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1cP-AL-LAD Facts

Psychedelic; Lysergamide; Serotonin 2A receptor agonist

Description

1cP-AL-LAD is a synthetic psychedelic of the lysergamide class. It activates serotonin receptors in the brain, producing the visual and cognitive shifts characteristic of classical psychedelics.

Subjective effects include geometric visual patterns, brightened colors, time alteration, accelerated thinking, and elevated mood. The experience follows the classical lysergamide arc — visually rich, cognitively expansive, with a light stimulant edge, shaped heavily by mindset and environment.

1cP-AL-LAD produces no physical dependence, and serotonergic psychedelics carry an extremely high physiological safety margin;[1] rapid tolerance after a single dose makes compulsive use self-limiting.[2] The primary risks are psychological — acute distress, rare persistent visual disturbances, and psychiatric destabilisation, amplified sharply by combinations with MAOIs or lithium.

Dose and durationby route · individual sensitivity varies

Oral(µg)
Threshold< 20 µgLight50 – 100 µgCommon100 – 225 µgStrong225 – 350 µgHeavy350+ µg

Starts in 20 – 60 minLasts 7 – 10 hoursAfter-effects 2 – 18 hours

Body and dependence

Acute toxicity
Negligible
Chronic toxicity
Negligible
Physical dependence
None
Psychological dependence
Negligible
Withdrawal
None recorded
Compulsive redosing
Negligible

Tolerance

Builds
Rapid
Fully resets after
14 days
Carries over to
LSD; psilocybin; mescaline; DMT; other serotonergic psychedelics

Effectslikely at a common dose

Perception
Auditory enhancement; Color alteration; Color enhancement; Environmental patterning; Geometry; Music enhancement; Tracers; Visual breathing; Visual drifting; +26 possible, including Spatial disorientation, Visual haze / noise, Vestibular distortion
Body
Body scan awareness; Pupil dilation; Stimulation; +24 possible, including Insomnia, Heart rate perception changes, Dizziness
Thinking
Aesthetic enhancement; Cognitive flexibility; Conceptual thinking; +31 possible, including Cognitive impairment, Decision impairment, Suggestibility enhancement
Feeling
none likely · 8 possible, including Emotional lability, Anxiety, Paranoia
Self
none likely · 9 possible, including Derealization, Depersonalization
Time
Time alteration; +3 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Psychotic disorders; Concurrent lithium use; Concurrent MAOI therapy
Relative
Serious cardiovascular conditions; History of HPPD; Unstable psychiatric conditions; Pregnancy or breastfeeding; Concurrent serotonergic medications

Combinations60 recorded

Lethal (1)
MAOIs
Dangerous (19)
MDMA, MDA; Buspirone; DXM; GHB, Baclofen; GHB, GBL; Ibogaine; Ketamine, DXM, PCP; Lithium; Local anesthetics; MDMA, Amphetamines; NDRIs (Wellbutrin); NRIs; NSAIDs; Psychedelics; Salvia, Ibogaine; SNRIs; SSRIs; Stimulants; Synthetic cannabinoids
Caution (36)
See full page: psychedex.org/substances/1cp-al-lad
Not graded (4)
Not listed never means safe.

Seek help immediately if

Most difficulty is psychological (intense fear, panic, confusion) and passes with calm support — the signs below mean seek emergency help:

  • Very high body temperature; hot, dry skin
  • Seizures
  • Chest pain; fast or irregular heartbeat
  • Severe muscle rigidity, tremor, or twitching (possible serotonin syndrome)
  • Cold, pale, or blue fingers/toes — severe vasoconstriction (notably NBOMe / DOx)
  • Persistent vomiting; unconsciousness; uncontrollable agitation or risk of self-harm

What to do

  1. Stay calm and reassure — remind them they took a drug and the effect will pass
  2. Move to a calm, quiet, safe space with low light; reduce noise and sensory input
  3. Keep them from harm — they may act on fear or confusion; stay with them, don't leave them alone
  4. Talk them down gently; don't grab or restrain unless they're in danger
  5. For the medical signs above (overheating, seizure, chest pain, vasoconstriction, unresponsive) call emergency services
  6. If overheating, cool the body; be ready to give rescue breaths / CPR

The experience is time-limited and usually resolves with calm reassurance in a safe setting — psychological first aid, not medication. Serious physical harm is uncommon for classic psychedelics (LSD, psilocybin) but real for some potent phenethylamines (NBOMe, DOx), where hyperthermia, seizures, and vasoconstriction warrant emergency care.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Luethi D, Liechti ME (2020) Designer drugs: mechanism of action and adverse effects — Archives of Toxicology doi:10.1007/s00204-020-02693-7
  2. [2]
    ^Buckholtz NS, Zhou DF, Freedman DX, Potter WZ (1990) Lysergic acid diethylamide (LSD) administration selectively downregulates serotonin2 receptors in rat brain — Neuropsychopharmacology PMID:1969270
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