Anodyne| Tyramine | |
|---|---|
 |
| Salts [] | |
|---|---|
| Tyramine hydrochloride | |
|
| Esters [] | |
|---|---|
| Tyramine acetate | |
|
| Molecular structure via molpic | |
| Conformer structure via 3Dmol.js | |
| Molecular formula | C8H11NO[1] |
|---|---|
| Molecular mass | 137.18 g/mol[1] |
| Appearance | CRYSTALS FROM BENZENE OR ALCOHOL[1] |
| Predicted LogP | 1.1[1] |
| Melting point | 164-165 °C[1] |
| Boiling point | 166 °C[1] |
| Solubility | SOL IN WATER /TYRAMINE HYDROCHLORIDE/[1] |
| Chirality | achiral[2] |
| Identifiers [] | |
|---|---|
| IUPAC name | 4-(2-aminoethyl)phenol[1] |
| SMILES | C1=CC(=CC=C1CCN)O[1] |
| InChI | InChI=1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2[1] |
| InChIKey | DZGWFCGJZKJUFP-UHFFFAOYSA-N[1] |
| Dosing |
|---|
Tyramine
Tyramine (also known as 4-Hydroxyphenethylamine, 2-(4-Hydroxyphenyl)ethylamine, Uteramine, Tyrosamine, Tocosine, Tyramin, Systogene, Phenol, 4-(2-aminoethyl)-, 4-Hydroxyphenylethylamine or p-(2-Aminoethyl)phenol) is a substance of the phenethylamine class.
Chemistry
Tyramine is typically found in the form of its hydrochloride salt or its acetate ester.
Stereochemistry
Tyramine is a achiral mixture