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
FEMA编号:
3658
Beilstein:
104974
EC 号:
欧洲委员会编号:
11225
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
3.007
生物来源
synthetic
等级
Halal
管理合规性
FDA 21 CFR 172.515
方案
≥85%
折射率
n20/D 1.445 (lit.)
沸点
65 °C/16 mmHg (lit.)
mp
−46 °C (lit.)
密度
0.887 g/mL at 25 °C (lit.)
应用
flavors and fragrances
文件
see Safety & Documentation for available documents
食品过敏原
no known allergens
性状检查
spicy; vanilla
SMILES字符串
CC(C)C12CCC(C)(CC1)O2
InChI
1S/C10H18O/c1-8(2)10-6-4-9(3,11-10)5-7-10/h8H,4-7H2,1-3H3/t9-,10+
InChI key
RFFOTVCVTJUTAD-AOOOYVTPSA-N
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一般描述
1,4-Cineole is a volatile monoterpene cyclic ether typically found in the plant essential oils. It is phytotoxic and shows potent allelopathic property.
警示用语：
Warning
危险声明
危险分类
Flam. Liq. 3
储存分类代码
3 - Flammable liquids
WGK
WGK 2
闪点(°F)
116.6 °F - closed cup
闪点(°C)
47 °C - closed cup
个人防护装备
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)
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
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
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
Y Asakawa et al.
Xenobiotica; the fate of foreign compounds in biological systems, 18(10), 1129-1134 (1988-10-01)
1. The metabolism of 1,4-cineole, a monoterpene ether, was studied in the rabbit. 2. Four neutral and one acidic metabolites were isolated from the urine and shown to be 9-hydroxy-1,4-cineole, 3,8-dihydroxy-1,4-cineole, 8,9-dihydroxy-1,4-cineole, 1,4-cineole-8-en-9-ol and 1,4-cineole-9-carboxylic acid.
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