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Decafluorobiphenyl

    • Product Name Decafluorobiphenyl
    • Alias Perfluorobiphenyl
    • Einecs 206-199-1
    • 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
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    Specifications

    HS Code

    367547

    Chemicalname Decafluorobiphenyl
    Casnumber 322-70-3
    Molecularformula C12F10
    Molecularweight 336.11 g/mol
    Appearance White crystalline solid
    Meltingpoint 81-83 °C
    Boilingpoint 209-210 °C
    Density 1.885 g/cm3
    Solubilityinwater Insoluble
    Refractiveindex 1.461
    Smiles C1(=C(C(=C(C(=C1F)F)F)F)F)C2=C(C(=C(C(=C2F)F)F)F)F

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

    Packing & Storage
    Packing Decafluorobiphenyl is supplied in a 25-gram amber glass bottle, sealed with a PTFE-lined cap, and labeled with hazard information.
    Shipping Decafluorobiphenyl is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent leaks and contamination. Packages are clearly labeled with appropriate hazard warnings and shipped in compliance with regulations for transporting hazardous chemicals, including documentation and handling instructions to ensure safety during transit.
    Storage Decafluorobiphenyl should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong bases and oxidizers. Keep it in a tightly sealed container made of compatible material, and clearly label the container. Store it away from direct sunlight and moisture, and use secondary containment to prevent accidental release or spills.
    Application of Decafluorobiphenyl

    Applications of Decafluorobiphenyl in Industrial Manufacturing

    Decafluorobiphenyl is an aromatic perfluorinated compound valued for its chemical stability, remarkable electron-withdrawing character, and performance as a specialty synthon in technical manufacturing. We directly supply this grade to key sectors utilizing its unique reactivity and compatibility for advanced synthesis, polymer modification, and specialty electronics.

    1. Electronic-Grade Liquid Crystal Alignment Layers

    Decafluorobiphenyl functions as a precursor in high-purity alignment layer materials for liquid crystal displays (LCDs) and organic electroluminescent panels. Its robust perfluorinated aromatic structure delivers controlled surface energy and anchoring properties critical for uniform LC orientation, enabling sharper contrast ratios in finished devices. Raw material addition requires strict moisture and contaminant controls to avoid impact on downstream photoalignment and polymerization quality within cleanroom environments.

    Industry compliance standards

    • SEMATECH Technology Roadmap (for display materials)
    • IEC 62341 (OLED display performance and reliability)
    • RoHS Directive for halogenated residues
    • ISO 9001:2015 for process traceability in LC films

    Typical usage ratio

    • 0.5–1.5% by mass in functional polymer layer formulations; slightly varied depending on target pretilt angle and film thickness requirements

    Downstream process integration

    • Introduced during prepolymer solution synthesis; dissolved fully in electronic-grade organic solvents and reacted under inert atmosphere conditions before coating onto substrates

    Final product types

    • LCD alignment films for consumer and automotive displays
    • OLED panel backplanes
    • Photoaligning agents for advanced display technologies

    2. High-Performance Fluorinated Polyimide Manufacturing

    As a difunctional monomer, decafluorobiphenyl participates in nucleophilic aromatic substitution to generate fluorinated polyimide chains for high dielectric strength films used in flexible circuit boards and thermal insulation. Its incorporation improves hydrophobicity and thermal oxidation resistance versus standard imide matrices, supporting demand for longer service life in electronics subjected to repeated flexing and extreme temperatures.

    Industry compliance standards

    • IPC-4101/41 (flexible base materials)
    • UL 94 VTM-0 (flame retardance for flexible films)
    • REACH regulation (perfluorinated chemical monitoring)
    • JIS C2318 (polyimide film testing)

    Typical usage ratio

    • 1.8–3.5 mol% of total dianhydride-diamine equivalent, tunable by molecular weight and film flexibility target

    Downstream process integration

    • Dissolved and reacted in mixed aprotic solvents with diamines; introduced at polyamic acid synthesis step prior to chemical imidization and film casting or spin-coating

    Final product types

    • Flexible printed wiring boards (FPCs)
    • High-temperature-resistant cable wraps
    • Thin-film insulation for aerospace and mobile electronics

    3. Pharmaceutical Intermediate – Nucleophilic Aromatic Couplings

    Decafluorobiphenyl provides a perfluorinated aromatic core for coupling sequences in medicinal chemistry R&D and pilot production. Its susceptibility to SNAr substitution supports attachment of amine- or thiol-containing ligands, giving access to novel moieties for radiolabeling or activation tagging in diagnostic tracer synthesis and molecular imaging probes.

