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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:
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

Signal Word

Warning

Hazard Statements

H226

Precautionary Statements

P210

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

138.2 °F

Flash Point(C)

59 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK6925
STBK3405
STBJ7116
STBH8323
STBH2228

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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)
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)
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)
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)
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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