Zinc ricinoleate
Names
IUPAC name
Zinc bis[(9Z,12R)-12-hydroxy-9-octadecenoate]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.032.632
UNII
  • InChI=1S/2C18H34O3.Zn/c2*1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21;/h2*9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21);/q;;+2/p-2/b2*12-9-;/t2*17-;/m11./s1
    Key: GAWWVVGZMLGEIW-GNNYBVKZSA-L
  • InChI=1/2C18H34O3.Zn/c2*1-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21;/h2*9,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21);/q;;+2/p-2/b2*12-9-;/t2*17-;/m11./s1
    Key: GAWWVVGZMLGEIW-AHLWSCBLBS
  • CCCCCC[C@@H](O)C/C=C\CCCCCCCC(=O)[O-].CCCCCC[C@@H](O)C/C=C\CCCCCCCC(=O)[O-].[Zn+2]
Properties
C36H66O6Zn
Molar mass 660.315
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Zinc ricinoleate is the zinc salt of ricinoleic acid, a major fatty acid found in castor oil. It is used in many deodorants as an odor-adsorbing agent. The mechanism of this activity is unclear.[1]

Zinc carboxylates adopt the basic zinc acetate structure but they are often depict, like here, as salts with naked Zn2+ and two ionized carboxylate anions.

References

  1. ↑ Kuhn, H.; F. Müller; J. Peggau; R. Zekorn (April 18, 2000). "Mechanism of the odor-adsorption effect of zinc ricinoleate. A molecular dynamics computer simulation". Journal of Surfactants and Detergents. Springer Berlin/Heidelberg. 3 (3): 335–343. doi:10.1007/s11743-000-0137-9. ISSN 1097-3958. S2CID 93526895.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.