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Merck

240834

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24854438
EC Number:
202-981-2
Beilstein/REAXYS Number:
1364620
MDL number:
MFCD00003034
Assay:
≥99%
Bp:
259 °C (lit.)
Vapor pressure:
<1 mmHg ( 20 °C)

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

crystalline

autoignition temp.

1144 °F

expl. lim.

1.5 %

dilution

(for general lab use)

refractive index

n20/D 1.579 (lit.)

bp

259 °C (lit.)

mp

25-27 °C (lit.)

solubility

alcohol: soluble(lit.)
benzene: soluble(lit.)
diethyl ether: soluble(lit.)
glacial acetic acid: soluble(lit.)
water: insoluble(lit.)

density

1.073 g/mL at 25 °C (lit.)

functional group

phenoxy

Quality Level

100

Gene Information

human ... TTR(7276)

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Application

Diphenyl ether can be used as:
  • An additive in the fabrication of thienothiophene-co-benzodithiophene polymer-based organic photovoltaics and isoindigo polymer-based organic solar cells.
  • A model compound to study the hydrodeoxygenation of ether linkages in the lignin fragments using various catalytic systems.
  • A solvent in the synthesis of FePd nanoparticles using modified polyol process.

General description

The diphenyl derivatives, having potency for inhibiting InhA (an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis), were studied.

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
SHBL5909
MKCF8863
MKCB1958V
MKBX0256V
MKBT9444V

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Transformation to L10 structure in FePd nanoparticles synthesized by modified polyol process
Watanabe K, et al.
Science and Technology of Advanced Materials, 7, 145-145 (2006)
P Kamsri et al.
SAR and QSAR in environmental research, 25(6), 473-488 (2014-05-03)
A series of diphenyl ether derivatives were developed and showed promising potency for inhibiting InhA, an essential enoyl acyl carrier protein reductase involved in mycolic acid biosynthesis, leading to the lysis of Mycobacterium tuberculosis. To understand the structural basis of
Thomas S Lisse et al.
NPJ Regenerative medicine, 5, 13-13 (2020-06-23)
Glial-cell-derived neurotrophic factor (GDNF) is a well-studied neuroregenerative factor; however, the degree to which it supports hair formation and skin wound repair is not known. By using a Gfra1 (GDNF family receptor alpha 1) knock-in reporter mouse line, GDNF signaling
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
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