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About This Item
Linear Formula:
CF3(CF2)5I
CAS Number:
Molecular Weight:
445.95
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-586-6
Beilstein/REAXYS Number:
1802118
MDL number:
Assay:
99%
Form:
liquid
Quality Level
assay
99%
form
liquid
refractive index
n20/D 1.329 (lit.)
bp
117 °C (lit.)
density
2.063 g/mL at 25 °C (lit.)
functional group
fluoro, iodo
SMILES string
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I
InChI
1S/C6F13I/c7-1(8,3(11,12)5(15,16)17)2(9,10)4(13,14)6(18,19)20
InChI key
BULLJMKUVKYZDJ-UHFFFAOYSA-N
General description
Perfluorohexyl iodide forms 1:1 complexes with a variety of hydrogen-bond acceptors. It has been grafted onto the isocitronellene/propene copolymer by radical reaction yielding a poly(α-olefin) with fluorinated side chains. The radical addition of perfluorohexyl iodide to vinyl acetate, using azo-bis( isobutyronitrile) (AIBN) as an initiator, has been investigated.
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
239.0 °F - closed cup
flash_point_c
115 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Effect of reaction conditions on the radical addition of perfluorohexyl iodide to vinyl acetate.
Napoli M, et al.
Journal of Fluorine Chemistry, 57(1), 219-227 (1992)
Rafel Cabot et al.
Chemical communications (Cambridge, England), (15)(15), 2005-2007 (2009-04-01)
Quantitative studies of the 1 : 1 complexes formed between perfluorohexyl iodide and a variety of hydrogen-bond acceptors have been used to probe the relationship between halogen bonding, hydrogen bonding, desolvation and the electrostatics of non-covalent interactions.
Zirconocene-MAO-catalyzed homo-and copolymerizations of linear asymmetrically substituted dienes with propene: A novel strategy to functional (co) poly (a-olefin) s.
Hackmann M, et al.
Macromolecular Chemistry and Physics, 199(8), 1511-1517 (1998)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 262145-5G | 04061837595394 |
| 262145-25G | 04061838348142 |