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Diclazepam (Ro5-3448), also known as chlorodiazepam and 2′-chloro-diazepam, is a benzodiazepine and functional analog of diazepam. It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960. It is not currently approved for use as a medication, but rather sold as an unscheduled substance. Efficacy and safety have not been tested in humans.

In animal models, its effects are similar to diazepam, possessing long-acting anxiolyticanticonvulsanthypnoticsedativeskeletal muscle relaxant, and amnestic properties

 

Diclazepam Powder (also known as chlorodiazepam) is a novel depressant substance of the benzodiazepine class and functional analog of diazepam. Diclazepam is reported to produce similar effects to diazepam.

Diclazepam (Ro5-3448), also known as chlorodiazepam and 2′-chloro-diazepam, is a benzodiazepine and functional analog of diazepam. It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960. It is not currently approved for use as a medication, but rather sold as an unscheduled substance. Efficacy and safety have not been tested in humans.

It is an analogue of the sedative diazepam (Valium), it is a benzodiazepine drug with, among others, hypnotic, sedative, and analytical properties. Part of the tranquilizer class.

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Buy Diclazepam Powder Online, Doses of diclazepam are suggested to be about 50 percent of These specified to youthful people and cure limited to an utmost of two weeks. Long-performing benzodiazepines for instance diazepam will not be recommended to the aged.[fourteen] Diazepam may also be risky in geriatric individuals owing to a big greater risk of falls

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Diazepam, as with other benzodiazepine medicine, can cause tolerance, physical dependence, substance use problems, and benzodiazepine withdrawal syndrome. Withdrawal from diazepam or other benzodiazepines generally leads to withdrawal symptoms similar to Those witnessed during barbiturate or alcohol withdrawal.

Oral diazepam might be employed adjunctively in convulsive Ailments, although it has not proved helpful as the sole therapy.

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The states of California and Florida offer diazepam to condemned inmates to be a pre-execution sedative as a portion in their lethal injection plan, Even though the state of California has not executed a prisoner because 2006.

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What is Diclazepam 

Diclazepam is also known as Chlorodiazepam. This research chemical falls under the benzodiazepine class. Diclazepam was first synthesized in the 1960s. Many researchers experiment with this chemical in order to witness results that are typical of other benzodiazepines.  Experiments with Diclazepam typically yield findings of muscle relaxation, sedation, disinhibition, anxiety suppression, thought deceleration, analysis suppression, dream potentiation, and residual sleepiness. Researchers should be well aware of the residual sleepiness findings before they begin experimenting with Diclazepam in their laboratories.  

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Here at Buy Chem Online, we have high-quality Diclazepam for sale. Our Diclazepam typically comes in powder form. However, if you prefer another form, you can contact us to see when we will have it available.  

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

Diclazepam, also known as chlorodiazepam and 2′-chloro-diazepam, is a benzodiazepine and functional analog of diazepam. It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960.

Diclazepam (chlorodiazepam) is the short name for 7-chloro-5-(2-chlorophenyl)-1-methyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one and can be considered both to be the 2′-chloro analogue of diazepam or the 1-methyl analogue of Delorazepam. This chemical is a novel research chemical and is not currently subject to any licensing controls or regulations in the UK when used for laboratory research and development purposes.

It is an analogue of the sedative diazepam (Valium), Diclazepam is a benzodiazepine drug with, among others, hypnotic, sedative, and anxiolytic properties. Part of the tranquiliser class.

Diclazepam is also available in pellet form, and can be used as a substitute for etizolam in comparable study conditions.

As 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 accidently ingested then immediate medical attention should be sought. Please ensure you adhere to standard laboratory safety practices including using suitable skin, eye and clothing protection.

Diclazepam, also known as chlorodiazepam and 2′-chloro-diazepam, is a benzodiazepine and functional analog of diazepam. It was first synthesized by Leo Sternbach and his team at Hoffman-La Roche in 1960.

Diclazepam (chlorodiazepam) is the short name for 7-chloro-5-(2-chlorophenyl)-1-methyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one and can be considered both to be the 2′-chloro analogue of diazepam or the 1-methyl analogue of Delorazepam. This chemical is a novel research chemical and is not currently subject to any licensing controls or regulations in the UK when used for laboratory research and development purposes.

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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.

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