    Industry compliance standards

    • ICH Q7 (GMP for APIs and pharmaceutical intermediates)
    • USP <467> (Residual Solvents in Pharmaceuticals)
    • Ph. Eur. monograph 2034 (Solvents for Synthesis)
    • ISO 17025 (analytical validation for traceability)

    Typical usage ratio

    • 0.25–0.6 molar equivalents relative to nucleophile, with precise adjustment based on stoichiometric demands and isolation yield

    Downstream process integration

    • Employed during parallel library construction or as a key reactant in batchwise aromatic substitution reactions; added to anhydrous reactor systems prior to base activation and purification of coupled products

    Final product types

    • Radiotracer synthesis intermediates
    • Activated perfluoroaryl moieties for molecular diagnostics
    • Specialty pharmaceutical building blocks for imaging agents

    4. Perfluorinated Surface Modification for Analytical Devices

    In microfluidics and sensor fabrication, decafluorobiphenyl acts as a surface modifier to reduce background adsorption of biomolecules and provide durable anti-fouling layers. Its aromatic ring binds selectively to pre-treated silica and polymer surfaces through covalent functionalization, protecting microchannel and capillary interiors under repeated wash cycles and exposure to analytical solvents.

    Industry compliance standards

    • ISO 13485 (medical device quality management)
    • FDA QSR 21 CFR Part 820 for laboratory consumables
    • RoHS 2015/863 (limitations on hazardous substances in test equipment)
    • ASTM F2459 (testing for surface cleanliness of biomaterial devices)

    Typical usage ratio

    • 0.1–0.5% w/v in coating baths, precisely determined by required monolayer thickness and device channel dimension

    Downstream process integration

    • Applied in post-manufacture microfluidic channel silanization; solution activated under mild heating to drive surface functionalization and rinsed before assembly or packaging

    Final product types

    • Lab-on-chip microfluidic devices
    • Capillary electrophoresis columns
    • Disposable biosensor cartridges
    • Diagnostic slide arrays with antifouling coatings

    5. Advanced Fluorinated Aromatic Crosslinkers for Specialty Coatings

    Decafluorobiphenyl supports formulation of chemically resistant coatings for high-value industrial surfaces including semiconductor tools, chemical reactors, and analytical instrument housings. As a multifunctional aromatic crosslinker, it imparts fluorinated character into polyaryl ether or epoxy matrices, significantly extending solvent resistance and lowering surface energy. Users must control addition rates to prevent phase separation and ensure uniform network formation during curing.

    Industry compliance standards

    • ASTM D6578 (chemical-resistance properties of coatings)
    • ISO 12944-6 (performance standards for protective paint systems)
    • FDA 21 CFR 175.300 (coatings for food contact surfaces, if relevant)
    • REACH Annex XVII (control of PFAS in coatings)

    Typical usage ratio

    • 1–7 phr (parts per hundred resin) depending on substrate and desired crosslink density; higher end used for harsh chemical-contact scenarios

    Downstream process integration

    • Added to fluoropolymer or epoxy pre-mixture before application by spray, spin, or dip–followed by controlled thermal or UV curing for polymer network formation

    Final product types

    • Chemical-resistant coatings for semiconductor wet benches
    • Analytical instrument housings
    • Fluorinated tank and reactor linings
    • Protective equipment surface films
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    Certification & Compliance
    More Introduction

    Decafluorobiphenyl: Practical Foundations, Proven Value

    The Reality of Decafluorobiphenyl in Chemical Manufacturing

    At our site, Decafluorobiphenyl doesn’t sit quietly on a shelf. It enters the reactors daily, moving through every process with a kind of reliability that isn’t just theoretical or confined to lab reports. This compound, commonly referenced by its chemical identity, C12F10, remains an essential substrate in our facility’s toolbox, particularly as the demand for robust, highly fluorinated building blocks rises across electronics, specialty coatings, and pharma. Our hands-on work with Decafluorobiphenyl started years ago, driven by a need for consistent high-purity raw material with uncompromising performance.

