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Melissic acid (CAS 506-50-3)

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Alternate Names:
Triacontanoic acid
Application:
Melissic acid is used in a study on identification and determination of very-long-chain polyunsaturated fatty acid
CAS Number:
506-50-3
Purity:
≥95%
Molecular Weight:
452.80
Molecular Formula:
CH3(CH2)28COOH
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Melissic acid was used in a study on identification and determination of very-long-chain polyunsaturated fatty acid. Melissic acid, a long-chain saturated fatty acid, is prevalent in various plant and animal sources. Its significance lies in its involvement in biological processes, including maintaining cell membrane structure and function, serving as energy storage, and participating in signal transduction. This versatile acid is not only an essential constituent of industrial products like soaps, lubricants, and surfactants but also an object of extensive scientific research. Researchers have utilized it to explore fatty acids′ impact on cell membrane structure and function, and its role in regulating gene expression. Additionally, investigations into melissic acid have revealed insights into energy metabolism and signal transduction regulation facilitated by fatty acids.


Melissic acid (CAS 506-50-3) References

  1. [Chemical constituents of Pericampylus glaucus (Lam.) Merr].  |  Liang, P., et al. 1998. Zhongguo Zhong Yao Za Zhi. 23: 39-40, 63. PMID: 11243154
  2. Chemical constituents of Selinum cryptotaenium.  |  Rao, GX., et al. 2006. J Asian Nat Prod Res. 8: 273-5. PMID: 16864434
  3. [Chemical constituents of the pericarp of Trichosanthes rosthornii Harms].  |  Chao, Z. and Liu, J. 1991. Zhongguo Zhong Yao Za Zhi. 16: 97-9, 127. PMID: 1872972
  4. Stabilization of Gas Bubbles Released from Water-Soluble Carbohydrates Using Amphiphilic Compounds: Preparation of Formulations and Acoustic Monitoring of Bubble Lifetime.  |  Hoff, L., et al. 2011. J Surfactants Deterg. 14: 585-593. PMID: 21957396
  5. Characterization of two long-chain fatty acid CoA ligases in the Gram-positive bacterium Geobacillus thermodenitrificans NG80-2.  |  Dong, Y., et al. 2012. Microbiol Res. 167: 602-7. PMID: 22694860
  6. Fatty acid profiles of ecotypes of hyperaccumulator Noccaea caerulescens growing under cadmium stress.  |  Zemanová, V., et al. 2015. J Plant Physiol. 180: 27-34. PMID: 25886397
  7. Fatty acid composition and antibacterial potential of Cassia tora (leaves and stem) collected from different geographic areas of India.  |  Shukla, S., et al. 2018. J Food Drug Anal. 26: 107-111. PMID: 29389545
  8. Composition of the neutral and phospholipid fractions from ginkgo nuts (Ginkgo biloba) and fatty acid composition of individual lipid classes.  |  Urakami, C., et al. 1976. J Am Oil Chem Soc. 53: 525-9. PMID: 8476
  9. Molecular sputtering and damage induced by kiloelectron ions in organic monolayer-metal systems  |  R. Galera, J.C. Blais, G. Bolbach. 1991. International Journal of Mass Spectrometry and Ion Processes. 107: 531-543.
  10. Dark-field electron microscopy of Langmuir-Blodgett films of fatty acids and their barium salts  |  Mutsuo Matsumoto, Natsu Uyeda, Yoshinori Fujiyoshi, Kazuhiro Aoyama. 1993. Thin Solid Films. 223: 358-367.
  11. Phase Behavior and Structure of Systems Based on Mixtures of n-Hentriacontane and Melissic Acid  |  Lourdes Liliana Serrato-Palacios, Jorge F. Toro-Vazquez, Elena Dibildox-Alvarado, Antonio Aragón-Piña, Maria del Rosario Morales-Armenta, Vrani Ibarra-Junquera, Jaime David Pérez-Martínez. 2015. https://doi.org/10.1007/s11746-015-2623-6. 92: 533-540.
  12. Solid–liquid phase transition in a Gibbs monolayer of melissic acid at the n-hexane–water interface  |  A. M. Tikhonov. 2015. JETP Letters. 102: 552–556.
  13. Diffuse X-ray scattering near a two-dimensional solid–liquid phase transition at the n-hexane–water interface  |  A. M. Tikhonov. 2016. JETP Letters. 104: 309–314.
  14. The Solid–Liquid Phase Diagram of Binary Mixtures Dissolved in an Inert Oil: Application to Ternary Blends that Can Form Organogels  |  Hermanus M. Schaink. 2020. Journal of the American Oil Chemists' Society. 97: 117-124.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Melissic acid, 100 mg

sc-215293
100 mg
$80.00

Melissic acid, 1 g

sc-215293A
1 g
$950.00