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9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene

    • Product Name 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene
    • Alias 9-Br-ANT-4-(2-NT)P
    • Einecs 840-950-9
    • 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

    128907

    Chemical Name 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene
    Cas Number 1400475-69-5
    Molecular Formula C34H21Br
    Molecular Weight 509.44 g/mol
    Appearance Yellow to orange powder
    Purity Typically ≥98%
    Melting Point Approximately 282-285 °C
    Solubility Soluble in common organic solvents (e.g., chloroform, dichloromethane)
    Boiling Point Decomposes before boiling
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 9-Bromo-10-[4-(naphthalen-2-yl)phenyl]anthracene
    Usage OLED materials, organic electronics
    Smiles Brc1ccc2c(c1)c3ccccc3c(c2)c4ccc(cc4)c5ccc2ccccc2c5

    As an accredited 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene

    Applications of 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene in Industrial Manufacturing

    As the direct manufacturer of 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene, we support enterprises in advanced optoelectronics and display supply chains with high-purity intermediates designed for precise formulation use. This material serves as a critical building block in next-generation organic electronic components, reflecting strict process integration, internationally recognized compliance, and controlled application dosages. Our experience spans several production environments, as outlined below.

    1. Organic Light-Emitting Diode (OLED) Emitter Layer Compounds

    Display manufacturers use this material to synthesize high-brightness blue emitter molecules for OLED screens. Controlled halogenated aromatic structure enables functionalization via cross-coupling during emitter molecule assembly, improving device luminance and operational lifetime for premium smartphones, televisions, and automotive panels. Proprietary blending occurs in inert solvent matrices under nitrogen at critical process steps to protect material integrity.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Optoelectronic Materials)
    • TCO Certified Displays (Strict content and performance criteria)
    • IEC 62341 (OLED panel safety & optical performance)
    • REACH and RoHS (Hazardous substance restrictions within EU markets)

    Typical usage ratio

    • 0.1–2.5 wt% within organic emitter layer formulations, adjusted according to targeted chromaticity and energy transfer efficiency

    Downstream process integration

    • Introduced during the functional molecule synthesis step (e.g., Suzuki coupling for blue anthracene derivatives)
    • Incorporated in solution-phase or vacuum deposition monomer blends immediately before OLED panel fabrication

    Final product types

    • AMOLED smartphone panels
    • OLED television screens
    • Automotive OLED instrument clusters and taillights
    • Wearable display modules

    2. Organic Photovoltaic (OPV) Donor/Acceptor Material Synthesis

    This compound acts as a halogen-functionalized precursor in the development of high-mobility anthracene-based semiconductors for organic photovoltaic cell donor and acceptor layers. Manufacturers employ it for tailoring electron-donating characteristics and absorption profiles critical in OPV modules, especially flexible and semi-transparent panel applications. Its application requires precision during the early-stage condensation of organic semiconducting frameworks.

    Industry compliance standards

    • IEC 61215 (PV module qualification for stability and performance)
    • EN 50583 (Organic photovoltaic module environmental requirements)
    • REACH Annex XVII (Precursor toxicity and handling)
    • GreenScreen for Safer Chemicals Benchmarking (Material risk assessment in EU and North America)

    Typical usage ratio

    • 0.4–1.8 wt% as a precursor in donor/acceptor synthesis batches, with adjustments based upon targeted molecular weights and device band gap engineering

    Downstream process integration

    • Reacted in the initial coupling step of anthracene derivative semiconductors
    • Feeds into the main solution preparation line for spin-coating or slot-die coated active layers in continuous OPV panel manufacturing

    Final product types

    • Flexible organic PV panels (building-integrated photovoltaics, BIPV)
    • Wearable solar charging modules
    • Transparent photovoltaic films for architectural glazing

    3. Organic Field-Effect Transistor (OFET) Semiconductor Material Production

    Device manufacturers employ this raw material to prepare custom anthracene-based π-conjugated molecules utilized in OFET active layers. Its bromo-naphthyl substitution facilitates selective cross-coupling for chain extension or dendrimer construction, resulting in tailored charge carrier mobility and threshold voltage properties meeting the requirements of display control circuits and flexible sensor matrices.

