Ethylvanillin

This colorless solid consists of a benzene ring with hydroxyl, ethoxy, and formyl groups on the 4, 3, and 1 positions, respectively.

Ethylvanillin is prepared from catechol, beginning with ethylation to give guaethol (1).

[1] As a flavorant, ethylvanillin is about three times as potent as vanillin and is used in the production of chocolate.

[1] The molecule revolutionized both the design and aesthetics of olfactory art; artist Jacques Guerlain added a large quantity of it to a bottle of Jicky (1889) perfume, creating the main accord for the perfume house's flagship fragrance, Shalimar (perfume) (1925).

This is one of the earliest uses of synthetic molecules that freed scent artists from the limits of natural materials.

Structural formula of ethylvanillin
Ball-and-stick model of the ethylvanillin molecule
Ball-and-stick model of the ethylvanillin molecule
NFPA 704 four-colored diamond Health 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroform Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen Special hazards (white): no code