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Merck
CN

113174

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847137
EC Number:
208-701-5
Beilstein/REAXYS Number:
1904359
MDL number:
MFCD00009502
Assay:
99%

Key Documents

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InChI key

PWATWSYOIIXYMA-UHFFFAOYSA-N

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

SMILES string

CCCCCc1ccccc1

assay

99%

Quality Level

200

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.)

functional group

phenyl

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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

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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Certificates of Analysis (COA)

Lot/Batch Number
0000466618
0000466618
0000454739
0000454739
0000273837

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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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