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3,4-dichlorometylofenidat

3,4-CTMP is approximately seven times more potent than methylphenidate and has a significantly longer duration of 6-18 hours. A critical safety concern is its agonist activity at 5-HT2B receptors, which can cause pulmonary hypertension and heart valve fibrosis with repeated use. Insufflation is strongly discouraged as the substance has low water solubility, is extremely caustic to nasal tissues, and has poor absorption leading to delayed onset that increases overdose risk. Users must use precise milligram scales due to the extremely low active doses. The very long onset (1-2 hours) and extended duration require careful dose timing to avoid unwanted sleep disruption and accidental overdoses from premature redosing.

Also known as: 3,4-ctmp, 3,4-dcmp, Dichloromethylphenidate

Classification

  • Chemical: Phenidate
  • Psychoactive: Stimulant
  • Tag: Habit-Forming
  • Tag: Research-Chemical
  • Tag: substituted phenidate

Effects

  • Stimulation
  • Increased Heart Rate
  • Vasoconstriction
  • Teeth Grinding
  • Headache
  • Pupil Dilation
  • Focus Enhancement
  • Motivation Enhancement
  • Wakefulness
  • Thought Acceleration
  • Analysis Enhancement
  • Time Distortion
  • Appetite Suppression
  • Dehydration
  • Increased Sexuality
  • Visual And Auditory Hallucinations
  • Double Vision
  • Disinhibition

Routes of Administration

Oral

Dosage

  • Threshold: 1-2 mg
  • Light: 2-4 mg
  • Common: 4-6 mg
  • Strong: 6-8 mg
  • Heavy: 6-10 mg

Duration

  • Onset: 1-2 h
  • Peak: 3-6 h
  • Offset: 4-8 h
  • After Effects: 2-24 h

Harm Reduction

Check interactions before mixing substances, pay attention to dose spacing and hydration, and treat all dosage guidance as approximate rather than guaranteed safe.

Sources

Substance data is aggregated from the following public harm-reduction and reference sources.

Links

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3,4-Dichloromethylphenidate - przewodnik po substancji DrugsPRO

3,4-Dichloromethylphenidate: 3,4-CTMP is approximately seven times more potent than methylphenidate and has a significantly longer duration of 6-18 hours. A critical safety concern is its agonist activity at 5-HT2B receptors, which can cause pulmonary hypertension and heart valve fibrosis with repea

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