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5027-32-7

2,5-Hexanedione, 3,4-diacetyl-

Catalog#: AR00I9OU  |   CAS#: 5027-32-7  |   MDL#: MFCD00031531  |   MF: C10H14O4  |   MW: 198.2158

Packsize Purity Price Availability Quantity
50mg 97% $15.00 Global Stock Buy Now Add To Cart
100mg 97% $16.00 Global Stock Buy Now Add To Cart
250mg 97% $26.00 Global Stock Buy Now Add To Cart
1g 97% $70.00 Global Stock Buy Now Add To Cart
5g 97% $207.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00I9OU
Chemical Name 2,5-Hexanedione, 3,4-diacetyl-
CAS Number 5027-32-7
Molecular Formula C10H14O4
Molecular Weight 198.2158
MDL Number MFCD00031531
SMILES CC(=O)C(C(C(=O)C)C(=O)C)C(=O)C
NSC Number 35137

The 3,4-Diacetylhexane-2,5-dione, also known as acetylacetone, is a widely used compound in chemical synthesis due to its versatile applications. This compound is commonly utilized as a β-diketone ligand in coordination chemistry, forming stable complexes with various metal ions. In addition, acetylacetone is a key building block in the synthesis of heterocyclic compounds, such as pyrazoles, pyridines, and pyrimidines.Furthermore, 3,4-Diacetylhexane-2,5-dione serves as a chelating agent in analytical chemistry, enabling the determination of metal ions in solution through complexation reactions. Its ability to form stable metal complexes makes it a valuable tool in metal extraction and separation processes. Additionally, acetylacetone is employed in organic synthesis as a carbonyl compound, participating in aldol condensation reactions and as a precursor in the formation of enolates for further transformations.Overall, the versatility of 3,4-Diacetylhexane-2,5-dione makes it a valuable reagent in various chemical synthesis applications, ranging from coordination chemistry to organic transformations.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H302-H315-H319-H335
Precautionary Statements P261-P280-P301+P312-P302+P352-P305+P351+P338
Class N/A
Packing Group N/A

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