Showing all 14 results

2C-B-FLY Pellets

2C-B-FLY is a lesser-known psychedelic substance of the phenethylamine and benzodihydrodifuran classes that produces an array of psychedelic and entactogenic effects when administered. Reports have characterized its effects profile as possessing features of 2C-B, mescaline and MDA, with a duration of 6–8 hours (or up to 12 hours in larger doses).

2C-B-FLY is a derivative of the 2C-x family of psychedelic phenethylamines, specifically 2C-B, of which it significantly differs from in terms of its potency, metabolism, and potential toxicity.

Physical effects
The physical effects of 2C-B-FLY are comparable to that of traditional phenethylamines such as 2C-E, mescaline and 2C-T-7 along with more pronounced side effects. There have been reports gastrointestinal disturbances following the use of this compound which include diarrhea, nausea, moderate to severe stomach bloating and general gassiness at moderate to heavy doses. These effects are comparable to that of 5-MeO-MiPT, 2C-T-7 and other compounds with suspected MAO-altering properties. This suggests that 2C-B-FLY may potentially have such MAO-altering properties of its own, which may make it dangerous to combine with certain substances.
Stimulation and Sedation
Spontaneous physical sensations
Physical euphoria
Tactile enhancement
Temperature regulation suppression
Increased bodily temperature
Bodily control enhancement
Bodily pressures
Increased blood pressure
Increased libido
Headaches
Stomach bloating
Stomach cramps
Nausea
Diarrhea
Dehydration
Excessive yawning
Watery eyes
Pupil dilation
Teeth grinding

2C-B-FLY is sold for research purposes only and is not be utilized for any other purposes.

Acetildenafil

Acetildenafil (hongdenafil) is a synthetic drug which acts as a phosphodiesterase inhibitor.It is an analog of sildenafil (Viagra) which has been detected in numerous different brands of supposedly “herbal” aphrodisiac products sold to boost libido and alleviate erectile dysfunction.

A range of designer analogs of licensed PDE5 inhibitors such as sildenafil and vardenafil have been detected in recent years in over-the-counter herbal aphrodisiac products in an apparent attempt to circumvent both the legal restrictions on sale of erectile dysfunction drugs, which are prescription-only medicines.

These compounds have been demonstrated to display PDE5 inhibitory activity in vitro and presumably have similar effects when consumed, but have undergone no formal testing in either humans or animals, and as such may represent significant health risks to consumers of these products due to their unknown safety profile.

Other similar types:
Aildenafil
Nitrosoprodenafil
Sulfoaildenafil

Acetildenafil is sold for research purposes only and is not be utilized for any other purposes.

Clonazolam

Clonazolam (also known as Clonitrazolam) is a depressant substance of the benzodiazepine chemical class which produces anxiolytic, sedative, muscle relaxant, and amnesic effects when administered. This compound is a research chemical derivative of the approved drugs clonazepam (Klonopin, Rivitrol) and alprazolam (Xanax). Clonazolam is reported to be roughly 2.5x as potent as alprazolam.

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 (ug).It is reported to have a medium-length onset of action (20 – 60 minutes).

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.

Clonazolam is reported to be similar to alprazolam and other benzodiazepines that suppress emotions and produce moderate-strong feelings of relaxation, pleasure and comfort in the body. This seems to present itself more often in those with pre-existing anxiety. Many anecdotal reports from users of this compound have stated it as being one of the most euphoric benzodiazepines.

Physical effects
Sedation
Motor control loss
Dizziness
Increased libido
Respiratory depression
Muscle relaxation

Clonazolam is sold for research purposes only and is not be utilized for any other purposes.

DeschloroEtizolam

Deschloroetizolam is a short-acting psychoactive substance of the thienodiazepine class which has been shown to produce depressants, anxiolytic, sedative, hypnotic, muscle relaxant, anticonvulsant, depressant and amnesic effects. Deschloroetizolam, like benzodiazepines, binds to modulatory sites on the GABA receptors. Deschloroetizolam is closely related to etizolam (Etilaam), triazolam (Halcion), and alprazolam (Xanax).

Deschloroetizolam has a relatively fast onset of action and symptomatic relief. It is half as potent as its parent compound etizolam with a duration which is twice as long. It also has a similar bioavailibility and a similar time to onset in comparison to the parent drug. 2mg of deschloroetizolam is thought to be of similar potency to 10mg of diazepam.

Deschloroetizolam is a structural relative of benzodiazepines, whereby the benzene ring has been replaced by a thiophene ring, classifying it as a thienodiazepine. It differs structurally from its parent compound etizolam through removal of the chlorine atom at the 2′ position on the phenyl ring.

Thienodiazepines 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.

Physical effects
Sedation
Respiratory depression
Muscle relaxation
Dizziness

Cognitive effects
Amnesia
Anxiety suppression
Thought deceleration
Analysis suppression
Disinhibition
Euphoria
Compulsive redosing
Emotion suppression

Deschloroetizolam is sold for research purposes only and is not be utilized for any other purposes.

