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1,2-Dibenzoylethane

    • Product Name 1,2-Dibenzoylethane
    • Alias DBE
    • Einecs 214-335-4
    • 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

    649925

    Cas Number 1451-23-0
    Molecular Formula C16H14O2
    Molecular Weight 238.28
    Appearance White to off-white crystalline powder
    Melting Point 94-97°C
    Boiling Point 391.8°C at 760 mmHg
    Density 1.189 g/cm3
    Solubility In Water Insoluble
    Refractive Index 1.603
    Flash Point 190.8°C
    Purity Typically ≥98%
    Synonyms Benzil monohydrate, 1,2-bis(phenyl)ethanone
    Ec Number 215-901-1

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

    Packing & Storage
    Packing A 100-gram amber glass bottle with a secure screw cap, labeled "1,2-Dibenzoylethane," including hazard symbols and safety instructions.
    Shipping 1,2-Dibenzoylethane should be shipped in tightly sealed containers, protected from light and moisture. It must be labeled according to relevant chemical transport regulations, and handled as a non-hazardous organic compound unless otherwise specified. Standard transport guidelines for laboratory chemicals apply, ensuring safe handling and prevention of leaks or spills during transit.
    Storage 1,2-Dibenzoylethane should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from sources of ignition and incompatible substances such as oxidizing agents. Ensure that the storage area is equipped with spill containment measures and labeled appropriately. Use only with proper ventilation and handle with suitable protective equipment.
    Application of 1,2-Dibenzoylethane

    Applications of 1,2-Dibenzoylethane in Industrial Manufacturing

    As an experienced manufacturer of 1,2-dibenzoylethane, we support a range of industrial sectors where advanced stabilization and processing requirements drive downstream demand. This material serves performance-driven functions in selected markets, underpinning product stability and compliance. The sections below address established downstream use cases based on formal regulatory acceptance, process integration, and end-market product design.

    1. PVC Processing – Heat Stabilization in Rigid and Flexible Formulations

    PVC manufacturers leverage 1,2-dibenzoylethane as an organic co-stabilizer to control thermal degradation during compounding and processing of both rigid (e.g., window profiles, pipes) and flexible (e.g., wire coatings, films) products. The additive works in tandem with calcium-zinc and organic tin systems, enabling compliance with halogen-free and low-lead regulatory frameworks while extending product clarity and mechanical properties under thermal stress. Process engineers tune addition levels based on the required color retention and thermal load by resin grade and line speed.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH Regulation (EC) No 1907/2006 (SVHC restrictions)
    • EN 71-3:2019 (Toy Safety - Migration of certain elements)
    • GB 4806.7-2016: National Food Safety Standard for Plastic Materials and Articles

    Typical usage ratio

    • 0.05%–0.5% by weight of total PVC resin; dosage adjusted based on thermal stability requirements, compounding method, and additive synergy with primary stabilizer system.

    Downstream process integration

    • Blended into the dry blend or paste resin mix prior to plastification, typically during high-speed premixing to ensure uniform dispersion before extrusion or calendaring.

    Final product types

    • Window and door profiles, potable water pipes, medical-grade tubing, wire and cable insulation, food contact packaging films

    2. Photoinitiation for UV-Curable Coatings and Adhesives

    For manufacturers of UV-cured coatings, inks, and adhesives, 1,2-dibenzoylethane acts as a Type II photoinitiator, facilitating the crosslinking of acrylate oligomers and monomers upon irradiation. This compound allows precise control over cure speed and depth, essential for electronics, graphic arts, and industrial flooring applications where light penetration and mobility of radical species are critical. Production chemists select this photoinitiator for systems requiring low-yellowing and specific wavelength responsiveness.

    Industry compliance standards

    • ISO 9001:2015 certified QC systems for coatings manufacturing
    • EN 71-3 (for toy coatings and inks)
    • Swiss Ordinance SR 817.023.21 (Printing Inks for Food Contact Materials)
    • FDA 21 CFR 175.300 (Resinous and Polymeric Coatings, for food packaging coating)

    Typical usage ratio

    • 0.1%–1.5% by weight of total binder solids; dosing optimized according to film thickness, pigment loading, and lamp intensity for required curing kinetics.

    Downstream process integration

    • Incorporated during the final blend of UV-curable formulations following pigment dispersion and prior to viscosity adjustment, ensuring complete dissolution before packaging or direct application.

    Final product types

    • UV-cured printing inks, protective industrial coatings, adhesive tapes, optical fiber coatings, UV lacquer for flooring

    3. Production of Polymer Additives for High-Performance Plastics

    Compounders and masterbatch producers utilize 1,2-dibenzoylethane as a key intermediate when manufacturing light stabilizers and custom antioxidant blends for engineering polymers such as ABS, PS, and polyolefins. Its molecular structure tailors absorption and stabilization profiles, especially in automotive and appliance components where low discoloration and long service life are mission-critical. Production is targeted at additive formulations for injection molding, extrusion, and blow-molding process windows.

    Industry compliance standards

    • ISO 14001 & 9001 for quality/environmental management during plastic compounding
    • UL 94 (Flammability of plastic materials for parts in devices and appliances)
    • Automotive OEM requirements (e.g., VW TL 527, GM GMW15572)
    • FDA 21 CFR 177.1520 (Polymers for food-contact plastics, for applicable grades)

    Typical usage ratio

    • 0.02%–0.3% of final polymer mass; tuned according to polymer type, anticipated UV exposure, and compatibility with pigments and fillers.

    Downstream process integration

    • Added during masterbatch production or direct compounding, co-milled with other stabilizer components before melt blending in twin-screw extruders, ensuring uniform dispersion in the polymer matrix.

    Final product types

    • Automotive interior components, appliance housings, outdoor furniture, electrical enclosures

    4. Synthesis of Pharmaceutical Intermediates in Specialty Chemical Manufacturing

    In pharmaceutical ingredient manufacturing, 1,2-dibenzoylethane functions as a building block for the synthesis of advanced intermediates, including diketone-based ligands and heterocyclic scaffolds with therapeutic potential. Its defined purity and batch traceability support use in GMP-compliant synthesis campaigns, particularly for custom active pharmaceutical ingredient (API) routes in pilot and commercial scale-up phases.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monograph requirements for starting material purity (as referenced in route documentation)
    • 21 CFR Part 211 (US FDA cGMP)
    • European Union EudraLex Volume 4 (EU GMP guidelines)

    Typical usage ratio

    • Synthesis-scale dependent; typically ranging from 0.1 to 1.8 molar equivalents relative to the target transformation, adjusted according to the step yield and stoichiometric needs in the synthetic pathway.

    Downstream process integration

    • Charged at the intermediate preparation stage of multi-step syntheses, reacted under controlled temperature and inert conditions, and subsequently purified by crystallization, extraction, or chromatography before further conversion.

    Final product types

    • Intermediates for pharmaceutical APIs, diketone-based chelating ligands, specialized fine chemicals for medicinal chemistry screening
    Free Quote

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