BOED

BOED
Clinical data
Other names4-Methyl-2,5-dimethoxy-β-ethoxyphenethylamine; 2,5-Dimethoxy-β-ethoxy-4-methylphenethylamine; 2,5-Dimethoxy-4-methyl-β-ethoxyphenethylamine; β-Ethoxy-2C-D; β-EtO-2C-D
Routes of
administration		Oral[1][2]
Drug classPsychoactive drug
ATC code
  • None
Pharmacokinetic data
Duration of action10 hours[1][2]
Identifiers
  • 2-(2,5-dimethoxy-4-methylphenyl)-2-ethoxyethan-1-amine
Chemical and physical data
FormulaC13H21NO3
Molar mass239.315 g·mol−1
3D model (JSmol)
  • CCOC(c1cc(OC)c(cc1OC)C)CN
  • InChI=1S/C13H21NO3/c1-5-17-13(8-14)10-7-11(15-3)9(2)6-12(10)16-4/h6-7,13H,5,8,14H2,1-4H3
  • Key:LZNFMACBNUDNGO-UHFFFAOYSA-N

BOED, also known as 4-methyl-2,5-dimethoxy-β-ethoxyphenethylamine or as β-ethoxy-2C-D, is a psychoactive drug of the phenethylamine, 2C, and BOx families.[1][2] It is the β-ethoxy derivative of 2C-D and homologue of BOD (β-methoxy-2C-D).[1][2] The drug was briefly described by Alexander Shulgin in his 1991 book PiHKAL (Phenethylamines I Have Known and Loved).[1][2] Its dose was said to be 70 to 75 mg orally and its duration was 10 hours.[1][2] The drug was said to be about 3-fold less potent than BOD.[1] Its effects included a highly intoxicated state, no visual effects, appetite suppression, and diuresis.[1] The chemical synthesis of the drug was also briefly described.[1] It is a controlled substance in Canada under phenethylamine blanket-ban language.[3]

See also

References

  1. ^ a b c d e f g h i Shulgin A, Shulgin A (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. https://erowid.org/library/books_online/pihkal/pihkal014.shtml "A parallel chemistry to all of this follows the addition of sodium ethoxide (rather than sodium methoxide) to the nitrostyrene. The final product, then, is the ethoxy homologue 2,5-dimethoxy-β-ethoxy-4-methylphenethylamine, or BOED. It is down in human potency by a factor of three, with a normal dosage being 70–75 milligrams. It has a ten-hour duration, and is both anorexic and diuretic. There have been no visual effects or insights reported, but rather simply a highly intoxicated state."
  2. ^ a b c d e f Trachsel D, Lehmann D, Enzensperger C (2013). Phenethylamine: von der Struktur zur Funktion [Phenethylamines: From Structure to Function]. Nachtschatten-Science (in German) (1 ed.). Solothurn: Nachtschatten-Verlag. pp. 833–834. ISBN 978-3-03788-700-4. OCLC 858805226. Archived from the original on 21 August 2025.
  3. ^ "Controlled Drugs and Substances Act". Department of Justice Canada. Retrieved 19 January 2026.
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