Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S2430

Propiophenone | 93-55-0 | Sarchem Labs

SKU: S2430

Description

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

Color Yellow
Boiling Point 216°C
Formula Weight 134.18
Physical Form Clear Liquid at 20°C
Chemical Name or Material Propiophenone

SPECIFICATION

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A

Safety Information

Classification of the substance or mixture

GHS Label elements, including precautionary statements

Hazards not otherwise classified (HNOC) or not covered by GHS

 

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Propiophenone | 93-55-0 FAQs

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.