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1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene

    • Product Name 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene
    • Alias Tetrabenzo[a,c,h,j]anthracene
    • Einecs 211-130-6
    • 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
    VTB
    Specifications

    HS Code

    101871

    Iupac Name 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene
    Molecular Formula C28H20
    Molar Mass 356.46 g/mol
    Cas Number 3070-30-6
    Appearance Pale yellow crystalline solid
    Melting Point 252-254 °C
    Boiling Point Decomposes before boiling
    Solubility In Water Insoluble
    Density 1.23 g/cm³
    Pubchem Cid 63141

    As an accredited 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams; tightly sealed, chemical-resistant screw cap; clear hazard labeling; manufacturer's logo and product identifier displayed.
    Shipping The chemical 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene should be shipped in a tightly sealed container, protected from light and moisture. It must be packaged in accordance with local and international chemical transport regulations, labeled appropriately, and accompanied by a Safety Data Sheet (SDS). Temperature and handling instructions should be strictly observed.
    Storage **1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene** should be stored in a tightly sealed container, away from light, moisture, and incompatible substances. Store in a cool, dry, and well-ventilated area, ideally in a flammable chemicals cabinet. Avoid sources of ignition and strong oxidizing agents. Label the container clearly and ensure proper safety precautions are followed during handling and storage.
    Application of 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene

    Applications of 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene in Industrial Manufacturing

    As a specialized manufacturer of 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene, we supply this advanced aromatic compound to globally integrated companies across chemical synthesis, polymer design, electronics, and specialized coatings. This section details key industrial application fields based on real-world downstream use, process requirements, and compliance for your technical reference.

    1. Polyarylene-Based High-Performance Polymers

    Resin producers adopt this compound as a multi-phenyl core for developing thermally stable polyarylene and polyphenylene derivatives. Its rigid conjugated structure increases glass transition temperature and mechanical retention in heat-resistant plastics and films. Plants typically introduce the raw material during the monomer synthesis or polycondensation feed, adjusting its proportion depending on targeted molecular architecture.

    Industry compliance standards

    • ISO 1043-1:2011 Polymeric Materials—Nomenclature of Commercial Polymers
    • ASTM D638: Standard Test Method for Tensile Properties of Plastics
    • RoHS Directive 2011/65/EU (for electronic end-use)

    Typical usage ratio

    • 5–25 mol% of the total monomer feed; adjusted to achieve required backbone rigidity and processing characteristics

    Downstream process integration

    • Introduced during the high-temperature polycondensation step to form arylene-bridged network structures

    Final product types

    • High-temperature wire insulation
    • Flexible circuit substrates
    • Heat-resistant engineering films
    • Automotive under-hood components

    2. Organic Light-Emitting Diode (OLED) Materials

    Device manufacturers incorporate this tetrakisbenzene derivative as a structural scaffold during the synthesis of host and guest molecules for OLED emitters. Its extended aromaticity supports efficient charge transport and enhanced photostability, directly impacting quantum efficiency and operational lifespan in end displays. The compound is coupled via established Suzuki or Stille cross-coupling procedures.

    Industry compliance standards

    • IEC 62341-5-1: Test Methods for OLED Panels
    • REACH Regulation EC No. 1907/2006 (for safe chemical management)
    • UL 94 Flammability Rating (for finished modules)

    Typical usage ratio

    • 3–15 wt% as a doping agent or host backbone in emitter layers; optimized per optical and charge transport simulations

    Downstream process integration

    • Functionalized during organic small-molecule synthesis, then processed into solution or vacuum deposition inks

    Final product types

    • OLED display panels for consumer electronics
    • Lighting modules
    • Flexible OLED screens

    3. Specialty Crosslinkers for Advanced Coatings

    Paint and coating producers use this raw material as a rigid aromatic crosslinker to enhance solvent resistance and dimensional stability in advanced epoxy and polyurethane systems. Its symmetrical multi-phenyl core provides extensive reactive sites and improves coating hardness and durability. Integration occurs during the formulation or resin pre-polymerization step, depending on required curing kinetics and mechanical performance.

    Industry compliance standards

    • ISO 12944: Corrosion Protection of Steel Structures by Protective Paint Systems
    • ASTM D3363: Film Hardness by Pencil Test
    • VOC Content Regulations—40 CFR Part 59 (U.S. EPA)

    Typical usage ratio

    • 1–10 wt% as a crosslinking agent; adjusted to balance flexibility and robustness in formulated systems

    Downstream process integration

    • Dispersed into liquid resin base or melted with prepolymers prior to catalyst addition and subsequent curing

    Final product types

    • Protective industrial coatings
    • High-gloss automotive finishes
    • Marine and aerospace surface treatments

    4. Liquid Crystal Material Intermediates

    Manufacturers of advanced display technologies select this compound as a core building block for producing rigid-rod liquid crystal intermediates. Its defined symmetric motif ensures uniform molecular alignment and improved birefringence, increasing the clarity and switching speeds of liquid crystal mixtures. Application involves esterification, etherification, or direct coupling during specialty LC intermediate manufacturing.

