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Substituted phenidates: Difference between revisions
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| [[4F-EPH]] || H || F || CH<sub>2</sub>CH<sub>3</sub> || [[File:4F-EPH.png|171px]] | | [[4F-EPH]] || H || F || CH<sub>2</sub>CH<sub>3</sub> || [[File:4F-EPH.png|171px]] | ||
|- | |- | ||
| [[Methylnaphthidate]] (HDMP-28) || CH=CH- || CH=CH- || CH<sub>3</sub> || [[File:Hdmp-28.png|170px]] | | [[Methylnaphthidate]] (''HDMP-28'') || CH=CH- || CH=CH- || CH<sub>3</sub> || [[File:Hdmp-28.png|170px]] | ||
|- | |- | ||
| Ethylnaphthidate || CH=CH- || CH=CH- || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethylnaphthidate.png|170px]] | | Ethylnaphthidate || CH=CH- || CH=CH- || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethylnaphthidate.png|170px]] | ||
Revision as of 00:46, 28 November 2016
Substituted phenidates, also known as phenidates, are a class of chemicals that include compounds with psychoactive effects.
Chemistry
Substituted phenidates are a chemical class based upon the molecule Methylphenidate. Methylphenidate is made up of a phenethylamine molecule with a carbon chain substitution at the Rα position that links to the RN position forming a piperidine ring, and a substitution at the Rβ position of methyl acetate.
List of substituted phenidates
| Compound | R3 | R4 | RO | Structure |
|---|---|---|---|---|
| Methylphenidate | H | H | CH3 | 
|
| Ethylphenidate | H | H | CH2CH3 | 
|
| Isopropylphenidate | H | H | CH(CH3)2 | 
|
| Propylphenidate | H | H | CH2CH2CH3 | 
|
| 4-Methyl Methylphenidate | H | CH3 | CH3 | 
|
| 3,4-CTMP | Cl | Cl | CH3 | 
|
| 4F-MPH | H | F | CH3 | 
|
| 4F-EPH | H | F | CH2CH3 | 
|
| Methylnaphthidate (HDMP-28) | CH=CH- | CH=CH- | CH3 | 
|
| Ethylnaphthidate | CH=CH- | CH=CH- | CH2CH3 | 
|