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Sigma-Aldrich

Iodopentafluorobenzene

99%

Synonym(s):

2,3,4,5,6-Pentafluoroiodobenzene, Pentafluoroiodobenzene

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About This Item

Empirical Formula (Hill Notation):
C6F5I
CAS Number:
827-15-6
Molecular Weight:
293.96
EC Number:
212-565-2
MDL number:
MFCD00001032
UNSPSC Code:
12352100
PubChem Substance ID:
24846596
NACRES:
NA.22

Assay

99%

refractive index

n20/D 1.496 (lit.)

bp

161 °C (lit.)

density

2.204 g/mL at 25 °C (lit.)

SMILES string

Fc1c(F)c(F)c(I)c(F)c1F

InChI

1S/C6F5I/c7-1-2(8)4(10)6(12)5(11)3(1)9

InChI key

OPYHNLNYCRZOGY-UHFFFAOYSA-N

General description

Iodopentafluorobenzene forms supramolecular complexes with aromatic electron donors by forming halogen bonds to form discrete heterodimeric aggregates.

Application

  • Iodopentafluorobenzene was used to study the formation of radical ions of iodopentafluorobenzene in aqueous solution.
  • It was used as solvent in a study to determine singlet oxgen lifetimes from phosphorescence decays in halogen substituted perfluorinated solvents by infrared emission spectrometery.
  • It has potential applications in plasma processing industry and in preparation of catalysts.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Formation and redox properties of radical ions of iodopentafluorobenzene in aqueous solution: a pulse radiolysis study
Mohan H and Mittal JP
The Journal of Physical Chemistry, 99(33), 12559-12564 (1995)
Co-crystals of iodopentafluorobenzene with nitrogen donors: 2-D molecular assemblies through halogen bonding and aryl-perfluoroaryl interactions.
Wasilewska A, et al.
CrystEngComm, 9(3), 203-206 (2007)
Influence of heavy atoms on the deactivation of singlet oxygen (1. DELTA. g) in solution
Schmidt R
Journal of the American Chemical Society, 111(18), 6983-6987 (1989)
Chenxin Ran et al.
Chemical Society reviews, 47(12), 4581-4610 (2018-04-24)
The rapid development of solar cells (SCs) based on organic-inorganic hybrid metal triiodide perovskite (MTP) materials holds great promise for next-generation photovoltaic devices. The demonstrated power conversion efficiency of the SCs based on MTP (PSCs for short) has reached over
Iodopentafluorobenzene: Electronic state spectroscopy by high-resolution vacuum ultraviolet photoabsorption and photoelectron spectroscopy.
Eden S, et al.
Chemical Physics, 359(1), 111-117 (2009)

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