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2C-G



2C-G
Chemical name 3,4-dimethyl-2,5-dimethoxyphenethylamine
Chemical formula C12H19NO2
Molecular mass 209.284 g/mol
CAS number 207740-18-9
SMILES Cc1c(OC)c(CCN)cc(OC)c1C


2C-G is a psychedelic phenethylamine of the 2C family. It was first synthesized by Alexander Shulgin, sometimes used as an entheogen. It has structural and pharmacodynamic properties similar to 2C-D and Ganesha. Like many of the phenethylamines in PiHKAL, 2C-G and its homologues (see below) have only been taken by Shulgin and a small test group, making it difficult to ensure completeness when describing effects.

Contents

Chemistry

2C-G is 3,4-dimethyl-2,5-dimethoxyphenethylamine, with the formula C12H19NO2. There are 209.284 grams of C12H19NO2 per mole.

Dosage and Effects

In Shulgin's book PiHKAL, the dosage range is listed as 20 to 35 mg. Effects are similar to the related Ganesha, and are extremely long lasting; the duration is 18-30 hours. Visual effects are muted or absent, and it is described in PiHKAL as an "insight-enhancher" [1]. Unlike other members of the 2C* family, 2C-G is nearly as potent as its amphetamine cousin.

Homologues

Several homologues of 2C-G were also synthesized by Shulgin. These include 2C-G-3, 2C-G-5, and 2C-G-N. Some, such as 2C-G-2 and 2C-G-4, are possible to synthesize in principle but impossible or extraordinarily difficult to do so in practice.

2C-G-3 CAS: 207740-19-0

Dosage: 16-25 mg
Duration: 12-24 hours
Effects: Some visual effects. General euphoria with an underlying sense of paranoia.

 
2C-G-5 CAS: 207740-20-3

Dosage: 10-16 mg
Duration: 32-48 hours
Effects: Similar to 2C-B for some users. General euphoria (sometimes followed by irritability), often leading to tiredness (likely due to duration).

 
2C-G-N CAS: 207740-21-4

Dosage: 20-40 mg
Duration: 20-30 hours
Effects: Stimulation similar to that caused by amphetamines. General sense of unease or unfriendliness for most.

 

Law

2C-G and all of its homologues are unscheduled and uncontrolled in the United States, but possession and sales of 2C-G (and homologues) will probably be persecuted under the Federal Analog Act because of their structural similarities to 2C-B.

2C-G and all other compounds featuring in PiHKAL are Class A drugs in the United Kingdom.

References

  1. ^ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. 

Categorization

v • d • e
2Cs
Halogenated2C-B • 2C-C • 2C-F • 2C-I
Alkylated2C-D • 2C-E • 2C-P • 2C-G
Alkoxylated2C-O • 2C-O-4
Alkylthiolated2C-T • 2C-T-2 • 2C-T-4 • 2C-T-7 • 2C-T-8 • 2C-T-9 • 2C-T-13 • 2C-T-15 • 2C-T-17 • 2C-T-21
Other2C-H • 2C-N • 2C-SE • 2C-TFM


See also
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "2C-G". A list of authors is available in Wikipedia.
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