Self-reflecting. Intensive. Close to L*D. But I never had the feeling of losing control. A very helpful experience.
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This is a research chemical and is therefore not intended for human consumption! Further information can be found in the description.
Tryptamines for the next generation: Our 4-PrO-MET Pellets stand for precise dosing, maximum purity, and a new generation of psychedelically inspired research chemicals.
4-PrO-MET belongs to the 4-substituted tryptamines – a class of compounds primarily known through psilocybin from so-called Magic Mushrooms. Structurally related to established substances like 4-AcO-DMT or 4-HO-MET, 4-PrO-MET is increasingly becoming the focus of modern research approaches dealing with altered perception models, consciousness processes, and sensory modulation. More on this can be found in our blog.
Our 4-PrO-MET Megadosing Pellets have been specially developed for research approaches that work with larger active substance units and extended observation models.
The advantages at a glance:
Accessible Characteristics: Appreciated in expert circles for its clear, pleasantly structured, and deep dynamics – ideal for macrodosing and demanding research models.
Synthetic Exactness: Unlike volatile natural extracts, pure synthesis guarantees absolute freedom from accompanying substances and fluctuating active substance contents.
Valid Experimental Conditions: Maximum purity and constant dosing ensure seamless reproducibility in long-term observation series.
Product: 4-PrO-MET Megadosing Pellets with 30 mg active ingredient each
Active Ingredient: 4-Propionoxy-N-Ethyl-N-Methyltryptamine fumarate
Empirical Formula: C20H26N2O6
Chemical Formula: C₂₀H₂₆N₂O₆
Molecular Mass: 390.43 g·mol⁻¹
IUPAC: 3-(2-(ethyl(methyl)amino)ethyl)-1H-indol-4-yl propionate fumarate
Form: Solid pellets for precise units within scientific investigations
Ingredients: 4-PrO-MET 30mg, microcrystalline cellulose, magnesium stearate, silicon dioxide, dicalcium phosphate
Each new batch of our 4-PrO-MET products is externally tested by a certified laboratory in Germany. The active ingredient is identified by mass spectrometric analysis after dissolving the substance in acetonitrile. In addition, the purity is checked to ensure consistently high research quality.
Confirmed are:
Analytics:
Quality control using HPLC / LC-MS / NMR
Application:
This reagent is typically used in chromatographic-mass spectrometric methods (GC-MS, LC-MS). Suitability for the respective application must be checked by the user.
Typical research approaches:
All information is provided exclusively in a scientific context and does not constitute a recommendation for use. 4-PrO-MET is not suitable for human consumption.
For optimal stability, we recommend the following storage conditions:
Numerous options:
Shipping is discreet and neutral via our logistics partner DHL from Germany. We use inconspicuous packaging without any indication of content or product category.
Sender and manufacturer information:
Awakening GmbH
Fidicinstrasse 44
DE-10965 Berlin
+49 (0) 178 5493 709
mail@psychedelika.club
General Questions:
If you have general questions about our products, please visit our Blog or Wikipedia.
4-PrO-MET is one of the 4-substituted tryptamines – a group of substances that became known primarily through psilocybin from so-called magic mushrooms.
Structurally related to established substances such as 4-AcO-DMT or 4-HO-MET, 4-PrO-MET is increasingly becoming the focus of modern research approaches dealing with altered perception models, consciousness processes, and sensory modulation.
The Narcotics Act (BtMG) generally covers substances by explicitly listing them in Annexes I to III. The New Psychoactive Substances Act (NpSG) also uses substance group definitions that describe specific chemical structures and their permissible substitution patterns.
For the substance group of indol-3-alkylamines, various substituents are explicitly named at specific positions on the indole ring system, particularly positions 4 to 7, including hydroxy, alkoxy, methylenedioxy, and acetoxy groups.
A propionoxy substitution is not listed in the wording of the relevant substance group definition. Therefore, based on an interpretation aligned with the legal text, a classification different from acetoxy-substituted compounds results.