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PROTONITAZENE .HCL
protonitazene is a benzimidazole derived opioid analgesic drug related to etonitazene, which has been sold as a designer drug. It has only around one third the potency of etonitazene in animal studies, but it is likely less potent in humans as was seen wi
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MDA-19
MDA-19 is a drug that acts as a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor, though with some variation between species. In animal studies it was effective for the treatment
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5F-MDA-19
5F-MDA-19 is a drug that acts as a potent and selective agonist for the cannabinoid receptor CB2, with reasonable selectivity over the psychoactive CB1 receptor, though with some variation between species. In animal studies it was effective for the treatm
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3C-P .HCL
3C-P is a psychedelic phenethylamine. It has structural and pharmacodynamic properties similar to the drugs escaline, proscaline. Little information exists on the human pharmacology of 3C-P, but a psychedelic dosage appears to be 20–40 mg, and is accompan
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Allylescaline .HCL
Allylescaline (4-allyloxy-3,5-dimethoxyphenethylamine) is a lesser-known psychedelic drug. It is closely related in structure to mescaline. Allylescaline was first synthesized by Otakar Leminger in 1972. The compound was later synthesized by Alexander Shu
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Deschloroclotizolam
Deschloroclotizolam is a thienotriazolodiazepine derivative which was first synthesised in 1979, but was never marketed. It has subsequently been sold as a designer drug, first being definitively identified in 2017. This product is intended for laborato
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FLUCLOTIZOLAM
Fluclotizolam is a thienotriazolodiazepine derivative which was first synthesised in 1979, but was never marketed. It has subsequently been sold as a designer drug, first being definitively identified in 2017. This product is intended for laboratory rese
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ETONITAZEPIPNE .HCL
ETONITAZEPIPNE is an kind of drug related to etonitazene, which was first reported in 1957,and has been shown to have approximately 100 times the potency of morphine by central routes of administration,but if used orally it has been shown to have approxi
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Nitromethaqualone
Nitromethaqualone is an kind of methaqualone that has similar sedative and hypnotic properties. It is significantly more potent (10x) compared to the parent compound; the typical dose is approximately 25 mg. However, the aromatic nitro group is metabolise
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Desmethylmoramide .HCL
Desmethylmoramide (INN) is an opioid analgesic related to dextromoramide (the active (+)-isomer of moramide) that was synthesized and characterized in the late 1950s but was never marketed… This product is intended for research and forensic applications.
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Methylmethaqualone
Methylmethaqualone (MMQ) is a quinazolinone and an kind of methaqualone that has similar sedative and hypnotic properties to its parent compound (resulting from its agonist activity at the β subtype of the GABAA receptor), and is around the same potency.
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Emylcamate
Emylcamate (marketed as Striatran by Merck) is an anxiolytic and muscle relaxant. It was patented in the US in 1961 (US Patent 2,972,564) and advertised for the treatment of anxiety and tension. It was claimed to be superior to meprobamate, which was the
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ALD-52 .HCL.POWDER
ALD-52, also known as 1-acetyl-LSD, is a chemical of lysergic acid diethylamide (LSD). It was originally discovered by Albert Hofmann but was not widely studied until the rise in popularity of psychedelics in the 1960s. ALD-52 gained public notoriety wh
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DIPYANONE. HCL
DIPYANONE is a strong opioid analgesic drug, used for very severe pain in cases where other analgesics are unsuitable, for instance where morphine is indicated but cannot be used due to the patient being allergic to morphine… This product is intended for
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3-CPM .LARGE CRYSTAL
3-Chlorinephenmetrazine is a halogenated phenmetrazine derivative. Halogenated amphetamines are psychostimulatory designer drugs that inhibit the uptake of monoamine neurotransmitters.The physiological and toxicological properties of this compound are not
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FLUBROMAZEPAM
Flubromazepam is a benzodiazepine derivative which was first synthesized in 1960, but was never marketed and did not receive any further attention or study until late 2012 when it appeared on the grey market as a novel designer drug. It is a structural
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4C-MAR .POWDER
4-Chlorine-4-methylaminorex (4C-4-MAR) is a stimulant drug of the 2-amino-5-aryloxazoline class that was first synthesized in 1960 by McNeil Laboratories 4C-MAR has effects comparable to methamphetamine but with a longer duration. It produces long-lasti
