Psychedelic Research Chemicals or RC Chems are new synthetic substances which are structurally similar to the original drug, while being functional analogs. Data on their effects limited due as they’re fairly new and do not have a lot of human consumption history.

Psychedelics are substances (natural or laboratory made) which cause profound changes in a one’s perceptions of reality. While under the influence of hallucinogens, users might hallcuniate visually and auditorily.

This is an Experimental Substance with little data. This is most likely because the substance is is not very old. Information is limite and incomplete.

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Description

DOET Also known as:

  • 1-(4-Ethyl-2,5-dimethoxyphenyl)-2-propanamin[German][ACD/IUPAC Name]
  • 1-(4-Ethyl-2,5-dimethoxyphenyl)-2-propanamine[ACD/IUPAC Name]
  • 1-(4-Éthyl-2,5-diméthoxyphényl)-2-propanamine[French][ACD/IUPAC Name]
  • 1-(4-Ethyl-2,5-dimethoxyphenyl)propan-2-amine
  • 4-ETHYL-2,5-DIMETHOXYAMPHETAMINE
  • Benzeneethanamine, 4-ethyl-2,5-dimethoxy-α-methyl-[ACD/Index Name]
  • Phenethylamine, 2,5-dimethoxy-4-ethyl-α-methyl-
  • (±)2-(4-Ethyl-2,5-dimethoxy-phenyl)-1-methyl-ethylamine
  • 2-(4-Ethyl-2,5-dimethoxy-phenyl)-1-methyl-ethylamine
  • 2,5-DIMETHOXY-4-ETHYLAMPHETAMIN
  • 2,5-Dimethoxy-4-ethylamphetamine
  • 2,5-dimethoxy-4-ethylamphetamine (''DOEt'')
  • 4-ethyl-2,5-dimethoxy-?-methyl-benzeneethanamine
  • 4-ethyl-2,5-dimethoxy-a-methyl-benzeneethanamine
  • 4-ethyl-2,5-dimethoxy-α-methyl-benzeneethanamine
  • 4-ethyl-2,5-dimethoxy-α-methyl-benzeneethanamine
  • DOET
  • DOET (exempt preparation)
  • DOET,(-)

A potent and long acting psychedelic stimulant and substituted amphetamine, similar in effects to other DOx compounds. First synthesised by Alexander Shulgin.

Chemistry

Common Name4-ETHYL-2,5-DIMETHOXYAMPHETAMINE
Systematic name4-ETHYL-2,5-DIMETHOXYAMPHETAMINE
FormulaC_{13}H_{21}NO_{2}
SMILESCCc1cc(c(cc1OC)CC(C)N)OC
Std. InChiInChI=1S/C13H21NO2/c1-5-10-7-13(16-4)11(6-9(2)14)8-12(10)15-3/h7-9H,5-6,14H2,1-4H3
Std. InChiKeyHXJKWPGVENNMCC-UHFFFAOYSA-N
Avg. Mass223.3113 Da
Molecular Weight223.3113
Monoisotopic Mass223.157227 Da
Nominal Mass223
ChemSpider ID25499

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Dose Chart

Oral
Threshold1mg
Light2-4mg
Common4-6mg
Strong6-10mg

Duration Chart

DOET Duration Data
Onset1-3 hours
Duration12-30 hours
After-effects12-72 hours

Sources

Resources

  1. 1717 CheMall OR054661
  2. 1717 CheMall OR132199
  3. ACToR: Aggregated Computational Toxicology Resource 15588-95-1
  4. Advanced Technology & Industrial 3570075
  5. Alfa Chemistry ACM22004326
  6. American Custom Chemicals Corp CHM0008079
  7. Aurora Fine Chemicals A31.062.997
  8. Aurora Fine Chemicals K13.731.026
  9. BGS International BG04243666
  10. BindingDB 81965
  11. Cayman Chemical 11141
  12. Cayman Chemical 11141.0
  13. Cayman Chemical 15704
  14. Cayman Chemical 15704.0
  15. ChemAdvisor OHS73354
  16. ChEMBL CHEMBL8224
  17. ChemIDplus 022004326
  18. ChemIDplus 22004326
  19. Chemspace CSC015231490
  20. CSDeposition Service DB01467
  21. DiscoveryGate 27402
  22. DrugBank DB01467
  23. FDA UNII - NLM 9SK6K682UL
  24. LabNetwork LN01307210
  25. MuseChem R054285
  26. NIST Spectra mainlib_335372
  27. NIST Spectra replib_247842
  28. PubChem 27402
  29. PubMed 1182040
  30. PubMed 1197576
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  40. Royal Society of Chemistry c0nj00228c
  41. Springer Nature 5HT-2 mediation of acute behavioral effects of hallucinogens in rats
  42. Springer Nature Cross-reactivities of 39 new amphetamine designer drugs on three abuse drugs urinary screening tests
  43. Springer Nature Cross-reactivities of 41 new amphetamine designer drugs to EMIT?? immunoassays
  44. Springer Nature Effects of the phenethylamine derivatives, BL-3912, fenfluramine, and Sch-12679, in rats trained with LSD as a discriminative stimulus
  45. Springer Nature Enantiomeric separation of amphetamine, methamphetamine and ring substituted amphetamines by means of a ??-cyclodextrin-chiral stationary phase
  46. Springer Nature MDA and DOM: Substituted amphetamines that do not produce amphetamine-like discriminative stimuli in the rat
  47. Springer Nature Relative potency of amphetamine derivatives and N,N-dimethyltryptamines
  48. Springer Nature The discriminative stimulus properties of 2,5-dimethoxy-4-methylamphetamine (DOM): Differentiation from amphetamine
  49. Springer Nature The effects of 2,5-dimethoxy-4-methylamphetamine (DOM), 2,5-dimethoxy-4-ethylamphetamine (DOET), d-amphetamine, and cocaine in rats trained with mescaline as a discriminative stimulus
  50. Thomson Pharma 00514010
  51. VulcanChem VC254849
  52. Wikidata Q947249
  53. Wikipedia 2,5-Dimethoxy-4-ethylamphetamine

Information made possible with:

  1. PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
  2. Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
  3. PubChem National Center for Bio Informatics
  4. Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
  5. Wikipedia

Additional APIs were used to construct this information. Thanks to ChemSpider, NCBI, PubChem etc.

Data is constantly updated so please check back later to see if there is any more available information on this substance.