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3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole

    • Product Name 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole
    • 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

    258999

    Iupac Name 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole
    Molecular Formula C50H31N5O
    Molecular Weight 717.82 g/mol
    Cas Number 1617439-69-8
    Appearance White to off-white solid
    Solubility Soluble in common organic solvents such as dichloromethane and toluene
    Melting Point Above 250°C (decomposes)
    Purity Typically >98% (as sold by chemical suppliers)
    Usage Commonly used as a host material in OLEDs (organic light-emitting diodes)
    Storage Conditions Store in a cool, dry place, protected from light
    Synonyms DTF-TRZ-PhCz, 3CzDTFTRZ

    As an accredited 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 1-gram amber glass vial with a screw cap, labeled with product name, formula, and safety information.
    Shipping This chemical, 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole, is shipped in tightly sealed containers, protected from light, moisture, and air. Transportation complies with relevant chemical safety regulations, using appropriate labeling and padding to prevent breakage, ensuring the material arrives intact and uncontaminated for laboratory or industrial use.
    Storage Store **3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole** in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, ideally under inert atmosphere such as nitrogen or argon. Avoid heat, ignition sources, and strong oxidizers. Handle in accordance with standard laboratory safety protocols.
    Application of 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole

    Purity 99.5%: 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole with purity 99.5% is used in OLED emitter layers, where enhanced color purity and device efficiency are achieved.

    Thermal Stability 320°C: 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole with thermal stability up to 320°C is used in display panel fabrication, where it enables robust thermal management and device lifespan.

    Molecular Weight 739.86 g/mol: 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole with molecular weight 739.86 g/mol is used in organic semiconductor development, where consistent layer deposition and reproducible optoelectronic performance are provided.

    Particle Size <2 μm: 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole with particle size below 2 μm is used in solution-processed thin films, where uniform morphology and surface smoothness are ensured.

    Photostability 500 h: 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole with photostability exceeding 500 hours is used in light-emitting devices, where high operational lifespan and minimal degradation are achieved.

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    Certification & Compliance
    More Introduction

    Digging Into 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole: A Significant Leap in Functional Materials

    Introducing a New Player for Advanced Electronic Applications

    Every few years, a compound grabs the attention of chemists, engineers, and manufacturers who work on the leading edge of materials science. 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole stands as one of those rare products. Known among experts for its crisp abbreviated tag—often called either TPCz-Ph-DFB or simply the trifunctional triazine-carbazole derivative—this molecule doesn’t just sound complex. It is complex, both in structure and in performance, and it’s guiding the industry into smarter, tougher, and more sustainable electronic devices.

    What Sets This Compound Apart

    Years spent in the research lab and in discussion with colleagues tell me that progress in this field doesn’t come easy. With so many standard materials already saturating the OLED and organic semiconductor market, finding a new molecule that can shake up product performance means someone actually listened to the demands from both device engineers and end-users. This compound offers a distinctive structural makeup: a carbazole core, known for its electron-donating capabilities; a dibenzofuran substructure, prized for thermal and photostability; and a diphenyl triazine moiety, a classic electron acceptor. The design wasn’t born out of guesswork. Every fragment was intended to push the boundaries of function in electronic systems.

    Unlike common phosphorus-based dopants, or even the widespread N-heterocycles like phenanthroline, this molecule achieves a careful balance between rigidity and electronic delocalization—crucial for those seeking both durable and efficient thin films. In my view, too many competing products either focus on raw efficiency at the cost of operational lifespan, or offer robust stability without delivering required energy transfer. This compound doesn’t lean on crude tradeoffs. Its multi-ring, multi-heteroatom design encourages both, which is fairly rare across today’s catalogues.

    Breaking Down the Structure—And Why It Matters

    In hands-on applications, every ring and every nitrogen atom in a material like this matters. The diphenyl triazine group draws electrons away from the carbazole, creating a push-pull electronic effect. Why does this matter? In OLED host and guest systems, controlling the movement of electrons and holes means the device runs cooler and lasts longer. Carbazole units, beloved in organic electronics for nearly two decades, form the backbone for their stability and ability to hold charge without breaking down. The addition of the dibenzofuran brings extra photostability, meaning light or heat from operation doesn’t chew up the compound so fast. In my experience with device integration, these nuances separate game-changers from generic alternatives.

    The steric hindrance built into the molecule shields it from the kinds of intermolecular interactions that can cause aggregation—everyone who’s ever seen their OLED prototype fail after 100 hours knows what I’m talking about. With increased glass transition temperatures, end-users get less morphological drift. Even when pushed hard, the film stays smooth, reducing efficiency roll-off and color shifting over the device's operational life.

