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The main application of diphenyl ether is as a eutectic mixture with biphenyl, used as a heat transfer fluid. Such a mixture is well-suited for heat transfer applications because of the relatively large temperature range of its liquid state. A eutectic mixture (commercially, Dowtherm A) is 73.5% diphenyl ether and 26.5% biphenyl. [9] [10]
This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.
A water miscible solvent often found in lithium batteries (b.p. 85 °C): Dioxane: A cyclic ether and high-boiling solvent (b.p. 101.1 °C). Tetrahydrofuran (THF) A cyclic ether, one of the most polar simple ethers that is used as a solvent. Anisole (methoxybenzene) An aryl ether and a major constituent of the essential oil of anise seed. Crown ...
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
i = 2.3 for calcium chloride in water, due to nearly full dissociation of CaCl 2 into Ca 2+ and 2Cl − (often simplified as 3) Non integer i factors result from ion pairs in solution, which lower the effective number of particles in the solution. Equation after including the van 't Hoff factor ΔT b = K b · b solute · i
Polybrominated diphenyl ethers or PBDEs, are a class of organobromine compounds that are used as flame retardants. Like other brominated flame retardants , PBDEs have been used in a wide array of products, including building materials, electronics, furnishings, motor vehicles, airplanes, plastics, polyurethane foams, [ 1 ] and textiles.
(E)-Stilbene, commonly known as trans-stilbene, is an organic compound represented by the condensed structural formula C 6 H 5 CH=CHC 6 H 5.Classified as a diarylethene, it features a central ethylene moiety with one phenyl group substituent on each end of the carbon–carbon double bond.
Benzil is a standard building block in organic synthesis.It condenses with amines to give diketimine ligands. A classic organic reaction of benzil is the benzilic acid rearrangement, in which base catalyses the conversion of benzil to benzilic acid.