Amyrin
From Infogalactic: the planetary knowledge core
![]() α-Amyrin
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![]() β-Amyrin
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Names | |
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IUPAC names
α: (3β)-Urs-12-en-3-ol
β: (3β)-Olean-12-en-3-ol |
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Other names
α: α-Amyrenol; α-Amirin; α-Amyrine; Urs-12-en-3β-ol; Viminalol
β: β-Amyrenol; β-Amirin; β-Amyrine; Olean-12-en-3β-ol; 3β-Hydroxyolean-12-ene |
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Identifiers | |
638-95-9 (α) ![]() 559-70-6 (β) ![]() |
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ChemSpider | 65935 (α) 65921 (β) |
Jmol 3D model | (α): Interactive image (β): Interactive image |
PubChem | 73170 (α) 73145 (β) |
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Properties | |
C30H50O | |
Molar mass | 426.73 g·mol−1 |
Melting point | α: 186 °C[1] β: 197-187.5 °C[2] |
Vapor pressure | {{{value}}} |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references | |
The amyrins are a pair of closely related natural chemical compounds of the triterpene class. They are designated α-amyrin and β-amyrin. Each has the chemical formula C30H50O. They are widely distributed in nature and have been isolated from a variety of plant sources. α-Amyrin is found in dandelion coffee.
References
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- ↑ Merck Index, 11th Edition, 653
- ↑ Merck Index, 11th Edition, 654
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- Secondary alcohols
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