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173495

Sigma-Aldrich

Geranyl acetate

≥97%

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Synonym(s):
trans-3,7-Dimethyl-2,6-octadien-1-yl acetate, trans-3,7-Dimethyl-2,6-octadienyl acetate
Linear Formula:
CH3CO2CH2CH=C(CH3)CH2CH2CH=C(CH3)2
CAS Number:
Molecular Weight:
196.29
EC Number:
MDL number:
PubChem Substance ID:

vapor density

6.8 (vs air)

Quality Level

vapor pressure

0.07 mmHg ( 20 °C)

Assay

≥97%

form

liquid

impurities

1-2% neryl acetate

refractive index

n20/D 1.461 (lit.)

bp

138 °C/25 mmHg (lit.)

density

0.916 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

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

InChI

1S/C12H20O2/c1-10(2)6-5-7-11(3)8-9-14-12(4)13/h6,8H,5,7,9H2,1-4H3/b11-8+

InChI key

HIGQPQRQIQDZMP-DHZHZOJOSA-N

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General description

Geranyl acetate is an aroma active rice volatile. It is one of the components of the essential oils of Daucus carota L. seeds.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Chronic 3 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

219.2 °F - closed cup

Flash Point(C)

104 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Nesrine Rokbeni et al.
Chemistry & biodiversity, 10(12), 2278-2290 (2013-12-12)
The essential oils of Daucus carota L. (Apiaceae) seeds sampled from ten wild populations spread over northern Tunisia were characterized by GC-FID and GC/MS analyses. In total, 36 compounds were identified in the D. carota seed essential oils, with a
Bruno Pandelo Brügger et al.
Scientific reports, 9(1), 8358-8358 (2019-06-09)
Podisus nigrispinus Dallas (Heteroptera: Pentatomidae), released in biological control programs, is a predator of Lepidopteran and Coleopteran species. Lemongrass essential oil and its constituents can be toxic to this natural enemy. The major constituents of lemongrass essential oil are neral
Shuai Liu et al.
Insect biochemistry and molecular biology, 127, 103485-103485 (2020-10-14)
The sensory neuron membrane protein, SNMP1, was initially discovered in moths and is associated with sex pheromone sensitive neurons, suggesting a role in the detection of these semiochemicals. Although DrosophilaSNMP1 has been reported to be involved in detecting of the
Satoshi Nojima et al.
PloS one, 6(3), e18178-e18178 (2011-04-06)
Semiochemicals are often produced in infinitesimally small quantities, so their isolation requires large amounts of starting material, not only requiring significant effort in sample preparation, but also resulting in a complex mixture of compounds from which the bioactive compound needs
Won-Il Cho et al.
Journal of food protection, 78(6), 1221-1225 (2015-06-04)
The sporicidal activities against Bacillus subtilis spores of surfactant components with hydrophilic and hydrophobic properties that can lead to the denaturation of various proteins comprising the spore structure were investigated. The reduction in spore numbers by each of the surfactant

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