2C-H

This article is a stub.

As such, it may contain incomplete or wrong information. You can help by expanding it.

This page has not been fully approved by the PsychonautWiki administrators.

It may contain incorrect information, particularly with respect to dosage, duration, subjective effects, toxicity and other risks. It may also not meet PW style and grammar standards.

2C-H (2,5-Dimethoxyphenethylamine) is a lesser-known substituted phenethylamine that is the traditional precursor to 2C-B, 2C-C and 2C-I. It was first synthesized in 1932 by Johannes S. Buck and was later studied by Alexander Shulgin, who later published his findings in his book PiHKAL. It it easily broken down my the MAO enzyme in the liver and is thus considered inactive. When combined with a MAOI, it is believed to have stimulant effects.

Chemical Nomenclature

Common names

2C-H, DMPEA

Substitutive name

2,5-Dimethoxyphenethylamine

Systematic name

2-(2,5-Dimethoxyphenyl)ethanamine

Class Membership

Psychoactive class

Stimulant / Psychedelic

Chemical class

Phenethylamine

Routes of Administration

WARNING: Always start with lower doses due to differences between individual body weight, tolerance, metabolism, and personal sensitivity. See responsible use section.

⇣ Oral
Dosage
Common	Unknown
Duration
Total	Unknowm

DISCLAIMER: PW's dosage information is gathered from users and resources for educational purposes only. It is not a recommendation and should be verified with other sources for accuracy.

Interactions

Summary sheet: 2C-H

Chemistry

This chemistry section is incomplete.

You can help by adding to it.

2C-H or 2,5-dimethoxyphenethylamine is a substituted phenethylamine featuring a phenyl ring bound to an amino (NH₂) group through an ethyl chain. 2C-H contains methoxy functional groups CH₃O- attached to carbons R₂ and R₅ as well as a hydrogen atom attached to carbon R₄ of the phenyl ring. 2C-H belongs to the 2C family of phenethylamines which contain methoxy groups on the 2 and 5 positions of the benzene ring, and is also their simplest member. It is commonly used as a precursor to other compounds of the 2C family, most notably 2C-B.

Pharmacology

This pharmacology section is incomplete.

You can help by adding to it.

Subjective effects

This subjective effects section is a stub.

As such, it is still in progress and may contain incomplete or wrong information.

You can help by expanding or correcting it.

The effects listed below are based upon the subjective effects index and personal experiences of PsychonautWiki contributors. The listed effects will rarely (if ever) occur all at once, but heavier dosages will increase the chances and are more likely to induce a full range of effects.

Physical effects

Cognitive effects

Visual effects

Hallucinatory states

Auditory effects

Toxicity and harm potential

This toxicity and harm potential section is a stub.

As a result, it may contain incomplete or even dangerously wrong information! You can help by expanding upon or correcting it.
Note: Always conduct independent research and use harm reduction practices if using this substance.

Legal issues

This legality section is a stub.