spec sheet10 rows
3-HO-PCP (3-hydroxyphencyclidine) is a hydroxylated analog of phencyclidine that acts as an NMDA receptor antagonist and, unusually for a dissociative, also displays notable mu-opioid receptor activity arising from its 3-hydroxy group; it is reported to be more potent than PCP itself. This dual mechanism can add opioid-like sedation and respiratory risk to the expected dissociative effects. Analytically confirmed case reports document severe toxicity, including hyperthermia, tachycardia, rhabdomyolysis, and serotonergic features, and forensic studies have quantified the drug and mapped its hepatic metabolism, noting brain concentrations exceeding those in blood. In silico work flags moderate acute toxicity and potential cardiotoxicity, while controlled human data remain absent.
- Dissociation
- Strong analgesia
- Opioid-like sedation and warmth
- Dissociative with added mu-opioid activity
- Respiratory depression risk
- Disorientation
- High potency and narrow margin
- Compulsive redosing
Mechanism
It acts as an receptor to produce dissociation, and its 3-hydroxyl substitution confers appreciable agonism at the mu-opioid receptor. This dual action means effects blend dissociation with opioid-like sedation and analgesia, and the opioid side brings respiratory-depression risk not typical of ketamine-type dissociatives.
receptor fingerprint
Antagonist
Mu-opioid receptorAgonist
Safetyrisks and cautions, not medical advice
The mu-opioid activity means 3-HO-PCP can suppress breathing, and that risk multiplies when combined with other depressants such as alcohol, benzodiazepines, or opioids. It is reportedly potent, so small dosing errors matter, and human safety data are scarce. Naloxone (a mu-opioid antagonist) may reverse the opioid-driven breathing suppression. Not medical advice.
Subjective profileweighing the evidence above
Treat this as an opioid at least as much as a dissociative. The mu activity brings breathing suppression that ketamine-type dissociatives do not, and it multiplies with alcohol, benzodiazepines or opioids. Potent enough that small measuring errors matter, with severe toxicity documented in case reports and scarce human safety data. Not a casual compound.
Resources
This entry is here for reference.
Research
- 1981first citedOn the opioid nature of phencyclidine and its 3-hydroxy derivative
- 2026most recentQualitative and quantitative in silico toxicity profiling of "angel dust": phencyclidine (PCP)…
- 1.On the opioid nature of phencyclidine and its 3-hydroxy derivative
- 2.Severe Toxicity to the New Psychoactive Substances 3-Hydroxyphencyclidine and N-Ethylhexedrone: an Analytically Confirmed Case Report
- 3.In vitro and in vivo metabolism and detection of 3-HO-PCP, a synthetic phencyclidine, in human samples and pooled human hepatocytes using high resolution mass spectrometry.
- 4.Phencyclidine-Like Abuse Liability and Psychosis-Like Neurocognitive Effects of Novel Arylcyclohexylamine Drugs of Abuse in Rodents.
- 5.Qualitative and quantitative in silico toxicity profiling of "angel dust": phencyclidine (PCP) analogues as new psychoactive substances (3-HO-PCP, 3-MeO-PCP, 4-MeO-PCP, 3-HO-PCE, 3-MeO-PCE, 4-MeO-PCE).
5 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What makes 3-HO-PCP different from other dissociatives?
It has real mu-opioid activity, so it can suppress breathing in a way ketamine-type dissociatives generally do not.
Is naloxone useful?
It may reverse the opioid component of a dangerous slowdown in breathing, though the compound is poorly studied.
How potent is it?
It is reported to be quite potent, so small differences in dose can have outsized effects.
Adverse effects
- Respiratory depression risk
- Disorientation
- High potency and narrow margin
- Compulsive redosing