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Substituted phenidates: Difference between revisions
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>Oskykins m Oskykins moved page Substituted Phenidate to Substituted phenidate without leaving a redirect: "Phenidate" should be lowercase as per the guidelines |
>Unity m Text replacement - "General formula" to "Generic structure" |
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[[File:sphenidate.png|thumb|right|301px|| | [[File:sphenidate.png|thumb|right|301px||Generic structure of a phenidate molecule.]] | ||
'''Substituted phenidates''', also known as '''phenidates''', are a class of chemicals that include compounds with psychoactive effects. | '''Substituted phenidates''', also known as '''phenidates''', are a class of chemicals that include compounds with psychoactive effects. | ||
Revision as of 21:15, 29 January 2017
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 | 
|