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BOD (psychedelic)

From Wikipedia, the free encyclopedia
Pharmaceutical compound
BOD
Clinical data
Other namesβ-Methoxy-2C-D; 4-Methyl-2,5,β-trimethoxyphenethylamine; β-MeO-2C-D
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action8–16 hours[1]
Identifiers
  • 2-(2,5-dimethoxy-4-methylphenyl)-2-methoxyethan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC12H19NO3
Molar mass225.288 g·mol−1
3D model (JSmol)
  • COc1cc(C)c(cc1C(CN)OC)OC
  • InChI=1S/C12H19NO3/c1-8-5-11(15-3)9(6-10(8)14-2)12(7-13)16-4/h5-6,12H,7,13H2,1-4H3 checkY
  • Key:VTEIFHQUZWABDE-UHFFFAOYSA-N checkY
  (verify)

BOD, also known as4-methyl-2,5,β-trimethoxyphenethylamine or asβ-methoxy-2C-D, is apsychedelic drug of thephenethylamine,2C, andBOx families.[1] It is the β-methoxyderivative of2C-D.[1] The drug is takenorally.[1]

Use and effects

[edit]

In his bookPiHKAL (Phenethylamines I Have Known and Loved),Alexander Shulgin lists BOD's dose range as 15 to 25 mgorally and itsduration as 8 to 16 hours.[1] Its reported effects include mildopen-eye and moderateclosed-eye visual changes, enhancement ofconversation and sense ofhumor, and unpleasant physical effects such asnausea andlethargy.[1]

Interactions

[edit]
See also:Psychedelic drug § Interactions, andTrip killer § Serotonergic psychedelic antidotes

Pharmacology

[edit]

Very little data exists about the pharmacological properties, metabolism, and toxicity of BOD.[1]

Chemistry

[edit]

Synthesis

[edit]

Thechemical synthesis of BOD has been described.[1]

Analogues

[edit]

Analogues of BOD includeBOHD (β-hydroxy-2C-D) andBOB (β-methoxy-2C-B), among others.[1]

History

[edit]

BOB was first described in thescientific literature byAlexander Shulgin,Peyton Jacob III, andDarrell Lemaire in 1985.[2] Subsequently, it was described in greater detail by Shulgin in his 1991 bookPiHKAL (Phenethylamines I Have Known and Loved).[1]

Society and culture

[edit]

Legal status

[edit]

United Kingdom

[edit]

This substance is a Class A drug in theDrugs controlled by the UK Misuse of Drugs Act.[3]

United States

[edit]

BOD is unscheduled in theUnited States, but purchase, sale, or possession for human consumption could be prosecuted under theFederal Analogue Act.[4]

See also

[edit]

References

[edit]
  1. ^abcdefghijkShulgin, Alexander;Shulgin, Ann (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.BOD Entry
  2. ^Lemaire D, Jacob P, Shulgin AT (August 1985). "Ring-substituted beta-methoxyphenethylamines: a new class of psychotomimetic agents active in man".J Pharm Pharmacol.37 (8):575–577.doi:10.1111/j.2042-7158.1985.tb03072.x.PMID 2864422.
  3. ^"UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved12 March 2014.
  4. ^"21 U.S. Code § 841 - Prohibited acts A",LII / Legal Information Institute, retrieved2016-08-02

External links

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