Diclazepam

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 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. At R1, diclazepam is substituted with methyl group.

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 diclazepam on the nervous system.

The anticonvulsant properties of benzodiazepines may be, in part or entirely, due to binding to voltage-dependent sodium channels rather than benzodiazepine receptors.

Physical effects
Muscle relaxation
Sedation
Motor control loss
Respiratory depression
Dizziness

Cognitive effects
Amnesia
Disinhibition
Anxiety suppression
Thought deceleration
Analysis suppression
Compulsive redosing
Emotion suppression

5-MeO-DiBF is sold for research purposes only and is not be utilized for any other purposes.

Etizolam

Etizolam (also known as Etilaam, Etizola, Sedekopan, Etizest, Pasaden or Depas) is a thienodiazepine derivative which is a benzodiazepine analog.

The etizolam molecule differs from a benzodiazepine in that the benzene ring has been replaced by a thiophene ring and triazole ring has been fused, making the drug a thienotriazolodiazepine.
It possesses amnesic,anxiolytic, anticonvulsant,hypnotic, sedative and skeletal muscle relaxant properties.

Etizolam, a thienodiazepine derivative, is absorbed fairly rapidly, with peak plasma levels achieved between 30 minutes and 2 hours. It has a mean elimination half life of about 3.5 hours.
In a study that compared the effectiveness of etizolam, alprazolam, and bromazepam for the treatment of generalized anxiety disorder, all three drugs retained their effectiveness over 2 weeks, but etizolam became more effective from 2 weeks to 4 weeks, a type of reverse tolerance.

Etizolam is sold for research purposes only and is not be utilized for any other purposes.

Flubromazepam

Flubromazepam is a long-lasting psychoactive substance of the benzodiazepine class which produces anxiolytic, sedative, muscle relaxant, depressant and amnesic effects.

Physical effects
Sedation – In terms of energy level alterations, this substance has the potential to become very sedating in a rapid-acting fashion. At higher doses, this can lead users to suddenly feel as if they are extremely sleep deprived and have not slept for days, forcing them to sit down and generally feel as if they are constantly on the verge of passing out. This sense of sleep deprivation increases proportional to dosage and eventually becomes powerful enough to force a person into complete unconsciousness.
Muscle relaxation
Physical euphoria
Motor control loss
Respiratory depression
Increased libido
Seizure suppression
Appetite enhancement – This effect is not particularly prominent, but is reported to occur in some people. It can have a synergistic effect when combined with cannabis.
Dizziness
Temporary erectile dysfunction

Paradoxical effects
Paradoxical reactions to benzodiazepines such as increased seizures (in epileptics), aggression, increased anxiety, violent behavior, loss of impulse control, irritability and suicidal behavior sometimes occur (although they are rare in the general population, with an incidence rate below 1%).[7][8]
These paradoxical effects occur with greater frequency in recreational abusers, individuals with mental disorders, children, and patients on high-dosage regimes.

Flubromazolam

Flubromazolam is a synthetic depressant substance of the benzodiazepine class which produces anxiolytic, disinhibiting, sedative, muscle relaxant, and memory suppressing effects when administered. It is incredibly potent (active in the microgram range) with an unusually long 18 hour duration.

Flubromazolam has been noted for its potential use in the short-term treatment of anxiety, insomnia, acute seizures, and the sedation of hospitalized patients.

It is worth noting that the sudden discontinuation of benzodiazepines can be potentially dangerous or life-threatening for individuals using regularly for extended periods of time, sometimes resulting in seizures or death.It is highly recommended to taper one’s dose by gradually lowering the amount taken each day for a prolonged period of time instead of stopping abruptly.

Flubromazolam is a chemical of the benzodiazepine class. Flubromazolam is named for the fluorine, bromine, and triazole substitutions on its core benzodiazepine skeleton (FLUorine-BROMine-AZOLe-AM).

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.

Flubromazolam has been described by some users as being one of the most euphoric benzodiazepines. It has been noted for its more pronounced sedative effects and hypnotic than anxiolytic effects.

Physical effects
Sedation
Motor control loss
Respiratory depression
Dizziness
Muscle relaxation

Flubromazolam is sold for research purposes only and is not be utilized for any other purposes.

Fluclotizolam

Fluclotizolam belongs to the Benzo class of chemicals, aka benzodiazepine.

A psychoactive substance, Fluclotizolam is available in 0.5mg blotter form. Its effects include hypnotic, sedative, and anticonvulsant attributes, and it is available for use by scientists interested in the pharmacology of benzodiazepines.

Fluclotizolam blotters and pellets are sold strictly for in vitro research only, and are not meant for human consumption.

Fluclotizolam (New)

Fluclotizolam Blotters belong to the Benzo class of chemicals, aka benzodiazepine.

