Date published: 2026-7-12

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11-Dodecenoic acid (CAS 65423-25-8)

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Datasheets
Alternate Names:
cis-11-Dodecenoic acid; 11-lauroleic acid; 11-cis-Dodecenoic acid
CAS Number:
65423-25-8
Molecular Weight:
198.3
Molecular Formula:
C12H22O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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11-Dodecenoic acid is a naturally occurring fatty acid abundant in numerous plants. It serves diverse purposes in the medical and food industries, as well as acts as an intermediate in compound synthesis. Scientific research has employed 11-Dodecenoic acid in various applications. It has been utilized in polymer synthesis for drug delivery, as well as in investigating the impact of fatty acids on cell membranes. Additionally, it serves as a model compound for studying the structure and function of biological membranes. Although the exact mechanism of action remains unclear, it is speculated that the compound affects cell membranes by enhancing fluidity and reducing permeability to specific molecules. Furthermore, 11-Dodecenoic acid is believed to function as a signaling molecule, influencing the activity of enzymes and proteins.


11-Dodecenoic acid (CAS 65423-25-8) References

  1. Regioselectivity of a plant lauric acid omega hydroxylase. Omega hydroxylation of cis and trans unsaturated lauric acid analogs and epoxygenation of the terminal olefin by plant cytochrome P-450.  |  Weissbart, D., et al. 1992. Biochim Biophys Acta. 1124: 135-42. PMID: 1543735
  2. The catalytic site of rat hepatic lauric acid omega-hydroxylase. Protein versus prosthetic heme alkylation in the omega-hydroxylation of acetylenic fatty acids.  |  CaJacob, CA., et al. 1988. J Biol Chem. 263: 18640-9. PMID: 3198593
  3. Differential inactivation of plant lauric acid omega- and in-chain-hydroxylases by terminally unsaturated fatty acids.  |  Salaün, JP., et al. 1988. Arch Biochem Biophys. 260: 540-5. PMID: 3341756
  4. Autocatalytic inactivation of plant cytochrome P-450 enzymes: selective inactivation of the lauric acid in-chain hydroxylase from Helianthus tuberosus L. by unsaturated substrate analogs.  |  Salaun, JP., et al. 1984. Arch Biochem Biophys. 232: 1-7. PMID: 6742847
  5. Fate of a terminal olefin with Drosophila microsomes and its inhibitory effects on some P-450 dependent activities.  |  Cuany, A., et al. 1995. Arch Insect Biochem Physiol. 28: 325-38. PMID: 7711301
  6. In vitro hydroxylation and epoxidation of some isomeric lauric acid analogs by rat liver microsomes. Identification of metabolites and effects of clofibrate or phenobarbital pretreatment.  |  Boucher, JL., et al. 1996. Drug Metab Dispos. 24: 462-8. PMID: 8801062
  7. Cytochrome P450-dependent desaturation of lauric acid: isoform selectivity and mechanism of formation of 11-dodecenoic acid.  |  Guan, X., et al. 1998. Chem Biol Interact. 110: 103-21. PMID: 9566728

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

11-Dodecenoic acid, 100 mg

sc-506295
100 mg
$136.00