TMPEA
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Molecular structure via molpic |
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Conformer structure via 3Dmol.js |
Molecular formula | C11H17NO3[1] |
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Molecular mass | 211.26 g/mol[1] |
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Appearance | Crystals. ... Takes up CO2 from the air and forms crystalline carbonate[1] |
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Predicted LogP | 0.7[1] |
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Melting point | 35-36 °C[1] |
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Boiling point | 180 °C[1] |
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Solubility | Moderately soluble in water; soluble in chloroform, benzene. Practically insoluble in ether, petroleum ether.[1] |
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Chirality | achiral[2] |
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Dosing |
Elimination half-life | 3.6 hours (range 2.6–5.3 hours) |
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Duration of action | 6.4–14 hours (range 3.0–22 hours) |
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Statistically derived dosages by Sernyl |
Mescaline
Mescaline (also known as Mescalin, Tmpea, 3,4,5-Trimethoxyphenethylamine, Mezcaline, 2-(3,4,5-Trimethoxyphenyl)ethanamine, 3,4,5-Trimethoxybenzeneethanamine, 3,4,5-Trimethoxyphenylethylamine, mescalina, mezcalina or Meskalin) is a psychedelic substance of the catecholamine class.
Chemistry
Mescaline is typically found in the form of its sulfate, hemisulfate and hydrochloride salts
or its acetate ester.
Stereochemistry
Mescaline is a achiral mixture
Legal status
- Australia: Mescaline is a Schedule 9.
- Brazil: Mescaline is a F2.[3]
- Canada: Mescaline is a Schedule III.
- Germany: Mescaline is a Anlage I.
- United Kingdom: Mescaline is a Class A.
- United States: Mescaline is a Schedule I under the "Controlled Substances Act (CSA)".
- United Nations: Mescaline is a Schedule I under the "Convention on Psychotropic Substances 1971".
See also
External links
References