Chemistry:Methionol
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Revision as of 13:14, 6 May 2022 by imported>Unex (url)
Names | |
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IUPAC name
3-methylsulfanylpropan-1-ol
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Identifiers | |
3D model (JSmol)
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1731208 | |
ChEBI | |
ChEMBL | |
ChemSpider | |
EC Number |
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PubChem CID
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UNII | |
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Properties | |
C4H10OS | |
Molar mass | 106.18 g·mol−1 |
Hazards | |
GHS pictograms | ![]() |
GHS Signal word | Warning |
H315, H319, H335 | |
P261, P264, P264+265Script error: No such module "Preview warning".Category:GHS errors, P271, P280, P302+352, P304+340, P305+351+338, P319Script error: No such module "Preview warning".Category:GHS errors, P321, P332+317Script error: No such module "Preview warning".Category:GHS errors, P337+317Script error: No such module "Preview warning".Category:GHS errors, P362+364Script error: No such module "Preview warning".Category:GHS errors, P403+233, P405, P501 | |
Related compounds | |
Related compounds
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1-(Methylthio)propane; Methional; Methionine; 1,3-Propanediol mono methyl ether; 4-(Methylsulfanyl)butanoic acid; 4-Thiapentanoic acid; |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Methionol (3-(Methylthio)-1-propanol) is a methyl sulfide derived from propan-1-ol. It is found in nature, including as a metabolite of yeast and bacillus anthracis.[2] It is a sulphurous aroma component of many foods, such as wine, cheese and roasted coffee.[3] It is classed as an irritant.[2] It has a very low olfactory threshold.[4]
References
- ↑ "Methionol" (in en). https://pubchem.ncbi.nlm.nih.gov/compound/Methionol#section=Safety-and-Hazards.
- ↑ 2.0 2.1 "Methionol". https://pubchem.ncbi.nlm.nih.gov/compound/10448.
- ↑ "Methionol (YMDB16045) - Yeast Metabolome Database". http://www.ymdb.ca/compounds/YMDB16045.
- ↑ Xiao, Deng-Rong; Liu, Rui-Sang; He, Long; Li, Hong-Mei; Tang, Ya-Ling; Liang, Xin-Hua; Chen, Tao; Tang, Ya-Jie (November 26, 2015). "Aroma improvement by repeated freeze-thaw treatment during Tuber melanosporum fermentation". Scientific Reports 5 (1): 17120. doi:10.1038/srep17120. PMID 26607288. Bibcode: 2015NatSR...517120X.
![]() | Original source: https://en.wikipedia.org/wiki/Methionol.
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