2-(2,5-Dimethoxyphenyl)ethanamine hydrochloride (1:1)
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Grundinformationen
- CAS
3166-74-3- Standard-SMILES
COc1ccc(OC)c(CCN)c1.Cl- InChIKey
PJMQBIMLDBAWRK-UHFFFAOYSA-N- Summenformel
- C10H16ClNO2
- Durchschnittliche Molmasse
- 217,696 g/mol
- Monoisotopische Masse
- 217,08695643
Namen und Bezeichner
- Bevorzugter Name
- 2-(2,5-Dimethoxyphenyl)ethanamine hydrochloride (1:1)
- IUPAC
- 2-(2,5-Dimethoxyphenyl)ethan-1-amine--hydrogen chloride (1/1)
- Englischer Name
- 2,5-Dimethoxyphenethylamine hydrochloride
- Summenformel
- C10H16ClNO2
- Molmasse
- 217.69
Namen und Synonyme
2C-H (hydrochloride)Dopamine Impurity 24 HCl2,5-DIMETHOXYPHENETHYLAMINE HCL2,5-Dimethoxyphenylethylamine HClDopamine hydrochloride impurity 352-(2,5-DiMethoxy-phenyl)-ethylaMine HCl2,5-dimethoxy-phenethylaminhydrochloride2C-H (hydrochloride) (exempt preparation)2,5-DIMETHOXY PHENETHYLAMINE HYDROCHLORIDE2,5-DIMETHOXY PHENETHYLAMINE HYDORCHLORIDE
Datenbank-Bezeichner
- CAS
3166-74-3- PubChem CID
- 76631
- DTXSID
DTXSID10185559- UNII
- P2Y262S9PP
Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 139 °C · 139 °C
- Löslichkeit
- 30 mg/ml; · DMF: 30 mg/ml; DMSO: 30 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 10 mg/ml
- Aggregatzustand
- 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 Datenbank
- 3166 · 3166-74-3(CAS DataBase Reference)
Chemie und Industrie
Anwendungen
BeschreibungA 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 illegal substances. 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). This product is intended for research and forensic applications.
VerwendenA 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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