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Cinnamaldehyde is used in agriculture because of its low toxicity, but it is a skin irritant. [25] Cinnamaldehyde may cause allergic contact stomatitis in sensitised individuals, however allergy to the compound is believed to be uncommon. [26] Cinnamaldehyde can contain traces of styrene, which arises during storage or transport. Styrene ...
Cinnamaldehyde decomposes, in high humidity and high temperatures, to styrene, [51] and, by reaction with oxygen as it ages, it darkens in colour and forms resinous compounds. [ 10 ] [ 52 ] Cinnamon constituents include some 80 aromatic compounds , [ 53 ] including eugenol, found in the oil from leaves or bark of cinnamon trees.
The commercial material often contains low levels of 2,6-di-tert-butyl-4-methoxyphenol as a stabilizer. It is a derivative of cinnamaldehyde with a hexyl substituent. One supplier reported that its hexyl cinnamaldehyde (or "hexyl cinnamic aldehyde") contained at least 90% trans isomer. [2]
It is obtained from oil of cinnamon, or from balsams such as storax. [4] It is also found in shea butter. [citation needed] Cinnamic acid has a honey-like odor; [2] and its more volatile ethyl ester, ethyl cinnamate, is a flavor component in the essential oil of cinnamon, in which related cinnamaldehyde is the major constituent.
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Cinnamaldehyde, an organic compound with the formula C 6 H 5 CH=CHCHO 1-Indanone , the organic compound with the formula C 6 H 4 (CH 2 ) 2 CO Index of chemical compounds with the same molecular formula
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Cinnamyl alcohol has a distinctive odor described as "sweet, balsam, hyacinth, spicy, green, powdery, cinnamic" and is used in perfumery [4] and as a deodorant. Cinnamyl alcohol is the starting material used in the synthesis of reboxetine .