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THJ-018
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HomePure Research Chemicals THJ-018
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THJ-018

$270 – $10,800

Specification

Product Name: THJ-018
IUPAC Name: 1-naphthalenyl(1-pentyl-1H-indazol-3-yl)-methanone
Other Names: 1-naphthalenyl(1-pentyl-1H-indazol-3-yl)-methanone
Cas Number: 1364933-55-0
Molecular Formula: C23H22N2O
Molar Mass: 342.4 g/mol
Effect: stimulant, psychedelic
Purity of the substance: 99.9%
Physical properties: Crystals, powder

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SKU: N/A Categories: Cannabinoids, Pure Research Chemicals Tags: Buy THJ-018 Online, THJ-018 Cannabinoid Australia, THJ-018 Cannabinoid UK, THJ-018 Cannabinoid USA
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Description

THJ-018 Synthetic Cannabinoid For Sale

THJ-018 (SGT-17) is an indazole derivative of JWH-018; it is a synthetic cannabinoid drug sold online as a designer drug.

SGT-17 is a synthetic cannabinoid that is the indazole analog of JWH-018. It has been sold online as a designer drug with no reported recreational use.

THJ-018 (SGT-17, AM-2233) is a synthetic cannabinoid that acts as a potent agonist for the cannabinoid receptors CB1 and CB2.

THJ-018 (SGT-17) is a synthetic cannabinoid indazole analog of JWH-018 and has been sold online as a designer drug. It has been associated with cases of intoxication and fatalities, particularly in the United States, before being regulated.

THJ-018 (SGT-17) is a synthetic cannabinoid indazole analog of JWH-018 and has been sold online as a designer drug. Propylhexedrine exhibits stimulant activity in animals, but it lacks both the piperidine group and a carbonyl group found in methamphetamine.

THJ-018 is a synthetic cannabinoid indazole analog of JWH-018 and has been sold online as a designer drug. The drug has never been properly researched in humans. Still, it is believed to act as a potent agonist for the cannabinoid receptors, as a full agonist at CB1 receptors and as a partial agonist at CB2 receptors. It has a high affinity for these sites, with an affinity for the human CB1 receptor approximately equal to that of JWH-018.

THJ-018 is a synthetic cannabinoid sold online as a designer drug. It has never been properly researched in humans, but it is believed to act as a potent agonist at the cannabinoid receptors and as a full agonist at CB1.

THJ-018 is a synthetic cannabinoid that acts as a potent agonist of the cannabinoid receptors. It binds to CB1 and CB2 receptors with high affinity and acts as a full agonist but shows a higher affinity for CB1 receptors than JWH-018.

THJ-018 is a synthetic cannabinoid that acts as a potent agonist for the CB1 and CB2 receptors, with a similar affinity to the cannabis derivative JWH-018.

Cannabinoids are a class of diverse chemical compounds active in the brain and throughout the peripheral nervous system. The best-known cannabinoid is the phytocannabinoid tetrahydrocannabinol (THC), the primary psychoactive compound in cannabis.

THJ-018 is a synthetic cannabinoid that was first reported in 2009.

THJ-018 is an indazole analog of JWH-018, invented by Alexandros Makriyannis at Northeastern University in 2009.

THJ-018 is a synthetic cannabinoid that binds to the CB1 receptor. Its chemical structure is similar to JWH-18 and AM-2201, which are illegal under the Controlled Substances Act. First detected in the Spring of 2013, THJ-018 has been involved in several documented intoxications, hospitalizations and deaths.

THJ-018 is a synthetic cannabinoid that resembles JWH-18, Pravadoline and Am-2201. It is often found in combination with other active ingredients.

THJ-018 is a synthetic cannabinoid that binds to CB1 cannabinoid receptors in the brain, which are responsible for pain perception, memory, coordination and time perception.

THJ-018, also known as APICA, is a synthetic cannabinoid drug chemically similar to JWH-18 and AM-2201. It is slightly less potent than JWH-18.

THJ-018 is a synthetic cannabinoid that is the indazole analog of JWH-018, a substance sold as a designer drug.

THJ-018 (SGT-17) is a synthetic cannabinoid indazole analog of JWH-018 and has been sold online as a designer drug. Commonly known as 4-methyl-naphthyl indazole, this compound was likely first synthesized by Pfizer in 2006.

This is a synthetic cannabinoid that is the indazole analog of JWH-018.

It is an analog of JWH-018, with a higher affinity for CB1 receptors and a lower affinity for CB2 receptors

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