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P9900

Sigma-Aldrich

Perfluorodecalin

95%

Synonym(s):

Octadecafluorodecahydronaphthalene (cis+trans), Perflunafene, Perfluorodecahydronaphthalene (cis+trans)

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About This Item

Empirical Formula (Hill Notation):
C10F18
CAS Number:
306-94-5
Molecular Weight:
462.08
Beilstein/REAXYS Number:
2067113
EC Number:
206-192-4
MDL number:
MFCD00010626
UNSPSC Code:
12352100
PubChem Substance ID:
24898930
NACRES:
NA.22

vapor density

17.5 (vs air)

Quality Level

100

assay

95%

refractive index

n20/D 1.3145 (lit.)

bp

142 °C (lit.)

mp

−10 °C (lit.)

density

1.908 g/mL at 25 °C (lit.)

SMILES string

FC1(F)C(F)(F)C(F)(F)C2(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C2(F)C1(F)F

InChI

1S/C10F18/c11-1-2(12,5(17,18)9(25,26)7(21,22)3(1,13)14)6(19,20)10(27,28)8(23,24)4(1,15)16

InChI key

UWEYRJFJVCLAGH-UHFFFAOYSA-N

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Application

Perfluorodecalin is a fluorous solvent generally used as a primary component of the fluorous biphasic system (FBS) or the fluorous multiphasic system (FMS) in synthetic chemistry. It is also used as an additive to increase oxygen solubility in fermentation media.

accessory

Product No.
Description
Pricing

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

pcodes

P210

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

138.2 °F

flash_point_c

59 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Certificates of Analysis (COA)

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Dilution-free analysis from picoliter droplets by nano-electrospray ionization mass spectrometry.
Ryan T Kelly et al.
Angewandte Chemie (International ed. in English), 48(37), 6832-6835 (2009-08-19)
Three-component one-pot synthesis of pyrimidinone derivatives in fluorous media: Ytterbium bis (perfluorooctanesulfonyl) imide complex catalyzed Biginelli-type reaction.
Hong M and Cai C
Journal of Heterocyclic Chemistry, 46(6), 1430-1432 (2009)
Sc [N (SO2C8F17) 2] 3 catalyzed condensation of β-naphthol and aldehydes in fluorous solvent: One-pot synthesis of 14-substituted-14H-dibenzo [a, j] xanthenes.
Hong M and Cai C
Journal of Fluorine Chemistry, 130(10), 989-992 (2009)
Improvement of antibiotic production by increased oxygen solubility through the addition of perfluorodecalin.
Elibol M.
Journal of Chemical Technology and Biotechnology, 76(4), 418-422 (2001)
Convenient electrophilic fluorination of functionalized aryl and heteroaryl magnesium reagents.
Yamada S, et al.
Angewandte Chemie (International Edition in English), 122(12), 2261-2264 (2010)
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