2,2,6,6-Tetramethylheptane-3,5-dione丨CAS 1118-71-4

2,2,6,6-Tetramethylheptane-3,5-dione丨CAS 1118-71-4
Product Introduction:
Catalog No.: SS139271
CAS No.: 1118-71-4
Purity(GC): 98.0% min.
Product Name: 2,2,6,6-Tetramethylheptane-3,5-dione
Molecular Formula: C11H20O2
Molecular Weight: 184.28br /> Synonym(s): 1,3-Di-tert-butyl-1,3-propanedione
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Technical Parameters
Description

Hangzhou Leap Chem Co., Ltd. is one of the most professional manufacturers and suppliers of 2,2,6,6-tetramethylheptane-3,5-dione丨cas 1118-71-4 in China. Welcome to wholesale bulk high quality chemical products at competitive price from our factory. If you have any enquiry about custom service, please feel free to email us.

 

Specifications

 

Appearance Colorless to light yellow liquid or solid
Purity (GC) 98.0% min
Loss on drying 0.5% max

 

 

 

Applications

 

2,2,6,6-Tetramethylheptane-3,5-dione is primarily used as a chelating ligand in the preparation of stable metal complexes with transition and rare earth metals, which find applications in catalysis, analytical chemistry, and materials science. The compound is also used in organometallic synthesis to generate metal β-diketonates that serve as precursors for metal oxide nanoparticles, thin films, and ceramics. In organic synthesis, it can act as a versatile intermediate for constructing heterocyclic compounds, diketone derivatives, and substituted enols. Additionally, it is used in research laboratories for studying coordination chemistry, reaction mechanisms, and developing new metal–organic frameworks (MOFs) or catalytic systems.

 

Benefits

 

One of the main benefits of 2,2,6,6-tetramethylheptane-3,5-dione is its strong chelating ability and sterically protected β-diketone structure, which improves the stability of metal complexes and prevents undesired side reactions. The steric hindrance around the carbonyl groups enhances thermal and chemical stability, making it suitable for high-temperature and harsh reaction conditions. Its solubility in common organic solvents facilitates easy handling, formulation, and incorporation into synthetic reactions. The compound's versatility allows selective functionalization and modification, supporting diverse applications in catalysis, material science, and organometallic chemistry. Furthermore, its well-defined structure provides reproducible performance in analytical, synthetic, and industrial processes.

 

Conclusion

 

2,2,6,6-Tetramethylheptane-3,5-dione is a valuable β-diketone intermediate widely used in metal complex synthesis, catalysis, and organic chemistry. Its sterically hindered structure, strong chelation properties, and thermal stability make it a key compound for developing advanced materials, organometallic complexes, and functional organic molecules. As demand grows for high-performance ligands and catalytic systems, this compound remains a significant tool in modern chemical and material research.

 

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