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Merck

W215902

Sigma-Aldrich

Bornyl acetate

≥98%, FG

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About This Item

Empirische Formel (Hill-System):
C12H20O2
CAS-Nummer:
Molekulargewicht:
196.29
FEMA-Nummer:
2159
EG-Nummer:
CoE-Nummer:
207
MDL-Nummer:
UNSPSC-Code:
12164502
PubChem Substanz-ID:
Flavis-Nummer:
9.017

Biologische Quelle

synthetic

Qualität

FG

Einhaltung gesetzlicher Vorschriften

EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117
FDA 21 CFR 172.515

Assay

≥98%

Optische Aktivität

[α]20/D −41°, neat

Brechungsindex

n20/D 1.4635 (lit.)

bp

228-231 °C (lit.)

Dichte

0.985 g/mL at 25 °C (lit.)

Anwendung(en)

flavors and fragrances

Dokumentation

see Safety & Documentation for available documents

Nahrungsmittelallergen

no known allergens

Organoleptisch

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

InChIKey

KGEKLUUHTZCSIP-HOSYDEDBSA-N

Rechtliche Hinweise

For R&D Use and/or Food Manufacturing only

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

192.0 °F - closed cup

Flammpunkt (°C)

88.89 °C - closed cup


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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
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
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
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

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