67334
ジフェニルエーテル
Selectophore™, ≥99.9%
別名:
ジフェニルオキシド, フェニルエーテル
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この商品について
化学式:
(C6H5)2O
CAS番号:
分子量:
170.21
UNSPSC Code:
26111700
NACRES:
NB.61
PubChem Substance ID:
EC Number:
202-981-2
Beilstein/REAXYS Number:
1364620
MDL number:
製品名
ジフェニルエーテル, Selectophore™, ≥99.9%
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
SMILES string
O(c1ccccc1)c2ccccc2
vapor density
>5.86 (25 °C, vs air)
vapor pressure
<1 mmHg ( 20 °C)
description
for ion-selective electrodes
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.)
Quality Level
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関連するカテゴリー
Application
Used as plasticizing solvent mediator for PVC-based membranes.
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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Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B
保管分類
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
ppe
dust mask type N95 (US), Eyeshields, Gloves
Chandra, S., Lang, H.
Sensors and Actuators B, Chemical, 114, 849-854 (2006)
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
Ariana Beste et al.
The Journal of organic chemistry, 74(7), 2837-2841 (2009-03-06)
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
Kostantinos Benekos et al.
Journal of biotechnology, 150(1), 195-201 (2010-07-20)
Plant glutathione transferases (GSTs) superfamily consists of multifunctional enzymes and forms a major part of the plants herbicide detoxification enzyme network. The tau class GST isoenzyme GmGSTU4 from soybean, exhibits catalytic activity towards the diphenyl ether herbicide fluorodifen and is
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