Pinolenic acid
Structural formula | ||||||||||
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General | ||||||||||
Surname | Pinolenic acid | |||||||||
other names |
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Molecular formula | C 18 H 30 O 2 | |||||||||
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properties | ||||||||||
Molar mass | 278.44 g mol −1 | |||||||||
Physical state |
firmly |
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safety instructions | ||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
The pinolenic acid is a polyunsaturated fatty acid with three non-conjugated cis - double bonds , the monocarboxylic acid is one of the alkenoic acids . The Trie acid counts - such as its isomer, attached to a C = C double bond is trans -configured columbinic (5 E , 9 Z , 12 Z ) -octadecatrienoic acid, it is often erroneously identified with the pinolenic acid - to the to - or polymethylene interrupted Isolenic Acids (NMI; Non-Methylene-Interrupted or PMI; Poly-Methylene-Interrupted). These also include B. sciadonic acid , coniferonic acid and taxolenic acid or dihomopinolenic acid .
The omega-6 fatty acid is an isomer of the group of natural conjugated linoleic acids belonging (CLN) calendic , Catalpinsäure , punicic and Jacarinsäure .
Pinolenic acid occurs esterified as triacylglyceride in cedar nut oil and pine nut oil , as well as in other seed and leaf lipids, especially in the pine family (Pinaceae), but also in cypress trees (Cupressaceae) and yew trees ( Taxus ). It also occurs in the esters of tall oil .
Individual evidence
- ↑ Johann Vollmann, Istvan Rajčan: Oil Crops. Springer, 2009, ISBN 978-0-387-77593-7 , p. 36 (nomenclature)
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ↑ 5,9,12-Octadecatrienoic acid from PlantFA Database, accessed November 15, 2017.
- ↑ Frank D. Gunstone, John L. Harwood, Albert J. Dijkstra: The Lipid Handbook. Third Edition, CRC Press, 2007, ISBN 978-0-8493-9688-5 , pp. 6, 64.