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Heneicosylic acid

From Wikipedia, the free encyclopedia
Heneicosylic acid
Names
Preferred IUPAC name
Henicosanoic acid
Other names
Heneicosylic acid
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.017.377Edit this at Wikidata
UNII
  • InChI=1S/C21H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23/h2-20H2,1H3,(H,22,23)
    Key: CKDDRHZIAZRDBW-UHFFFAOYSA-N
  • InChI=1S/C21H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23/h2-20H2,1H3,(H,22,23)
    Key: CKDDRHZIAZRDBW-UHFFFAOYSA-N
  • CCCCCCCCCCCCCCCCCCCCC(=O)O
Properties
C21H42O2
Molar mass326.55 g/mol
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Heneicosylic acid, orheneicosanoic acid, is theorganic compound with the formulaCH3(CH2)19CO2H. It is the straight-chain 21-carbonsaturated fatty acid. It is a colorless solid.

It has shown relevance in the production offoams,paints, and related viscous materials.[1] A laboratory preparation involves permanganate oxidation of1-docosene (CH3(CH2)19CH=CH2).[2]

See also

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References

[edit]
  1. ^Ghaskadvi, R.S.; Dennin, Michael (2000). "Alternate Measurement of the Viscosity Peak in Heneicosanoic Acid Monolayers".Langmuir.16 (26):10553–10555.doi:10.1021/la0006925.
  2. ^Donald G. Lee; Shannon E. Lamb; Victor S. Chang (1981)."Carboxylic Acids from the Oxidation of Terminal Alkenes by Permanganate: Nonadecanoic Acid".Organic Syntheses.60: 11.doi:10.15227/orgsyn.060.0011.
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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