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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:
97-53-0
Molecular Weight:
164.20
Beilstein:
1366759
EC Number:
202-589-1
MDL number:
MFCD00008654
UNSPSC Code:
12352100
PubChem Substance ID:
24894609
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
GHS07

Signal Word

Warning

Hazard Statements

H317,H319

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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Clove oil

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C8392

Clove oil

Eugenol United States Pharmacopeia (USP) Reference Standard

USP

1268965

Eugenol

Eugenol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1269

Eugenol

β-Caryophyllene ≥80%, FCC, FG

Sigma-Aldrich

W225207

β-Caryophyllene

Isoeugenol 98%, mixture of cis and trans

Sigma-Aldrich

I17206

Isoeugenol

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)
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)
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)
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