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Merck
CN

P24101

Diphenyl ether

99%, crystals, ReagentPlus®

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
NACRES:
NA.21
PubChem Substance ID:
57654511
UNSPSC Code:
12352100
EC Number:
202-981-2
MDL number:
MFCD00003034
Beilstein/REAXYS Number:
1364620

Key Documents

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Product Name

Diphenyl ether, ReagentPlus®, 99%

InChI key

USIUVYZYUHIAEV-UHFFFAOYSA-N

InChI

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

SMILES string

O(c1ccccc1)c2ccccc2

vapor density

>5.86 (25 °C, vs air)

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

Quality Level

200

Gene Information

human ... TTR(7276)

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Application

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

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.

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H319,H410

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

239.0 °F - closed cup

flash_point_c

115 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ7951
SDBB3842
SDBB0491
MKCV5118
STBL1397

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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)
Takayuki Yonezawa et al.
Bioorganic & medicinal chemistry letters, 21(11), 3248-3251 (2011-05-10)
Osteogenic activity of six diarylheptanoids, acerogenin A (1), (R)-acerogenin B (2), aceroside I (3), aceroside B(1) (4), aceroside III (5) and (-)-centrolobol (6) and two phenolic compounds; (+)-rhododendrol (7) and (+)-cathechin (8), isolated from the stem bark of Acer nikoense
Robert C Hale et al.
Environment international, 29(6), 771-779 (2003-07-10)
North America consumes over half of the world's production of polybrominated diphenyl ether (PBDE) flame retardants. About 98% of global demand for the Penta-BDE mixture, the constituents of which are the most bioaccumulative and environmentally widespread, resides here. However, research
Tony Ly et al.
Analytical chemistry, 80(13), 5059-5064 (2008-05-24)
Selective noncovalent adduct protein probing (SNAPP) mass spectrometry was recently developed to study solution-phase conformations of proteins by exploiting the specific affinity between 18-crown-6 ether (18C6) and lysine side chains. To obtain more detailed information about protein tertiary structure, a
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