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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:
Molecular Weight:
196.29
FEMA Number:
2159
EC Number:
Council of Europe no.:
207
MDL number:
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.017
Pricing and availability is not currently available.

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 Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

192.0 °F - closed cup

Flash Point(C)

88.89 °C - closed cup


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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
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
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.
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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