Atomfair 1,6-Diiodoperfluorohexane C6F12I2 CAS 375-80-4

1,6-Diiodoperfluorohexane (CAS No. 375-80-4) is a highly fluorinated organic compound with the molecular formula C6F12I2. Its IUPAC name is 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodohexane , reflecting its fully fluorinated backbone and terminal iodine atoms. This compound is characterized by its exceptional chemical stability, hydrophobicity, and resistance to thermal degradation, making it a valuable intermediate in advanced synthetic chemistry and materials science. With a purity grade suitable for research and industrial applications, our 1,6-Diiodoperfluorohexane is rigorously tested to ensure consistency and reliability. It is commonly used in the synthesis of fluorinated polymers, surfactants, and specialty chemicals. The compound’s unique perfluorinated structure also lends itself to…

Description

1,6-Diiodoperfluorohexane (CAS No. 375-80-4) is a highly fluorinated organic compound with the molecular formula C6F12I2. Its IUPAC name is 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodohexane, reflecting its fully fluorinated backbone and terminal iodine atoms. This compound is characterized by its exceptional chemical stability, hydrophobicity, and resistance to thermal degradation, making it a valuable intermediate in advanced synthetic chemistry and materials science.

With a purity grade suitable for research and industrial applications, our 1,6-Diiodoperfluorohexane is rigorously tested to ensure consistency and reliability. It is commonly used in the synthesis of fluorinated polymers, surfactants, and specialty chemicals. The compound’s unique perfluorinated structure also lends itself to applications in surface modification, nanotechnology, and as a precursor for further functionalization.

Packaged under inert conditions to maintain stability, this product is ideal for researchers and scientists working in organofluorine chemistry, catalysis, and high-performance material development. Available in various quantities to suit laboratory and bulk requirements.

Properties

  • CAS Number: 375-80-4
  • Complexity: 338
  • IUPAC Name: 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodo-hexane
  • InChI: InChI=1S/C6F12I2/c7-1(8,3(11,12)5(15,16)19)2(9,10)4(13,14)6(17,18)20
  • InChI Key: JOQDDLBOAIKFQX-UHFFFAOYSA-N
  • Exact Mass: 553.78978
  • Molecular Formula: C6F12I2
  • Molecular Weight: 553.85
  • SMILES: C(C(C(C(F)(F)I)(F)F)(F)F)(C(C(F)(F)I)(F)F)(F)F
  • Monoisotopic Mass: 553.78978
  • Synonyms: 1,6-Diiodoperfluorohexane, 375-80-4, 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodohexane, T7E2MA3AD2, Hexane, 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodo-, EINECS 206-794-7, DTXSID90190949, DTXCID80113440, 206-794-7, 1,6-diiodododecafluorohexane, Dodecafluoro-1,6-diiodohexane, 1,6-Diiododecafluorohexane, C6F12I2, Perfluoro-1,6-diiodohexane, MFCD00042264, UNII-T7E2MA3AD2, SCHEMBL51180, 1,1,2,2,3,3,4,4,5,5,6,6-dodecafluoro-1,6-diiodo-hexane, AKOS015853706, DB-049140, D2333, NS00011020, D83410

Application

1,6-Diiodoperfluorohexane is widely employed as a key building block in the synthesis of fluorinated polymers and surfactants, offering enhanced chemical and thermal resistance. Its terminal iodine atoms facilitate nucleophilic substitution reactions, enabling the creation of complex fluorinated architectures. Researchers utilize this compound in surface modification to impart hydrophobic and oleophobic properties to materials. Additionally, it serves as a precursor in the development of advanced nanomaterials and specialty chemicals for high-performance applications.

Safety and Hazards

GHS Hazard Statements

  • Not Classified
  • Reported as not meeting GHS hazard criteria by 47 of 52 companies (only 9.6% companies provided GHS information). For more detailed information, please visit ECHA C&L website.

Hazard Classes and Categories

  • Not Classified

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