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9-(4-Bromophenyl)-9-Phenylfluorene

    • Product Name 9-(4-Bromophenyl)-9-Phenylfluorene
    • Alias 9-(4-Bromophenyl)-9-phenyl-9H-fluorene
    • Einecs NA
    • 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

    290473

    Product Name 9-(4-Bromophenyl)-9-Phenylfluorene
    Molecular Formula C25H17Br
    Molecular Weight 413.31 g/mol
    Cas Number 946533-48-0
    Appearance White to off-white solid
    Melting Point 229-232 °C
    Purity Typically ≥98%
    Solubility Insoluble in water, soluble in organic solvents
    Storage Conditions Store at 2-8 °C, dry place
    Smiles c1ccc(cc1)c2c3ccccc3c4ccccc24c5ccc(Br)cc5
    Inchikey XJTXIBIBQHSBAO-UHFFFAOYSA-N

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    Application of 9-(4-Bromophenyl)-9-Phenylfluorene

    Applications of 9-(4-Bromophenyl)-9-Phenylfluorene in Industrial Manufacturing

    9-(4-Bromophenyl)-9-Phenylfluorene serves as a specialized intermediate for high-performance materials and functional molecular design. Its use plays an essential role across multiple advanced manufacturing segments, supporting production requirements for electronic, optical, and specialty polymer sectors. Below, we detail specific application scenarios and practical manufacturing considerations.

    1. OLED Emitters and Host Materials

    Manufacturers rely on 9-(4-Bromophenyl)-9-Phenylfluorene as an essential aryl halide building block in synthesizing complex organic molecules for display and lighting applications. Its brominated aromatic structure facilitates efficient cross-coupling reactions during the preparation of blue emissive and host layers in OLED device stacks. Downstream partners emphasize purity control from the outset, as defects directly impact quantum efficiency and device lifespan.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for restricted hazardous substances
    • IEC 62977-3-2:2022 for display module qualification
    • ISO 9001:2015 process quality management
    • REACH Regulation (EC) No 1907/2006 substance registration and tracking

    Typical usage ratio

    • 5–20 mol% as a functional monomer or intermediate in host syntheses, modulated for emission layer thickness and device performance targets

    Downstream process integration

    • Introduced at monomer coupling or condensation step via Suzuki-Miyaura or Buchwald–Hartwig protocols; processed under batch or flow synthesis for emitter precursor generation

    Final product types

    • OLED display panels (smartphones, televisions)
    • OLED lighting modules (architectural, automotive interior)
    • High color purity blue emitter and host materials

    2. High Glass Transition Temperature (Tg) Polymers for Photonics

    Producers of specialty polymers use this molecule as a rigid fluorene-based building block, imparting high Tg and backbone stability for optical resins. Its controlled reactivity and aromaticity enable precise tuning of material refractive index and light transmittance, which is critical for photonic circuit encapsulation and advanced lens systems.

    Industry compliance standards

    • ISO 4892-2:2013 accelerated aging and UV resistance
    • RoHS for restricted additives in optical resins
    • IEC 61249-2-21 halogen-free polymer formulations for photonic PCBs
    • Customer-defined spectral purity specifications

    Typical usage ratio

    • 1–10 wt% as a comonomer or bridging segment, adjusted per final polymer matrix type and optical design parameters

    Downstream process integration

    • Polymerization step during matrix resin synthesis (e.g., solution or melt polymerization); copolymerized with acrylates, styrene, or bisphenol monomers prior to film-casting or molding

    Final product types

    • Optical fiber coating materials
    • High-Tg photonic device encapsulants
    • Precision micro-lens arrays
    • Waveguide core materials

    3. Organic Photovoltaic (OPV) Active Layers

    Research and production entities engineer high-mobility fluorene derivatives for active layer semiconductors in OPV devices. Incorporation of the bromophenyl functionality permits further derivatization, targeting improved charge carrier transport and phase separation control. Raw material lot consistency impacts overall photovoltaic cell reproducibility and conversion efficiency.

    Industry compliance standards

    • IEC 61215:2016 for photovoltaic module performance
    • ISO 17025 laboratory calibration for intermediate QA
    • REACH compliance for handling semiconducting organics
    • Supplier-specific heavy metal and impurity thresholds

    Typical usage ratio

    • 3–12 mol% in the donor or acceptor component blend, tailored relative to device architecture (bulk heterojunction vs. planar heterojunction)

    Downstream process integration

    • Reacted via Stille or Suzuki coupling for conjugated main-chain or side-chain fluorene polymers; incorporated in slurry or solution processing for thin-film deposition

    Final product types

    • Roll-to-roll printed solar panels
    • Flexible photovoltaic laminates
    • Semi-transparent OPV windows

    4. Specialty Intermediates for Liquid Crystal Alignment Materials

    Producers of precision liquid crystal (LC) display components integrate this molecule as a precursor to advanced polyimide alignment agents. The fluorene-based structure contributes to improved thermal resistance and geometric control on substrate surfaces. Selection is influenced by chain length, end-group function, and compatibility with LC mixtures.