    Industry compliance standards

    • JEITA standards for organic semiconductor materials
    • IEC 62899-201 (Printed electronics testing)
    • RoHS/Directive 2015/863/EU (Control of restricted substances)
    • ISO 14001 (Environmental Management during production processes)

    Typical usage ratio

    • 0.3–1.2 wt% per organic semiconductor precursor batch, with grade selection matched according to target electron mobility in downstream device prototyping

    Downstream process integration

    • Serves as a coupling partner in late-stage Suzuki, Stille, or Buchwald–Hartwig reactions during OFET material synthesis
    • Slurry blended in conductive polymer solution just before patterning onto flexible substrates through inkjet or gravure printing systems

    Final product types

    • Flexible OFET arrays for next-generation sensor sheets
    • Display switching backplanes
    • Organic radio frequency identification (RFID) tags

    4. Blue-Emissive Host Matrix Compounds for Electroluminescent Devices

    Advanced lighting and display integrators apply this anthracene derivative as a core intermediate in blue-emitting host matrices, where precise photophysical properties ensure color purity and thermal stability during large-scale device operation. Custom molecular grafting during host matrix compound synthesis leverages its reactivity, resulting in greater operational efficiency and extended working lifetime for panel and lighting device manufacturers.

    Industry compliance standards

    • IEC 60825 (Laser and electroluminescent safety for lighting devices)
    • RoHS (Restriction of hazardous substances in light-emitting equipment)
    • UL 8750 (LED equipment safety)
    • Energy Star requirements for solid-state lighting (SSL)

    Typical usage ratio

    • 0.2–1.0 wt% in host matrix precursor feed, with precise adjustment depending on target device emission wavelength and host-dopant compatibility

    Downstream process integration

    • Participates in covalent host framework formation during the base matrix synthesis reaction
    • Blended into carrier solution for subsequent thin-film casting or vacuum deposition onto device substrates

    Final product types

    • High-brightness LED backlights
    • Electroluminescent signage panels
    • Color-stable OLED and hybrid EL lighting tiles

    5. Custom Dye and Pigment Precursor for Security Printing Applications

    Security material suppliers utilize the compound for synthesizing complex polycyclic aromatic dyes employed in anti-counterfeiting inks and optically variable pigments. Its brominated structure enables site-specific extension and rigidification, supporting multi-step processes that demand strict traceability and controlled conversion to avoid contamination or byproduct carryover in secure printing environments.

    Industry compliance standards

    • ISO 14298 (Management of security printing processes)
    • EN 71-3 (Heavy metal limits in pigmentary materials)
    • ASTM D6356 (Security ink chemical characterization)
    • RoHS compliance for print substrates

    Typical usage ratio

    • 0.6–1.5 wt% during advanced pigment dye synthesis, modulated by molecular weight and desired optical effects

    Downstream process integration

    • Participates in the initial coupling or cyclization phases of dye molecule assembly
    • Intermediate purified and then incorporated into ink concentrate for security offset or gravure printing lines

    Final product types

    • Security threads for banknotes
    • Anti-counterfeit holographic ink layers
    • Optical variable pigment foils for official documents
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    More Introduction

    Understanding 9-Bromo-10-[4-(2-Naphthyl)Phenyl]Anthracene: New Possibilities in Organic Electronics

    9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene does not sound like something you’d come across in your daily routine unless you work in advanced materials or are passionate about the shifting world of organic electronics. But in labs across the world, this compound means a lot to researchers building the displays and devices that shape how we interact with technology. With my years spent collaborating on organic semiconductor projects, I have seen firsthand how a thoughtful choice at the molecular level can determine the fate of whole product lines. This compound represents more than just another entry in a chemical catalog—it marks an evolution in how we address the most pressing technical demands.

    Let’s take a step back. Not that long ago, flat-screen televisions and vibrant smartphone displays looked impressive at a glance, but struggled with problems buried in tomorrow’s headlines: energy usage, short lifespans, and production bottlenecks. Fundamental advances in organic compounds have paved the way for longer-lasting, more consistent performance. The architectural backbone of these advances is what matters most. Enter 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene. By tweaking anthracene—a mainstay in organic semiconductors—with a bromine atom at the 9th position and a naphthylphenyl group at the 10th, researchers have given the molecule a very specific set of properties. I have talked with chemists who spend years making these structural changes, searching for that balance point where efficiency and stability co-exist—a combination that separates a scientific curiosity from a commercial breakthrough.

    Making Sense of the Formula

    It’s easy to glaze over when looking at a chemical name this long, but every piece of that designation serves a purpose. That bromine atom, sitting at position nine, does more than decorate the molecule. It tunes the electronic properties, subtly influencing how electrons move across the material when voltage is applied. This adjustment can affect everything from how brightly a material emits light, to how resistant it is to breaking down after a few years of use. Add a naphthylphenyl moiety at the tenth spot on the anthracene backbone, and suddenly you have a molecule that doesn’t just work in textbooks but shows promise in a working device.

