What is 6-APDB ?

6-APDB ,6-(2-Aminopropyl)-2,3-dihydrobenzofuran (4-Desoxy-MDA, EMA-3) is a stimulant and entactogen drug of the phenethylamine and amphetamine classes. It’s an analogue of MDA where the heterocyclic 4-position oxygen from the 3,4-methylenedioxy ring has been replaced with a methylene bridge. 5-APDB (3-Desoxy-MDA) is an analogue of 6-APDB where the 3 position oxygen has been replaced with a methylene instead. It along with 5-APDB, was first synthesized by David E. Nichols in the early 1990s while investigating non neurotoxic MDMA analogues. Buy 6-APDB online

6-APDB Buy 6-APDB online

In animal studies, 6-APDB fully substitutes for MBDB and MMAI but not for amphetamine or LSD. In vitro, 6-APDB shown to inhibit the reuptake of serotonin, dopamine, and norepinephrine with IC50 values of 322 nM, 1,997 nM, and 980 nM, respectively. These values are very similar to those of MDA, but with those for the catecholamines slightly lower in comparison, perhaps more similarly to MDMA. In contrast, 5-APDB is highly selective for serotonin. Though 6-APDB does not substitute for amphetamine in rats at the doses used in referenced study, based on its in vitro profile it suggested that it may have amphetamine-like effects at higher doses. Buy 6-APDB online overnight without prescription 

6-APDB Buy 6-APDB online

The unsaturated benzofuran derivative 6-APB, or 6-(2-aminopropyl)benzofuran also known. But the difference in pharmacological effects between 6-APB and 6-APDB is unclear. 6-APDB is a class B drug in the UK since June 10, 2013. It banned by a blanket law on benzofurans and related compounds. 6-(2-Aminopropyl)-2,3-dihydrobenzofuran ( 4-Desoxy-MDA, EMA-3) is a stimulant and entactogen drug of the phenethylamine and amphetamine classes. It is an analogue of MDA where the heterocyclic 4-position oxygen from the 3,4-methylenedioxy ring replaced with a methylene bridge. 5-APDB (3-Desoxy-MDA) is an analogue of it where the 3-position oxygen replaced with a methylene instead. It along with 5-APDB, was first synthesized by David E. Nichols in the early 1990s while investigating non-neurotoxic MDMA analogues.