Icosane

Icosane
Names
	Preferred IUPAC name Icosane
	Other names Eicosane
Identifiers
CAS Number	112-95-8 ;
3D model (JSmol)	Interactive image;
Beilstein Reference	1700722
ChEBI	CHEBI:43619 ;
ChEMBL	ChEMBL1233983 ;
ChemSpider	7929 ;
ECHA InfoCard	100.003.653
EC Number	204-018-1;
MeSH	eicosane
PubChem CID	8222;
UNII	3AYA9KEC48 ;
CompTox Dashboard (EPA)	DTXSID1025227 ;
	SMILES CCCCCCCCCCCCCCCCCCCC;
Properties
Chemical formula	C20H42
Molar mass	282.56 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
kH	31 μmol Pa−1 kg−1
Thermochemistry
Standard molar; entropy So298	558.6 J K−1 mol−1
Specific heat capacity, C	602.5 J K−1 mol−1 (at 6.0 °C)
Hazards
	1 0 0
Flash point	>
Related compounds
Related {{{label}}}	{{{value}}}
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Icosane, also commonly spelled eicosane, is an alkane or a hydrocarbon with the chemical formula H₂₀C₄₂.^[2]^[3] It has 366,319 structural isomers. Its high flash point makes it a hard to light fuel, so it is not much use in the petrochemical industry.^[4] However, an isomer of icosane, n-Icosane (the straight-chain structural isomer of icosane) is the shortest compound found in paraffin waxes (C_nH_2n+2, where $n=\mathbb {Z} ={[20,40]}$ ) used to form candles. Icosane's phase transition at a moderate temperature makes it a candidate for PCM, which is used to store thermal energy and control temperature.

Icosane is a non-polar molecule: quite unreactive except when it burns (see the NFPA Diamond in the infobox). It is also way less dense than insoluble in water. This also means it shares properties with its smaller alkaline counterparts.

Icosane can also be detected in the body odor of people diagnosed with Parkinson's Disease.^[4]

The compound is found in the highest concentrations in plants such as Mexican ageratum, licorice, and the Bayrum tree.^[5]

References

↑ 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.
↑ PubChem. "Eicosane". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-05-20.
↑ "PDBeChem: Ligand Dictionary (PDB Ligand Chemistry - chemical component dictionary)". www.ebi.ac.uk. Retrieved 2021-06-03.
↑ ^4.0 ^4.1 "icosane (CHEBI:43619)". www.ebi.ac.uk. Retrieved 2021-05-20.
↑ "Activities of a Specific Chemical Query". 2015-09-23. Archived from the original on 2015-09-23. Retrieved 2021-05-21.{{cite web}}: CS1 maint: bot: original URL status unknown (link)

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[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] PubChem. "Eicosane". pubchem.ncbi.nlm.nih.gov. Retrieved 2021-05-20.

[3] "PDBeChem: Ligand Dictionary (PDB Ligand Chemistry - chemical component dictionary)". www.ebi.ac.uk. Retrieved 2021-06-03.

[:0-4] 4.0 ^4.1 "icosane (CHEBI:43619)". www.ebi.ac.uk. Retrieved 2021-05-20.

[5] "Activities of a Specific Chemical Query". 2015-09-23. Archived from the original on 2015-09-23. Retrieved 2021-05-21.{{cite web}}: CS1 maint: bot: original URL status unknown (link)

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