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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 | 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. |
Applications of Decacyclene in Industrial ManufacturingDecacyclene 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 SynthesisLeading 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
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2. Specialty Polymer Precursors for High-Performance CompositesHigh-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
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3. Photochemical Research: Singlet Fission and Light-Harvesting SystemsAdvanced 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
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4. Chemical Synthesis Intermediates for Advanced Aromatic DerivativesProducers 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
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