2-Acetyl-1-pyrroline
Names | |
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Preferred IUPAC name
1-(3,4-Dihydro-2H-pyrrol-5-yl)ethan-1-one | |
Other names
1-(3,4-Dihydro-2H-pyrrol-5-yl)ethanone
2-Acetyl-1-pyrroline | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
MeSH | 2-Acetyl-1-pyrroline |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C6H9NO | |
Molar mass | 111.144 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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2-Acetyl-1-pyrroline (2AP) is an aroma compound and flavor that gives white bread, jasmine rice and basmati rice, the spice pandan (Pandanus amaryllifolius), and bread flowers (Vallaris glabra) their customary smell.[1] Many observers describe the smell as similar to "hot, buttered popcorn", and it is credited for lending this odor to the scent of binturong (bearcat) urine.[2] Fresh MF (Marking fluid) and urine of the tiger (Indian, Amur or Siberian) and Indian leopard also have a strong aroma due 2AP.[3]
2AP and its structural homolog, 6-acetyl-2,3,4,5-tetrahydropyridine of similar smell, can be formed by Maillard reactions during heating of food such as the baking of bread dough. Both compounds have odor thresholds below 0.06 ng/l.[4]
Structure and properties
2AP is a substituted pyrroline and a cyclic imine as well as a ketone.
References
- ^ S. Wongpornchai; T. Sriseadka; S. Choonvisase (2003). "Identification and quantitation of the rice aroma compound, 2-acetyl-1-pyrroline, in bread flowers (Vallaris glabra Ktze)". J. Agric. Food Chem. 51 (2): 457–462. doi:10.1021/jf025856x. PMID 12517110.
- ^ "Why bearcats smell like buttered popcorn". Duke University/Eurekalert. 2016-04-13.
- ^ Brahmachary, Poddar-Sarkar. "Fifty years of tiger pheromone research" (PDF). Archived from the original (PDF) on 2015-06-27. Retrieved 2017-03-25.
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suggested) (help) - ^ T. J. Harrison; G. R. Dake (2005). "An expeditious, high-yielding construction of the food aroma compounds 6-acetyl-1,2,3,4-tetrahydropyridine and 2-acetyl-1-pyrroline". J. Org. Chem. 70 (26): 10872–10874. doi:10.1021/jo051940a. PMID 16356012.