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Diphenyl ether

Selectophore™, ≥99.9%

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:
26111700
PubChem Substance ID:
329760547
NACRES:
NB.61

grade

for ion-selective electrodes

Quality Level

200

vapor density

>5.86 (25 °C, vs air)

vapor pressure

<1 mmHg ( 20 °C)

product line

Selectophore™

Assay

≥99.9% (GC)
≥99.9%

form

solid

autoignition temp.

1144 °F

expl. lim.

1.5 %

refractive index

n20/D 1.579 (lit.)

bp

259 °C (lit.)

mp

25-27 °C (lit.)
27-29 °C

density

1.073 g/mL at 25 °C (lit.)

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

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General description

Diphenyl ether (diphenyl oxide) belongs to the family of aromatic homomonocyclic compounds. It is colorless, exists as crystalline solid or liquid (above 82°F) and has a geranium-like odor. Diphenyl ether is present in alcoholic beverages. It is used as a flavouring ingredient and is found in vanilla, green tea, muscat grapes, potato chips, grilled beef, buckwheat, and lemon balm. It is a starting material in the production of phenoxathiin via the Ferrario reaction.. In similar reactions, diphenyl ether is a significant side product in the high-pressure hydrolysis of chlorobenzene during production of phenol. Also several polybrominated diphenyl ethers (PBDEs) are useful flame retardants.
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Application

Used as plasticizing solvent mediator for PVC-based membranes.

Legal Information

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

H319,H360Fd,H410

Hazard Classifications

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

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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
BCCK6749
BCCJ3686
BCCC6197
BCCB1954
BCCB7624

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Chandra, S., Lang, H.
Sensors and Actuators B, Chemical, 114, 849-854 (2006)
Julie B Herbstman et al.
Environmental health perspectives, 115(12), 1794-1800 (2007-12-19)
Recent studies have reported blood levels of polybrominated diphenyl ethers (PBDEs) in the U.S. population. Information about neonatal levels and about the relationship to polychlorinated biphenyls (PCBs) exposures is limited. The objective was to characterize levels and determinants of fetal
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
Manfred Pöhlein et al.
Journal of chromatography. A, 1203(2), 217-228 (2008-08-09)
Two versatile and fast methods to identify and quantify brominated flame retardants (BrFRs) in styrenic polymers were developed. Gas chromatography/mass spectrometry (GC/MS) as well as gas chromatography with electron-capture detection (GC/ECD), both following ultrasonic-supported dissolution and precipitation (USDP), were applied.
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