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Sigma-Aldrich

Perfluoro-1,3-dimethylcyclohexane

technical grade, 80%

Synonym(s):

Decafluoro-1,3-bis(trifluoromethyl)cyclohexane, Hexadecafluoro-1,3-dimethylcyclohexane, Hexadecafluoro-1,3-dimethylcyclohexane (cis+trans)

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About This Item

Linear Formula:
C6F10(CF3)2
CAS Number:
335-27-3
Molecular Weight:
400.06
Beilstein/REAXYS Number:
2064147
EC Number:
206-386-9
MDL number:
MFCD00001469
UNSPSC Code:
12352100
PubChem Substance ID:
24857038
NACRES:
NA.22

grade

technical grade

vapor density

14 (vs air)

assay

80%

form

liquid

refractive index

n20/D 1.3 (lit.)

bp

101-102 °C (lit.)

mp

−55 °C (lit.)

density

1.828 g/mL at 25 °C (lit.)

SMILES string

FC(F)(F)C1(F)C(F)(F)C(F)(F)C(F)(F)C(F)(C(F)(F)F)C1(F)F

InChI

1S/C8F16/c9-1(7(19,20)21)3(11,12)2(10,8(22,23)24)5(15,16)6(17,18)4(1,13)14

InChI key

LOQGSOTUHASIHI-UHFFFAOYSA-N

General description

Quenching of the second excited singlet state of xanthione in inert, nonpolar perfluoro-1,3-dimethylcyclohexane has been studied using picosecond time-resolved fluorescence decay methods.

Application

Perfluoro-1,3-dimethylcyclohexane has been used in:
  • the preparation of amorphous fluorocarbon films by plasma polymerization
  • hydroformylation of linear terminal alkenes using rhodium based catalysts under fluorous biphasic conditions in the presence and absence of toluene

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Electrical and optical properties of amorphous fluorocarbon films prepared by plasma polymerization of perfluoro-1, 3-dimethylcyclohexane.
Weber A, et al.
Journal of Vacuum Science & Technology. A, Vacuum, Surfaces, And Films, 16(4), 2120-2124 (1998)
Hydroformylation in perfluorinated solvents; improved selectivity, catalyst retention and product separation.
<BIG>Foster DF, et al. </BIG>
Tetrahedron, 58(20), 3901-3910 (2002)
Transient effects in the fluorescence quenching of xanthione in perfluoro-1, 3-dimethylcyclohexane.
Maciejewski A, et al.
International Journal of Radiation Applications and Instrumentation, Part B: Nuclear Medicine and Biology, 39(1), 155-158 (1992)
Meagan M Gadzuk-Shea et al.
The journal of physical chemistry. B, 122(43), 9947-9955 (2018-10-24)
Understanding the structures of proteins in the gas phase is essential for using gas-phase measurements to infer the properties of proteins in solution. Using serum albumin as a model, this study aims to expand our understanding of this relationship for
Antonelle Pardo et al.
Journal of chromatography. A, 1364, 128-139 (2014-09-10)
Molecularly imprinted polymers (MIPs) based on quercetin and synthesized by either bulk, precipitation or suspension polymerization were characterized in terms of size and shape by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). After a study of rebinding protocols

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