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Names | |
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IUPAC name
(R)-1-(3,4-Dimethoxyphenyl)-2-(dimethylamino)ethanol
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII | |
CompTox Dashboard (
EPA)
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Properties | |
C12H19NO3 | |
Molar mass | 225.288 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Macromerine is a phenethylamine derivative. It was first identified from the cactus Coryphantha macromeris. [1] It can also be found in C. runyonii, [2] C. elephantidens, and other related members of the family Cactaceae.
Macromerine is a phenethylamine derivative with the molecular formula C12H19NO3.
At least one study found macromerine to be non-psychoactive, [3] however as a phenethylamine derivative, it may be psychoactive.
![]() | |
Names | |
---|---|
IUPAC name
(R)-1-(3,4-Dimethoxyphenyl)-2-(dimethylamino)ethanol
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C12H19NO3 | |
Molar mass | 225.288 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Macromerine is a phenethylamine derivative. It was first identified from the cactus Coryphantha macromeris. [1] It can also be found in C. runyonii, [2] C. elephantidens, and other related members of the family Cactaceae.
Macromerine is a phenethylamine derivative with the molecular formula C12H19NO3.
At least one study found macromerine to be non-psychoactive, [3] however as a phenethylamine derivative, it may be psychoactive.