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ETONITAZEPYNE .HCL
ETONITAZEPYNE is an analgesic drug related to etonitazene, which was first reported in 1957,and has been shown to have approximately 200 times the potency of morphine by central routes of administration,but if used orally it has been shown to have approxi
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4B-MAR .POWDER
4-Bromo-4-methylaminorex (4B-4-MAR) is a stimulant drug of the 2-amino-5-aryloxazoline class that was first synthesized in 1960 by McNeil Laboratories 4B-MAR has effects comparable to methamphetamine but with a longer duration. It produces long-lasting
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BUTONITAZENE .HCL
BUTONITAZENE is an analgesic drug related to etonitazene, which was first reported in 1957,and has been shown to have approximately 50 times the potency of morphine by central routes of administration,but if used orally it has been shown to have approxima
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A-PiHP .LARGE CRYSTAL
α-PHiP (also known as α-PiHP), is a stimulant drug of the cathinone class that has been sold online as a designer drug. It is a structural isomer of pyrovalerone, with the methyl group shifted from the 4-position of the aromatic ring to the 4-position of
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5-Chloro-αMT .HCL
5-Chloro-α-methyltryptamine (5-Chloro-αMT), also known as PAL-542, is a tryptamine derivative related to α-methyltryptamine (αMT) and one of only a few known specific serotonin-dopamine releasing agents (SDRAs).It has been investigated in animals as a pot
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4F-MAR .POWDER
4-Fluoro-4-methylaminorex (4F-4-MAR) is a stimulant drug of the 2-amino-5-aryloxazoline class that was first synthesized in 1960 by McNeil Laboratories 4F-MAR has effects comparable to methamphetamine but with a longer duration. It produces long-lasting
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ETAZENE .HCL
Desnitroetonitazene (Etazen, Etazene, Etazone) is a benzimidazole derived opioid analgesic drug, which was originally developed in the late 1950s alongside etonitazene and a range of related derivatives. It is many times less potent than etonitazene itsel
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A-D2PV .LARGE CRYSTAL
Alpha- D2PV is a synthetic stimulant drug of the cathinone class developed in the middle of 2020 which has been reported as a novel designer drug. α- D2PV is a substituted homologue of α-PVP, having an Phenylacetyl replaced the alkyl side chain,regarding
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Deschloroetizolam
Deschloroetizolam (also known as Etizolam-2) is a thienotriazolodiazepine that is the dechlorinated of the closely related to etizolam. The compound has been sold as a designer drug… This product is intended for laboratory research purposes only and are
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3-CL-PCP .LARGE CRYSTAL
3-Chlorophencyclidine (3-CL-PCP) is a dissociative anesthetic drug with hallucinogenic and sedative effects that has been sold as a research chemical. It is around the same potency as phencyclidine, but has slightly different effects due to its altered bi
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METONITAZENE .HCL
Metonitazene is an analgesic drug related to etonitazene, which was first reported in 1957,and has been shown to have approximately 100 times the potency of morphine by central routes of administration,but if used orally it has been shown to have approxim
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FLUONITAZENE.HCL
FLUONITAZENE.HCL: Formal Name : N,N-diethyl-2-(2-(4-fluorobenzyl)-5-nitro-1H-benzo[d]imidazol-1-yl)ethan-1-amine Chemical Formula: C20H23FN4O2 Molecular Weight: 370.43
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25B-NBOH .HCL
25B-NBOH .HCL Iupac name: 2-({[2-(4-bromo-2,5-dimethoxyphenyl)ethyl]amino}methyl)phenol CAS number: 1335331-46-8 Molecular Weight:365.06 g/mol Chemical Formula: C17H20BrNO3
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3-FLUORO-PCP .LARGE CRYSTAL
3-FLUORO-PCP .LARGE CRYSTAL IUPAC Name: 1-(1-(3-fluorophenyl)cyclohexyl)piperidine Molecular Formula: C17H24FN Molecular Mass: 261.38
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5-CL-DMT .FUMARATE
5-CL-DMT .FUMARATE: Iupac name: 2-(5-chloro-1H-indol-3-yl)-N,N-dimethylethan-1-amine Synonyms: 5-CL-N,N-dimethyltryptamine Chemical Formula: C12H15ClN2 Molecular Weight: 222.72
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5-Bromo-DMT .FUMARATE
5-Bromo-DMT .FUMARATE: Iupac name: 2-(5-Bromo-1H-indol-3-yl)-N,N-dimethylethan-1-amine Synonyms: 5-bromo-N,N-dimethyltryptamine CAS NO: 17274-65-6 Chemical Formula: C12H15BrN2 Molecular Weight: 267.170 g•mol−1
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METODESNITAZENE.HCL
METODESNITAZENE is an analgesic drug related to Metonitazene which was first reported in 1957… Its effects are similar to other opioids like fent including analgesia, euphoria, sleepiness Adverse effects include vomiting, and respiratory depression that
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CLONAZOLAM
Clonazolam, also called Clonitrazolam,is a drug which is a benzodiazepine derivative related to Clonazepam. This product is intended for laboratory research purposes only and are not to be used for any other purposes.
