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W215902

Sigma-Aldrich

Bornyl acetate

≥98%, FG

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About This Item

Empirical Formula (Hill Notation):
C12H20O2
CAS Number:
76-49-3
Molecular Weight:
196.29
FEMA Number:
2159
EC Number:
200-964-4
Council of Europe no.:
207
MDL number:
MFCD00135944
UNSPSC Code:
12164502
PubChem Substance ID:
24900675
Flavis number:
9.017

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

SMILES string

CC(=O)O[C@@H]1C[C@@H]2CC[C@@]1(C)C2(C)C

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

InChI key

KGEKLUUHTZCSIP-HOSYDEDBSA-N

Legal Information

For R&D Use and/or Food Manufacturing only

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

192.0 °F - closed cup

flash_point_c

88.89 °C - closed cup

Certificates of Analysis (COA)

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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
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
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
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
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