Valeric acid: Difference between revisions

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'''Valeric Acid'''
{{Short description|A carboxylic acid with a pungent odor}}
{{Chembox
| verifiedfields = changed
| verifiedrevid = 477002303
| ImageFile = Valeric_acid_acsv.svg
| ImageSize = 150px
| ImageAlt = Skeletal formula of valeric acid
| IUPACName = Pentanoic acid
| OtherNames = Valeric acid
}}


Valeric acid, also known as [[Pentanoic acid]], is a straight-chain [[alkyl]] [[carboxylic acid]] with the chemical formula CH3(CH2)3COOH. It is named after the plant genus ''[[Valeriana]]'', from which it was first isolated. Valeric acid is found naturally in several plants and herbs, and it is a colorless, oily liquid with an unpleasant odor.
'''Valeric acid''', also known as '''pentanoic acid''', is a [[carboxylic acid]] with the chemical formula C<sub>5</sub>H<sub>10</sub>O<sub>2</sub>. It is a colorless liquid with a pungent odor and is found naturally in the [[Valerian (herb)|valerian]] plant, from which it derives its name.


==Chemical Properties==
==Structure and properties==
 
Valeric acid is a straight-chain [[saturated fatty acid]] with five carbon atoms. It is a member of the [[alkanoic acids]] and is classified as a [[short-chain fatty acid]]. The acid is miscible with [[water]], [[ethanol]], and [[ether]].
Valeric acid is a [[carboxylic acid]], which means it has a -COOH group. It is a weak acid, with a [[pKa]] of 4.82. It is miscible with water and organic solvents. It is a volatile substance, which means it can easily evaporate at room temperature.


==Production==
==Production==
Valeric acid can be produced by the [[oxidation]] of [[valeraldehyde]] or by the [[fermentation]] of [[glucose]] using certain [[bacteria]]. Industrially, it is often synthesized from [[butyric acid]] through the [[Koch reaction]].


Valeric acid is produced industrially by the [[oxidation]] of [[valeraldehyde]]. It can also be obtained by the hydrolysis of [[pentanoic esters]], which are derived from renewable resources.
==Applications==
 
Valeric acid is used in the manufacture of [[esters]] for [[flavoring]] and [[fragrance]] applications. It is also used as a precursor in the synthesis of [[pharmaceuticals]] and [[plasticizers]].
==Uses==
 
Valeric acid is used in the synthesis of various chemicals, including [[plasticizers]], [[flavors]], and [[perfumes]]. It is also used as a food additive, where it acts as a flavoring agent.
 
==Health Effects==


Exposure to valeric acid can cause irritation to the skin, eyes, and respiratory tract. Ingestion can lead to gastrointestinal discomfort. Long-term exposure can lead to more serious health effects.
==Safety==
Valeric acid is an irritant and should be handled with care. It can cause skin and eye irritation upon contact and may be harmful if ingested or inhaled.


==See Also==
==Related compounds==
* [[Isovaleric acid]]
* [[Butyric acid]]
* [[Caproic acid]]


==Related pages==
* [[Carboxylic acid]]
* [[Carboxylic acid]]
* [[Valeraldehyde]]
* [[Fatty acid]]
* [[Pentanoic esters]]
* [[Valerian (herb)]]


==References==
==References==
 
{{Reflist}}
<references />


[[Category:Carboxylic acids]]
[[Category:Carboxylic acids]]
[[Category:Chemical compounds]]
[[Category:Fatty acids]]
[[Category:Industrial chemicals]]
[[Category:Flavors]]
[[Category:Food additives]]
 
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Revision as of 12:01, 9 February 2025

A carboxylic acid with a pungent odor


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Valeric acid, also known as pentanoic acid, is a carboxylic acid with the chemical formula C5H10O2. It is a colorless liquid with a pungent odor and is found naturally in the valerian plant, from which it derives its name.

Structure and properties

Valeric acid is a straight-chain saturated fatty acid with five carbon atoms. It is a member of the alkanoic acids and is classified as a short-chain fatty acid. The acid is miscible with water, ethanol, and ether.

Production

Valeric acid can be produced by the oxidation of valeraldehyde or by the fermentation of glucose using certain bacteria. Industrially, it is often synthesized from butyric acid through the Koch reaction.

Applications

Valeric acid is used in the manufacture of esters for flavoring and fragrance applications. It is also used as a precursor in the synthesis of pharmaceuticals and plasticizers.

Safety

Valeric acid is an irritant and should be handled with care. It can cause skin and eye irritation upon contact and may be harmful if ingested or inhaled.

Related compounds

Related pages

References

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