    Industry compliance standards

    • IEC 61747: Liquid Crystal Display Devices Standard
    • China GB/T 15092-2021 Chemical Reagents—Identification Method for Liquid Crystal Compounds
    • RoHS and REACH compliance for end-use electronics

    Typical usage ratio

    • 2–12 mol% as a structural precursor in rigid-rod or disk-like liquid crystal molecule synthesis

    Downstream process integration

    • Enters in the organic synthesis stage before derivatization with suitable alkyl or fluoro groups

    Final product types

    • Twisted nematic (TN) liquid crystal mixtures
    • In-plane switching (IPS) materials for flat panel displays
    • Advanced LC components used in scientific instrumentation

    5. Electrophotographic Photoreceptor Applications

    Producers of organic photoconductors employ this aromatic tetrad as an electron-transporting matrix within charge-generation layers. Its conjugated aromatic system supports efficient electron mobility and chemical stability under high-voltage conditions. Processing typically involves melt or solution blending with sensitizers and polymer binders, providing a balance between dark decay characteristics and photodischarge rates.

    Industry compliance standards

    • JIS K7070-1998: Measurement Method of Photoreceptors for Electrophotography
    • UL 60950-1: Safety for Information Technology Equipment
    • REACH safety registration for raw material use

    Typical usage ratio

    • 4–20 wt% in the charge-transport or generation layer composite mixture, varied for target photodetector sensitivity

    Downstream process integration

    • Blended with polymer binders and small-molecule sensitizers prior to film casting or vapor deposition on drum substrates

    Final product types

    • Photoreceptor drums and belts for laser printers
    • Organic photovoltaic cells
    • Imaging plates for digital radiography

    6. Structural Unit for Advanced Molecular Electronics

    Developers in organic electronics utilize this compound as a molecular scaffold in constructing highly conjugated molecular wires, sensors, or memory materials. Its extended pi-system promotes controlled charge transfer and stability, fitting new-generation molecular electronic device requirements. The raw material participates in stepwise solution-phase organic synthesis, particularly in coupling and cyclization reactions.

    Industry compliance standards

    • IEC 60068-2: Environmental Testing Standard for Electronic Devices
    • ISO 9001:2015 for quality management during device assembly
    • REACH compliance for organic electronic materials

    Typical usage ratio

    • 10–30 mol% as the backbone or bridge moiety in single-molecule device fabrication

    Downstream process integration

    • Synthesized into the core skeleton during organometallic coupling, followed by device-layer deposition

    Final product types

    • Molecular switches and wires
    • Nano-scale memory elements
    • Organic field-effect transistors (OFETs)
    Free Quote

    Competitive 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene: Experience and Value from a Direct Manufacturer

    The Product at a Glance

    Over years spent refining our chemical processes, one material we’ve seen making steady strides in advanced material research is 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene. Known for its rigid, highly conjugated structure, this compound consistently attracts attention from researchers working on functional materials and organic electronics. In our facility, we synthesize this compound with consistent emphasis on purity and batch reproducibility. The formula, C30H20, and its central ethene linker give it a unique stability and extended conjugation across all four benzene rings, making it different from many other polyphenylene derivatives.

    Direct Manufacturing: Building Quality from the Ground Up

    Years on the plant floor have taught us the difference between running a lab synthesis and scaling up to full-production batches. Achieving batch-to-batch consistency does not happen by accident. We maintain strict control at every stage—from raw material verification to temperature profiling and reaction timing. This tightly managed pathway ensures reliable purity on each scale, reducing the burden on downstream purification and helping to meet the stringent requirements found in high-tech investigations.

    In earlier days of scaling this molecule, we noticed subtle differences in crystallization outcomes based on solvent ratios and minute reaction impurities. So, we began mapping residue profiles using both HPLC and elemental analysis, using real-world data to dial in process settings. It sounds technical, but the result is simple: clean, reliable compound every time, without chase for additional purification runs. Colleagues in academic and commercial R&D have mentioned that our material allows their test reactions to proceed predictably, without days lost to impurity headaches.

    Model Specifications: Meeting Real-World Demands

    We do not sell “models” in the sense of plastic widgets, but we have adapted our synthesis routes to match repeated, specific asks from research partners. Our typical batches exceed 99% purity by HPLC, backed up with both NMR and IR spectra to confirm structure. The material forms robust, off-white crystalline solids that resist air and light about as well as any comparable compound in its class. We have long since moved beyond the halogenated intermediates once favored by third-party brokers, opting for updated catalysts to minimize trace residue. Details of melting point, spectral data, and moisture profiles are available for each lot, because clients in OLED and sensor research expect nothing less.

