Date published: 2026-5-25

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Methyl ricinelaidate (CAS 7706-01-6)

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CAS Number:
7706-01-6
Molecular Weight:
312.49
Molecular Formula:
C19H36O3
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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Methyl ricinelaidate, with the CAS number 7706-01-6, is a methyl ester derived from ricinelaidic acid, a trans isomer of the naturally occurring ricinoleic acid found in castor oil. This compound is particularly notable in the fields of organic chemistry and materials science due to its distinctive molecular structure, featuring a long carbon chain with a trans double bond. This structural attribute significantly influences its physical and chemical properties, making it a subject of interest for various applications. In research, methyl ricinelaidate is extensively used to study the effects of trans fatty acid esters on the physical properties of biodiesel, such as viscosity and freezing point, which are critical for the performance and stability of biofuels. The presence of the trans double bond in methyl ricinelaidate affects the crystallization behavior of the ester, which is crucial for understanding and improving low-temperature performance in biodiesel applications. Additionally, this compound serves as a model for synthesizing other complex esters and polymers, providing insights into reaction mechanisms and the kinetics of esterification processes. Researchers also explore its potential in developing new materials with specific properties, such as enhanced lubricity or modified surface characteristics, which are valuable for industrial applications in coatings and plasticizers.


Methyl ricinelaidate (CAS 7706-01-6) References

  1. Synthesis and nuclear magnetic resonance properties of all geometrical isomers of conjugated linoleic acids.  |  Jie, MS., et al. 1997. Lipids. 32: 1041-4. PMID: 9358429
  2. Anomalous Behavior of Methyl 12-Hydroxy-9, 10-Octadecenoates in Iodine Number Determinations  |  Skell, P. S., & Radlove, S. B. 1946. Industrial & Engineering Chemistry Analytical Edition. 18(1): 67-68.
  3. Determination of Allyl Groups in Polyallyl Ethers and Esters  |  Boyd, H. M., & Roach, J. R. 1947. Analytical Chemistry. 19(3): 158-159.
  4. Ricinelaidic acid and methyl ricinelaidate. Their preparation and determination by infrared spectroscopy  |  McCutchon, Marian A., et al. 1959. Journal of the American Oil Chemists' Society. 36(3): 115-118.
  5. The cyanoethylation and infrared spectra of some ricinoleic acid derivatives  |  Dupuy, H. P., Calderón, R., McCall, E. R., O'Connor, R. T., & Goldblatt, L. A. 1959. Journal of the American Oil Chemists Society. 36(12): 659-663.
  6. Antimicrobial activity of some ricinoleic acid oleic acid derivatives  |  Novak, A. F., Clark, G. C., & Dupuy, H. P. 1961. Journal of the American Oil Chemists Society. 38(6): 321-324.
  7. Analysis of the geometric isomers of methyl linoleate by gas chromatography  |  Litchfield, C., Isbell, A. F., & Reiser, R. 1962. Journal of the American Oil Chemists' Society. 39(7): 330-334.
  8. The analysis of Cis-trans fatty acid isomers using gas-liquid chromatography  |  Litchfield, C., Reiser, R., & Isbell, A. F. 1963. Journal of the American Oil Chemists' Society. 40(7): 302-309.
  9. NMR Spectra of Methyl Ricinoleate and Methyl Ricinelaidate  |  SUZUKI, O., HASHIMOTO, T., & HAYAMIZU, K. 1970. Journal of Japan Oil Chemists' Society. 19(3): 140-144.
  10. Confirmation of the carbon chemical shifts of ethylenic carbon atoms in methyl ricinoleate and methyl ricinelaidate  |  Lie Ken Jie, M. S. F., & Cheng, A. K. L. 1993. Natural Product Letters. 3(1): 65-69.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl ricinelaidate, 1 g

sc-280986
1 g
$345.00
US: Only available in the US