Ganesha (2,5-dimethoxy-3,4-dimethylamphetamine) is a lesser-known psychedelic drug. It is also a substituted amphetamine. It was first synthesized by Alexander Shulgin.[citation needed] In his book PiHKAL, the dosage range is listed as 24–32 mg.[1] The drug is usually taken orally, although other routes such as rectally may also be used.[citation needed] Ganesha is synthesized from 2,5-dimethoxy-3,4-dimethylbenzaldehyde. Ganesha is the amphetamine analog of 2C-G. It is a particularly long lasting drug, with the duration listed in PiHKAL as being 18–24 hours, which might make it undesirable to some users. It is named after the Hindu deity, Ganesha. Very little is known about the dangers or toxicity of ganesha. Effects of ganesha include:[1]
- Strong closed-eye visuals
- An increased appreciation of music
- Powerful relaxation and tranquility
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Names | |||
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Preferred IUPAC name
1-(2,5-Dimethoxy-3,4-dimethylphenyl)propan-2-amine | |||
Other names
3,4-Dimethyl-2,5-dimethoxyamphetamine;
2-(3,4-Dimethyl-2,5-dimethoxyphenyl)-1-methyl-1-aminoethane | |||
Identifiers | |||
3D model (JSmol)
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ChEMBL | |||
ChemSpider | |||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C13H21NO2 | |||
Molar mass | 223.316 g·mol−1 | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Homologues
editG-3
edit2,5-Dimethoxy-3,4-(trimethylene)amphetamine:[2]
- Dosage: 12–18 mg
- Duration: 8-12 h
- Effects: Enhancement of reading, no visuals or body load.
- 2C analog: 2C-G-3
G-4
edit2,5-Dimethoxy-3,4-(tetramethylene)amphetamine:[3]
G-5
edit3,6-Dimethoxy-4-(2-aminopropyl)benzonorbornane:[4]
G-N
edit1,4-Dimethoxynaphthyl-2-isopropylamine:[5]
Legality
editUnited Kingdom
editThis substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[6]
See also
editReferences
edit- ^ a b Ganesha Entry in PiHKAL
- ^ G-3 entry in PiHKAL
- ^ G-4 entry in PiHKAL
- ^ G-5 entry in PiHKAL
- ^ G-N entry in PiHKAL
- ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.