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Diphenyl ether is the organic compound with the formula (C 6 H 5) 2 O. It is a colorless, low-melting solid. It is a colorless, low-melting solid. This, the simplest diaryl ether , has a variety of niche applications.
The simplest member of the phenyl ether family is diphenyl ether (DPE), also called diphenyl oxide, the structure of which is provided in Figure 4. Low molecular weight polyphenyl ethers and thioethers are used in a variety of applications, and include high-vacuum devices, optics, electronics, and in high-temperature and radiation-resistant ...
Diethyl ether has higher water solubility of 8 g per 100 mL, versus diphenyl ether, with a solubility of 0.002 g per 100 mL. [ 3 ] [ 4 ] The presence of the aromatic ring also draws electrons away from the ethereal oxygen, making the hydrolysis of a phenol ether significantly more difficult than that of an alkyl ether. [ 5 ]
2,3',6-tribromodiphenyl ether 337513-53-8 JUPZALSVNWJHII-UHFFFAOYSA-N PBDE-28 C 12 H 7 Br 3 O: 2,4,4'-tribromodiphenyl ether 41318-75-6 UPNBETHEXPIWQX-UHFFFAOYSA-N PBDE-29 C 12 H 7 Br 3 O: 2,4,5-tribromodiphenyl ether 337513-56-1 LTMKAFUXYKEDLR-UHFFFAOYSA-N PBDE-30 C 12 H 7 Br 3 O: 2,4,6-tribromodiphenyl ether 155999-95-4 TVZAPPGLBLTACB ...
Poly(2,6-diphenylphenylene oxide) is a low bleeding material with a low level of impurities, and has a high thermal stability (up to 350 °C). Before use poly(2,6-diphenylphenylene oxide) should be thermally conditioned with a high purity gas at elevated temperatures to remove any residual components.
Bis[(2-diphenylphosphino)phenyl] ether, also known as DPEphos, is a wide bite angle diphosphine ligand used in inorganic and organometallic chemistry.The name DPEphos is derived from diphenyl ether (DPE) which makes up the ligand's backbone.
[15] [16] In particular the Krafft point of the high 2-phenyl product (i.e. the least branched isomer) remains below 0 °C up to 25% LAS whereas the low 2-phenyl cloud point is ~15 °C. [17] This behavior is often exploited by producers to create either clear or cloudy products.
As is typical of ethers, dipropyl ether may slowly form explosive organic peroxides over long periods in storage. [2] Antioxidants such as butylated hydroxytoluene are often added to ethers to prevent this process. [4] Due to the shock and light sensitive nature of organic peroxides, dipropyl ether should never be boiled or evaporated to dryness.