Isoeugenol
Names | |
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IUPAC names
2-methoxy-4-(prop-1-en-1-yl)phenol (trans isomer shown) | |
Other names
4-hydroxy-3-methoxy-1-propenylbenzene 2-methoxy-4-propenylphenol 4-propenylguaiacol | |
Identifiers | |
97-54-1 | |
ChEBI | CHEBI:18224 |
ChEMBL | ChEMBL445206 |
ChemSpider | 21106129 (trans) |
EC Number | 202-590-7 |
Jmol interactive 3D | (trans): Image |
KEGG | C10469 |
PubChem | 7338 |
UNII | 5M0MWY797U |
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Properties | |
C10H12O2 | |
Molar mass | 164.201 |
Appearance | oily liquid |
Density | 1.080 |
Melting point | −10 °C (14 °F; 263 K) |
Boiling point | 266 °C (511 °F; 539 K) |
Pharmacology | |
ATCvet code | QN01 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Isoeugenol is a phenylpropene, a propenyl-substituted guaiacol. A phenylpropanoid, it occurs in the essential oils of plants such as ylang-ylang (Cananga odorata). It can be synthesized from eugenol and has been used in the manufacture of vanillin. It may occur as either the cis (Z) or trans (E) isomer. Trans (E) isoeugenol is crystalline while cis (Z) isoeugenol is a liquid.
Allergy
Some individuals experience a hives-like reaction to long-term exposure to Isoeugenol, which is named as Fragrance in the ingredients of consumer products such as soaps, shampoos and detergents, bath tissue, and topical cosmetic applications. Sensitivity to isoeugenol (Fragrance) may be identified with a clinical patch test.[1]
References
- ↑ AllergEAZE. "PF137 Isoeugenol" (PDF). AllergEAZE. Retrieved 2015-08-25.
- The Merck Index, 12th edition, Merck & Co, Whitehouse Station, New Jersey, USA, 1996.
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