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
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
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
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
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
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.
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