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W208620

Sigma-Aldrich

Anethol

natural, 99%, FG

Sinonimo/i:

trans-Anethole, 4-Propenylanisole, trans-1-Methoxy-4-(1-propenyl)benzene

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About This Item

Formula condensata:
CH3CH=CHC6H4OCH3
Numero CAS:
4180-23-8
Peso molecolare:
148.20
Numero FEMA:
2086
Beilstein:
774229
Numero CE:
224-052-0
Numero MDL:
MFCD00009284
Codice UNSPSC:
12164502
ID PubChem:
329830449
Numero Flavis:
4.010
NACRES:
NA.21

Grado

FG
Fragrance grade
Halal
Kosher
natural

agenzia

follows IFRA guidelines

Conformità normativa

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FDA 21 CFR 117

Saggio

99%

Composizione

contains trans-Anethole

Indice di rifrazione

n20/D 1.561 (lit.)

P. eboll.

234-237 °C (lit.)

Punto di fusione

20-21 °C (lit.)

Densità

0.988 g/mL at 25 °C (lit.)

applicazioni

flavors and fragrances

Documentazione

see Safety & Documentation for available documents

Allergene alimentare

no known allergens

Allergene in fragranze

trans-anethole

Organolettico

anise; sweet

Stringa SMILE

COc1ccc(\C=C\C)cc1

InChI

1S/C10H12O/c1-3-4-9-5-7-10(11-2)8-6-9/h3-8H,1-2H3/b4-3+
RUVINXPYWBROJD-ONEGZZNKSA-N

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Azioni biochim/fisiol

Naturally occurring phenylpropene derivative that is estrogenic at lower concentrations and cytotoxic at higher concentrations to cancer cell lines. The cytotoxicity is related to the metabolism of trans-anethole to 4-hydroxy-1-propenylbenzene.

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H317,H411

Classi di pericolo

Aquatic Chronic 2 - Skin Sens. 1

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

213.8 °F

Punto d’infiammabilità (°C)

101 °C

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Certificati d'analisi (COA)

Lot/Batch Number
SHBN7544
SHBN0036
SHBL2872
MKCG7098
MKCG4923

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Riham Gharib et al.
Food chemistry, 267, 67-74 (2018-06-24)
The effect of hydrogenation of phospholipids on the characteristics of freeze-dried liposomes was investigated using hydroxypropyl-ß-cyclodextrin (HP-ß-CD) as membrane protectant. The ethanol-injection method was applied to prepare liposomes using hydrogenated (Phospholopion-90H and 80H) and non-hydrogenated phospholipids (Lipoid-S100) in combination with
Riham Gharib et al.
The Journal of membrane biology, 250(3), 259-271 (2017-04-24)
The effect of structurally closely related phenylpropenes (PPs), estragole, anethole, eugenol, and isoeugenol, on the fluidity of dipalmitoyl phosphatidyl choline (DPPC) liposome membrane was investigated by DSC, Raman, and fluorescence anisotropy of 1,6-diphenyl-1,3,5-hexatriene (DPH). Liposomes were prepared by thin-film hydration
Camila Fernanda Estevão-Silva et al.
Journal of natural medicines, 68(3), 567-575 (2014-05-03)
The aim of this study was to investigate the effect of anethole (AN) and eugenol (EUG) on leukocyte migration using in vitro chemotaxis and in situ microcirculation assays. BALB/c mice were used for the in vitro chemotaxis assay, and Wistar
Kyu-Sik Chang et al.
Journal of medical entomology, 51(4), 804-810 (2014-08-15)
An assessment was made of the toxicity of 12 insecticides and three essential oils as well as Bacillus thuringiensis subsp. israelensis (Bti) alone or in combination with the oil major constituents (E)-anethole (AN), (E) -cinnamaldehyde (CA), and eugenol (EU; 1:1
Matthias Onghena et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 31(12), 2090-2102 (2014-11-20)
In 2011, the European Union prohibited the production of polycarbonate (PC) baby bottles due to the toxic effects of the PC monomer bisphenol-A. Therefore, baby bottles made of alternative materials, e.g. polypropylene (PP) or polyethersulphone (PES), are currently marketed. The

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