Date published: 2026-5-25

1-800-457-3801

SCBT Portrait Logo
Seach Input

R-Palmitoyl-(1-methyl) Ethanolamide (CAS 142128-47-0)

0.0(0)
Write a reviewAsk a question

Alternate Names:
R-1 PMA; N-(2-hydroxy-1R-methylethyl)-hexadecanamide
Application:
R-Palmitoyl-(1-methyl) Ethanolamide is a synthetic analog of PEA
CAS Number:
142128-47-0
Molecular Weight:
313.52
Molecular Formula:
C19H39NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

R-Palmitoyl-(1-methyl) Ethanolamide, with the CAS number 142128-47-0, is a specialized fatty acid amide belonging to the broader class of N-acylethanolamines (NAEs). This chemical is structurally related to naturally occurring NAEs, which are known to play roles in intracellular signaling and the modulation of various physiological processes. In research contexts, R-Palmitoyl-(1-methyl) Ethanolamide is utilized to study the bioactivity and function of NAEs, particularly focusing on how these molecules interact with specific receptors or intracellular pathways. One key area of investigation involves understanding how the structural modifications, like the addition of a methyl group in this compound, influence its interaction with targets such as cannabinoid-like receptors, which are implicated in regulating pain, inflammation, and other cellular responses. Furthermore, this compound is of interest in exploring the mechanisms of lipid signaling pathways that impact cellular processes such as apoptosis and cell proliferation. By analyzing how R-Palmitoyl-(1-methyl) Ethanolamide affects these pathways, researchers can gain insights into the modulatory roles of fatty acid derivatives in cell signaling, potentially leading to broader understandings of cellular regulation, lipid metabolism, and the intracellular effects of structurally modified lipids.


R-Palmitoyl-(1-methyl) Ethanolamide (CAS 142128-47-0) References

  1. Palmitoylethanolamide increases after focal cerebral ischemia and potentiates microglial cell motility.  |  Franklin, A., et al. 2003. J Neurosci. 23: 7767-75. PMID: 12944505
  2. Anti-inflammatory activity on compounds obtained from egg yolk, peanut oil, and soybean lecithin.  |  GANLEY, OH., et al. 1958. J Lab Clin Med. 51: 709-14. PMID: 13539486
  3. Human test models for bioequivalence of topical corticosteroids: a review.  |  Olsen, EA. 1992. Int J Dermatol. 31 Suppl 1: 9-13. PMID: 1428469
  4. Prioritizing potential endocrine active high resolution mass spectrometry (HRMS) features in Minnesota lakewater.  |  Guyader, ME., et al. 2019. Sci Total Environ. 670: 814-825. PMID: 30921715
  5. Synthesis, Molecular Modeling and Biological Evaluation of Metabolically Stable Analogues of the Endogenous Fatty Acid Amide Palmitoylethanolamide.  |  D'Aloia, A., et al. 2020. Int J Mol Sci. 21: PMID: 33260658
  6. (R)-methanandamide: a chiral novel anandamide possessing higher potency and metabolic stability.  |  Abadji, V., et al. 1994. J Med Chem. 37: 1889-93. PMID: 8021930

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

R-Palmitoyl-(1-methyl) Ethanolamide, 5 mg

sc-205482
5 mg
$28.00

R-Palmitoyl-(1-methyl) Ethanolamide, 50 mg

sc-205482A
50 mg
$224.00