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MDAI – is also known as 5,6-Methylenedioxy-2-aminoindane, and is a compound developed in the 1990s by a team led by David E. Nichols at Purdue University. It acts as a non-neurotoxic and highly selective serotonin releasing agent (SSRA) in vitro and produces entactogen effects in humans.

The chemical structure of MDAI is indirectly derived from that of the illicit drug MDA, but the alpha-methyl group of the alkylamino amphetamine side chain has been bound back to the benzene nucleus, to form an indane ring system, which changes its pharmacological properties substantially.

MDAI, can be produced from 3-(3,4-Methylenedioxyphenyl)propionic acid which is converted to the acid chloride and then heated to produce 5,6-Methylenedioxy-1-indanone. Treatment of the indanone with amyl nitrite in methanol with HC1 afforded the hydroxyimino ketone. This is reduced to the 2-aminoindan following a modification of Nichols’ earlier method from a paper discussing DOM analogues, using a Pd/C catalyst in glacial acetic acid with catalytic H2SO4.

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MDAI POWDER is not for human consumption.



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Buy Mdai; Chemically, MDAI is very similar to 3,4-methylenedioxyamphetamine (MDA), which is principally use as a recreational drug, the main difference being the existence of a bond between the alpha-methyl group of the alkylamino amphetamine side chain and the benzene nucleus (Indane ring). A simple of MDA otherwise known as MDMA, It is a psychoactive research concoction that has stimulant properties.

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Utilized in research, It is a viable substitute for other none legitimate chemicals because of its comparative structure.

Doorbell Pharmacy sells MDAI for in vitro research purposes as it were. It isn’t reasonable for human utilization.

Ethylphenidate Acting as

 In addition Ethylphenidate acts as both a dopamine reuptake inhibitor and norepinephrine reuptake inhibitor. meaning it effectively boosts the levels of the norepinephrine and dopamine neurotransmitters in the brain. by binding to, and partially blocking the transporter proteins that normally remove those monoamines from the synaptic cleft.

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