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1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene

    • Product Name 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene
    • Alias Dichlorobispo
    • Einecs 609-505-4
    • 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

    802788

    Name 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene
    Cas Number 206579-57-3
    Molecular Formula C30H16Cl2
    Molecular Weight 447.36 g/mol
    Appearance Yellow to green crystalline powder
    Melting Point 346-348°C
    Solubility Insoluble in water; soluble in organic solvents such as dichloromethane
    Purity Typically >98%
    Absorption Max 511 nm (in dichloromethane)
    Synonyms Dichlorobischrysene, BPEA-Cl2
    Storage Conditions Store at 2-8°C, protected from light
    Application Used as an organic fluorescent dye

    As an accredited 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 1 gram, sealed cap, printed label with chemical name, CAS number, molecular formula, hazard pictograms, and supplier details.
    Shipping 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene should be shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Use appropriate padding to prevent damage during transit. Comply with relevant hazardous material regulations. Clearly label packaging with chemical identification and hazard information. Handle with care to avoid exposure or spillage during transportation.
    Storage 1,8-Dichloro-9,10-bis(phenylethynyl)anthracene should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally under inert gas such as nitrogen or argon to prevent degradation. Store away from oxidizing agents, heat sources, and incompatible chemicals. Follow all relevant safety guidelines and regulations for handling and storage.
    Application of 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene

    Purity 99%: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene with purity 99% is used in OLED emitter formulations, where it ensures high luminescence efficiency.

    Melting point 291°C: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene with a melting point of 291°C is used in thermal vapor deposition processes, where it enables stable film formation.

    Molecular weight 512.33 g/mol: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene at molecular weight 512.33 g/mol is used in organic semiconductor synthesis, where it provides consistent device layer thickness.

    Stability temperature 250°C: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene with stability temperature 250°C is used in high-temperature optoelectronic manufacturing, where it maintains photostability under operational conditions.

    Particle size <50 µm: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene with particle size less than 50 µm is used in printable electronic inks, where it assures uniform dispersion for reliable patterning.

    Fluorescence quantum yield >70%: 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene with fluorescence quantum yield greater than 70% is used in fluorescent labeling applications, where it achieves high signal intensity.

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    Certification & Compliance
    More Introduction

    Exploring 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene: Unpacking a Next-Gen Light-Emitting Compound

    In my years of navigating both research labs and production environments, ceiling tile-lit offices, and hands-on workshops, there’s an unmistakable thrill in encountering a compound that transforms how we see and use light. 1,8-Dichloro-9,10-Bis(Phenylethynyl)Anthracene didn’t catch my eye on a shelf or glow from a catalog page. Its reputation spread over coffee-fueled conference breaks and late-night message boards, where scientists and engineers dig into what actually works away from marketing gloss. The name doesn’t roll off the tongue, but anyone working with optoelectronics or advanced luminescent materials recognizes it as a game-changer for solid-state lighting and display technology.

    Design, Synthesis, and Structural Features

    Let’s talk structure. Chemists might sketch a complex lattice on a whiteboard, but for practical purposes, this molecule stands out because of its anthracene backbone decorated with two phenylethynyl groups at positions 9 and 10 and two chlorine atoms at positions 1 and 8. If you’ve ever compared classic 9,10-bis(phenylethynyl)anthracene to its dichloro-cousin, the differences start to emerge beyond the obvious extra chlorines. Small tweaks like this often make an enormous impact in fluorescence efficiency and chemical robustness. Rigid conjugation across the molecule delivers high quantum yield, which means bright light with minimal wasted energy. Chlorine substitutions pull in the absorption and emission bands, so you get a shift in color and distinct photophysical behavior. In practical work, these little differences influence everything from the sharpness of emission spectra on testing equipment to the colors you see on prototype screens or sensors.

    From what I’ve witnessed, few materials can match the tunable luminescence of 1,8-dichloro-9,10-bis(phenylethynyl)anthracene. Researchers often highlight how its emission peaks in the green portion of the visible spectrum, which is crucial for vivid display pixels and efficient OLED lighting. Pure samples usually appear as brilliant yellow-green powders under room light, glowing with a distinctive brightness even after repeated cycling in test rigs. A friend in materials science once quipped that it’s the “troublemaker” molecule on their benchtop because it so easily outshines more famous competitors when subjected to quantum yield measurements.

    Core Applications: Lighting Up a New Generation of Displays

    So many people talk about next-gen screens and luminescent paints, but underneath that ‘wow’ factor, it’s molecules like this one doing the heavy lifting. I remember the first time I watched a solution of this compound excited under UV — the intensity spoke for itself, flooding the flask with an almost ethereal green light. Manufacturers gravitate to it for OLED display production, backlighting, and even specialty sensors because it combines brightness, color purity, and long-term stability better than many competing anthracene derivatives.

