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Lignoceric acid

From Wikipedia, the free encyclopedia
Lignoceric acid
Names
Preferred IUPAC name
Tetracosanoic acid
Other names
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard100.008.347Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C24H48O2/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/h2-23H2,1H3,(H,25,26) checkY
    Key: QZZGJDVWLFXDLK-UHFFFAOYSA-N checkY
  • InChI=1/C24H48O2/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/h2-23H2,1H3,(H,25,26)
    Key: QZZGJDVWLFXDLK-UHFFFAOYAH
  • O=C(O)CCCCCCCCCCCCCCCCCCCCCCC
Properties
C24H48O2
Molar mass368.63 g/mol
Melting point84.2 °C (183.6 °F; 357.3 K)[1]
Related compounds
Behenic acid (C22:0)
Cerotic acid (C26:0)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Lignoceric acid, ortetracosanoic acid, is thesaturated fatty acid with formulaC23H47COOH. It is found inwood tar, variouscerebrosides, and in small amounts in most naturalfats. The fatty acids ofpeanut oil contain small amounts of lignoceric acid (1.1% – 2.2%).[1] This fatty acid is also a byproduct oflignin production.

Reduction of lignoceric acid yieldslignoceryl alcohol.

See also

[edit]

References

[edit]
  1. ^abBeare-Rogers, J. L.; Dieffenbacher, A.; Holm, J. V. (2001)."Lexicon of lipid nutrition (IUPAC Technical Report)".Pure and Applied Chemistry.73 (4):685–744.doi:10.1351/pac200173040685.S2CID 84492006.
Saturated
ω−3 Unsaturated
ω−5 Unsaturated
ω−6 Unsaturated
ω−7 Unsaturated
ω−9 Unsaturated
ω−10 Unsaturated
ω−11 Unsaturated
ω−12 Unsaturated

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