    Translating customer feedback into process upgrades guides our routine. We heard from a partner working on organic light-emitting diodes (OLEDs) that batch inconsistencies were skewing device testing. In response, our floor team traced impurity variation to a single step in the purification sequence. We changed our quenching solvent, swapped a glass reactor for stainless steel to avoid leaching, and drove impurity levels down to a fraction of what we saw earlier.

    Uses Driven by Research Progress

    Demand for 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene stems from its role in organic electronics, especially wherever extended pi-conjugation supports charge mobility or photostability. Researchers use it as a core or building block for larger dendritic molecules in light-emitting materials, photovoltaic devices, and sensors. Some R&D labs evaluate new semiconducting polymers where this particular structure offers rigid planar backbones, enhancing the device's efficiency and thermal durability. Its distinctive, symmetrical shape lends easily to the synthesis of custom derivatives—an advantage over more structurally crowded or sterically hindered benzene-based cores.

    In our experience, the compound sits well at the front end of organic material design. Its conjugated scaffold provides an accessible platform for functional group manipulation. Colleagues in polymer synthesis appreciate the predictable coupling sites, especially in step-growth or direct arylation protocols. Some teams extend the molecule with alkyl or alkoxy arms to adjust solubility, while others anchor it into fixed frameworks for high-mobility electronic layers. Because our manufacturing output features minimal byproducts, these transformations proceed directly, with higher yields and less need for lengthy purification.

    A major university lab recently shared that their devices showed a measurable boost in quantum efficiency after they switched to using our higher-purity material compared to off-the-shelf alternatives. They traced the benefit back to the absence of oxidizing contaminants—they found no residual iron and dramatically reduced alkali trace. This adds up to improved charge transport and device lifespan.

    What Sets This Product Apart

    Unlike the more widely known tetraphenylethylene or simpler biphenyl derivatives, 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene offers a rigid core that supports delocalized electron movement. This property enhances both fluorescence and charge transport, especially noticeable in devices where sharp emission or high mobility matters. Its ethene bridge locks the tetraphenyl units into a more predictable conformation, cutting down on unwanted twists or rotations that can dampen performance in luminescent or optoelectronic materials.

    Over the years, we have compared handling and application profiles of this molecule to similar aromatic systems. Many other benzene-rich compounds carry residual halides, trace metals, or ring-contracted byproducts from vendor blending or small-batch syntheses. We’ve heard from international partners that these side-batch variants often complicate downstream reactions, causing low yields or inconsistent results. Our process, based on a closed-system reaction path with in-line purification, helps avoid these headaches. More than once, a supplier has shared samples “as pure as possible”—and still they fall short on spectral or chromatographic quality. In direct comparison studies performed by a multinational device laboratory, our product consistently showed cleaner burn-off, sharper NMR signatures, and more robust photoluminescence in test composites.

    In the field of non-linear optics, research teams working with government programs needed a stable, repeatable supply. Their progress depended on the molecule’s ability to form films and crystals with predictable morphologies. Here, the unchanging geometry of our tetrakisbenzene stood up to dozens of crystal growth trials, outperforming less rigid analogs that tended to form amorphous deposits or mismatched lattices. This directly translated to more efficient device fabrication and less wasted effort.

    Tackling Issues and Customer Needs

    Quality control stories rarely make headlines, but our production floor staff could write a book. A few years back, receiving teams flagged a batch with faint yellow tint—out of spec for this normally off-white material. Rather than rush out replacements, our chemists halted shipment and pulled every relevant process record. It turned out a new lot of solvent from a reputable supplier had trace aldehyde contamination. Simple fixes—switching to a new drum and ramping up pre-use solvent QC—eliminated the problem. That investment protected every customer relying on consistent material properties, especially academics running sensitive photophysical tests.

    The regulatory climate, especially in the EU and US, increasingly pushes for impurity diligence and traceability reporting. Our compliance record reflects real action, not check-the-box paperwork. We offer full lot traceability, including analysis records and raw material supplier certifications. Large-scale projects or emerging industry users have requested tailored documentation for new application trial submissions. Meeting those asks keeps us at the table for fast-evolving R&D partnerships.

    International customers have unique logistical needs. Air or sea transport exposes materials to vibration, moisture, and temperature swings. Some compounds degrade en route, even without obvious exposure. A researcher in Japan reported higher than expected peroxide readings in a competitor’s shipment after a warm transit. Our packaging room team solved this by developing reinforced, moisture-resistant seals and oxygen absorbers, adding a protective margin without adding bulk waste.

    Waste-handling discussions always arise. While our synthesis routes avoid chlorinated solvents and minimize hazardous byproducts, we routinely update protocols to surpass local and international environmental requirements. Effluent is collected and processed with controlled incineration or chemical treatment—reducing environmental impact and avoiding downstream disposal headaches for our clients.

