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User:SirBrahms/Articles by SirBrahms/Ethyl nonanoate

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Ethyl nonanoate
Names
IUPAC name
Ethyl nonanoate
Other names
Ethyl pelargonate
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C11H22O2/c1-3-5-6-7-8-9-10-11(12)13-4-2/h3-10H2,1-2H3
    Key: BYEVBITUADOIGY-UHFFFAOYSA-N
  • C(CCCCCCCC)(OCC)=O
Properties
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)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
0
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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

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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

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  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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