2-Octanol: Difference between revisions

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= 2-Octanol =
{{DISPLAYTITLE:2-Octanol}}
 
== 2-Octanol ==


[[File:2-Octanol.svg|thumb|right|Structural formula of 2-Octanol]]
[[File:2-Octanol.svg|thumb|right|Structural formula of 2-Octanol]]


'''2-Octanol''' is an [[organic compound]] with the chemical formula C_H__O. It is a secondary [[alcohol]] and is one of the isomers of [[octanol]].
'''2-Octanol''', also known as '''sec-octanol''', is an [[alcohol]] with the chemical formula C_H__O. It is a secondary alcohol, meaning the hydroxyl group (-OH) is attached to a secondary carbon atom. This compound is part of the [[octanol]] isomer family, which consists of several isomers with the same molecular formula but different structural arrangements.


== Structure and Properties ==
== Structure and Properties ==
2-Octanol is a [[secondary alcohol]], meaning the hydroxyl group (-OH) is attached to the second carbon in the carbon chain. This structure gives 2-Octanol its unique chemical properties compared to other isomers of octanol, such as [[1-octanol]].


The compound is a [[colorless]] liquid at room temperature and has a characteristic odor. It is slightly soluble in water but more soluble in organic solvents such as [[ethanol]] and [[diethyl ether]].
2-Octanol is a [[chiral]] molecule, which means it can exist in two enantiomeric forms: (R)-2-octanol and (S)-2-octanol. These enantiomers have identical physical properties except for their interaction with plane-polarized light and reactions in chiral environments.
 
The structural formula of 2-Octanol is depicted in the image to the right. The molecule consists of an eight-carbon chain with a hydroxyl group attached to the second carbon atom. This structure gives 2-Octanol its characteristic properties as a secondary alcohol.


== Synthesis ==
== Synthesis ==
2-Octanol can be synthesized through the [[hydration]] of [[1-octene]] in the presence of an acid catalyst. This process involves the addition of a water molecule across the double bond of 1-octene, resulting in the formation of 2-octanol.
 
2-Octanol can be synthesized through various methods, including the [[hydration]] of [[1-octene]] or the reduction of 2-octanone. Industrially, it is often produced by the [[hydrogenation]] of 2-octanone using a suitable catalyst.


== Applications ==
== Applications ==
2-Octanol is used in the production of [[plasticizers]], [[surfactants]], and [[lubricants]]. It is also used as a solvent and an intermediate in the synthesis of other chemical compounds.
 
2-Octanol is used in the production of [[plasticizers]], [[surfactants]], and [[lubricants]]. It is also employed as a solvent in the [[chemical industry]] and as an intermediate in the synthesis of other chemical compounds.


== Safety and Handling ==
== Safety and Handling ==
As with many organic solvents, 2-Octanol should be handled with care. It is important to use appropriate [[personal protective equipment]] (PPE) such as gloves and goggles when handling the compound. It should be stored in a cool, well-ventilated area away from sources of ignition.
 
As with many alcohols, 2-Octanol should be handled with care. It is flammable and can cause irritation to the skin and eyes upon contact. Proper [[safety precautions]] should be taken when working with this chemical, including the use of [[personal protective equipment]] such as gloves and goggles.


== Related Pages ==
== Related Pages ==
* [[Alcohol]]
* [[Octanol]]
* [[Octanol]]
* [[Alcohol (chemistry)]]
* [[Chirality (chemistry)]]
* [[Organic chemistry]]
* [[Hydrogenation]]
* [[Solvent]]


[[Category:Alcohols]]
[[Category:Alcohols]]
[[Category:Organic compounds]]
[[Category:Organic compounds]]

Latest revision as of 03:44, 13 February 2025


2-Octanol[edit]

Structural formula of 2-Octanol

2-Octanol, also known as sec-octanol, is an alcohol with the chemical formula C_H__O. It is a secondary alcohol, meaning the hydroxyl group (-OH) is attached to a secondary carbon atom. This compound is part of the octanol isomer family, which consists of several isomers with the same molecular formula but different structural arrangements.

Structure and Properties[edit]

2-Octanol is a chiral molecule, which means it can exist in two enantiomeric forms: (R)-2-octanol and (S)-2-octanol. These enantiomers have identical physical properties except for their interaction with plane-polarized light and reactions in chiral environments.

The structural formula of 2-Octanol is depicted in the image to the right. The molecule consists of an eight-carbon chain with a hydroxyl group attached to the second carbon atom. This structure gives 2-Octanol its characteristic properties as a secondary alcohol.

Synthesis[edit]

2-Octanol can be synthesized through various methods, including the hydration of 1-octene or the reduction of 2-octanone. Industrially, it is often produced by the hydrogenation of 2-octanone using a suitable catalyst.

Applications[edit]

2-Octanol is used in the production of plasticizers, surfactants, and lubricants. It is also employed as a solvent in the chemical industry and as an intermediate in the synthesis of other chemical compounds.

Safety and Handling[edit]

As with many alcohols, 2-Octanol should be handled with care. It is flammable and can cause irritation to the skin and eyes upon contact. Proper safety precautions should be taken when working with this chemical, including the use of personal protective equipment such as gloves and goggles.

Related Pages[edit]