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Documenti fondamentali

67334

Supelco

Diphenyl ether

for ion-selective electrodes, Selectophore, ≥99.9%

Sinonimo/i:

Diphenyl oxide, Phenyl ether

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About This Item

Formula condensata:
(C6H5)2O
Numero CAS:
Peso molecolare:
170.21
Beilstein:
1364620
Numero CE:
Numero MDL:
Codice UNSPSC:
26111700
ID PubChem:
NACRES:
NB.61

Grado

for ion-selective electrodes

Livello qualitativo

Densità del vapore

>5.86 (25 °C, vs air)

Tensione di vapore

<1 mmHg ( 20 °C)

Nome Commerciale

Selectophore

Saggio

≥99.9% (GC)
≥99.9%

Stato

solid

Temp. autoaccensione

1144 °F

Limite di esplosione

1.5 %

Indice di rifrazione

n20/D 1.579 (lit.)

P. ebollizione

259 °C (lit.)

Punto di fusione

25-27 °C (lit.)
27-29 °C

Densità

1.073 g/mL at 25 °C (lit.)

Stringa SMILE

O(c1ccccc1)c2ccccc2

InChI

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

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Descrizione generale

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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Applicazioni

Used as plasticizing solvent mediator for PVC-based membranes.

Note legali

Selectophore is a trademark of Merck KGaA, Darmstadt, Germany

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

239.0 °F - closed cup

Punto d’infiammabilità (°C)

115 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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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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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
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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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