2CE-5iPrO

2CE-5iPrO is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and documented in his book PiHKAL.

Chemistry

2CE-5iPrO, or 2,5-dimethoxy-4-(5-isopropoxy)-phenethylamine, is a synthetic phenethylamine featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain. 2CE-5iPrO contains methoxy functional groups CH3O- attached to carbons R2 and R5 as well as an isopropoxy group attached to carbon R4 of the phenyl ring. 2CE-5iPrO belongs to the 2C family of phenethylamines which are characterized by their phenyl ethylamine backbone.

Pharmacology

The exact mechanism of action of 2CE-5iPrO is not fully understood. However, it is believed to work primarily by binding to the serotonin 5-HT2A receptor, which plays a key role in the regulation of mood, anxiety, and consciousness. This receptor is also the primary target of other psychedelic substances such as LSD and psilocybin.

Effects

The effects of 2CE-5iPrO can vary greatly depending on the dose, set, and setting. Common effects reported by users include visual hallucinations, enhanced sensory perception, altered sense of time, and introspective experiences. These effects are similar to those of other psychedelic substances.

Risks

As with all psychedelic substances, 2CE-5iPrO carries risks. These can include psychological distress, panic attacks, and rare cases of psychosis in predisposed individuals. It is also possible for users to experience physical discomfort such as nausea, headache, and increased heart rate.

Legal Status

The legal status of 2CE-5iPrO varies by country. In many places, it is considered a controlled substance and its possession, sale, or use may be punishable by law.

See Also

• 2C-B
• 2C-E
• 2C-I
• 2C-T-2
• 2C-T-7

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