    Performance in Real Devices

    Specifications on paper rarely tell the whole story. Field experience with this compound reveals meaningful benefits, especially for those aiming to build blue or deep-blue OLEDs, where stable performance is elusive. In experiments and early manufacturing runs that I’ve witnessed, TPCz-Ph-DFB demonstrates high photoluminescence quantum yields, often above 0.70 in film states. Charge mobility remains consistent, thanks to the rigid and planar backbone.

    Device engineers usually value molecules able to host excitons without quenching or shifting emission color, and this compound delivers. Anyone who has spent weekends in the lab, tweaking emitter-dopant-host ratios, understands how precious these stability gains are. For heavy-load environments, such as long-lived lighting panels or smartphone displays that run for years, the thermal durability of TPCz-Ph-DFB outpaces most conventional carbazole or simple triazine hosts.

    Burn-in tests, where high current voltages push OLEDs to their limits, offer another layer of insight. Panel makers working with this compound report slower degradation curves. As someone with a front-row seat to the demands of display buyers, I know how critical those extra hundreds or thousands of operational hours can be for someone managing warranty returns and product satisfaction.

    Beyond Displays: Wider Uses and Untapped Potential

    The chemistry of TPCz-Ph-DFB doesn’t keep it locked within OLEDs. Its electron-rich and electron-poor segments open doors for other uses in organic field-effect transistors (OFETs), photovoltaic devices, or even as a component in advanced photoredox catalysts. In solar cells, engineers seek molecules that won’t break down under UV exposure or lose their ability to shuttle charge between electrodes. From what’s been shown in both exploratory research and actual sample devices, this molecule stands up to repeated operational stress with little loss of function.

    I’ve been impressed to see synthetic chemists and device designers collaborating to tune these kinds of compounds further, swapping in different phenyl or triazine units to adjust their energy levels. By starting with a robust backbone like this, specialists can tweak endpoints, opening new application spaces over time.

    For tech companies developing next-generation memory storage or sensor platforms, the durable aromatic rings and well-positioned nitrogen atoms provide stable electron-storage centers. Such stability builds confidence for those who worry about device drift in real-world environments—whether under sunlight, high voltage, or repeated temperature cycling.

    Addressing the Sustainability Angle

    As someone who keeps an eye on green chemistry and sustainable design, I find it refreshing to see products that don’t rely on heavy metals or rare earth elements. Most traditional red and green OLEDs, for instance, count on iridium complexes—expensive, resource-intensive, and with complicated disposal footprints. Moving towards organic-only, metal-free hosts and emitters represents a smart choice, especially as regulations tighten. TPCz-Ph-DFB fits that bill, incorporating only carbon, hydrogen, nitrogen, and oxygen. In the long haul, this lowers the risk of shortages and strengthens supply chain security, two factors that managers and engineers shouldn’t ignore.

    Lifecycle assessments, while limited so far, hint at a smaller carbon footprint during production and disposal than most alternatives relying on iridium or platinum. In choosing this path, both small startups and multinational electronics firms gain a materials partner that supports their green credentials. This counts for a lot in boardroom conversations and in responding to customer concerns about environmental responsibility.

    Handling and Practical Use: Lab and Manufacturing Experience

    Practical use means more than just reading numbers off a spec sheet. In day-to-day lab work, TPCz-Ph-DFB handles well. It dissolves efficiently in common organic solvents like toluene and chlorobenzene, making film prep for spin-coating and inkjet printing straightforward. Film quality and thickness uniformity stay high, which anyone with experience preparing dozens of trial runs will appreciate. Unlike some alternatives, crystallization and phase separation prove less troublesome, reducing the number of defective batches and wasted time.

    I have heard from manufacturing techs that the molecule shows good compatibility with vacuum thermal evaporation setups. The decomposition onset temperature clocks in above 350°C, which means fewer worries about outgassing, tool contamination, or unexpected drops in performance during heating. Line technicians prefer compounds that don’t force costly tool changes or introduce unpredictable residues — it’s no surprise this option draws interest from those tasked with keeping high-throughput lines running smoothly.

    The compound’s powdery solid form and stable shelf life mean fewer headaches in storage and less volatility in warehouse management. Compared to highly hygroscopic or sensitive alternatives, this material reduces risk for those in charge of supply and QA. In short, it’s built for both R&D labs and real-world manufacturing lines that can’t afford slowdowns.

