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Merck
CN

P9900

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:
Molecular Weight:
462.08
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-192-4
Beilstein/REAXYS Number:
2067113
MDL number:
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Product Name

Perfluorodecalin, 95%

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

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

vapor density

17.5 (vs air)

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.)

Quality Level

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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.

pictograms

Flame

signalword

Warning

hcodes

pcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

138.2 °F

flash_point_c

59 °C

ppe

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

Regulatory Information

危险化学品
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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)
Helen G Pennington et al.
PLoS pathogens, 15(3), e1007620-e1007620 (2019-03-12)
The biotrophic fungal pathogen Blumeria graminis causes the powdery mildew disease of cereals and grasses. We present the first crystal structure of a B. graminis effector of pathogenicity (CSEP0064/BEC1054), demonstrating it has a ribonuclease (RNase)-like fold. This effector is part
Palladium-Catalyzed Oxidation and Cyclization of Carbon-Carbon Triple Bonds in Fluorous Media Using Molecular Oxygen.
Wen Y, et al.
Synlett, 2011(07), 1023-1027 (2011)
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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