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20735-15-3

20735-15-3 Structure

20735-15-3 Structure
IdentificationBack Directory
[Name]

1-PHENYL-2-BUTANAMINE HYDROCHLORIDE
[CAS]

20735-15-3
[Synonyms]

1-benzyl-propylamine
Butanphenamine hydrochloride
1-PHENYL-2-BUTANAMINE HYDROCHLORIDE
1-phenylbutan-2-amine:hydrochloride
2-Amino-1-phenylbutane (hydrochloride)
[Molecular Formula]

C10H16ClN
[MDL Number]

MFCD00274068
[MOL File]

20735-15-3.mol
[Molecular Weight]

185.694
Chemical PropertiesBack Directory
[Melting point ]

143-144°C
[solubility ]

DMF: 30 mg/ml; DMSO: 25 mg/ml; Ethanol: 30 mg/ml; PBS (pH 7.2): 5 mg/ml
[form ]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H319
[Precautionary statements ]

P264-P270-P280-P301+P312-P305+P351+P338-P337+P313
[Hazard Codes ]

Xn
[Risk Statements ]

22-36
[Safety Statements ]

26
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Amphetamines are chemical compounds characterized by an α-methylphenethylamine base structure. D-amphetamine is a stimulant that binds the norepinephrine and dopamine transporters (EC50s = 7.1 and 24.8 nM, respectively). 2-Amino-1-phenylbutane is an amphetamine characterized by having an ethyl group in the alpha position. It has emerged as a potential recreational drug. This product is a mixture of the D and L isomers. The D isomer of this compound partially substitutes for D-amphetamine in an animal discrimination analysis, suggesting that it weakly mimicks the signaling and stimulant properties of D-amphetamine. This product is intended for forensic and research applications.
[Uses]

1-Phenyl-2-butanamine Hydrochloride is a derivative of Amphetamine (A634248); a CNS stimulant and anorexic.
[Synthesis Reference(s)]

Journal of Medicinal Chemistry, 31, p. 824, 1988 DOI: 10.1021/jm00399a024
[References]

[1] JAESIN LEE. Identification of N-ethyl-α-ethylphenethylamine in crystalline powder seized for suspected drug trafficking: a research chemical or a new designer drug?[J]. Forensic Toxicology, 2012, 31 1: 54-58. DOI: 10.1007/s11419-012-0158-1
[2] PIETER A. COHEN  Bastiaan J V  John C Travis. A methamphetamine analog (N,α-diethyl-phenylethylamine) identified in a mainstream dietary supplement[J]. Drug Testing and Analysis, 2013, 6 7-8: 805-807. DOI: 10.1002/dta.1578
[3] ROBERT OBERLENDER  David E N. Structural variation and (+)-amphetamine-like discriminative stimulus properties[J]. Pharmacology Biochemistry and Behavior, 1991, 38 3: Pages 581-586. DOI: 10.1016/0091-3057(91)90017-v
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