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[Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene

    • Product Name [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene
    • Alias PIFA
    • Einecs 802-104-0
    • 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
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    Specifications

    HS Code

    317305

    Product Name [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene
    Cas Number 27195-49-3
    Molecular Formula C10F10IO4
    Molecular Weight 494.99 g/mol
    Appearance White to off-white solid
    Melting Point 88-92°C
    Solubility Soluble in organic solvents (e.g., dichloromethane, acetonitrile)
    Boiling Point Decomposes before boiling
    Purity Typically ≥97%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms Pentafluorophenylbis(trifluoroacetoxy)iodine
    Chemspider Id 57444427

    As an accredited [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25 g of [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene is packaged in a sealed amber glass bottle with a tamper-evident cap.
    Shipping [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene is shipped in tightly sealed, chemical-resistant containers to prevent moisture and air exposure. It is transported under cool, dry conditions and labeled as an oxidizing agent. Due to its reactivity, shipping complies with relevant chemical safety and hazardous materials regulations, ensuring safe handling and delivery.
    Storage [Bis(Trifluoroacetoxy)Iodo]pentafluorobenzene should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep the container tightly closed and segregated from incompatible substances, such as strong reducing agents and bases. Use chemically resistant containers, and ensure storage in a designated area for oxidizers. Always follow standard laboratory safety protocols.
    Application of [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene

    Applications of [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene in Industrial Manufacturing

    [Bis(Trifluoroacetoxy)Iodo]Pentafluorobenzene supports advanced synthesis needs as a modern hypervalent iodine reagent. Its strong oxidative properties and selective transfer capacity underpin a range of downstream molecular transformations and specialty material applications in regulated industrial environments.

    1. Pharmaceutical Intermediates Synthesis

    Process chemists use this reagent for arylations, oxidative coupling, and fluorinated arene functionalizations, especially for constructing unique scaffolds in active pharmaceutical ingredient (API) development. Its oxidative profile provides orthogonal reactivity for late-stage functional group modifications during multi-step organic synthesis, leading to building blocks for next-generation pharmaceuticals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. FDA 21 CFR Part 210/211
    • EU EudraLex Volume 4, GMP Guidelines
    • Japan Pharmacopoeia (JP), European Pharmacopoeia (EP) specifications for intermediates

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents relative to substrate; ratio adjusted based on the electron density of the aromatic ring and desired conversion at bench and pilot scale.

    Downstream process integration

    • Added during late-stage intermediate transformations, often as the key oxidant or electrophilic fluorinating agent in sealed reactors under temperature-controlled conditions.

    Final product types

    • Regioselectively functionalized arene intermediates for small molecule APIs
    • Precursors for kinase inhibitors and CNS drugs
    • Complex heterocyclic intermediates for oncology therapeutics
    • API intermediate stock solutions for process R&D scale-up

    2. Agrochemical Active Ingredient Modification

    Specialty pesticide and herbicide development leverages the reagent’s selective trifluoroacetoxylation and aryl-iodine exchange reactions to introduce fluorinated functional groups, modulating compound metabolic stability and improving bioactivity. Manufacturers specify this step to enhance physicochemical properties of proprietary crop protection molecules.

    Industry compliance standards

    • FAO/WHO specifications for technical grade active ingredients
    • REACH Regulation (EC) No. 1907/2006 for chemical safety
    • ISO 9001:2015 Quality Management for agrochemical production
    • OECD Good Laboratory Practice (GLP) for regulated studies

    Typical usage ratio

    • 0.5 to 1.5 molar equivalents per target substrate; the precise loading determined by reactivity of the base molecule and product purification requirements.

    Downstream process integration

    • Employed in final synthetic step or penultimate step before formulation, after core skeleton assembly, under strictly controlled stoichiometry to minimize by-product formation.

