W365807
1,4-桉叶素
≥85%
别名:
1-甲基-4-(1-甲乙基)-7-氧杂二环[2.2.1]庚烷
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关于此项目
经验公式（希尔记法）:
C10H18O
化学文摘社编号:
分子量:
154.25
PubChem Substance ID:
UNSPSC Code:
12164502
Council of Europe no.:
11225
FEMA Number:
3658
Flavis number:
3.007
EC Number:
207-428-9
MDL number:
Beilstein/REAXYS Number:
104974
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
biological source
synthetic
grade
Halal
reg. compliance
FDA 21 CFR 172.515
assay
≥85%
refractive index
n20/D 1.445 (lit.)
bp
65 °C/16 mmHg (lit.)
mp
−46 °C (lit.)
density
0.887 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
spicy; vanilla
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General description
1,4-Cineole is a volatile monoterpene cyclic ether typically found in the plant essential oils. It is phytotoxic and shows potent allelopathic property.
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
新产品
此项目有
Allelopathic effects of volatile cineoles on two weedy plant species.
Romagni JG, et al.
Journal of Chemical Ecology, 26(1), 303-313 (2000)
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
Abdul Ahad et al.
Current drug delivery, 8(2), 213-224 (2011-01-18)
The purpose of this study was to investigate the effectiveness and mechanism(s) of percutaneous absorption of propranolol hydrochloride (PHCL) across rat and human cadaver skin using seven novel terpenes with reference to marker terpene 1,8-cineole. In-vitro skin permeation studies were
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
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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