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Methyl eugenol
[CAS# 93-15-2]

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Complete supplier list of Methyl eugenol
Identification
Classification Chemical reagent >> Organic reagent >> Ether
Name Methyl eugenol
Synonyms 1,2-Dimethoxy-4-(2-propenyl)benzene; 4-Allyl-1,2-dimethoxybenzene; 4-Allylveratrole
Molecular Structure CAS # 93-15-2, Methyl eugenol, 1,2-Dimethoxy-4-(2-propenyl)benzene, 4-Allyl-1,2-dimethoxybenzene, 4-Allylveratrole
Molecular Formula C11H14O2
Molecular Weight 178.23
CAS Registry Number 93-15-2
EC Number 202-223-0
FEMA 2475
SMILES COC1=C(C=C(C=C1)CC=C)OC
Properties
Water solubility insoluble
Density 1.0±0.1 g/cm3, Calc.*, 1.036 g/mL (Expl.)
Melting point -4 ºC (Expl.)
Index of Refraction 1.500, Calc.*, 1.534 (Expl.)
Boiling Point 254.7±0.0 ºC (760 mmHg), Calc.*, 254-255 ºC (Expl.)
Flash Point 87.1±22.7 ºC, Calc.*, 110 ºC (Expl.)
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol symbol   GHS07;GHS08 Warning    Details
Hazard Statements H302-H317-H341-H351    Details
Precautionary Statements P203-P261-P264-P270-P272-P280-P301+P317-P302+P352-P318-P321-P330-P333+P317-P362+P364-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
CarcinogenicityCarc.2H351
Germ cell mutagenicityMuta.2H341
Skin sensitizationSkin Sens.1H317
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
CarcinogenicityCarc.1BH350
Acute hazardous to the aquatic environmentAquatic Acute2H401
SDS Available
up Discovory and Applicatios
Methyl eugenol, chemically known as 1,2-dimethoxy-4-(prop-2-enyl)benzene, is a naturally occurring phenylpropene compound found in various plants, including basil, cinnamon, and cloves. It is the methyl ether derivative of eugenol and is characterized by its distinctive aroma and flavor. Methyl eugenol has been utilized in various applications, particularly in the fragrance and flavor industries, where it serves as a key ingredient in perfumes, soaps, and food products.
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