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Citronellyl formate

From Wikipedia, the free encyclopedia
Citronellyl formate
Names
IUPAC name
3,7-dimethyloct-6-enyl formate
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.036 Edit this at Wikidata
EC Number
  • 203-338-9
KEGG
UNII
  • InChI=1S/C11H20O2/c1-10(2)5-4-6-11(3)7-8-13-9-12/h5,9,11H,4,6-8H2,1-3H3
    Key: DZNVIZQPWLDQHI-UHFFFAOYSA-N
  • CC(CCC=C(C)C)CCOC=O
Properties[1]
C11H20O2
Molar mass 184.279 g·mol−1
Appearance colourless
Odor strong, fruity, floral
Density 0.897 g/cm3
Boiling point 235 °C (455 °F; 508 K)
insoluble
Solubility soluble in alcohol, most fixed oils
slightly soluble in propylene glycol
insoluble in glycerin
log P 3.800
1.443-1.452
Hazards
GHS labelling:[1]
GHS07: Exclamation mark
Warning
H315, H317
P261, P264, P272, P280, P302+P352, P321, P333+P317, P362+P364, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Citronellyl formate is a terpenoid ester derived from citronellol and formic acid.

Occurrence

[edit]

Citronellyl formate is an important component of geranium oil from Pelargonium graveolens. In two studies, its concentration was around 10% (9.7% and 11%).[2][3] Citronellyl formate is also found in kumquats, albeit in small amounts, but it is a characteristic component.[4]

Usage

[edit]

The compound is used as a fragrance, with worldwide usage in this area ranging from 10 to 100 tonnes per year.[5] In the EU, it is approved under FL number 09.078 as a general food flavoring and may contain citronellol for this application.[6]

References

[edit]
  1. 1 2 PubChem. "Citronellyl formate". pubchem.ncbi.nlm.nih.gov. Retrieved 2026-09-26.
  2. ↑ O. A. Lawal, A. H. Hutchings, O. Oyedeji (November 2010), "Chemical Composition of the Leaf Oil of Plectranthus neochilus Schltr.", Journal of Essential Oil Research, vol. 22, no. 6, pp. 546–547, doi:10.1080/10412905.2010.9700396{{citation}}: CS1 maint: multiple names: authors list (link)
  3. ↑ V Rana (December 2002), "Chemical constituents of essential oil of Pelargonium graveolens leaves", International Journal of Aromatherapy, vol. 12, no. 4, pp. 216–218, doi:10.1016/S0962-4562(03)00003-1
  4. ↑ Hyang-Sook Choi (2005-03-01), "Characteristic Odor Components of Kumquat (Fortunella japonica Swingle) Peel Oil", Journal of Agricultural and Food Chemistry, vol. 53, no. 5, pp. 1642–1647, Bibcode:2005JAFC...53.1642C, doi:10.1021/jf040324x, PMID 15740053
  5. ↑ A.M. Api, D. Belsito, D. Botelho, M. Bruze, G.A. Burton, J. Buschmann, M.A. Cancellieri, M.L. Dagli, M. Date, W. Dekant, C. Deodhar, A.D. Fryer, L. Jones, K. Joshi, M. Kumar, A. Lapczynski, M. Lavelle, I. Lee, D.C. Liebler, H. Moustakas, M. Na, T.M. Penning, G. Ritacco, J. Romine, N. Sadekar, T.W. Schultz, D. Selechnik, F. Siddiqi, I.G. Sipes, G. Sullivan, Y. Thakkar, Y. Tokura (December 2021), "RIFM fragrance ingredient safety assessment, citronellyl formate, CAS Registry number 105-85-1", Food and Chemical Toxicology, vol. 158, doi:10.1016/j.fct.2021.112621, PMID 34673180{{citation}}: CS1 maint: multiple names: authors list (link)
  6. ↑ "Food and Feed Information Portal Database | FIP". Retrieved 2024-02-03.