| Weight | 164.204 g/mol |
|---|---|
| Formula | C10H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 3 |
eugenol (97-53-0)
Score:
#374 in Biology
,
#392 in Chemistry
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- INHIBITION OF GROWTH AND AFLATOXIN PRODUCTION BY CINNAMON AND CLOVE OILS. CINNAMIC ALDEHYDE AND EUGENOL (Journal of Food Science, 1977)
- Studies on the inhibitory effects of curcumin and eugenol on the formation of reactive oxygen species and the oxidation of ferrous iron. (Molecular and Cellular Biochemistry, 1994)
- THERAPEUTIC USES OF OCIMUM SANCTUM LINN (TULSI) WITH A NOTE ON EUGENOL AND ITS PHARMACOLOGICAL ACTIONS: A SHORT REVIEW (Indian journal of physiology and pharmacology, 2005)
- Changes in membrane fatty acids composition of microbial cells induced by addiction of thymol, carvacrol, limonene, cinnamaldehyde, and eugenol in the growing media. (Journal of Agricultural and Food Chemistry, 2006)
- Eugenol (an essential oil of clove) acts as an antibacterial agent against Salmonella typhi by disrupting the cellular membrane. (Journal of Ethnopharmacology, 2010)
- Mechanisms of bactericidal action of cinnamaldehyde against Listeria monocytogenes and of Eugenol against L. monocytogenes and Lactobacillus sakei (Applied and Environmental Microbiology, 2004)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H317: May cause an allergic skin reaction
Warning Sensitization, Skin - Category 1 - H412: Harmful to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard - Category 3 -
SMILESCOC1=C(C=CC(=C1)CC=C)O
-
InChIKeyRRAFCDWBNXTKKO-UHFFFAOYSA-N
- Pubchem - eugenol
- Wikipedia - eugenol
Eugenol is a phenylpropene, an allyl chain-substituted guaiacol. Eugenol is a member of the phenylpropanoids class of chemical compounds. It is a colourless to pale yellow, aromatic oily liquid extracted from certain essential oils especially from clove oil, nutmeg, cinnamon, basil and bay leaf.
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Alternate Names
Estimated Properties
| Boiling Point | 256.39 C | EPA T.E.S.T. |
|---|---|---|
| Density | 1.07 g/cm3 | EPA T.E.S.T. |
| Flash Point | 114.35 C | EPA T.E.S.T. |
| Water Solubility | 1516.7 mg/L | EPA T.E.S.T. |
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Synthesis
Reactant
+
Methyl hydroperoxide
(Dakin oxidation)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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(1131-94-8)
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(21714-26-1)
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(5208-87-7)
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(7149-10-2)
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(2478-38-8)
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(19924-43-7)
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eugenol
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