2C-C: Difference between revisions
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'''2C-C''' is a psychedelic | == Overview == | ||
[[File:2C-C.svg|thumb|right|Chemical structure of 2C-C]] | |||
'''2C-C''' is a psychedelic phenethylamine of the 2C family. It was first synthesized by [[Alexander Shulgin]] and is known for its hallucinogenic properties. The chemical name of 2C-C is 2,5-dimethoxy-4-chlorophenethylamine. | |||
==Chemical | == Chemical Properties == | ||
2C-C is | 2C-C is a member of the [[2C (psychedelics)|2C family]] of drugs, which are characterized by their phenethylamine backbone. The presence of a chlorine atom at the 4-position of the phenyl ring distinguishes 2C-C from other compounds in the series. Its molecular formula is C10H14ClNO2. | ||
==Pharmacology== | == Pharmacology == | ||
2C-C acts primarily as a [[serotonin receptor]] agonist, particularly at the | 2C-C acts primarily as a [[serotonin receptor]] agonist, particularly at the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects. The drug is typically consumed orally, and its effects can last between 4 to 8 hours. | ||
==Effects== | == Effects == | ||
The effects of 2C-C are | The effects of 2C-C are similar to those of other psychedelics, including altered perception of time and space, visual hallucinations, and changes in mood and thought patterns. Users may experience enhanced sensory perception and a sense of euphoria. | ||
== | == Legal Status == | ||
2C-C | The legal status of 2C-C varies by country. In some jurisdictions, it is classified as a controlled substance, while in others it may be legal or unregulated. It is important to be aware of local laws regarding the possession and use of 2C-C. | ||
== | == 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 aromatic ring. The synthesis of 2C-C should only be performed by trained chemists in a controlled laboratory setting. | |||
==Related | == Related Compounds == | ||
2C-C is related to other compounds in the 2C series, such as [[2C-B]], [[2C-I]], and [[2C-E]]. These compounds share a similar chemical structure but differ in their substituents, leading to variations in their pharmacological effects. | |||
== See Also == | |||
* [[Psychedelic drug]] | * [[Psychedelic drug]] | ||
* [[Phenethylamine]] | |||
* [[Alexander Shulgin]] | |||
== Related Pages == | |||
* [[2C (psychedelics)]] | |||
* [[Serotonin receptor]] | |||
* [[Hallucinogen]] | |||
[[Category:Psychedelic phenethylamines]] | [[Category:Psychedelic phenethylamines]] | ||
[[Category:2C (psychedelics)]] | [[Category:2C (psychedelics)]] | ||
Latest revision as of 03:26, 13 February 2025
Overview[edit]
2C-C is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin and is known for its hallucinogenic properties. The chemical name of 2C-C is 2,5-dimethoxy-4-chlorophenethylamine.
Chemical Properties[edit]
2C-C is a member of the 2C family of drugs, which are characterized by their phenethylamine backbone. The presence of a chlorine atom at the 4-position of the phenyl ring distinguishes 2C-C from other compounds in the series. Its molecular formula is C10H14ClNO2.
Pharmacology[edit]
2C-C acts primarily as a serotonin receptor agonist, particularly at the 5-HT2A receptor, which is believed to be responsible for its psychedelic effects. The drug is typically consumed orally, and its effects can last between 4 to 8 hours.
Effects[edit]
The effects of 2C-C are similar to those of other psychedelics, including altered perception of time and space, visual hallucinations, and changes in mood and thought patterns. Users may experience enhanced sensory perception and a sense of euphoria.
Legal Status[edit]
The legal status of 2C-C varies by country. In some jurisdictions, it is classified as a controlled substance, while in others it may be legal or unregulated. It is important to be aware of local laws regarding the possession and use of 2C-C.
Synthesis[edit]
2C-C can be synthesized from 2,5-dimethoxybenzaldehyde through a series of chemical reactions, including the addition of a chlorine atom to the aromatic ring. The synthesis of 2C-C should only be performed by trained chemists in a controlled laboratory setting.
Related Compounds[edit]
2C-C is related to other compounds in the 2C series, such as 2C-B, 2C-I, and 2C-E. These compounds share a similar chemical structure but differ in their substituents, leading to variations in their pharmacological effects.
