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2C-G


FieldValue
Verifiedfieldschanged
Watchedfieldschanged
verifiedrevid477216206
image2C-G.svg
image_classskin-invert-image
width200px
image22C-G-3d-sticks.png
image_class2bg-transparent
width2175px
routes_of_administrationOral
classSerotonergic psychedelic; Hallucinogen
ATC_prefixNone
legal_statusIn general Unscheduled
duration_of_action18–30 hours
CAS_number_Ref
CAS_number207740-18-9
PubChem22238091
ChemSpiderID_Ref
ChemSpiderID21106224
UNII_Ref
UNIIDTG7FMO01J
ChEMBL_Ref
ChEMBL127202
synonyms2C-G-0; 2,5-Dimethoxy-3,4-dimethylphenethylamine; 3,4-Dimethyl-2,5-dimethoxyphenethylamine; 3-Methyl-2C-D
IUPAC_name2-(2,5-dimethoxy-3,4-dimethylphenyl)ethan-1-amine
C12H=19N=1O=2
SMILESCOc1c(C)c(C)c(cc1CCN)OC
StdInChI_Ref
StdInChI1S/C12H19NO2/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3/h7H,5-6,13H2,1-4H3
StdInChIKey_Ref
StdInChIKeyNFOHGLKGLZIHJQ-UHFFFAOYSA-N

| Drugs.com =

| elimination_half-life =

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. First synthesized by Alexander Shulgin, it has structural and pharmacodynamic properties similar to 2C-D and Ganesha (G). The drug has a number of known homologues, which are known as the 2C-G series of compounds.

Use and effects

In Alexander Shulgin's book PiHKAL (Phenethylamines I Have Known and Loved), the dose range is listed as 20 to 35mg orally. Effects are similar to the related Ganesha, and are extremely long lasting; the duration is 18 to 30hours. Visual effects are muted or absent, and it is described as an "insight-enhancer". Unlike other members of the 2C series, 2C-G is nearly as potent as its amphetamine form.

Interactions

Chemistry

Synthesis

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

Homologues

Several homologues of 2C-G (2C-G-0) were also synthesized and/or tested by Alexander Shulgin. These include 2C-G-3, 2C-G-5, and 2C-G-N. 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.

CompoundDetailsStructure
2C-G-1*CAS #*: 2888537-47-9
[[File:2C-G-1.png125pxclass=skin-invert-image]]
2C-G-2*CAS #*: 2888537-48-0
[[File:2C-G-2.png125pxclass=skin-invert-image]]
[2C-G-3](2c-g-3)*CAS #*: 207740-19-0
[[File:2C-G-3-Chemdraw.png125pxclass=skin-invert-image]]
[2C-G-4](2c-g-4)*CAS #*: 952006-59-6
[[File:2C-G-4.svg125pxclass=skin-invert-image]]
[2C-G-5](2c-g-5)*CAS #*: 207740-20-3
[[File:2C-G-5.svg125pxclass=skin-invert-image]]
2C-G-6*CAS #*: 2888537-49-1
[[File:2C-G-6.png125pxclass=skin-invert-image]]
[2C-G-N](2c-g-n)*CAS #*: 207740-21-4
[[File:2C-G-N-Chemdraw.png125pxclass=skin-invert-image]]

History

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

Society and culture

Canada

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

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.

References

References

  1. (1991). "PiHKAL: A Chemical Love Story". Transform Press.
  2. (4 May 2016). "Regulations Amending the Food and Drug Regulations (Part J — 2C-phenethylamines)".
  3. (February 2023). "Lists of: Scheduling Actions - Controlled Substances - Regulated Chemicals". Drug Enforcement Administration.
  4. [[Drug Enforcement Administration]]. (3 December 2007). "Definition of “Positional Isomer” as It Pertains to the Control of Schedule I Controlled Substances".
Info: Wikipedia Source

This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.

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