    Our entire approach begins with sourcing high-quality starting materials. We run multiple purification steps—fractional distillation stands out as our most trusted method. This ensures each lot of Decafluorobiphenyl (CAS 307-07-1) leaves our plant within a purity specification above 99.5%. Any operator can confirm, strict control at each checkpoint is what minimizes variability. The careful hands running these columns know a batch off specification holds up customer processes and increases waste, so there’s no room for loose ends or hope-based QC. We back every drum with batch-level data, no shortcuts.

    Structure and What Makes It Work

    The structure says a lot: two benzene rings joined by a single bond, every hydrogen replaced by fluorine. Decafluorobiphenyl stands apart chemically. We don’t see unwanted side reactions creeping in as with less-fluorinated biphenyls; the ten fluorines shut down reactive sites and bring high chemical stability. This is appreciated in downstream coupling, where reliability reduces troubleshooting and waste. In our reactors, there’s immediate payoff in yields and consistency.

    We introduced Decafluorobiphenyl to our workflow largely because traditional biphenyls (or even partially fluorinated analogs) kept returning inconsistent results. Side reactions, instability, and unpredictable byproducts were costing time and cleanup. Full fluorination brought true inertness, gave us higher yields in Suzuki-type coupling, and saved maintenance on filtration equipment by producing fewer residues. These aren’t theoretical wins—they turn up in manufacturing KPIs and cleaner product streams.

    Real Differences in Practice

    Field work tells the story better than datasheets. Many manufacturers are familiar with biphenyl or tetrafluorobiphenyl. The fully fluorinated Decafluorobiphenyl marks a significant jump. Its melting point sits considerably higher than its partially fluorinated relatives. As a solid at room temperature (with a melting point typically around 48–52°C), it handles easily in standard chemical processing environments. Its exceptional chemical and thermal stability means fewer risks of decomposition or unwanted interaction—a trait every experienced operator values, especially during high-temperature reactions.

    Another practical difference, seldom spelled out in technical summaries, appears during storage and handling. Decafluorobiphenyl shows remarkable resistance to environmental influences—minimal discoloration, no noticeable hydrolysis under ambient humidity, and practically no emission of offensive odors. Both material handlers and process engineers have remarked on its benign storage profile, compared to especially more volatile or malodorous alternatives. This translates to real benefits in safety and maintenance.

    In production settings focused on pharmaceuticals, specialty polymers, and electronic intermediates, a compound’s true value reveals itself under pressure. Our chemists still recall early runs with tetrafluorobiphenyls; unpredictable color bodies, slow crystallization, residual smells—none of these have materialized since moving over to Decafluorobiphenyl as the staple. Instead, we now see greater reproducibility batch over batch. Analyses of reaction byproducts over the past year confirm the point: lower impurity profiles and higher downstream processability.

    Applications from Daily Experience

    Each factory line tells its own Decafluorobiphenyl story, but there are some universals. In our experience, the major use turns up as a robust arylating agent in advanced coupling chemistry, particularly for creating highly fluorinated aromatic frameworks. The electronics sector leans heavily on these structures for manufacturing OLEDs, liquid crystal displays, and high-performance polymers. Consistent feedback from electronic material producers highlighted Decafluorobiphenyl’s role in improving contrast, dielectric constants, and durability of end products.

    It’s also a backbone component in pharmaceutical R&D. Our collaboration with medicinal chemists clarified the value: the fully fluorinated nature reduces metabolic vulnerability, helping lead compounds maintain their structure under both in vitro and in vivo conditions. This advantage often trims months off drug candidate iteration cycles. Researchers we supply have consistently pointed to Decafluorobiphenyl as a preferred starting point for synthesizing heavily fluorinated pharmacophores, where high C–F bond energy blocks unwanted metabolic breakdown.

    Some special polymer lines rely on Decafluorobiphenyl in condensation reactions to impart unusual toughness and inertness. Operators who work these lines note improvements in polymer solution viscosity control and cleaner phase separations. In practice, the stability and solid-state properties mean easier storage and less frequent equipment cleaning, adding up to measurable operating efficiency.

    Material Properties You Notice in Production

    Every property listed on a data sheet eventually meets its test during routine operation. For Decafluorobiphenyl, the most commented-upon practical properties are its purity, its chemical inertness, and its relatively straightforward solid handling.

    Purity matters more than anyone first thinks. With fully fluorinated biphenyl, any tiny impurity—unreacted precursor, side-chain isomer, traces of metal catalyst—magnifies as the synthesis scale grows. From our hands-on perspective, running regular GC-MS and NMR controls on each shipment uncovers trends before they become problems. In the years we’ve handled this molecule, we’ve noticed that frequent, rigorous analytic oversight catches minute batch drift long before it leads to out-of-spec downstream product.

    Chemical inertness emerges clearly. During high-temperature Suzuki and Buchwald-Hartwig couplings, other biphenyl analogs degrade, darken, or shed hydrogen fluoride. Decafluorobiphenyl stands up to both base and acid, resists oxidative environments, and never clouds the product stream. We see lower fouling and nearly nonexistent polymer formation on reactor walls, making each cleanout faster and less hazardous.

    As a solid, Decafluorobiphenyl ships and dispenses easily. Powder flow tests across various batch sizes confirm strong flowability with minimal caking. Our packing crew no longer battles hard clumps or dust-up issues during drumming. A consistent granule size and stable bulk density smooth out both internal logistics and downstream processing, keeping every stage moving predictably.

    Consistent Handling and Logistics Experiences

    Handling Decafluorobiphenyl demonstrates the real-plant difference between a well-designed molecule and a problematic one. From the moment it’s unpacked on the floor, warehouse teams note the lack of any significant odor and the predictable response to standard containment. It avoids both stickiness and dust hazards seen in less-pure or more hygroscopic analogs. Material remains free-flowing across a broad temperature range, never leaving residues on utensils or transfer equipment. Workers switching from less fluorinated biphenyls mention fewer respiratory complaints, and OSHA logs confirm a lower number of handling-related incidents over the years.

    Shipping brings its own challenges with specialty chemicals. Many aromatic compounds require tightly monitored containers or inert atmosphere packaging. Our internal monitoring shows Decafluorobiphenyl ships safely in standard fluoropolymer drums, without aggressive secondary containment or inerting step. Packages reach buyers unchanged, which maximizes shelf life and reduces costs tied to special packaging or insurance surcharges.

    On rare occasions involving long-distance seafreight, we track for potential degradation markers. Real-world stability studies—backed by several years of monthly sample analysis—have yet to show measurable drop in product quality. This stability lowers the total landed cost for our buyers, freeing them from time-critical inventory pressure or risk of writing down batches exposed to shipping delays.

    Comparison with Other Aromatic Fluorocarbons

    Biphenyl chemistry includes a broad family of partially and fully fluorinated materials. From hands-on experience, Decafluorobiphenyl stands apart, not just on paper but on the factory floor and in purchasing records.

    Partially fluorinated biphenyls—like tetrafluorobiphenyl—still show occasional reactivity. They pick up moisture and sometimes darken upon long storage. Chlorinated biphenyls or other halogenated analogs introduce toxicity or challenging disposal issues, making waste management a recurring headache. Our own environmental compliance team tracks no special emissions controls for Decafluorobiphenyl—waste streams are both predictable and manageable.

    In terms of process chemistry, Decafluorobiphenyl’s clean reaction profile means less purification, which reduces solvent use, saves energy, and translates into fewer process interruptions. Customers processing electronics-grade intermediates often point to Decafluorobiphenyl as uniquely suited for high-purity applications where trace reactivity ruins yields. Further, our downstream partners note fewer instances of fouled chromatography columns and less loss in high-throughput automated systems than with partially fluorinated alternatives.

    Safety and Environmental Performance in Action

    Every chemical plant weighs material safety during both normal and abnormal conditions. Having handled thousands of kilograms over years, we know Decafluorobiphenyl doesn’t invite the sort of acute hazards posed by some high-vapor-pressure aromatics. Our air monitoring records consistently show workplace values well below occupational exposure limits, and handling protocols remain straightforward. The lack of volatility means no frequent exposure incidents—no sudden spikes needing emergency action.

    As for environmental responsibilities, this compound’s high stability pays dividends. It does not break down easily in the environment, so waste incineration protocols neutralize it thoroughly. Regular emissions testing at our plant and downstream in our customers’ operations has confirmed that stack outputs stay well within legal parameters, and no unusual remediation steps have been called for historically. Being able to rely on such consistent performance means safety officers and process engineers spend their time optimizing for throughput rather than incident response.

