| Boiling Point | 216°C |
| Color | Yellow |
| Formula Weight | 134.18 |
| Physical Form | Clear Liquid at 20°C |
| Chemical Name or Material | Propiophenone |
| 7148 |
Synonym : propiophenone, ethyl phenyl ketone, propionylbenzene, 1-phenyl-1-propanone, 1-propanone, 1-phenyl, phenyl ethyl ketone, ketone, ethyl phenyl, propionphenone, usaf ek-1235, 1-phenyl-propan-1-one
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A propane chain links a benzene ring to a carbonyl group, forming propiophenone. This typical aromatic ketone, with a molecular formula of C9H10O, has several uses in chemical synthesis.
Many medications, perfumes, and agrochemicals use propiophenone, an aromatic ketone with many potential uses, as an intermediary in their production. Due to its stability and reactivity, propiophenone is useful in both laboratory and industrial contexts.
A Propiophenone molecular weight of 134.18 g/mol is assigned to propiophenone. This property, which results from its molecular formula C9H10O, is very important for its reactivity and use in chemical synthesis and scientific study.
Propiophenone's aromatic and nonpolar nature causes it to have low water solubility. Nevertheless, its excellent solubility in organic solvents allows it to be used in a wide variety of chemical reactions.
One typical method for producing propiophenone involves acylating benzene with propionyl chloride and a Lewis acid catalyst, like aluminium chloride, in the Friedel-Crafts reaction. This effective process produces the aromatic ketone in a very pure form.
Propiophenone is not very volatile, yet it is still important to handle it carefully. Wear protective eyewear and gloves because it might irritate the skin or eyes. Avoid oxidizing substances and bright sunshine, and always keep it in a cold, dry area.
