6070-16-2

Usage

Uses

Used in Food and Beverage Industry:
(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is used as a flavoring agent for its fruity and minty aroma, enhancing the taste and smell of various food and beverage products.
Used in Perfume and Fragrance Industry:
(1beta,2alpha,4alpha)-p-menth-2-yl hexanoate is used in the production of perfumes and fragrances due to its pleasant and refreshing scent, contributing to the overall appeal and attractiveness of these products.

Upstream product

• 15356-70-4 menthol 
• 142-62-1 hexanoic acid 
• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 142-61-0 Hexanoyl chloride 
• 628-02-4 Caproamide 
• 2216-51-5 (-)-menthol 

Downstream Products

• 15356-60-2 (1S,2R,5S)-(+)-menthol 
• 142-62-1 hexanoic acid 
• 2216-51-5 (-)-menthol 

Relevant academic research and scientific papers

d-menthol fatty acid ester derivative, application thereof and preparation method for d-menthol fatty acid ester derivative

The invention belongs to the technical field of medicines and relates to a d-menthol fatty acid ester derivative, an application thereof and a preparation method for the d-menthol fatty acid ester derivative. The d-terpineol fatty acid ester is prepared through carrying out an esterification reaction on d-menthol and straight-chain fatty acid. The method comprises the steps of firstly, carrying out a reaction on fatty acid and thionyl chloride so as to prepare acyl chloride, and then, subjecting acyl chloride to a reaction with d-menthol, there by preparing the ester. The d-menthol ester is applied to external preparations such as plasters, cataplasm, ointment, gels, sprays and liniment as a penetration enhancer, so that the percutaneous absorption capacity of drugs, particularly, chiral drug enantiomers is increased; and the d-menthol ester is a very good percutaneous absorption penetration enhancer and has a broad application prospect.

Scandium triflate catalyzed ester synthesis using primary amides

A scandium triflate (ScOTf)3 catalyzed methodology has been developed to synthesize esters from primary amides. Various primary and secondary aliphatic alcohols have been shown to react in n-heptane with a range of primary amides for 24 h.

Recyclable hypervalent iodine(III) reagent iodosodilactone as an efficient coupling reagent for direct esterification, amidation, and peptide coupling

A hypervalent iodine(III) reagent plays a novel role as an efficient coupling reagent to promote the direct condensation between carboxylic acids and alcohols or amines to provide esters, macrocyclic lactones, amides, as well as peptides without racemization. The regeneration of iodosodilactone (1) can also be readily achieved. The intermediate acyloxyphosphonium ion C from the activation of a carboxylic acid is thought to be involved in the present esterification reaction.

Quantitative Analyses of Biochemical Kinetic Resolution of Enantiomers. 2. Enzyme-Catalyzed Esterification in Water-Organic Solvent Biphasic Systems

New quantitative expressions, which relate the kinetic and thermodynamic parameters that govern the stereospecificity of enzyme-catalyzed resolution of enantiomers in biphasic aqueous-organic media, have been developed.The theoretical predictions have been verified experimentally, and the technical merit of this esterification methodology has been assessed in relation to the more conventional hydrolytic procedure.