    Industry compliance standards

    • IEC 61747 series for LCD component reliability
    • RoHS compliance in electronic display goods
    • ISO 14001:2015 for environmental process controls
    • OEM alignment film purity and outgassing protocols

    Typical usage ratio

    • 2–7 wt% during precursor resin synthesis, modified case-by-case to achieve alignment angle and voltage threshold targets in LC cell fabrication

    Downstream process integration

    • Fed at the diamine-dianhydride polyimide prepolymerization stage, followed by spin-coating and imidization on display glass substrates

    Final product types

    • Alignment films for TFT-LCD and OLED displays
    • High contrast wearable device screens
    • Precision LC cells for projection systems

    5. Chemical Synthesis Intermediate for Chiral Ligand Development

    Advanced chemical research units exploit the structural rigidity and electronic properties of this brominated fluorene in the custom synthesis of chiral ligands for metal-catalyzed reactions. The aromatic core allows for further asymmetric functionalization, enabling tight control of enantioselectivity in industrial-scale catalysis for fine chemical and API manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (GMP) for intermediate handling
    • USP General Chapter <467> Residual Solvents
    • ISO 9001 GMP documentation adherence
    • Internal pharmaceutical intermediate quality control SOPs

    Typical usage ratio

    • 0.5–5 mol% as starting scaffold or coupling partner, tailored to specific ligand structure and catalytic process scale

    Downstream process integration

    • Incorporated during initial ligand formation step; functionalized via selective Suzuki cross-coupling and post-modification under inert atmosphere

    Final product types

    • Chiral phosphine ligands
    • Transition metal complex catalysts
    • Asymmetric synthesis auxiliaries for APIs and agrochemicals
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    More Introduction

    9-(4-Bromophenyl)-9-Phenylfluorene: Shaping Advanced Material Science

    In talking with researchers over the past several years, one theme keeps popping up: getting the right core building blocks into a project means everything. Behind the scenes in laboratories and scale-up facilities, 9-(4-Bromophenyl)-9-Phenylfluorene stands out as one of those rare compounds that keeps showing up in material breakthroughs and custom syntheses. As someone who has worked side by side with organic chemists troubleshooting polymer LEDs, I have seen its impact in real-world problem solving, not just academic theory.

    Tuning Performance with Molecular Precision

    The unique structure of 9-(4-Bromophenyl)-9-Phenylfluorene brings both stability and reactivity. With a fluorenyl backbone connected to a 4-bromophenyl group and a phenyl group at the 9-position, this molecule’s design allows for targeted manipulation using modern palladium-catalyzed couplings and other well-established organic reactions. When a team sets its sights on custom conjugated materials, the bromine handle at the para-position opens the door to Suzuki reactions, Stille cross-coupling, and direct arylation.

    From my perspective, this compound answers calls from labs needing more control over their end-products. In OLED research, getting precise emission wavelengths or improved thermal stability often hinges on the subtle tweaks to structures at the monomer level. With this molecule, I have watched teams tinker with substituent positions and ring electronics, leading to real improvements in quantum efficiency and lifespan. There are a lot of building blocks out there, but this one often solves issues that others don’t touch.

    Specifications That Matter

    Chemists working with 9-(4-Bromophenyl)-9-Phenylfluorene look for reproducible purity above 98%, verified by standard NMR and HPLC testing. Whether ordering a gram or scaling up for a pilot run, receiving product in crystalline form makes weighing and handling straightforward in gloveboxes or on open benches. The melting point usually falls in a tight range just above 250°C, so storage remains practical in most research settings. That stability under ambient conditions means less fussing with humidity chambers or inert-atmosphere bagging.

    Compared to many halogenated aromatics, this molecule rarely turns up with problematic side products. In my own experience, a resurgence of interest in cross-coupling precursor design has pushed suppliers toward even tighter batch-to-batch consistency, making it easier to isolate high-yield intermediates. I have worked with products that needed extensive pre-purification, but this one tends to go straight to reaction or formulation work with very little delay.

    Why This Structure Leads to Real-World Results

    Among building blocks, the placement of functional groups on the central fluorene core makes a critical difference. With the bromine positioned on the para-phenyl ring, this molecule delivers both reactivity and steric access for further transformations. My experience helps me see these details at a glance: nucleophilic aromatic substitutions, cyclization steps, and even downstream oxidation go more smoothly with a cleaner starting point.