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PYRAZOLAM
Pyrazolam (SH-I-04)is a benzodiazepine derivative originally developed by a team led by Leo Sternbach at Hoffman-La Roche in the 1970s, and subsequently "rediscovered" and sold as a designer drug starting in 2012. Pyrazolam has structural similarities t
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Cannabidiol (CBD).POWDER
Cannabidiol (CBD) is a phytocannabinoid discovered in 1940. It is one of 113 identified cannabinoids in cannabis plants and accounts for up to 40% of the plant's extract.In 2018, clinical research on cannabidiol included preliminary studies of anxiety, co
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A-PCYP .LARGE CRYSTAL
alpha -pcyp is a synthetic stimulant drug of the cathinone class developed in the middle of 2019 which has been reported as a novel designer drug. α-pcyp is a substituted homologue of α-PVP, having an cyclohexane replaced the alkyl side chain,regarding t
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BTCP. CRYSTAL
Benocyclidine (BTCP) is a derivative of phencyclidine with a benzothiophenyl group instead of a phenyl ring. It acts as a potent and selective dopamine reuptake inhibitor (IC50 = 8 nM) with negligible affinity for the NMDA receptor-linked phencyclidine r
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4-AcO-EPT .FUMARATE
4- Acetoxy -N-ethyl-N-propyltryptamine (also known as 4-AcO-EPT) is a novel synthetic psychedelic substance of the tryptamine chemical class that produces psychedelic effects when administered. It is structurally related to (4-ACO-DMT), the active compone
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4-AcO-DET .FUMARATE
4-Acetoxy-DET (4-Acetoxy-N,N-diethyltryptamine), also known as ethacetin, ethylacybin or 4-AcO-DET is a psychedelic tryptamine. It was first synthesized in 1958 by Albert Hofmann in the Sandoz lab. It is expected that the compound is quickly into the fr
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adb-butinaca
ADB-BUTINACA is a cannabinoid designer drug that is an ingredient in some synthetic cannabis products. It is a potent agonist of the CB1 receptor and CB2 receptor with EC50 values of 0.52 nM and 0.88 nM respectively. Like MDMB-BUTINACA, this compound cont
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MDPEP .POWDER
MDPEP is a stimulant of the cath class originally developed in the 1960s,which has been reported as a novel designer drug. It is closely related to the potent stimulant MDPV though with slightly milder effects, and has been used as an alternative in some
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Sl-164
SL-164 is methaqualone developed in the late 1960s by a team at Sumitomo. SL-164 has similar sedative, hypnotic and anticonvulsant properties to the parent compound, but was never marketed for clinical use. This product is intended for laboratory resear
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2F-VIMINOL.FREEBASE WITH CYCLODEXTRIN COATED
2F-VIMINOL is an opioid analgesic developed by a team at the drug company Zambon in the 1960s.. 2F-VIMINOL is based on the α-pyrryl-2-aminoethanol structure, unlike any other class of opioids… 2F-VIMINOL has both antitussive (cough suppressing) and anal
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NDH.CRYSTAL
NDH (also known as n-isobutyl-hexedrone) is a stimulant research chemical belonging to the cathinone group. isobutyl-hexedrone's stimulation is believed to be caused by its affinity as an NDRI (norepinephrine-dopamine reuptake inhibitor); however, there h
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2-METHYL-AP-237.HCL .LARGE CRYSTAL
2-METHYL-AP-237 is an opioid analgesic drug that was widely used in China to treat pain in cancer patients as of 1986.It is one of the most potent compound among a series of analgesic acyl piperazines compounds first synthesized and reported in Japan in
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PIPERIDYLTHIAMBUTENE .HCL
Piperidylthiambutene (Piperidinohton) is an opioid analgesic drug from the thiambutene family, which has around the same potency as morphine. If sold / was obtained for the purpose of human consumption it could be considered a controlled substance in some
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4F-MPH. HCL. POWDER
