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5,6-Methylenedioxy-2-aminoindane�(also known as�MDAI) is a lesser-known novel�entactogen�substance of the�aminoindane�class.mdai research,buy mdai,mdai for sale,mdai effects,mda

Notably, this compound primarily produces the non-stimulating effects of prototypical entactogens like�MDMA�such as�sedation,�muscle relaxation, and�tactile enhancement.

MDAI was developed in the 1990s by a team led by�David E. Nichols�at Purdue University.

It acts as a putatively non-neurotoxic and highly selective�serotonin�releasing agent�(SSRA) with neglible effects on�dopamine�and�norepinephrine.

This reportedly limits its potential at producing overtly invigorating, prosocial or�euphoric�effects.

MDAI has been marketed alongside�research chemical�entactogens�like�5-MAPB,�5-APB, and�6-APB�as a legal, grey-market alternative to�MDMA.

Very little data exists about the pharmacological properties, metabolism, and toxicity of MDAI, and it has a limited history of human use. It is highly advised to use�harm reduction practices�if using this substance.

MDAI, or 5,6-methylenedioxy-2-aminoindane, is a synthetic molecule of the�aminoindane�class with structural similarity to�amphetamines.mdai research,buy mdai,mdai for sale,mdai effects,mda

It features the R3�terminal carbon of the propane chain of amphetamine bound to the benzene ring.

This creates an indane group, a bicyclic moeity containing a benzene ring fused to a pentane ring. MDAI contains an amino group NH2�bound to R2�of the indane ring.

MDAI also contains two oxygen substitutions at R5�and R6 joined by a methylene bridge to form a methylenedioxy group. MDAI is structurally related to�2-AI, differing by a methylenedioxy ring.

MDAI has been shown to�inhibit the reuptake�of�serotonin�and has a selective affinity for the serotonin�receptor. Studies have shown that the brains of animals treated with MDAI have greater extracellular concentrations of�monoamine neural transmitters, most significantly�serotonin.

For comparison, MDAI is similar in potency with releasing serotonin to�MDA, but significantly less potent than�MDMA.

This is done by inhibiting the reuptake and reabsorption of the neurotransmitters after they have performed their function of transmitting a neural impulse, essentially allowing them to accumulate, be reused and cause�entactogenic�effects.

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All products found on this website are distributed for the purpose of research and education.

None of our products is sold for human or animal utilization, consumption or for any type of illegal usage.

Today chemplaza.gubpharm Chemical Employ more than 70 full-time staff, of which approximately 20 are PhD�s and MSc�s working for pharmaceutical ingredient reference and other special chemicals for researchers in global universities, research institutes, pharmaceutical manufacturers.

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