Date published: 2026-9-11

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Petroselinyl alcohol (CAS 2774-87-0)

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CAS Number:
2774-87-0
Molecular Weight:
268.48
Molecular Formula:
C18H36O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Petroselinyl alcohol, identified by the CAS number 2774-87-0, is an organic compound classified under the group of unsaturated fatty alcohols. This chemical is characterized by its unique structural element, the petroselinic acid derivative, which is an omega-12 monounsaturated fatty acid commonly found in the seeds of certain plants such as parsley and coriander. In research, petroselinyl alcohol is of considerable interest due to its distinct chemical properties that stem from the presence of a double bond in its long carbon chain. This structural feature makes it a valuable subject in the study of lipid chemistry, particularly in understanding the physical and chemical behavior of unsaturated alcohols in biological and industrial systems. Researchers utilize petroselinyl alcohol to explore its potential as a bio-based starting material for the synthesis of environmentally friendly surfactants and emulsifiers. Its applications extend to the field of green chemistry, where it is investigated for its ability to serve as a precursor for the production of biodegradable plastics, coatings, and other polymer materials. The study of this alcohol also enhances understanding of the lipid metabolism in plants, providing insights into the biosynthesis pathways and the role of unsaturated lipids in plant physiology and adaptation.


Petroselinyl alcohol (CAS 2774-87-0) References

  1. Fatty Acids and Their Derivatives as Modulators of Appressorium Formation in Magnaporthe grisea.  |  Eilbert, F., et al. 1999. Biosci Biotechnol Biochem. 63: 879-83. PMID: 27385571
  2. Synthesis and reactivity of (. eta. 5-C5Me5)(PMe3) Ir (CH2): a monomeric (pentamethylcyclopentadienyl) iridium methylene complex  |  Klein, D. P., & Bergman, R. G. 1989. Journal of the American Chemical Society. 111(8): 3079-3080.
  3. Glycidyl derivatives as chiral C3 synthons. Ring opening catalyzed by boron trifluoride etherate  |  Guivisdalsky, P. N., & Bittman, R. 1989. Journal of the American Chemical Society. 111(8): 3077-3079.
  4. An efficient stereocontrolled route to both enantiomers of platelet activating factor and analogs with long-chain esters at C-2: saturated and unsaturated ether glycerolipids by opening of glycidyl arenesulfonates  |  Guivisdalsky, P. N., & Bittman, R. 1989. The Journal of Organic Chemistry. 54(19): 4643-4648.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Petroselinyl alcohol, 100 mg

sc-281127
100 mg
$46.00