46128
Eucalyptol
Ph. Helv.
Synonym(s):
Cineolum, 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octane, 1,8-Cineole, 1,8-Epoxy-p-menthane
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About This Item
Empirical Formula (Hill Notation):
C10H18O
CAS Number:
Molecular Weight:
154.25
EC Number:
207-431-5
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
105109
MDL number:
agency
Ph. Helv., USP/NF
refractive index
n20/D 1.457 (lit.)
bp
176-177 °C (lit.)
mp
1-2 °C (lit.)
density
0.921 g/mL at 25 °C (lit.)
SMILES string
C[C@]12CC[C@H](CC1)C(C)(C)O2
InChI
1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3/t8-,10+
InChI key
WEEGYLXZBRQIMU-WAAGHKOSSA-N
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signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3 - Skin Sens. 1
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
125.6 °F - closed cup
flash_point_c
52 °C - closed cup
Regulatory Information
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Anke Fähnrich et al.
Plant molecular biology, 85(1-2), 135-145 (2014-02-05)
Nicotiana species of the section Alatae emit a characteristic floral scent comprising the' cineole cassette' monoterpenes 1,8-cineole, limonene, myrcene, β-pinene, α-pinene, sabinene and α-terpineol. All previously isolated 'cineole cassette'-monoterpene synthase genes are multi product enzymes that synthesize the seven compounds
Zerihun A Demissie et al.
Plant molecular biology, 79(4-5), 393-411 (2012-05-18)
Several members of the genus Lavandula produce valuable essential oils (EOs) that are primarily constituted of the low molecular weight isoprenoids, particularly monoterpenes. We isolated over 8,000 ESTs from the glandular trichomes of L. x intermedia flowers (where bulk of
Hee-jin Jun et al.
Bioorganic & medicinal chemistry letters, 23(2), 579-583 (2012-12-19)
We investigated the effect of cineole on the expression of genes related to reverse cholesterol transport and hepatic fatty acid metabolism. Cineole, a small aroma compound in teas and herbs, significantly stimulated the transactivation of liver X receptor modulator (LXR)-α