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Decacyclene

    • Product Name Decacyclene
    • Alias coronene
    • Einecs 207-006-5
    • 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

    184653

    Iupac Name Tricyclo[12.4.0.02,7]octadeca-1,3,5,7,9,11,13,15,17-nonaene
    Common Name Decacyclene
    Chemical Formula C18H12
    Molar Mass 228.29 g/mol
    Appearance Yellow crystalline solid
    Melting Point 409-411 °C
    Solubility In Water Insoluble
    Cas Number 3446-89-7
    Structure Type Polycyclic aromatic hydrocarbon
    Boiling Point Decomposes before boiling

    As an accredited Decacyclene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Decacyclene is packaged in a 1-gram amber glass vial with a tightly sealed cap, labeled with safety and identification information.
    Shipping Decacyclene should be shipped in tightly sealed containers, protected from light, moisture, and sources of ignition. Transport in compliance with local, national, and international regulations for hazardous chemicals. Use appropriate labeling and documentation, ensuring handling by trained personnel. Store in a cool, dry place during transit to prevent decomposition or hazardous reactions.
    Storage Decacyclene should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Store it in tightly sealed containers, protected from light and moisture. Proper labeling and secure shelving are important to prevent spills or accidental exposure. Use appropriate personal protective equipment when handling or transferring the substance.
    Application of Decacyclene

    Applications of Decacyclene in Industrial Manufacturing

    Decacyclene functions as a polycyclic aromatic hydrocarbon with unique structural and electronic properties. Its high stability and π-conjugation enable advanced applications across specialty polymers, electronic materials, photochemistry, and research-grade intermediates. As the original manufacturer, we support customers with precise formulation guidance, compliance integration, and dedicated technical service.

    1. Organic Electronics: Semiconductor Material Synthesis

    Leading manufacturers employ Decacyclene as a core building block for organic semiconductors used in field-effect transistors and organic light-emitting diodes (OLEDs). Its rigid polycyclic structure facilitates high charge-carrier mobility and enhanced morphological stability in thin-film applications. Manufacturers precisely incorporate this raw material in the advanced stages of small-molecule synthesis for device-grade performance, closely controlling purity to eliminate electronic traps and defects in the end devices.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 62474 Declarable Substances List for electronic components
    • IPC-4101B Specification for Base Materials for Printed Boards
    • ISO 9001:2015 Certified Quality Management

    Typical usage ratio

    • 5-25 wt% in organic layer formulations, adjusted based on desired mobility and film-forming properties; higher concentrations may be needed in high-purity single-crystal applications.

    Downstream process integration

    • Added during final synthetic stages for small-molecule active layers
    • Employed in solvent cast or vapor deposition for thin-film electronics
    • Subject to additional purification through sublimation when used in device fabrication

    Final product types

    • Organic light-emitting diode (OLED) panels and modules
    • Organic field-effect transistors (OFETs)
    • Printed and flexible electronic circuits
    • Electronic display backplane materials

    2. Specialty Polymer Precursors for High-Performance Composites

    High-end composite manufacturers utilize Decacyclene to introduce extended aromatic domains and crosslinkable sites in specialty polymers. This application targets advanced matrix systems for aerospace, automotive, and high-frequency electronic laminates. The rigidity and high molecular weight enhance dimensional stability and load-transferring capacity. Producers strategically incorporate this molecule in polycondensation or in-situ copolymerization reactions to achieve superior heat resistance and dielectric performance.

    Industry compliance standards

    • ASTM D3965 Standard for Polymeric Materials
    • UL 94 Flammability Classification for plastics
    • REACH EC No 1907/2006 (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • SAE International AMS standards for aerospace-grade composites

    Typical usage ratio

    • 3-10 mol% as a comonomer or crosslinker in specialty polymer blends; proportional adjustment based on required thermal resistance and dielectric constant.

    Downstream process integration

    • Introduced during controlled polycondensation reactions for thermosetting networks
    • Blended at melt compounding stage in engineering resin formulations
    • Dispersed as a functional additive in prepreg materials for composite layup

    Final product types

    • High-frequency printed circuit board (PCB) laminates
    • Aerospace structural composites
    • Lightweight automotive components
    • Heat-resistant resin systems for power electronics

    3. Photochemical Research: Singlet Fission and Light-Harvesting Systems

    Advanced material research teams select Decacyclene for photophysical studies focused on singlet fission, triplet generation, and light-harvesting. Its planar aromatic structure allows controlled tuning of electronic coupling and excited-state dynamics. Laboratories typically use this compound as a molecular standard or core chromophore within prototype photovoltaic assemblies and optoelectronic devices. Precise synthetic protocols ensure high batch purity, necessary for reproducible research outcomes and scalable IP-validated processes.

    Industry compliance standards

    • GLP (Good Laboratory Practice) Compliance OECD Principles
    • ISO/IEC 17025 Testing and Calibration Laboratories
    • EU CLP Regulation (EC) No 1272/2008 for chemicals used in research
    • Institutional synthetic approval cycles and safety panel verification

    Typical usage ratio

    • 1-15 mg/mL in preparative solutions for film casting or microcrystal growth; final concentration varies based on spectroscopic requirements.

    Downstream process integration

    • Dissolved in high-purity solvents for thin-film photophysical measurements
    • Integrated into device prototypes during singlet fission efficiency screening
    • Employed in combinatorial libraries for synthetic chromophore variants

    Final product types

    • Reference standards for photophysical analysis
    • Laboratory-scale light-harvesting assemblies
    • Next-generation organic photovoltaic cell prototypes
    • Synthesized chromophore libraries for device patent development

    4. Chemical Synthesis Intermediates for Advanced Aromatic Derivatives

    Producers of custom aromatic compounds employ Decacyclene as an advanced intermediate in multistep syntheses, especially where control of extended conjugation and molecular symmetry is critical. Its robust ring system serves as a scaffold for regioselective functionalization, including halogenation, alkylation, and oxidative coupling. Chemists follow detailed protocols to integrate this precursor at specific stages, allowing efficient transformation toward high-performance materials, molecular wires, and reference standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemicals
    • GMP guidelines for chemical intermediates (if required for API R&D)
    • EU REACH registration and inventory rules
    • Custom synthesis compliance under customer mutual NDA

    Typical usage ratio

    • 0.05–1.2 equivalents depending on transformation efficiency and scale; adjusted for targeted yield and downstream purification requirements.

    Downstream process integration

    • Reacted in controlled batch or semi-batch reactors during custom syntheses
    • Subjected to metal-catalyzed cross-coupling or oxidative polymerization
    • Post-functionalized for ligand, porphyrin, or macrocyclic chemistry

    Final product types

    • Branched polyaromatic derivatives for high-end materials
    • Cyclic or linear π-conjugated systems for sensor development
    • Organic optoelectronic components
    • Benchmarked analytical standards for advanced organic chemistry
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