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Icosane

Chemical compound From Wikipedia, the free encyclopedia

Icosane (alternative spelling eicosane and eichosane[2]) is an alkane with the chemical formula C20H42. It has 366,319 constitutional isomers.

Quick Facts Names, Identifiers ...
Icosane
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Names
Preferred IUPAC name
Icosane[1]
Other names
Eicosane, Eichosane
Identifiers
3D model (JSmol)
1700722
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.653
EC Number
  • 204-018-1
MeSH eicosane
UNII
  • InChI=1S/C20H42/c1-3-5-7-9-11-13-15-17-19-20-18-16-14-12-10-8-6-4-2/h3-20H2,1-2H3 Y
    Key: CBFCDTFDPHXCNY-UHFFFAOYSA-N Y
  • CCCCCCCCCCCCCCCCCCCC
Properties
C20H42
Molar mass 282.556 g·mol−1
Appearance Colorless, waxy crystals
Odor Odorless
Melting point 36 to 38 °C; 97 to 100 °F; 309 to 311 K
Boiling point 343.1 °C; 649.5 °F; 616.2 K
log P 10.897
31 μmol Pa−1 kg−1
Thermochemistry
602.5 J K−1 mol−1 (at 6.0 °C)
558.6 J K−1 mol−1
Hazards
NFPA 704 (fire diamond)
ThumbHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
1
0
Flash point > 113 °C (235 °F; 386 K)
Related compounds
Related alkanes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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n-Icosane (the straight-chain structural isomer of icosane) is the shortest compound found in paraffin waxes used to form candles. It can be isolated from Agave attenuate leaves. It is also found in Vanilla madagascariensis and Gymnodinium nagasakiense.[3]

Icosane's size, state or chemical inactivity does not exclude it from the traits its smaller alkane counterparts have. It is a colorless or white, non-polar molecule, nearly unreactive except when it burns. It is less dense than and insoluble in water. Its non-polar trait means it can only perform weak intermolecular bonding (hydrophobic/van der Waals forces).

Icosane's phase transition at a moderate temperature makes it a candidate phase change material, or PCM which can be used to store thermal energy and control temperature.

It can be detected in the body odor of persons suffering from Parkinson's disease.[4]

Naming

IUPAC currently recommends icosane,[5] whereas Chemical Abstracts Service and Beilstein use eicosane.[6]

See also

References

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