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Sigma-Aldrich

Dibenzyl ether

purum, ≥98.0% (GC)

Synonym(s):

Benzyl ether

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About This Item

Linear Formula:
(C6H5CH2)2O
CAS Number:
Molecular Weight:
198.26
Beilstein:
1911156
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

purum

Quality Level

Assay

≥98.0% (GC)

form

liquid

refractive index

n20/D 1.562

bp

158-160 °C/10 mmHg (lit.)

mp

1.5-3.5 °C (lit.)

density

1.043 g/mL at 20 °C (lit.)

SMILES string

C(OCc1ccccc1)c2ccccc2

InChI

1S/C14H14O/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2

InChI key

MHDVGSVTJDSBDK-UHFFFAOYSA-N

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General description

Thermolysis of dibenzyl ether in water was studied to probe into volatiles obtained from the reaction of coal in supercritical water. Diffusion coefficients of dibenzyl ether at infinite dilution in CO2 and ethanol mixtures has been measured.

Application

  • Green synthesis route: Research demonstrated a green synthesis route using dibenzyl ether for the formation of benzyl phenyl sulfide, emphasizing environmentally friendly methods in chemical synthesis processes (Wu et al., 2023).
  • Nanoparticle synthesis by thermal decomposition: Dibenzyl ether was used in the thermal decomposition process for the synthesis of manganese oxide nanoparticles, showcasing its utility in facilitating controlled chemical reactions (Martinez de la Torre and Bennewitz, 2020).

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1B

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

278.6 °F - Pensky-Martens closed cup

Flash Point(C)

137 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Diffusion of benzyl acetate, 2-phenylethyl acetate, 3-phenylpropyl acetate, and dibenzyl ether in mixtures of carbon dioxide and ethanol.
Suarez-Iglesias O, et al.
Industrial & Engineering Chemistry Research, 46(11), 3810-3819 (2007)
Dibenzyl ether as a probe into the supercritical fluid solvent extraction of volatiles from coal with water.
Townsend SH and Klein MT.
Fuel: The Science and Technology of Fuel and Energy, 64(5), 635-638 (1985)
Hui-Ling Dai et al.
Chemical & pharmaceutical bulletin, 57(1), 84-86 (2009-01-06)
Ten single benzyl phenyl ethers were synthesized and evaluated as human immunodeficiency virus-1 (HIV-1) inhibitors in vitro for the first time. Among these compounds, especially 4-nitrobenzyl phenyl ether (3h) exhibited the highest anti-HIV-1 activity with EC50 (concentration of drug that
Ya-Ping Tu
The Journal of organic chemistry, 71(15), 5482-5488 (2006-07-15)
It is often found in mass spectrometry that when a molecule is protonated at the thermodynamically most favorable site, no fragmentation occurs, but a major reaction is observed when the proton migrates to a different position. For benzophenones, acetophenones, and
Hosamani Basavaprabhu et al.
Organic & biomolecular chemistry, 10(13), 2528-2533 (2012-03-01)
An application of the classical Ritter reaction for the synthesis of unsymmetrical di and trisubstituted ureas catalyzed by FeCl(3) is described. The protocol is of significant interest in view of the easy availability of precursors, mild reaction conditions employed and

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