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HS Code |
232034 |
| Cas Number | 5699-09-8 |
| Molecular Formula | C21H16O |
| Molecular Weight | 284.35 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 117-120 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | C1=CC=C(C=C1)C=CC=CC(=O)C=CC=CC2=CC=CC=C2 |
| Inchi | InChI=1S/C21H16O/c22-21(14-10-16-6-2-1-3-7-16)15-11-17-8-4-12-18(5-9-17)19-13-20-21/h1-15H |
| Storage Temperature | Room temperature |
| Synonyms | 1,9-diphenyl-1,3,6,8-nonatetraen-5-one |
As an accredited 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle with screw cap, labeled "1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One, 10g, For Laboratory Use Only," with safety warnings. |
| Shipping | 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One is shipped in tightly sealed containers under dry, cool conditions to prevent degradation. The chemical is protected from direct sunlight and moisture. Proper labeling and documentation accompany each shipment, and handling is conducted in accordance with local, national, and international hazardous material regulations. |
| Storage | **1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One** should be stored in a tightly sealed container, away from light, moisture, and incompatible materials such as strong oxidizing agents. Store at room temperature in a cool, dry, and well-ventilated area. Clearly label the container and keep it in a designated chemical storage cabinet to ensure safety and prevent contamination. |
Applications of 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One in Industrial ManufacturingAs a direct manufacturer of 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One, we support downstream customers across select industrial sectors where this specialty intermediate enables structural and performance attributes essential to value-added products. Below, we detail focused, proven applications across key industries, including applicable regulatory standards, formulation guidelines, integration steps, and finished product formats. 1. OLED Display Material SynthesisOur material is widely incorporated as a key structural subunit in the synthesis of advanced electroluminescent compounds used in organic light-emitting diode (OLED) devices. Its extended conjugation and phenyl substitution assist in tuning bright emission, high carrier mobility, and device longevity, especially in blue and green-emitting layers. Downstream formulators employ the compound during the creation of host or emitter molecules for deposition in thin-film transistor displays, flat panels, and display modules for consumer electronics. Industry compliance standards
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2. Photonic Dye for Laser Gain MediaRecognized for its extended π-conjugated backbone, the compound is synthesized into highly efficient fluorescent dyes for use as laser gain media, particularly in dye lasers requiring broad emission tuning in the visible region. Research and industry customers rely on its photostability and color purity for applications ranging from spectroscopy equipment to medical diagnostic instruments, where dye lifetimes and quantum yields directly influence end-use performance. Industry compliance standards
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3. Fluorescent Marker Synthesis in Analytical ReagentsOur compound is a precursor in the synthesis of tailored fluorescent markers used in analytical chemistry, chromatography, and bioimaging reagents. Its molecular framework allows downstream laboratories to derivatize and attach target-functional groups, generating fluorescent probes with distinct absorption/emission characteristics. Purity and batch consistency are critical for these applications, as end uses range from analytical reference standards to labeled biomolecule kits. Industry compliance standards
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4. Organic Photovoltaic Material ProductionDownstream manufacturers use our product as an intermediate in synthesizing small molecule donors or acceptors for organic photovoltaic (OPV) cells. This application leverages the compound’s planar structure and electron transport capacity to improve photon harvesting, blend miscibility, and charge mobility characteristics within the active layer of OPV devices. The focus remains on maximizing conversion efficiency and operational stability under solar exposure. Industry compliance standards
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5. Sensitizing Agent in Photopolymerization SystemsChemical formulators adopt our compound as a sensitizing agent in photopolymerization protocols requiring extended absorption for UV-curable resins and coatings. Its molecular structure allows it to transfer energy efficiently, speeding up radical generation and crosslinking in formulations for microelectronics, advanced printing, and coating technologies. Product usage hinges on spectral match and quantum efficiency needs for specific cure processes. Industry compliance standards
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