Showing 81–96 of 106 results

Methiopropamine (MPA)

Methiopropamine (MPA) is a thiophene ring-based structural analogue of methamphetamine. Chemically, it is not a phenethylamine or amphetamine, nor is it their functional analog.

Methiopropamine, or 1-(thiophen-2-yl)-2-methylaminopropane, is a synthetic molecule of the thiophene class. It is a structural analogue to methamphetamine. It contains a thiophene ring bound to an amino (NH2) group through an ethyl chain with an additional methyl substitution at Rα. Methiopropamine contains an additional methyl substitution at RN (similarly to MDMA and methamphetamine).

Physical effects
Stimulation – In terms of its effects on the physical energy levels of the user, methiopropamine is usually considered to be mildly to moderately energetic and stimulating in a fashion that is considerably weaker in comparison to that of traditional recreational stimulants such as amphetamine, MDMA or cocaine.
Spontaneous tactile sensations
Increased heart rate
Appetite suppression
Increased perspiration
Increased libido
Temperature regulation suppression
Teeth grinding

Cognitive effects
Focus enhancement
Cognitive euphoria
Wakefulness
Thought acceleration
Thought organization
Analysis enhancement
Motivation enhancement
Compulsive redosing
Increased music appreciation

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

Methoxetamine (MXE)

3-MeO-2′-Oxo-PCE (commonly known as Methoxetamine, MXE, Mexxy, among others) is a dissociative substance of the arylcyclohexylamine class that produces ketamine-like dissociative effects when administered. It is structurally related to ketamine, PCE, and 3-MeO-PCP.

Methoxetamine, or (RS)2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone, is classed as an arylcyclohexylamine. Arylcyclohexylamines are named for their structures which include a cyclohexane ring bound to an aromatic ring along with an amine group.

MXE acts as a non-competitive NMDA receptor antagonist and serotonin-reuptake inhibitor.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 an almost identical equivalent of the famous “k-hole.” MXE was reported to be similar to ketamine, despite being stronger and having a longer duration.

Because of its structural similarity to 3-HO-PCP, it was falsely believed to carry opioid properties.

Physical effects
Sedation
Spontaneous bodily sensations
Perception of bodily lightness
Motor control loss
Spatial disorientation
Tactile suppression
Pain relief
Physical autonomy
Dizziness
Nausea
Optical sliding
Orgasm suppression

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

Methoxphenidine (MXP)

Methoxphenidine (also known as MXP) is a lesser-known dissociative substance of the diarylethylamine class that produces dissociative and hallucinogenic effects when administered. It is structurally related to diarylethylamines like diphenidine and ephenidine.

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

Methoxphenidine along with related diarylethylamines have been studied as treatments for neurotoxic injuries.

Physical effects
Tactile disconnection – This results in typical states of progressive physical disconnection but is far more consciously controllable than that of other dissociatives.
Pain relief
Spontaneous physical sensations
Tactile suppression
Motor control loss
Euphoria
Perception of bodily lightness
Dizziness – Although uncommon, some people report dizziness under the influence of MXP.
Physical autonomy
Spatial disorientation
Orgasm suppression
Gait alteration

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

Methylone

3,4-Methylenedioxy-N-methcathinone (also known as M1, MDMC, βk-MDMA, and Methylone) is an entactogenic and stimulant substance of the cathinone chemical class that produces a mixture of entactogenic, stimulating, and euphoric effects when administered.
This compound is often used as a substitute for MDMA due to similarities in their effects.

Methylone, or 3,4-methylenedioxy-N-methylcathinone, is a synthetic molecule of the cathinone family. Cathinones are structurally similar to amphetamines, they contain a phenethylamine core featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain with an additional methyl substitution at Rα.
Methylone contains an methyl substitution at RN, a substitution which is shared with MDMA, mephedrone, and certain other stimulants. Methylone contains additional substitutions at R3 and R4 of the phenyl ring with oxygen groups.

