Beta-D

Pharmaceutical compound From Wikipedia, the free encyclopedia

Beta-D, or β-D, also known as 3,4,5-trimethoxy-β,β-dideuterophenethylamine or as β,β-dideuteromescaline, is a psychedelic drug of the scaline family related to mescaline.[1][2][3] It is the isotopologue of mescaline in which the two hydrogen atoms at the β position have been replaced with the deuterium isotopes.[1][2][3]

Other namesβ-D; β,β-Dideuteromescaline; 3,4,5-Trimethoxy-β,β-dideuterophenethylamine
ATC code
  • None
Quick facts Clinical data, Other names ...
Beta-D
Clinical data
Other namesβ-D; β,β-Dideuteromescaline; 3,4,5-Trimethoxy-β,β-dideuterophenethylamine
Routes of
administration
Oral[1]
Drug classSerotonergic psychedelic; Hallucinogen
ATC code
  • None
Pharmacokinetic data
Duration of action12 hours[1]
Identifiers
  • 2-(3,4,5-trimethoxyphenyl)(2,2-2H2)ethan-1-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC11H15D2NO3
Molar mass213.272 g·mol−1
3D model (JSmol)
  • COc1c(cc(cc1OC)C([2H])([2H])CN)OC
  • InChI=1S/C11H17NO3/c1-13-9-6-8(4-5-12)7-10(14-2)11(9)15-3/h6-7H,4-5,12H2,1-3H3/i4D2 checkY
  • Key:RHCSKNNOAZULRK-APZFVMQVSA-N checkY
  (verify)
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In his book PiHKAL (Phenethylamines I Have Known and Loved) and other publications, Alexander Shulgin lists β-D's dose as 200 to 400 mg orally in the case of the sulfate salt or 178 to 356 mg orally in the case of the hydrochloride salt and its duration as 12 hours.[1][2][3] The onset ranged from 15 minutes to 1.5 hours.[1] The drug produces hallucinogenic effects similarly to mescaline, with these effects of β-D having been thoroughly described.[1] It is thought to be very similar or indistinguishable in terms of properties, effects, and metabolism compared to mescaline.[1][2][3]

The chemical synthesis of β-D has been described.[1] Other deuterated isotopologues of mescaline are also known, such as 4-D (4-trideuteromescaline) and α-D (alpha-D; α,α-dideuteromescaline), among others.[1][2][3] α-D may be resistant to the oxidative deamination that is known to occur with mescaline, which may result in it being more potent than mescaline.[1][2][3] However, α-D is not known to have been studied.[1][2][3]

β-D was described by Shulgin in his book PiHKAL in 1991.[1] It does not seem to be a controlled substance in Canada as of 2025.[4]

See also

References

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