Valeric acid: Difference between revisions

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{{Short description|A carboxylic acid with a pungent odor}}
{{short description|An organic compound known as pentanoic acid}}
{{Chembox
{{DISPLAYTITLE:Valeric acid}}
| 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 [[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.
[[File:Valeric_acid_acsv.svg|thumb|right|Structural formula of valeric acid]]


==Structure and properties==
'''Valeric acid''', also known as '''pentanoic acid''', is a straight-chain alkyl 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]].
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]].
 
==Chemical properties==
Valeric acid is a [[carboxylic acid]], which means it contains a carboxyl group (_COOH). It is a weak acid, meaning it does not completely dissociate in water. The acid is soluble in organic solvents and slightly soluble in water.


==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 can be produced by the oxidation of [[valeraldehyde]] or by the hydrolysis of [[valerate esters]]. Industrially, it is often synthesized from [[butyric acid]] through the [[Koch reaction]].


==Applications==
==Uses==
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]].
Valeric acid is used in the production of [[esters]] for the flavor and fragrance industry. These esters, such as [[ethyl valerate]], have fruity odors and are used in perfumes and as food additives. Additionally, valeric acid is used as a precursor in the synthesis of [[pharmaceuticals]] and [[pesticides]].
 
==Biological role==
In nature, valeric acid is found in the [[Valerian (herb)|valerian plant]], which has been used for centuries as a herbal remedy for its sedative properties. The acid itself is not responsible for the sedative effects, but it is one of the many compounds present in the plant.


==Safety==
==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.
Valeric acid is corrosive and can cause skin and eye irritation. It should be handled with care, using appropriate [[personal protective equipment]] such as gloves and goggles.
 
==Related compounds==
* [[Isovaleric acid]]
* [[Butyric acid]]
* [[Caproic acid]]


==Related pages==
==Related pages==
* [[Valerian (herb)]]
* [[Carboxylic acid]]
* [[Carboxylic acid]]
* [[Fatty acid]]
* [[Ester]]
* [[Valerian (herb)]]
* [[Valeraldehyde]]
 
==References==
{{Reflist}}


[[Category:Carboxylic acids]]
[[Category:Carboxylic acids]]
[[Category:Fatty acids]]
[[Category:Organic compounds]]
[[Category:Flavors]]

Latest revision as of 11:03, 15 February 2025

An organic compound known as pentanoic acid



Structural formula of valeric acid

Valeric acid, also known as pentanoic acid, is a straight-chain alkyl carboxylic acid with the chemical formula C5H10O2. It is a colorless liquid with a pungent odor and is found naturally in the valerian plant.

Chemical properties[edit]

Valeric acid is a carboxylic acid, which means it contains a carboxyl group (_COOH). It is a weak acid, meaning it does not completely dissociate in water. The acid is soluble in organic solvents and slightly soluble in water.

Production[edit]

Valeric acid can be produced by the oxidation of valeraldehyde or by the hydrolysis of valerate esters. Industrially, it is often synthesized from butyric acid through the Koch reaction.

Uses[edit]

Valeric acid is used in the production of esters for the flavor and fragrance industry. These esters, such as ethyl valerate, have fruity odors and are used in perfumes and as food additives. Additionally, valeric acid is used as a precursor in the synthesis of pharmaceuticals and pesticides.

Biological role[edit]

In nature, valeric acid is found in the valerian plant, which has been used for centuries as a herbal remedy for its sedative properties. The acid itself is not responsible for the sedative effects, but it is one of the many compounds present in the plant.

Safety[edit]

Valeric acid is corrosive and can cause skin and eye irritation. It should be handled with care, using appropriate personal protective equipment such as gloves and goggles.

Related pages[edit]