Lacceroic acid

Lacceroic acid

Names
Preferred IUPAC name Dotriacontanoic acid
Identifiers
CAS Number	3625-52-3^Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:76215^N
ChemSpider	18168^N
PubChem CID	19255
UNII	PB0234915O^Y
CompTox Dashboard (EPA)	DTXSID30189791
InChI InChI=1S/C32H64O2/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(33)34/h2-31H2,1H3,(H,33,34)^N Key: ICAIHSUWWZJGHD-UHFFFAOYSA-N^N InChI=1/C32H64O2/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(33)34/h2-31H2,1H3,(H,33,34) Key: ICAIHSUWWZJGHD-UHFFFAOYAW
SMILES CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O
Properties
Chemical formula	C32H64O2
Molar mass	480.85 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 ^YN ?) Infobox references

Lacceroic acid (or dotriacontanoic acid) is a saturated fatty acid.

Sources

Lacceroic acid can be derived by saponification of lacceryl lacceroate or by oxidation of 1-Dotriacontanol (lacceryl) and purification of the product.^[1] It can also be isolated from stick lac wax, from which the name is derived.^[2]

Derivatives

Ethyl lacceroate can be obtained as a crystalline solid (rhombic plates, mp 76 °C) by the action of HCl gas on lacceroic acid in boiling absolute alcohol.^[1]

See also

• List of saturated fatty acids

References

1. "Chemical Abstracts". Chemical Abstracts. 16 (1). American Chemical Society: 50. 1922-01-10. Retrieved 2010-05-10.
2. Markley, Klare (1960). Fatty acids: Their chemistry, properties, production, and uses. Part 1. (2nd ed.). New York: Interscience. p. 48.

External links

• Lacceroic acid at the Nature Lipidomics Gateway