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Cinnamaldehyde - Structure and physical properties | | Cinnamaldehyde - Structure and physical properties: Encyclopedia II - 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 cinnemaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde.
An aromatic hydrocarbon and aldehyde, cinnamaldehyde has a mono-substituted benzene ring. A conjugated double bond (alkene) makes geometry of the compound planar. Cinnam ...
See also:Cinnamaldehyde, Cinnamaldehyde - Structure and physical properties, Cinnamaldehyde - Applications | | | Cinnamaldehyde, Cinnamaldehyde - Applications, Cinnamaldehyde - Structure and physical properties | | |
| | | Cinnamaldehyde: Encyclopedia II - Cinnamaldehyde - Structure and physical properties
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 cinnemaldehyde is excreted in urine as cinnamic acid, an oxidized form of cinnamaldehyde.
An aromatic hydrocarbon and 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 arromatic 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 condensation of benzaldehyde and acetaldehyde.
Other related archives1884, Aldehydes, Alkenes, Almond, Cinnamomum, Disclaimer and references, Flavors, Fungicides, Plant toxin insecticides, SI, acetaldehyde, agriculture, alcohol, aldehyde, alkene, alloys, apricot, aromas, aromatic hydrocarbon, bark, benzaldehyde, benzene, beverages, butterscotch, camphor, candy, carbonyl, carcinogen, cassia, cats, chemical, chewing gum, cinnamic acid, cinnamon, compound, condensation, corrosion inhibitor, corrosive, crops, dogs, double bond, flavouring, fruity, fungicide, genus, geometry, grams, ice cream, insecticide, oxidized, perfumes, planar, ppm, root, scents, solvents, spice, standard, steam distillation, steel, surfactants, sweet, trans, trees, viscous
 Adapted from the Wikipedia article "Structure and physical properties", under the G.N U Free Docmentation License. Please also see http://en.wikipedia.org/wiki |
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