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Merck

53801

Sigma-Aldrich

Eucalyptol

tested according to Ph. Eur.

Synonym(e):

Cineolum, 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan, 1,8-Cineol, 1,8-Epoxy-p-menthan

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About This Item

Empirische Formel (Hill-System):
C10H18O
CAS-Nummer:
Molekulargewicht:
154.25
Beilstein:
105109
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352212
PubChem Substanz-ID:
NACRES:
NA.21

Agentur

tested according to Ph. Eur.

Qualitätsniveau

Brechungsindex

n20/D 1.457 (lit.)

bp

176-177 °C (lit.)

mp (Schmelzpunkt)

1-2 °C (lit.)

Dichte

0.921 g/mL at 25 °C (lit.)

SMILES String

C[C@]12CC[C@H](CC1)C(C)(C)O2

InChI

1S/C10H18O/c1-9(2)8-4-6-10(3,11-9)7-5-8/h8H,4-7H2,1-3H3/t8-,10+

InChIKey

WEEGYLXZBRQIMU-WAAGHKOSSA-N

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Piktogramme

FlameExclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Flam. Liq. 3 - Skin Sens. 1

WGK

WGK 2

Flammpunkt (°F)

closed cup

Flammpunkt (°C)

closed cup


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(−)-Menthol puriss., meets analytical specification of Ph. Eur., BP, USP, 98.0-102.0%

Sigma-Aldrich

15785

(−)-Menthol

(+)-Carvon analytical standard

Supelco

22070

(+)-Carvon

α-Pinen 98%

Sigma-Aldrich

147524

α-Pinen

β-Cyclodextrin powder, BioReagent, suitable for cell culture, ≥97%

Sigma-Aldrich

C4805

β-Cyclodextrin

Acetophenon analytical standard

Supelco

42163

Acetophenon

Eugenol ReagentPlus®, 99%

Sigma-Aldrich

E51791

Eugenol

Fumarsäure ≥99.0% (T)

Sigma-Aldrich

47910

Fumarsäure

Lisa A Shipley et al.
Journal of chemical ecology, 38(9), 1178-1189 (2012-10-12)
Pygmy rabbits (Brachylagus idahoensis) are one of only three vertebrates that subsist virtually exclusively on sagebrush (Artemisia spp.), which contains high levels of monoterpenes that can be toxic. We examined the mechanisms used by specialist pygmy rabbits to eliminate 1,8-cineole
Hee-jin Jun et al.
Bioorganic & medicinal chemistry letters, 23(2), 579-583 (2012-12-19)
We investigated the effect of cineole on the expression of genes related to reverse cholesterol transport and hepatic fatty acid metabolism. Cineole, a small aroma compound in teas and herbs, significantly stimulated the transactivation of liver X receptor modulator (LXR)-α
Zerihun A Demissie et al.
Plant molecular biology, 79(4-5), 393-411 (2012-05-18)
Several members of the genus Lavandula produce valuable essential oils (EOs) that are primarily constituted of the low molecular weight isoprenoids, particularly monoterpenes. We isolated over 8,000 ESTs from the glandular trichomes of L. x intermedia flowers (where bulk of
Jossana Pereira de Sousa et al.
International journal of food microbiology, 158(1), 9-13 (2012-07-17)
This study aimed to investigate the effects of sublethal concentrations of carvacrol (CAR) and 1,8-cineole (CIN) alone and in combination on the morphology, cell viability and membrane permeability of Pseudomonas fluorescens ATCC 11253 cultivated in a vegetable-based broth. Transmission and
Xun Hu et al.
Bioresource technology, 123, 249-255 (2012-09-04)
Bio-oil from pyrolysis of mallee (Eucalyptus loxophleba ssp. gratiae) leaves differs from that obtained with wood by its content of cyclic ethers, terpenoids and N-containing organic compounds. Upgrading of the leaf bio-oil in methanol with a solid acid catalyst was

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