Prenol: Difference between revisions
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{{DISPLAYTITLE:Prenol}} | |||
[[File:Prenol_structure.png|thumb|right|Prenol structure]] | |||
Prenol | |||
'''Prenol''' is a type of organic compound that belongs to the class of [[terpenes]]. It is a simple [[alcohol]] with the chemical formula C<sub>5</sub>H<sub>10</sub>O. Prenol is also known as 3-methyl-2-buten-1-ol and is a primary alcohol with a [[molecular structure]] that includes a [[hydroxyl group]] attached to a carbon atom that is part of an isoprene unit. | |||
Prenol is | |||
== | ==Structure and Properties== | ||
Prenol is | Prenol is a colorless liquid with a mild odor. It is soluble in organic solvents and slightly soluble in water. The structure of prenol consists of a five-carbon chain with a terminal hydroxyl group. The presence of the double bond in the isoprene unit gives prenol its characteristic reactivity. | ||
[[File:Prenol-3D-balls.png|thumb|left|Prenol 3D molecular model]] | |||
== | ==Synthesis== | ||
Prenol | Prenol can be synthesized through several methods. One common method involves the [[hydroformylation]] of isoprene, followed by hydrogenation. Another method is the reduction of prenal, which is the corresponding aldehyde of prenol. | ||
== | [[File:Isoprenol_prepn.png|thumb|right|Isoprenol preparation]] | ||
==Applications== | |||
Prenol is used as an intermediate in the synthesis of various [[fragrances]] and [[flavors]]. It is also used in the production of [[vitamins]] and other [[biologically active compounds]]. Due to its structure, prenol can undergo polymerization and is used in the manufacture of certain types of [[plastics]] and [[resins]]. | |||
==Biological Role== | |||
In nature, prenol is a building block for the biosynthesis of [[terpenoids]], which are a large and diverse class of naturally occurring organic chemicals derived from five-carbon isoprene units. Terpenoids are found in all classes of living things and are the largest group of natural products. | |||
==Safety and Handling== | |||
Prenol should be handled with care, as it is a flammable liquid. It should be stored in a cool, well-ventilated area away from sources of ignition. Proper protective equipment, such as gloves and goggles, should be used when handling prenol to prevent skin and eye contact. | |||
[[File:Prenol_prepn.png|thumb|left|Prenol preparation]] | |||
==Related Pages== | |||
* [[Terpene]] | * [[Terpene]] | ||
* [[ | * [[Alcohol]] | ||
* [[ | * [[Isoprene]] | ||
* [[Hydroformylation]] | |||
{{Organic-compound-stub}} | |||
[[Category:Terpenes]] | |||
[[Category:Alcohols]] | [[Category:Alcohols]] | ||
[[Category: | [[Category:Monoterpenes]] | ||
Latest revision as of 18:59, 23 March 2025
Prenol is a type of organic compound that belongs to the class of terpenes. It is a simple alcohol with the chemical formula C5H10O. Prenol is also known as 3-methyl-2-buten-1-ol and is a primary alcohol with a molecular structure that includes a hydroxyl group attached to a carbon atom that is part of an isoprene unit.
Structure and Properties[edit]
Prenol is a colorless liquid with a mild odor. It is soluble in organic solvents and slightly soluble in water. The structure of prenol consists of a five-carbon chain with a terminal hydroxyl group. The presence of the double bond in the isoprene unit gives prenol its characteristic reactivity.
Synthesis[edit]
Prenol can be synthesized through several methods. One common method involves the hydroformylation of isoprene, followed by hydrogenation. Another method is the reduction of prenal, which is the corresponding aldehyde of prenol.
Applications[edit]
Prenol is used as an intermediate in the synthesis of various fragrances and flavors. It is also used in the production of vitamins and other biologically active compounds. Due to its structure, prenol can undergo polymerization and is used in the manufacture of certain types of plastics and resins.
Biological Role[edit]
In nature, prenol is a building block for the biosynthesis of terpenoids, which are a large and diverse class of naturally occurring organic chemicals derived from five-carbon isoprene units. Terpenoids are found in all classes of living things and are the largest group of natural products.
Safety and Handling[edit]
Prenol should be handled with care, as it is a flammable liquid. It should be stored in a cool, well-ventilated area away from sources of ignition. Proper protective equipment, such as gloves and goggles, should be used when handling prenol to prevent skin and eye contact.
Related Pages[edit]
