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The synthesis of clonazolam was first reported in 1971. It was described as the most active compound in the series tested. Clonazolam is reputed to be highly potent, and concerns have been raised that it and flubromazolam may pose comparatively higher risks than other designer benzodiazepines due to their ability to produce strong sedation and amnesia at oral doses as low as 0.5 mg, or 500 micrograms (µg). It is reported to have a medium-length onset of action (20 – 60 minutes). Buy Clonazolam powder for sale
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Very little is known about this substance, but it has recently become easily accessible through online research chemical vendors where it is being sold as a designer drug. Due to its extremely high potency, it is often found on blotter paper or in volumetrically dosed solutions. Ingestion of raw clonazolam powder is unsafe due to its microgram-range potency and the ease in which it can lead to multi-day blackouts.
Sudden discontinuation of benzodiazepines can cause seizures (which may be life-threatening in certain cases) for individuals who have been heavily using them for a prolonged period of time. For this reason, it is recommended to gradually lower the daily dose over a period of time instead of stopping abruptly — a technique known as tapering. Buy Clonazolam powder for sale
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Due to the high dependence-forming and addiction potential that this substance shares with other members of the benzodiazepine class, as well as its alcohol-like ability to induce dangerously disinhibited black-out states, it is strongly advised to use proper harm reduction practices if choosing to use this substance. Clonazolam is a drug of the benzodiazepine class. Benzodiazepine drugs contain a benzene ring fused to a diazepine ring, which is a seven membered ring with the two nitrogen constituents located at R1 and R4. The benzyl ring of clonazolam is substituted at R8 with a nitro group, NO2-. Further, the diazepine ring is bonded at R6 to a 2-chlorinated phenyl ring. Buy Clonazolam powder for sale
Clonazolam also contains a 1-methylated triazole ring fused to and incorporating R1 and R2 of its diazepine ring. Clonazolam belongs to a class of benzodiazepines containing this fused triazole ring, called triazolobenzodiazepines, distinguished by the suffix “-zolam.” Clonazolam is also a nitrobenzodiazepine, a subclass of benzodiazepines which contain a nitro (NO2-) group. Other nitrobenzodiazepines include clonazepam and flunitrazepam.
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Benzodiazepines produce a variety of effects by binding to the benzodiazepine receptor site and magnifying the efficiency and effects of the neurotransmitter gamma aminobutyric acid (GABA) by acting on its receptors. As this site is the most prolific inhibitory receptor set within the brain, its modulation results in the sedating (or calming effects) of Clonazolam on the nervous system.
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The other physical and cognitive effects that it would release on the human body include respiratory depression, dizziness, muscle relaxation, seizure control, spasms control, loss of coordination.
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Clonazolam is a benzodiazepine that is similar to clonazepam (Klonopin) in results, however, it is significantly more potent. In fact, clonazolam is known as the most potent benzodiazepine that is available in the world today. This means that only extremely experienced chemical researchers should experiment with clonazolam. Clonazolam was first created in 1971.
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Clonazolam has varying legal statuses around the world. In Sweden, it has been proposed to be made a hazardous substance. In the United Kingdom, it is a Class C drug
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Product Name:Clonazolam
IUPAC Name:Clonazolam
Other Names:Clonazolam
Cas Number:33887-02-4
Molecular Formula:C17H12ClN5O2
Molar Mass:353.77 g/mol
Effect:sedative
Purity of the substance:99.9%
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