Methylone acts as a mixed reuptake inhibitor/releasing agent of serotonin, norepinephrine, and dopamine.These neurotransmitters are thought to be responsible for regulating pleasure, motivation, focus, and sense of well-being.
In comparison to MDMA, it has approximately 3x lower affinity for the serotonin transporter.

Stimulation – In terms of its effects on the user’s physical energy levels, methylone is commonly considered to be extremely stimulating and energetic. This encourages activities such as running, climbing and dancing in a way that makes methylone a popular choice for musical events such as festivals and raves.
Spontaneous physical sensations
Tactile enhancement
Increased heart rate
Increased perspiration
Increased blood pressure
Temperature regulation suppression
Increased bodily temperature
Dehydration

Methylone 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.

Mexedrone

BUY IT NOW: BRCShops.com has Mexedrone Crystal in stock ready to sell, a EU legal Cathinone

Mexedrone is 100% legal across Europe (NOT including UK).

The chemical name is: 3methoxy-2 (methylamino)-1-(p-tolyl)propan-1-one or AKA: 4-mmc-oMe

Research Chemicals such as Mexedrone are for research only. Not human consumption!

Mextasy

Buyrcbathsalts.com now stocks Mextasy Pellets, 250mg Mexedrone per pellet..

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

MMB-CHMINACA

MDMB-CHMICA (also incorrectly known as MMB-CHMINACA) is an indole-based synthetic cannabinoid that is a potent agonist of the CB1 receptor and has been sold online as a designer drug.While MDMB-CHMICA was initially sold under the name “MMB-CHMINACA”,the compound corresponding to this code name (i.e. the isopropyl instead of t-butyl analogue of MDMB-CHMINACA).

MDMB-CHMICA acts as a highly potent full agonist of the CB1 receptor with an efficacy of 94% and an EC50 value of 0.14 nM, which is approximately 8 times lower than the EC50 of JWH-018 (1.13 nM) and twofold lower than AB-CHMINACA (0.27 nM).

MDMB-CHMICA’s main metabolic reactions comprise mono-hydroxylations and hydrolysis of the carboxylic ester function.

Side effects such as unconsciousness or coma, hyperemesis, nausea, seizures, convulsions, tachycardia, bradycardia, mydriasis, syncope, spontaneous urinating and defecating, shortness of breath, somnolence, respiratory acidosis, metabolic acidosis, collapse, lower limbs paralysis, chest pain, aggression and severe disturbance of behaviour were reported.

MDMB-CHMICA is sold for research purposes only and is not be utilized for any other purposes.

Modafiendz

N-Methyl-4,4′-difluoro-modafinil (also known as N-Methylbisfluoromodafinil, Dehydroxyfluorafinil, and Modafiendz) is an obscure nootropic of the benzhydryl class with no history of research. Although it is closely related on a structural level to adrafinil and modafinil, neither a pharmacological nor a safety-profile similarity should be assumed.

N-methyl-4,4-difluoro-modafinil, or 2-{[bis(4-fluorophenyl)methyl]sulfinyl}-N-methylacetamide, is a synthetic molecule of the benzhydryl class. Benzhydryl compounds are comprised of two benzene rings attached to a single carbon molecule. N-methylbisfluoromodafinil contains a fluorine group bound to each benzene ring at R4.

Physical effects
Stimulation – In terms of its effects on the user’s physical energy levels, N-methylbisfluoromodafinil is commonly considered to be stimulating and energetic, but can be considered as much less stimulating when compared to amphetamine. This stimulation encourages physical movement and activities such as running, playing sports, socializing, and/or exercising.
Dehydration
Headaches
Appetite suppression
Diarrhea
Increased heart rate
Dizziness
Nausea

Cognitive effects
Focus enhancement
Wakefulness
Thought acceleration
Memory enhancement
Motivation enhancement
Increased music appreciation
Emotion enhancement
Anxiety

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

MPA & 5MD

A unique blend of 5-MeO-Dalt (5-MD) and MPA (Methiopropamine), these pellets offer an excellent opportunity for researchers to study the ways in which the two chemicals work together.

As they both bind to the same family of receptors, it presents an ideal method by which to discover how they compete with, as well as react to, one another, without the need to source and weigh the constituent elements.

The effects of 5-MD & MPA pellets are said to be similar to that of Benzo Fury and M&Ms, with euphoria and increased energy being common.

Buyrcbathsalts.com sells 5-MD & MPA pellets for research purposes only. It is not meant for human ingestion.

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.

Nitracaine

Nitracaine is a chemical which many compare to the Dimethoaine series.

Early testing on Nitracaine indicates that it works to inhibit the reuptake of dopamine and possibly also as a dopamine receptor ligand.

It is closely related to dimethocaine.

This chemical is sold only for use in approved laboratory settings and not for human consumption!

NM-2201

NM-2201 (also known as CBL-2201) is an indole-based synthetic cannabinoid that presumably has similar properties to the closely related 5F-PB-22 and NNE1, which are both full agonists and unselectively bind to CB1 and CB2 receptors with low nanomolar affinity.

NM-2201 acts as a full agonist with a binding affinity of 0.332nM at CB1 and 0.732nM at CB2 cannabinoid receptors.

NM-2201 is similar to

EAM-2201
MAM-2201
THJ-2201
SDB-005

NM-2201 is sold for research purposes only and is not be utilized for any other purposes.

NM-2AI

NM-2-AI (N-methyl-2-aminoindane) is a psychoactive drug and research chemical with stimulant properties of the aminoindane chemical class.

In comparison to the more prevalent close chemical relative known as 2-AI, this compound has a lower potency, a longer duration and very similar effects. Besides this, very little is known about this substance.

NM-2-AI, or N-methyl-2-AI, is the N-methylated derivative of 2-Aminoindane and is analogous to amphetamine. It features the R3 terminal carbon of the propane chain of amphetamine bound to the benzene ring.

Physical effects
Stimulation – In terms of its effects on the physical energy levels of the user, NM-2-AI is usually considered to be energetic and stimulating in a fashion that is similar to that of amphetamine but stronger than that of modafinil or caffeine.
Increased heart rate
Dehydration
Appetite suppression
Nausea
Temporary erectile dysfunction
Increased perspiration
Increased blood pressure
Teeth grinding

After effects
Anxiety
Cognitive fatigue
Depression
Irritability
Motivation suppression
Thought deceleration
Wakefulness

NM-2-AI is sold for research purposes only and is not be utilized for any other purposes.

Pentedrone

Pentedrone (also known as drone) is a lesser-known stimulant substance of the cathinone class. Pentedrone belongs to a group of compounds known as substituted cathinones. Pentedrone acts as a norepinephrine-dopamine reuptake inhibitor (NDRI).

Pentedrone is known to come in the form of either a white powder or crystallized shards which users can ingest to produce a powerful, fast-acting but short-lived euphoric stimulant effects which are comparable to those of crack-cocaine, N-ethylpentedrone and a-PVP-type compounds, particularly when they are insufflated, vaporized or injected.

Starting with the advent of MDPV, research chemical stimulants like pentedrone have gained notoriety for its tendency to induce compulsive redosing and addictive behaviors in a seemingly significant percentage of its users as well the ability to readily induce paranoid, delusional states and stimulant psychosis when abused.

Physical effects
Stimulation – In terms of its effects on the user’s physical energy levels, pentedrone can be considered to be very stimulating and energetic.
Spontaneous physical sensations
Physical euphoria
Dehydration
Vasoconstriction
Tactile enhancement
Abnormal heartbeat
Increased heart rate
Increased blood pressure
Increased perspiration
Appetite suppression
Focus enhancement
Temporary erectile dysfunction
Teeth grinding – At common doses, this component has been reported considerably to less intense when compared with that of MDMA or other cathinones like a-PHP or NEP.

Pentedrone 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.