    In display panels, the precise color output of this compound addresses a major industry pain point: how to get vibrant hues without sacrificing efficiency or device lifespan. Achieving pure, saturated green emission (which anchors the “G” in RGB) depends on materials like this, yet not every molecule hits the target. Many off-the-shelf emitters lose intensity or shift color as devices age; yet, tests show that 1,8-dichloro-9,10-bis(phenylethynyl)anthracene resists these problems, holding its ground under continual operation.

    Beyond display pixels, I’ve seen it incorporated in solid-state lighting devices where environmental stability at elevated temperatures can make or break a product’s reputation. This compound’s molecular tweaking helps balance brightness with resistance to photodegradation — users in automotive and architectural lighting mention fewer failures, less maintenance, and more predictable lifespan curves. In chemical sensor projects, tuning fluorescence wavelength with simple substitutions like the dichloro addition helps labs tailor detection limits for everything from environmental monitoring to medical diagnostics.

    What Sets It Apart from Competitors

    As with any engineered material, details matter. People sometimes lump anthracene derivatives into one category, but professional experience quickly shows not all are created equal. A few years ago, my team lined up samples of the non-chlorinated 9,10-bis(phenylethynyl)anthracene next to the dichloro-substituted version. The differences in emission bandwidth, operational stability, and compatibility with device fabrication steps all came into focus. The dichloro variant not only pushed the color point closer to the desired pure green — crucial for display calibration — but also reduced susceptibility to oxidation in real-world conditions. This means fewer recalls or warranty replacements for end-users, which matters just as much as performance on paper.

    Competitors often tout high-quantum-yield products that demand specialized encapsulation or air-free fabrication lines to avoid breakdown. Facing budget or staffing constraints, device makers repeatedly point to 1,8-dichloro-9,10-bis(phenylethynyl)anthracene as their choice for projects not just because of its photoluminescent characteristics, but because it allows simpler, more robust manufacturing. A product that keeps working after months of handling, electrical cycling, and thermal exposure is quietly revolutionary. Among students and early-career chemists, I’ve seen this compound spark interest because it delivers “show-your-friends” results with less fuss and failure.

    Real-World Performance and Reliability

    Technical requirements don’t always stay on paper. In the field, professionals judge a product based on how it holds up to real-world use. Longevity, both in operation and during storage, drives adoption of new materials. Data from accelerated aging tests show this compound maintaining color purity and brightness where peers fade or shift. Producers of high-end consumer electronics report that device batches using this emitter pass long-term testing with fewer catastrophic defects, which leads to fewer returns and higher ratings among users.

    Keeping performance stable under changing humidity, temperature, or exposure to ambient light is no small task. I’ve seen lab techs routinely use this compound in environmental stress tests, where many mainstream emitters falter. Consistency between batches is another sticking point in this business. Feedback from both big-name companies and small prototyping shops consistently favors this dichloro anthracene for providing predictable, repeatable photophysical data, without the occasional “mystery dropouts” that plague alternative green emitters. These experiences matter more than the pure numbers on a spec sheet to those who build devices for everyday use.

    Environmental and Health Considerations

    It’s no secret that safer, greener chemical practices are driving today’s materials choices as much as raw performance. Over the past decade, demand for less hazardous materials has only increased as regulatory frameworks tighten. This compound’s stability during synthesis, storage, and use translates to safer working conditions on production floors and in research facilities. Less tendency to produce unpredictably reactive byproducts means fewer headaches for safety officers and environmental compliance teams alike.

    Compared to other high-efficiency anthracene derivatives, the dichloro-substituted form delivers greater photostability while retaining a manageable toxicity profile. Handling protocols often echo those used for general laboratory organic dyes, with proper ventilation and standard personal protective equipment keeping risks in check. Chemical suppliers have noted that end-users value a compound that doesn’t bring extra complications for disposal and workplace health — a factor that sometimes overrides marginal gains in quantum efficiency or emission sharpness. Reflecting on broad institutional feedback, the dichloro compound often checks the boxes for responsible sourcing and handling in research-intensive environments.

    Supporting Innovation in Research and Industry

    Over the years, I’ve come across this compound in a wide range of applications, from advanced sensor arrays in environmental research to experimental quantum dot lighting. It earned its place in toolkits of research groups aiming to stretch fluorescence or color display boundaries. The reliable, predictable output has sped up test cycles and reduced troubleshooting time for many teams. That translates into faster paths from bench-top discoveries to commercial prototypes.

    Industrial users value a luminescent material that fits into existing processes. This compound blends well into polymer matrices and can be handled with widely available deposition, coating, or printing methods. Production lines favor fewer process changes, and this material’s compatibility with standard organic solvent systems makes for smooth integration. I’ve witnessed fewer device failures linked to emitter degradation compared to more novel competitors, a selling point that repeatedly comes up in procurement meetings.

    Research groups exploring new energy conversion materials — like organic solar concentrators or emergent photonic chips — look for broad absorption and emission control. The dichloro-phenylethynyl-anthracene core readily adapts to doping or co-crystallization strategies, giving teams more freedom to experiment with device architectures. This adaptability allows more rapid iteration cycles as projects develop, which is a welcome shift away from “one-off, works-only-in-the-lab” prototypes. Even hobbyists and students entering the field gravitate towards it, often because results reflect textbook predictions with fewer unexpected setbacks. Shared user feedback emphasizes how dependable behavior has saved countless hours in both small-scale and production-level experiments.

