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E5000000

Eugenol

European Pharmacopoeia (EP) Reference Standard

Synonyme(s) :

2-méthoxy-4-(2-propényl)phénol, 4-allylguaiacol

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About This Item

Formule linéaire :
4-(H2C=CHCH2)C6H3-2-(OCH3)OH
Numéro CAS:
97-53-0
Poids moléculaire :
164.20
Numéro Beilstein :
1366759
Numéro MDL:
MFCD00008654
Code UNSPSC :
41116107
ID de substance PubChem :
329799063
Nomenclature NACRES :
NA.24

Qualité

pharmaceutical primary standard

Famille d'API

eugenol

Fabricant/nom de marque

EDQM

Indice de réfraction

n20/D 1.541 (lit.)

Point d'ébullition

254 °C (lit.)

Pf

−12-−10 °C (lit.)

Densité

1.067 g/mL at 25 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-8°C

Chaîne SMILES 

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

Clé InChI

RRAFCDWBNXTKKO-UHFFFAOYSA-N

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Description générale

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.

Application

Eugenol EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.

Conditionnement

The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.

Autres remarques

Sales restrictions may apply.

Produit(s) apparenté(s)

Réf. du produit
Description
Tarif

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H317,H319

Classification des risques

Eye Irrit. 2 - Skin Sens. 1

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

255.2 °F - closed cup

Point d'éclair (°C)

124 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number

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Guy P Kamatou et al.
Molecules (Basel, Switzerland), 17(6), 6953-6981 (2012-06-26)
Eugenol is a major volatile constituent of clove essential oil obtained through hydrodistillation of mainly Eugenia caryophyllata (=Syzygium aromaticum) buds and leaves. It is a remarkably versatile molecule incorporated as a functional ingredient in numerous products and has found application
Keng Hong Tan et al.
Journal of insect science (Online), 12, 56-56 (2012-09-12)
This review discusses the occurrence and distribution (within a plant) of methyl eugenol in different plant species (> 450) from 80 families spanning many plant orders, as well as various roles this chemical plays in nature, especially in the interactions
Kristin Herrmann et al.
Carcinogenesis, 35(4), 935-941 (2013-12-10)
Methyleugenol--a natural constituent of herbs and spices--is hepatocarcinogenic in rodent models. It can form DNA adducts after side-chain hydroxylation and sulfation. We previously demonstrated that human sulfotransferases (SULTs) 1A1 and 1A2 as well as mouse Sult1a1, expressed in Salmonella target
K Markowitz et al.
Oral surgery, oral medicine, and oral pathology, 73(6), 729-737 (1992-06-01)
Eugenol-containing dental materials are frequently used in clinical dentistry. When zinc oxide-eugenol (ZOE) is applied to a dentinal cavity, small quantities of eugenol diffuse through the dentin to the pulp. Low concentrations of eugenol exert anti-inflammatory and local anesthetic effects
W R Hume
Journal of oral rehabilitation, 21(4), 469-473 (1994-07-01)
The diffusion gradient which develops across dentine and the clearance into the capillary circulation at the pulpal side of the tissue both reduce the concentration of potential toxins applied to dentine, thus protecting pulpal cells. The data presented on eugenol
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