Ethylphenidate

Pharmacology

Pharmacokinetics

Ethylphenidate metabolizes into methylphenidate and ritalinic acid.

Tiny amounts of ethylphenidate can be formed in vivo when ethanol and methylphenidate are coingested, via hepatic transesterification. Ethylphenidate formation appears to be more common when large quantities of methylphenidate and alcohol are consumed at the same time, such as in non-medical use or overdose scenarios. However, the transesterification process of methylphenidate to ethylphenidate, as tested in mice liver, was dominant in the inactive (−)-enantiomer but showed a prolonged and increased maximal plasma concentration of the active (+)-enantiomer of methylphenidate. Additionally, only a small percentage of the consumed methylphenidate is converted to ethylphenidate.

This carboxylesterase-dependent transesterification process is also known to occur when cocaine and alcohol are consumed together, forming cocaethylene.

Pharmacodynamics

All available data on ethylphenidate's pharmacodynamics are drawn from studies conducted on rodents. Ethylphenidate is more selective to the dopamine transporter (DAT) than methylphenidate, having approximately the same efficacy as the parent compound, but has significantly less activity on the norepinephrine transporter (NET). Its dopaminergic pharmacodynamic profile is nearly identical to methylphenidate, and is primarily responsible for its euphoric and reinforcing effects.

The eudysmic ratio for ethylphenidate is superior to that of methylphenidate.

The following is ethylphenidate's binding profile in the mouse, alongside methylphenidate's. Figures for both the racemic and the dextrorotary enantiomers are given:

Legality

• Ethylphenidate is a schedule II drug under the Convention on Psychotropic Substances.
• Ethylphenidate is illegal in the Netherlands, as the Opium Law List I covers it, as of April 27, 2018
• In the United States, effective November 21, 2024, Etheylphenidate was placed in Schedule I of the Controlled Substances Act.
  • On September 22, 2023, the DEA filed a proposed rule for placement of Ethylphenidate into Schedule I status. Public commenting opened on September 22, 2023, and closed on November 21, 2023.
• Ethylphenidate was made schedule I at the state level in Alabama on March 18th, 2014.
• Ethylphenidate is illegal in Sweden as of December 15, 2012.
• Ethylphenidate is illegal to manufacture, distribute or import in the UK, as of 10 April 2015 it has been placed under a Temporary Class Drug Order which automatically places it in a Class-B-like category. Though ordinarily the TCDO would only last 1 year, the ACMD reported that since its invocation prevalence of MPA had significantly decreased, and that it had been challenging to collect information about the drug. As a result of this, they requested that the TCDO be extended a further year from 26 June 2016.
• Ethylphenidate is illegal in Jersey under the Misuse of Drugs (Jersey) Law 1978.
• Australian state and federal legislation contains provisions that mean that analogues of controlled drugs are also covered by the legislation. Ethylphenidate would be an analogue of methylphenidate under this legislation.
• Ethylphenidate is controlled in Canada under the Controlled Drugs and Substances Act under Schedule III as of May 5, 2017.
• Ethylphenidate is illegal in Germany as of May 7, 2013.
• Ethylphenidate is illegal in Austria by the "Neue Psychoaktive Substanzen Gesetz" (New Psychoactive Substances Act) NPSG since 1 January 2012
• Ethylphenidate is illegal in Denmark as of February 1, 2013.
• Ethylphenidate is illegal in Poland by "the Act on Counteracting Drug Addiction" since July 1, 2015.
• It is illegal in Lithuania to use, buy, possess, transport, sell or import Ethylphenidate from 2015
• As of October 2015, ethylphenidate is a controlled substance in China.
• In Finland ethylphenidate is scheduled in government decree on substances, preparations and plants considered to be narcotic drugs.

References

References

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