Ethyl decadienoate
Names
Preferred IUPAC name
Ethyl (2E ,4Z )-deca-2,4-dienoate
Other names
Ethyl (2E ,4Z )-2,4-decadienoate Pear ester Ethyl 2-trans -4-cis -decadienoate
Identifiers
ChEBI
ChemSpider
ECHA InfoCard
100.019.254
UNII
InChI=1S/C12H20O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h8-11H,3-7H2,1-2H3/b9-8-,11-10+
Key: OPCRGEVPIBLWAY-QNRZBPGKSA-N
InChI=1/C12H20O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h8-11H,3-7H2,1-2H3/b9-8-,11-10+
Key: OPCRGEVPIBLWAY-QNRZBPGKBN
Properties
C 12 H 20 O 2
Molar mass
196.290 g·mol−1
Appearance
Colorless liquid[ 1]
Boiling point
70–72 °C (158–162 °F; 343–345 K) (0.05 mmHg)[ 2] 81–82 °C (178–180 °F) (0.1 mmHg)[ 3] 83–88 °C (181–190 °F) (0.1 mmHg)[ 4]
8.588 mg/L (est.)[ 5]
Hazards
Flash point
113 °C (235 °F)[ 2]
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Ethyl decadienoate , also known as pear ester , is an organic chemical compound used in flavors and perfumery for its pear -like taste and odor.
Occurrence and preparation
Ethyl decadienoate is found in apples , Bartlett pears , Concord grapes , beer , pear brandy and quince .[ 1]
It can also be prepared synthetically from 1-octyn-3-ol[ 4] or from ethyl propiolate .[ 3]
Uses
Ethyl decadienoate is used in natural flavors and fragrances for its intense fruity flavor. In the United States, as a food additive it is listed as generally recognized as safe (GRAS).[ 6]
References
^ a b Michael Zviely (August 23, 2011). "Pear Ester: Ethyl (E,Z)-2,4-decadienoate" . Perfumer & Flavorist.
^ a b
"Ethyl 2-trans-4-cis-decadienoate" . Sigma-Aldrich .
^ a b
Alexakis, A.; Cahiez, G.; Normant, J.F. (1980). "Vinyl-copper derivatives—XI". Tetrahedron . 36 (13): 1961. doi :10.1016/0040-4020(80)80209-2 .
^ a b
S. Tsuboi, T. Masuda, S. Mimura, and A. Takeda (1988). "Ethyl (E,Z)-2,4-Decadienoate" . Organic Syntheses . 66 : 22 {{cite journal }}
: CS1 maint: multiple names: authors list (link ) ; Collected Volumes , vol. 8, p. 251 .
^ "Ethyl (E,Z)-2,4-decadienoate" . Good Scents Company.
^ "ETHYL DECADIENOATE, NATURAL" . natural-advantage.net. Archived from the original on 2011-01-04. Retrieved 2012-09-27 .