Date published: 2026-4-24

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Ricinoleyl Alcohol (CAS 540-11-4)

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CAS Number:
540-11-4
Molecular Weight:
284.5
Molecular Formula:
C18H36O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
Available in US only.
* Refer to Certificate of Analysis for lot specific data.

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Ricinoleyl alcohol is a monounsaturated fatty alcohol derived from castor oil, finding extensive applications in cosmetics, pharmaceuticals, agriculture, and various industrial fields. With its unique chemical and physical properties, Ricinoleyl alcohol has been a subject of thorough scientific research. It serves as a versatile surfactant in drug delivery systems, an effective emulsifier in cosmetics, and a reliable lubricant in machinery. Furthermore, its potential as a biofuel and as a starting material for chemical synthesis has been explored. The distinctive structure of Ricinoleyl alcohol, encompassing a polar hydroxyl group and a non-polar hydrocarbon chain, allows it to interact with both polar and non-polar molecules. Notably, it exhibits inhibitory effects on enzymes like lipase and lipoxygenase, while also demonstrating antioxidant and anti-inflammatory properties.


Ricinoleyl Alcohol (CAS 540-11-4) References

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  2. Actions of ricinoleic acid and structurally related fatty acids on the gastrointestinal tract. II. Effects on water and electrolyte absorption in vitro.  |  Gaginella, TS., et al. 1975. J Pharmacol Exp Ther. 195: 355-61. PMID: 1185605
  3. Separation of oxygenated fatty compounds by thin-layer chromatography.  |  SUBBARAO, R., et al. 1962. J Chromatogr. 9: 295-300. PMID: 13979033
  4. INSECT SEX ATTRACTANTS. IV. THE DETERMINATION OF GYPLURE IN ITS MIXTURES BY ADSORPTION AND GAS CHROMATOGRAPHY.  |  JONES, WA. and JACOBSON, M. 1964. J Chromatogr. 13: 22-7. PMID: 14155338
  5. The structure of the glycerides of ergot oils.  |  Morris, LJ. and Hall, SW. 1966. Lipids. 1: 188-96. PMID: 17805610
  6. Maximization of bioconversion of castor oil into ricinoleic acid by response surface methodology.  |  Goswami, D., et al. 2009. Bioresour Technol. 100: 4067-73. PMID: 19419859
  7. Synthesis and physical properties of estolide ester using saturated Fatty Acid and ricinoleic Acid.  |  Salimon, J., et al. 2011. J Autom Methods Manag Chem. 2011: 263624. PMID: 22007150
  8. Chemoenzymatic synthesis and properties of novel lactone-type anionic surfactants.  |  Mori, K. and Matsumura, S. 2012. J Oleo Sci. 61: 609-20. PMID: 23138250
  9. Characterization of Two VAO-Type Flavoprotein Oxidases from Myceliophthora thermophila.  |  Ferrari, AR., et al. 2018. Molecules. 23: PMID: 29303991
  10. Metabolism of hydroxy fatty acids. V. Metabolic conversion of homoricinoleic and homoricinelaidic acids by Escherichia coli K 12.  |  Mizugaki, M., et al. 1965. J Biochem. 58: 273-8. PMID: 5324013
  11. Gypsy moth sex attractants: a reinvestigation.  |  Jacobson, M., et al. 1970. J Econ Entomol. 63: 943-5. PMID: 5431687
  12. Susceptibility of eggs and young adults of Cryptolestes ferrugineus and C. turcicus to hydrogen phosphide.  |  Barker, PS. 1969. J Econ Entomol. 62: 363-5. PMID: 5778302
  13. Enzymatic synthesis of wax esters by cell-free preparations from Sinapis alba L roots.  |  Zimowski, J., et al. 1982. Acta Biochim Pol. 29: 27-36. PMID: 7180324

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Ricinoleyl Alcohol, 100 mg

sc-296270
100 mg
$61.00
US: Only available in the US

Ricinoleyl Alcohol, 1 g

sc-296270A
1 g
$255.00
US: Only available in the US