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Dokumente

113174

Sigma-Aldrich

Pentylbenzol

99%

Synonym(e):

1-Phenyl-pentan

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About This Item

Lineare Formel:
C6H5(CH2)4CH3
CAS-Nummer:
538-68-1
Molekulargewicht:
148.24
Beilstein:
1904359
EG-Nummer:
208-701-5
MDL-Nummer:
MFCD00009502
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847137
NACRES:
NA.22

Assay

99%

Brechungsindex

n20/D 1.488 (lit.)

bp

205 °C (lit.)

mp (Schmelzpunkt)

−75 °C (lit.)

Löslichkeit

H2O: insoluble
alcohol: soluble
benzene: miscible
diethyl ether: miscible

Dichte

0.863 g/mL at 25 °C (lit.)

SMILES String

CCCCCc1ccccc1

InChI

1S/C11H16/c1-2-3-5-8-11-9-6-4-7-10-11/h4,6-7,9-10H,2-3,5,8H2,1H3

InChIKey

PWATWSYOIIXYMA-UHFFFAOYSA-N

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Anwendung

Pentylbenzene can be eluted using the bisphenol A dimethacrylate (BADMA) monolithic column.

Angaben zur Herstellung

Pentylbenzene is soluble in lithium 1-perfluoroundecanoate micelles which can be measured by increasing the surfactant concentration.

Piktogramme

Environment
GHS09

H-Sätze

H411

Gefahreneinstufungen

Aquatic Chronic 2

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

149.0 °F - closed cup

Flammpunkt (°C)

65 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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2-Methylnaphthalin (β) 95%

Sigma-Aldrich

M57006

2-Methylnaphthalin (β)

1,3,5-Triethyl-benzol ≥97%

Sigma-Aldrich

132071

1,3,5-Triethyl-benzol

2-Methylnaphthalin analytical standard

Supelco

45796

2-Methylnaphthalin

Take'uchi et al.
Journal of colloid and interface science, 197(2), 230-235 (1998-02-19)
The solubilization of benzene, toluene, ethylbenzene, n-propylbenzene, n-butylbenzene, n-pentylbenzene, n-hexylbenzene, and some arenes into lithium 1-perfluoroundecanoate micelles was measured with increasing the surfactant concentration. Concentrations of all the solubilizates in equilibrium were determined spectrophotometrically at 293.2, 298.2, 303.2, and 308.2
Yuanyuan Li et al.
Journal of chromatography. A, 1218(10), 1399-1408 (2011-02-08)
Highly cross-linked networks resulting from single crosslinking monomers were found to enhance the concentrations of mesopores in, and the surface areas of, polymeric monoliths. Four crosslinking monomers, i.e., bisphenol A dimethacrylate (BADMA), bisphenol A ethoxylate diacrylate (BAEDA, EO/phenol=2 or 4)
Reza Zadmard et al.
Journal of chromatographic science, 53(5), 702-707 (2014-10-15)
In this work, we present a new method for synthesis of silica gel stationary phases based on calix[4]arene derivatives. In order to achieve it, 25,27-dipropoxy-26,28-bis-[3-propyloxydimethylsililoxy]calix[4]arene has been synthesized in six steps and immobilized on silica via chlorotrimethylsilane. Stationary phases were
Flavio A Franchina et al.
Journal of chromatography. A, 1402, 102-109 (2015-06-03)
The present research is focused on the use and evaluation of a novel helium ionization detector, defined as barrier discharge ionization detector (BID), within the context of (low-)flow modulation comprehensive two-dimensional gas chromatography (FM GC×GC). The performance of the BID
K Elias Ikonen et al.
Journal of chromatography. A, 1614, 460705-460705 (2019-11-23)
An update for ASTM D2425, "Standard Test Method for Hydrocarbon Types in Middle Distillates by Mass Spectrometry," was recently released to expand its scope by adding modern mass spectrometric instrumentation and a new sample type, synthesized hydrocarbons. While the method
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