    Final product types

    • Fluorinated aromatic herbicide actives
    • Enhanced insecticide intermediates
    • Protected fungicide scaffolds
    • Advanced screening compounds for agricultural field trials

    3. Electronic Materials – High-Performance Polymer Precursors

    Manufacturers in the microelectronics and display sector apply this reagent to introduce perfluorinated groups onto aromatic rings, generating specialty monomers for polymeric dielectric films and fluoropolymer coatings. Its strong nucleofugic character ensures clean incorporation into polymer backbones, vital for material consistency in dielectrics and protective layers.

    Industry compliance standards

    • IPC-4101/42 for base materials for printed circuits
    • RoHS 2 Directive 2011/65/EU on hazardous substances
    • ISO 14001:2015 Environmental Management
    • SEMI C95 standards for electronic chemical purity

    Typical usage ratio

    • 0.4 to 1.0 molar equivalents per monomer batch; loading defined by monomer structure and desired functionalization density for target polymer grade.

    Downstream process integration

    • Introduced at the monomer synthesis/re-functionalization step, preceding polymerization or copolymerization, typically under anhydrous and inert atmosphere conditions.

    Final product types

    • Perfluorinated polyimide dielectric films
    • Photoresist polymer backbones for lithography
    • Fluoropolymer coatings for integrated circuitry
    • Functionalized oligomers for advanced microfabrication

    4. Specialty Fluorinated Fine Chemicals

    Custom synthesis firms utilize this reagent for targeted introduction of fluorinated and trifluoroacetoxy moieties during pilot plant and specialty chemicals manufacturing. It supports stepwise, controlled oxidations and arene modifications, providing access to a range of advanced intermediates leveraged as key starting points in high-value product lines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine and specialty chemical production
    • OECD Test Guidelines for environmental and human safety assessment
    • U.S. TSCA Section 5 inventory regulations where applicable
    • Custom client QC release and in-process controls

    Typical usage ratio

    • 0.6 to 1.3 molar equivalents, optimized in route scouting; adjusted depending on substrate concentration, target cost, and product profile for each campaign.

    Downstream process integration

    • Charged during transformation of aromatic precursors, following protection/deprotection steps or oxidation-sensitive functional group introduction; implemented at kilogram to multi-kilogram scale with temperature and pressure monitoring.

    Final product types

    • Trifluoroacetoxylated aromatics for custom reagents
    • Fluorinated intermediates for pharmaceutical, agrochemical, or performance additive development
    • Building blocks for advanced lubricants and surfactants
    • Contract synthesis products for downstream users

    5. Advanced Organic Fluorination Reactions (Research & Pilot Production)

    Academic and industrial R&D centers conducting scale-up of novel fluorination methodologies apply this hypervalent iodine reagent to achieve site-selective introduction of –OC(O)CF3 and pentafluorophenyl groups in aromatic compounds. This approach underpins high-value pilot campaigns for next-generation catalysts and reference standards.

    Industry compliance standards

    • Internal SOP compliance (GLP for R&D; relevant to ISO/IEC 17025 accredited labs)
    • Hazardous chemical management per local/national regulation (e.g. OSHA 29 CFR 1910.1200)
    • Documentation for scale transfer complying with technology transfer guidelines (e.g. ICH Q10)
    • Custom in-house analytical validation protocols (NMR, HPLC, GC-MS)

    Typical usage ratio

    • 0.2 to 1.0 molar equivalents, tailored case-by-case per substrate and desired level of functionalization; adjusted for scale-up validation from gram to multi-kilogram scale.

    Downstream process integration

    • Employed in batch reactors during pre-functionalization or direct arylation stages, often as a final or penultimate reaction step before purification and scale-up to pilot plant quantities.

