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
Eri Matsubara et al.
Biomedical research (Tokyo, Japan), 32(2), 151-157 (2011-05-10)
(-)-Bornyl acetate is the main volatile constituent in numerous conifer oils and has a camphoraceous, pine-needle-like odor. It is frequently used as the conifer needle composition in soap, bath products, room sprays, and pharmaceutical products. However, the psychophysiological effects of
G P Young et al.
Journal of chemical ecology, 35(1), 74-80 (2009-01-21)
Potential allelopathic compounds of Juniperus ashei Buchh. (Ashe juniper) and their effect on a native grass were determined in laboratory and field studies. Solid-phase microextraction and gas chromatography/mass spectrometry were used to determine if monoterpenes found in the essential oils
T Hirata et al.
Phytochemistry, 55(3), 197-202 (2001-01-06)
A peroxidase was purified from the culture medium of a suspension culture of Marchantia polymorpha (liverwort) after treatment with bornyl acetate, which acts as a chemical stress agent to the cells. The peroxidase was characterised as a glycoprotein of molecular
Leo A Paquette et al.
The Journal of organic chemistry, 68(18), 6905-6918 (2003-08-30)
An intramolecular anionic oxy-Cope rearrangement (44 --> 46) serves as the key step in a synthetic approach to the insect antifeedant dumsin. Initial investigations clarified the manner in which (--)-bornyl acetate may be transformed into the exo-norbornenol 44. Two routes
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
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