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Diclazepam (also known as Chlorodiazepam) is a synthetic depressant substance of the benzodiazepine chemical class that produces effects similar to diazepams, such as anxiety suppression, disinhibition, anticonvulsant, hypnotic, muscle relaxing, and amnesia when administered.

It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960. In animal models, it has a potency of approximately ten times that of diazepam, of which it is a structural analog.

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With all the chemicals that we stock, Diclazepam is not approved for any type of in-vivo research (i.e. not in humans or animals) or for clinical trials, and therefore if accidentally ingested then immediate medical attention should be sought.

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It is basically a synthetic depressant substance that belongs to a chemical class of benzodiazepines and is related to diazepam in its properties.

Benzodiazepines contain a basic benzene ring that is linked to a seven-membered diazepine ring, having two nitrogen constituents located at R1 and R4. Chemically, it has the same structure, instead of being in the R1 position, it is replaced by a methyl group.

The benzodiazepine ring is attached to a 2-chlorinated phenyl ring at R5, and also a chloro group is attached to R7 of the benzyl ring. Diclazepam also contains a ketone group that is formed by the double bond of the oxygen group to the diazepine ring in the R2 position.