Allylescaline

Allylescaline

Allylescaline

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Description

Allylescaline

Also known as:

  • 2-(4-Allyloxy-3,5-dimethoxy-phenyl)-ethylamine
  • 2-[4-(Allyloxy)-3,5-dimethoxyphenyl]ethanamin[German][ACD/IUPAC Name]
  • 2-[4-(Allyloxy)-3,5-dimethoxyphenyl]ethanamine[ACD/IUPAC Name]
  • 2-[4-(Allyloxy)-3,5-diméthoxyphényl]éthanamine[French][ACD/IUPAC Name]
  • 4-Allyloxy-3,5-dimethoxyphenethylamine
  • Benzeneethanamine, 3,5-dimethoxy-4-(2-propen-1-yloxy)-[ACD/Index Name]
  • 2-(3,5-dimethoxy-4-prop-2-enoxyphenyl)ethanamine
  • 2-(4-(Allyloxy)-3,5-dimethoxyphenyl)ethanamine
  • 2-{3,5-Dimethoxy-4-[(prop-2-en-1-yl)oxy]phenyl}ethan-1-amine
  • 3,5-Dimethoxy-4-(2-propenyloxy)benzeneethanamine
  • 3,5-Dimethoxy-4-(2-propenyloxy)benzeneethanamine hydrochloride
  • 3,5-dimethoxy-4-(allyloxy)phenethylamine
  • 3,5-Dimethoxy-4-allyloxy-??-phenoaethylamin
  • Benzeneethanamine, 3,5-dimethoxy-4-(2-propenyloxy)-
  • MFCD12829242

Mescaline analogue with a much lower dose, that seems to rely heavily on colours.

Summary

It is relatively uncommon and has little to no history of human usage. Very little data exists about the pharmacological properties, metabolism, and toxicity of allylescaline. The effects of this compound were first described by Alexander Shulgin in his book PiHKAL: A Chemical Love Story.

He lists the dosage range as 20 – 35 mg orally and describes the duration of action to be 8 - 12 hours.

History

Chemistry

Allylescaline

Allylescaline

Escaline contains two methoxy functional groups CH3O- which are attached to carbons R3, and R5 and an additional allyloxy group at carbon R4 of the phenyl ring.

Allylescaline is the 4-allyloxy analog of mescaline.

Common NameAllylescaline
Systematic nameAllylescaline
FormulaC_{13}H_{19}NO_{3}
SMILESCOc1cc(cc(c1OCC=C)OC)CCN
Std. InChiInChI=1S/C13H19NO3/c1-4-7-17-13-11(15-2)8-10(5-6-14)9-12(13)16-3/h4,8-9H,1,5-7,14H2,2-3H3
Std. InChiKeyJNUAYHHGCXYBHX-UHFFFAOYSA-N
Avg. Mass237.2949 Da
Molecular Weight237.2949
Monoisotopic Mass237.13649 Da
Nominal Mass237
ChemSpider ID21106254

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Dosing Guide

Oral
Threshold15-20mg
Light20-30mg
Common30-40mg
Strong40-60mg+

Duration

Allylescaline Duration Data
Onset45-240 minutes
Duration8-12 hours
After-effects1-16 hours

Interactions and Synergies

There are no existing interaction or synergy data for this drug.

General Information

Experiences
Oral
Vaporization
Come up
Dosage
EffectsEuphoria, empathy, insight, brightened colour, Closed/Open eye visuals, enhanced tactile sensation, mental/physical stimulation, decreased appetite, pupil dilation, restlessness, change in perception, ego softening, sweating/chills, muscle tension, confusion, insomnia.
After Effects
Avoid
Warning
Risks
Test Kits
Marguis Test Result
Tolerance
Detection
Half-life
Advice
Note
Note 2:
Note 3:

Effects

Pharmacological Effects

Allylescaline acts as a 5-HT2A partial agonist. The psychedelic effects are believed to come from allylescaline’s efficacy at the 5-HT2A receptors. However, the role of these interactions and how they result in the psychedelic experience continues to remain elusive.

Subjective Effects

Physical Effects

Psychological Effects

Visual Effects

Enhancements

Distortions

Geometry

Hallucinatory states

Auditory Effects

Sensory Effects

Transpersonal Effects

Legal Status


References

  1. https://www.erowid.org/library/books_online/pihkal/pihkal002.shtml | Allylescaline (TiHKAL)
  2. "Neunte Verordnung zur Änderung betäubungsmittelrechtlicher Vorschriften" (in German). Bundesanzeiger Verlag. Retrieved December 10, 2019.
  3. "Anlage I BtMG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
  4. "§ 29 BtMG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
  5. Psychoactive Substances Act 2016 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/2016/2/contents/enacted

Sources

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 for 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.