|
|||
Names | |||
---|---|---|---|
Preferred IUPAC name
Benzenecarboperoxoic acid
|
|||
Other names
Peroxybenzoic acid
Perbenzoic acid (no longer recommended) Benzoperoxoic acid |
|||
Identifiers | |||
3D model (JSmol)
|
|||
ChemSpider | |||
ECHA InfoCard | 100.002.056 | ||
EC Number | 202-260-2 | ||
MeSH | C017611 | ||
PubChem CID
|
|||
|
|||
|
|||
Properties | |||
C7H6O3 | |||
Molar mass | 138.12 g/mol | ||
Melting point | 41 to 42 °C (106 to 108 °F; 314 to 315 K) | ||
Acidity (pKa) | 7.8 | ||
Related compounds | |||
Related compounds
|
m-Chloroperoxybenzoic acid; hydrogen peroxide; benzoic acid | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|||
what is ?) | (|||
Infobox references | |||
Peroxybenzoic acid is a simple peroxy acid. It may be synthesized from benzoic acid and hydrogen peroxide, or by the treatment of benzoyl peroxide with sodium methoxide, followed by acidification.
Like other peroxyacids, it may be used to generate epoxides, such as styrene oxide from styrene: