Showing 49–64 of 106 results

Cannabis Seeds (Feminized)

Grow a high percentage (98% ) of feminized cannabis plants via our seeds here. You can save wasted time and efforts. Space and cultivation time as there’s no need to classify male and female plants.

Feminized cannabis seeds are designed to produce only female plants.

Usually, a cannabis seed can develop into a male or female plant; the entire process is determined by the sex expressing X and Y chromosomes. “Feminization” is a process of conditioning female plants to obtain male pollen needed for seed production.

A plant with two X chromosomes will be female 99% of the time, while regular cannabis seeds (XY genetic set) sometimes have a tendency to produce more male than female individuals.

Charge Plus

Buyrcbathsalts provides Charge Plus in powder form and in branded packaging.

Charge Plus contains a blend of several however the active chemical is: Ethylphenidate (EP).

Research Chemicals such as Charge Plus are for research only. No human consumption!

Ching

BRCShops.com provides Ching in powder form and in branded packaging.

Ching Powder contains a blend of several chemicals but the active chemical is: Ethylphenidate (EP).

Research Chemicals such as GoGaine are for research only. No human consumption!

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.

CXT-54 Herbal Blend

New CXT-54 blend on sale now in over 10 flavours.

All blends are supplied at our high strength blends with CXT-54.

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.

Diphenidine

Diphenidine is a lesser-known dissociative substance of the diarylethylamine class that produces dissociative and hallucinogenic effects when administered. It is structurally related to methoxphenidine and ephenidine.

Diphenidine is classified as an NMDA receptor antagonist. Members of this class induce a state known as “dissociative anesthesia” and are used in both medical and recreational contexts. These include arylcyclohexylamines like ketamine and phencyclidine (PCP), as well as dextromethorphan (DXM).

Anecdotal reports describe high doses of diphenidine producing “bizarre somatosensory phenomena and transient anterograde amnesia.

Diphenidine is a molecule of the diarylethylamine class. It contains a substituted phenethylamine skeleton with an additional phenyl ring bound to Rα. The terminal amino group of the phenethylamine chain is incorporated into a piperidine ring. Hence, diphenidine belongs to the piperidine dissociative class of compounds. Diphenidine is structurally analogous to MXP, lacking a 2-methoxy substitution on one of its phenyl rings.

Diphenidine acts as an NMDA receptor antagonist.NMDA receptors allow for electrical signals to pass between neurons in the brain and spinal column; for the signals to pass, the receptor must be open. Dissociatives close the NMDA receptors by blocking them. This disconnection of neurons leads to loss of feeling, difficulty moving, and eventually the famous “hole”.

Subjective effects
The general head space of diphenidine is often described as euphoric and clear-headed in comparison to that of ketamine and reminiscent of ephenidine at lower dosages. Moderate or higher dosages can sometimes unwillingly turn very confusing and dysphoric without any apparent cause.

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

Doob

Our new blends replace Doob.

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

Dr Buzz Pellets (New)

Dr Buzz, these pellets contain 85mg 6-APB and 15mg Nutmeg!

6-APB is similar to MDA, and is part of the phenethylamine/amphetamine classes, and the effects said to range from euphoria through to increased energy and empathy towards others.

BRCShops.com offers Dr Buzz Pellets with the active amount of 6-APB set at 85mg per pellet. It is not sold for human consumption.

Please check our local laws before ordering as 6-APB is not legal everywhere. This product ships from the Netherlands.

EG-018

EG-018 Previously an ingredient in some synthetic cannabis blends, this substance acts upon the cannabinoid receptors, and is a fairly potent agonist.

The chemical formula for EG-018 is C28H25NO.

As there has been little research carried out on 2NE1, it offers a great opportunity for you to study its effects, and gain a greater understanding of one of the newer cannabinoids on the market.

Formal Name
naphthalen-1-yl(9-pentyl-9H-carbazol-3-yl)methanone
Molecular Formula
C28H25NO
Formula Weight
391.5
Purity
≥98%
Formulation
A crystalline solid
λmax
219, 234, 277, 299, 340 nm
SMILES
O=C(C1=CC=CC2=C1C=CC=C2)C3=CC(C(C=CC=C4)=C4N5CCCCC)=C5C=C3
InChI Code
InChI=1S/C28H25NO/c1-2-3-8-18-29-26-15-7-6-13-23(26)25-19-21(16-17-27(25)29)28(30)24-14-9-11-20-10-4-5-12-22(20)24/h4-7,9-17,19H,2-3,8,18H2,1H3
InChI Key
FJMMDJDPNLZYLA-UHFFFAOYSA-N

We sell EG-018 for research purposes only. It should be applied in vitro, and is not suitable for human consumption.

