Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

DOTMA

From Wikipedia, the free encyclopedia
Pharmaceutical compound
DOTMA
Clinical data
Other names2,5-Dimethoxy-3,4,6-trimethylamphetamine; Julia; 3,6-Dimethyl-DOM; 6-Methyl-Ganesha
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic;Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action7–9 hours[1]
Identifiers
  • 1-(2,5-dimethoxy-3,4,6-trimethylphenyl)propan-2-amine
Chemical and physical data
FormulaC14H23NO2
Molar mass237.343 g·mol−1
3D model (JSmol)
  • COc1c(C)c(CC(N)C)c(c(c1C)C)OC
  • InChI=1S/C14H23NO2/c1-8(15)7-12-11(4)13(16-5)9(2)10(3)14(12)17-6/h8H,7,15H2,1-6H3
  • Key:ROGMRKPRWZWOSW-UHFFFAOYSA-N

DOTMA, also known as2,5-dimethoxy-3,4,6-trimethylamphetamine or asJulia, is apsychedelic drug of thephenethylamine,amphetamine, andDOx families related toDOM.[1] It is the 3,6-dimethylderivative of DOM and the 6-methyl derivative ofGanesha.[1] The drug is said to be the first and only known active phenethylamine psychedelic with a fullysubstitutedphenyl ring.[1] However, thecyclizedFLY phenethylamines such as2C-B-FLY also have a fully substituted phenyl ring.[1]

DOTMA's dose is approximately 70 mgorally and itsduration is 7 to 9 hours.[1] It is lesspotent than DOM, which is active at doses of 3 to 10 mg, and has a shorter duration than DOM, which lasts 14 to 20 hours.[1] Similarly, DOTMA is less potent and shorter-acting than Ganesha, which has a dose of 20 to 32 mg and a duration of 18 to 24 hours.[1]

DOTMA was described in thescientific literature byDaniel Trachsel in 2013.[1] The6-methyl-DOManalogue of DOTMA and Ganesha,Juno, is relatively unknown but may be an active psychedelic as well.[1] DOTMA, or Julia, is closely related toAlexander Shulgin's "ten classic ladies".[2][3] It is acontrolled substance inCanada due to phenethylamine blanket-ban language[4] but is not explicitly controlled in theUnited States.[5]

See also

[edit]

References

[edit]
  1. ^abcdefghijkTrachsel 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. 936–937.ISBN 978-3-03788-700-4.OCLC 858805226. Archived fromthe original on 21 August 2025.
  2. ^Shulgin, Alexander;Shulgin, Ann (September 1991).PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press.ISBN 0-9630096-0-5.OCLC 25627628.
  3. ^Ger A, Ger D."Triple Goddess of the Night".British Neuroscience Association Bulletin.63:28–30.
  4. ^"Controlled Drugs and Substances Act".Department of Justice Canada. 5 December 2025. Retrieved20 January 2026.
  5. ^Orange Book: List of Controlled Substances and Regulated Chemicals (January 2026)(PDF),United States: U.S.Department of Justice:Drug Enforcement Administration (DEA): Diversion Control Division, January 2026

External links

[edit]
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
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

Thishallucinogen-related article is astub. You can help Wikipedia byadding missing information.

Retrieved from "https://en.wikipedia.org/w/index.php?title=DOTMA&oldid=1334211267"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2026 Movatter.jp