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Merck
CN

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:
4128-17-0
Molecular Weight:
264.40
NACRES:
NA.22
PubChem Substance ID:
24860818
UNSPSC Code:
12352100
MDL number:
MFCD00036516
Assay:
95%
Form:
liquid

Key Documents

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Product Name

trans,trans-Farnesyl acetate, 95%

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+

SMILES string

CC(=O)OC\C=C(/C)CC\C=C(/C)CC\C=C(\C)C

InChI key

ZGIGZINMAOQWLX-NCZFFCEISA-N

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

Quality Level

100

Related Categories

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

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCR7080
MKCD7979
MKBL0894V
MKAA2334
12926KD

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Asymmetric dihydroxylation of geranyl, neryl and< i> trans, trans</i>-farnesyl acetates.
Vidari G, et al.
Tetrahedron Letters, 34(40), 6485-6488 (1993)
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
Pingping Liu et al.
Pest management science, 76(9), 2986-2993 (2020-04-05)
Thrips, Megalurothrips usitatus, usually display aggregation behavior, which is probably mediated by a male-produced aggregation pheromone. Aggregation pheromones are species-specific, and can be used to develop commercial lures for monitoring and mass-trapping of pests. The active components of the aggregation
Fangfang Zeng et al.
Insect biochemistry and molecular biology, 113, 103213-103213 (2019-08-24)
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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