W250910
乙酸香叶酯
natural, FCC
别名:
反-3,7-二甲基-2,6-辛二烯-1-醇乙酸酯, 反-3,7-二甲基-2,6-辛二烯乙酸酯
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线性分子式:
CH3CO2CH2CH=C(CH3)CH2CH2CH=C(CH3)2
化学文摘社编号:
分子量:
196.29
FEMA Number:
2509
Council of Europe no.:
201
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.011
EC Number:
203-341-5
NACRES:
NA.21
MDL number:
Organoleptic:
green; waxy; floral; rose
Grade:
Halal, Kosher, natural
Food allergen:
no known allergens
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
grade
Halal, Kosher, natural
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
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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.
wgk
WGK 2
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 3 - Skin Irrit. 2 - Skin Sens. 1
存储类别
10 - Combustible liquids
flash_point_f
219.2 °F - closed cup
flash_point_c
104 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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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