Names | |
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Preferred IUPAC name
Diphenylethanedione | |
Systematic IUPAC name
1,2-Diphenylethane-1,2-dione | |
Other names
Diphenylethane-1,2-dione
Benzil Dibenzoyl Bibenzoyl Diphenylglyoxal | |
Identifiers | |
3D model (JSmol)
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608047 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.004.689 |
EC Number |
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PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C14H10O2 | |
Molar mass | 210.232 g·mol−1 |
Appearance | yellow crystalline powder |
Density | 1.23 g/cm3, solid (1.255 g/cm3, x-ray) |
Melting point | 94.0 to 96.0 °C; 201.2 to 204.8 °F; 367.1 to 369.2 K |
Boiling point | 346.0 to 348.0 °C; 654.8 to 658.4 °F; 619.1 to 621.1 K |
insoluble | |
Solubility in ethanol | soluble |
Solubility in diethyl ether | soluble |
Solubility in benzene | soluble |
-118.6·10−6 cm3/mol | |
Structure | |
P31,221[1] | |
3.8 D[2] | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Irritant |
GHS labelling: | |
Warning | |
H315, H319, H335 | |
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
NFPA 704 (fire diamond) | |
Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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>3 g/kg (mouse, oral)[3] |
Related compounds | |
Related diketones
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diacetyl |
Related compounds
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benzophenone glyoxal bibenzil |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Benzil (i.e. Bz2, systematically known as 1,2-diphenylethane-1,2-dione) is the organic compound with the formula (C6H5CO)2, generally abbreviated (PhCO)2. This yellow solid is one of the most common diketones. Its main use is as a photoinitiator in polymer chemistry.[4]