3,4-Methylenedioxy-N-isopropylamphetamine: Difference between revisions

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{{Short description|Chemical compound}}
'''3,4-Methylenedioxy-N-isopropylamphetamine''' (MDIP) is a synthetic compound belonging to the [[amphetamine]] class of [[psychoactive drugs]]. It is structurally related to [[3,4-methylenedioxyamphetamine]] (MDA) and [[3,4-methylenedioxymethamphetamine]] (MDMA), which are well-known for their stimulant and [[empathogenic]] effects.
{{Drugbox
| verifiedfields = changed
| verifiedrevid = 477318123
| IUPAC_name = 1-(1,3-Benzodioxol-5-yl)-N-isopropylpropan-2-amine
| image = MDIP.svg
| image_size = 200px
| image_alt =
| legal_status =
| routes_of_administration =
| CAS_number = 74698-46-5
| PubChem = 4433
| ChemSpiderID = 4278
| UNII =
| KEGG =
| ChEMBL = 2104665
| C=12
| H=17
| N=1
| O=2
| smiles = CC(C)NC(C)Cc1ccc2OCOc2c1
| InChI = 1S/C12H17NO2/c1-9(2)13-8(3)7-10-4-5-11-12(6-10)15-14-11/h4-6,8-9,13H,7H2,1-3H3
| InChIKey = ZJQZQXKZVZVQFZ-UHFFFAOYSA-N
}}


'''3,4-Methylenedioxy-N-isopropylamphetamine''' ('''MDIP''') is a chemical compound belonging to the [[substituted amphetamines]] class. It is structurally related to [[3,4-methylenedioxyamphetamine]] (MDA) and other [[phenethylamines]].
== Chemical Structure ==


==Chemical structure and properties==
MDIP is characterized by the presence of a methylenedioxy group attached to the phenyl ring, similar to other compounds in the [[methylenedioxyphenethylamine]] family. The isopropyl group is attached to the nitrogen atom of the [[amphetamine]] backbone, distinguishing it from other related compounds such as [[MDMA]], which has a methyl group instead.
MDIP is characterized by the presence of a [[methylenedioxy]] group attached to the benzene ring, which is a common feature in many psychoactive compounds. The compound also contains an [[isopropyl]] group attached to the nitrogen atom, distinguishing it from other related compounds such as [[MDMA]] and [[MDA]].


==Pharmacology==
== Pharmacology ==
The pharmacological properties of MDIP are not well-documented, but it is believed to act as a [[serotonin]] and [[dopamine]] releasing agent, similar to other compounds in the substituted amphetamines class. The presence of the methylenedioxy group suggests potential [[entactogenic]] effects, although specific studies on MDIP are lacking.


==Synthesis==
The pharmacological profile of MDIP is not well-documented, but it is presumed to act as a [[serotonin]] and [[dopamine]] releasing agent, similar to other methylenedioxy-substituted amphetamines. These compounds typically increase the release of [[neurotransmitters]] in the brain, leading to their characteristic psychoactive effects.
MDIP can be synthesized through various chemical pathways, typically involving the reaction of [[safrole]] with isopropylamine. The synthesis process requires careful control of reaction conditions to ensure the correct formation of the methylenedioxy bridge and the isopropylamine substitution.


==Legal status==
== Effects ==
The legal status of MDIP varies by country. In many jurisdictions, it may be considered a controlled substance due to its structural similarity to other regulated amphetamines. Researchers and chemists must be aware of local regulations when handling or studying this compound.
 
The effects of MDIP are not extensively studied, but it is likely to produce stimulant and empathogenic effects similar to those of [[MDMA]] and [[MDA]]. Users may experience increased energy, enhanced mood, and heightened sensory perception. However, the specific effects and their intensity can vary based on dosage and individual differences.
 
== Legal Status ==
 
The legal status of MDIP varies by country. In many jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated amphetamines. It is important to consult local laws to determine its legal status in a specific region.
 
== Related Compounds ==
 
MDIP is part of a broader class of compounds known as [[substituted amphetamines]]. Other related compounds include:


==Related compounds==
* [[3,4-Methylenedioxyamphetamine]] (MDA)
* [[3,4-Methylenedioxyamphetamine]] (MDA)
* [[3,4-Methylenedioxymethamphetamine]] (MDMA)
* [[3,4-Methylenedioxymethamphetamine]] (MDMA)
* [[3,4-Methylenedioxy-N-methylamphetamine]] (MDMA)
* [[3,4-Methylenedioxy-N-methylamphetamine]] (MDMA)
* [[Substituted amphetamines]]


==See also==
== Related Pages ==
* [[Phenethylamine]]
 
* [[Amphetamine]]
* [[Psychoactive drug]]
* [[Psychoactive drug]]
* [[Entactogen]]
* [[Serotonin]]
* [[Dopamine]]


==Gallery==
{{Psychoactive drugs}}
 
[[Category:Amphetamines]]
[[Category:Psychoactive drugs]]
== 3,4-Methylenedioxy-N-isopropylamphetamine gallery ==
<gallery>
<gallery>
File:MDIP.svg|Chemical structure of MDIP
File:MDIP.svg|MDIP structure
</gallery>
</gallery>
[[Category:Substituted amphetamines]]
[[Category:Psychoactive drugs]]
[[Category:Serotonin releasing agents]]

Latest revision as of 06:17, 3 March 2025

3,4-Methylenedioxy-N-isopropylamphetamine (MDIP) is a synthetic compound belonging to the amphetamine class of psychoactive drugs. It is structurally related to 3,4-methylenedioxyamphetamine (MDA) and 3,4-methylenedioxymethamphetamine (MDMA), which are well-known for their stimulant and empathogenic effects.

Chemical Structure[edit]

MDIP is characterized by the presence of a methylenedioxy group attached to the phenyl ring, similar to other compounds in the methylenedioxyphenethylamine family. The isopropyl group is attached to the nitrogen atom of the amphetamine backbone, distinguishing it from other related compounds such as MDMA, which has a methyl group instead.

Pharmacology[edit]

The pharmacological profile of MDIP is not well-documented, but it is presumed to act as a serotonin and dopamine releasing agent, similar to other methylenedioxy-substituted amphetamines. These compounds typically increase the release of neurotransmitters in the brain, leading to their characteristic psychoactive effects.

Effects[edit]

The effects of MDIP are not extensively studied, but it is likely to produce stimulant and empathogenic effects similar to those of MDMA and MDA. Users may experience increased energy, enhanced mood, and heightened sensory perception. However, the specific effects and their intensity can vary based on dosage and individual differences.

Legal Status[edit]

The legal status of MDIP varies by country. In many jurisdictions, it may be classified as a controlled substance due to its structural similarity to other regulated amphetamines. It is important to consult local laws to determine its legal status in a specific region.

Related Compounds[edit]

MDIP is part of a broader class of compounds known as substituted amphetamines. Other related compounds include:

Related Pages[edit]



3,4-Methylenedioxy-N-isopropylamphetamine gallery[edit]