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经验公式(希尔记法):
C10H18O
化学文摘社编号:
分子量:
154.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-428-9
Beilstein/REAXYS Number:
104974
MDL number:
产品名称
1,4-桉叶素, technical, mixture of isomers, ≥85% (GC)
InChI key
RFFOTVCVTJUTAD-AOOOYVTPSA-N
InChI
1S/C10H18O/c1-8(2)10-6-4-9(3,11-10)5-7-10/h8H,4-7H2,1-3H3/t9-,10+
SMILES string
CC(C)C12CCC(C)(CC1)O2
grade
technical
assay
≥85% (GC)
form
liquid
composition
1,4-cineol, ~75%
1,8-cineol, ~15%
refractive index
n20/D 1.445 (lit.)
n20/D 1.447
bp
65 °C/16 mmHg (lit.)
mp
−46 °C (lit.)
density
0.887 g/mL at 25 °C (lit.)
functional group
ether
Quality Level
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General description
1,4-Cineole is present in eucalyptus oil. It activated both human TRPA1 (a sensor of noxious cold) and human TRPM 8 (a thermosensitive receptor). It is a natural monoterpene that inhibits plant growth.
signalword
Warning
hcodes
Hazard Classifications
Flam. Liq. 3
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
116.6 °F - closed cup
flash_point_c
47 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
L Ji et al.
Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica, 22(8), 489-492 (1997-08-01)
The essential oils from the dried stems of Ephedra sinica, E. intermedia and E. equisetina were analyzed by GC-MS qualitatively and GC quantitatively. One hundred and twenty-seven constituents were identified, l-alpha-terpineol (31.64%) in E. sinica, 1,4-cineole (12.80%) in E. intermedia
W Liu et al.
Applied and environmental microbiology, 59(11), 3889-3893 (1993-11-01)
A cytochrome P-450-dependent monooxygenase system that catalyzes the stereospecific hydroxylation of the monoterpene substrate 1,4-cineole was demonstrated in cell-free preparations of Bacillus cereus UI-1477. 1,4-Cineole hydroxylations were catalyzed by a 100,000 x g (1-h)-centrifuging soluble, hexane-inducible enzyme that activated and
M Miyazawa et al.
Xenobiotica; the fate of foreign compounds in biological systems, 31(10), 713-723 (2001-11-07)
1. Oxidation of 1,4-cineole, a monoterpene cyclic ether, was studied in rat and human liver microsomes and recombinant cytochrome P450 (P450 or CYP) enzymes expressed in insect cells in which human P450 and NADPH-P450 reductase cDNAs have been introduced. On
Janine K Reinert et al.
Frontiers in behavioral neuroscience, 13, 267-267 (2020-01-11)
Behavioral phenotyping of mice is often compromised by manual interventions of the experimenter and limited throughput. Here, we describe a fully automated behavior setup that allows for quantitative analysis of mouse olfaction with minimized experimenter involvement. Mice are group-housed and
Patrícia Bezerra Gomes et al.
Pharmacology, biochemistry, and behavior, 96(3), 287-293 (2010-07-31)
Recent studies have shown that some monoterpenes exert anxiolytic- and depressant-like actions, however, these effects from monoterpene 1,4-cineole are still unknown. This work aimed to study the effects of 1,4-cineole in classic animal models for depression- and anxiety-like behavior, specifically
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