    Final product types

    • Reference standards for analytical chemistry
    • Novel organofluorine catalysts
    • Library compounds for pharmaceutical screening
    • Intermediates for subsequent downstream fluorination or coupling reactions
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    Certification & Compliance
    More Introduction

    Introducing Bis(Trifluoroacetoxy)IodoPentafluorobenzene: Experience Direct from the Source

    In the business of building chemistry that lasts, even subtle changes in reagent structure can shape outcomes in ways that years of experience reveal best. We manufacture Bis(Trifluoroacetoxy)IodoPentafluorobenzene, known to our R&D and production teams as a reliable, high-performance hypervalent iodine reagent. Every batch developed in our facility takes into account the priorities faced by researchers and process engineers: high purity, predictable reactivity, and shelf stability. The demand for clean electrophilic fluorination and selective oxidations keeps climbing, and our expertise in organofluorine chemistry reflects our commitment to advancing the frontier, not just following it. Working with this molecule daily — in tons, not grams — reinforces what we already know: nuanced chemistry deserves reagents that simply work the way you need them to, run after run.

    Model, Grade, and Specifications Straight from Production

    The Bis(Trifluoroacetoxy)IodoPentafluorobenzene batches we produce run at consistently high purity, confirmed by in-house GC-MS, NMR, and HPLC. Material comes as a pale solid, free-flowing, with moisture content controlled through every phase of handling. Internal benchmarks demand iodination levels above 99%, fluorine content within a tight margin, and rigorous particle size control to support easy weighing and smooth transfer into your processes. We oversee raw materials from fluorine sources right through to the final crystalline product, since shortcuts in starting material quality erode not just yield, but reproducibility. Every container carries the batch’s analytical fingerprint, so your lab or plant gets the same results we’ve validated on-site.

    How We See Usage: Not Trends, But Proven Value

    Our customers tell us the real-world value of Bis(Trifluoroacetoxy)IodoPentafluorobenzene comes through in transformation steps where conventional oxidants tend to fizzle. You notice this immediately in aromatic fluorination—whether you’re enhancing biological activity in a pharmaceutical intermediate or aiming for a tighter selectivity in a materials science route. In our own application trials, this molecule opens up efficient oxidative cross-couplings and clean functionalizations, even with tricky heteroaromatics or electron-rich arenes. We’ve seen solid performance, particularly in oxidative coupling, direct C-H activation, and as a fluorinating tool when you want to avoid harsh metals or moisture-sensitive conditions. Researchers trust it for scalable conversions too, since the product’s solubility profile means consistent performance in both small glassware and larger steel reactors.

    From decades of synthesis scale-up and troubleshooting, we appreciate what it means for a hypervalent iodine reagent to deliver without fuss—no surprise side-products, no headaches in work-up or purification. As a manufacturer, we prefer to keep things grounded and measurable, steering clear of theoretical value and focusing on what delivers reliable chemistry under pressure.

    Why We Produce It: Understanding Where It’s Different

    Plenty of hypervalent iodine oxidants exist, and over the years we’ve produced several in scale. Our technical team knows that structure matters, not just in reactivity, but in how reagents handle throughout the entire chemical lifecycle. Bis(Trifluoroacetoxy)IodoPentafluorobenzene stands out for two practical reasons. The pentafluorobenzene core drives both reactivity and selectivity in electrophilic transformations. Unlike products based on simple iodobenzenes or less fluorinated scaffolds, this reagent resists undesired side-reductions, thanks to the electron-deficient ring system. You notice reduced byproduct formation, especially in late-stage functionalizations where every percent matters. Our analysis also confirms that trifluoroacetoxy ligands confer greater leaving group capability, translating to more efficient substrate activation and cleaner recoveries.

    From process chemistry to medicinal chemistry labs, the switch to this molecule cuts down on purification hassle. Many in the industry still rely on more generic hypervalent iodine reagents like PIFA or PIDA, which have their strengths but tend to leave more aromatic iodinated byproducts or require more aggressive scavenging. With Bis(Trifluoroacetoxy)IodoPentafluorobenzene, researchers return to us reporting sharper, more reproducible NMR and LC outputs, less column time, and easier mass-balance reconciliation. The distinctive pentafluorophenyl structure clears up bottlenecks where typical iodine-based oxidants fall short, in part due to better solubility in organic solvents and a reduced profile of problematic heavy-metal co-products.

