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67334

Supelco

Diphenyl ether

Selectophore™, ≥99.9%

Synonyma:

Diphenyl oxide, Phenyl ether

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About This Item

Lineární vzorec:
(C6H5)2O
Číslo CAS:
101-84-8
Molekulová hmotnost:
170.21
Beilstein/REAXYS Number:
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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Související kategorie

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

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

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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Osvědčení o analýze (COA)

Lot/Batch Number
BCCK6749
BCCJ3686
BCCC6197
BCCB1954
BCCB7624

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Supelco

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p-Anisaldehyde

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Sigma-Aldrich

L8274

Lipopolysaccharides from Escherichia coli O26:B6

Chlorobenzene anhydrous, 99.8%

Sigma-Aldrich

284513

Chlorobenzene

Tetrahydrofuran inhibitor-free, suitable for HPLC, &#8805;99.9%

Sigma-Aldrich

34865

Tetrahydrofuran

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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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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
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Lignin is an abundant natural resource that is a potential source of valuable chemicals. Improved understanding of the pyrolysis of lignin occurs through the study of model compounds for which phenethyl phenyl ether (PhCH(2)CH(2)OPh, PPE) is the simplest example representing
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Protoporphyrinogen oxidase (PPO, EC 1.3.3.4), which has been identified as a significant target for a great family of herbicides with diverse chemical structures, is the last common enzyme responsible for the seventh step in the biosynthetic pathway to heme and
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