Jump to content

Melissic acid

From Wikipedia, the free encyclopedia
(Redirected from C30H60O2)
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).
☒N verify (what is checkY☒N ?)

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

[edit]

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

Self-assembly

[edit]

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

See also

[edit]

References

[edit]
  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.
[edit]