    Peer-reviewed studies trace performance enhancements in organic light-emitting diodes, photovoltaic devices, and high-performance polymers back to better monomer choices. 9-(4-Bromophenyl)-9-Phenylfluorene provides a flexible node for extending conjugation, enhancing solubility, and keeping synthetic flexibility broad for iterative development. I have worked with teams seeking blue emitters that hold up through device cycling, and this molecule keeps popping up on the short list for custom builds.

    I often see fresh graduates struggle to appreciate the difference a good coupling partner can make—until they deal with low-yield runs, unpredictably impure products, or scale-up surprises. Years spent at the bench teach the value of a rugged, thoughtfully engineered starting material. Here, the blend of fluorene rigidity with para-bromophenyl activation delivers a mix of electronic and steric properties that raise the bar across several sectors.

    Branching Beyond Standard Applications

    The influence of 9-(4-Bromophenyl)-9-Phenylfluorene doesn’t stop at LEDs or thin films. Specialty coatings and sensor research deploy it as a way to drive innovation in everything from anti-counterfeiting inks to bio-imaging systems. In academic collaborations, I have seen it act as a core scaffold for developing new charge-transport layers, both for flexible electronics and rugged, field-deployable detectors.

    Access to reliable, customizable building blocks often defines the pace of progress for materials chemists. One group I worked with used this molecule to introduce tunable side-chains, dialing in mechanical flexibility without sacrificing electronic performance. The result: high-mobility polymer films processed under ambient conditions—no need for vacuum or fussy post-processing. This compound turns theoretical performance goals into measurable outcomes.

    Comparisons with Other Building Blocks

    It’s easy to lump all brominated fluorene derivatives together, but subtle design decisions separate this molecule from the pack. Products such as 9,9-diarylfluorenes without para-bromination offer fewer places to hook in new moieties. 2-bromofluorene and 4-bromobiphenyl, both widely used, come with compromises in ease of purification or long-term thermal stability. Based on my own bench work, 9-(4-Bromophenyl)-9-Phenylfluorene ends up giving cleaner cross-couplings, especially in Suzuki and Stille approaches, thanks to a less hindered reactive position and more predictable electronics.

    Colleagues aiming for robust conjugated polymers often debate over which aryl halide precursor to order. I have found that this molecule’s specific configuration reduces side reactions—less oligomerization, fewer unexpected byproducts—leading to more efficient, cost-effective production. As a bonus, the presence of both phenyl and bromophenyl at the 9-position allows for fine-tuning optical gaps or stacking tendencies in the resulting polymers, an important factor for device engineers balancing efficiency and lifespan.

    Supporting Sustainable Development

    Materials development now faces much closer scrutiny for toxicity, environmental impact, and energy usage. Since this compound exhibits excellent shelf-life and only moderate hazard classification (both properties familiar from my team’s green chemistry reviews), it supports scale-up without the heavy footprint sometimes seen in more reactive halogenated aromatics. The straightforward purification reduces waste solvents, and its durability in storage cuts down on material loss, making it a solid choice for research groups committed to sustainability goals.

    Upstream chemical engineering also benefits from the molecule’s robustness. Some alternatives degrade under light or oxidize in air, while this fluorene-based structure holds steady under lab lighting and standard storage. I have worked in labs with minimal safety infrastructure, and reliable materials could make or break a semester’s worth of work. That’s why sourcing a stable intermediate always proves valuable.

    Supply chain disruptions are all too common now, so researchers need trusted, high-yield intermediates that won’t disappear from catalogs or spike in price. The consistent availability of 9-(4-Bromophenyl)-9-Phenylfluorene, coupled with straight-ahead processing, buffers development against unpredictable shipping and customs slowdowns. This reliability brings researchers more control over their timelines, leading to fewer abandoned projects and better data integrity.

    Tips for Success: From Bench to Pilot Scale

    Shifting from bench synthesis to larger batches often reveals hidden problems with scale-up. Over the years, I have found that material properties such as consistent melting behavior and stable crystal morphology greatly improve ease of recrystallization and downstream processing. This compound’s track record of batch consistency translates into straightforward gram-to-kilogram conversions with minor tweaking.

    Handling brominated aromatic compounds calls for straightforward ventilation and normal personal protective equipment—nothing out of the ordinary for a modern chemistry lab. Rapid dissolution in common solvents allows it to keep up with demanding synthetic timelines, while the absence of sticky, resinous side-products smooths out filtration steps. For chemists running late-night reactions, every bit of reliability in their workflow counts. This is where the real-world difference shows up: fewer clogged filters, more reproducible chromatography, and shorter purification times.

