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Pentafluorobenzene

    • Product Name Pentafluorobenzene
    • Alias PFB
    • Einecs 205-924-1
    • 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

    201113

    Iupac Name Pentafluorobenzene
    Cas Number 363-72-4
    Molecular Formula C6HF5
    Molar Mass 168.06 g/mol
    Appearance Colorless liquid
    Density 1.542 g/cm3
    Boiling Point 84 °C
    Melting Point -37 °C
    Solubility In Water Low
    Flash Point 28 °C
    Vapor Pressure 60 mmHg (20 °C)
    Refractive Index 1.402 (20 °C)
    Smiles C1=C(C(=C(C(=C1F)F)F)F)F

    As an accredited Pentafluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Pentafluorobenzene, 100 mL amber glass bottle, tightly sealed with PTFE-lined cap, labeled with hazard symbols and chemical identification.
    Shipping Pentafluorobenzene should be shipped as a hazardous chemical, packed in tightly sealed containers compatible with organic solvents. It must be labeled according to relevant regulations (such as UN 2619, class 3, flammable liquid), and handled with care to avoid leaks, exposure, and ignition sources during transport. Store upright, away from heat or incompatible materials.
    Storage Pentafluorobenzene should be stored in a tightly sealed container, away from moisture, heat, and incompatible materials such as strong oxidizing agents. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight and sources of ignition. Use chemical-resistant storage containers and ensure proper labeling. Follow local regulations for flammable and environmentally hazardous chemicals during storage and handling.
    Application of Pentafluorobenzene

    Applications of Pentafluorobenzene in Industrial Manufacturing

    Pentafluorobenzene serves as a critical building block in multiple industrial manufacturing sectors that require highly fluorinated aromatics. Its unique chemical structure and fluorination pattern make it suitable only for certain advanced applications where specific reactivity and stability are necessary. Below, we detail the primary downstream application scenarios where this material delivers consistent performance and meets strict regulatory and formulation demands.

    1. Agrochemical Intermediate Synthesis

    Leading crop protection companies utilize pentafluorobenzene in the synthesis of fluorinated phenyl scaffolds, critical for selective herbicides and insecticides. This aromatic serves as a precursor for constructing complex active molecules via direct arylation or nucleophilic aromatic substitution, providing both electronic deactivation and site-selective reactivity. Its precise integration requires strict control during multi-step synthesis and full compliance with pesticide registration protocols in major agricultural markets.

    Industry compliance standards

    • FAO Specification for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 on placing plant protection products on the market
    • US EPA National Pesticide Standards
    • ISO 10668 for active pesticide ingredients

    Typical usage ratio

    • 5–15% of precursor formulation by mole, adjusted based on target molecule yield and downstream conversion selectivity.

    Downstream process integration

    • Introduced during Stage 1 or 2 of active ingredient assembly; reacts under controlled conditions (120–150°C, inert atmosphere) via catalytic or nucleophilic aromatic substitution.

    Final product types

    • Selective herbicides (triazinyl-, oxadiazolyl-based actives)
    • Fluorinated phenyl-pyrazole insecticides
    • Intermediates for fungicide actives

    2. Pharmaceutical API Intermediate Production

    Pharmaceutical manufacturers use pentafluorobenzene to assemble advanced intermediates for APIs—especially those requiring strong carbon-fluorine bond contributions to metabolic stability or receptor affinity. Integration occurs mainly in the synthesis of rare disease and oncology molecules, demanding validated impurity profiles and reproducible batch-to-batch quality. Regulatory dossier submission requires rigorous tracking of precursor quality and trace-level impurity carryover.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.) monograph compliance where applicable
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 3–10% by mass in multi-step synthesis; precise level depends on route optimization and desired fluorine incorporation.

    Downstream process integration

    • Reaction as the first or second aromatic component under Pd-catalyzed coupling or SNAr conditions, followed by protective group removal and downstream functionalization, with inline HPLC monitoring.

    Final product types

    • API intermediates for kinase inhibitors
    • Small-molecule drugs with high-fluorine content
    • Final APIs in oncology and antiviral segments

    3. Specialty Polymer Monomer Manufacturing

    Producers of high-performance fluorinated polymers rely on pentafluorobenzene as a monomer or functional comonomer in the creation of specialty copolymers. This component imparts remarkable chemical resistance and low surface energy, key for demanding environments such as diaphragms, membranes, or advanced barrier films. Such incorporation requires precise reactivity assessment to avoid unwanted polymer branching and guarantee uniform distribution of fluorinated functionalities.

