340480
trans,trans-Farnesyl acetate
95%
Synonym(s):
(E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-ol acetate, (E,E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-yl acetate
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About This Item
Linear Formula:
CH3CO2CH2CH=C(CH3)CH2CH2CH=C(CH3)CH2CH2CH=C(CH3)2
CAS Number:
Molecular Weight:
264.40
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95%
form
liquid
refractive index
n20/D 1.477 (lit.)
bp
115-125 °C/0.3 mmHg (lit.)
density
0.914 g/mL at 25 °C (lit.)
functional group
ester
SMILES string
CC(=O)OC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C
InChI
1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10+,16-12+
InChI key
ZGIGZINMAOQWLX-NCZFFCEISA-N
General description
trans,trans-Farnesyl acetate is one of the most odor-active or key compounds of Hyuganatsu aroma in Hyuganatsu (Citrus tamurana Hort. ex Tanaka) peel oil. Asymmetric dihydroxylation of trans,trans-farnesyl acetate using the new Sharpless′ ligand has been studied.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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H S Choi et al.
Journal of agricultural and food chemistry, 49(5), 2404-2408 (2001-05-23)
The volatile components of Hyuganatsu (Citrus tamurana Hort. ex Tanaka) peel oil, isolated by cold-pressing, were investigated by chemical and sensory analyses. According to chemical analysis by GC and GC-MS, limonene (84.0%) was the most abundant compound, followed by gamma-terpinene
Asymmetric dihydroxylation of geranyl, neryl and< i> trans, trans</i>-farnesyl acetates.
Vidari G, et al.
Tetrahedron Letters, 34(40), 6485-6488 (1993)
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Mosquitoes rely heavily on the olfactory system to find a host for a bloodmeal, plants for a source of energy and suitable sites for oviposition. Here, we examined a cluster of eight odorant receptors (ORs), which includes one OR, CquiOR1
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