A psychoactive substance, Flunitrazolam is available in 0.25mg blotter form. Its effects show is should include sedative and anticonvulsant effect, and it is available for use by scientists interested in the pharmacology of benzos.

Flunitrazolam blotters and pellets are sold strictly for in vitro research only, and are not meant for human consumption.

Isopropylphenidate (IPD)

Isopropylphenidate (also known as IPH, IPPH, and IPPD) is synthetic stimulant of the piperidine chemical class that produces stimulating, motivating, and focus enhancing effects when administered. It is a structural analog of the widely-prescribed ADHD medication methylphenidate and is reported to produce near identical cognitive and physical effects, albeit with less of a euphoric “rush” component and a drawn-out duration of action, properties that many find preferable for use as a study-aid or productivity enhancer.

Isopropylphenidate has been investigated for its potential use as a replacement for methylphenidate in the treatment of ADHD and related disorders.

Isopropylphenidate is a synthetic molecule of the substituted phenethylamine and piperidine classes. It contains a phenethylamine core featuring a phenyl ring bound to an amino (NH2) group via an ethyl chain. It is structurally similar to amphetamine, featuring a substitution at Rα which is then incorporated into a piperidine ring ending at the terminal amine of the phenethylamine chain.

These differences result in the substance having more notable dopaminergic activity than adrenergic activity compared to methylphenidate at equivalent effective dosages, and in the substance having a longer duration than methylphenidate and a greater potency than methylphenidate at a given dosage.

Isopropylphenidate is sold for research purposes only and is not be utilized for any other purposes.

Metizolam

Metizolam (also known as Desmethyletizolam) is a synthetic depressant of the thienodiazepine chemical class that reportedly produces etizolam-like effects such as anxiety suppression, disinhibition, sedation, muscle relaxation and memory suppression when administered. It is half as potent and has a 60% longer half-life than etizolam.

Metizolam, or desmethyletizolam, is a structural relative of benzodiazepines whereby the benzene ring has been replaced by a thiophene ring, classifying it as a thienodiazepine. It differs structurally from its parent compound etizolam through the removal of the methyl group on the triazole ring.

Metizolam contains a thiophene ring fused to a diazepine ring, which is a seven member ring with the two nitrogen constituents located at R1 and R4. Thiophene is a five member aromatic ring with one sulfur atom. This forms the thienodiazepine core of metizolam. An ethyl chain is bound to this bicyclic structure at R7.

Thienzodiazepines 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.[6] As this site is the most prolific inhibitory receptor set within the brain, its modulation results in the sedating (or calming effects) of metizolam on the nervous system.

Physical effects
Sedation
Motor control loss
Respiratory depression
Muscle relaxation
Dizziness

Cognitive effects
Anxiety suppression
Disinhibition
Thought deceleration
Analysis suppression
Euphoria
Compulsive redosing
Amnesia
Emotion suppression

Metizolam is sold for research purposes only and is not be utilized for any other purposes.

Nifoxipam

Nifoxipam is a synthetic depressant substance of the benzodiazepine chemical class that produces long-lived, typical benzodiazepine effects such as anxiety suppression, disinhibition, anticonvulsant, hypnotic, muscle relaxing, and amnesia when administered.

Nifoxipam has potential use for the short-term treatment of anxiety, insomnia, acute seizures, and the sedation of hospitalized patients.

Due to the high dependence-forming and addiction potential that this substance shares with members of the closely related benzodiazepine class, as well as its alcohol-like ability to induce dangerous disinhibitory black-out states, it is highly advised to use proper harm reduction practices if choosing to use this substance.

Nifoxipam 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. Nifoxipam, or 3-hydroxydesmethylflunitrazepam, is an active metabolite of flunitrazepam.

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.

Physical effects
Sedation
Motor control loss
Muscle relaxation
Dizziness
Respiratory depression

Nifoxipam is sold for research purposes only and is not be utilized for any other purposes.

Pyrazolam

Pyrazolam is a benzodiazepine derivative and subsequently “rediscovered” and sold as a research chemical starting in 2012.It is mainly an anxiolytic,but has also shown muscle relaxant,depressant and hypnotic effects at high doses.

It’s worth noting that the sudden discontinuation of benzodiazepines can be potentially dangerous or life-threatening for individuals using regularly for extended periods of time, sometimes resulting in seizures.
It is highly recommended to taper one’s dose by gradually lowering the amount taken each day for a prolonged period of time instead of stopping abruptly.

Pyrazolam 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.

Physical effects:
Sedation – In terms of energy level alterations, pyrazolam is considerably less sedating than other substances of the same class unless it is taken at heavy doses.
Dizziness
Motor control loss
Muscle relaxation
Respiratory depression

Paradoxical effects
Cognitive effects
Amnesia
Anxiety suppression
Thought deceleration
Analysis suppression
Disinhibition
Compulsive redosing
Delusions of sobriety
Dream potentiation

Pyrazolam is sold for research purposes only and is not be utilized for any other purposes.