3C-E

3C-E
Legal status
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;
Identifiers
	IUPAC name 1-(4-Ethoxy-3,5-dimethoxyphenyl)propan-2-amine;
CAS Number	146849-92-5 ;
PubChem CID	44350137;
ChemSpider	21106237;
UNII	W9QX56V5RU;
ChEMBL	ChEMBL128038;
CompTox Dashboard (EPA)	DTXSID40658382 ;
Chemical and physical data
Formula	C13H21NO3
Molar mass	239.315 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES CCOc1c(cc(cc1OC)CC(C)N)OC;
	InChI 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]^[2] The duration of action was stated to be 8–12 hours.^[1]

This compound is the amphetamine analog of escaline.

References

^ ^a ^b PiHKAL entry
^ Halberstadt AL, Chatha M, Klein AK, Wallach J, Brandt SD (May 2020). "Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species" (PDF). Neuropharmacology. 167: 107933. doi:10.1016/j.neuropharm.2019.107933. PMC 9191653. PMID 31917152. Table 4 Human potency data for selected hallucinogens. [...]

This hallucinogen-related article is a stub. You can help Wikipedia by expanding it.

[PiHKAL-1] PiHKAL entry

[HalberstadtChathaKlein2020-2] Halberstadt AL, Chatha M, Klein AK, Wallach J, Brandt SD (May 2020). "Correlation between the potency of hallucinogens in the mouse head-twitch response assay and their behavioral and subjective effects in other species" (PDF). Neuropharmacology. 167: 107933. doi:10.1016/j.neuropharm.2019.107933. PMC 9191653. PMID 31917152. Table 4 Human potency data for selected hallucinogens. [...]

[1]

[2]

See also

References