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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 ...
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]
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.
Aldehyde structure. In organic chemistry, an aldehyde (/ ˈ æ l d ɪ h aɪ d /) is an organic compound containing a functional group with the structure R−CH=O. [1] The functional group itself (without the "R" side chain) can be referred to as an aldehyde but can also be classified as a formyl group.
Cinnamaldehyde, an essential oil extracted from C. osmophloeum, has numerous commercial uses. Also, it is a xanthine oxidase inhibitor , hence a potential drug for treatment of hyperuricemia and related medical conditions including gout .
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Compounds found in curry tree leaves, stems, bark, and seeds include cinnamaldehyde, [14] and numerous carbazole alkaloids, including mahanimbine, [15] girinimbine, [16] and mahanine. Nutritionally, the leaves are a rich source of carotenoids, beta-carotene, calcium and iron.
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