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  2. Cinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Cinnamaldehyde

    Cinnamaldehyde is an organic compound with the formula or C₆H₅CH=CHCHO. Occurring naturally as predominantly the trans ( E ) isomer, it gives cinnamon its flavor and odor . [ 1 ] It is a phenylpropanoid that is naturally synthesized by the shikimate pathway . [ 2 ]

  3. Cinnamyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl_alcohol

    Cinnamyl alcohol or styron [2] is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure.

  4. Hydrocinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydrocinnamaldehyde

    Toggle the table of contents. Hydrocinnamaldehyde. ... Melting point: −42 °C (−44 °F; 231 K) ... It is produced by the hydrogenation of cinnamaldehyde.

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  6. Cinnamic acid - Wikipedia

    en.wikipedia.org/wiki/Cinnamic_acid

    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.

  7. How to Extend the Life of Baked Goods, According to Experts - AOL

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    As Keiry Palma, chef-instructor of Pastry & Baking Arts at the Institute of Culinary Education’s New York City campus, explains, it all depends on the type of baked goods. For cakes and cupcakes ...

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  9. α-Hexylcinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Α-Hexylcinnamaldehyde

    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]