E51791
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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-589-1
Beilstein/REAXYS Number:
1366759
MDL number:
Assay:
99%
Form:
liquid
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)
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
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Sens. 1
Storage Class
10 - Combustible liquids
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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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 antimicrobial activity of 6-triazolo-6-deoxy eugenol glucosides
de Souza TB, et al.
Carbohydrate Research, 410(20), 1-8 (2015)
Synthesis and characterization of novel bio-based benzoxazines from eugenol
Thirukumaran P, et al.
Royal Society of Chemistry Advances, 4(16), 7959-7966 (2014)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E51791-500G | 04061835556748 |
| E51791-5G | 04061835556755 |
| E51791-100G | 04061835564095 |