Cumene hydroperoxide
Names | |
---|---|
IUPAC name
2-hydroperoxypropan-2-ylbenzene | |
Other names
Cumyl Hydroperoxide CHP | |
Identifiers | |
80-15-9 | |
ChEBI | CHEBI:78673 |
ChemSpider | 6377 |
| |
Jmol-3D images | Image |
PubChem | 6629 |
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Properties | |
Molecular formula |
C9H12O2 |
Molar mass | 152.19 g·mol−1 |
Appearance | colorless to pale yellow liquid |
Density | 1.02 g/cm3 |
Melting point | −9 °C (16 °F; 264 K) |
Boiling point | 153 °C (307 °F; 426 K) |
1.5 g / 100 mL | |
Vapor pressure | 14 mmHg at 20 °C |
Hazards | |
MSDS | sigmaaldrich.com |
GHS pictograms | |
GHS signal word | DANGER |
H242, H302, H312, H314, H331, H373, H411 | |
P220, P261, P273, P280, P305+351+338, P310 | |
NFPA 704 | |
Flash point | 57 °C (135 °F; 330 K) |
Except where noted otherwise, data is given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
verify (what is: / ?) | |
Infobox references | |
Cumene hydroperoxide is an intermediate in the cumene process for developing phenol and acetone from benzene and propylene. It is typically used as an oxidizing agent.[2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone and cumyl alcohol.[3] Its formula is C6H5C(CH3)2OOH.
One of the key uses for the material is as a free radical initiator for acrylate and methacrylates monomers.
References
- ↑ University, Safety Officer in Physical Chemistry at Oxford (2005). "Safety (MSDS) data for cumene hydroperoxide". Retrieved 2009-05-13.
- ↑ Richard J. Lewis, Richard J. Lewis (Sr.), Hazardous chemicals desk reference, Publisher Wiley-Interscience, 2008, ISBN 0-470-18024-2, ISBN 978-0-470-18024-2, 1953 pages (page 799)
- ↑ Cumene Hydroperoxide at the Organic Chemistry Portal
Related terms
External links
- Cumene hydroperoxide
- Cumene hydroperoxide at International Chemical Safety Cards