MAL Stats & Data
NCCc1cc(OC)c(OCC(C)=C)c(OC)c1FOXJFBFFGULACD-UHFFFAOYSA-NReceptor Profile
Receptor Actions
Effect Profile
Curated + 21 ReportsStrong visuals, headspace, auditory effects, and body load
Community Effects
TripSitTolerance & Pharmacokinetics
drugs.wikiTolerance Decay
Rapid tolerance develops to classical psychedelics and cross‑tolerance is well‑documented between LSD and mescaline; MAL is inferred to follow a similar 5‑HT2A‑mediated pattern. Values above are heuristic for planning intervals, not pharmacokinetic half‑life. Data quality primarily anecdotal with inference from classic literature.
Cross-Tolerances
Experience Report Analysis
ErowidDemographics
Gender Distribution
Age Distribution
Reports Over Time
Effect Analysis
ErowidEffects aggregated from 21 experience reports (21 Erowid)
Effect Sentiment Distribution
Confidence Distribution
Positive Effects 9
Adverse Effects 9
Dosage Distribution
Dose distribution from experience reports
Real-World Dose Distribution
62K DosesFrom 25 individual dose entries
Oral (n=23)
Form / Preparation
Most common forms and preparations reported
Body-Weight Dosing
Dose relative to body weight from reports with weight data
Redose Patterns
Redosing behavior across 13 reports
Harm Reduction
drugs.wiki- Identity and nomenclature: MAL is 3,5-dimethoxy-4-methallyloxyphenethylamine; the methallyl (2‑methylallyl) ether at the 4-position makes it an escaline-family analogue. This specific naming helps distinguish it from mescaline analogues with 3,4,5-trimethoxy patterns. (Source: PiHKAL·info entry and IUPAC listing).
- Very slow, sometimes deceptive onset (60–120 min) is frequently reported; premature redosing is a common cause of excessive body-load and adverse effects—avoid any redose before 3 hours and consider split-dosing only after prior experience. (Anecdotal consensus across BL/Erowid).
- Long duration (10–16 h) plus residual after-effects can impact sleep and next-day function; don’t drive, cycle, swim, or operate machinery during and after. Plan an unhurried, temperature‑controlled setting with trusted support.
- Nausea and GI cramping are common in the first hours; bland pre-meal, ginger/peppermint, and avoiding heavy fats can help. Some find sublingual/insufflation reduces nausea but increases stimulation and local irritation. (Anecdotal).
- Peripheral stimulation/vasoconstriction and mild hypertension can occur; combining with stimulants (including high-dose caffeine) increases cardiovascular strain—avoid such mixes, especially if you have cardiovascular risk factors. (General HR + TripSit chart rationale).
- Urinary retention has been repeatedly reported anecdotally with moderate–high doses; inability to void for many hours is a red flag. Avoid anticholinergics (e.g., diphenhydramine), stay hydrated with electrolytes, and seek urgent care if painful retention persists (>6–8 h), if there’s flank pain, or if you feel systemically unwell. Do not self‑medicate with prescription alpha‑blockers without medical supervision. (Anecdotal; community warnings).
- Salt forms: “MAL fumarate” has appeared in drug checking contexts and can be laid on blotter. Salt form changes mg‑for‑mg potency by mass; if unknown, titrate from the low end and do an allergy test with each new batch.
- Reagent/drug checking: MAL has been found on blotter, a format often used for long‑acting phenethylamines; always test. Reagents may not be definitive; GC/MS (e.g., DrugsData) or a local service provides confirmation.
- Allergy test: For any new batch, especially RCs, start with 1–2 mg to screen idiosyncratic reactions, then stepwise titrate on a different day.
- Mental set: As with other psychedelics, strong alterations in thought and perception occur; having a sober sitter, a plan for anxiety management (breathing, environment control), and avoiding emotionally charged settings reduces risk.
- Medical cautions: People with BPH/prostate issues, urinary tract problems, uncontrolled hypertension, or significant cardiovascular disease should avoid MAL without medical clearance due to retention and BP risks.
- Do not mix with lithium (seizure/coma risk reported with psychedelics) or MAOIs (unpredictable potentiation and hypertension risk). Tramadol is risky due to serotonergic and seizure‑threshold effects.
- Hydration: Sip fluids regularly; add electrolytes if sweating or active. Overhydration can be harmful—avoid chugging large volumes rapidly.
- Sleep protection: Expect sleep disruption; prepare a dark, quiet space and non-pharmacologic sleep hygiene rather than sedative stacking post‑trip.
References
Cited References
- Bluelight: The Big & Dandy Methallylescaline Thread
- Erowid Experience Vault: Methallylescaline
- PIHKAL Entry #99: Methallylescaline
- PsychonautWiki: Methallylescaline
- Smolecule: Methallylescaline Chemical Profile
- TripSit Wiki: Drug Combinations Chart
- Wikipedia: Methallylescaline
- Bluelight: Big & Dandy Methallylescaline Thread
- TripSit Factsheet: Methallylescaline
- PiHKAL Mirror: Pihkal
Drugs.wiki References
- PiHKAL·info entry for Methallylescaline (names/IUPAC; links; MAL fumarate noted)
- Erowid Methallylescaline Experience Vault (dose/duration user ranges; slow onset)
- Bluelight Big & Dandy Methallylescaline Thread (dose ranges, slow come up, nausea/body load)
- Bluelight MAL dosing discussion (typical 40–60 mg oral; redose cautions)
- Reddit: MAL urinary retention/kidney function warning ( community anecdotal)
- Reddit: Managing MAL urinary retention (anecdotal tamsulosin post; not advice)
- Reddit MAL ROA anecdotes – insufflated 50 mg strong; sublingual 5–10 mg mild
- TripSit drug combinations chart (general HR rationale re: psychedelics + stimulants)
- Bluelight: Main LSD & Lithium thread (seizure/coma risk reports)
- Erowid Extracts / classic text: cross‑tolerance between LSD and mescaline
- Erowid DrugsData project overview (GC/MS checking resource)
- PubChem entry (synonyms/identifier)