    Industry compliance standards

    • ISO 9001:2015 for polymer manufacturing
    • ASTM D7799 (Standard Test Method for Flammability properties of high-fluorine polymers)
    • REACH Regulation (EC) No 1907/2006 for chemical registration in Europe
    • Food Contact Notification (FCN) standards when polymers are used for food contact applications

    Typical usage ratio

    • 0.5–8% by monomer feed weight; finalized after reactivity ratio testing and mechanical property validation according to downstream usage.

    Downstream process integration

    • Feeds as a co-monomer during bulk or emulsion polymerization, typically under controlled atmosphere and elevated pressure; followed by melt-compounding and extrusion for film or membrane fabrication.

    Final product types

    • Fluorinated ion-exchange membranes
    • Fuel cell and battery separator films
    • Specialty coatings for electronics and aerospace

    4. Electronic Chemical Synthesis for Liquid Crystal Materials

    Advanced electronic chemical manufacturers incorporate pentafluorobenzene into the synthesis of highly fluorinated liquid crystal (LC) monomers, tailored for high-precision display panels and electro-optic devices. Its unique fluorination allows for the tuning of dielectric anisotropy and viscosity, essential in achieving high contrast and rapid switching times in LCD fabrication. Stringent trace impurity management and batch traceability are enforced during precursor handling and downstream functionalization steps.

    Industry compliance standards

    • IEC 61249-2-43 (Halogen-free electronic materials specification)
    • RoHS Directive 2011/65/EU (for LC device components)
    • JEDEC JESD22 standard for moisture and contaminant control
    • ISO 14644 for cleanroom processing

    Typical usage ratio

    • 2–7% per LC functional group synthesis, ratio optimized for dielectric and optical requirements in target LC blends.

    Downstream process integration

    • Used in aromatic nucleophilic substitution for LC core structure assembly; enters at initial LC monomer synthesis before esterification/functionalization and LC blend formulation.

    Final product types

    • TFT-LCD display panels
    • Electro-optical LC films
    • High-frequency communication substrates with LC polymers
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    Certification & Compliance
    More Introduction

    Pentafluorobenzene: Stepping Forward in Specialty Chemistry

    Our Perspective on Pentafluorobenzene

    Years of involvement in fluorination chemistry taught us that quality in specialty organofluorines begins at synthesis, not just in a lab notebook but in each vessel, under every fume hood. Pentafluorobenzene belongs to a fascinating class of compounds—aromatic rings where substitution changes how molecules behave. With the molecular formula C6HF5 and a purity exceeding 99.5% GC, this compound highlights the shift from legacy halogen chemistry towards better performance in demanding applications.

    Pentafluorobenzene isn’t a base chemical folks reach for in bulk commodity trades. Chemists in the field often seek out this product for its para-fluorine activation, which most see as a clear path to further functionalization. We produce pentafluorobenzene as a colorless liquid, typically bottled in fluoropolymer-lined steel containers or amber glass to avoid light-triggered decomposition. Our material leaves the facility tested for residual acid, trace metals, and GC purity, because downstream catalytic or pharmaceutical work doesn’t tolerate inconsistency.

    What Sets Pentafluorobenzene Apart?

    Pick up a bottle of standard fluorinated aromatics and you’ll spot the difference in both aroma and reactivity. Chlorobenzene, for instance, doesn’t match the activity or electron deficiency seen in pentafluorobenzene. Here, five fluorines pull electron density away from the ring far more aggressively than other halogens, creating an excellent entry point for nucleophilic aromatic substitution. That’s why researchers in agrochemical labs and pharmaceutical R&D often insist on this molecule instead of less-substituted alternatives.

    Handling this product through the years, our technicians have noticed the contrast in stability during storage compared with other polyfluorinated benzenes. Lower levels of acid residue mean better shelf-life and less risk of contamination downstream. That small difference can determine whether a kilo of a new API intermediate works or ends up wasted. Our batch-to-batch consistency stems not only from synthetic finesse, but also from old-fashioned diligence—centralized cold storage, closed-loop transfer lines, and hands-on sample testing in a monitored facility.

    Main Uses: Where Pentafluorobenzene Carries Its Weight

    Organic chemists around the globe reach for pentafluorobenzene at the crucial step of N- or O-arylation, often exploiting the ring’s strong activating effect for nucleophilic substitution. For example, it enables straightforward introduction of amine, ether, or thiol functionalities at positions usually stubborn in non-fluorinated compounds. Agrochemical labs pursue it to develop herbicide and insecticide leads where metabolic robustness matters.

