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Contents

   



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1 See also  




2 References  













Heneicosylic acid






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From Wikipedia, the free encyclopedia
  

Heneicosylic acid
Names
Preferred IUPAC name

Henicosanoic acid

Other names

Heneicosylic acid

Identifiers

CAS Number

3D model (JSmol)
ChemSpider
ECHA InfoCard 100.017.377 Edit this at Wikidata

PubChem CID
UNII

CompTox Dashboard (EPA)

  • 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

Chemical formula

 C21H42O2
Molar mass 326.55 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Infobox references

Heneicosylic acid, or heneicosanoic acid, is the organic compound with the formula CH3(CH2)19CO2H. It is the straight-chain 21-carbon saturated fatty acid. It is a colorless solid.

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

See also[edit]

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.
  • ^ 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.


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    • Retrieved from "https://en.wikipedia.org/w/index.php?title=Heneicosylic_acid&oldid=1184465172"
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