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113174

Sigma-Aldrich

Pentylbenzene

99%

Sinónimos:

1-Phenylpentane

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About This Item

Fórmula lineal:
C6H5(CH2)4CH3
Número de CAS:
538-68-1
Peso molecular:
148.24
Beilstein/REAXYS Number:
1904359
EC Number:
208-701-5
MDL number:
MFCD00009502
UNSPSC Code:
12352100
PubChem Substance ID:
24847137
NACRES:
NA.22

Quality Level

200

assay

99%

refractive index

n20/D 1.488 (lit.)

bp

205 °C (lit.)

mp

−75 °C (lit.)

solubility

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

density

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

InChI key

PWATWSYOIIXYMA-UHFFFAOYSA-N

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Application

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

Preparation Note

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

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

149.0 °F - closed cup

flash_point_c

65 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificados de análisis (COA)

Lot/Batch Number
MKCP6112
MKCK8494
MKCF6103
MKCF2227
MKBW9238V

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Sigma-Aldrich

M57006

2-Methylnaphthalene (β)

1,3,5-Triethylbenzene ≥97%

Sigma-Aldrich

132071

1,3,5-Triethylbenzene

Perylene analytical standard

Supelco

45798

Perylene

2-Methylnaphthalene analytical standard

Supelco

45796

2-Methylnaphthalene

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
Pavel Jandera et al.
Journal of chromatography. A, 1410, 76-89 (2015-08-05)
We studied possibilities of prediction of the gradient elution data for alkylbenzenes, flavones and phenolic acids on two short octadecyl silica gel monolithic columns, namely a Chromolith Flash C18, 25×4.6mm, and a "new generation" Chromolith High Resolution C18, 50×4.6mm, in
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