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.
Disclaimer: Psychedelic drugs offer some of the most powerful and intense psychological experiences. Additionally these substances are illegal in many places. We understand that even though these substances are illegal, their use occurs frequently. We do not condone breaking of the law. By providing accurate information about these substances, we encourage the user to make responsible decisions and practice harm reduction.
Description
EPT Also known as:
- 1H-Indole-3-ethanam
ine, N-ethyl-N-prop [ACD/Index Name]yl-
- N-Ethyl-N-[2-(1H-in
dol-3-yl)ethyl]-1-p [German][ACD/IUPAC Name]ropanamin
- N-Ethyl-N-[2-(1H-in
dol-3-yl)ethyl]-1-p [ACD/IUPAC Name]ropanamine
- N-Éthyl-N-[2-(1H-in
dol-3-yl)éthyl]-1-p [French][ACD/IUPAC Name]ropanamine
- EPT
- N-ethyl-N-propyl-1H
-indole-3-ethanamine
Ethylpropyltryptamine a novel tryptamine, that is the structural homologue of DMT.
Summary
EPT is chemically related to DMT and belongs to a series of psychedelic compounds known as unsubstituted tryptamines. The original synthesis date of EPT is unknown. It first appeared for sale on the online research chemical market in 2016.
Unlike most research chemicals, EPT has no documentation in the scientific literature. It appears to be an entirely novel product of clandestine drug design. Initial reports describe the effects of EPT as mild and indistinct compared to structurally similar base tryptamines such as DMT, DET and DPT, all of which are highly powerful psychedelics.
Of these, it is reported to be most similar to DPT, albeit less potent and with a less immersive headspace. Virtually no data exists about the pharmacological properties, metabolism, and toxicity of EPT. It is highly advised to use harm reduction practices if using this substance.
Chemistry
Tryptamines share a core structure comprised of a bicyclic indole heterocycle attached at R3 to an amino group via an ethyl side chain.
EPT features one propyl and one ethyl groups bound to the terminal amine RN of its tryptamine backbone. EPT is the N-ethyl analog of DPT and the N-propyl analog of DET.
It is also an analog of 4-HO-EPT and [4-AcO-EPT]].
Common Name | N-Ethyl-N-[2-(1H-indol-3-yl)ethyl]-1-propanamine |
Systematic name | N-Ethyl-N-[2-(1H-indol-3-yl)et |
Formula | C_{15}H_{22}N_{2} |
SMILES | CCN(CCC)CCC1=CNC2=CC=CC=C12 |
Std. InChi | InChI=1S/C13H20O/c1-2-3-4-5-6-7-12-8-10-13(14)11-9-12/h8-11,14H,2-7H2,1H3 |
Std. InChiKey | KNDDEFBFJLKPFE-UHFFFAOYSA-N |
Avg. Mass | 230.3486 Da |
Molecular Weight | 230.3486 |
Monoisotopic Mass | 230.178299 Da |
Nominal Mass | 230 |
ChemSpider ID | 81407759 |
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Dose Chart
Oral | |
---|---|
Light | 50-75mg |
Common | 75-100mg |
Strong | 100mg+ |
Duration Chart
Oral | |
---|---|
Onset | 20-60 minutes |
Duration | 2-4 hours |
After-effects | 1-6 hours |
Legal Status
Due to its relative obscurity, the possession and sale of EPT is unscheduled in most countries.
Sources
References
- "Anlage NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
- "Verordnung zur Änderung der Anlage des Neue-psychoaktive-Stoffe-Gesetzes und von Anlagen des Betäubungsmittelgesetzes" (PDF). Bundesgesetzblatt Jahrgang 2019 Teil I Nr. 27 (in German). Bundesanzeiger Verlag. July 17, 2019. pp. 1083–1094. Retrieved January 1, 2020.
- "§ 4 NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz [Federal Ministry of Justice and Consumer Protection]. Retrieved December 10, 2019.
- "Part I: Class A Drugs". "Misuse of Drugs Act 1971". UK Government. Retrieved January 7, 2020.
Resources
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1717 CheMall LP107992
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1717 CheMall OR003566
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abcr AB116991
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ABI Chemicals AC2A00B0J
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Advanced Technology & Industrial 1100222
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Advanced Technology & Industrial 4149355
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AK Scientific 6518AL
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AKos AKOS002685653
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Alfa Aesar A15407
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Alfa Chemistry 1987-50-4
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Alfa Chemistry ACM1987504
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Alichem A019146476
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Amadis Chemical A814024
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Ambeed A658227
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American Custom Chemicals Corp CHM0025739
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Angene AG-A-75546
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Angene AGN-PC-0JKCPH
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Anward ANW-23836
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Apollo Scientific Limited OR24676
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Ark Pharm, Inc. AK167106
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Cayman Chemical CM280057
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Jalor-Chem I01-6623
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KEGG C14698
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LabNetwork LN01364012
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Labseeker SC-76441
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LGC Standards DRE-C14136500
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Mcule MCULE-1814167078
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MMDB 6722
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MMDB 6722.7
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Molport MolPort-000-183-590
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MuseChem M124080
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NIST Chemistry WebBook 4020916700
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NIST Spectra mainlib_301632
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NIST Spectra nist ri
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Parchem – fine & specialty chemicals 44579
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PDB EPT
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PIChemicals PI-11987
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PubChem 16143
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Rosewachem RW078480
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Royal Society of Chemistry b403124e
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