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Chemical compound From Wikipedia, the free encyclopedia
N,N-Dimethylphenethylamine (N,N-DMPEA) is a substituted phenethylamine that is used as a flavoring agent. It is an alkaloid that was first isolated from the orchid Eria jarensis.[1] Its aroma is described as "sweet, fishy". It is mainly used in cereal, cheese, dairy products, fish, fruit and meat.[2] It is also being used in pre-workout and bodybuilding supplements with claims of a stimulant effect.[3]
Names | |
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Preferred IUPAC name
N,N-Dimethyl-2-phenylethan-1-amine | |
Other names
N,N-Dimethyl-2-phenylethanamine N,N-Dimethyl-β-phenylethylamine N,N-DMPEA | |
Identifiers | |
3D model (JSmol) |
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ChEBI | |
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.156.869 |
EC Number |
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PubChem CID |
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UNII | |
CompTox Dashboard (EPA) |
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Properties | |
C10H15N | |
Molar mass | 149.237 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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There is also evidence suggesting that N,N-DMPEA acts as a TAAR1 agonist in humans,[4] and as a 5-HT1A ligand in rats. Some less conclusive research also indicated that it had interaction with MAO-B, most likely as an enzyme substrate and not an inhibitor.[5]
N,N-DMPEA is a positional isomer of methamphetamine. Instead of the methyl group attached to the alpha position of phenylethylamine, it's attached to the nitrogen group. Both substances have the chemical formula C10H15N.
N,N-DMPEA has been found to be safe for use as a flavoring agent by the Flavor and Extract Manufacturers Association (FEMA) Expert Panel[6] and also by the Joint Expert Committee on Food Additives (JECFA)[7]—a collaboration between the Food and Agricultural Organization of the United Nations (FAO) and the World Health Organization.[8]
In the United States, N,N-DMPEA may be considered a Schedule II substance as a positional isomer of methamphetamine (C10H15N), due to the Schedule II definition of methamphetamine defined as "any quantity of methamphetamine, including its salts, isomers, and salts of isomers".[9] [10][11]
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