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  2. Cinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Cinnamaldehyde

    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 ...

  3. Cinnamyl acetate - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl_acetate

    Cinnamyl acetate (3-phenylprop-2-enyl acetate) is a chemical compound of the cinnamyl ester family, in which the variable R group is substituted by a methyl group. As a result of the non-aromatic carbon-carbon double bond, cinnamyl acetate can exist in a Z and an E configuration : [ 9 ]

  4. 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.

  5. Aldehyde - Wikipedia

    en.wikipedia.org/wiki/Aldehyde

    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.

  6. 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.

  7. Hydrocinnamaldehyde - Wikipedia

    en.wikipedia.org/wiki/Hydrocinnamaldehyde

    Chemical formula. C 9 H 10 O: Molar mass: 134.178 g·mol −1 ... It is produced by the hydrogenation of cinnamaldehyde. The compound is used in many mechanistic ...

  8. 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]

  9. Cinnamyl-alcohol dehydrogenase - Wikipedia

    en.wikipedia.org/wiki/Cinnamyl-alcohol_dehydrogenase

    In enzymology, a cinnamyl-alcohol dehydrogenase (EC 1.1.1.195) is an enzyme that catalyzes the chemical reaction. cinnamyl alcohol + NADP + cinnamaldehyde + NADPH + H +. Thus, the two substrates of this enzyme are cinnamyl alcohol and NADP +, whereas its 3 products are cinnamaldehyde, NADPH, and H +.

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