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Description
4-AcO-MET Also known as:
- 4-Acetoxy-N-methyl-
N-ethyltryptamine
- 1445751-40-5[RN]
- 1H-Indol-4-ol, 3-[2
-(ethylmethylamino) [ACD/Index Name]ethyl]-, acetate (e ster)
- 3-{2-[Ethyl(methyl)
amino]ethyl}-1H-ind [ACD/IUPAC Name]ol-4-yl acetate
- 3-{2-[Ethyl(methyl)
amino]ethyl}-1H-ind [German][ACD/IUPAC Name]ol-4-yl-acetat
- 4-ACETOXYETHYLMETHY
LTRYPTAMINE
- 4-Acetoxy-MET
- 4-AcO-MET[Wiki]
- Acétate de 3-{2-[ét
hyl(méthyl)amino]ét [French][ACD/IUPAC Name]hyl}-1H-indol-4-yle
- Metacetin
- PCJ17NV1P0
- 3-{2-[Ethyl(methyl)
amine]ethyl}-1H-ind [ACD/IUPAC Name]ol-4-yl acetate
- UNII:PCJ17NV1P0
A rare psychedelic tryptamine which is thought to be metabolised into 4-HO-MET. Onset and duration, intensity will vary but effect profile is largely the same.
Chemistry
Tryptamines share a core structure comprised of a bicyclic indole heterocycle attached at R3 to an amino group via an ethyl side chain.
4-AcO-MET is substituted at R4 of its indole heterocycle with an acetoxy (AcO) functional group CH3COO−.
It also contains a methyl group and an ethyl chain bound to the terminal amine RN of its tryptamine backbone (MET).
4-AcO-MET is an acetate ester analog of 4-HO-MET and the N-substituted ethyl homolog of 4-AcO-DMT.
Common Name | 4-Acetoxy-N-methyl-N-ethyltryptamine |
Systematic name | 4-Acetoxy-N-methyl-N-ethyltryp |
Formula | C_{15}H_{20}N_{2}O_{2} |
SMILES | CCN(C)CCc1c[nH]c2c1c(ccc2)OC(=O)C |
Std. InChi | InChI=1S/C15H20N2O2/c1-4-17(3)9-8-12-10-16-13-6-5-7-14(15(12)13)19-11(2)18/h5-7,10,16H,4,8-9H2,1-3H3 |
Std. InChiKey | OMDKHOOGGJRLLX-UHFFFAOYSA-N |
Avg. Mass | 260.3315 Da |
Molecular Weight | 260.3315 |
Monoisotopic Mass | 260.152466 Da |
Nominal Mass | 260 |
ChemSpider ID | 26633897 |
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Dose Chart
Oral | |
---|---|
Light | 12-18mg |
Common | 20-25mg |
Heavy | 25-35+mg |
Duration Chart
4-AcO-MET Duration Data | |
---|---|
Onset | 20-40 minutes |
Duration | 4-6 hours |
After-effects | 2-12 hours |
Legal Status
Sources
References
- Talaie, H.; Panahandeh, R.; Fayaznouri, M. R.; Asadi, Z.; Abdollahi, M. (2009). "Dose-independent occurrence of seizure with tramadol". Journal of Medical Toxicology. 5 (2): 63–67. :10.1007/BF03161089. 1556-9039.
- "Verordnung zur Änderung der Anlage des Neue-psychoaktive-Stoffe-Gesetzes und von Anlagen des Betäubungsmittelgesetzes" (PDF) (in German). Bundesanzeiger Verlag. Retrieved December 10, 2019.
- "Anlage NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
- "§ 4 NpSG" (in German). Bundesministerium der Justiz und für Verbraucherschutz. Retrieved December 10, 2019.
- Misuse of Drugs Act 1971 (Legislation.gov.uk) | http://www.legislation.gov.uk/ukpga/1971/38/schedule/2/part/I/paragraph/3
- Misuse of Drugs Act 1971 (Legislation.gov.uk) |http://www.legislation.gov.uk/ukpga/1971/38/schedule/2/part/I#reference-M_F_c7632653-ddad-4420-f307-e3da1e36d30e
Resources
Information made possible with:
- PsychonautWiki is a community-driven online encyclopedia that aims to document the field of psychonautics in a comprehensive, scientifically-grounded manner.
- Erowid is a non-profit educational & harm-reduction resource with 60 thousand pages of online information about psychoactive drugs
- PubChem National Center for Bio Informatics
- Chemspider is a free chemical structure database providing fast access to over 34 million structures, properties and associated information.
- 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.