Diphenyl sulfone

Diphenyl sulfone
Names
	Preferred IUPAC name 1,1′-Sulfonyldibenzene
	Other names Diphenyl sulphone
Identifiers
CAS Number	127-63-9 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:78360;
ChemSpider	29117;
ECHA InfoCard	100.004.413
PubChem CID	31386;
UNII	V25W2CFS3M ;
CompTox Dashboard (EPA)	DTXSID6041892 ;
	InChI InChI=1S/C12H10O2S/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H Key: KZTYYGOKRVBIMI-UHFFFAOYSA-N; InChI=1/C12H10O2S/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H Key: KZTYYGOKRVBIMI-UHFFFAOYAU;
	SMILES O=S(=O)(c1ccccc1)c2ccccc2;
Properties
Chemical formula	C12H10O2S
Molar mass	218.27 g·mol−1
Melting point	123 °C (253 °F; 396 K)
Boiling point	379 °C (714 °F; 652 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Diphenyl sulfone is an organosulfur compound with the formula (C₆H₅)₂SO₂. It is a white solid that is soluble in organic solvents. It is used as a high temperature solvent. Such high temperature solvents are useful for processing highly rigid polymers, e.g., PEEK, which only dissolve in very hot solvents.

It is produced by the sulfonation of benzene with sulfuric acid and oleum. For typical processes, benzenesulfonic acid is an intermediate.^[1] It is also produced from benzenesulfonyl chloride and benzene.^[2]

References edit

^ Otto Lindner, Lars Rodefeld "Benzenesulfonic Acids and Their Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a03_507
^ Roger Adams, C. S. Marvel, H. T. Clarke, G. S. Babcock, and T. F. Murray (1921). "Benzenesulfonyl chloride". Organic Syntheses. 1: 21{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 1, p. 84.

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[1] Otto Lindner, Lars Rodefeld "Benzenesulfonic Acids and Their Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry 2005, Wiley-VCH, Weinheim. doi:10.1002/14356007.a03_507

[2] Roger Adams, C. S. Marvel, H. T. Clarke, G. S. Babcock, and T. F. Murray (1921). "Benzenesulfonyl chloride". Organic Syntheses. 1: 21{{cite journal}}: CS1 maint: multiple names: authors list (link); Collected Volumes, vol. 1, p. 84.

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