Para-Methoxyphenylpiperazine

Clinical data
Other names	pMeOPP; pMPP; p-MeOPP; p-MPP; 4-MeOPP; 4-MPP; MeOPP; MPP; Paraperazine
Routes of administration	Oral
ATC code	none
Legal status
Legal status	DE: NpSG (Industrial and scientific use only) NZ: Class C
Pharmacokinetic data
Metabolism	The human liver P450 CYP2D6 converts para-methoxyphenylpiperazine by demethylation to para-hydroxyphenylpiperazine.
Excretion	Renal
Identifiers
IUPAC name 1-(4-methoxyphenyl)piperazine
CAS Number	38212-30-5 Y
PubChemCID	269722
ChemSpider	237180 N
UNII	P385M92GYG
CompTox Dashboard(EPA)	DTXSID30191591
ECHA InfoCard	100.048.918
Chemical and physical data
Formula	C11H16N2O
Molar mass	192.262 g·mol−1
3D model (JSmol)	Interactive image
SMILES C1=CC(=CC=C1N2CCNCC2)OC
InChI InChI=1S/C11H16N2O/c1-14-11-4-2-10(3-5-11)13-8-6-12-7-9-13/h2-5,12H,6-9H2,1H3 N Key:MRDGZSKYFPGAKP-UHFFFAOYSA-N N
NY (what is this?)  (verify)

para-Methoxyphenylpiperazine (pMeOPP), also known as4-methoxyphenylpiperazine (4-MeOPP), is asubstituted piperazinederivative withstimulant effects which has been sold as an ingredient in "Party pills", initially inNew Zealand and subsequently in other countries around the world.^[1]

pMeOPP is anecdotally said to induce significantly less anxiety than similar piperazines, and is usually taken at doses between 120–200 mg. However it is often mixed with stimulant piperazine derivatives such asbenzylpiperazine (BZP) for a combined effect.

pMeOPP has been foundin vitro toinhibit thereuptake and induce therelease of themonoamineneurotransmitters. This is a mechanism of action shared with drugs of abuse such asamphetamines, and pMeOPP produces somewhat similar effects although it is much less potent and is thought to have relatively insignificant abuse potential.^[2] Piperazine derivatives such astrifluoromethylphenylpiperazine (TFMPP) have also been shown to exert a major part of their mechanism of action as nonselectiveserotonin receptor agonists, and pMeOPP has also been demonstrated to act in this way.^[3]

Scheduled in the "government decree on psychoactive substances banned from the consumer market".^[4]

Based on the recommendation of the EACD, the New Zealand government has passed legislation which placed BZP, along with a number of other piperazine derivatives into Class C of the New Zealand Misuse of Drugs Act 1975. A ban was intended to come into effect in New Zealand on December 18, 2007, but the law change did not go through until the following year, and the sale of BZP and the other listed piperazines became illegal in New Zealand as of 1 April 2008. An amnesty for possession and usage of these drugs remained until October 2008, at which point they became completely illegal.^[5]

pMeOPP is not scheduled at the federal level in theUnited States.^[6]

"Methoxyphenylpiperazine" is a Schedule Icontrolled substance in the state ofFlorida making it illegal to buy, sell, or possess in Florida.^[7]

• Substituted piperazine

• Media related toPara-Methoxyphenylpiperazine at Wikimedia Commons

• Drugs not assigned an ATC code
• Designer drugs
• Monoamine releasing agents
• 1-Phenylpiperazines
• Serotonin receptor agonists

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