W215902
乙酸冰片酯
≥98%, FG
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关于此项目
经验公式（希尔记法）:
C12H20O2
化学文摘社编号:
分子量:
196.29
FEMA Number:
2159
Council of Europe no.:
207
UNSPSC Code:
12164502
PubChem Substance ID:
EC Number:
200-964-4
Flavis number:
9.017
MDL number:
SMILES string
CC(=O)O[C@@H]1C[C@@H]2CC[C@@]1(C)C2(C)C
InChI key
KGEKLUUHTZCSIP-HOSYDEDBSA-N
InChI
1S/C12H20O2/c1-8(13)14-10-7-9-5-6-12(10,4)11(9,2)3/h9-10H,5-7H2,1-4H3/t9-,10+,12+/m0/s1
biological source
synthetic
grade
FG
reg. compliance
EU Regulation 1334/2008 & 178/2002, FDA 21 CFR 117, FDA 21 CFR 172.515
assay
≥98%
optical activity
[α]20/D −41°, neat
refractive index
n20/D 1.4635 (lit.)
bp
228-231 °C (lit.)
density
0.985 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
woody; sweet
Legal Information
For R&D Use and/or Food Manufacturing only
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
192.0 °F - closed cup
flash_point_c
88.89 °C - closed cup
法规信息
新产品
此项目有
K P Adam et al.
Archives of biochemistry and biophysics, 354(1), 181-187 (1998-06-20)
The incorporation of 13C-labeled glucose into borneol, bornyl acetate, the sesquiterpenes cubebanol and ricciocarpin A, phytol, and stigmasterol has been studied in axenic cultures of the liverworts Ricciocarpos natans and Conocephalum conicum. Quantitative 13C NMR spectroscopic analysis of the resulting
Nicolas Baldovini et al.
Phytochemical analysis : PCA, 14(4), 241-244 (2003-08-02)
The enantiomeric differentiation of bornyl acetate was carried out by 13C-NMR spectroscopy using a chiral lanthanide shift reagent. The technique was successfully applied to the determination of the enantiomer of bornyl acetate present in the essential oil of Inula graveolens.
Xiaosong Wu et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 28(6), 505-507 (2005-10-08)
To study the analgesic effect and mechanism of bornyl acetate, the main ingredient of Amomum Villosum Volatile oil. The analgesic effects were tested by pressing tail method. The I, and II phase pain were observed with the pain model caused
E Tachikawa et al.
Biochemical pharmacology, 60(3), 433-440 (2000-06-17)
The crude extract of magnolia bark, an herbal drug, inhibited the secretion of catecholamines from bovine adrenal chromaffin cells stimulated by acetylcholine (ACh) in a concentration-dependent manner (200-900 microg/mL). The extract also diminished the secretion induced by high K(+), which
Na Chen et al.
The Journal of surgical research, 186(1), 436-445 (2013-10-15)
Bornyl acetate is a bicyclic monoterpene present in numerous conifer oils. In this study, we aimed at clarifying the potential anti-inflammatory function and mechanism of bornyl acetate by using lipopolysaccharide (LPS)-induced acute lung injury murine model and RAW 264.7 cells.
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