Chemistry:Octyldodecanol

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Octyldodecanol
Octyldodecanol.svg
Names
IUPAC name
2-Octyldodecan-1-ol[1]
Other names
2-Octyl-1-dodecanol, 2-Octyldodecanol, Eutanol G, Guerbet C20, Isofol 20, Kalcohl 200G
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
DrugBank
EC Number
  • 226-242-9
KEGG
UNII
Properties
C20H42O
Molar mass 298.555 g·mol−1
Appearance yellow oil
Density 0.84
Melting point 1 °C (34 °F; 274 K)
Boiling point 382 °C (720 °F; 655 K)
1.454
Hazards
Flash point 113 °C (235 °F; 386 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
Tracking categories (test):

Octyldodecanol is a branched-chain primary alcohol used as the isomer 2-octyl-1-dodecanol in cosmetics such as lipstick,[2] or as an anti-blooming agent in facepowder.[3] It is a medium spreading emollient, with equilibrium spreading pressure of 17.0 dyne/cm.[4] Octyldodecanol is in the class of Guerbet alcohols, because it has the branch at the β position.[5] Compared to arachidyl alcohol, the linear alcohol of the same molecular weight, it has a lower melting point, yet retains low volatility.[5]

Production

2-Octyldodecanol is produced by the Guerbet condensation of decyl alcohol.[6]

Reactions

When octyldodecanol is melted with an alkali it yields octyldodecanoic acid by a dehydrogenation reaction.[5]

References

  1. "2-Octyl-1-dodecanol". https://pubchem.ncbi.nlm.nih.gov/compound/2-Octyl-1-dodecanol#section=IUPAC-Name. 
  2. Milne, G. W. A. (2005) (in en). Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties. John Wiley & Sons. p. 456. ISBN 9780471736615. https://books.google.com/books?id=oWdc2qcb3QsC&pg=PA456. 
  3. Williams, S. D. (1996) (in en). Chemistry and Technology of the Cosmetics and Toiletries Industry. Springer Science & Business Media. p. 164. ISBN 9780751403343. https://books.google.com/books?id=q1W7VtF8rJgC&pg=PA164. 
  4. Kroke, H. P. (April 1978). "Oily components in cosmetics from a European view". Journal of the American Oil Chemists' Society 55 (4): 444–446. doi:10.1007/BF02911910. 
  5. 5.0 5.1 5.2 O'Lenick, Anthony J. (July 2001). "Guerbet chemistry". Journal of Surfactants and Detergents 4 (3): 311–315. doi:10.1007/s11743-001-0185-1. 
  6. Williams (1996), p. 26.