Melissic acid
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 434945288
| ImageFile=Melissic acid.svg
| ImageSize=300
| PIN=Triacontanoic acid
| OtherNames=
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo=506-50-3
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = HLT2OTQ105
| PubChem=10471
| SMILES= CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 10039
| 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)
| InChIKey = VHOCUJPBKOZGJD-UHFFFAOYAR
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 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)
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = VHOCUJPBKOZGJD-UHFFFAOYSA-N
}}
|Section2={{Chembox Properties
| Formula=C30H60O2
| MolarMass=452.46 g/mol
| Appearance=
| Density=
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|Section3={{Chembox Hazards
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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
n-Triacontanoic acid was synthesized by Bleyberg and Ulrich (1931) and by G.M. Robinson.{{cite journal | title = The isolation of n-triacontanol from lucerne wax | journal = Biochemical Journal | year = 1933 | first = Albert Charles | last = Chibnall |author2=Ernest Frank Williams |author3=Alfred Louis Latner |author4=Stephen Harvey Piper | volume = 27 | issue = 6 | pages = 1885–1888| doi = 10.1042/bj0271885 | pmid = 16745314 | pmc = 1253114}}
Self-assembly
Triacontanoic acid and triacontanamide (CH3(CH2)28-CONH2) can be self-assembled.{{cite journal | title = Self-assembled Langmuir monolayers and trilayers at the air-formamide interface | journal = Journal of Physical Chemistry | date = May 1993 | first = Susan P. | last = Weinbach |author2=Kristian Kjaer |author3=Jens Als-Nielsen |author4=Meir Lahav |author5=Leslie Leiserowitz | volume = 97 | issue = 20 | pages = 5200–5203| doi = 10.1021/j100122a003}}
See also
References
{{reflist}}
External links
- [http://www.lipidmaps.org/data/LMSDRecord.php?LMID=LMFA01010030 Melissic acid] at the Nature Lipidomics Gateway
{{Fatty acids}}