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Merck

W246719

Eugenol

greener alternative

natural, ≥98%, FG

Sinónimos:

2-Methoxy-4-(2-propenyl)phenol, 4-Allyl-2-methoxyphenol, 4-Allylguaiacol

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Fórmula lineal:
4-(H2C=CHCH2)C6H3-2-(OCH3)OH
Número CAS:
Peso molecular:
164.20
FEMA Number:
2467
Council of Europe no.:
171
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
4.003
EC Number:
202-589-1
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
1366759
Organoleptic:
clove; woody; spicy; sweet
Grade:
FG, Fragrance grade, Halal, Kosher, natural
Agency:
follows IFRA guidelines, meets purity specifications of JECFA
Food allergen:
no known allergens
Servicio técnico
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Quality Segment

grade

FG, Fragrance grade, Halal, Kosher, natural

agency

follows IFRA guidelines, meets purity specifications of JECFA

reg. compliance

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

assay

≥98%

form

liquid

composition

contains IFRA and EU 1223/2009 restricted Eugenol

greener alternative product characteristics

Less Hazardous Chemical Syntheses
Use of Renewable Feedstocks
Learn more about the Principles of Green Chemistry.

refractive index

n20/D 1.541 (lit.)

bp

254 °C (lit.)

mp

−12-−10 °C (lit.)

density

1.067 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

eugenol

greener alternative category

organoleptic

clove; woody; spicy; sweet

SMILES string

COc1cc(CC=C)ccc1O

InChI

1S/C10H12O2/c1-3-4-8-5-6-9(11)10(7-8)12-2/h3,5-7,11H,1,4H2,2H3

InChI key

RRAFCDWBNXTKKO-UHFFFAOYSA-N

Gene Information

human ... UGT1A4(54657)

General description

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives . This product is a Biobased products, showing key improvements in Green Chemistry Principles “Less Hazardous Chemical Syntheses” and “Use of Renewable Feedstock”.
Eugenol is one of the key volatile constituents of cinnamon and clove oils.

Application


  • Methoxyeugenol Protects Against Lung Inflammation and Suppresses Neutrophil Extracellular Trap Formation in an LPS-Induced Acute Lung Injury Model.: This research highlights the protective effects of methoxyeugenol against lung inflammation and its potential to suppress neutrophil extracellular trap formation, indicating its therapeutic potential in inflammatory conditions (Antunes et al., 2022) (Antunes et al., 2022).

  • Methoxyeugenol regulates the p53/p21 pathway and suppresses human endometrial cancer cell proliferation.: This research uncovers the ability of methoxyeugenol to regulate the p53/p21 pathway and inhibit the proliferation of human endometrial cancer cells, indicating its potential as an anticancer agent (Costa et al., 2021) (Costa et al., 2021).



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pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Clase de almacenamiento

10 - Combustible liquids

wgk

WGK 1

flash_point_f

255.2 °F - closed cup

flash_point_c

124 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter



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Certificados de análisis (COA)

Lot/Batch Number

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