My watch list
my.bionity.com  
Login  

Cinnamaldehyde



Cinnamaldehyde
IUPAC name (E)-3-phenyl-2-propenal
Other names Cinnamic aldehyde; cinnamaldehyde
Identifiers
CAS number 104-55-2
RTECS number GD6475000
SMILES O=C/C=C/c1ccccc1
Properties
Molecular formula C9H8O
Molar mass 132.16 g/mol
Appearance Yellow oil
Density 1.05 g/ml
Melting point

-7.5 °C

Boiling point

248 °C

Solubility in water Slightly Soluble
Viscosity  ? cP at ?°C
Hazards
MSDS External MSDS
R-phrases R36 R37 R38
S-phrases S26 S36
Flash point 71 °C
Related Compounds
Related compounds Cinnamic acid
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox disclaimer and references

Cinnamic aldehyde or cinnamaldehyde (more precisely trans-cinnamaldehyde, the only naturally-occurring form) is the chemical compound that gives cinnamon its flavor and odor.[1]

Additional recommended knowledge

Cinnamaldehyde occurs naturally in the bark of cinnamon trees and other species of the genus Cinnamomum like camphor and cassia. These trees are the natural source of cinnamon, and the essential oil of cinnamon bark is about 90% cinnamaldehyde.

Structure and physical properties

A yellow oily liquid more viscous than water, cinnamaldehyde smells strongly of cinnamon.

Concentrated cinnamaldehyde is a skin irritant, and the chemical is toxic in large doses, but no agencies suspect the compound is a carcinogen or poses a long-term health hazard. Most cinnamaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde.

Both aromatic and an aldehyde, cinnamaldehyde has a mono-substituted benzene ring. A conjugated double bond (alkene) makes geometry of the compound planar. Cinnamaldehyde is technically trans-cinnamaldehyde because the terminal carbonyl is on the opposite side of the aromatic ring over the rigid double bond.

A technique to synthesize cinnamaldehyde was published in 1884. Several methods of synthesis are now known, but cinnamaldehyde is most economically obtained from the steam distillation of the oil of cinnamon bark. The compound can be prepared from related compounds like cinnamyl alcohol, (the alcohol form of cinnamaldehyde), but the first synthesis from unrelated compounds was the aldol condensation of benzaldehyde and acetaldehyde.

Applications

The most obvious application for cinnamaldehyde is as a flavoring. 50 grams can be purchased for around US$20.00, and concentrations required for flavoring food items like chewing gum, ice cream, candy, and beverages range from 9 to 4900 ppm (that is, less than 0.5%).

Cinnamaldehyde is used in some perfumes of natural, sweet, or fruity scents. Almond, apricot, butterscotch, and other aromas may partially employ the compound for their pleasant smells.

Cinnamaldehyde is also used as a fungicide.[2] Proven effective on over 40 different crops, cinnamaldehyde is typically applied to the root systems of plants. Its low toxicity and well-known properties make it ideal for agriculture. To a lesser extent, cinnamaldehyde is an effective insecticide, and its scent is also known to repel animals like cats and dogs.[2]

Cinnamaldehyde is also known as a corrosion inhibitor for steel and other ferrous alloys in corrosive fluids. It can be used in combination with additional components such as dispersing agents, solvents and other surfactants.

Cinnamaldehyde can be used as a food adulterant; powdered beechnut husk aromatized with cinnamaldehyde can be marketed as powdered cinnamon.

Being widely available, it could be used to manufacture amphetamine cheaply, through reduction, oxidation and amination.

References

  1. ^ Cinnamon. Transport Information Service. Gesamtverband der Deutschen Versicherungswirtschaft e.V.. Retrieved on 2007-10-23.
  2. ^ a b Cinnamaldehyde Use. PAN Pesticides Database. Retrieved on 2007-10-23.
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Cinnamaldehyde". A list of authors is available in Wikipedia.
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE