Description

2-Bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)pentane (CAS No. 22528-67-2) is a highly fluorinated brominated alkane with the molecular formula C₆BrF₁₃. This specialized organofluorine compound features a unique structure with a bromine substituent at the 2-position and a trifluoromethyl group, making it a valuable intermediate in advanced synthetic chemistry applications. Its high fluorine content and stability under extreme conditions make it suitable for use in fluoropolymer modification, specialty solvents, and as a precursor for further functionalization. The compound is supplied as a high-purity liquid (>98%) with strict quality control to ensure consistency for research and industrial applications. Store under inert conditions to maintain stability.

Properties

• CAS Number: 22528-67-2
• Complexity: 343
• IUPAC Name: 2-bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)pentane
• InChI: InChI=1S/C6BrF13/c7-1(4(12,13)14,5(15,16)17)2(8,9)3(10,11)6(18,19)20
• InChI Key: LMULIUNHVQIBGA-UHFFFAOYSA-N
• Exact Mass: 397.89758
• Molecular Formula: C6BrF13
• Molecular Weight: 398.95
• SMILES: C(C(C(C(F)(F)F)(F)F)(F)F)(C(F)(F)F)(C(F)(F)F)Br
• Monoisotopic Mass: 397.89758
• Synonyms: 22528-67-2, 2-bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)pentane, DTXSID90371231, DTXCID10322265, 2-Bromoperfluoro(2-methylpentane), 2-Bromodecafluoro-2-(trifluoromethyl)pentane, Pentane,2-bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)-, 2-bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethyl)-pentane, perfluoro-2-bromo-2-methylpentane, perfluoro-t-hexyl bromide, SCHEMBL10346353, MFCD00077551, AKOS005258175, NS00111904, A816246, Heptafluoro-1,1-bis(trifluoromethyl)butyl bromide, 2-bromo-1,1,1,3,3,4,4,5,5,5-decafluoro-2-(trifluoromethy)pentane, 2-bromanyl-1,1,1,3,3,4,4,5,5,5-decakis(fluoranyl)-2-(trifluoromethyl)pentane

Application

This compound is primarily used as a fluorinated building block in the synthesis of advanced materials, including fluoropolymers and surfactants. Its reactivity with nucleophiles makes it useful for introducing fluorinated segments into complex molecules. Researchers also explore its potential as a flame retardant additive due to its high thermal stability and bromine content. Additionally, it may serve as a specialty solvent in electrochemical applications.

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