    Pharmaceutical synthesis requires building blocks stable to oxidation, with predictable substitution behavior. Pentafluorobenzene delivers both, and its use spans heterocycle construction, radiolabeling for PET tracers, and creation of drug fragments unlikely to metabolize through unwanted pathways. Researchers keep an eye on supply chain reliability for this compound; we respond by synchronizing our runs to match seasonal upticks from universities and biotech companies, something third-party traders rarely manage without factory-level control.

    Insights: Processing, Handling, and Real-World Concerns

    Many of us remember the shift a decade ago, when smaller reactors and better venting allowed growth in the production of high-purity pentafluorobenzene. Demand didn’t skyrocket overnight, but as more research groups uncovered the utility of polyfluorinated rings, feedback bounced straight to manufacturing. Historically, early suppliers struggled with HF contamination and oxidized impurities. That made for troublesome purification and lower safety margins, especially in scale-up settings. We solved this using improved scrubbing towers and precise temperature profiling.

    Tightly controlling reaction atmosphere limits side reactions, a lesson learned from batches lost to moisture ingress. Open-flask techniques common in other aromatic syntheses don’t hold up for reactive fluorinated aromatics. Our operators stick to closed transfer under nitrogen or argon, which guarantees that each drum or bottle leaves with less than 50 ppm water by Karl Fischer titration. End-users appreciate this care; downstream derivatizations stop stalling, and finished actives reach market trials on time.

    Specification Details Gleaned From the Field

    Spec sheets list melting point at -26°C, boiling point near 85°C under ambient conditions, and density close to 1.6 g/cm3. These aren’t just numbers—we track them batch after batch, spotting subtle deviations that can warn us about heat exchanger fouling or contamination upstream. Purity above 99.5% ensures almost complete consumption in substitution reactions; after lowering trace THC and HF to below industry benchmarks, chromatography columns last longer and scaling up new processes takes less effort.

    Many buyers ask about color stability and odor. Pure pentafluorobenzene gives a faint, sweet and almost medicinal smell—very different from the acrid notes of chlorinated aromatics like hexachlorobenzene. If a batch turns faintly yellow, we check for polymerized impurities. Addressing batch color early nips potential oxidative breakdown in the bud, which keeps the focus on actual chemistry rather than troubleshooting supply chain headaches.

    Comparisons With Related Aromatics

    Pentafluorobenzene offers tangible advantages against trifluorobenzene or even perfluorobenzene. The extra fluorine atoms create a more pronounced electron-withdrawing effect, enhancing reactivity at the one available hydrogen site. That lone hydrogen, accessible only on the 1-position, leads to highly directed, predictable substitution patterns—critical for synthetic planning in complex molecule construction.

    Perfluorobenzene lacks any hydrogen, closing off direct substitution and limiting its use as a precursor for more complex products. On the other hand, trifluorobenzene comes in multiple isomers; getting a consistent substitution pattern is not reliable, so pentafluorobenzene’s straightforward reactivity provides immediate value for scale-up processes. Our customers point out that, compared to other fluorinated aromatics, purification flows more smoothly and reaction conditions require less fine-tuning.

    Manufacturing: Why Real-World Experience Matters

    Working in this sector day after day, direct exposure to the challenges of fluorinated chemistry gives valuable insight. The literature can mention idealized routes, but only through repeated campaigns have we optimized columns, resin beds, and reactor linings suitable for this class of molecules. Customers frequently share stories of batches sourced from outside the original manufacturer that arrived degraded, often because traders repack or warehouse material under suboptimal conditions.

    We stick to original packaging engineered for volatile, corrosive liquids—meaning new fluoropolymer liners and cleanroom filling. Trace acids in the product are more than an annoyance; they can halt an entire pilot plant or block up a chromatography column. Our protocol checks each batch by both GC and NMR to confirm not just purity but molecular identity—important, since near-identical contaminants can slip past basic quality control. If a drum fails our own standards, it never leaves the premises.

    Challenges in Shipping and Storage

    Pentafluorobenzene’s volatility brings some logistical challenges. Temperature-controlled transport ensures stability, while specialist carriers prevent leaks or exposure. Unlike lower-boiling or highly reactive products, pentafluorobenzene tolerates cross-continent shipping with minimal risk of decomposition, given correct storage. But careless handling increases the odds of hydrolysis or accidental contamination; that’s why we ship directly, skipping trans-shipments or unnecessary repacking.

