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Phenibut

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Identification
Molecular formula
C10H13NO2
CAS number
1078-21-3
IUPAC name
4-amino-3-phenyl-butanoic acid
State
State

At room temperature, Phenibut is a solid substance.

Melting point (Celsius)
194.00
Melting point (Kelvin)
467.15
Boiling point (Celsius)
343.70
Boiling point (Kelvin)
616.85
General information
Molecular weight
179.22g/mol
Molar mass
179.2180g/mol
Density
1.0990g/cm3
Appearence

Phenibut typically appears as a white crystalline powder. It may be slightly hygroscopic and often has a bitter taste.

Comment on solubility

Solubility of 4-amino-3-phenyl-butanoic acid

4-amino-3-phenyl-butanoic acid, commonly known as phenylalanine, exhibits intriguing solubility characteristics that are vital for its applications in biochemistry and nutrition.

In terms of its solubility profile:

  • Water solubility: 4-amino-3-phenyl-butanoic acid is moderately soluble in water, facilitated by the presence of its amino group which can engage in hydrogen bonding with water molecules.
  • Solubility in organic solvents: This compound shows limited solubility in non-polar organic solvents, owing to its polar functional groups which disrupt cohesive forces in these hydrophobic solvents.
  • Temperature dependence: Its solubility is sensitive to temperature; typically, solubility increases with rising temperature, a characteristic that can influence its stability and usability.

Overall, as emphasized by its solubility traits, the properties of 4-amino-3-phenyl-butanoic acid make it a versatile compound in both dietary applications and various biochemical environments. Understanding its solubility plays a vital role in maximizing its effectiveness and functionality in scientific and nutritional contexts.

Interesting facts

Interesting Facts about 4-Amino-3-phenyl-butanoic acid

4-Amino-3-phenyl-butanoic acid, often referred to by its abbreviation, is a fascinating compound in the field of organic chemistry. Here are some noteworthy insights:

  • Composition: This compound belongs to the class of amino acids, which are the building blocks of proteins. It features both an amino group and a carboxylic acid, making it crucial for various biochemical processes.
  • Biological Relevance: Amino acids play key roles in metabolism and serve as precursors for the synthesis of hormones, neurotransmitters, and other essential molecules. 4-Amino-3-phenyl-butanoic acid may have biological significance in certain metabolic pathways.
  • Pharmaceutical Applications: Compounds like 4-amino-3-phenyl-butanoic acid can be explored for their potential therapeutic properties. They may have uses in the development of pharmaceuticals or nutraceuticals due to their structural characteristics.
  • Stereochemistry: The compound's stereochemistry can significantly influence its biological activity. Understanding the 3D orientation of its atoms is vital for drug design and function.

As one delves deeper into the chemistry of 4-amino-3-phenyl-butanoic acid, it becomes clear that its study is not only essential due to its structure but also for its potential applications in various scientific fields. "Each amino acid has a story to tell," and this compound is no exception.

Researchers continue to investigate the myriad of ways such compounds can impact health and technology, ensuring that our understanding of this and similar molecules evolves as science progresses.

Synonyms
4-Amino-3-phenylbutanoic acid
Phenibut
1078-21-3
Fenibut
4-Amino-3-phenylbutyric acid
PhGaba
Phenylgamma
phenigamma
Fenigam
Fenigama
Phenigam
Phenylgam
Pgaba
phenygam
Phenigama
beta-Phenyl-gamma-aminobutyric acid
beta-(Aminomethyl)hydrocinnamic acid
beta-Phenyl-gamma-aminobutyrate
beta-(Aminomethyl)benzenepropanoic acid
Benzenepropanoic acid, beta-(aminomethyl)-
EINECS 214-079-6
BRN 2804903
T2M58D6LA8
Dl-4-amino-3-phenylbutanoic acid
PHENIBUT [WHO-DD]
phenyl-GABA
BUTYRIC ACID, 4-AMINO-3-PHENYL-
Benzenepropanoic acid, .beta.-(aminomethyl)-
DTXSID70870838
4-14-00-01723 (Beilstein Handbook Reference)
phenybut
fenibut citrate
4-AMINO-3-PHENYLBUTYRIC ACID [MI]
.BETA.-(AMINOMETHYL)HYDROCINNAMIC ACID
.BETA.-PHENYL-.GAMMA.-AMINOBUTYRIC ACID
.BETA.-(AMINOMETHYL)BENZENEPROPANOIC ACID
citrocard
noophen
(+-)-FENIBUT
(+-)-BETA-PHENYL-GABA
DTXCID80818524
(+-)-.BETA.-PHENYL-GABA
214-079-6
Benzenepropanoic acid, b-(aminomethyl)-
(3R)-4-amino-3-phenylbutanoic acid
(3S)-4-amino-3-phenylbutanoic acid
UNII-T2M58D6LA8
Phenibut; Fenibut
Oprea1_183000
Oprea1_381119
(+/-)-FENIBUT
SCHEMBL340838
3-phenyl-4-aminobutanoic acid
CHEMBL315818
EX-A734
CHEBI:136039
GLXC-20028
HMS3886K05
butanoic acid, 4-amino-3-phenyl-
ALBB-022462
BCP10710
BBL000576
MFCD00456233
s4892
STK182861
(+/-)-.BETA.-PHENYL-GABA
3-amino-2-phenylpropanecarboxylic acid
AKOS000555914
AKOS016347357
CCG-266416
DB13455
GS-3145
3-[3-(Aminomethyl)phenyl]propionic acid
FA130469
NS00018243
D10509
D96082
EN300-110013
Q419559
BRD-A66920069-001-01-3
Z1255487817