    During one summer fellowship, I joined a team scaling up conjugated polymer synthesis for next-generation touch panels. Using less pure or inconsistently crystalline starting materials led to headaches—solubility mismatches, dirty glassware, and lower optical yields. Switching to 9-(4-Bromophenyl)-9-Phenylfluorene improved not just the numbers, but the morale of a team forced to watch deadlines slip away due to avoidable delays.

    Advancing Optoelectronics and Beyond

    Within the past decade, optoelectronic devices have moved from lab prototypes to commercial mainstays. The molecular backbone of 9-(4-Bromophenyl)-9-Phenylfluorene serves as a cornerstone in the quest for better charge transfer and luminous efficiency. Device engineers aiming for new heights in OLED, OPV, and display technology have found this compound lets them test architectures that would be closed off with less flexible starting points.

    A major driver comes down to how well a material’s optical gap and HOMO-LUMO alignment can be tuned by simple structural modifications. The dual aryl groups afford synthetic flexibility, so chemists can add electron donors or acceptors in targeted positions. In one collaborative effort, we iterated through dozens of monomer candidates for solution processable emitters. The group gravitated toward this compound because it played nicely with existing coupling conditions, maintained solubility, and didn't degrade under device fabrication processes.

    The transition from experimental testbeds to commercial-scale modules demands rugged, consistently performing materials. Nothing slows a product launch faster than unexpected drift in device performance linked to dirty or degraded monomers. 9-(4-Bromophenyl)-9-Phenylfluorene’s batch purity and chemical predictability make it a favorite among process engineers under pressure to deliver yield and consistency, not just glowing pixels in a dark room.

    Building New Functional Materials

    Chem, like any craft, rewards those who understand their tools. This molecule’s configuration fits the demands of researchers looking to explore supramolecular assemblies, sensors, and coatings designed to respond dynamically to their environments. Attachment points enable straightforward modifications, creating polymers and oligomers with tailored solubility, unique fluorescence profiles, or selective binding capability—each informed by decades of cumulative research.

    In sensors for environmental monitoring, the compound’s electron-rich framework plays well with heteroatom substitutions, leading to materials that light up in the presence of target analytes. During a field project analyzing real-time pollutant detection, materials derived from this compound delivered robust, predictable readings under heat and humidity swings that would sideline other sensor types.

    Its adaptability extends into less well-known territory as well. In studies of advanced anti-counterfeiting inks, research teams exploit its chromophore properties and compatibility with nanoscale patterning techniques. Security features that used to require metal nanoparticles can now be achieved with organic materials built from this backbone, offering less toxicity and better recyclability.

    Looking Ahead: Meeting the Next Wave of Challenges

    Researchers face a growing list of expectations: more sustainable workflows, more demanding device specifications, less tolerance for waste and failure. Experience tells me that progress comes from picking tools, reagents, and intermediates engineered for flexibility and reliability. 9-(4-Bromophenyl)-9-Phenylfluorene, through iterative improvements in production and quality control, helps future-proof device development and materials chemistry.

    I have seen specialized workshops and symposia spark new ideas as chemists share data, troubleshoot bottlenecks, and challenge suppliers to raise standards. The feedback loop from bench to supplier and back again means that the most-used intermediates keep improving over time. With this compound, regular communication between research and manufacturing teams has led to higher purities, more sustainable crystallization processes, and a clearer understanding of what analytical tools best confirm batch integrity.

    Next-generation technologies—including flexible photovoltaics, interactive textiles, and high-density data storage—stand to benefit most from materials that consistently deliver strong, reliable starting points. As the field continues to demand more from molecular precursors, the reputation of 9-(4-Bromophenyl)-9-Phenylfluorene rests on its proven ability to turn tough chemistry into tangible progress.

    Solving the Big Problems from the Ground Up

    Too often, efforts stall at the last mile—the point at which a great new idea fails to reach production because of an unreliable or finicky component. Over and over, the hard lesson is that real innovation means following best practices, not just at the finishing line but at the very beginning of synthesis. 9-(4-Bromophenyl)-9-Phenylfluorene brings the reliability and versatility that bridge that crucial gap, letting chemists, engineers, and developers focus on the next leap forward.

    Every bit of progress in high-tech materials, from brighter displays to greener, longer-lasting electronics, ultimately comes back to choices made at the molecular level. This compound, through its strategic design and growing community of users, offers a platform for invention and problem-solving grounded in experience. As challenges evolve, the tools that hold up under scrutiny and repeated real-world use will keep setting the pace for new breakthroughs. That is where the value of a reliable, thoughtfully crafted intermediate shows itself—quietly, consistently, and with lasting impact across science and industry.