinal chemists aiming to manipulate lipophilicity, metabolic pathways, or receptor binding. In electronic materials, this substitution delivers big shifts in energy levels or dielectric properties, whether working on new display materials or semiconductors.

    Subtle changes in substitution affect everything from melting point to electronic distribution. Our tetravalent product delivers less nucleophilic ring carbons, slows down many metabolic enzymes, and shifts reactivity in cross-coupling reactions. Those features mean it functions differently than the more common 4’-fluoroacetophenone or its trifluoro analog. Tetrafluorination gives almost complete resistance to oxidative degradation, granting a much longer shelf and device life for high-value products.

    Applications: Not Just “Another Intermediate”

    2',3',4',5'-Tetrafluoroacetophenone rarely works alone. Most of our customers use it as a building block or intermediate. Medicinal chemists see its core used in experiments to dial in drug candidate activity and stability. Lead discovery teams approach us for custom scaling when a hit in the early lead phase moves to formal development, and a consistent, traceable grade becomes non-negotiable.

    Organic electronics teams have told us this molecule finds its way into small-molecule emitters for OLED displays, where it brings needed stability and electron-accepting power. In battery R&D, the fluorinated acetyl fragment helps modulate electrochemical properties, often reducing unwanted side reactions. R&D chemists modifying this building block create compounds with enhanced moisture and oxygen tolerance—critical when pushing the frontier on new materials.

    A recent example: clients in the specialty coatings field developed ambiphilic ligands using this acetophenone, lending enhanced chemical resistance and suitability for extreme-use environments. Consistently delivering on purity and controlled moisture levels allows those innovations to reach their full potential.

    Lessons from Production: Flow Chemistry, Waste Reduction, and Scalability

    Large-scale fluorination means wrestling not just with yields but also with safe handling and byproduct minimization. In our journey scaling up 2',3',4',5'-Tetrafluoroacetophenone, we've moved from traditional batch syntheses to using more flow chemistry setups. This change cuts exposure to hazardous conditions, improves heat management, and provides tighter control over reaction time and stoichiometry.

    Our waste streams have shrunk, and our purification cycles grow more efficient. The process generates less acid waste than older methods using excess fluorinating agents, which speaks not only to safer workplace conditions but also smoother regulatory audits. Consistent feedback from end-users informs every single production upgrade. Every scale-up stage, from gram to multi-kilo, ties back to our core philosophy: deliver the cleanest product, with the lowest possible environmental impact, at the scale chemists genuinely need.

    Technical Nuances Experienced Each Day

    Challenges don’t just stop at synthesis. Storage and transport of highly fluorinated aromatics bring their own set of lessons. This acetophenone resists hydrolysis well, but we always use certified fluoropolymer linings for containers—early tests with standard gaskets or liners showed subtle leaching or discoloration over months. Complete transparency about recommended storage and handling comes not just from manuals but years of hands-on testing and customer post-delivery audits.

    The Value in Real Partnerships with Chemists

    We think beyond selling a bottle. Any experienced producer knows recurring technical requests matter as much as any sales order. Customers call when they want extra data on impurity profiles, reaction byproducts, or residual solvents. We've set up rapid sample turnaround, accepting requests for HPLC, GC, or custom NMR scans before a purchase moves forward. This responsiveness doesn’t stem from a script—it comes from watching promising research hinge on the smallest details.

    Feedback from labs on solubility or volatility drives how we ship, label, and even how we update our safety literature. Once, an unexpected interaction with certain amines at customer sites led us to tweak both drying procedures and packaging, helping avoid costly downtime on their end. Direct, open dialogue shortens development cycles for everybody.

    Supporting Innovation and Predictability in Research

    R&D is often a race against time and uncertainty. Our job as a producer means demystifying a sophisticated intermediate like 2',3',4',5'-Tetrafluoroacetophenone. When a chemist wants a kilo lot, we share not just purity certificates but real-world insights about how the molecule handles at scale. How quickly it distills, shelf life under inert gas, containers that best suit their application—all these shape faster project timelines and fewer dead ends.

    Academic research often asks for detailed byproduct analyses that commercial scales overlook. Supporting those projects helps keep the molecule’s growing reputation strong. As a result, this acetophenone backbone keeps showing up in patents, high-impact papers, and emerging syntheses for next-generation pharmaceuticals or performance polymers.

    Comparing with Standard Acetophenones—A Stepwise Advantage

    Where regular acetophenone offers a simple chemical handle, our tetrafluorinated grade directly improves metabolic robustness and changes the chemistry game in cross-coupling reactions. Other analogs won’t match this product’s electron-withdrawing power or ability to block metabolic oxidation at the para and ortho sites. That translates to extended half-life in drug candidates or superior stability under high-voltage device test.

    Certain difluorinated versions present inconsistent reactivity, especially in Suzuki or Buchwald-Hartwig couplings. Tetrafluoroacetophenone stays predictable, letting teams scale up with fewer surprises. Teams working in battery and polymer R&D point to repeatable, high-quality product as a non-negotiable. They reach for this molecule not just due to its structure but because we maintain batch reproducibility time after time.

    Foresight on Regulations and Sustainability

    With scrutiny mounting on both halogenated solvents and intermediates, we track regulatory shifts closely. Recent trends push for full traceability on raw materials, transparency about byproduct composition, and a commitment to waste minimization. Our facilities invest continually in emissions monitoring, solvent recycling, and energy recovery from exothermic steps. Each lot shipped comes with clear upstream information because we recognize research doesn’t happen in a vacuum—compliance failures upstream can ripple into a partner’s pipeline or delay product launches.

    On sustainability, we’re refining greener synthesis routes, seeking fluorine sources aligned with modern regulations, and engaging with customers developing biodegradable or partially recyclable end products. This molecule—once viewed simply as a rigid fluorinated intermediate—becomes part of bigger stories about safer chemistry and environmental stewardship.

    What Continual Production Has Taught Us

    Over years of making 2',3',4',5'-Tetrafluoroacetophenone, the lessons pile up. No two production runs bring exactly the same batch curve—ambient factors, reagent grades, reaction vessel cleanout routines, and downstream handling each show up in analytical results. Our teams maintain tight batch logs and QA thresholds knowing that every deviation, no matter how small, risks customer trust and future collaborations.

    True value, we realize, comes from commitment to process detail, not just the end molecule. From solvent drying protocols to packaging validation, every lesson gets captured and passed on. This approach has earned us a reputation for not just purity, but predictability. For researchers and process engineers who depend on this acetophenone, every incremental improvement in quality or supply chain reliability adds real value to their timelines and innovations.

    Looking Forward: Enabling Next-Generation Chemistry

    Innovation cycles move faster every year. As projects incorporate more fluorine chemistry to create smarter medicines, durable coatings, and advanced electronic materials, supplying high-quality intermediates means keeping pace with evolving research. With 2',3',4',5'-Tetrafluoroacetophenone, our plant teams and technical support staff see the compound not as a finished good, but as a crucial tool for others to build transformative new products.

    Demands will only rise for increased batch sizes, new derivative compounds, and custom purity grades. Our ongoing dialogue with researchers, process scale-up specialists, and formulation teams shapes how and what we deliver. Each new customer project, feedback call, or analytical challenge adds to what we know—and improves the reliability and reach of everything we produce.

    Real manufacturing isn’t magic. It’s accountability, precise execution, and an appreciation for the unique fingerprint that every molecule can have. 2',3',4',5'-Tetrafluoroacetophenone, as we’ve seen through years of collaborative progress, is more than a line item—it’s a bridge to new research, better materials, and a more dynamic industry.