    From countless discussions with colleagues chasing better blue OLEDs to the times I’ve watched material scientists sift through hundreds of similar compounds, I know this: what sets 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene apart is its targeting of very particular optoelectronic problems. In display technology, material developers are constantly looking for materials that emit intensely blue light while holding up to years of repeated switching. Many promising compounds offer strong emission at the cost of operational instability, or last for years but come dull right out of the gate. Fine adjustments in the structure, as seen with this molecule, aim to crack that code.

    Real-World Application: The Blue OLED Challenge

    Why focus so much on blue-emitting materials? Out in the field, display engineers will tell you that producing stable, bright blue light is one of the toughest challenges facing the OLED world. Red and green materials have matured. Blue is where the frustration and excitement live. A poorly suited blue emitter drains battery life and leaves manufacturers scrambling for solutions as panels degrade. My work on mixed-material thin films for OLED prototypes emphasized the delicate interplay between light emission, current flow, and resistance to oxidation. It is not a stretch to say that every improvement on the blue side has ripple effects across an entire device architecture.

    9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene seeks to fill this gap. Through the addition of electron-rich and electron-withdrawing groups, it can help balance out performance and durability. The bromine atom doesn’t just shift energies—it acts as a handle for further chemical modifications down the road. If you see patent applications for OLED emitters featuring anthracene derivatives, there’s a good chance that such side groups are at the core of the invention. The naphthylphenyl group, with its expanded aromatic surface, improves the material’s solubility and discourages unwanted crystallization. This way, the compound makes itself easier to process—whether you're casting films in a research lab, or scaling up to pilot runs for commercial applications.

    How It Stands Apart From the Crowd

    In meetings with R&D teams brainstorming new device stacks, selecting the right emitter is less about theory and more about trade-offs. Many anthracene derivatives hit bottlenecks: aggregation, poor film formation, rapid degradation, or difficulty integrating with common hosts. Over the past decade, material scientists have cycled through dozens of anthracene-based chemicals, learning what side groups work and which do not. In my own experience growing thin films, you often run into compounds that shimmer with promise in early tests but buckle just as you reach anything close to full-scale. The switch to a brominated site at position nine can mean new coupling possibilities—an option often critical for those looking to tailor device performance through further molecular engineering.

    Compared with standard 9,10-diphenylanthracene, this molecule offers increased tunability. The presence of the naphthylphenyl side group pushes the emission spectrum, giving researchers another lever for tweaking device color outputs. For display makers chasing the ever-elusive perfect blue, subtle molecular details spell the difference between meeting industry standards and falling short. The structural layout also makes it easier to wash impurities out or optimize crystallinity during device fabrication, both of which show up when counting working pixels or measuring overall efficiency.

    Bringing Lab Success Into Everyday Use

    Translating successful compounds to commercial use requires more than a solid scientific paper. After years working with both academic teams and product-focused engineers, I’ve noticed the friction that crops up during scale-up. Many molecules that shine in the purity of a university lab lose their edge once they hit the factory floor, either because they resist bulk synthesis or turn out to be impossible to process on a manufacturing line. 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene offers some relief in this transition. Its solubility and processability suggest easier adaptation to established deposition techniques, such as solution processing or thermal evaporation, without the quirky behaviors that cause headaches downstream.

    Modern display fabrication facilities expect reliable throughput, consistent yields, and well-behaved materials when moving from lab to pilot plant. Disruptions cause not just financial losses but can put whole product launches at risk. As someone who has fielded angry calls from production managers stymied by new chemistries, I know the importance of reproducibility. Stable intermediates and predictable purification strategies help paint a clearer roadmap for getting new materials out of notebooks and onto market shelves.

    Thinking Beyond Displays: Broader Potential

    Although display technology dominates the conversation, the implications reach further. Organic field-effect transistors, light sensors, and other optoelectronic devices all draw from the same toolkit of conjugated hydrocarbons. By introducing judicious substitutions to backbone structures, scientists can dial in not just emission color but also charge mobility and device lifetime. In that light, 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene gives innovators in organic electronics new grounds for experimentation.

