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Conclusions: After 4, 8, and 12 hours, the patient’s blood levels of clonazolam were 0.077 mg/L, 0.015 mg/L, and 0.009 mg/L, respectively, based on three measurements. Since the toxicity of clonazolam to humans is still unknown, any cases of poisoning should be carefully investigated.
Keywords: Blood confirmation; Clonazolam; New designer benzodiazepine; Buy Diclazepam Powder Online.

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Diclazepam (Ro5-3448) is a benzodiazepine and the functional analog of diazepam. It is sometimes referred to as chlorodiazepam and 2′-chloro-diazepam. Leo Sternbach and his colleagues at Hoffman-La Roche synthesized it for the first time in 1960. It is now marketed as an unscheduled substance rather than one that is authorized for use as medicine. Human testing has not been done on efficacy or safety.

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Metabolism

After this compound is metabolized, it is discovered that diclorazepam has an approximate 42-hour elimination half-life and that it is N-demethylated to dilorazepam, which is detectable in urine for six days after the parent drug is administered. Additional metabolites found in the urine were lorazepam and lormetazepam, which were present for 19 and 11 days, respectively, suggesting that hydroxylation by cytochrome P450 enzymes was taking place at the same time as N-demethylation.

Formal Name: 1-methyl-2H-1,3-dihydro-1-chloro-5-(2-chlorophenyl)-1,4-benzodiazepin-2-one

Number of CAS: 2894-68-0

Cl2N2O C16H12 is the molecular formula.

Weight of Formula: 319.2

98+% purity

Formulation: A tidy, firm

Solubility (Discover How Solubility Varies)

30 mg/ml DMF

30 mg/ml of DMSO

0.5 mg/ml of DMSO:PBS (pH 7.2) (1:1)

10 mg/ml of ethanol

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Background: Experienced designer drug users are increasingly drawn to the new wave of psychoactive compounds that have emerged in recent times. A notable subset consists of derivatives of benzodiazepines, which are not prescribed drugs but are abused by individuals who experiment with novel and traditional psychoactive chemicals.

Case presentation: The purpose of the paper is to present the instance of a non-benzodiazepine-habitual user ingesting clonazolam. The main side effects of the ingestion were a prolonged coma, reduced muscular tone, and deep tendon reflexes; there was no concurrent toxicity or cardio-respiratory failure.