Clonazolam is a medication of the benzodiazepine course. Benzodiazepine drugs include a benzene engagement ring fused to a diazepine wedding ring, which really is a seven membered wedding ring with both nitrogen constituents located at R1 and R4. The benzyl engagement ring of clonazolam is substituted at R8 with a nitro group, NO2-. Further, the diazepine band is bonded at R6 to a 2-chlorinated phenyl wedding ring.

Clonazolam also includes a 1-methylated triazole wedding ring fused to and incorporating R1 and R2 of its diazepine wedding ring. Clonazolam belongs to a school of benzodiazepines made up of this fused triazole diamond ring, called triazolobenzodiazepines, recognized by the suffix "-zolam." Clonazolam is also a nitrobenzodiazepine, a subclass of benzodiazepines that have a nitro (NO2-) group. Other nitrobenzodiazepines include clonazepam and flunitrazepam.

This product is intended for research and forensic applications. Warning - this product is not for human or veterinary use.

Benzodiazepines create a variety of results by binding to the benzodiazepine receptor site and magnifying the efficiency and ramifications of the neurotransmitter gamma aminobutyric acid solution (GABA) by functioning on its receptors. As this web site is the most prolific inhibitory receptor place within the mind, its modulation brings about the sedating (or soothing results) of clonazelam on the stressed system.

The anticonvulsant properties of benzodiazepines may be, partly or entirely, credited to binding to voltage-dependent sodium programs alternatively than benzodiazepine receptors
Clonazolam (also called Clonitrazolam) is a book depressant compound of the benzodiazepine substance course which produces anxiolytic, sedative, muscle relaxant, and amnesic results when implemented. This element is a novel research chemical substance derivative of the FDA-approved drugs clonazepam (Klonopin, Rivitrol) and alprazolam (Xanax). Clonazolam is reported to be about 2.5x as effective as alprazolam.

The formation of clonazolam was initially reported in 1971. It had been referred to as the most dynamic element in the series examined. Clonazolam is respected to be highly powerful, and concerns have been increased which it and flubromazolam may create comparatively higher hazards than other creator benzodiazepines because of their ability to create strong sedation and amnesia at dental doses only 0.5 mg, or 500 micrograms. It really is reported to truly have a medium-length starting point of action (20 - 60 minutes).

Very little is well known about this compound, but it has become easy to get at through online research chemical substance sellers where it has been sold as a creator drug. Because of its extremely high strength, it is entirely on blotter newspaper or in volumetrically dosed alternatives. Ingestion of natural clonazolam natural powder is unsafe because of its microgram-range strength and the decrease where it can result in multi-day blackouts.
The rapid discontinuation of benzodiazepines can result in life-threatening seizures for those who have been with them regularly, in heavy dosages, or for long periods of time.


Clonazolam, otherwise called Clonitrazolam is a medium-term psychoactive medication that additionally has a place with the class of benzodiazepines. The first ever synthesis of clonazolam powder was conducted in 1971 and was put under the tested series of most active compounds . It produces anxiolytic, sedative, hypnotic, muscle relaxant, anticonvulsant, depressant, and amnesic effects. It is a derivative of the FDA-approved benzodiazepines clonazepam and alprazolam.

Clonazolam = Clonitrazolam
PubChem: 12317881
Molecular formula: C17H12ClN5O2
Molecular weight: 353.766 g/mol
IUPAC: 6-(2-chlorophenyl)-1-methyl-8-nitro-4H-[1,2,4]triazolo[4,3-a][1,4]benzodiazepine

Contrasted with the other specified medications, in any case, clonazolam has been accounted for to be all the more quick acting and its belongings can be felt inside 20 to a hour. It also has the reputation of being highly potent as it produces very strong sedation and effects even when taken in small doses such as 0.5 mg. As such, it may be more dangerous than the other benzodiazepines available in the market.

Similarly as with most benzodiazepines, unexpected stopping of utilization can present genuine dangers to the continuous clients including seizures and sudden demise. It is medically recommended that one’s dose is tapered off gradually before it is stopped altogether.

The combination of clonazolam and depressants such as alcohol, barbiturates, and opioids can cause fatal respiratory depression. Depressants have the tendency to maximize the sedative and muscle relaxant effects of clonazolam. The combined effect can produce unexpected loss of consciousness when taken at higher doses.


Some pharmacology information exists, but none elucidating its activity at specific receptors. We do know the drug can cause a potent benzodiazepine-like response in animals. Coupled with its known effects in humans and its structure, clonazolam is most likely a benzodiazepine receptor agonist.


Clonazolam is a benzodiazepine that is basically like clonazepam. The two mixes include a nitro assemble at the 7 position on the benzodiazepine ring structure, making them both nitrobenzodiazepines, and they additionally highlight a chlorine gather at the 2 prime position of every one of their separate structures. Clonazolam varies fundamentally clonazepam by the substitution of a triazole ring onto the benzodiazepine ring structure to yield a triazolobenzodiazepine ring structure; along these lines, clonazolam can likewise be alluded to as a triazolobenzodiazepie.

Comments: 0
No comments
Leave a Reply

Your email address cannot be published. Required fields are marked*