25iP-NBOMe
25iP-NBOMe is a synthetic psychedelic of the substituted phenethylamine class, specifically an N-benzylated derivative of the hallucinogen 2C-iP. It has emerged as a rarely encountered novel designer drug1 and remains largely unresearched. Reported to be extremely potent with stimulating qualities, it may produce uncomfortable body load and potentially dangerous vasoconstriction at higher doses. Very limited information is available regarding its safety profile and pharmacological properties.
Dosage & Duration
Dosage
Duration
Subjective Effects
25iP-NBOMe produces a stimulating psychedelic experience broadly typical of the NBOMe series, combining euphoria, empathy, and a sense of insight with prominent open and closed-eye visuals. The headspace involves a general shift in perception and a softening of the ego, though confusion can also occur. As with other N-benzylphenethylamines, the substance is active at sub-milligram doses and its subjective profile remains only sparsely documented.
Physical
The body experience carries a distinct stimulation with restlessness, muscle tension, and decreased appetite. Pupil dilation, sweating and chills, and difficulty sleeping are also reported.
Stimulation
Uncomfortable
Cognitive
The mental state is stimulating and euphoric, with enhanced empathy, a sense of insight, and a mild softening of the sense of self. Confusion is possible, particularly at stronger doses.
Emotional
Visual
Visual effects include brightened colors and both open and closed-eye visuals.
Tactile
Sense of touch is enhanced.
Pharmacology
Pharmacodynamics
25iP-NBOMe produced off-target μ-opioid receptor activation in two cell-based assay systems, but the result was weak in the receptor-proximal β-arrestin-2 assay: about 6% of the hydromorphone reference response at 100 μM, without a plateau from which a reliable EC50 could be calculated.2
Its apparently high response in the calcium-release assay was accompanied by the strongest non-MOR-mediated signal among the tested analogues, so that response cannot be treated as clean μ-opioid receptor efficacy.2
Because μ-opioid activity in this series occurred only at high concentrations, the investigators considered clinically relevant opioid toxicity from this mechanism unlikely at physiologically relevant concentrations.2
Pharmacokinetics
Dangerous
Highest riskThese combinations are considered extremely harmful and should always be avoided. Reactions to these drugs taken in combination are highly unpredictable and have a potential to cause death.
Unsafe
AvoidThere is considerable risk of physical harm when taking these combinations, they should be avoided where possible.
Caution
Use cautionThese combinations are not usually physically harmful, but may produce undesirable effects, such as physical discomfort or overstimulation. Extreme use may cause physical health issues. Synergistic effects may be unpredictable. Care should be taken when choosing to use this combination.
Tolerance
Serotonergic psychedelics, 5-HT2A agonists
Harm Potential
Toxicity
May cause potentially dangerous vasoconstriction at high doses; the extreme potency of this compound increases the risk of accidental overdose leading to cardiovascular complications.
History & Culture
25iP-NBOMe emerged as a novel designer drug and was first documented in the scientific literature around 2014. Like other members of the NBOMe series, it represents an N-benzyl modification of an existing 2C-x compound—in this case, 2C-iP. The substance remains relatively obscure compared to more widely encountered NBOMe compounds such as 25I-NBOMe or 25C-NBOMe,1 with limited information available regarding its history of human use or cultural significance.
Legality
International
The 2025 Green List separately lists 25I-NBOMe in 1971 Convention Schedule I as 2-(4-iodo-2,5-dimethoxyphenyl)-N-(2-methoxybenzyl)ethanamine. That is not 25iP-NBOMe and does not establish structural coverage of 25iP-NBOMe. Complete current 1961, 1971, and 1988 INCB lists were inspected before reaching this absence finding.
By Country
References
Source Pages
Citations
- Prevalence of use and acute toxicity associated with the use of NBOMe drugs. Clin Toxicol (Phila), 53(2), 85–92 (February 2015). https://doi.org/10.3109/15563650.2015.100417912
- Deventer MH, Persson M, Laus A, Pottie E, Cannaert A, Tocco G, Gréen H, & Stove CP. (2023). Off-target activity of NBOMes and NBOMe analogs at the μ opioid receptor. Archives of Toxicology, 97(5), 1367–1384. https://doi.org/10.1007/s00204-023-03465-9123
- Controlled Drugs and Substances Act, Schedule III, item 35. laws-lois.justice.gc.ca (n.d.). https://laws-lois.justice.gc.ca/eng/acts/c-38.8/page-11.html1
- Neue-psychoaktive-Stoffe-Gesetz (NpSG), Anlage 1 Nr. 1. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/BJNR261510016.html1
- Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 2. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__2.html1
- Neue-psychoaktive-Stoffe-Gesetz (NpSG), § 3. gesetze-im-internet.de (n.d.). https://www.gesetze-im-internet.de/npsg/__3.html1
- Cabinet of Ministers Resolution No. 770: List of narcotic drugs, psychotropic substances and precursors, Table I, List No. 2. zakon.rada.gov.ua (n.d.). https://zakon.rada.gov.ua/laws/show/770-2000-%D0%BF1
- Cabinet of Ministers Resolution No. 600 of 10 July 2019: amendments to the List of narcotic drugs, psychotropic substances and precursors. zakon.rada.gov.ua (n.d.). https://zakon.rada.gov.ua/laws/show/600-2019-%D0%BF1
- Misuse of Drugs Act 1971, Schedule 2, Part I, paragraph 1(f), as inserted by the Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014. legislation.gov.uk (n.d.). https://www.legislation.gov.uk/uksi/2014/11061
- Misuse of Drugs Act 1971, Schedule 2, Part I, paragraph 1(f), as inserted by the Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014. legislation.gov.uk (n.d.). https://www.legislation.gov.uk/ukpga/1971/38/schedule/21
- Misuse of Drugs Act 1971 — Schedule 4 (Prosecution and Punishment of Offences). legislation.gov.uk (1971). https://www.legislation.gov.uk/ukpga/1971/38/schedule/412
- The Misuse of Drugs Act 1971 (Ketamine etc.) (Amendment) Order 2014 (SI 2014/1106). (2014). https://www.legislation.gov.uk/uksi/2014/1106/made1
Further Reading
Ettrup A et al. 'Structure-Activity Relationships of NBOMe 5-HT2A Agonists' Journal of Neurochemistry 2013
King LA 'New phenethylamines in Europe' Drug Testing and Analysis 2014
Nichols DE 'Psychedelics' Pharmacological Reviews 2016
Nichols DE. ‘Psychedelics’ Pharmacol Rev 2016 (general NBOMe toxicity)
Poulie CBM et al. 'Correlating the Metabolic Stability of Psychedelic 5-HT2A Agonists with Anecdotal Reports of Human Oral Bioavailability' Neurochemical Research 2014
Rickli A et al. 'Receptor interaction profiles of novel N-2-methoxybenzyl (NBOMe) derivatives of 2,5-dimethoxy-substituted phenethylamines (2C drugs)' Neuropharmacology 2015
Zawilska JB, Kacela M, Adamowicz P 'NBOMes–Highly Potent and Toxic Alternatives of LSD' Frontiers in Neuroscience 2020
Automated synthesisInformation aggregated and synthesized using an autonomous workflow built by Josie Kins.
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