2C-E

2C-E
Clinical data
Other names	4-Ethyl-2,5-dimethoxyphenethylamine; 2,5-Dimethoxy-4-ethylphenethylamine; 2C-DOET; 2C-DOEt; Aquarust
Routes of; administration	Oral
Drug class	Serotonin 5-HT2 receptor agonist; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen
ATC code	None;
Legal status
Legal status	BR: Class F2 (Prohibited psychotropics); CA: Schedule III; DE: Anlage I (Authorized scientific use only); NZ: Class C; UK: Class A; US: Schedule I;
Pharmacokinetic data
Onset of action	<2 hours
Duration of action	8–12 hours
Identifiers
	IUPAC name 2-(4-ethyl-2,5-dimethoxyphenyl)ethan-1-amine;
CAS Number	71539-34-9 ;
PubChem CID	24729233;
ChemSpider	21106222 ;
UNII	I190284UXX;
ChEMBL	ChEMBL124063 ;
CompTox Dashboard (EPA)	DTXSID40221772 ;
ECHA InfoCard	100.221.016
Chemical and physical data
Formula	C12H19NO2
Molar mass	209.289 g·mol−1
3D model (JSmol)	Interactive image;
Solubility in water	>70 mg/mL (20 °C)
	SMILES COc1cc(CC)c(cc1CCN)OC;
	InChI InChI=1S/C12H19NO2/c1-4-9-7-12(15-3)10(5-6-13)8-11(9)14-2/h7-8H,4-6,13H2,1-3H3 ; Key:VDRGNAMREYBIHA-UHFFFAOYSA-N ;
	(verify)

2C-E, also known as 4-ethyl-2,5-dimethoxyphenethylamine, is a psychedelic drug of the phenethylamine and 2C families. It is taken orally.

2C-E was first synthesized by Alexander Shulgin in 1977 and was documented in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).