Icosane
Structural formula of icosane
Ball and stick model of the icosane molecule
Names
Preferred IUPAC name
Icosane[1]
Other names
Eicosane
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 checkY
    Key: CBFCDTFDPHXCNY-UHFFFAOYSA-N checkY
  • 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)
NFPA 704 four-colored diamond
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).
☒N verify (what is checkY☒N ?)
Infobox references

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

Icosane has little use in the petrochemical industry, as its high flash point makes it an inefficient fuel. n-Icosane (the straight-chain structural isomer of icosane) is the shortest compound found in paraffin waxes used to form candles.

Icosane's size, state or chemical inactivity does not exclude it from the traits its smaller alkane counterparts have. It is a colorless, 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.[2]

Naming

IUPAC currently recommends icosane,[3] whereas Chemical Abstracts Service and Beilstein use eicosane.[4]

See also

References

  1. ↑ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 59. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
  2. ↑ Trivedi, Drupad K.; Sinclair, Eleanor; Xu, Yun; Sarkar, Depanjan; Walton-Doyle, Caitlin; Liscio, Camilla; Banks, Phine; Milne, Joy; Silverdale, Monty; Kunath, Tilo; Goodacre, Royston; Barran, Perdita (2019). "Discovery of Volatile Biomarkers of Parkinson's Disease from Sebum". ACS Central Science. 5 (4): 599–606. doi:10.1021/acscentsci.8b00879. PMC 6487537. PMID 31041379.
  3. ↑ "Table 11 Basic numerical terms (multiplying affixes)". IUPAC. Retrieved 2011-02-16.
  4. ↑ "Footnote for Table 11". IUPAC. Retrieved 2011-02-16.
  • Icosane at Dr. Duke's Phytochemical and Ethnobotanical Databases
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.