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W250910

Sigma-Aldrich

Geranyl acetate

greener alternative

natural, FCC

Synonym(s):

trans-3,7-Dimethyl-2,6-octadien-1-yl acetate, trans-3,7-Dimethyl-2,6-octadienyl acetate

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About This Item

Linear Formula:
CH3CO2CH2CH=C(CH3)CH2CH2CH=C(CH3)2
CAS Number:
Molecular Weight:
196.29
FEMA Number:
2509
EC Number:
Council of Europe no.:
201
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.011
NACRES:
NA.21

grade

Halal
Kosher
natural

Quality Level

reg. compliance

FCC
FDA 21 CFR 117

vapor density

6.8 (vs air)

vapor pressure

0.07 mmHg ( 20 °C)

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

refractive index

n20/D 1.461 (lit.)

bp

138 °C/25 mmHg (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

greener alternative category

Organoleptic

green; waxy; floral; rose

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

We are committed to bringing you greener alternative products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is Biobased and thus aligns with "Less Hazardous Chemical Syntheses" and "Use of Renewable Feedstocks".

Application


  • Differentiation of action mechanisms between natural and synthetic repellents through neuronal electroantennogram and proteomic in Aedes aegypti (Diptera: Culicidae).: This study investigates the different mechanisms of action between natural and synthetic repellents, including Geranyl acetate, using neuronal electroantennogram and proteomic analysis in Aedes aegypti. It provides insights into the biochemical pathways affected by these repellents (Portilla Pulido et al., 2022).

  • Hydrodistillation-headspace solvent microextraction, a new method for analysis of the essential oil components of Lavandula angustifolia Mill.: This paper introduces a novel method combining hydrodistillation and headspace solvent microextraction for analyzing essential oil components, including Geranyl acetate, in Lavandula angustifolia. It enhances the efficiency and accuracy of essential oil analysis (Fakhari et al., 2005).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

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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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
Bio-degradation of acetates of geraniol, nerol & citronellol by P. incognita: isolation & identification of metabolites.
K M Madyastha et al.
Indian journal of biochemistry & biophysics, 20(3), 136-140 (1983-06-01)
Luca Nicolotti et al.
Journal of chromatography. A, 1360, 264-274 (2014-08-19)
Comprehensive two-dimensional gas chromatography (GC×GC) coupled with Mass Spectrometry (MS) is one of today's most powerful analytical platforms for detailed analysis of medium-to-high complexity samples. The column set usually consists of a long, conventional-inner-diameter first dimension ((1)D) (typically 15-30m long
Emilie Deletre et al.
Parasites & vectors, 8, 316-316 (2015-06-13)
Laboratory and field studies showed that repellent, irritant and toxic actions of common public health insecticides reduce human-vector contact and thereby interrupt disease transmission. One of the more effective strategies to reduce disease risk involves the use of long-lasting treated

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