    Clients have occasionally reported issues with shipments handled by non-manufacturers—repeat exposure to sunlight, poor repackaging into inadequate glassware, or loss caused by condensation. Those issues reinforce the lesson that direct line-of-sight from synthesis to user makes all the difference, especially for custom derivatives or time-sensitive projects. In-house logistics teams keep a clear record of batch movements, and downstream clients receive not just the product, but the assurance of traceability and reliability.

    Supporting Innovation, Not Just Delivering Chemicals

    Over the years, pentafluorobenzene evolved from a specialty research reagent to a key intermediate for advanced materials, pharmaceuticals, and agrochemical products. Our involvement goes beyond synthesis—we support application development, echoing the needs of both academic research and industrial innovation. Many research groups develop new coupling partners and invent ligands or catalysts built around this core. Sharing best practices in purification or storage often saves clients avoidable setbacks.

    Customers value the exchange of real-world tips: storing under inert atmosphere, avoiding long-term exposure to light, using proper safety shielding when scaling up. Some forward-looking teams experiment with green synthetic routes, using defluorination techniques or recycling spent reagents. Our plant continuously reviews greener alternatives for reagents and solvents, investing in solvent recycling and emission capture that drive down waste and lower energy consumption—a response rooted in feedback from end-users and regulatory changes on halogenated waste.

    Regulatory Trends and Market Outlook

    Sustained market growth appears likely as both pharma and agrochemical industries advance toward more metabolically stable and potent molecules. Regulatory change in key jurisdictions emphasizes both worker safety and environmental compliance. Unlike older halogenated chemicals, pentafluorobenzene faces fewer restrictions around environmental persistence, though careful tracking and waste-handling remain central to responsible production. Regular audits keep us in line with both international regulatory bodies and local environmental authorities.

    We’ve set up dedicated emission controls and solvent recovery systems to limit the environmental footprint. Continuous improvement in handling and process design also keeps us ahead as new guidelines emerge, especially for waste management of spent acids and fluorinated residues. Regulatory teams work in tandem with chemical engineers, closing gaps fast—because compliance doesn’t happen in a vacuum, and downstream customers shouldn’t bear the risk of outdated practices.

    Direct Customer Feedback Shapes the Product

    Listening to experienced chemists and technicians helped us refine both the synthetic and logistical side of pentafluorobenzene. Some R&D labs pointed out minor variations in impurity levels when switching between suppliers; that motivated tighter specification thresholds in our own facility. Others noted problems during scale-up, where trace hydrofluoric acid led to equipment corrosion and slower throughput. We responded by lowering HF residue and adopting more frequent in-line analysis.

    Crowdsourcing feedback from process development teams, we adapted our storage guidance, improving inert gas blanketing, and reducing headspace to lower oxidative stress during shipment. New project managers appreciate having access to staff who’ve handled both kilo-lab and ton-scale orders—offering not just material but actual troubleshooting tips gleaned from years of hands-on experience. This responsiveness, in turn, inspires confidence for clients stretching into new applications or complex syntheses.

    Building Relationships—Not Just Transactions

    Making pentafluorobenzene in volume involves technical skill, but maintaining trust with chemists and researchers working downstream matters just as much. For one-off orders, we keep channels open for post-delivery technical follow-up. Ongoing partnerships see regular site visits and audits, drawing on shared risk management—because, for most projects, the cost of a missed deadline or contaminated intermediate outweighs the price of the raw material itself.

    By advocating direct communication between synthetic teams and production engineers, we cut down on the headaches that come from miscommunication across supply chains. Providing real, up-to-date batch records and transparent handling advice minimizes avoidable surprises and keeps research moving forward. Every batch that leaves our warehouse reflects decades of technical refinement and the benefit of lessons learned from clients pushing the limits of modern fluorinated chemistry.

    A Future for Pentafluorobenzene—Shaped By Real Needs

    Manufacturing pentafluorobenzene doesn’t stand still. Each year brings changes in application scope, safety expectations, and customer priorities. Today, expanding use in nucleophilic aromatic substitution and the creation of metabolically robust molecules drives both production volume and technical development. Researchers investigating new medical imaging agents, or environmental scientists in search of durable tracers, turn to us for material that meets not just a standard, but a promise of reliability.

    By drawing on direct manufacturing experience and responding to concrete feedback from the lab bench, we continue to raise standards in purity, consistency, and safe handling. Pentafluorobenzene stands out for its practical value in real-world syntheses, owing not just to its unique chemical structure but to careful preparation and the trust of chemists worldwide.