γ-Butyrolactone

GHB acts as a central nervous system (CNS) depressant with effects similar to those of barbiturates.

[9] γ-Butyrolactone is produced industrially by dehydrogenation of 1,4-butanediol at a temperature of 180–300 °C and atmospheric pressure in the presence of a copper catalyst.

When treated with a non-nucleophilic base, such as lithium diisopropylamide, GBL undergoes deprotonation of the alpha carbon atom to the carbonyl.

[5] Butyrolactone, with its wide liquid range, chemical stability, and high dielectric constant, is used in electrolytic capacitors as the organic solvent.

It is frequently mixed with a small ratio of ethylene glycol, "9:1" being common, to vary internal resistivity.

GBL has a distinctive taste and odor, described as being comparable to stale water, synthetic melon aroma or burnt plastic.

[27] Due to the fact that those with limited chemistry knowledge can make GBL with easy-to-get precursors, it has become quite popular among young people in French nightclubs.

[35] Frequent use of GHB or GBL, even when taken long-term and in moderate doses, does not appear to cause significant physical dependency in the majority of its users.

However, when consumed in excessive amounts with a high frequency of dosing, physical and psychological dependence can develop.

Legislation entering into force on 1 April 2011 made it possible to handle narcotics for industrial purposes and enabled GBL and 1,4-Butanediol to be classified as controlled substances.

Schedule VI of the "Controlled Drugs and Substances Act" requires vendors to collect information regarding purchases of GBL.

Possession is not illegal, but may be punished according to the Medicines Act, when intended to be sold for human consumption or synthesis of GHB.

Any person who is found to have in his possession of it not in accordance with this Ordinance can be liable, on conviction upon indictment, a fine of HK$1,000,000 and to imprisonment for 7 years.

Possession is not illegal but may be punished according to the Medicines Act, when intended to be sold for human consumption or synthesis of GHB.

[44] People's Republic of China: GBL was regulated as a Class III drug precursor since 7 June 2021.

Although recently passed legislation to enter into force on 1 April 2011 will make it possible to handle narcotics for industrial purposes will enable GBL and 1,4-Butanediol to be classified as controlled substances.

[50] Sales and distribution of this product for industrial use is tightly regulated and requires quantity tracing, lock and key storage and 24 hour surveillance and is limited to a very few suppliers who have appropriate DEA registrations and as of 2021 included only Ashland, BASF, and Miami Chemical.

NFPA 704 four-colored diamond Health 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroform Flammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oil Instability 1: Normally stable, but can become unstable at elevated temperatures and pressures. E.g. calcium Special hazards (white): no code
2-Methyl-4-chlorophenoxybutyric acid is an herbicide produced from butyrolactone.
Metabolic pathway of 1,4-butanediol , GBL and GHB
Jugs of seized GBL
FDA warning against products containing GHB and its prodrugs, such as GBL