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379247

Sigma-Aldrich

Tetradecafluorohexane

A mixture of perfluorinated hexanes, 95%

Synonym(s):

Perfluorohexane

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About This Item

Linear Formula:
CF3(CF2)4CF3
CAS Number:
355-42-0
Molecular Weight:
338.04
Beilstein:
1802113
EC Number:
206-585-0
MDL number:
MFCD00000437
UNSPSC Code:
12352100
PubChem Substance ID:
24863232
NACRES:
NA.22

Quality Level

100

Assay

95%

form

liquid

impurities

5% perfluoropentane

refractive index

n20/D 1.252 (lit.)

bp

58-60 °C (lit.)

mp

-74 °C (lit.)

density

1.669 g/mL at 25 °C (lit.)

SMILES string

FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C6F14/c7-1(8,3(11,12)5(15,16)17)2(9,10)4(13,14)6(18,19)20

InChI key

ZJIJAJXFLBMLCK-UHFFFAOYSA-N

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General description

Tetradecafluorohexane in the gas phase reacts spontaneously with lithium amalgam, to give a solid and intimate mixture of lithium fluoride and elemental polymeric carbon with a small amount of superstoichiometric lithium.

Application

Tetradecafluorohexane may be used as a fluorocarbon organic solvent in the preparation of temperature-induced phase-separation solution.

Other Notes

Contains perfluorocyclohexane

Hazard Statements

H412

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Chronic 3

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Koichi Kitaguchi et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 30(6), 687-690 (2014-06-13)
A fluorocarbon and hydrocarbon organic solvent mixture is known as a temperature-induced phase-separation solution. When a mixed solution of tetradecafluorohexane as a fluorocarbon organic solvent and hexane as a hydrocarbon organic solvent (e.g., 71:29 volume ratio) was delivered in a
Hermann Fromme et al.
Environmental science & technology, 41(22), 7928-7933 (2007-12-14)
Because dietary intake is supposed to be an important route of human exposure we quantified the dietary intake of perfluorooctane sulfonate (PFOS), perfluorooctanoate (PFOA), perfluorohexane sulfonate (PFHxS), perfluorohexanoate (PFHxA), and perfluorooctane sulfonamide (PFOSA) using 214 duplicate diet samples. The study
Ondine S von Ehrenstein et al.
Reproductive toxicology (Elmsford, N.Y.), 27(3-4), 239-245 (2009-05-12)
Polyfluoroalkyl chemicals (PFCs) comprise a group of man-made organic compounds, some of which are persistent contaminants with developmental toxicity shown in laboratory animals. There is a paucity of human perinatal exposure data. The US EPA conducted a pilot study (Methods
Kyunghee Ji et al.
Environment international, 45, 78-85 (2012-05-15)
Perfluorinated compounds (PFCs) have been frequently detected in both the environment and biota, and have become a growing concern. However, information is limited on the potential sources and human health implications of such exposure. We evaluated the exposure levels of
Liselotte M Kornmann et al.
Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging, 10(5), 264-270 (2008-06-10)
We investigated in vitro the potential of macrophages to act as targeted vehicle for ultrasound molecular imaging. Murine bone marrow-derived macrophages (BMM), incubated for 3 h with different concentrations of perfluorohexane (PFH) emulsions, were monitored by microscopy, flow cytometry, and
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