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241989

Sigma-Aldrich

Ethoxybenzene

99%

Sinónimos:

Phenetole, Ethoxybenzene, Ethyl phenyl ether

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About This Item

Fórmula lineal:
C6H5OC2H5
Número de CAS:
103-73-1
Peso molecular:
122.16
Beilstein/REAXYS Number:
636270
EC Number:
203-139-7
MDL number:
MFCD00009090
UNSPSC Code:
12352100
PubChem Substance ID:
24854525
NACRES:
NA.22

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.)

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

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Categorías relacionadas

Application

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

pictograms

Flame
GHS02

signalword

Warning

hcodes

H226

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 2

flash_point_f

134.6 °F - closed cup

flash_point_c

57 °C - closed cup

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

293296

Butyl benzoate

Diphenyl ether ≥99%, FG

Sigma-Aldrich

W366706

Diphenyl ether

1,3-Diiodobenzene 98%

Sigma-Aldrich

475262

1,3-Diiodobenzene

Anisole analytical standard

Supelco

96109

Anisole

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
H Ohi et al.
Xenobiotica; the fate of foreign compounds in biological systems, 22(11), 1329-1337 (1992-11-01)
1. The effects of oxygen concentration were studied on the metabolic pathways of anisole homologues (anisole, phenetole and isopropoxybenzene) catalysed by liver microsomes from phenobarbital-treated rats. 2. With increase of oxygen concentration, the rate of anisole o-hydroxylation reached a plateau
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
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
Saken Sherkhanov et al.
Nature communications, 11(1), 4292-4292 (2020-08-29)
Cost competitive conversion of biomass-derived sugars into biofuel will require high yields, high volumetric productivities and high titers. Suitable production parameters are hard to achieve in cell-based systems because of the need to maintain life processes. As a result, next-generation
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