COMPOUNDS / PSYCHEDELIC / ETH-LAD
PSYCHEDELIC

ETH-LAD

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ETH-LAD · N6-ETHYL-NOR-LSD · N-ETHYL-6-NOR-LSD · 6-ETHYL-6-NOR-LYSERGIC ACID DIETHYLAMIDE · N6-ETHYLNORLYSERGIC ACID N,N-DIETHYLAMIDE · N-ETHYL-N-NORLYSERGIC ACID DIETHYLAMIDE
PsychedelicLysergamideResearch Chemical5-HT2A AgonistNPS

A potent lysergamide psychedelic and N6-ethyl analogue of LSD, reported as more intense and visually oriented than LSD.

ROUTE / DOSAGE
LOW30-60mcg
STANDARD60-150mcg
HIGH150-225mcg
Note: Most common route; typically distributed on blotter paper. Potency slightly higher than LSD.
CYCLE
Max 1x per week 2-week tolerance reset recommended
BIOAVAILABILITY
~70% oral (estimated based on lysergamide class)
ACTIVE DURATION
8-12h (subjective)
STORAGE
Room temperature dry away from light refrigerate for long-term storage of bulk material
HALF-LIFE
~5h (plasma)
DURATION BREAKDOWN
Total8-12 hours
Onset20-40 min
Come up45-90 min
Peak2-4 hours
Offset2-4 hours
After effects4-8 hours
Duration varies by route, dose, and individual. Source: community reports.
§ 01 — EFFECTS
8 documented
Intense visual hallucinations with geometric patterns
Altered perception of time and space
Profound introspective and philosophical thinking
Enhanced color perception and sensory synthesis
Ego dissolution at higher doses
Stimulation and increased energy
Rapid mood shifts and emotional lability
Long duration of 8-12 hours
§ 02 — RISKS
Severe acute toxicity including aggression, unconsciousness, and persistent psychosis as documented in a clinical case report
Prolonged psychiatric effects requiring extended hospitalization and intensive care
HPPD (hallucinogen persisting perception disorder) risk with repeated use
Cardiovascular stimulation and vasoconstriction
Difficult or overwhelming psychological experiences at high doses
Unpredictable potency and purity in unregulated market sources
§ 03 — INTERACTIONS
No interaction with your stack
VIEW STACK
CAUTION
Cannabis
Stimulants
AVOID · DANGEROUS
Lithium
Tramadol
§ 04 — SCIENCE

ETH-LAD is an N6-ethyl derivative of LSD that emerged on the new psychoactive substances market, typically distributed on blotter paper. Analytical characterization via GC-MS, LC-MS, NMR, and IR spectroscopy has confirmed its identity and distinguished it from structural isomers such as EIPLA. In vitro metabolism studies show N-dealkylation and hydroxylation predominantly catalyzed by CYP1A2 and CYP3A4, with parent compounds or metabolites not reliably detected in rat urine using standard screening approaches. A 2016 Global Drug Survey analysis found LSD analogues including ETH-LAD had similar onset and duration to LSD but were rated lower in strength and pleasurable effects. A 2026 case report documented severe toxicity including acute aggression, unconsciousness, metabolic disturbances, and persistent psychosis requiring 17 days of hospitalization and psychiatric transfer, suggesting ETH-LAD may carry higher acute toxicity risk than LSD. Evidence remains limited to analytical characterization, self-report surveys, a single clinical case report, and preclinical animal data; no controlled human trials have been conducted.

§ 06 — SOURCES
[1]
Return of the lysergamides. Part III: Analytical characterization of ETH-LAD and 1P-ETH-LAD
pubmed.ncbi.nlm.nih.gov ↗
[2]
Analytical and behavioral characterization of EIPLA, an isomer of ETH-LAD
pubmed.ncbi.nlm.nih.gov ↗
[3]
An ETH-LAD trip with unfavourable consequences: A case report
pubmed.ncbi.nlm.nih.gov ↗
[4]
Genie in a blotter: A comparative study of LSD and LSD analogues' effects and user profile
pubmed.ncbi.nlm.nih.gov ↗
[5]
Identification and Analysis of LSD Derivatives in Illegal Products as Paper Sheet
pubmed.ncbi.nlm.nih.gov ↗
[6]
In vitro metabolic fate of nine LSD-based new psychoactive substances
pubmed.ncbi.nlm.nih.gov ↗
[7]
PsychonautWiki - ETH-LAD
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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