    Cost Dynamics and Value to Users

    For most buyers, Decafluorobiphenyl aligns cost with delivered value. Initial quotes occasionally elicit questions about price vs. commodity aromatic substrates, but we see the full picture on a process-wide basis. Batches run with Decafluorobiphenyl deliver higher yields, predictability in timelines, and lower operating costs from less downtime. This compresses the true cost per kilo of finished specialty polymer or active pharmaceutical ingredient. Several users formerly on tetrachloro- or mixed-halogen biphenyls have cut waste disposal expenses and analytical runs, trading up for the security and operational visibility that comes with Decafluorobiphenyl.

    By far, our most cost-conscious partners—those tracking every input on high-value targets—have found their spend justified after just a few campaigns. Their internal cost-benefit regressions show real bottom-line gain, beyond just cost/kg.

    Challenges We’ve Faced and Addressed

    No real-world chemical is perfect, and Decafluorobiphenyl presents a few recurring operational challenges. Early in our scale-up work, we found that the commercial manufacturing route required particular care with catalyst recovery. Trace metals, even at ppm levels, altered performance in downstream reactions. We overhauled process trains with upgraded extraction and filtration, which paid off in tighter control, less scrap, and faster turnaround times. Process optimization remains ongoing—our continuous improvement teams work on reducing solvent usage and upgrading to greener purification solvents as waste regulations evolve.

    Also, like most fluorinated aromatics, Decafluorobiphenyl demands strict inventory tracking and preventive machine maintenance. Dust control, even with such a stable compound, remains significant during bulk transfer and pneumatic conveying. Installing localized dust extraction and switching to lined transfer equipment allowed us to avoid cross-contamination entirely; since those changes, batch variability has dropped noticeably.

    Feedback loops with integrators, especially in pharma and electronics, have kept us alert to trace impurity drift in both input and product. Recent investments into in-line spectroscopy and upgraded GC-MS mean routine identification of outlier batches and smarter segregation, so our partners encounter less rework.

    Responsible Stewardship and Knowledge Sharing

    We recognize that producing a compound like Decafluorobiphenyl isn’t just about filling up drums. Stewardship matters. Continuous engagement happens through our technical support teams and regular feedback from R&D partners. Whether troubleshooting a stubborn reaction or facilitating tech transfer, we share application data and best practices honed from years in operation.

    Among our various outreach programs, training for handlers and buyers stands out. We provide updated guides, drawing from recurring plant observations, real incident logs, and first-hand operability tests. Much of our operator and customer guidance comes directly from lessons learned during scale-up: don’t take shortcut filtration, always monitor storage temperature, and check transfer lines for particulate buildup quarterly. These are not slogans—they’re best practices written in sweat and real-world experience.

    As regulations shift toward greener manufacturing, Decafluorobiphenyl’s minimal waste and emission profile offers a bridge to both compliance and competitive differentiation. Emerging guidance from environmental bureaus increasingly gravitates toward high-purity, low-volatility intermediates, and Decafluorobiphenyl fits this evolution. Regular dialogue with environmental and safety professionals helps us keep the process aligned with upcoming requirements, while ensuring no corners are cut.

    Open collaboration continues as our process teams and those of our partners trade technical know-how—on everything from improved solvent recovery to faster crystallization flows. This willingness to share gives both us and our buyers a leg up on both efficiency and compliance.

    Pathways Forward and Ongoing Improvements

    With Decafluorobiphenyl continuing to play a vital role in chemistry-driven industries, ongoing investments shape its production future. Process automation and better analytical controls have shortened batch release cycles, giving end-users more responsive service. Our next steps focus on ramping throughput capacity—already supported by modern distillation and filtration systems—to meet global expansion in electronics, pharma, and engineered materials.

    Sustaining reliability, purity, and safety ranks above all. Our operational audit cycles now include rigorous reviews not just of product quality, but also the environmental footprint. Technology pilots explore waste stream valorization, and our R&D pipeline looks for new catalyst platforms to trim even marginal material waste. The ultimate goal: Decafluorobiphenyl that always delivers, with less footprint and broader positive impact throughout the supply chain.

    For those building tomorrow’s advanced materials, working with Decafluorobiphenyl day after day has taught us that real-world fit means more than an impressive formula. Every ton handed over to a partner represents a culmination of hands-on know-how, years of continuous improvement, and open dialogue with the end-users shaping their fields.

    This experience, more than the sum of numbers or certificates, underpins why Decafluorobiphenyl remains central to our operation. Its difference lies not just in its chemical make-up, but in the way it performs, day after day, under the stress and demands of true industrial life.