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241989

Ethoxybenzene

Name: Ethoxybenzene
Brand: ALDRICH

99%

Synonym(s):

Phenetole, Ethoxybenzene, Ethyl phenyl ether

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About This Item

Linear Formula:

C₆H₅OC₂H₅

CAS Number:

103-73-1

Molecular Weight:

122.16

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24854525

EC Number:

203-139-7

Beilstein/REAXYS Number:

636270

MDL number:

MFCD00009090

Assay:

99%

Form:

liquid

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Properties

Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.507 (lit.)

bp

169-170 °C (lit.)

mp

−30 °C (lit.)

solubility

alcohol: freely soluble(lit.), diethyl ether: freely soluble(lit.), water: insoluble(lit.)

density

0.966 g/mL at 25 °C (lit.)

functional group

phenoxy

SMILES string

CCOc1ccccc1

InChI

1S/C8H10O/c1-2-9-8-6-4-3-5-7-8/h3-7H,2H2,1H3

InChI key

DLRJIFUOBPOJNS-UHFFFAOYSA-N

Description

Application

Ethoxybenzene (Phenetole) was used as an analyte in assaying the performance of the porous graphitic carbon (PGC) particles.

pictograms

GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

134.6 °F - closed cup

flash_point_c

57 °C - closed cup

Regulatory Information

危险化学品

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Study of the competitive isotherm model and the mass transfer kinetics for a BET binary system.

Wojciech Piatkowski et al.

Journal of chromatography. A, 1003(1-2), 73-89 (2003-08-06)

The competitive adsorption behavior of the binary mixture of phenetole (ethoxy-benzene) and propyl benzoate in a reversed-phase system was investigated. The adsorption equilibrium data of the single-component systems were acquired by frontal analysis. The same data for binary mixtures were

Detailed analysis of the vibronic structure of phenetole in its first excited state and ionic ground state.

Niklas Helle et al.

European journal of mass spectrometry (Chichester, England), 25(1), 142-156 (2019-02-19)

The vibronic structure of the first electronically excited state S1 and ionic ground state D0 of phenetole has been investigated by means of resonance enhanced multi photon ionization (REMPI) and mass analyzed threshold ionization (MATI) spectroscopy. The vibronic levels were

Functionalization/passivation of porous graphitic carbon with di-tert-amylperoxide.

David S Jensen et al.

Journal of chromatography. A, 1218(46), 8362-8369 (2011-10-19)

Porous graphitic carbon (PGC) particles were functionalized/passivated in situ in packed beds at elevated temperature with neat di-tert-amylperoxide (DTAP) in a column oven. The performance of these particles for high performance liquid chromatography (HPLC) was assayed before and after this

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Global Trade Item Number

SKU	GTIN
241989-100ML	04061825560762
241989-500ML	04061837632938