is the organic compound
with the formula O
. The molecule is subject to reactions typical of other phenyl
rings, including hydroxylation
, and Friedel-Crafts alkylation or acylation
. This simple diaryl ether enjoys a variety of niche applications.
Diphenyl ether and many of its properties were first reported as early as 1901.
It is synthesized by Williamson ether synthesis
, here the reaction of phenol
in the presence of base
and a catalytic
amount of copper
- PhONa + PhBr → PhOPh + NaBr
Involving similar reactions, diphenyl ether is a significant side product in the high-pressure hydrolysis
in the production of phenol.
The main application of diphenyl ether is as a eutectic
mixture with biphenyl
, used as a heat transfer
medium. Such a mixture is well-suited for heat transfer applications because of the relatively large temperature range of its liquid state.
Diphenyl ether is a starting material in the production of phenoxathiin via the Ferrario reaction. Phenoxathiin is used in polyamide and polyimide production.
Because of its odor reminiscent of geranium, as well as its stability and low price, diphenyl ether is used widely in soap perfumes. Diphenyl ether is also used as a processing aid in the production of polyesters.
Several polybrominated diphenyl ethers (PBDEs) are useful flame retardants. Of penta-, octa-, and decaBDE, the three most common PBDEs, only decaBDE is still in widespread use since its ban in the European Union in 2003. DecaBDE, also known as decabromodiphenyl oxide, is a high-volume industrial chemical with over 450,000 kilograms produced annually in the United States. Decabromodiphenyl oxide is sold under the trade name Saytex 102 as a flame retardant in the manufacture of paints and reinforced plastics.