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1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One

    • Product Name 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One
    • Alias Dibenzalacetone
    • Einecs 249-112-3
    • 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

    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 & Storage
    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.
    Application of 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One

    Applications of 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One in Industrial Manufacturing

    As 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 Synthesis

    Our 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

    • RoHS Directive (2011/65/EU) for hazardous substances in electronic equipment
    • REACH Regulation (EC 1907/2006) for chemical substance registration and safety
    • IEC 62321 standard for substances in electrical and electronic products
    • ISO 9001 certified quality management systems for electronic materials

    Typical usage ratio

    • 3%–12% w/w in host–guest OLED emitting layer formulations, adjusted for color purity and luminance performance targets

    Downstream process integration

    • Incorporated during organic synthesis of emitter molecules, then blended into solution for spin-coating or vacuum deposition onto ITO-coated substrates under a cleanroom-controlled atmosphere

    Final product types

    • OLED display panels for smartphones, tablets, TVs, and automotive dashboard screens
    • Wearable electronics with flexible display modules
    • High-end signage and miniature display units

    2. Photonic Dye for Laser Gain Media

    Recognized 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

    • EN 60825-1:2014 for laser product safety
    • ISO 10110-17 for optics and photonics components
    • ASTM F519 for stress corrosion and chemical compatibility
    • RoHS compliance for photonic components in European markets

    Typical usage ratio

    • 0.1–0.4 mM (30–120 mg/L) within solvent-based dye matrices, adjusted based on required lasing threshold and emission wavelength

    Downstream process integration

    • Added to solvent mixtures and filtered, then filled into quartz cells or incorporated into solid-state polymer matrices during gain media fabrication

    Final product types

    • Tunable dye lasers for academic and industrial research
    • Analytical instrumentation for fluorescence spectroscopy
    • Pulsed laser devices for medical and surgical applications

    3. Fluorescent Marker Synthesis in Analytical Reagents

    Our 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

    • ISO 17034:2016 for production of reference materials
    • Ph. Eur. General Chapter 2.2.25 for fluorescence spectrophotometry
    • IUPAC nomenclature and analytical reagent purity requirements
    • Good Laboratory Practice (GLP) protocols

    Typical usage ratio

    • Varies between 1–10 μmol per labeling reaction, adjusted per target molecule size and required signal intensity

    Downstream process integration

    • Undergoes chemical modification and coupling in solution-phase syntheses, then purified and formulated into ready-to-use analytical or biolabeling reagents

    Final product types

    • Fluorescent labeling kits for nucleic acids and proteins
    • Certified analytical reference dyes
    • Calibration standards for chromatography and flow cytometry

    4. Organic Photovoltaic Material Production

    Downstream 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

    • IEC 61215 for photovoltaic module design qualification
    • UL 1703 for safety of flat-plate photovoltaic modules
    • ISO 14001 environmental management systems for solar component manufacturing
    • RoHS and REACH compliance for materials in solar cell assemblies

    Typical usage ratio

    • 4%–9% wt/wt in donor–acceptor blend formulations, optimized for specific device architectures and light-absorbing layers

    Downstream process integration

    • Introduced during small molecule or polymer synthesis, then dispersed in organic solvents for slot-die coating or roll-to-roll printing onto conductive substrates in controlled production environments

    Final product types

    • Flexible organic solar cells and photovoltaic modules
    • Portable solar charging units
    • Photovoltaic layers for building-integrated solar windows

    5. Sensitizing Agent in Photopolymerization Systems

    Chemical 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

    • ISO 13655 for spectral measurement in graphic technology
    • IEC 60432 for safety in ultraviolet lamps and photopolymerization equipment
    • REACH chemical safety requirements for UV/EB curable systems
    • DIN EN 71-3 for migration of certain elements in coatings for children’s toys (where relevant)

    Typical usage ratio

    • 0.5%–2% w/w in photoinitiator blends for resins, with exact level determined by resin type and lamp wavelength

    Downstream process integration

    • Incorporated directly into resin or ink masterbatches before UV/EB curing, followed by application using automated coating, printing, or molding lines

    Final product types

    • UV-cured printed circuit boards and solder masks
    • High-definition inkjet printing inks
    • UV-cured coatings for electronic and automotive parts
    Free Quote

    Competitive 1,9-Diphenyl-1,3,6,8-Nonatetraen-5-One prices that fit your budget—flexible terms and customized quotes for every order.

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