Date published: 2026-2-24

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Methyl palmitelaidate (CAS 10030-74-7)

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Alternate Names:
Methyl hexadec-9-enoate
Application:
Methyl palmitelaidate is a fatty ester
CAS Number:
10030-74-7
Purity:
≥98%
Molecular Weight:
268.43
Molecular Formula:
C17H32O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Methyl palmitelaidate (MPTA) is an intriguing synthetic compound that has garnered attention in recent years due to its versatile applications across scientific disciplines. Derived from palmitic acid, Methyl palmitelaidate comprises a palmitic acid moiety and a methyl group. Its potential applications span the fields of biochemistry, physiology, and chemical synthesis, making it a subject of extensive research and development. In the realm of biochemistry, Methyl palmitelaidate holds promise as a surfactant in cell culture media and a stabilizer in protein solutions. Its applications in physiology include exploration as a drug delivery system and an adjuvant in vaccine formulations. Furthermore, Methyl palmitelaidate has been investigated in chemical synthesis as a catalyst in organic reactions and a reagent in synthetic processes. Although the precise biochemical and physiological effects of Methyl palmitelaidate are still being elucidated, it is believed to exhibit surfactant and stabilizing properties, function as a drug delivery system and vaccine adjuvant, and potentially possess anti-inflammatory, antioxidant, and cancer therapeutic applications. The mechanism through which Methyl palmitelaidate operates is not yet fully understood however, it is hypothesized that its binding to proteins and other cellular molecules, facilitated by the methyl group, induces structural and functional alterations.


Methyl palmitelaidate (CAS 10030-74-7) References

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  2. Kinetic barriers of H-atom transfer reactions in alkyl, allylic, and oxoallylic radicals as calculated by composite ab initio methods.  |  Hayes, CJ. and Burgess, DR. 2009. J Phys Chem A. 113: 2473-82. PMID: 19281146
  3. Endogenous fatty acids in olfactory hairs influence pheromone binding protein structure and function in Lymantria dispar.  |  Nardella, J., et al. 2015. Arch Biochem Biophys. 579: 73-84. PMID: 26032337
  4. Separation of the main flavonoids and essential oil from seabuckthorn leaves by ultrasonic/microwave-assisted simultaneous distillation extraction.  |  Li, C., et al. 2018. R Soc Open Sci. 5: 180133. PMID: 30109070
  5. A Network Pharmacology Study Based on the Mechanism of Citri Reticulatae Pericarpium-Pinelliae Rhizoma in the Treatment of Gastric Cancer.  |  Song, S., et al. 2021. Evid Based Complement Alternat Med. 2021: 6667560. PMID: 33953786
  6. Exploring Active Compounds and Mechanisms of Angong Niuhuang Wan on Ischemic Stroke Based on Network Pharmacology and Molecular Docking.  |  Zhang, Y., et al. 2022. Evid Based Complement Alternat Med. 2022: 2443615. PMID: 35388303
  7. Prediction of the Medicinal Mechanisms of Pinellia ternata Breitenbach, a Traditional Medicine for Gastrointestinal Motility Disorders, through Network Pharmacology.  |  Choi, NR., et al. 2022. Plants (Basel). 11: PMID: 35631773
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  10. Structure and biosynthesis of the hydroxy fatty acids of cutin in Vicia faba leaves.  |  Kolattukudy, PE. and Walton, TJ. 1972. Biochemistry. 11: 1897-907. PMID: 5025632

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl palmitelaidate, 100 mg

sc-215363
100 mg
$138.00

Methyl palmitelaidate, 500 mg

sc-215363A
500 mg
$321.00