2C-G, or 2C-G-0, also known as 3,4-dimethyl-2,5-dimethoxyphenethylamine or as 3-methyl-2C-D, is a psychedelic phenethylamine of the 2C family.[1] First synthesized by Alexander Shulgin, it has structural and pharmacodynamic properties similar to 2C-D and Ganesha (G).[1] The drug has a number of known homologues, which are known as the 2C-G series of compounds.[1]

Use and effects

In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists 2C-G's dose range as 20 to 35 mg orally and its duration as 18 to 30 hours.[1] The time to peak effects was described as being 2 hours.[1] The effects of 2C-G have been reported to include little in the way of visuals, being a "true psychedelic", mental changes, insights, altered sense of taste, "energy tremor", stomach queasiness, and a feeling of heat in the upper back.[1] The drug is said to have very similar properties and effects as its amphetamine homologue Ganesha (G).[1] Its similar potency to Ganesha is in contrast to other 2Cs and psychedelic phenethylamines, which are less potent than their amphetamine homologues.[1]

Interactions

Chemistry

Synthesis

The chemical synthesis of 2C-G has been described.[1]

Homologues

Several homologues of 2C-G (2C-G-0) were also synthesized and/or tested by Alexander Shulgin.[1] These include 2C-G-3, 2C-G-5, and 2C-G-N.[1] Some, such as 2C-G-1, 2C-G-2, 2C-G-4, and 2C-G-6, are possible to synthesize in principle but impossible or extraordinarily difficult to do so in practice.[1]

CompoundDetailsStructure
2C-G-1 CAS #: 2888537-47-9

The synthesis of this compound has not been reported, but it is described prophetically in WO2022271982
DOx analogue: None

2C-G-2 CAS #: 2888537-48-0

The synthesis of this compound has not been reported, but it is described prophetically in WO2022271982
DOx analogue: None

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

Dose: 16–25 mg
Duration: 12–24 hours
Effects: Some visual effects. General euphoria with an underlying sense of paranoia.
DOx analogue: G-3

2C-G-4 CAS #: 952006-59-6

Partially synthesized but not tested.
DOx analogue: G-4

2C-G-5 CAS #: 207740-20-3

Dose: 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).
DOx analogue: G-5

2C-G-6 CAS #: 2888537-49-1

The synthesis of this compound has not been reported, but it is described prophetically in WO2022271982
DOx analogue: None

2C-G-N CAS #: 207740-21-4

Dose: 20–40 mg
Duration: 20–30 hours
Effects: Stimulation similar to that caused by amphetamines. General sense of unease or unfriendliness for most. 2C-G-N is sometimes called 2C-NPH due to the naphthalene portion of the molecule.
DOx analogue: G-N

History

2C-G was first described in the literature by Alexander Shulgin in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).[1]

Society and culture

Canada

As of October 31, 2016; 2C-G is a controlled substance (Schedule III) in Canada.[2]

United Kingdom

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

United States

In the United States 2C-G is considered a Schedule I controlled substance as a positional isomer of 2C-E and DOM.[3][4]

See also

References

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 Shulgin AT, Shulgin A (1991). "2C-G". PiHKAL: A Chemical Love Story (1st ed.). Berkeley, CA: Transform Press. ISBN 978-0-9630096-0-9. OL 22859055M.
  2. "Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)". 4 May 2016.
  3. "Lists of: Scheduling Actions - Controlled Substances - Regulated Chemicals" (PDF). Drug Enforcement Administration. February 2023.
  4. Drug Enforcement Administration (3 December 2007). "Definition of "Positional Isomer" as It Pertains to the Control of Schedule I Controlled Substances". Federal Register.