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Vigabatrin

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Identification
Molecular formula
C6H11NO2
CAS number
60643-86-9
IUPAC name
4-aminohex-5-ynoic acid
State
State

At room temperature, 4-aminohex-5-ynoic acid is in a solid state.

Melting point (Celsius)
171.00
Melting point (Kelvin)
444.15
Boiling point (Celsius)
410.00
Boiling point (Kelvin)
683.15
General information
Molecular weight
129.16g/mol
Molar mass
129.1610g/mol
Density
1.0362g/cm3
Appearence

4-aminohex-5-ynoic acid, commonly known as Vigabatrin, typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-aminohex-5-ynoic Acid

4-aminohex-5-ynoic acid, with the formula C6H11NO2, exhibits a notable solubility profile in various solvents. The solubility of this compound can be described with the following key points:

  • Water Solubility: This compound is expected to have moderate solubility in water due to the presence of both an amino group and a carboxylic acid group, which can facilitate interactions with water molecules through hydrogen bonding.
  • Organic Solvents: 4-aminohex-5-ynoic acid is likely to be soluble in polar organic solvents such as ethanol and methanol. This property is attributed to the hydrophilic nature of the functional groups.
  • pH Influence: The solubility may significantly change with pH variations. In acidic environments, the carboxylic group may be protonated, potentially enhancing solubility, while in alkaline conditions, it can deprotonate, which might also affect solubility dynamics.

As a general observation, compounds with similar structural motifs often follow the trend of increased solubility with enhanced polarity. Therefore, it is prudent to conduct empirical tests to precisely ascertain the solubility in various conditions to capture the complete solubility profile of this intriguing compound.

Interesting facts

Interesting Facts About 4-Aminohex-5-ynoic Acid

4-Aminohex-5-ynoic acid is a fascinating compound that is part of the family of amino acids. This molecule offers a unique combination of functional groups that contributes to its diverse chemical reactivity and potential applications in various fields.

Key Characteristics:

  • Amino Acid Nature: As an amino acid, it plays a crucial role in biological processes. Amino acids are the building blocks of proteins, which are essential for life.
  • Acetylenic Structure: The presence of a triple bond in its structure (the "ynoic" part) allows it to engage in fascinating chemical reactions, making it a subject of interest for organic synthesis.
  • Potential Therapeutic Uses: Similar compounds have been explored for their roles in drug discovery. The versatility of this molecule could suggest contributions to medicinal chemistry.
  • Synthesis Opportunities: Scientists are often intrigued by the synthesis of such compounds from simpler precursors, presenting an exciting challenge in reaction mechanisms.

One noteworthy aspect of 4-aminohex-5-ynoic acid is its potential in the development of bioactive molecules, which are compounds capable of affecting biological processes. This characteristic opens the door for research in drug design and development, particularly in the realm of treatments for various diseases, including cancer.

In summary, 4-aminohex-5-ynoic acid represents a unique intersection of biological significance and chemical versatility. As we delve deeper into the study of such compounds, we continue to unveil the intricacies of their behavior and their contributions to science.

Synonyms
gamma-Acetylenic gaba
4-Aminohex-5-ynoic acid
4-Amino-5-hexynoic acid
gamma-Acetylinic GABA
57659-38-8
5-Hexynoic acid, 4-amino-
UNII-PG9G3XCD6P
PG9G3XCD6P
.GAMMA.-ACETYLENIC GABA
DTXSID40973249
4-aminohexynoate
MDL-71645
gamma-acetylenic-gamma-aminobutyric acid
(+/-)-.GAMMA.-ACETYLENIC GABA
.GAMMA.-ACETYLENIC-.GAMMA.-AMINOBUTYRIC ACID
gamma-acetylenic-GABA
.GAMMA.-ACETYLENIC-.GAMMA.-AMINOBUTYRIC ACID, (+/-)-
RMI 71645
RMI-71645
Acetylenic GABA-7
4-ami-nohex-5-ynoic acid
4-Amino-hex-5-ynoic acid
Lopac0_000138
SCHEMBL690785
CHEMBL330129
BDBM81477
DTXCID20834182
HMS3260K18
Tox21_500138
PDSP1_000142
PDSP2_000141
(+/-)-GAMMA-ACETYLENIC GABA
AKOS006272245
CCG-204233
LP00138
SDCCGSBI-0050126.P002
NCGC00015019-02
NCGC00015019-03
NCGC00015019-04
NCGC00015019-05
NCGC00093628-01
NCGC00093628-02
NCGC00260823-01
CAS_57659-38-8
DB-229043
HY-131693
CS-0138522
EU-0100138
SR-01000075598
SR-01000075598-1
Q27286546
GAMMA-ACETYLENIC-GAMMA-AMINOBUTYRIC ACID, (+/-)-
637-345-7