4-Fluoromethylphenidate (also known as 4-FMPH and 4F-MPH) is a stimulant drug that acts as a higher potency dopamine reuptake inhibitor than the closely related methylphenidate 4-Fluoromethylphenidate was studied further along with of (TMP) to assess th
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3-HO-PCP .LARGE CRYSTAL
3-Hydroxyphencyclidine (3-HO-PCP) is a dissociative hallucinogen of the arylcyclohexylamine class related to PCP that has been sold online as a designer drug. This product is intended for laboratory research purposes only and are not to be used for any o
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25E-NBOH .HCL
25E-NBOH (NBOH-2C-E) is a derivative of the phenethylamine 2C-E. It acts in a similar manner to related compounds such as 25I-NBOH which are potent agonists at the 5HT2A receptor.25E-NBOH has been sold as a drug and produces similar effects in humans to r
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4-FEA .POWDER
4-Fluoroethamphetamine (also known as 4-FEA) is a novel synthetic ring-substituted fluorinated am compound that produces a mixture of entactogenic and stimulant effects when administered. 4-FEA is structurally related to a series of designer fluorinated s
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ISOPROPYLPHENIDATE.HCL.CRYSTAL
ISOPROPYLPHENIDATE (also known as IPH and IPPD) is a piperidine based stimulant RC, closely related to ethylphenidate, but with the ethyl ester replaced by an isopropyl ester. This product is intended for forensic and research purposes.
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PRE-084 .HCL
PRE-084 is a sigma receptor agonist, selective for the σ1 subtype. It has nootropic and antidepressant actions in animal studies, as well as antitussive and reinforcing effects.PRE-084 increases the expression of GDNF… High affinity, selective σ1 agonist
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vx-809
VX-809 is a novel CFTR corrector that modulates the folding and trafficking of CFTR protein. VX-809 stabilizes an N-terminal domain in CFTR that contains only MSD1 (membrane-spanning domain 1) and efficaciously restores function to CFTR forms that have mi
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O-DSMT .HCL
O-Desmethyltramadol (O-DSMT) is an opioid analgesic and an active metabolite ,It has little to no history of human usage but is easily accessible through the use of certain online research chemical vendors. In comparison to tramadol, O-DSMT lacks any stim
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BROMAZOLAM
BROMAZOLAM is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative, and antidepressant properties, it was never FDA approved and was never available to the public. This product is intended for laboratory research purposes only
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FLUNITRAZOLAM
Flunitrazolam is a benzodiazepine derivative. It possesses anxiolytic, anticonvulsant, sedative, and antidepressant properties, Super potent, very hypnotic, king of benzos. it was never FDA approved and was never available to the public. This product is
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3-HYDROXYPHENAZEPAM
3-HYDROXYPHENAZEPAM is a benzodiazepine with hypnotic, sedative, anxiolytic, and anticonvulsant properties, Relative to phenazepam, 3-hydroxyphenazepam has diminished myorelaxant properties, but is about equivalent in most other regards.Like other benzodi
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4-AcO-DMT .FUMARATE
4-AcO-DMT (also known as O-Acetylpsilocin, 4-Acetoxy-DMT, or Psilacetin) is a synthetically produced psychedelic drug which has been suggested by David Nichols to be a potentially useful alternative to psilocybin for pharmacological studies as they are bo
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4-HO-MET .FUMARATE
4-HO-MET belonging to the class of Tryptamines, it is said to have effects almost identical to psilocin according to Alexander Shulgin who first synthesized the compound,it is not scheduled in the United States. This product is intended for research and
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DPT .HCL
DPT belonging to the tryptamine family, first reported in 1973,It is found either as its crystalline hydrochloride salt or as an oily or crystalline base,it is legal worldwide currently. This product is intended for research and forensic applications.
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