Lumequeic acid
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| Names | |
|---|---|
| IUPAC name (Z)-triacont-21-enoic acid | |
| Other names 21-Triacontenoic acid | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
| |
| |
| Properties | |
| C30H58O2 | |
| Molar mass | 450.792 g·mol−1 |
| Melting point | 50.5–50.9 °C (122.9–123.6 °F; 323.6–324.0 K) |
| soluble | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Lumequeic acid is a chemical compound with the chemical formula C30H58O2.[1] Its delta notation is Δ21-30:1. This is a monounsaturated fatty acid and very long chain fatty acid with a 30-carbon chain with a cis-configured double bond at the 21st position.[2]
The acid has been found in Ximenia americana (yellowplum). The genus is named after the Spanish priest Francisco Ximénez (1666–1729).[3] Also, the acid has been identified in cured vanilla beans (Vanilla planifolia species).[4] The lumequeic acid is named after lumeque seed of West African Ximenia species.[5]
Synthesis
Synthetic method
Lumequic acid synthesis involves extending shorter fatty acids by adding carbon units using enzymes or chemical catalysts, leading to the creation of very long-chain fatty acids.[6]
Industrial method
Industrial-scale production of this compound relies on biotechnological methods, specifically microbial fermentation. The process involves genetically engineering microorganisms to produce the desired fatty acid, a method chosen for its efficiency and environmental sustainability.[6]
Uses
The acid is primarily used in biochemical research, pharmaceutical development, and environmental science.[6]
References
- ^ "NCATS Inxight Drugs — LUMEQUEIC ACID". drugs.ncats.io. Retrieved 2 April 2025.
- ^ "NP-MRD: Showing NP-Card for lumepueic acid (NP0202499)". np-mrd.org. Retrieved 2 April 2025.
- ^ The Etymology of Chemical Names: Tradition and Convenience vs. Rationality in Chemical Nomenclature. Walter de Gruyter GmbH & Co KG. 8 October 2019. p. 283. ISBN 978-3-11-061271-4. Retrieved 1 April 2025.
- ^ Ravindran, P. N.; Sivaraman, K.; Devasahayam, S.; Babu, K. Nirmal (24 June 2024). Handbook of Spices in India: 75 Years of Research and Development. Springer Nature. p. 555. ISBN 978-981-19-3728-6. Retrieved 2 April 2025.
- ^ The Etymology of Chemical Names: Tradition and Convenience vs. Rationality in Chemical Nomenclature. Walter de Gruyter GmbH & Co KG. 8 October 2019. p. 278. ISBN 978-3-11-061271-4. Retrieved 2 April 2025.
- ^ a b c "Buy Lumequic acid | 67329-09-3 | BenchChem". benchchem.com. Retrieved 2 April 2025.