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Melissic acid

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Melissic acid
Names
Preferred IUPAC name
Triacontanoic acid
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.312 Edit this at Wikidata
UNII
  • InChI=1S/C30H60O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30(31)32/h2-29H2,1H3,(H,31,32) ☒N
    Key: VHOCUJPBKOZGJD-UHFFFAOYSA-N ☒N
  • InChI=1/C30H60O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30(31)32/h2-29H2,1H3,(H,31,32)
    Key: VHOCUJPBKOZGJD-UHFFFAOYAR
  • CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O
Properties
C30H60O2
Molar mass 452.46 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Melissic acid (or triacontanoic acid) is the organic compound with the formula CH3(CH2)28CO2H. It is classified as a very long chain fatty acid, a subset of saturated fatty acids. It is a white solid that is soluble in organic solvents. Melissic acid gets its name from the Greek word melissa meaning bee, since it was found in beeswax.

Synthesis

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n-Triacontanoic acid was synthesized by Bleyberg and Ulrich (1931) and by G.M. Robinson.[1]

Self-assembly

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Triacontanoic acid and triacontanamide (CH3(CH2)28-CONH2) can be self-assembled.[2]

See also

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References

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  1. ^ Chibnall, Albert Charles; Ernest Frank Williams; Alfred Louis Latner; Stephen Harvey Piper (1933). "The isolation of n-triacontanol from lucerne wax". Biochemical Journal. 27 (6): 1885–1888. doi:10.1042/bj0271885. PMC 1253114. PMID 16745314.
  2. ^ Weinbach, Susan P.; Kristian Kjaer; Jens Als-Nielsen; Meir Lahav; Leslie Leiserowitz (May 1993). "Self-assembled Langmuir monolayers and trilayers at the air-formamide interface". Journal of Physical Chemistry. 97 (20): 5200–5203. doi:10.1021/j100122a003.
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