Jump to content
Wikipedia The Free Encyclopedia

2C-DB

From Wikipedia, the free encyclopedia
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.
Pharmaceutical compound
2C-DB
Clinical data
Other names2-Bromo-2C-B; 2,5-Dimethoxy-4,6-dibromophenethylamine; 2,4-Dibromo-3,6-dimethoxyphenethylamine
Routes of
administration
Oral [1]
Drug class Serotonergic psychedelic; Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action 6–8 hours[1]
Identifiers
  • 2-(2,4-dibromo-3,6-dimethoxyphenyl)ethan-1-amine
Chemical and physical data
Formula C10H13Br2NO2
Molar mass 339.027 g·mol−1
3D model (JSmol)
  • NCCc1c(OC)cc(c(c1Br)OC)Br
  • InChI=1S/C10H13Br2NO2/c1-14-8-5-7(11)10(15-2)9(12)6(8)3-4-13/h5H,3-4,13H2,1-2H3
  • Key:ISCLQOQPPGRPTK-UHFFFAOYSA-N

2C-DB, also known as 2,5-dimethoxy-4,6-dibromophenethylamine or as 6-bromo-2C-B, is a psychedelic drug of the phenethylamine and 2C families related to 2C-B.[1] It is the 6-bromo derivative of 2C-B and the 4,6-dibromo derivative of 2,5-dimethoxyphenethylamine (2C-H).[1] The drug has a dose range of 20 to 35 mg orally and a duration of 6 to 8 hours.[1] For comparison, 2C-B has a dose of 12 to 24 mg and a duration of 4 to 8 hours.[1] 2C-DB is described as having largely the same effects as 2C-B.[1] However, it is said that the drug may have somewhat greater visual effects than 2C-B.[1] 2C-DB was synthesized and tested by P. Rausch in the 1990s or 2000s.[1] [2] It was described in the scientific literature by Daniel Trachsel in 2013, who cited personal communication with Rausch as the source for the information.[1]

See also

References

  1. ^ a b c d e f g h i j 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. p. 921. ISBN 978-3-03788-700-4. OCLC 858805226. Archived from the original on 21 August 2025.
  2. ^ Rausch P (January 1995). Leuner H, Schlichting M (eds.). Jahrbuch des Europäischen Collegiums für Bewußtseinsstudien: 1995 [Yearbook of the European College for the Study of Consciousness: 1995] (in German and English). Vol. 4. Berlin: VWB. ISBN 3861354071. ISSN 0942-7600. OCLC 28636362.
Tryptamines
No ring subs.
4-Hydroxytryptamines
5-Hydroxytryptamines
5-Methoxytryptamines
Other ring subs.
α-Alkyltryptamines
Others
Cyclized
Bioisosteres
Phenethylamines
Scalines
2C-x
3C-x
DOx
4C-x
Ψ-PEA
MDxx
FLY
25x-NB (NBOMes)
Others
Cyclized
Lysergamides
  • Bioisosteres: JRT
Others
Natural sources
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Stub icon

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

AltStyle によって変換されたページ (->オリジナル) /