    Manufacturing Perspective: From Raw Materials to Finished Product

    From our bench-scale methods decades back, we learned that controlling every variable in hypervalent iodine chemistry reduces headaches for our customers. We keep tight control over raw material purity, especially sources of pentafluorobenzene and trifluoroacetic anhydride, since trace metals and organic residues can spark side-reactions in sensitive downstream chemistry. Our reactors run at low temperature to avoid undesired overoxidation, and in-line monitoring checks both fluoride content and free iodine levels. This zero-tolerance policy for cross-contaminants isn’t marketing—batch batches that drift from spec get reprocessed or trashed. Unwavering control means you see fewer failures, especially at kilo-scale and beyond, where “almost good enough” batches sink expensive runs.

    Storing and shipping highly fluorinated organoiodine compounds requires planning for moisture and light sensitivity. We developed amber glass and bulk carbon-lined containers after seeing how shelf vibrancy fades with slipshod packing. Even short journeys under suboptimal packing lead to measurable degradation, so our logistics team packs according to the same standards they apply to our own R&D stock. That way, our customers receive fresh, free-flowing material, even after overseas air freight or ground handling. We check for peroxide and acid formation at release, meaning your reagents don’t just meet numbers—they actually work the way they’re supposed to, right from unsealing.

    What Experience Taught Us About Applications

    Direct feedback loops from advanced materials scientists, process chemists, and pharmaceutical teams sharpened our approach to manufacturing Bis(Trifluoroacetoxy)IodoPentafluorobenzene. Discovery teams favor it for late-stage aromatic fluorinations and complex oxidations. In-house, we’ve observed a practical edge in transformations such as O-alkylations, oxidative dearomatizations, and transition-metal-free coupling of electron-deficient systems. As process scale increases, so do minor byproducts. The tight control over side product generation here stands out versus other hypervalent iodine options, especially when trace contaminants could cost a campaign weeks or even months. We share data openly as part of our tech transfer process, feeding real-world lessons into every new production loop.

    Sometimes, customers expect miracles from new reagents. But after hundreds of pilot runs and process development meetings, we’ve found that realistic, incremental victories matter most. Bis(Trifluoroacetoxy)IodoPentafluorobenzene performs reliably across a range of solvents, even handling well in polar aprotic “workhorse” media like DMF and acetonitrile. Product loss drops and isolation steps shorten, often saving days on mid-scale synthesis timelines. Batch-to-batch reproducibility – measured right here in our plant, not guessed in a marketing office – remains high, which is why contract synthesis partners and production technologists build it into their mainline processes instead of relegating it to niche applications. Tracking returned product numbers dropped off after we introduced our new filtration and drying step three years ago, and customer complaints on mixability — once a minor headache — now rarely occur.

    Common Questions: Our Take, Not Scripted Answers

    Visitors touring our facility often ask what makes this compound a better choice than the usual PIDA, PIFA, or other market stalwarts. The difference lies in handling and performance, not just tables and theory: old standards deliver fine for textbook oxidations, but costs start mounting when isolating products free of iodine residues or heavy aromatic byproducts drags down yield. Some syntheses demand both high selectivity and minimal heavy atom footprint. Even at kilogram scale, Bis(Trifluoroacetoxy)IodoPentafluorobenzene leaves less to manage post-reaction, cutting waste disposal costs and purification cycles. Environmentally, this translates to lower burdens, with easier compliance in regulated workflows.

    We’ve weighed complaints about price, too—premium reagents cost more up front, but our own process chemists insist that quality inputs trim far larger losses in failed runs or costly troubleshooting. For projects on a tight schedule or locked to a crouched budget, the math favors predictability, not surprise salvage efforts. This hypervalent iodine’s thermal stability rating ranks unusually high, thanks to the pentafluorobenzene core, so shelf life stretches comfortably past lower-grade alternatives. Even after repeated uncapping, our QC teams consistently measure full reactivity after two years in storage, under recommended dry conditions and away from direct sunlight.

