User:SirBrahms/Articles by SirBrahms/Ethyl nonanoate

Ethyl nonanoate
Names
	IUPAC name Ethyl nonanoate
	Other names Ethyl pelargonate
Identifiers
CAS Number	123-29-5 ;
3D model (JSmol)	Interactive image;
ChemSpider	28991 ;
PubChem CID	31251;
	InChI InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3 Key: BYEVBITUADOIGY-UHFFFAOYSA-N;
	SMILES C(CCCCCCCC)(OCC)=O;
Properties
Chemical formula	C11H22O2
Molar mass	186.29 g/mol
Density	0.863 g/cm3 at 20 °C
Melting point	−44.5 °C (−48.1 °F; 228.7 K)
Boiling point	119 °C (246 °F; 392 K)
Solubility	Soluble in Propylene glycol, insoluble in Water
Hazards
NFPA 704 (fire diamond)	0 0 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Ethyl nonanoate, also known by the common name Ethyl pelargonate,^[1] is an organic compound. It also has a biological role as a metabolite.^[2]

Uses

Ethyl nonanoate is used in cosmetics as a skin conditioner, due to its low toxicity.^[3] It is also used as a flavouring agent,^[4] described as having a floral flavour.^[5]

References

^ PubChem. "Ethyl Nonanoate". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-10-25.
^ "ethyl nonanoate (CHEBI:87501)". www.ebi.ac.uk. Retrieved 2024-10-23.
^ Johnson, Wilbur; Heldreth, and Bart; Bergfeld, Wilma F.; Belsito, Donald V.; Klaassen, Curtis D.; Hill, Ronald; Liebler, Daniel; Marks, James G.; Shank, Ronald C.; Slaga, Thomas J.; Snyder, Paul W.; Andersen, F. Alan (December 2011). "Final Report of the Cosmetic Ingredient Review Expert Panel on the Safety Assessment of Pelargonic Acid (Nonanoic Acid) and Nonanoate Esters". International Journal of Toxicology. 30 (6_suppl): 228S–269S. doi:10.1177/1091581811428980. ISSN 1091-5818.
^ "Substances Added to Food (formerly EAFUS)". www.hfpappexternal.fda.gov. Retrieved 2024-10-25.
^ "ETHYL NONANOATE | FEMA". www.femaflavor.org. Retrieved 2024-10-25.

[1] PubChem. "Ethyl Nonanoate". pubchem.ncbi.nlm.nih.gov. Retrieved 2024-10-25.

[2] "ethyl nonanoate (CHEBI:87501)". www.ebi.ac.uk. Retrieved 2024-10-23.

[3] Johnson, Wilbur; Heldreth, and Bart; Bergfeld, Wilma F.; Belsito, Donald V.; Klaassen, Curtis D.; Hill, Ronald; Liebler, Daniel; Marks, James G.; Shank, Ronald C.; Slaga, Thomas J.; Snyder, Paul W.; Andersen, F. Alan (December 2011). "Final Report of the Cosmetic Ingredient Review Expert Panel on the Safety Assessment of Pelargonic Acid (Nonanoic Acid) and Nonanoate Esters". International Journal of Toxicology. 30 (6_suppl): 228S–269S. doi:10.1177/1091581811428980. ISSN 1091-5818.

[4] "Substances Added to Food (formerly EAFUS)". www.hfpappexternal.fda.gov. Retrieved 2024-10-25.

[5] "ETHYL NONANOATE | FEMA". www.femaflavor.org. Retrieved 2024-10-25.

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