| Identification | More | [Name]
2,5-Dimethoxyphenethylamine hydrochloride | [CAS]
3166-74-3 | [Synonyms]
2-(2,5-DIMETHOXYPHENYL)ETHYLAMINE HYDROCHLORIDE
2,5-DIMETHOXYPHENETHYLAMINE HCL
2,5-DIMETHOXY PHENETHYLAMINE HYDROCHLORIDE
2,5-dimethoxyphenethylamine monohydrochloride
BENZENEETHANAMINE,2,5-DIMETHOXY-MONOHYDROCHLORIDE
2,5-dimethoxy-phenethylaminhydrochloride
2,5-DIMETHOXY PHENETHYLAMINE HYDORCHLORIDE | [EINECS(EC#)]
-0 | [Molecular Formula]
C10H16ClNO2 | [MDL Number]
MFCD01708299 | [Molecular Weight]
217.69 | [MOL File]
3166-74-3.mol |
| Chemical Properties | Back Directory | [Melting point ]
139 °C | [solubility ]
DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 10 mg/ml | [form ]
A crystalline solid | [InChI]
InChI=1S/C10H15NO2.ClH/c1-12-9-3-4-10(13-2)8(7-9)5-6-11;/h3-4,7H,5-6,11H2,1-2H3;1H | [InChIKey]
PJMQBIMLDBAWRK-UHFFFAOYSA-N | [SMILES]
C1(CCN)=C(OC)C=CC(OC)=C1.[H+].[Cl-] | [CAS DataBase Reference]
3166-74-3(CAS DataBase Reference) |
| Hazard Information | Back Directory | [Description]
A series of 2,5-phenethylamines, collectively referred to as 2Cs, have psychoactive effects.1,2 The most effective 2C compounds are 2,5-dimethoxy-4-substituted phenethylamines; many are scheduled as illegal substances.3,4 2C-H is described formally as 2,5-dimethoxyphenethylamine. Unlike the 4-substituted 2-C forms, it has little effect on serotonin receptors, activating the 5-HT2C receptor to 20% that induced by serotonin (pEC50 = 5.93).2 This product is intended for research and forensic applications. | [Uses]
A series of 2,5-phenethylamines, collectively referred to as 2Cs, have psychoactive effects. The most effective 2C compounds are 2,5-dimethoxy-4-substituted phenethylamines; many are scheduled as ille
gal substances. This product is intended for research and forensic applications. |
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