Perfluoro(decahydronaphthalene), cis + trans, 95%, Thermo Scientific Chemicals

Name: Perfluoro(decahydronaphthalene), cis + trans, 95%, Thermo Scientific Chemicals
SKU: A18288.14

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Catalog number A18288.14

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25 g

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Chemical Identifiers

CAS306-94-5

IUPAC Nameoctadecafluoro-decahydronaphthalene

Molecular FormulaC10F18

InChI KeyUWEYRJFJVCLAGH-UHFFFAOYSA-N

SMILESFC1(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

Specifications

Specification Sheet

Assay (GC)≥94.0% (sum of isomers)

Identification (FTIR)Conforms

Appearance (Color)Clear colorless

FormLiquid

Refractive Index1.3115-1.3175 @ 20?C

Perfluoro(decahydronaphthalene) is used to dissolve gases. Due to its gas carrying capacity, it is utilized to increase oxygen delivery during cell culture. It acts as an ingredient in fluosol which is an artificial blood product. It is also used to dissolve Teflon.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Perfluoro(decahydronaphthalene) is used to dissolve gases. Due to its gas carrying capacity, it is utilized to increase oxygen delivery during cell culture. It acts as an ingredient in fluosol which is an artificial blood product. It is also used to dissolve Teflon.

Solubility
Insoluble in water.

Notes
Incompatible with strong oxidizing agents.

RUO – Research Use Only

General References:

The ability of perfluorinated solvents to solubilize gases, together with their unique phase properties, have been exploited in a system for oxidation of aldehydes to acids, sulfides to sulfoxides and sulfones, and alkenes to epoxides. The reactions are carried out in the presence of dissolved O₂, using a transition metal (Ru, Ni) catalyst with perfluorinated ligands, in a perfluoro(decahydronaphthalene)/toluene solvent mixture under monophasic conditions at 64°C. On cooling, phase separation takes place, enabling the product to be isolated from the toluene phase, and the catalyst system to be recycled in the fluorous phase: Angew. Chem. Int. Ed., 36, 1454 (1997).
Trindade, A. C.; De Figueiredo, J. A. P.; Steier, L.; Weber, J. B. B. Photodynamic Therapy in Endodontics: A Literature Review. Photomed. Laser Surg. 2015, 33 (3), 175-182.
George, S.; Kishen, A. Augmenting the antibiofilm efficacy of advanced noninvasive light activated disinfection with emulsified oxidizer and oxygen carrier. J. Endod. 2008, 34 (9), 1119-1123.