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Short description: Psychedelic drug
3C-E |
Legal status |
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Legal status |
- CA: Schedule I
- DE: NpSG (Industrial and scientific use only)
- UK: Class B
- US: Analogue of a Schedule I drug, possibly illegal under the Federal Analog Act
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Identifiers |
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1-(4-Ethoxy-3,5-dimethoxyphenyl)propan-2-amine
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CAS Number | |
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PubChem CID | |
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ChemSpider | |
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UNII | |
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ChEMBL | |
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Chemical and physical data |
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Formula | C13H21NO3 |
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Molar mass | 239.315 g·mol−1 |
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3D model (JSmol) | |
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CCOc1c(cc(cc1OC)CC(C)N)OC
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InChI=1S/C13H21NO3/c1-5-17-13-11(15-3)7-10(6-9(2)14)8-12(13)16-4/h7-9H,5-6,14H2,1-4H3 Key:AHLXCGRWNKUNTQ-UHFFFAOYSA-N
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3C-E (3,5-Dimethoxy-4-ethoxyamphetamine) is a psychedelic of the amphetamine class. It was first synthesized by Alexander Shulgin. In his book PiHKAL, Shulgin lists the dosage range as 30 to 60 mg, consumed orally.[1] The duration of action was stated to be 8–12 hours.[1]
This compound is the amphetamine analog of escaline.
See also
References
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Psychedelics (5-HT2A agonists) | Benzofurans | |
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Lyserg‐ amides | |
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Phenethyl‐ amines | 2C-x | 25x-NBx | 25x-NB3OMe | |
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25x-NB4OMe | |
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25x-NBF | |
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25x-NBMD | |
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25x-NBOH | |
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25x-NBOMe | |
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Atypical structures | |
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3C-x | |
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4C-x | |
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DOx | |
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HOT-x | |
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MDxx | |
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Mescaline (subst.) | |
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TMAs |
- TMA
- TMA-2
- TMA-3
- TMA-4
- TMA-5
- TMA-6
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Others | |
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Piperazines | |
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Tryptamines | alpha-alkyltryptamines | |
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x-DALT | |
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x-DET | |
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x-DiPT | |
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x-DMT |
- 4,5-DHP-DMT
- 2,N,N-TMT
- 4-AcO-DMT
- 4-HO-5-MeO-DMT
- 4,N,N-TMT
- 4-Propionyloxy-DMT
- 5,6-diBr-DMT
- 5-AcO-DMT
- 5-Bromo-DMT
- 5-MeO-2,N,N-TMT
- 5-MeO-4,N,N-TMT
- 5-MeO-α,N,N-TMT
- 5-MeO-DMT
- 5-N,N-TMT
- 7,N,N-TMT
- α,N,N-TMT
- (Bufotenin) 5-HO-DMT
- DMT
- Norbaeocystin
- (Psilocin) 4-HO-DMT
- (Psilocybin) 4-PO-DMT
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x-DPT | |
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Ibogaine-related | |
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x-MET | |
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x-MiPT | |
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Others | |
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Others | |
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Dissociatives (NMDAR antagonists) | |
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Deliriants (mAChR antagonists) | |
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Others | |
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| Original source: https://en.wikipedia.org/wiki/3C-E. Read more |