Ethchlorvynol

Ethchlorvynol was indicated to treat insomnia, and was widely prescribed in the 1960s and 1970s; prescriptions had fallen significantly by 1990, however, as other hypnotics that were considered safer and less dangerous in overdose became more common. Availability Ethchlorvynol is no longer prescribed in the United States due to unavailability, but is still available in some countries, and would still be considered legal to possess and use with a valid prescription. == Adverse effects ==

Along with expected sedative effects (e.g. relaxation and drowsiness), reported adverse effects of ethchlorvynol include gastrointestinal upset (including nausea and vomiting), dizziness, blurred or altered vision, numbness or tingling, and unsteadiness or impaired coordination. Hypersensitivity reactions such as skin rash have also been reported. Misuse by injection has been associated with serious acute toxicity. Reports describe severe noncardiogenic pulmonary oedema and haemodynamic effects following intravenous injection of ethchlorvynol (Placidyl), and public health sources have warned of cardiovascular or pulmonary injury arising from improper intravenous or intra-arterial injection of the drug. Overdose There is no specific antidote for ethchlorvynol overdose; management is primarily supportive and broadly parallels the approach used for other sedative-hypnotic overdoses (including barbiturate toxicity), with particular attention to airway, breathing, and circulation. Reported features of ethchlorvynol overdose include confusion, slurred speech, unsteady gait or impaired coordination, slow or troubled breathing (respiratory depression), and slow heartbeat, along with severe poisoning that may progress to coma and death. Withdrawal Ethchlorvynol withdrawal following prolonged or high-dose use has been reported to produce a distinct withdrawal syndrome, particularly after abrupt discontinuation. Case reports describe symptoms including confusion and perceptual disturbances, as well as severe presentations involving psychosis, delirium, and seizures. In some cases, withdrawal symptoms have been reported to occur after a delayed onset following discontinuation. Severe ethchlorvynol withdrawal has been described as resembling withdrawal syndromes associated with other sedative-hypnotic drugs and may carry a risk of serious or potentially fatal complications without appropriate medical management.. Secondary pharmacology references have noted that chronic use of ethchlorvynol may lead to physical dependence, with withdrawal effects comparable to those of barbiturate-class sedative-hypnotics, reinforcing the clinical significance of these reports ==Chemistry==

Ethchlorvynol is a member of the class of sedative-hypnotic carbinols, which includes methylparafynol and tert-amyl alcohol. It is not a benzodiazepine, carbamate, or barbiturate, and its molecular structure is considerably simpler. The systematic name of ethchlorvynol is usually given as ethyl 2-chlorovinyl ethynyl carbinol or 1-chloro-3-ethylpent-1-en-4-yn-3-ol. Its empirical formula is C7H9ClO. Ethchlorvynol is synthesized by an ethynylation reaction using lithium acetylide and 1-chloro-1-penten-3-one in liquid ammonia, followed by acidic work-up. : The analogous compound consisting of a carbamate derived from the hydroxy group was investigated and was shown to have a slower onset, longer duration, and increased potency, but was not developed commercially. == References ==