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/REAXYS Number:
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

hazcat

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

Synthesis and characterization of a renewable cyanate ester/polycarbonate network derived from eugenol
Harvey BG, et al.
Polymer, 55(20), 5073-5079 (2014)
Synthesis of ibuprofen eugenol ester and its microemulsion formulation for parenteral delivery
Zhao X, et al.
Chemical & Pharmaceutical Bulletin, 53(10), 1246-1250 (2005)
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 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)

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