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Sigma-Aldrich

Pentylbenzene

99%

Synonym(s):

1-Phenylpentane

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About This Item

Linear Formula:
C6H5(CH2)4CH3
CAS Number:
538-68-1
Molecular Weight:
148.24
Beilstein:
1904359
EC Number:
208-701-5
MDL number:
MFCD00009502
UNSPSC Code:
12352100
PubChem Substance ID:
24847137
NACRES:
NA.22

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

Hazard Statements

H411

Precautionary Statements

P273 - P391 - P501

Hazard Classifications

Aquatic Chronic 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

149.0 °F - closed cup

Flash Point(C)

65 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
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