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About MDAI

Description of MDAI

5,6-Methylenedioxy-2-aminoindane (commonly known as MDAI) is an entactogen substance of the aminoindane chemical class that produces entactogenic effects when administered.Notably, this compound primarily produces the non-stimulating effects of prototypical entactogens like MDMA such as sedation, muscle relaxation, and tactile enhancement.

5,6-methylenedioxy-2-aminoindane, 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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.
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About MDAI

Description of MDAI

Contents Buy Cheap MDAI Online

 

Buy Cheap MDAI Online 5,6-methylenedioxy-2-aminoindane, 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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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 also contains two oxygen substitutions at R5 and R6 joined by a methylene bridge to form a methylenedioxy group.

 

It has been shown to inhibit the reuptake of serotonin and has a selective affinity for the serotonin receptor.

 

For comparison,

is similar in potency with releasing serotonin to MDA, Buy Cheap MDAI Online

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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

This creates an indane group,

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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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.

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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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 also contains two oxygen substitutions at R5 and R6 joined by a methylene bridge to form a methylenedioxy group.

 

It has been shown to inhibit the reuptake of serotonin and has a selective affinity for the serotonin receptor.

MDAI also contains two oxygen substitutions at R5 and R6 joined by a methylene bridge to form a methylenedioxy group.

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.

5,6-methylenedioxy-2-aminoindane,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 5,6-methylenedioxy-2-aminoindane,, and it has a limited history of human use.
It is highly advised to use harm reduction practices if using this substance.

is a synthetic molecule of the aminoindane class with structural similarity to amphetamines.

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 also contains two oxygen substitutions at R5 and R6 joined by a methylene bridge to form a methylenedioxy group.

 

It has been shown to inhibit the reuptake of serotonin and has a selective affinity for the serotonin receptor.

It has been shown to inhibit the reuptake of serotonin and has a selective affinity for the serotonin receptor.

Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status

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