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Pyrazolam
Overview
Research chemical benzodiazepine discovered by Hoffman-LaRoche in the 1970's. It has been reported to be sold on the research chemical market in the early 2010's. At lower doses it acts mainly as an anxiolytic compound, and at higher doses it has been reported to have sedating, hypnotic, amnesic effects while also lowering inhibitions. The drug is structurally similar to alprazolam, bromazepam, and triazolam. The drug is 12x as potent as diazepam.
Sources & licencesPsychonautWiki·TripSit·PubChem chemical identifiers
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The SMILES and basic chemical identifiers are resolved from the linked PubChem record. Fracton renders the molecule locally as inline SVG.
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Rendered locally from the bundled SMILES string.
Show SMILES
CC1=NN=C2N1C3=C(C=C(C=C3)Br)C(=NC2)C4=CC=CC=N4Dose
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Safety
- Addiction potential
- extremely physically and psychologically addictive
- Full tolerance
- within a couple of days of continuous use
- Zero tolerance
- 7 - 14 days
- Cross-tolerance with
- benzodiazepines
EffectsPsychonautWikiEffectIndex
Cognitive
7Amnesia
Amnesia is a global impairment in the ability to acquire new memories regardless of sensory modality, and a loss of some memories, especially recent ones, from the period before amnesia began. It is most commonly induced under the influence of heavy dosages of GABAergic depressants, such as alcohol, benzodiazepines, GHB, and zolpidem.
Open full explainer on EffectIndex↗Analysis suppression
Analysis suppression is a distinct decrease in a person's overall ability to process information and logically or creatively analyze concepts, ideas, and scenarios. It is most commonly induced under the influence of heavy dosages of antipsychotic compounds, and is associated with long term use of such drugs like quetiapine, haloperidol, and risperidone.
Open full explainer on EffectIndex↗Anxiety suppression
Anxiety suppression (also known as anxiolysis or minimal sedation) is medically recognized as a partial to complete suppression of a person’s ability to feel anxiety, general unease, and negative feelings of both psychological and physiological tension. It is most commonly induced under the influence of moderate dosages of anxiolytic compounds which primarily include GABAergic depressants, such as benzodiazepines, alcohol, GHB, and gabapentinoids.
Open full explainer on EffectIndex↗Compulsive redosing
Compulsive redosing is the experience of a powerful and difficult to resist urge to continuously redose a psychoactive substance in an effort to increase or maintain the subjective effects which it induces. It is most commonly induced under the influence of moderate dosages of a wide variety of compounds, such as opioids, stimulants, GABAergics, and entactogens.
Open full explainer on EffectIndex↗Disinhibition
Disinhibition is medically recognized as an orientation towards immediate gratification, leading to impulsive behavior driven by current thoughts, feelings, and external stimuli, without regard for past learning or consideration of future consequences. It is most commonly induced under the influence of moderate dosages of GABAergic depressants, such as alcohol, benzodiazepines, phenibut, and GHB.
Open full explainer on EffectIndex↗Dream potentiation
Dream potentiation is an effect that increases the subjective intensity, vividness, and frequency of sleeping dream states. It is most commonly induced under the influence of moderate dosages of oneirogenic compounds, a class of hallucinogen that is used to specifically potentiate dreams when taken before sleep.
Open full explainer on EffectIndex↗Thought deceleration
Thought deceleration is the process of thought being slowed down significantly in comparison to that of normal sobriety. It is most commonly induced under the influence of heavy dosages of depressant compounds, such as GABAergics, antipsychotics, and opioids.
Open full explainer on EffectIndex↗Emotional & social
1Respiratory depression
Respiratory depression can be described as a reduced urge to breathe that can be fatal depending on its intensity. It is most commonly induced under the influence of heavy dosages of depressant compounds, particularly opioids, such as heroin and fentanyl, or GABAergics, such as alcohol and GHB. However, it is worth noting that otherwise safe dosages of these compounds can become fatal when combined with even small amounts of other classes of depressant.
Open full explainer on EffectIndex↗Physical & bodily
4Dizziness
Dizziness can be described as the perception of a spinning or swaying motion which typically causes a difficulty in standing or walking. It is most commonly induced under the influence of heavy dosages of GABAergic depressant compounds, such as benzodiazepines, alcohol, and GHB.
Open full explainer on EffectIndex↗Motor control loss
Motor control loss can be described as feeling as if there has been a distinct decrease in a person's ability to control their physical body with precision, balance, coordination, and dexterity. Motor control loss is often accompanied by other coinciding effects such as sedation and disinhibition. It is most commonly induced under the influence of moderate dosages of GABAergic depressant compounds, such as, alcohol, benzodiazepines, GHB, and phenibut.
Open full explainer on EffectIndex↗Muscle relaxation
Muscle relaxation can be described as the experience of muscles losing their rigidity or tenseness while becoming relaxed and comfortable. It is most commonly induced under the influence of moderate dosages of depressant compounds, such as various benzodiazepines, GABAergics, and opioids.
Open full explainer on EffectIndex↗Sedation
Sedation can be described as a decrease in a person's physical energy levels which are interpreted as discouraging when it comes to wakefulness, movement, performing tasks, talkativeness, and general exercise. It is most commonly induced under the influence of moderate dosages of depressant compounds, such as opioids, GABAergics, and antipsychotics.
Open full explainer on EffectIndex↗No effects match that search.
Timing
Only onset and total duration are available for this route, so an intensity curve would be misleading.
Testing
Reagent test reference
The colour bars follow the written reaction sequence from the source. Rows without a bar are explicit results recorded by the source, not missing data. Reagents cannot establish identity, purity, or potency.
Reported appearance: Brownish.
Reported appearance: Light yellow.
Reported appearance: Light yellow.
Reported appearance: Light yellow.
Reported appearance: Light yellow.
Reported appearance: Dark purple or black.
Reported appearance: Pale green.
No color change
No color change
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