Zinc ricinoleate

Zinc ricinoleate
Names
	IUPAC name Zinc bis[(9Z,12R)-12-hydroxy-9-octadecenoate]
Identifiers
CAS Number	13040-19-2;
3D model (JSmol)	Interactive image;
ChemSpider	4942331;
ECHA InfoCard	100.032.632
PubChem CID	6437808;
CompTox Dashboard (EPA)	DTXSID30891887 ;
	InChI InChI=1S/2C18H34O3.Zn/c21-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21;/h29,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21);/q;;+2/p-2/b212-9-;/t217-;/m11./s1 Key: GAWWVVGZMLGEIW-GNNYBVKZSA-L; InChI=1/2C18H34O3.Zn/c21-2-3-4-11-14-17(19)15-12-9-7-5-6-8-10-13-16-18(20)21;/h29,12,17,19H,2-8,10-11,13-16H2,1H3,(H,20,21);/q;;+2/p-2/b212-9-;/t217-;/m11./s1 Key: GAWWVVGZMLGEIW-AHLWSCBLBS;
	SMILES CCCCCC[C@@H](O)C/C=C\CCCCCCCC(=O)[O-].CCCCCC[C@@H](O)C/C=C\CCCCCCCC(=O)[O-].[Zn+2];
Properties
Chemical formula	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]

References

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.

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