Photoanethole: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
Tags: mobile edit mobile web edit
 
CSV import
 
Line 1: Line 1:
'''Photoanethole''' is a [[chemical compound]] that is derived from [[anethole]], a compound that is primarily responsible for the flavor of [[anise]] and [[fennel]]. It is a clear to pale yellow liquid that is insoluble in water but soluble in [[alcohol]] and [[ether]]. Photoanethole is used in the [[food industry]] as a flavoring agent and in the [[pharmaceutical industry]] for its medicinal properties.
{{DISPLAYTITLE:Photoanethole}}


==Chemical Properties==
== Photoanethole ==
Photoanethole is a [[phenylpropene]], a type of [[phenolic compound]] that is a derivative of [[propene]]. It has a molecular formula of C10H12O and a molecular weight of 148.20 g/mol. It is a clear to pale yellow liquid that has a strong, sweet, anise-like odor. It is insoluble in water but soluble in alcohol and ether.
[[File:Photoanethole.svg|thumb|right|Chemical structure of photoanethole]]
'''Photoanethole''' is an organic compound that belongs to the class of [[phenylpropanoids]]. It is a derivative of [[anethole]], which is a major component of the essential oil of [[anise]] and [[fennel]]. Photoanethole is known for its role in the [[photochemistry]] of anethole, where it acts as a photochemical intermediate.


==Uses==
== Chemical Structure ==
Photoanethole is used in the food industry as a flavoring agent. It is used to impart a sweet, anise-like flavor to foods and beverages. It is also used in the pharmaceutical industry for its medicinal properties. It has been found to have [[antimicrobial]] and [[antifungal]] properties, and it has been used in traditional medicine for its [[analgesic]] and [[anti-inflammatory]] effects.
Photoanethole has a chemical structure similar to that of anethole, with the addition of a photoactive group. The structure consists of a phenyl group attached to a propenyl chain, which is characteristic of phenylpropanoids. The presence of a methoxy group on the phenyl ring contributes to its chemical properties.


==Health Effects==
== Synthesis ==
Photoanethole is generally considered safe for consumption. However, excessive consumption can lead to [[gastrointestinal]] upset, including nausea, vomiting, and diarrhea. It can also cause skin irritation if applied topically in high concentrations.
Photoanethole can be synthesized through the [[photochemical reaction]] of anethole. This process involves the exposure of anethole to [[ultraviolet light]], which induces a structural change in the molecule, resulting in the formation of photoanethole. This reaction is of interest in the study of [[photochemistry]] and the behavior of organic compounds under light exposure.


==See Also==
== Applications ==
Photoanethole is primarily studied in the context of its photochemical properties. It serves as a model compound for understanding the behavior of similar phenylpropanoids under light exposure. Research into photoanethole can provide insights into the stability and reactivity of essential oils and their components when subjected to light.
 
== Related Compounds ==
* [[Anethole]]
* [[Anethole]]
* [[Phenylpropene]]
* [[Estragole]]
* [[Food industry]]
* [[Phenylpropanoids]]
* [[Pharmaceutical industry]]


==References==
== Related Pages ==
<references/>
* [[Photochemistry]]
* [[Essential oils]]
* [[Anise]]
* [[Fennel]]


[[Category:Chemical compounds]]
[[Category:Phenylpropanoids]]
[[Category:Flavoring agents]]
[[Category:Photochemistry]]
[[Category:Pharmaceutical ingredients]]
{{Chem-stub}}
{{medicine-stub}}

Latest revision as of 11:32, 15 February 2025


Photoanethole[edit]

Chemical structure of photoanethole

Photoanethole is an organic compound that belongs to the class of phenylpropanoids. It is a derivative of anethole, which is a major component of the essential oil of anise and fennel. Photoanethole is known for its role in the photochemistry of anethole, where it acts as a photochemical intermediate.

Chemical Structure[edit]

Photoanethole has a chemical structure similar to that of anethole, with the addition of a photoactive group. The structure consists of a phenyl group attached to a propenyl chain, which is characteristic of phenylpropanoids. The presence of a methoxy group on the phenyl ring contributes to its chemical properties.

Synthesis[edit]

Photoanethole can be synthesized through the photochemical reaction of anethole. This process involves the exposure of anethole to ultraviolet light, which induces a structural change in the molecule, resulting in the formation of photoanethole. This reaction is of interest in the study of photochemistry and the behavior of organic compounds under light exposure.

Applications[edit]

Photoanethole is primarily studied in the context of its photochemical properties. It serves as a model compound for understanding the behavior of similar phenylpropanoids under light exposure. Research into photoanethole can provide insights into the stability and reactivity of essential oils and their components when subjected to light.

Related Compounds[edit]

Related Pages[edit]