Hexanoic anhydride

　　Main Uses

　　Acylation reagent in organic synthesis:

　　Reacts with alcohols to form hexanoate esters (e.g., ethyl hexanoate, butyl hexanoate), which can be used as fragrances, solvents, or plasticizers. For example, hexanoic acid reacts with benzyl alcohol under the catalysis of hexanoic anhydride to produce benzyl hexanoate, which has fruity and floral notes and is used in cosmetic fragrances.

　　Reacts with amines to form hexanamide, serving as an organic intermediate in the synthesis of pharmaceuticals or dyes.

　　Polymer modification:

　　Used for the acylation modification of natural polymers such as cellulose and starch, introducing long-chain acyl groups (-CO (CH₂)₄CH₃) to improve their fat solubility and thermal stability, and broadening their applications in plastics and coatings.

　　Pharmaceuticals and fine chemicals:

　　Participates as an intermediate in the synthesis of certain drugs, for example, introducing the hexanoyl group in the structural modification of antibiotics and steroid drugs to regulate the drug's lipophilicity and bioavailability.

　　Used to prepare surfactants; its derivatives (e.g., reaction products of hexanoic anhydride with polyols) can serve as emulsifiers or detergent components.

　　Other applications:

　　Acts as a dehydrating agent to promote intramolecular or intermolecular dehydration in certain organic reactions (e.g., in the preparation of cyclic ethers or lactones). Used to prepare metal soaps (e.g., zinc hexanoate, aluminum hexanoate) as coating driers or plastic stabilizers.

CAS NO: 2051-49-2

EC NO: 218-121-4

Molecular Formula: C₁₂H₂₂O₃

Molecular Weight: 214.3013

Aliases: Hexanoic anhydride; Hexanoyl anhydride; Caproic anhydride; Caproic anhydride;

Structural Formula: