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879-36-7

879-36-7 Structure

879-36-7 Structure
IdentificationBack Directory
[Name]

3-(2-AMINOPROPYL)INDOLE MONOHYDROCHLORIDE
[CAS]

879-36-7
[Synonyms]

U 14 Hy
NSC 97069 Hydrochloride
3-(2-AMINOPROPYL)INDOLE HCl
α-MethyltryptaMine Hydrochloride
α-methyl Tryptamine hydrochloride
(±)-α-MethyltryptaMine Hydrochloride
3-(2-AMinopropyl)indole Hydrochloride
3-(2-AMinopropyl)-1H-indole Hydrochloride
3-(2-AMINOPROPYL)INDOLE MONOHYDROCHLORIDE
.alpha.-methyl Tryptamine (hydrochloride)
1-(1H-indol-3-yl)propan-2-amine hydrochloride
1-(1H-indol-3-yl)-2-propanamine hydrochloride
2-(1H-Indol-3-yl)-1-MethylethylaMine Hydrochloride
α-Methyltryptamine (hydrochloride) (exempt preparation)
α-methyl Tryptamine (hydrochloride) (exempt preparation)
.alpha.-methyl Tryptamine (hydrochloride) (exempt preparation)
[Molecular Formula]

C11H15ClN2
[MDL Number]

MFCD01719208
[MOL File]

879-36-7.mol
[Molecular Weight]

210.703
Chemical PropertiesBack Directory
[Melting point ]

217 °C
[solubility ]

DMF: 11 mg/ml; DMSO: 11 mg/ml; Ethanol: 20 mg/ml; PBS (pH 7.2): 5 mg/ml
[form ]

A crystalline solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312+H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P321-P330-P362+P364-P501
Hazard InformationBack Directory
[Description]

α-methyl Tryptamine is a psychedelic drug that has schedule I status in the United States. It potently stimulates the release of monoamines from synaptosomes and inhibits their re-uptake (IC50s = 0.73, 0.38, and 0.4 μM for dopamine, serotonin, and norepinephrine, respectively). This product is intended for forensic use.
[Chemical Properties]

Light Beige Solid
[Uses]

3-(2-Aminopropyl)indole monohydrochloride is used as a Intermediate in organic syntheses.
[Uses]

α-Methyltryptamine is a methylated Tryptamine with psychedelic, stimulant and entactogenic properties. α-Methyltryptamine is a non-selective serotonin receptor agonist. α-Methyltryptamine acts as relatively balanced releasing agent of serotonin, norepinephrine, and dopamine.
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