2C-C: Difference between revisions

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File:2C-C.svg|Diagram of the chemical structure of 2C-C, a psychedelic phenethylamine.
File:2C-C.svg|Diagram of the chemical structure of 2C-C, a psychedelic phenethylamine.
File:2C-C_3D_ball.png|3D ball-and-stick model of the 2C-C molecule.
File:2C-C_synthesis.png|Illustration of a possible synthesis pathway for 2C-C.
File:2C-C_spectra.png|Spectral data of 2C-C, showing its characteristic peaks.
File:2C-C_crystals.jpg|Photograph of 2C-C crystals under a microscope.
File:2C-C_dosage_chart.png|Chart showing the dosage range and effects of 2C-C.
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Revision as of 06:07, 12 February 2025

A psychedelic phenethylamine of the 2C family


2C-C
File:2C-C.svg
INN
Drug class
Routes of administration Oral, Insufflation
Pregnancy category
Bioavailability
Metabolism
Elimination half-life
Excretion
Legal status Unscheduled
CAS Number 28234-80-8
PubChem 4433
DrugBank
ChemSpider 4280
KEGG


2C-C is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and is known for its relatively mild psychedelic effects compared to other compounds in the same class.

Chemical structure and properties

2C-C is chemically known as 2-(4-chloro-2,5-dimethoxyphenyl)ethanamine. It belongs to the 2C family of phenethylamines, which are characterized by a phenyl ring with two methoxy groups and an ethylamine chain. The presence of a chlorine atom at the 4-position of the phenyl ring distinguishes 2C-C from other 2C compounds.

Pharmacology

2C-C acts primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor. This action is responsible for its psychedelic effects, which include alterations in perception, mood, and cognition. The compound is known for its relatively short duration of action, typically lasting between 4 to 8 hours.

Effects

The effects of 2C-C are considered to be milder than those of other psychedelics such as LSD or psilocybin. Users report visual enhancements, increased empathy, and a sense of well-being. The compound is often described as having a "gentle" psychedelic experience, making it a choice for those new to psychedelics.

Synthesis

2C-C can be synthesized from 2,5-dimethoxybenzaldehyde through a series of chemical reactions, including the addition of a chlorine atom to the 4-position of the phenyl ring. The synthesis process requires careful handling of reagents and conditions to ensure the purity and safety of the final product.

Legal status

The legal status of 2C-C varies by country. In some jurisdictions, it is classified as a controlled substance, while in others, it remains unscheduled. Users should be aware of the legal implications of possessing or using 2C-C in their respective regions.

Related pages

2C-C Image Gallery