Benzenesulfonate

Benzenesulfonic acid

Names
Preferred IUPAC name Benzenesulfonic acid
Other names Benzene sulphonic acid; Benzenesulphonic acid; Phenylsulfonic acid; Phenylsulphonic acid; Besylic acid
Identifiers
CAS Number	98-11-3 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:64455
ChemSpider	7093 Y
ECHA InfoCard	100.002.399
EC Number	202-638-7
PubChem CID	7371
RTECS number	DB4200000
UNII	685928Z18A Y
UN number	2583, 2585, 1803
InChI InChI=1S/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9) Y Key: SRSXLGNVWSONIS-UHFFFAOYSA-N Y InChI=1/C6H6O3S/c7-10(8,9)6-4-2-1-3-5-6/h1-5H,(H,7,8,9) Key: SRSXLGNVWSONIS-UHFFFAOYAJ
SMILES c1ccc(cc1)S(=O)(=O)O
Properties
Chemical formula	C6H6O3S
Molar mass	158.17 g·mol−1
Appearance	Colorless crystalline solid
Density	1.32 g/cm3 (47 °C)
Melting point	* 44 °C (hydrate) 51 °C (anhydrous)
Boiling point	190 °C (374 °F; 463 K)
Solubility in water	Soluble
Solubility in other solvents	Soluble in alcohol, insoluble in non-polar solvents
Acidity (pKa)	−2.8
Hazards
Main hazards	Corrosive
Safety data sheet	External MSDS
GHS pictograms
GHS signal word	Danger
GHS hazard statements	H290, H302, H314, H315, H319, H335
GHS precautionary statements	P234, P260, P261, P264, P270, P271, P280, P301+312, P301+330+331, P302+352, P303+361+353, P304+340, P305+351+338, P310
Flash point	> 113 °C
Related compounds
Related sulfonic acids	Sulfanilic acid p-Toluenesulfonic acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y  (what is YN ?)
Infobox references

Benzenesulfonic acid (conjugate base benzenesulfonate) is an organosulfur compound with the formula C₆H₅SO₃H. It is the simplest aromatic sulfonic acid. It forms white deliquescent sheet crystals or a white waxy solid that is soluble in water and ethanol, slightly soluble in benzene and insoluble in nonpolar solvents like diethyl ether. It is often stored in the form of alkali metal salts. Its aqueous solution is strongly acidic.

Benzenesulfonic acid is prepared from the sulfonation of benzene using concentrated sulfuric acid:

This conversion illustrates aromatic sulfonation, which has been called "one of the most important reactions in industrial organic chemistry."

Benzenesulfonic acid exhibits the reactions typical of other aromatic sulfonic acids, forming sulfonamides, sulfonyl chloride, and esters. The sulfonation is reversed above 220 °C. Dehydration with phosphorus pentoxide gives benzenesulfonic acid anhydride ((C₆H₅SO₂)₂O). Conversion to the corresponding benzenesulfonyl chloride (C₆H₅SO₂Cl) is effected with phosphorus pentachloride.

It is a strong acid, being almost fully dissociated in water.