1,8-Octanediol: Difference between revisions
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== 1,8-Octanediol == | |||
[[File:1,8-Octanediol.svg|thumb|right|Structural formula of 1,8-Octanediol]] | |||
'''1,8-Octanediol''' is a [[diol]] with the chemical formula C_H__O_. It is a type of [[glycol]] that consists of an eight-carbon chain with hydroxyl groups (-OH) attached to the first and eighth carbon atoms. This compound is also known as '''octamethylene glycol'''. | |||
1,8-Octanediol is a [[ | |||
== Chemical Properties == | |||
1,8-Octanediol is a [[linear molecule]] with two [[hydroxyl groups]], which makes it a [[bifunctional]] compound. The presence of these hydroxyl groups allows it to participate in various [[chemical reactions]], such as [[esterification]] and [[etherification]]. | |||
1,8-Octanediol is | |||
=== Physical Properties === | |||
1,8-Octanediol is a [[white crystalline solid]] at room temperature. It has a melting point of approximately 60°C and a boiling point of around 250°C. The compound is [[soluble]] in water and many organic solvents, which makes it useful in various [[industrial applications]]. | |||
== Applications == | |||
==Safety and Handling== | 1,8-Octanediol is used in the production of [[polymers]], [[plasticizers]], and [[lubricants]]. It serves as a [[monomer]] in the synthesis of [[polyesters]] and [[polyurethanes]]. Additionally, it is used in the formulation of [[cosmetics]] and [[personal care products]] due to its [[moisturizing]] properties. | ||
== Synthesis == | |||
The synthesis of 1,8-Octanediol can be achieved through several methods, including the [[hydrogenation]] of [[suberic acid]] or its esters. Another method involves the [[reduction]] of [[1,8-octanedione]] using suitable reducing agents. | |||
== Safety and Handling == | |||
1,8-Octanediol should be handled with care, as with all chemical substances. It is important to use appropriate [[personal protective equipment]] (PPE) when handling this compound to prevent skin and eye contact. In case of exposure, affected areas should be rinsed thoroughly with water. | |||
== Related Pages == | |||
* [[Diol]] | * [[Diol]] | ||
* [[Glycol]] | |||
* [[Polyester]] | * [[Polyester]] | ||
* [[Polyurethane]] | * [[Polyurethane]] | ||
[[Category:Diols]] | [[Category:Diols]] | ||
Latest revision as of 11:35, 15 February 2025
1,8-Octanediol[edit]
1,8-Octanediol is a diol with the chemical formula C_H__O_. It is a type of glycol that consists of an eight-carbon chain with hydroxyl groups (-OH) attached to the first and eighth carbon atoms. This compound is also known as octamethylene glycol.
Chemical Properties[edit]
1,8-Octanediol is a linear molecule with two hydroxyl groups, which makes it a bifunctional compound. The presence of these hydroxyl groups allows it to participate in various chemical reactions, such as esterification and etherification.
Physical Properties[edit]
1,8-Octanediol is a white crystalline solid at room temperature. It has a melting point of approximately 60°C and a boiling point of around 250°C. The compound is soluble in water and many organic solvents, which makes it useful in various industrial applications.
Applications[edit]
1,8-Octanediol is used in the production of polymers, plasticizers, and lubricants. It serves as a monomer in the synthesis of polyesters and polyurethanes. Additionally, it is used in the formulation of cosmetics and personal care products due to its moisturizing properties.
Synthesis[edit]
The synthesis of 1,8-Octanediol can be achieved through several methods, including the hydrogenation of suberic acid or its esters. Another method involves the reduction of 1,8-octanedione using suitable reducing agents.
Safety and Handling[edit]
1,8-Octanediol should be handled with care, as with all chemical substances. It is important to use appropriate personal protective equipment (PPE) when handling this compound to prevent skin and eye contact. In case of exposure, affected areas should be rinsed thoroughly with water.
