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Hexafluoroacetylacetone (HFA)

  • Appearance colourless liquid
  • Purity,% ≧99.0
  • CAS number 1522-22-1

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Physical and chemical properties

Chemical formula C5H2F6O2
Molar mass 208.06 g/mol
Appearance colourless liquid
Density 1.47 g/mL
Boiling point 70 to 71 °C (158 to 160 °F; 343 to 344 K)
Solubility in water organic solvents

product description

Hexafluoroacetylacetone (HFA or hfac) is a key β-diketone compound widely used in various fields due to its unique chemical properties, such as strong electron-withdrawing effects, high volatility, and excellent chelating ability. Its major applications include:  

1. Organometallic Chemistry & Materials Science
   - Precursor Compounds:  
     Metal complexes of HFA (e.g., Cu(hfac)₂, Pt(hfac)₂) are commonly used in **chemical vapor deposition (CVD)** and **atomic layer deposition (ALD)** to produce thin metal films (e.g., copper, platinum, nickel) for semiconductors, nanomaterials, and conductive coatings.  
   - Volatile Complexes:  
     These metal chelates exhibit low-temperature volatility, making them ideal for high-purity metal synthesis.  

2. Electronics Industry 
   - Etching & Cleaning Agents:  
     HFA derivatives (e.g., cobalt hexafluoroacetylacetonate) serve as **etchants** or **cleaners** in semiconductor manufacturing, removing metal oxide residues (e.g., copper oxide).  
   - Photoresist Additives:  
     Used to enhance the resolution of photolithography processes.  

3. Nuclear Fuel & Radioactive Element Processing 
   - Extraction of Actinides:  
     HFA forms stable complexes with uranium (U), thorium (Th), and plutonium (Pu), aiding in **nuclear fuel recycling** and **radioactive waste treatment**.  

4. Analytical Chemistry
   - Derivatization Reagent:  
     Improves sensitivity and selectivity in **mass spectrometry (MS)** and **gas chromatography (GC)** by chelating metal ions (e.g., Al³⁺, Fe³⁺).  
   - Sensor Materials:  
     Used in fluorescent or electrochemical sensors for metal ion detection.  

5. Catalysis & Ligands 
   - Organic Reaction Catalyst:  
     Acts as a **Lewis acid ligand** in oxidation, polymerization, or cyclization reactions (e.g., olefin epoxidation).  
   - Asymmetric Synthesis:  
     Chiral HFA derivatives enable **asymmetric catalysis**.  

6. Other Applications 
   - Stabilizer:  
     Prevents thermal degradation in polymers.  
   - Pharmaceutical Intermediate:  
     Used in synthesizing **fluorinated drugs** or bioactive molecules.  

Key Advantages  
HFA’s **strong electron-withdrawing fluorine atoms** contribute to its high stability, volatility, and strong metal-coordinating ability, making it indispensable in advanced industrial and scientific research.

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