163333
Géraniol
98%
Synonyme(s) :
trans-3,7-Diméthyl-2,6-octadiène-1-ol
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A propos de cet article
Formule linéaire :
(CH3)2C=CHCH2CH2C(CH3)=CHCH2OH
Numéro CAS:
Poids moléculaire :
154.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-377-1
Beilstein/REAXYS Number:
1722456
MDL number:
Assay:
98%
Form:
liquid
Service technique
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Laissez-nous vous aidervapor density
5.31 (vs air)
Quality Level
vapor pressure
~0.2 mmHg ( 20 °C)
assay
98%
form
liquid
refractive index
n20/D 1.474 (lit.)
bp
229-230 °C (lit.)
solubility
water: soluble 0.1 g/L at 25 °C
density
0.879 g/mL at 20 °C (lit.)
functional group
hydroxyl
SMILES string
C\C(C)=C\CC\C(C)=C\CO
InChI
1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+
InChI key
GLZPCOQZEFWAFX-JXMROGBWSA-N
General description
Geraniol undergoes oxidation with molecular oxygen in supercritical carbon dioxide catalyzed by chromium containing mesoporous molecular sieve to yield citral.
Application
Geraniol was used in field evaluation of synthetic herbivore-induced plant volatiles as attractants to beneficial insects. It was used to evaluate the tumor-suppressive potency of isoprenoids in vitro and in vivo.
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Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
Classe de stockage
10 - Combustible liquids
flash_point_f
226.4 °F - closed cup
flash_point_c
108 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Contenu apparenté
Ying Zhou et al.
Biomolecules, 9(12) (2019-12-06)
When insects attack plants, insect-derived elicitors and mechanical damage induce the formation and emission of plant volatiles that have important ecological functions and flavor properties. These events have mainly been studied in model plants, rather than crop plants. Our study
L He et al.
The Journal of nutrition, 127(5), 668-674 (1997-05-01)
Sundry mevalonate-derived constituents (isoprenoids) of fruits, vegetables and cereal grains suppress the growth of tumors. This study estimated the concentrations of structurally diverse isoprenoids required to inhibit the increase in a population of murine B16(F10) melanoma cells during a 48-h
Maria Cristina Bonferoni et al.
Pharmaceutics, 11(3) (2019-03-06)
The pharmacological activities of geraniol include anticancer and neuroprotective properties. However, its insolubility in water easily induces separation from aqueous formulations, causing administration difficulties. Here we propose new emulsified formulations of geraniol by using the amphiphilic polymer chitosan-oleate (CS-OA) as