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E51791

Sigma-Aldrich

Eugenol

ReagentPlus®, 99%

Synonym(s):
2-Methoxy-4-(2-propenyl)phenol, 4-Allylguaiacol, 4-Allyl-2-methoxyphenol
Linear Formula:
4-(H2C=CHCH2)C6H3-2-(OCH3)OH
CAS Number:
Molecular Weight:
164.20
Beilstein:
1366759
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

product line

ReagentPlus®

assay

99%

form

liquid

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.)

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)

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General description

Eugenol is a natural phenolic compound found in clove oil.

Application

Eugenol can be used in the synthesis of:
  • bio-based benzoxazines
  • ibuprofen eugenol ester (IEE)
  • polycarbonate/cyanate ester blends
  • 1,2,3-triazole eugenol glucosides

Packaging

5, 100, 500 g in glass bottle

Legal Information

ReagentPlus is a registered trademark of Sigma-Aldrich Co. LLC

Pictograms

Exclamation markHealth hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Asp. Tox. 1 - Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK Germany

WGK 1

Flash Point(F)

255.2 °F - closed cup

Flash Point(C)

124 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Antifungal efficacy of thymol, carvacrol, eugenol and menthol as alternative agents to control the growth of food-relevant fungi.
Abbaszadeh S, et al.
Journal de mycologie medicale, 24(2), e51-e56 (2014)
Synthesis and characterization of novel bio-based benzoxazines from eugenol
Thirukumaran P, et al.
Royal Society of Chemistry Advances, 4(16), 7959-7966 (2014)
Synthesis and antimicrobial activity of 6-triazolo-6-deoxy eugenol glucosides
de Souza TB, et al.
Carbohydrate Research, 410(20), 1-8 (2015)
Poly (DL?lactide?co?glycolide)(PLGA) nanoparticles with entrapped trans?cinnamaldehyde and eugenol for antimicrobial delivery applications.
Gomes C, et al.
Journal of Food Science, 76(2) (2011)
Synthesis and characterization of a renewable cyanate ester/polycarbonate network derived from eugenol
Harvey BG, et al.
Polymer, 55(20), 5073-5079 (2014)

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