2C-G

This article relies largely or entirely on a single source. Relevant discussion may be found on the talk page. Please help by introducing citations to additional sources. Find sources:  –  ·  ·  · scholar · JSTOR (January 2017)

2C-G

Names
Preferred IUPAC name 2-(2,5-Dimethoxy-3,4-dimethylphenyl)ethan-1-amine
Identifiers
CAS Number	207740-18-9 Y
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL127202 Y
ChemSpider	21106224 Y
PubChem CID	22238091
UNII	DTG7FMO01J Y
CompTox Dashboard (EPA)	DTXSID70174848
InChI InChI=1S/C12H19NO2/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3/h7H,5-6,13H2,1-4H3 Y Key: NFOHGLKGLZIHJQ-UHFFFAOYSA-N Y InChI=1/C12H19NO2/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3/h7H,5-6,13H2,1-4H3 Key: NFOHGLKGLZIHJQ-UHFFFAOYAX
SMILES COc1c(C)c(C)c(cc1CCN)OC
Properties
Chemical formula	C12H19NO2
Molar mass	209.289 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YN ?)
Infobox references

2C-G is a psychedelic phenethylamine of the 2C family. First synthesized by Alexander Shulgin,^[1] it is 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 homologs have only been taken by Shulgin and a small test group, making it difficult to ensure completeness when describing effects.

Chemistry[]

2C-G is 3,4-dimethyl-2,5-dimethoxyphenethylamine, with the formula C
₁₂H
₁₉NO
₂.

Dosage and effects[]

In Shulgin's book PiHKAL, the dosage range is listed as 20 to 35 mg.^[1] 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-enhancer".^[1] Unlike other members of the 2C family, 2C-G is nearly as potent as its amphetamine cousin.

Homologs[]

Several homologs 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-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.

2C-G-1	CAS: not available The synthesis of this compound has not been reported	2C-G-1
2C-G-2	CAS: not available The synthesis of this compound has not been reported	2C-G-2
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-3
2C-G-4	CAS: 952006-59-6 Synthesized but not tested.	2C-G-4
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-5
2C-G-6	CAS: not available The synthesis of this compound has not been reported	2C-G-6
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. 2C-G-N is sometimes called 2C-NPH due to the Naphthalene portion of the molecule.	2C-G-N

Legal status[]

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[]

2C-G and all of its homologs are unscheduled in the United States, but possession and sales of 2C-G and homologs might be prosecuted under the Federal Analog Act because of their close structural similarities to 2C-B, which is a Schedule I controlled substance.

See also[]

• Phenethylamine
• Ganesha

References[]

External links[]

• [1], [2], [3], [4] PiHKAL entries on the homologues
• 2C-G Entry in PiHKAL • info
• 2C-G-3 Entry in PiHKAL • info
• 2C-G-4 Entry in PiHKAL • info
• 2C-G-5 Entry in PiHKAL • info
• 2C-G-N Entry in PiHKAL • info