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Ethchlorvynol

This article is a stubmissing:
Subjective Effects
Interactions
Tolerance
Ethchlorvynol molecule structureEthchlorvynol molecule structure
Chemical Class

Ethchlorvynol is a sedative-hypnotic depressant of the alcohol class that was produced in the 1950s. It has been used for short-term management of insomnia,1 although other hypnotics largely supersede it2. It belongs to the sedative-hypnotic carbinols and has a simpler molecular structure than benzodiazepines, carbamates, or barbiturates. It is habit-forming, and its replacement by other hypnotics partly reflects their greater perceived safety in overdose.

Dosage & Duration

Dosage

Doses are population estimates that vary widely between individuals.

Threshold~100 mg
Light100-200 mg
Moderate200-500 mg
Strong500-750 mg
Heavy750+ mg

Duration

Onset15-45 minutes
After Effects1-6 hours
Total6-9 hours

Subjective Effects

Subjective Effects not written up yet

Pharmacology

Pharmacodynamics

Ethchlorvynol depresses central nervous system activity3 and is described as a positive allosteric modulator of GABA-A receptors,4 although its exact mechanism remains uncertain.5 Antagonist actions are also reported at the GABA-A receptor α1 and β2 subunits.

Pharmacokinetics

Ethchlorvynol is rapidly absorbed from the gastrointestinal tract and is 35-50% protein bound. About 90% of a dose is metabolized in the liver,6 with possible additional metabolism in the kidneys. Ethchlorvynol and its metabolites undergo extensive enterohepatic recirculation,6 cycling between the intestine and liver. Its plasma half-life is approximately 10-20 hours,6 while its terminal half-life is 21-100 hours. Computational predictions suggest inhibition of CYP2C19.

Metabolitesnone documented yet

Interactions

Interactions not written up yet

An unlisted combination is an unknown one, not a safe one. Check a dedicated combination chart before mixing.

Check TripSit

Tolerance

Tolerance not written up yet

Harm Potential

Addiction & Dependence

Psychological

Ethchlorvynol may become habit-forming if too much is taken7 and has been associated with widespread abuse.

Physical

Hospitalization for ethchlorvynol detoxification has been reported in two individuals.

Toxicity

Lethal Dosage

Extreme overdoses can cause coma and death.8 Intravenous or intra-arterial injection can also be fatal.

Blood

Ethchlorvynol overdose can cause thrombocytopenia.8

Respiratory system

Ethchlorvynol overdose can cause respiratory depression.7

Cardiovascular system

Ethchlorvynol overdose can slow the heartbeat.7

Nervous system

Ethchlorvynol overdose can cause confusion, peripheral numbness and weakness, impaired coordination and muscle control, and slurred speech;7 extreme overdoses can cause coma.8

Vascular system

Intravenous or intra-arterial injection of ethchlorvynol can cause severe vascular injury, including injury requiring limb amputation, and death.

History & Culture

Pfizer developed ethchlorvynol in the 1950s, and research chemists at Abbott Laboratories in the United States identified it in 1956. A synthesis patent credited to A. Bayley and W. M. McLamore was issued on May 22, 1956, and assigned to Chas. Pfizer & Co., Inc. A related carbamate compound was…

Legality

By Country

Illegal1
United States flagUnited StatesIllegal

Article Status

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