Ephenidine

Ephenidine (also known as NEDPA and EPE) is a lesser-known dissociative substance of the diarylethylamine class. Ephenidine is an NMDA receptor antagonist that is structurally related to diarylethylamines like diphenidine and methoxphenidine. Notable effects include sedation, hallucinations, anesthesia, and out-of-body states, referred to as “dissociative anesthesia”.

Ephenidine and related diarylethylamines have been studied in humans as treatments for neurotoxic injuries.

Ephenidine is a molecule of the diarylethylamine class. It contains a substituted phenethylamine skeleton with an additional phenyl ring bound to Rα. An ethyl chain is bound to the terminal amine RN of the phenethylamine. Ephenidine is structurally analogous to diphenidine and MXP, but is not a piperidine dissociative. Ephenidine shares a diphenylethylamine skeleton with diphenidine and MXP, but lacks a piperidine substitution.

Ephenidine acts as an antagonist of the NMDA receptor (Ki = 66.4 nM).
The NMDA (N-methyl-D-aspartate) receptor is one of the major receptor subtypes for glutamate, the major excitatory neurotransmitter in the central nervous system (CNS). When NMDA channels are blocked,a loss of feeling (anesthesia), difficulty moving (immobilization), and at higher doses, the compound’s equivalent of the “K-hole” results.

Physical effects
Stimulation – This compound produces stimulating effects at lower doses which are less intense than that of diphenidine or methoxphenidine.
Tactile disconnection
Spatial disorientation
Pain relief
Cough suppression
Appetite suppression
Nausea

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

ETH-LAD (New)

6-Ethyl-6-nor-lysergic acid diethylamide (also known as N-Ethyl-nor-lysergic acid N,N-diethylamide,N-Ethyl-nor-LSD, and ETH-LAD is a lesser-known novel psychedelic of the lysergamide class.ETH-LAD is chemically similar to LSD and has a similar mechanism of action, acting primarily by stimulating serotonin receptors in the brain.

ETH-LAD has been shown to be moderately to significantly more potent than LSD itself in animal studies with an active dose reported at between 40 and 100 micrograms.

ETH-LAD has also been reported to more readily produce adverse physical effects such as severe and persisting nausea, temperature dysregulation, and generalized bodily discomfort, particularly at higher doses.This has been speculated to owe itself to an unusually sensitive and unpredictable dose-response curve, as low to common dose experiences are generally described as being very manageable and non-threatening.

While the subjective effects of ETH-LAD are reported to largely overlap with those of LSD, it has been noted for the tendency to be more visually and auditorily distortive, introspective, analytical and immersive yet with the capacity to produce pronounced discomforting physical effects like severe and persisting nausea, and temperature dysregulation past the common dose range in a seemingly unpredictable manner.

ETH-LAD is sold for research purposes only and is not be utilized for any other purposes

Ethylphenidate

Ethylphenidate (also known as EPH) is a stimulant substance of the piperidine class that produces traditional stimulant effects when administered.

It is a closely related analog of methylphenidate (brand names Ritalin, Concerta). The two substances have very similar pharmacological mechanisms but discernible differences in their subjective effects with ethylphenidate often considered to be recreational.

Physical effects
Stimulation – Ethylphenidate is usually reported to be energetic and stimulating in a fashion that is distinct but much weaker than that of amphetamine or methamphetamine and stronger than that of modafinil and caffeine.

Dehydration
Appetite suppression
Vasoconstriction– Norepinephrine reuptake inhibition causes the sympathetic nervous system to constrict vessels and puts strain on the cardiovascular system with prolonged use.
Increased heart rate
Increased blood pressure
Teeth grinding

Cognitive effects
Focus enhancement – This component is most effective at low to moderate dosages as anything higher will usually impair concentration.
Euphoria – The euphoric rush associated with ethylphenidate use, as result of dopamine reuptake inhibition, is very short-lived and compulsive, similarly to that of cocaine.
Time distortion – This can be described as the experience of time speeding up and passing much quicker than it usually would when sober.
Thought acceleration
Analysis enhancement
Wakefulness
Motivation enhancement
Increased music appreciation

Ethylphenidate 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.

Evoke

With its blend of research chemicals, including Ethylphenidate, Evoke is a branded psychostimulant suitable for research into the effects of multiple chemicals working in conjunction with one another.

A 100mg dose is enough to provide an extensive data set, such as whether there is any competitive binding for the same receptor when applied to an in vitro membrane.

Evoke is sold in powder form, and is available for research purposes only. It is NOT intended for human consumption.