(E)-3-(3-Hydroxy-4-methoxyphenyl)-2-propenoic acid ethyl ester
Ethyl isoferulate
CAS: 155401-23-3
Molecular Formula: C12H14O4
(E)-3-(3-Hydroxy-4-methoxyphenyl)-2-propenoic acid ethyl ester - Names and Identifiers
(E)-3-(3-Hydroxy-4-methoxyphenyl)-2-propenoic acid ethyl ester - Physico-chemical Properties
| Molecular Formula | C12H14O4 |
| Molar Mass | 222.24 |
| Density | 1.173 |
(E)-3-(3-Hydroxy-4-methoxyphenyl)-2-propenoic acid ethyl ester - Introduction
Ethyl isoferulate, also known as keraldehyde acetate, is an organic compound. The following is an introduction to the nature, use, formulation and safety information of Ethyl isoferulate:
Nature:
Ethyl isoferulate is a colorless to pale yellow liquid with a special aroma. It is highly irritating and can irritate the eyes, respiratory system and skin.
Use:
Ethyl isoferulate is widely used in the fragrance industry. It is commonly used in the manufacture of chewing gum, toothpaste, soap, perfume and other products, giving it a spicy, fresh smell. In addition, it can also be used as an insect attractant to attract insects for chemical control.
Method:
Ethyl isoferulate can be synthesized by reacting isoferulic acid (also known as kerataldehyde) with ethanol. The reaction is generally carried out at a relatively low temperature, and a basic catalyst is often used to promote the reaction.
Safety Information:
Ethyl isoferulate is highly irritating and should avoid contact with eyes, skin and respiratory system. Safety measures must be taken during use, including wearing protective gloves and goggles, and maintaining good ventilation. In addition, it is also a flammable liquid and needs to be kept away from open flames and high temperature objects.
Nature:
Ethyl isoferulate is a colorless to pale yellow liquid with a special aroma. It is highly irritating and can irritate the eyes, respiratory system and skin.
Use:
Ethyl isoferulate is widely used in the fragrance industry. It is commonly used in the manufacture of chewing gum, toothpaste, soap, perfume and other products, giving it a spicy, fresh smell. In addition, it can also be used as an insect attractant to attract insects for chemical control.
Method:
Ethyl isoferulate can be synthesized by reacting isoferulic acid (also known as kerataldehyde) with ethanol. The reaction is generally carried out at a relatively low temperature, and a basic catalyst is often used to promote the reaction.
Safety Information:
Ethyl isoferulate is highly irritating and should avoid contact with eyes, skin and respiratory system. Safety measures must be taken during use, including wearing protective gloves and goggles, and maintaining good ventilation. In addition, it is also a flammable liquid and needs to be kept away from open flames and high temperature objects.
Last Update：2024-04-09 20:52:54
