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Valerophenone CAS 1009-14-9

Molecular Formula: C11H14O
Molecular Weight:  162.23
Appearance: colorless liquid
Purity: ≥95%
MOQ: 1KG
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What is Valerophenone (CAS 1009-14-9)?

Valerophenone(CAS 1009-14-9), also known as butyl phenyl ketone, is an aromatic ketone with the chemical formula C11H14O.Valerophenone is a colourless liquid, soluble in organic solvents, with a melting point of -9.4°C and a boiling point of 105 to 107°C. In practice, valerophenone is usually prepared by acylating benzene using valeryl chloride.

Valerophenone(CAS 1009-14-9) Product Parameter

Product Name: Valerophenone
CAS NO: 1009-14-9
Molecular Weight: 162.23
Molecular Formula: C11H14O
Boiling Point: 244-245 °C(lit.)
Melting point: -9 °C
Density: 0.975 g/mL at 20 °C(lit.)
Appearance: colorless liquid
Solubility: Chloroform (Sparingly), Ethyl Acetate (Slightly)

Valerophenone synonyms

MFCD00009480; Pentanophenone; Butyl Phenyl Ketone; EINECS 213-767-3; Valerophenone; 1-Phenylpentan-1-one

How to store Valerophenone (CAS 1009-14-9)

1. Valerophenone should be stored in a cool, well-ventilated place at an ambient temperature not exceeding 30°C. It is recommended that Valerophenone be kept away from open flames or heat sources and in sealed containers.
2. It is recommended that Valerophenone be kept away from open flames or heat sources and stored in tightly closed containers.
3. Do not store Valerophenone with oxidising agents, reducing agents or bases.

valerophenone uses

Valerophenone is an aromatic ketone that finds utility as a valuable tool for investigating different photochemical reactions. It serves as a crucial intermediate in the synthesis of liquid crystals, which have applications in display technologies. Additionally, valerophenone acts as an effective inhibitor of the enzyme carbonyl reductase. Its diverse range of applications in photochemistry, liquid crystal synthesis, and enzymology highlights its versatility and significance in scientific research and industrial processes.

valerophenone synthesis

Valerophenone is prepared from benzene and valeryl chloride by friedel-crafts reaction or from methyl benzoate by the Grignard reaction.

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