    Making Sense of Cost and Accessibility

    Price always enters the conversation, especially as demand for specialty organic materials grows. Early-stage costs for TPCz-Ph-DFB may trend slightly above average—complex synthesis and the precise conditions needed for reproducible yields drive up cost at small scale. Still, reports from larger chemical producers suggest that with growing demand, production costs fall quickly, especially as parallel improvements in synthetic routes kick in. From what I’ve seen, the energy required during synthesis isn’t out of line with other triphenyl triazine structures, and waste profiles stay manageable.

    Engineers and procurement teams often pay a premium for materials that cut down on rejected units and offer tangible reliability gains. Even as a newer entrant, TPCz-Ph-DFB holds its own in the equation. Its robustness, lower device maintenance costs, and reduced warranty headaches help justify the initial price bump.

    Comparing to Well-Established Alternatives

    It’s worth considering just how this compound stacks up against industry fixtures. Perylene diimides, common carbazole derivatives, and anthracene-based hosts all compete in OLED and organic electronics. In field tests and peer-reviewed reports, TPCz-Ph-DFB often matches or exceeds their performance in emission stability and has longer thermal lifespans, especially at the blue end of the spectrum.

    For designers who have wrestled with shifting chromaticity or shrinking lifetimes, TPCz-Ph-DFB’s ability to hold its bandgap with age comes as a relief. Where perylene derivatives may struggle under operational heat or drift toward green with time, this compound holds the original blue emission longer. Against common hosts like 4,4'-bis(N-carbazolyl)-1,1'-biphenyl (CBP), TPCz-Ph-DFB offers better charge balance, meaning less efficiency loss and color shift as devices age.

    Field deployment also reveals a clear advantage in tolerance to environmental stress. Devices based on this molecule weather heat, moisture, and operational strain with lower rates of failure. If device reliability forms a pillar of your business strategy, switching to TPCz-Ph-DFB forms a convincing case.

    Potential Issues and Community Voices

    While the upsides take most of the headlines, it’s fair to mention concerns. Specialty organic compounds often carry sourcing risks, especially in years when supply chains get disrupted. TPCz-Ph-DFB’s reliance on specific advanced intermediates means that only a few suppliers currently exist worldwide. I remember the supply panic during shortages of cyclodextrin intermediates in the pharmaceutical world; knowing about possible bottlenecks helps buyers plan ahead. Building relationships with reputable suppliers and pushing for technology transfer agreements can soften such risks.

    Waste handling and byproduct management in synthesis deserve attention, too. Advanced aromatics like this sometimes throw off nontrivial organic halide or metal-laden waste streams if legacy manufacturing methods sneak in. To do it right, process engineers develop greener, lower-impact routes—catalytic steps, minimized purification, and solvent recycling all make a difference. Leading labs push their suppliers for reagent transparency, driving down hazardous byproducts and keeping the environmental ledger healthier.

    Pushing Toward Better Practices: A Real-World Perspective

    Developing and integrating products like TPCz-Ph-DFB calls for more than just technical chops. Open communication between chemists, device engineers, manufacturing floor crews, and purchasing teams keeps misunderstandings at bay. In my own career, I’ve seen too many projects stall or misfire due to siloed information. Sharing performance data and lessons from failed attempts increases the hit rate, speeding up adoption and reducing costly trial-and-error.

    Training also deserves mention. New compounds demand new handling protocols, measurement standards, and safety guidelines. By working together on workshops and hands-on demos, teams build shared muscle memory and can troubleshoot in real time. More than once, I’ve seen discoveries happen by accident—in a hands-on session, noticing a better way to dissolve or deposit a molecule, or keeping a film free from contamination because someone tried an alternative cleaning step.

    Good partnerships with academic collaborators also feed the progress loop. Direct feedback from those doing extended durability testing or deep-dive spectroscopy accelerates improvements and flags up any red flags early. Over the years, building these relationships pays dividends, especially as product generations evolve.

    The Road Ahead: Challenges and Optimism

    Taking a big-picture view, the story of TPCz-Ph-DFB mirrors much of the modern electronics industry—advancing not just by improving technical metrics, but by listening to those who build, use, and depend on the end products. Chemistry advances, but so does the willingness to adopt smarter, safer, and more sustainable materials.

    What strikes me most about this compound is its adaptability. From roundtable meetings with product managers to late-night lab troubleshooting, I keep encountering users who appreciate its reliability and relative ease of integration. Not every new molecule gets that kind of reception. As processes mature and production scales, the community will likely see costs fall and availability improve.

    For those looking to future-proof devices, reduce environmental impact, and build electronics that last through years of careful use, 3-[9-(4,6-Diphenyl-1,3,5-triazin-2-yl)-dibenzofuran-2-yl]-9-phenyl-9H-carbazole sets a solid example. From where I stand, its continued adoption signals a broader shift toward high-performance, sustainable, and user-driven product development in the field of functional organic materials.