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113174

Pentylbenzene

Name: Pentylbenzene
Brand: ALDRICH

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%

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Properties

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.)

functional group

phenyl

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

Description

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.

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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

0000532586

0000466618

0000454739

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Preparation of monoliths from single crosslinking monomers for reversed-phase capillary chromatography of small molecules.

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)

Solubilization of n-Alkylbenzenes into Lithium 1-Perfluoroundecanoate Micelles

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

Separation of amino acids by high performance liquid chromatography based on calixarene-bonded stationary phases.

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

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Global Trade Item Number

SKU	GTIN
113174-25G	04061838700834
113174-100G	04061838700827