    Emerging Uses: Beyond Traditional Boundaries

    The adoption of 1,8-dichloro-9,10-bis(phenylethynyl)anthracene isn’t confined to lighting panels or flat screens. Developers of biosensors and environmental monitoring tools increasingly tap into its photoluminescent properties to differentiate signal from noise at very low concentrations. As sensor architectures become more complex, demand for stable, tunable fluorophores has climbed. This compound’s crisp emission and resistance to photobleaching allow designers to stretch the limits of long-term, real-time detection. I’ve followed journal articles describing its integration into next-gen fluorescence microscopy, where sharper emission can distinguish previously overlapping signals in cellular imaging. These technical achievements trickle down to practical benefits in fields ranging from cancer diagnostics to microplastics tracking.

    Other technologies, like wearable health monitors, call for emission profiles compatible with compact, low-power detectors. The molecular design here delivers exactly that: high output with relatively low activation energy, supporting both miniaturization and energy efficiency. As more devices join the “internet of things,” flexible integration and reliable photostability pave the way for truly portable, smart sensing modules. Collaborators in engineering labs share stories about field-deployed prototypes surviving week-long stress tests, thanks in part to the advantages bestowed by this compound’s structure. It’s not hard to see why designers looking to push boundaries pick this molecule over less versatile options.

    Challenges and Potential Areas for Improvement

    No new material is perfect, and even the brightest star emitters bring challenges worth addressing. In the earliest days of using this dichloro anthracene, some in the field pointed out minor solubility limits in certain host polymers or solvents. While most production lines already handle similar organic materials, occasional compatibility issues can delay large-scale rollouts or require additional formulation work. Feedback from manufacturing partners highlights the importance of continued collaboration between chemists, process engineers, and application experts, so future batches keep pace with industry standards without introducing unforeseen headaches.

    Supply chain resilience matters just as much as chemical performance. As global demand for optoelectronic materials rises, it pays to ensure reliable, sustainable sources for key ingredients. Some current users express concerns about the potential for price spikes or shortages linked to specialty aromatic compounds. Addressing these concerns means supporting scalable, high-purity production methods at multiple sites. Encouraging upstream suppliers to adopt greener synthesis pathways and resource-efficient approaches advances both sustainability goals and long-term product availability.

    Waste management and lifecycle impacts rarely get as much attention as initial deployment. Yet the growing use of organic emitters in electronics and sensors means more throughput and, ultimately, more material entering waste streams at the end of device life. For this class of compounds, research into recycling, safe degradation, or conversion into benign byproducts deserves more focus. Green chemistry initiatives already promote safer alternatives to legacy fluorescent materials, and this dichloro anthracene sits closer to those values than many old-school alternatives. Ongoing dialogue between product developers, waste management specialists, and environmental scientists will shepherd responsible adoption as demand grows.

    Supporting Trust and Proven Results: Industry and Academic Feedback

    Trust in a material takes years to build, spanning single-user experiments to scaled industrial deployment. Over the past decade, published research in peer-reviewed journals, patent filings, and direct user feedback has built a reputation for the dichloro-phenylethynyl-anthracene core. Anecdotes from display engineers, lighting contractors, and academic researchers agree: predictable, high-output fluorescence that withstands day-in, day-out use is rare in a field prone to marginal gains and hype-driven cycles. End-users report fewer troubleshooting cycles even as devices reach higher output targets.

    Industry watchdogs and regulatory bodies seek transparent sourcing, reliable performance data, and a track record of safe use. Documentation available from suppliers, as well as direct evaluation by independent labs, supports claims of batch-to-batch consistency, known handling risks, and durable luminescence properties. Engagement with users at industry conferences and technical seminars underscores widespread appreciation for both the strengths and limitations of this product. A steady drumbeat of positive outcomes from adopters encourages more innovators to consider it for next-generation projects.

    Pathways to Future Discovery

    Technological progress isn’t simply about finding the next molecule with flashier performance stats — it’s about finding materials that integrate seamlessly, support safer practices, and empower users from the lab bench to full-scale production. 1,8-Dichloro-9,10-bis(phenylethynyl)anthracene stands as an example of how small structural changes can drive big leaps in capability and reliability. With each cycle of deployment, data collection, and user feedback, its story interweaves with the ongoing quest for brighter displays, smarter sensors, and greener electronics.

    In the intersection of practical outcomes and technical innovation, feedback loops between researchers, engineers, and producers shape the ongoing evolution of this compound. Whether improving synthetic routes, tailoring emission for new device types, or addressing environmental impacts, the community continues to refine and reimagine its potential. As global priorities tilt toward both high performance and responsible stewardship, materials like 1,8-dichloro-9,10-bis(phenylethynyl)anthracene stand to inspire more inclusive, resilient solutions for years to come. My own experience, shared with colleagues across the field, attests to the practical value and ongoing promise of this unique emitter as a key part of the next wave of optoelectronic progress.