    Feedback Loops: Continuous Improvement from Real Use

    No matter how many applications we test in-house, the most valuable lessons come from direct, constructive talks with experienced chemists. One pharmaceutical team recently streamlined a late-stage arene fluorination step with our reagent, boosting yield and slashing byproducts. They reported fewer chromatography cycles and higher purity of their target compound—metrics we care about ourselves. Analytical chemists working on specialty monomers found that pulsed additions of Bis(Trifluoroacetoxy)IodoPentafluorobenzene gave sharper control over reaction exotherms than other iodine sources, reducing thermal runaway risks. Several material science groups credit the product’s solubility window with opening new fluorinated scaffolds, some even previously written off as impossible with competing oxidants.

    It’s easy to overlook details—humidity, dosing rate, or even stirrer speed. But years fielding help calls taught us how minor parameters shift outcomes. For those scaling up from gram to kilo, trustworthy technical data and predictable particle morphology stop blunders before they start. After integrating customer suggestions, our current lots disperse cleanly, even in challenging continuous-flow systems. This isn’t marketing, just response to the lessons the chemistry community shares back with us.

    A Manufacturer’s Eye for Quality Control

    We guard each step of the process carefully, aware that hypervalent iodine reagents don’t forgive sloppiness. Producing at industrial scale brings challenges seldom seen at bench scale. Moisture pick-up and oxygen exposure degrade many oxidants quickly—a reality our early batches made all too clear. Aggressive nitrogen blanketing, in-process water scrubbing, and low-light conditions now form part of our standard workflow. In-process controls watch not just main product formation, but also build-up of iodo byproducts or potentially explosive intermediates. A decade ago, we accepted higher fractions of waste; now, emerging sensor tech and improved isolation steps let us cut unnecessary loss and raise effective yield.

    Documentation and transparency remain part of our promise to buyers. With complex molecules like this, open access to batch data arms chemists with the confidence to adjust process parameters without risking costly setbacks or compliance nightmares. Internally, we train every shift on reagent-specific hazards and safe storage—practices learned the hard way, by cleaning up spills and tracking purity drift after rough handling.

    Solutions for Common Adoption Barriers

    Some research teams hesitate to switch reagents, wary of any hiccup in established syntheses. We address this concern with samples, detailed tech packets, and open channels for method sharing. Support means more than providing an MSDS—it’s hands-on troubleshooting, site visits, or even splitting pilot lots for in-house validation. As manufacturers, we maintain pilot reactors for rapid turnaround of custom formulations, particle sizes, or targeted impurity levels, since nobody benefits from a one-size-fits-all approach for complex oxidative needs. Our internal reactivity database gets updated with each new customer feedback loop, matching application with performance data.

    Waste management always comes up in these discussions, particularly from teams scaling beyond gram quantities. With Bis(Trifluoroacetoxy)IodoPentafluorobenzene, lower inherent iodine and metal residue result in cleaner aqueous waste after quenching, translating to easier, less costly disposal. Our EHS specialists monitor downstream impact and help partner labs adapt quenching or neutralization to local rules, so compliance doesn’t blindside anyone mid-campaign. The continued shift toward greener chemistry finds this reagent a better choice when teams want to avoid heavy-metal co-oxidants or persistent organic residues. Every batch ships with an eye to total lifecycle, not just immediate use.

    Looking Forward: The Manufacturer’s Perspective

    Building a reputation for trustworthy hypervalent iodine chemistry means more than shipping reliable material—it takes learning from mistakes and never underestimating the fine details. Cleaner transformations, higher selectivity, and robust safety profiles grow out of relentless attention at every link in the chain, from raw chemical purity through shipping and storage to support after the sale. The fact that more and more innovators return to Bis(Trifluoroacetoxy)IodoPentafluorobenzene with new challenges tells us that chemistry thrives when supported by direct, honest manufacturing experience. No market trends or empty promises—just proven, practical value from one lab to another, from our floor to yours.