Γ-Butyrolactone: Difference between revisions

From WikiMD's Wellness Encyclopedia

CSV import
Tags: mobile edit mobile web edit
 
CSV import
 
Line 24: Line 24:
[[Category:Solvents]]
[[Category:Solvents]]
{{Chemistry-stub}}
{{Chemistry-stub}}
== Γ-Butyrolactone ==
<gallery>
File:Industrial_synthesis_of_gamma-butyrolactone.svg|Industrial synthesis of gamma-butyrolactone
File:MCPB.png|MCPB
File:GHB_metabolic_pathway.svg|GHB metabolic pathway
File:GBLjugs.jpg|GBL jugs
File:Dangerous_dietary_supplements.gif|Dangerous dietary supplements
</gallery>

Latest revision as of 23:58, 24 February 2025

Γ-Butyrolactone (GBL) is a hygroscopic colorless liquid with a weak characteristic odor and profoundly bitter taste. It is a common solvent and reagent in chemistry and is used as an aroma compound, as a stain remover, as a superglue remover, and as a solvent in some wet aluminium electrolyte capacitors.

Chemical Properties[edit]

GBL is a lactone. It is hydrolyzed under basic conditions, for example in a sodium hydroxide solution into sodium gamma-hydroxybutyrate, the sodium salt of gamma-hydroxybutyric acid. Under acidic conditions, it forms an equilibrium mixture of both compounds. These compounds then may go on to form the polymer poly(4-hydroxybutyrate).

Uses[edit]

GBL is not active in its own right; its mechanism of action stems from its identity as a prodrug of gamma-hydroxybutyric acid (GHB). The hypnotic effect of GHB is enhanced by combination with alcohol. A 2003 rat study showed that GBL in combination with ethanol showed a potentiated hypnotic effect, as the sleep-timing measure was longer than both of the individual components combined.

Safety[edit]

Overdose of GBL can cause adverse effects, including sedation, vertigo, nausea, and death. GBL has a distinctive taste and odor, described as being comparable to stale water, synthetic melon aroma, or burnt plastic. This differs significantly from GHB, which is described as having a decidedly salty taste. People who ingest GBL may not be aware they are consuming a drug.

Legal Status[edit]

In many countries, including the United States and Canada, the production, sale, and possession of GBL are illegal since it can be used as a prodrug of GHB. In the United Kingdom, GBL is classified as a Class C drug.

See Also[edit]

This article is a stub related to chemistry. You can help WikiMD by expanding it!


Γ-Butyrolactone[edit]