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Methyl melissate (CAS 629-83-4)

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Alternate Names:
Methyl Triacontanate
CAS Number:
629-83-4
Purity:
>95%
Molecular Weight:
466.83
Molecular Formula:
C31H62O2
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 melissate, a naturally occurring compound derived from the lavender plant, has been extensively studied in various scientific research applications due to its unique chemical properties and biological activities. Researchers have employed this compound to investigate its mechanisms of action in plant biology, biochemistry, and environmental science. Specifically, studies have shown that methyl melissate can modulate the activity of enzymes involved in plant defense responses, such as lipoxygenases and hydroperoxide lyases, and regulate the expression of genes involved in plant stress responses. Additionally, this compound has been used as a model system to study the mechanisms of plant-pollinator interactions, including the role of volatile organic compounds in attracting pollinators. Furthermore, methyl melissate has been used in the study of environmental pollution, enabling researchers to investigate the effects of pollutants on plant growth and development. In particular, this compound has been used as a substrate in enzymatic assays to study the activity of enzymes involved in plant metabolism, providing insights into the regulation of plant growth and development under stress conditions. Overall, the scientific research applications of methyl melissate have contributed significantly to our understanding of plant biology, biochemistry, and environmental science.


Methyl melissate (CAS 629-83-4) References

  1. Lipoxygenase inhibiting ethyl substituted glycoside from Symplocos racemosa.  |  Abbasi, MA., et al. 2005. Nat Prod Res. 19: 509-15. PMID: 15938197
  2. The Chemical Constituents of Australian Flindersia Species. XV. The Constituents of Flindersia acuminata CT White.  |  White, C. T., et al. 1961. Australian Journal of Chemistry. 14.3: 469-470.
  3. Composition of leaf surface waxes of Triticum species: variation with age and tissue.  |  Tulloch, Alexander P. 1973. Phytochemistry. 12.9: 2225-2232.
  4. 15, 18, 21, 24-triacontatetraenoic and 15, 18, 21, 24, 27-triacontapentaenoic acids: New C 30 fatty acids from the marine sponge Cliona celata.  |  Litchfield, Carter, et al. 1979. Lipids. 14: 619-622.
  5. The epitaxial growth of the methyl triacontanoate crystal.  |  Ueda, Yasukiyo. 1986. Bulletin of the Chemical Society of Japan. 59.12: 3775-3779.
  6. Bis (2, 2′-bipyridine)(4, 4′-diuntriacontanyl-2, 2′-bipyridine)-ruthenium (II) chloride and related hydrophobic complexes.  |  Seddon, Kenneth R. and Yousif Z. Yousif. 1986. Transition Metal Chemistry. 11: 443-446.
  7. The Effect of the Chain Length and the End-Groups on the Epitaxial Growth of Long-Chain Molecules.  |  Ueda, Yasukiyo. 1987. Bulletin of the Chemical Society of Japan. 60.6: 2011-2017.
  8. Epicuticular waxes of Abies balsamea and Picea glauca: occurrence of long-chain methyl esters.  |  Tulloch, Alexander P. 1987. Phytochemistry. 26.4: 1041-1043.
  9. A NEW ROUTE FOR SYNTHESIS OF 1-TRIACONTANOL.  |  Rao, B. V. S. K. and R. Supharao. 1992. Organic preparations and procedures international. 24.1: 67-70.
  10. Novel synthesis of 1-triacontanol, a plant growth stimulator, by crossed Kolbe coupling.  |  Kida, Yoshishige, et al. 1995. Journal of Japan Oil Chemists' Society. 44.3: 203-206.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Methyl melissate, 100 mg

sc-328872
100 mg
$213.00

Methyl melissate, 1 g

sc-328872A
1 g
$1165.00