COMPOUNDS / PSYCHEDELIC / 1P-LSD
PSYCHEDELIC

1P-LSD

MEDIUM RISK
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1P-LSD · 1-PROPIONYL-LSD · 1-PROPIONYL-LYSERGIC ACID DIETHYLAMIDE · 1P-LAD
PsychedelicLysergamideProdrugResearch ChemicalNPS

A prodrug for LSD that converts to LSD in vivo, producing classic psychedelic effects lasting 8-12 hours.

ROUTE / DOSAGE
LOW25-75mcg
STANDARD75-150mcg
HIGH150-300mcg
Note: Most common route; typically on blotter paper
CYCLE
Max 1x per week 2-week reset recommended
BIOAVAILABILITY
~100% oral (as prodrug for LSD)
ACTIVE DURATION
8-12h (subjective)
STORAGE
Dark cool dry place refrigerate for long-term protect from light and heat to prevent hydrolysis to LSD
HALF-LIFE
~6.4h (as LSD) (plasma)
DURATION BREAKDOWN
Total8-12 hours
Onset20-60min
Come up45-120 min
Peak2-4 hours
Offset2-4 hours
After effects4-12 hours
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
7 documented
Visual hallucinations and enhanced color perception
Altered sense of time and space
Profound introspective and philosophical thinking
Euphoria and mood elevation
Synesthesia
Increased heart rate and pupil dilation
Anxiety or paranoia at higher doses
§ 02 — RISKS
Psychological distress including anxiety, paranoia, and panic reactions
Risk of triggering latent psychiatric conditions in predisposed individuals
Distressing hallucinations and perceptual disturbances lasting 8-12 hours
Predicted hematotoxicity based on in silico modeling requiring empirical validation
Dangerous interactions with lithium and tramadol
Impaired judgment during acute effects may lead to risky behavior
§ 03 — INTERACTIONS
No interaction with your stack
VIEW STACK
CAUTION
Cannabis
Stimulants
AVOID · DANGEROUS
Lithium
Tramadol
§ 04 — SCIENCE

Human pharmacokinetic studies in two volunteers demonstrated that oral 1P-LSD is efficiently converted to LSD with near 100% bioavailability, producing subjective effects comparable to LSD with a terminal elimination half-life of approximately 6.4 hours (PMID 32415750). Animal studies confirm 5-HT2A-mediated head-twitch response, with 1P-LSD showing approximately 38% of LSD's potency by molar dose, consistent with prodrug conversion (PMID 26456305, 31756337). However, human data is limited to a single two-subject study, and the full toxicological profile remains largely unexplored. In silico predictions suggest potential hematotoxicity (76% probability) and moderate acute toxicity, though these findings require empirical validation (PMID 41915184). Long-term safety data is absent.

§ 06 — SOURCES
[1]
Stability studies of ALD-52 and its homologue 1P-LSD (PMID 36779453)
pubmed.ncbi.nlm.nih.gov ↗
[2]
Pharmacokinetics and subjective effects of 1P-LSD in humans after oral and intravenous administration (PMID 32415750)
pubmed.ncbi.nlm.nih.gov ↗
[3]
Validation of an LC-MS/MS method for the quantitative analysis of 1P-LSD and its tentative metabolite LSD (PMID 31181490)
pubmed.ncbi.nlm.nih.gov ↗
[4]
The toxicity of psychedelic LSD derivatives: prediction of toxicological parameters (PMID 41915184)
pubmed.ncbi.nlm.nih.gov ↗
[5]
Forensic Aspects of Designer LSD Analogs Identification by GC-MS (PMID 39683876)
pubmed.ncbi.nlm.nih.gov ↗
[6]
Return of the lysergamides Part I: Analytical and behavioural characterization of 1P-LSD (PMID 26456305)
pubmed.ncbi.nlm.nih.gov ↗
[7]
Pharmacological and biotransformation studies of 1-acyl-substituted derivatives of d-LSD (PMID 31756337)
pubmed.ncbi.nlm.nih.gov ↗
[8]
PsychonautWiki - 1P-LSD
psychonautwiki.org ↗
Disclaimer. Protokol.wiki is an informational reference. Nothing on this site is medical advice. Compounds listed may be unapproved, unregulated, or illegal in your jurisdiction. Consult a licensed physician before use. Data compiled from peer-reviewed literature.
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