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P24101

Sigma-Aldrich

Diphenyl ether

ReagentPlus®, 99%

Synonym(s):

Diphenyl oxide, Phenyl ether

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About This Item

Linear Formula:
(C6H5)2O
CAS Number:
101-84-8
Molecular Weight:
170.21
Beilstein:
1364620
EC Number:
202-981-2
MDL number:
MFCD00003034
UNSPSC Code:
12352100
PubChem Substance ID:
57654511
NACRES:
NA.21

vapor density

>5.86 (25 °C, vs air)

Quality Level

200

vapor pressure

<1 mmHg ( 20 °C)

product line

ReagentPlus®

Assay

99%

form

crystals

autoignition temp.

1144 °F

expl. lim.

1.5 %

refractive index

n20/D 1.579 (lit.)

bp

259 °C (lit.)

mp

25-27 °C (lit.)

density

1.073 g/mL at 25 °C (lit.)

functional group

phenoxy

SMILES string

O(c1ccccc1)c2ccccc2

InChI

1S/C12H10O/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H

InChI key

USIUVYZYUHIAEV-UHFFFAOYSA-N

Gene Information

human ... TTR(7276)

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General description

Diphenyl ether (DPE) is a bridged-phenyl molecule. The conformational analysis of using resonance-enhanced two-photon ionization method DPE has been reported.

Application

Diphenyl ether may be used to synthesize dibenzofuran via intramolecular cyclization in the presence of palladium acetate.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H319,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

239.0 °F - closed cup

Flash Point(C)

115 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB0491
MKCV5118
STBL1397
STBK6041
MKCS1080

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A REMPI investigation of the minimum energy conformations of diphenyl ether.
Paiva ACS, et al.
International Journal of Mass Spectrometry, 221(2), 107-115 (2002)
Palladium-promoted cyclization of diphenyl ether, diphenylamine, and related compounds.
Akermark B, et al.
The Journal of Organic Chemistry, 40(9), 1365-1367 (1975)
Xingyu Wang et al.
ChemSusChem, 5(8), 1455-1466 (2012-05-03)
The conversion of lignin, the most recalcitrant of the biopolymers, is necessary for a carbon-efficient utilization of lignocellulosic materials. In this context, hydrogenolysis of lignin is a process receiving increasing attention. In this report, the solvent effects on the hydrogenolysis
Sindra L Summoogum et al.
Chemosphere, 85(2), 143-150 (2011-07-09)
This article examines the thermal decomposition of alpha-cypermethrin, one of the most common pyrethroid pesticides. The objective was to identify its decomposition pathways and to gain an understanding into the formation of toxic species in the environment, including those that
Hua Xu et al.
Biochemistry, 47(14), 4228-4236 (2008-03-14)
Approximately one-third of the world's population carries Staphylococcus aureus. The recent emergence of extreme drug resistant strains that are resistant to the "antibiotic of last resort", vancomycin, has caused a further increase in the pressing need to discover new drugs
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