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  • Toxicological assessment of 3-chloropropane-1,2-diol and glycidol fatty acid esters in food.

Toxicological assessment of 3-chloropropane-1,2-diol and glycidol fatty acid esters in food.

Molecular nutrition & food research (2011-02-26)
Nadiya Bakhiya, Klaus Abraham, Rainer Gürtler, Klaus Erich Appel, Alfonso Lampen
ABSTRACT

Fatty acid esters of 3-chloropropane-1,2-diol (3-MCPD) and glycidol are a newly identified class of food process contaminants. They are widespread in refined vegetable oils and fats and have been detected in vegetable fat-containing products, including infant formulas. There are no toxicological data available yet on the 3-MCPD and glycidol esters, and the primary toxicological concern is based on the potential release of 3-MCPD or glycidol from the parent esters by lipase-catalyzed hydrolysis in the gastrointestinal tract. Although 3-MCPD is assessed as a nongenotoxic carcinogen with a tolerable daily intake (TDI) of 2 μg/kg body weight (bw), glycidol is a known genotoxic carcinogen, which induces tumors in numerous organs of rodents. The initial exposure estimates, conducted by Federal Institute for Risk Assessment (BfR) under the assumption that 100% of the 3-MPCD and glycidol are released from their esters, revealed especially that infants being fed commercial infant formula could ingest harmful amounts of 3-MCPD and glycidol. However, the real oral bioavailability may be lower. As this gives rise for toxicological concern, the currently available toxicological data of 3-MCPD and glycidol and their esters are summarized in this review and discussed with regard to data gaps and further research needs.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Glycidol, 96%
Sigma-Aldrich
(R)-(−)-3-Chloro-1,2-propanediol, 97%, optical purity ee: 98% (GLC)
Supelco
(±)-Glycidol, analytical standard
Sigma-Aldrich
(S)-(+)-3-Chloro-1,2-propanediol, 97%, optical purity ee: 97% (GLC)
Supelco
(±)-3-Chloro-1,2-propanediol, analytical standard
Sigma-Aldrich
(±)-3-Chloro-1,2-propanediol, 98%
Levodropropizine impurity C, European Pharmacopoeia (EP) Reference Standard