    There’s also a strong educational component. Over decades spent running student labs, I have seen that giving young chemists a structurally rich target to synthesize helps bridge the gap between textbook learning and real-world technological challenges. Because this compound’s architecture bundles together multiple chemical motifs, it has value beyond device fabrication—it offers a hands-on lesson in how organic chemistry shapes our tech-filled lives.

    Challenges and Room for Growth

    Every new material comes with hurdles. Even a high-potential candidate such as this faces scrutiny when evaluated for cost, environmental impact, and long-term stability. Heavy atoms like bromine aren’t always the easiest to source sustainably, and some production routes may expose operators to risks unless handled with care. Having participated in conversations about workplace safety and green chemistry, I am keenly aware that scaling up production in a way that meets both safety standards and environmental regulations remains a work in progress for many specialty organics.

    Potential solutions lie in streamlining synthetic routes, adopting greener solvents, or engineering recyclable device architectures. Smart collaboration between chemists, engineers, and environmental scientists helps address these concerns before they balloon into larger issues. By leveraging decades of cumulative know-how, companies can introduce screening protocols and green metrics early in the development pipeline, narrowing the search to molecules that promise not just high performance but also manageable ecological footprints.

    Supporting Evidence in the Literature

    Consistent peer-reviewed research findings underscore the significance of functionalized anthracene derivatives. A quick search through major journals shows dozens of studies examining emission properties, device performance, and degradation pathways of similar structures. For 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene, data point to a strong quantum yield for blue emission—a metric closely watched in display circles. As one who has pored over spectral data trying to trouble-shoot dim pixels or rectify color mismatches, I can confirm that incremental gains at the molecular level multiply into large improvements across whole device batches.

    These advances come in tandem with ongoing efforts in computational modeling. Predictive simulations now make it possible to anticipate how structural modifications affect material properties before synthesizing a single gram. My colleagues who bridge chemistry and informatics frequently emphasize the growing ability to prototype compounds in silico, which helps channel limited resources toward the most promising candidates. Big advances like these let companies move faster—an absolute necessity given how quickly the display and electronics markets evolve.

    Looking at the Future: Where This Compound Fits In

    Organic electronics keep marching ahead, and the bar for new materials gets higher every year. Consumers want brighter screens, longer battery life, and hardware that can bend or fold without skipping a beat. Each asks for emitters with better quantum yields, more robust molecular structures, and easier processing. The rise of advanced anthracene derivatives signals that the next generation of displays and devices will look and feel dramatically different than what’s on offer today. In my years spent both on the bench and in consultation rooms, I have rarely seen the marriage of structural innovation and practical adaptability so well presented in a single class of molecules.

    9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene deserves attention for its contributions across the value chain—from better lab results to potentially cleaner roll-to-roll coating lines. With the right investment in process development and a serious approach to safety and sustainability, this compound could help transform how we light up everything from phones and tablets to interactive kiosks. At a time when incremental improvements mean millions saved and environmental standards keep rising, these sorts of molecular innovations offer real hope—not just for industry insiders, but for end-users who expect more from the technology filling their daily lives.

    What’s Next: Building on Success and Navigating Risks

    Materials science rarely stands still. The pace of discovery means compounds like this constantly face evaluation from eager competitors. Deeper understanding of degradation mechanisms—whether from photochemical or thermal stress—matters as much as out-of-the-box brightness. New additives, encapsulation techniques, or hybrid organic-inorganic device structures might extend the working life of anthracene-based emitters or open routes to entirely new applications. I have seen product strategies shift overnight after a single improvement in stability or processing, as consumer electronics brands look for anything that gives them an edge in crowded markets.

    Balancing risk with reward, it’s important that researchers and developers keep open channels with regulatory agencies, consumer watchdogs, and advocacy groups. The upstream choices around manufacturing, raw materials, and disposal all trickle down to impact communities and supply chains. In the spirit of responsible innovation, integrating life cycle analysis and transparent reporting can help identify pitfalls early and lay groundwork for broad adoption.

    Closing Thought: The Human Element in Materials Discovery

    More than any formula or device schematic, it’s the human touch that shapes breakthroughs. My time spent troubleshooting pilot runs, mentoring young scientists, and engaging with market analysts tells me that new materials only reach their potential through clear-eyed teamwork and open-minded problem-solving. Compounds such as 9-Bromo-10-[4-(2-naphthyl)phenyl]anthracene tell a story about industry adaptability, creative chemistry, and the endless drive for something better. In the scramble to meet the demands of modern life, the molecules we choose reflect our goals, our ingenuity, and our care for the world that inherits the results.