모든 사진(1)
About This Item
실험식(Hill 표기법):
C10H18O
CAS Number:
Molecular Weight:
154.25
FEMA Number:
3658
Beilstein:
104974
EC Number:
유럽평의회 번호:
11225
MDL number:
UNSPSC 코드:
12164502
PubChem Substance ID:
플래비스(Flavis) 번호:
3.007
추천 제품
생물학적 소스
synthetic
Grade
Halal
규정 준수
FDA 21 CFR 172.515
분석
≥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.)
응용 분야
flavors and fragrances
문건
see Safety & Documentation for available documents
식품 알레르기항원
no known allergens
감각 수용성의
spicy; vanilla
SMILES string
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
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
1,4-Cineole is a volatile monoterpene cyclic ether typically found in the plant essential oils. It is phytotoxic and shows potent allelopathic property.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point (°F)
116.6 °F - closed cup
Flash Point (°C)
47 °C - closed cup
개인 보호 장비
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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
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
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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