The occurrence of 3-monochloropropane-1,2-diol esters and glycidyl esters in vegetable oils during frying. 2022

Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
Product Development and Advisory Services Division, Malaysian Palm Oil Board, Kajang, Selangor, Malaysia.

3-monochloropropane-1,2-diol esters (3-MCPDE) and glycidyl esters (GE) are processed-developed contaminants presence in vegetable oils after undergo refining process under excessive heat. Refined oils are extensively used in various frying applications, nevertheless, the reservation against their quality and safety aspects are of major concern to consumers and food industry. Realizing the importance to address these issues, this article deliberates an overview of published studies on the manifestation of 3-MCPDE and GE when vegetable oils undergo for frying process. With the modest number of published frying research associated to 3-MCPDE and GE, we confined our review from the perspectives of frying conditions, product properties, antioxidants and additives, pre-frying treatments and frying oil management. Simplicity of the frying process is often denied by the complexity of reactions occurred between oil and food which led to the development of unwanted contaminants. The behavior of 3-MCPDE and GE is closely related to physico-chemical characteristics of oils during frying. As such, relationships between 3-MCPDE and/or GE with frying quality indices - i.e. acidity in term of free fatty acid or acid value); secondary oxidation in term of p-anisidine value, total polar compounds and its fractions, and refractive index - were also discussed when oils were subjected under intermittent and continuous frying conditions.

UI MeSH Term Description Entries
D010938 Plant Oils Oils derived from plants or plant products. Oils, Plant,Oils, Vegetable,Plant Oil,Vegetable Oil,Vegetable Oils,Oil, Plant,Oil, Vegetable
D004952 Esters Compounds derived from organic or inorganic acids in which at least one hydroxyl group is replaced by an –O-alkyl or another organic group. They can be represented by the structure formula RCOOR’ and are usually formed by the reaction between an acid and an alcohol with elimination of water. Ester
D006358 Hot Temperature Presence of warmth or heat or a temperature notably higher than an accustomed norm. Heat,Hot Temperatures,Temperature, Hot,Temperatures, Hot
D000517 alpha-Chlorohydrin A chlorinated PROPANEDIOL with antifertility activity in males used as a chemosterilant in rodents. alpha-Chlorhydrin,3-Chloro-1,2-propanediol,3-Chloropropanediol,3-MCPD,3-Monochloropropane-1,2-diol,Glycerol alpha-Monochlorohydrin,U-5897,3 Chloro 1,2 propanediol,3 Chloropropanediol,3 Monochloropropane 1,2 diol,Glycerol alpha Monochlorohydrin,U 5897,U5897,alpha Chlorhydrin,alpha Chlorohydrin,alpha-Monochlorohydrin, Glycerol

Related Publications

Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
October 2021, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment,
Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
September 2020, Scientific reports,
Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
September 2023, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment,
Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
March 2020, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment,
Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
June 2019, Plant foods for human nutrition (Dordrecht, Netherlands),
Azmil Haizam Ahmad Tarmizi, and Ainie Kuntom
January 2014, Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment,
Copied contents to your clipboard!