Methional
| Names | |
|---|---|
| Preferred IUPAC name
3-(Methylsulfanyl)propanal | |
| Other names
3-(Methylmercapto)propionaldehyde; 3-(Methylthio)propionaldehyde; 3-(Methylthio)propanal
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| Identifiers | |
3D model (JSmol)
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| ECHA InfoCard | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value).Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C4H8OS | |
| Molar mass | 104.17 g·mol−1 |
| Appearance | Colorless liquid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Methional is an organic compound with the formula CH3SCH2CH2CHO. It is a colorless liquid that is a degradation product of methionine. It is a notable flavor in potato-based snacks, namely potato chips, one of the most popular foods containing methional.[1] Traces of the compound can also be found in black tea and green tea based products. Methional contains both aldehyde and thioether functional groups. It is readily soluble in alcohol solvents, including propylene glycol and dipropylene glycol.
Occurrence
[edit | edit source]In nature, methional is a thermally-induced volatile flavor compound. For instance, the heat-initiated Maillard reaction of reducing sugars and amino acids forms the initial basis of methional's composition. The formation of methional stems from the interaction of α-dicarbonyl compounds (intermediate products in the Maillard reaction) with methionine (Met) by the Strecker degradation reaction:[1]
- CH3SCH2CH2(NH2)CHCO2H + O → CH3SCH2CH2(HN=)CCO2H + H2O
- CH3SCH2CH2(HN=)CCO2H + H2O → CH3SCH2CH2CHO + NH3 + CO2
Methional easily degrades into methanethiol, which then oxidizes into dimethyl disulfide. Dimethyl disulfide is partly responsible for the "reactive sulfur" that contributes to the taste of potatoes. Furthermore, the methionine resulting from the Strecker degradation reaction produces alkyl pyrazines, which contribute to the flavors in roasted, toasted, or thermally processed foods. Due to the ease of its decomposition, a large portion of methional is lost during potato processing.
Similarly, in the presence of flavin mononucleotide (FMN) and light, methionine is nonenzymatically oxidized into methional, ammonia, and carbon dioxide.[2]
- CH3SCH2CH2(NH2)CHCO2H → CH3SCH2CH2CHO + NH3 + CO2
Preparation and reactions
[edit | edit source]Methional is synthesized commercially by the reaction of methanethiol and acrolein.[3]
- CH3SH + CH2=CHCHO → CH3SCH2CH2CHO
Using the Strecker synthesis, methional is converted to methionine. For the purpose of animal feed supplements, enantiopure methionine is not required.[3]
Methional is a versatile reagent in organic chemistry.[4]
Biological routes
[edit | edit source]Because of their high cost, methional or its precursor methionine are not added during potato processing.[1] In order to intensify flavoring of heat-processed potato foods, biotechnological approaches are used to increase methionine levels, and thus methional levels, in potato foods.
The enzyme aminotransferase acts on methionine to remove the amine and form an α-keto-γ-methylthiobutyric acid. As catalyzed by α-keto acid decarboxylase, this ketomethylthiobutyric acid converts to methional.[5]
- CH3S(CH2)2CH(NH2)CO2H + O → CH3S(CH2)2COCO2H + NH3
- CH3S(CH2)2COCO2H → CH3S(CH2)2CHO + CO2
References
[edit | edit source]- ^ a b c Faith C. Belanger, Rong Di & Daphna Havkin-Frenkel (2009) Increasing the Methional Content in Potato through Biotechnology, Biotechnology in Flavor Production, 185-188, Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ S. F. Yang, H. S. Ku & H. K. Pratt (1967) Photochemical Production of Ethylene from Methionine and Its Analogues in the Presence of Flavin Mononucleotide, The Journal of Biological Chemistry, 242, 5274-5280.
- ^ a b Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ María Del Carmen Martínez-Cuesta , Carmen Peláez & Teresa Requena (2013) Methionine Metabolism: Major Pathways and Enzymes Involved and Strategies for Control and Diversification of Volatile Sulfur Compounds in Cheese, Critical Reviews in Food Science and Nutrition, 53:4, 366-385. Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).