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4-Amino-3-phenylbutanoic acid hydrochloride

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4-Amino-3-phenylbutanoic acid hydrochloride Basic information

Product Name:
4-Amino-3-phenylbutanoic acid hydrochloride
Synonyms:
  • FENIBUT
  • 4-AMINO-3-PHENYLBUTIRIC ACID
  • 4-AMINO-3-PHENYL-BUTYRIC ACID
  • 3-Amino-4-phenylbutyric acid hydrochloride
  • Phenibut Hydrochloride
  • Benzenepropanoic acid, b-(aMinoMethyl)-, hydrochloride(1:1)
  • TIMTEC-BB SBB001567
  • 3-AMINO-4-PHENYLBUTYRIC ACID HCL
CAS:
3060-41-1
MF:
C10H14ClNO2
MW:
215.68
EINECS:
214-079-6
Product Categories:
  • 1
Mol File:
3060-41-1.mol
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4-Amino-3-phenylbutanoic acid hydrochloride Chemical Properties

Melting point:
194-201°C
storage temp. 
Sealed in dry,Room Temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Solid
color 
White to Off-White
InChI
InChI=1S/C10H13NO2.ClH/c11-7-9(6-10(12)13)8-4-2-1-3-5-8;/h1-5,9H,6-7,11H2,(H,12,13);1H
InChIKey
XSYRYMGYPBGOPS-UHFFFAOYSA-N
SMILES
C(C1C=CC=CC=1)(CN)CC(=O)O.Cl
CAS DataBase Reference
3060-41-1(CAS DataBase Reference)
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Safety Information

HS Code 
2916399090
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4-Amino-3-phenylbutanoic acid hydrochloride Usage And Synthesis

Uses

Phenibut is a derivative of γ-Aminobutyric Acid (A602920); an important inhibitory neurotransmitter. Phenibut possesses neuroprotective activity.

General Description

4-Amino-3-phenyl-butyric acid hydrochloride is a derivative of γ-Aminobutyric Acid which possesses neuroprotective activity. It is an organic compound characterized by the presence of both a carboxylic acid and an amine group. It′s an amino acid and holds substantial importance in the fields of biochemistry and physiology. Its versatile nature allows for a broad spectrum of applications in scientific research, particularly in studies involving enzyme inhibition and receptor activation.

Synthesis

1198-97-6

3060-41-1

GENERAL METHOD: 4-phenyl-2-pyrrolidone (0.4 mmol) and 10 mL of HCl (6.0 mol/L) were added to a round bottom flask. The reaction mixture was magnetically stirred under reflux conditions for 12 hours. After completion of the reaction, the solvent was removed by evaporation under reduced pressure to give 3-phenyl-4-aminobutyric acid hydrochloride.

References

[1] New Journal of Chemistry, 2015, vol. 39, # 3, p. 1643 - 1653
[2] Journal of the Brazilian Chemical Society, 2017, vol. 28, # 2, p. 285 - 298
[3] RSC Advances, 2014, vol. 4, # 5, p. 2538 - 2545

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