Cas no 13429-24-8 (Hexafluoropropene Dimer)

Hexafluoropropene Dimer (C6F12) is a fluorinated hydrocarbon formed by the dimerization of hexafluoropropene. This compound exhibits exceptional thermal and chemical stability due to its perfluorinated structure, making it suitable for high-performance applications. Its low surface energy and inertness contribute to its use as a lubricant, dielectric fluid, or processing aid in demanding environments. The dimer's resistance to oxidation, acids, and solvents enhances its utility in semiconductor manufacturing, aerospace, and specialty coatings. Additionally, its non-flammable and non-reactive properties ensure safety in critical industrial processes. The product's precise synthesis and high purity further support its role in advanced material science and electronics applications.
Hexafluoropropene Dimer structure
Hexafluoropropene Dimer structure
Product Name:Hexafluoropropene Dimer
CAS No:13429-24-8
MF:C6F12
MW:300.045043945313
CID:49233
PubChem ID:83439
Update Time:2025-05-19

Hexafluoropropene Dimer Chemical and Physical Properties

Names and Identifiers

    • Hexafluoropropylene dimer
    • 1,1,2,3,3,3-Hexafluoro-1-propene dimer
    • DIMERS OF HEXAFLUOROPROPENE
    • 1,1,1,3,4,4,5,5,5-nonafluoro-2-(trifluoromethyl)pent-2-ene
    • 1,1,2,3,3,3-hexafluoroprop-1-ene
    • 1-Propene, 1,1,2,3,3,3-hexafluoro-, dimer
    • Dodecafluoro-2-methyl-2-pentene
    • HEXAFLUOROPROPENE
    • Dimer Hexafluoropropylene oxide
    • 1,1,2,3,3,3-Hexafluoro-1-propene, dimer
    • Hexafluoropropylene
    • 13429-24-8
    • FS-4223
    • SCHEMBL2836890
    • HEXAFLUOROPROPENEDIMER
    • AKOS025213552
    • FT-0625022
    • Perfluoroprop-1-ene
    • DTXSID70894291
    • Hexafluoropropene Dimer
    • Inchi: 1S/2C3F6/c2*4-1(2(5)6)3(7,8)9
    • InChI Key: PBVZTJDHQVIHFR-UHFFFAOYSA-N
    • SMILES: FC(/C(=C(\F)/F)/F)(F)F.FC(/C(=C(\F)/F)/F)(F)F

Computed Properties

  • Exact Mass: 299.980838
  • Monoisotopic Mass: 299.980838
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 12
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 0
  • Complexity: 126
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 0

Experimental Properties

  • Density: 1.622
  • Boiling Point: 53-61 oC
  • Flash Point: 10 oF
  • LogP: 4.53220
  • Vapor Pressure: 234.7±0.1 mmHg at 25°C

Hexafluoropropene Dimer Security Information

  • Signal Word:warning
  • Hazard Statement: Irritant
  • Warning Statement: P264+P280+P305+P351+P338+P337+P313
  • Hazardous Material transportation number:UN 1993
  • Hazard Category Code: R11
  • Safety Instruction: S16;S29;S33
  • Hazardous Material Identification: F
  • Risk Phrases:R11
  • Safety Term:S16;S29;S33
  • Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)

Hexafluoropropene Dimer Pricemore >>

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Hexafluoropropene Dimer Related Literature

Additional information on Hexafluoropropene Dimer

Hexafluoropropene Dimer: A Comprehensive Overview

Hexafluoropropene dimer, also known by its CAS number 13429-24-8, is a compound of significant interest in various scientific and industrial applications. This compound is a dimer of hexafluoropropene, which itself is a highly fluorinated alkene with the chemical formula C3F6. The dimerization process results in a molecule with the formula C6F12, which exhibits unique chemical and physical properties that make it valuable in numerous fields.

The synthesis of hexafluoropropene dimer typically involves the reaction of hexafluoropropene under specific conditions, such as high pressure or catalytic processes, to form the dimer. Recent studies have explored novel synthesis methods that enhance the efficiency and scalability of this process, making it more viable for industrial applications. These advancements are particularly relevant in the context of increasing demand for fluorinated compounds in various industries.

One of the most notable applications of hexafluoropropene dimer is in the field of materials science, where it serves as a precursor for the production of advanced polymers and composites. The high fluorine content of this compound imparts exceptional thermal stability and chemical resistance to the resulting materials, making them ideal for use in harsh environments such as aerospace and automotive industries.

In addition to its role in polymer production, hexafluoropropene dimer has found applications in electronic manufacturing. Its ability to act as a precursor for fluorinated thin films has made it valuable in the production of high-performance electronics, including semiconductors and optoelectronic devices. Recent research has focused on optimizing the deposition processes to achieve better film quality and uniformity, further enhancing its utility in this sector.

The chemical stability of hexafluoropropene dimer also makes it a promising candidate for use in refrigeration and insulation systems. Its low global warming potential (GWP) and ozone-friendly properties align with current environmental regulations and sustainability goals, positioning it as a viable alternative to traditional refrigerants.

From a research perspective, hexafluoropropene dimer has been extensively studied to understand its structural properties, reactivity, and potential for further functionalization. Computational chemistry techniques have been employed to model its molecular structure and predict its behavior under various conditions, providing valuable insights for both academic and industrial applications.

In conclusion, hexafluoropropene dimer, with its unique properties and versatile applications, continues to be a focal point in scientific research and industrial development. As advancements in synthesis methods and application technologies progress, the potential for this compound to contribute to emerging technologies remains vast and promising.

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