Methylpentynol

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Methylpentynol.svg

Methylpentynol is a tertiary alcohol and a sedative and hypnotic drug. It is also known by its chemical name, 2-methyl-3-butyn-2-ol. Methylpentynol has been used in the past for its anxiolytic and muscle relaxant properties.

Chemical Properties[edit | edit source]

Methylpentynol is a colorless liquid with a characteristic odor. It is soluble in water and has a molecular formula of C5H8O. The molecular weight of methylpentynol is 84.12 g/mol. It has a boiling point of 120-122°C and a melting point of -50°C.

Pharmacology[edit | edit source]

Methylpentynol acts on the central nervous system (CNS) to produce its sedative and hypnotic effects. It is believed to enhance the activity of the gamma-aminobutyric acid (GABA) neurotransmitter, which is the primary inhibitory neurotransmitter in the CNS. This action results in a calming effect on the brain and body.

Medical Uses[edit | edit source]

Methylpentynol was historically used as a sedative and hypnotic for the treatment of insomnia and anxiety. It was also used as a muscle relaxant in certain medical conditions. However, due to the development of newer and safer medications, the use of methylpentynol has significantly declined.

Side Effects[edit | edit source]

The use of methylpentynol can lead to several side effects, including drowsiness, dizziness, nausea, and headache. In higher doses, it can cause respiratory depression, hypotension, and coma. Long-term use can lead to tolerance and dependence.

Synthesis[edit | edit source]

Methylpentynol can be synthesized through the reaction of acetylene with acetone in the presence of a catalyst such as sodium amide. The reaction produces 2-methyl-3-butyn-2-ol as the main product.

Regulation[edit | edit source]

Due to its potential for abuse and the availability of safer alternatives, the use of methylpentynol is regulated in many countries. It is classified as a controlled substance in some jurisdictions.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]


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