1-Tridecanol: Difference between revisions
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'''1-Tridecanol''' is a fatty alcohol with the chemical formula C₁₃H₂₈O. It is a long-chain alcohol that is part of the aliphatic alcohol family, which are compounds characterized by a hydroxyl group (-OH) attached to a saturated carbon chain. | '''1-Tridecanol''' is a fatty alcohol with the chemical formula C₁₃H₂₈O. It is a long-chain alcohol that is part of the aliphatic alcohol family, which are compounds characterized by a hydroxyl group (-OH) attached to a saturated carbon chain. | ||
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== References == | == References == | ||
* Environmental Protection Agency (EPA). (2021). ''Chemical Safety and Pollution Prevention''. Retrieved from [https://www.epa.gov/chemical-safety] | * Environmental Protection Agency (EPA). (2021). ''Chemical Safety and Pollution Prevention''. Retrieved from [https://www.epa.gov/chemical-safety] | ||
[[Category:Fatty Alcohols]] | [[Category:Fatty Alcohols]] | ||
[[Category:Organic Compounds]] | [[Category:Organic Compounds]] | ||
Revision as of 02:26, 26 October 2024
1-Tridecanol is a fatty alcohol with the chemical formula C₁₃H₂₈O. It is a long-chain alcohol that is part of the aliphatic alcohol family, which are compounds characterized by a hydroxyl group (-OH) attached to a saturated carbon chain.
Chemical Structure and Properties
1-Tridecanol is a linear alcohol with the following structure:
- Molecular Formula: C₁₃H₂₈O
- Molecular Weight: 200.36 g/mol
- IUPAC Name: Tridecan-1-ol
- CAS Number: 112-70-9
Physical Properties
- Appearance: White, waxy solid
- Melting Point: 32-36 °C
- Boiling Point: 270-280 °C
- Solubility: Insoluble in water, soluble in organic solvents such as ethanol and ether
Chemical Properties
1-Tridecanol is a primary alcohol, meaning the hydroxyl group is attached to the first carbon of the alkyl chain. This configuration allows it to undergo typical alcohol reactions, such as oxidation to form aldehydes or carboxylic acids, and esterification to form esters.
Synthesis
1-Tridecanol can be synthesized through several methods, including:
- Hydrogenation of Tridecanoic Acid: This process involves the catalytic hydrogenation of tridecanoic acid, reducing the carboxylic acid group to a primary alcohol.
- Reduction of Tridecanal: Tridecanal can be reduced using reducing agents such as sodium borohydride (NaBH₄) or lithium aluminum hydride (LiAlH₄) to yield 1-tridecanol.
Applications
1-Tridecanol is used in various industrial and commercial applications, including:
- Surfactants and Detergents: It is used as a raw material in the production of surfactants and detergents due to its ability to lower surface tension and enhance cleaning properties.
- Lubricants: The compound is used in the formulation of lubricants, providing smoothness and reducing friction in mechanical systems.
- Cosmetics and Personal Care: 1-Tridecanol is used in the formulation of creams, lotions, and other personal care products for its emollient properties.
- Plasticizers: It is used as a plasticizer in the production of plastics, improving flexibility and durability.
Safety and Handling
1-Tridecanol is generally considered to be of low toxicity. However, as with all chemical substances, it should be handled with care. Appropriate personal protective equipment (PPE) such as gloves and goggles should be worn to prevent skin and eye contact.
- Storage: Store in a cool, dry place away from sources of ignition.
- Disposal: Dispose of in accordance with local environmental regulations.
Environmental Impact
1-Tridecanol is biodegradable and is not expected to persist in the environment. However, its production and use should be managed to minimize any potential environmental impact.
Conclusion
1-Tridecanol is a versatile fatty alcohol with a range of applications in industrial and consumer products. Its chemical properties make it useful in the synthesis of various compounds, and its low toxicity profile makes it a relatively safe chemical to handle in controlled environments.
References
- Environmental Protection Agency (EPA). (2021). Chemical Safety and Pollution Prevention. Retrieved from [1]