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CAS 1522-22-1

Hexafluoroacetylacetone TCI H0476

Hexafluoroacetylacetone TCI H0476

Chemical Identity

Other names
1,1,1,5,5,5-Hexafluoro-2,4-pentanedione
CAS No.
1522-22-1
PubChem
CID 73706·SID 87570873
Formula
C5H2F6O2
Molecular weight
208.06 g/mol
Purity
>95.0%(GC)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1,1,1,5,5,5-hexafluoropentane-2,4-dione
SMILES
C(C(=O)C(F)(F)F)C(=O)C(F)(F)F
InChIKey
QAMFBRUWYYMMGJ-UHFFFAOYSA-N
MDL
MDL00000426
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Hexafluoroacetylacetone (HFAA) is a versatile organofluorine compound widely used in chemical laboratories as a building block for complex syntheses. It plays a crucial role in organic chemistry by enabling the formation of fluorinated compounds through its reactive nature. This compound is particularly valuable in reactions that require high reactivity and specificity, making it a key component in advanced synthetic processes. Its unique chemical structure allows it to participate in various reaction mechanisms, including nucleophilic and electrophilic pathways, enhancing its utility in laboratory settings.

The properties of HFAA that make it a preferred choice include its solubility in organic solvents and its ability to undergo a wide range of chemical transformations. Its fluorinated nature provides enhanced stability and reactivity, which are essential for synthesizing complex fluorinated molecules. Additionally, HFAA exhibits good thermal stability under controlled conditions, allowing for reliable use in a variety of experimental setups. These characteristics make it an indispensable reagent for researchers working with fluorinated compounds and complex organic syntheses.

In Indonesian laboratories, Hexafluoroacetylacetone is commonly used in organic chemistry research, especially in the synthesis of fluorinated compounds and in reactions that require a reactive and specific building block. Its availability and reliability make it a standard reagent in both academic and industrial research settings. Its role in facilitating complex chemical transformations underscores its importance in the field of fluorinated chemistry.

TCI brochures (PDF)

  • Organic synthesis of fluorinated compounds due to its reactivity and ability to form complex structures.
  • Use in nucleophilic and electrophilic reactions as a versatile building block for fluorinated molecules.
  • Application in Friedel-Crafts-type reactions for the formation of aromatic fluorinated derivatives.
  • Utilization in the preparation of metal complexes due to its ability to coordinate with various metal ions.
  • Support for research in pharmaceutical and agrochemical development through its role in fluorinated compound synthesis.

Brand TCI
CAS number 1522-22-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible materials

Hexafluoroacetylacetone should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of materials compatible with fluorinated compounds, such as glass or high-density polyethylene. The compound should be kept in a well-ventilated area to prevent the accumulation of vapors. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. Avoid contact with incompatible substances, such as strong oxidizers or bases, to ensure safe storage and use in the laboratory.

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