Description
A benzodiazepine derivative. Which is mostly an anxiolytic substance, without strong hypnotic properties that most benzodiazepines have. Its active metabolite is N-desmethylmetaclazepam, which is the main metabolite. Slightly more effective as an anxiolytic than Bromazepam.
Effects & Dosing
Dosage
Oral
| Light | Common | Strong |
|---|---|---|
| 9.5-18.75 mg | 18.75-18.75 mg | 35-50 mg+ |
Duration
Oral
After Effects 1h - 24h
Safety & Risks
Safer Use
- All other CNS depressants.
Detection Times
| Method | Detection Window |
|---|---|
| Urine | 3–7 days |
Note: Benzodiazepine with a thio-substituted structure. Cross-reactivity with standard immunoassays may vary.
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