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E51791

Sigma-Aldrich

Eugenol

ReagentPlus®, 99%

Synonym(s):

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

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About This Item

Linear Formula:
4-(H2C=CHCH2)C6H3-2-(OCH3)OH
CAS Number:
Molecular Weight:
164.20
Beilstein:
1366759
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1

Storage Class Code

10 - Combustible liquids

WGK

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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 a renewable cyanate ester/polycarbonate network derived from eugenol
Harvey BG, et al.
Polymer, 55(20), 5073-5079 (2014)

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