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Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 1
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 2
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 3
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 4
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 1
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 2
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 3
Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade 4

Acetylacetone (2,4-Pentanedione) 99.5% CAS NO. 123-54-6 Industrial & Pharmaceutical Grade

This high-purity Acetylacetone is a colorless to pale yellow liquid with a characteristic ketone-like odor, featuring a purity exceeding 99.5%. As a β-diketone compound, it exists predominantly in its enol form and exhibits exceptional chelating properties, forming stable complexes with various metal ions. It serves as a critical intermediate in pharmaceutical synthesis, a metal chelating agent, and a versatile building block in organic synthesis. Its high reactivity and excellent purity make it indispensable for advanced chemical manufacturing applications.

Scope of Application
· This product is widely used as a pharmaceutical intermediate in the synthesis of antiviral agents, antibacterials, anti-inflammatory drugs, and vitamin B6.
· It serves as a metal chelating agent for extracting and separating metal ions, including transition metals and lanthanides, in hydrometallurgy and analytical chemistry.
· It can be used as a ligand in the preparation of metal-organic frameworks (MOFs), coordination complexes, and catalysts for polymerization reactions.
· It is also employed as a crosslinking agent in polymer modification, a stabilizer in PVC production, and a curing agent in epoxy resin systems.
· It finds applications in the synthesis of agrochemicals, dye intermediates, and as an acetylating agent in organic transformations.

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    Product Features

    This Acetylacetone is produced via advanced condensation and purification technologies, ensuring consistent quality and batch-to-batch stability. With a purity exceeding 99.5% (verified by GC analysis) and a high enol content (>95%), it offers exceptional reactivity and chelating efficiency. The product features low water content and strict control of organic impurities, ensuring optimal performance in sensitive synthesis applications. Its unique β-diketone structure enables the formation of stable six-membered ring chelate complexes with over 60 different metal ions. Advanced analytical instruments including Gas Chromatography (GC) and Gas Chromatography-Mass Spectrometry (GC-MS) are employed to ensure the product meets stringent pharmaceutical and industrial standards. The product maintains excellent stability when stored under recommended conditions.

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    Packaging and Transportation

    · The products are packaged in clean, epoxy-lined drums, stainless steel drums, or ISO tanks to preserve product purity.

    · Customized packaging options, including HDPE containers for smaller quantities, are available upon customer request.

    Safety and Storage

    · Store in a cool, well-ventilated warehouse away from direct sunlight, heat sources, and open flames.

    · Keep container tightly sealed and properly grounded when handling to prevent static discharge. Keep away from strong oxidizing agents, strong bases, and amines.

    · The storage area should be equipped with appropriate fire-fighting equipment (alcohol-resistant foam, dry powder, carbon dioxide) and spill containment materials.

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    FAQ

    1
    What makes Acetylacetone unique among diketones?
    Acetylacetone is unique due to its high enol content (typically >95% at room temperature), which results from the stabilization of the enol form through intramolecular hydrogen bonding. This enol form readily deprotonates to form anionic ligands that create stable six-membered chelate rings with metal ions. This property makes it one of the most versatile and widely used chelating agents in coordination chemistry.
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