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| Oleic acid | |
|---|---|
| IUPAC name | (9Z)-Octadec-9-enoic acid |
| Other names | (9Z)-Octadecenoic acid (Z)-Octadec-9-enoic acid cis-9-Octadecenoic acid cis-Δ9-Octadecenoic acid Oleic acid 18:1 cis-9 |
| Identifiers | |
| CAS number | [112-80-1] |
| SMILES |
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| Properties | |
| Molecular formula | C18H34O2 |
| Molar mass | 282.4614 g/mol |
| Appearance | Pale yellow or brownish yellow oily liquid with lard-like odor |
| Density | 0.895 g/mL |
| Melting point |
13-14 °C (286 K) |
| Boiling point |
360 °C (633 K) (760mm Hg)[1] |
| Solubility in water | Insoluble |
| Solubility in methanol | Soluble |
| Hazards | |
| MSDS | ScienceLab.com |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox references |
|
Oleic acid is a monounsaturated omega-9 fatty acid found in various animal and vegetable sources. It has the formula C18H34O2 (or CH3(CH2)7CH=CH(CH2)7COOH).[2] The saturated form of this acid is stearic acid.
Contents |
Occurrence
Oleic acid makes up 55-80% of olive oil, though there may be only 0.5-2.5% or so as actual free acid, and 15-20% of grape seed oil and sea buckthorn oil.[3] Oleic acid may be responsible for the hypotensive (blood pressure reducing) effects of olive oil.[4]
The Brazilian palmberry, açaí, contains one of the highest contents known for oleic acid in the pulp of a fruit (56%).[5]
Oleic acid is emitted by the decaying corpses of a number of insects, including bees and Pogonomyrmex ants and triggers the instincts of living workers to remove the dead bodies from the hive. If a live bee[6] or ant[7] is daubed with oleic acid, it is dragged off as if it were dead.
Chemistry
Oleic acid shares the normal reactions of fatty acids and alkenes.
Reduction of oleic acid at the carboxyl end yields oleyl alcohol.
Salts of oleic acid are called oleates.
If dropped onto water, oleic acid spreads out into a very thin layer, only a molecule thick if allowed.citation needed
Uses
Oleic acid may hinder the progression of ALD, or Adrenoleukodystrophy, a fatal disease that affects the brain and adrenal glands.[8]
References
- ^ Oleic acid, Chemical Laboratory Information Profile, American Chemical Society
- ^ Bishop, Paul L. (2000). Pollution Prevention: Chapter 2 - Properties and Fates of Environmental Contaminants, instructional slides to accompany Pollution Prevention:Fundamentals and Practice, by Paul L. Bishop (ISBN 0-07-366147-3). Retrieved 2005-03-07.
- ^ Li, Thomas S. C. (1999). Sea buckthorn: New crop opportunity, from Perspectives on new crops and new uses by J. Janeck (ed.) Retrieved 2006-10-28.
- ^ Terés, S; Barceló-Coblijn, G; Benet, M; Alvarez, R; Bressani, R; Halver, Je; Escribá, Pv (Sep 2008). "Oleic acid content is responsible for the reduction in blood pressure induced by olive oil". Proceedings of the National Academy of Sciences of the United States of America. doi:. PMID 18772370.
- ^ Schauss AG, Wu X, Prior RL, Ou B, Patel D, Huang D, Kababick JP. Phytochemical and nutrient composition of the freeze-dried amazonian palm berry, Euterpe oleraceae Mart. (acai). J Agric Food Chem. 2006 Nov 1;54(22):8598-603. [1]
- ^ Anies Hannawati Purnamadjaja, R. Andrew Russell (2005). "Pheromone communication in a robot swarm: necrophoric bee behaviour and its replication". Robotica 23 (6): 731–742. doi:.
- ^ Ayasse, M, Paxton, R (2002) Brood protection in social insects. In: Hilker, M, Meiners, T (eds.). Chemoecology of Insect Eggs and Egg Deposition. Blackwell, Berlin, 117-148.
- ^ "Adrenoleukodystrophy: oleic acid lowers fibroblast saturated C22-26 fatty acids". National Center for Biotechnology Information (1986 March 3). Retrieved on 7 October 2008.
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Wikipedia content modification information:
- This page was last modified on 7 October 2008, at 22:40.
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