Levopimaric acid
From Wikipedia, the free encyclopedia
| Names | |
|---|---|
| IUPAC name
Abieta-11,13-dien-18-oic acid | |
| Systematic IUPAC name
(1R,4aR,4bS,10aR)-1,4a-Dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,9,10,10a-decahydrophenanthrene-1-carboxylic acid | |
| Other names
13-isopropylpodocarpa-8(14),12-dien-15-oic acid; D6,8(14)-abietadienoic acid; l-pimaric acid; β-pimaric acid; l-sapietic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C20H30O2 | |
| Molar mass | 302.458 g·mol−1 |
| Appearance | Orthorhombic crystals |
| Melting point | 150 °C (302 °F; 423 K) |
| Practically insoluble in water | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Levopimaric acid is an abietane-type of diterpene resin acid.[1] It is a major constituent of pine oleoresin with the chemical formula of C20H30O2. In general, the abietene types of diterpene resin acid have various biological activities, such as antibacterial, cardiovascular and antioxidant. Levopimaric acid accounts for about 18 to 25% of pine oleoresin.[2] The production of oleoresin by conifer species is an important component of the defense response against insect attack and fungal pathogen infection.[3]
Resin acid is the general name for all kinds of acids that share the same basic skeleton, a three-fused ring and the empirical formula C20H30O2. The resin acids may be classified into two types, abietic and pimaric. The abietic-type group include levopimaric, l-abietic and neoabietic. The structure of these compounds differ only in the position of the conjugated double bond system. This feature influences their chemical reactivity. The pimaric-type acids are dextropimaric and isodextropimaric.[4]
Extraction from pine resin
Levopimaric acid can be extracted from longleaf pine oleoresin by first dissolving it in a solution of acetone and 2-amino-2-methyl-1-propanol, then acidifying with phosphoric acid.[2]