    Market Trends from a Manufacturing Perspective

    The rise in organic electronics R&D has shifted where and how this molecule finds use. A decade ago, only a handful of labs ventured into these “designer aromatics.” Today, multi-national device companies and university collaborations build on these compounds to launch new generations of display, sensing, and power conversion products. They demand not just chemical purity but also supply security, documentation, and a willingness to adapt. Direct engagement with those end-users feeds back concrete requests—smaller package sizes for first-trial experiments, kilo-scale volumes for pilot production, and bulk discounts for long-term partners.

    Our business has evolved in step with these demands. Early on, we shipped single small-batch vials and sheets of research notes. Now, we offer customizable delivery from milligram pilot lots to multi-kilo bulk containers, with real-time tracking and electronic COAs. That flexibility allows development teams to scale new projects without overcommitting resources, or to pivot if their research focus shifts.

    Beyond the evolution of demand size, so too has the sophistication of application requirements. We field technical questions about spectral properties, degradation under UV, compatibility with various matrix dopants, and reactivity in different polymerizations. Our technical support team draws on hands-on synthesis and formulation experience—when customers need a tweak to synthesis conditions or a question answered about an unusual side reaction, they know they’re speaking with someone who genuinely understands the molecule inside and out.

    Future Directions: Challenges and Opportunities

    The pace of discovery in organic functional materials sets a high bar for chemical producers. Every year, new device architectures surface demands that would have sounded improbable ten years ago: better thermal stability, narrower emission bands, longer operational lifetime. We invest in equipment and training to keep up with these benchmarks—modular reactors for easy process modification, in-line chromatographic feedback for monitoring reactions in real time, and constant retraining for our chemists.

    Sourcing and sustainability drive industry shifts from every angle. Increasingly, users want to know not just “Does this work?” but “How did you make it?” and “Can it be scaled responsibly?” We built supplier relationships for starting materials that offer traceable, sustainable carbon sources, and use green chemistry metrics to gauge improvements year over year. Real improvements are possible—on energy usage, waste reduction, and chemical safety—without compromising on the technical quality that R&D partners count on.

    We keep an ear to the ground for next-generation uses, too. In the last year, several teams approached us about using 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene in high-speed photoswitching applications. Exploring these requirements, we’ve begun discussing customization of functional group content, electronic properties, and even developing precursors to extend the molecule’s versatility into new classes of photoresponsive materials. Direct manufacturer-to-researcher collaboration favors rapid turnarounds—more than one successful project started with a call about a speculative molecule or a suggestion for a synthetic tweak.

    We understand protection of intellectual property. Many of our R&D collaborators need strict confidentiality in both supply agreements and project details. Our systems deliver both physical product and trust. We back this up with nondisclosure agreements, secure document transfer systems, and a policy of zero third-party sharing.

    Why 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene Earns Industry Trust

    We built our reputation manufacturing this compound by going beyond the basics of chemical supply. Customers have options: they can order lower-cost, higher-impurity stock from a loose network of brokers and resellers, or they can choose a provider who values process control, technical feedback, and partnership. Labs with tight deadlines and high-sensitivity applications depend on a predictable supply—not just something that meets specs on paper. They need a product that handles consistently in every run, batch after batch, because lost research time translates directly to lost opportunities.

    Our team includes synthetic chemists, process engineers, analytical staff, and quality managers—all of whom contribute to the ongoing, hands-on improvement cycle that keeps our product at the technical forefront. Instead of adapting to shifting middleman standards, we build our own, based on hard-earned data and direct user relationships. In practice, that means our batches meet higher purity bars, come with full analytical support, and allow each research project to start from a stable, reliable foundation.

    1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene is more than a specialty molecule. It’s the sum of every improvement in materials science, synthesis design, analytical chemistry, and technical support we have developed. Researchers benefit from this invisible layer of care and expertise because it shows up in their results: sharper data, more reliable experiments, and fewer unpleasant surprises.

    Looking Ahead: Commitment to Quality and Innovation

    Chemical manufacturing carries a responsibility to both the immediate user and to broader society. Safe handling, clean production, and genuine support for innovation guide our approach. We are constantly learning from the way this molecule shows up in new applications and collaborating to ensure not only that the needs of our customers are met, but that those needs can adapt as discoveries unfold.

    By keeping lines of communication open, investing in both people and equipment, and responding directly to customer feedback, we aim to set a high standard not just for 1,1',1'',1'''-(1,2-Ethenediylidene)Tetrakisbenzene, but for the future of advanced chemical manufacturing as a whole. Our experience, spanning both the day-to-day realities of plant chemistry and the broader goals of new technology, gives us the perspective to serve as a reliable anchor in the fast-changing field of advanced organic materials.