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Contents

   



(Top)
 


1 References  





2 See also  














Beta-D






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From Wikipedia, the free encyclopedia
 


Beta-D
Names
Preferred IUPAC name

2-(3,4,5-Trimethoxyphenyl)(2,2-2H2)ethan-1-amine

Other names

3,4,5-Trimethoxy-beta-dideuterophenethylamine
3,4,5-Trimethoxy-1-ethyl-(beta-dideutero)amine

Identifiers

CAS Number

3D model (JSmol)

ChemSpider

PubChem CID

UNII

CompTox Dashboard (EPA)

  • 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

  • InChI=1/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

    Key: RHCSKNNOAZULRK-APZFVMQVEB

  • COc1c(cc(cc1OC)C([2H])([2H])CN)OC

Properties

Chemical formula

C11H15D2NO3 or C11H152H2NO3
Molar mass 213.27 g/mol

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

checkY verify (what is checkY☒N ?)

Infobox references

Beta-D (3,4,5-trimethoxy-β-dideuterophenethylamine) is a lesser-known psychedelic drug. It is one of the few phenethylamines used as a recreational drug that is enriched in deuterium. Beta-D can be prepared as a sulfate salt or as a hydrochloride salt. It is the beta-dideutero analogofmescaline. Beta-D was first synthesized by Alexander Shulgin. In his book PiHKAL, the dosage is listed as approximately 200–400 mg for the sulfate salt, and 178–356 mg for the hydrochloride salt. Its effects last for 12 hours. Beta-D has a very rapid onset. It produces an increased appreciation of music and a strong connection with God.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of Beta-D.

References

[edit]
  1. ^ Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

See also

[edit]
Retrieved from "https://en.wikipedia.org/w/index.php?title=Beta-D&oldid=1226028594"

Categories: 
Psychedelic phenethylamines
Deuterated compounds
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This page was last edited on 28 May 2024, at 04:35 (UTC).

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