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372439

Sigma-Aldrich

Perfluoro(methyldecalin), mixture of isomers

technical grade, 80%

Sinonimo/i:

Heptadecafluorodecahydro(trifluoromethyl)naphthalene

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About This Item

Formula empirica (notazione di Hill):
C11F20
Numero CAS:
51294-16-7
Peso molecolare:
512.09
Codice UNSPSC:
12352100
ID PubChem:
24863035
NACRES:
NA.22

Grado

technical grade

Saggio

80%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.317 (lit.)

P. eboll.

137-160 °C (lit.)

Punto di fusione

−40 °C (lit.)

Densità

1.95 g/mL at 25 °C (lit.)

Stringa SMILE

FC(F)(F)C1(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.FC(F)(F)C3(F)C(F)(F)C(F)(F)C(F)(F)C4(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C34F

InChI

1S/C11F20/c12-1-2(13,6(19,20)10(27,28)9(25,26)4(1,15)16)5(17,18)8(23,24)7(21,22)3(1,14)11(29,30)31
LWRNQOBXRHWPGE-UHFFFAOYSA-N

Descrizione generale

Perfluoro(methyldecalin) is a fluorinated solvent.

Applicazioni

Perfluoro(methyldecalin is suitable reagent used to investigate the reactions of iodide anions and anions derived from glow discharge ionization of perfluoro(methyldecalin) with positive ions derived from poly(ethylene glycol). It is suitable reagent used for the oxidation of alcohols with the ruthenium porphyrin at higher temperatures (140ºC) and elevated oxygen pressures (50psi). Perfluoro(methyldecalin (Perfluoro-1-Methyldecalin) may be used in the preparation of undecafluoro-6-trifluoromethyltetralin via defluorination.

Altre note

Contains perfluorodecalin

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.0 °F - closed cup

Punto d’infiammabilità (°C)

112.80 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Perfluoro-1-methyldecalin as a potential oxygen carrier with fluid scleral lenses.
M F Refojo et al.
Current eye research, 4(6), 732-733 (1985-06-01)
Michinao Hashimoto et al.
Small (Weinheim an der Bergstrasse, Germany), 3(10), 1792-1802 (2007-09-25)
A method is described for the formation of stable, composite aqueous emulsions of 1) combinations of distinct families of bubbles of nitrogen, 2) combinations of distinct families of droplets of an organic fluid (either perfluoro(methyl)decalin or hexadecane), and 3) combinations
M K Bakulin et al.
Mikrobiologiia, 75(3), 371-376 (2006-07-29)
The isolates of pseudomonads (56) and of Plesiomonas shigelloides (7) exhibiting ice-forming activity were isolated from plant leaves and rhizosphere. The theoretical possibility of the application of perfluorocarbons (PFC) with a gas-transporting function (perfluorodecalin, carbogal, and perfluoromethyldecalin) for the cultivation
Reactions of poly (ethylene glycol) cations with iodide and perfluorocarbon anions.
Stephenson Jr JM and McLuckey SA.
Journal of the American Society For Mass Spectrometry, 9(9), 957-965 (1998)
D J McIver et al.
Biochimica et biophysica acta, 751(1), 74-80 (1983-03-22)
An effective substitute for pulmonary surfactant must be able to reduce water-vapour surface tensions to under 1 mN/m and it must spread rapidly and spontaneously at the air interface from the aqueous phase. Pure dipalmitoylphosphatidylcholine meets the former requirement, but
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