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Thiodiglycolic acid

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Identification
Molecular formula
C3H5NO2S
CAS number
123-93-3
IUPAC name
2-[dithiocarboxy(methyl)amino]acetic acid
State
State
This compound is generally a solid at room temperature, forming colorless crystals.
Melting point (Celsius)
74.00
Melting point (Kelvin)
347.15
Boiling point (Celsius)
162.00
Boiling point (Kelvin)
435.15
General information
Molecular weight
135.14g/mol
Molar mass
136.1700g/mol
Density
1.5100g/cm3
Appearence

Thiodiglycolic acid appears as a colorless crystalline solid. The texture may vary but is generally similar to small crystals or powder.

Comment on solubility

Solubility of 2-[dithiocarboxy(methyl)amino]acetic acid (C3H5NO2S)

The solubility of 2-[dithiocarboxy(methyl)amino]acetic acid is influenced by its unique chemical structure. This compound features both amine and thiocarboxylic functional groups, which can interact with polar solvents. Here are some key points regarding its solubility:

  • Solvent Compatibility: It tends to have better solubility in polar solvents such as water due to the presence of the amine group, which can engage in hydrogen bonding.
  • Temperature Influence: Increased temperature may enhance solubility by providing the necessary energy for the compound to overcome intermolecular interactions.
  • pH Dependency: The solubility may vary with pH since the amine group can become protonated under acidic conditions, potentially increasing solubility in acidic environments.
  • Concentration Effects: At higher concentrations, solubility might reach a limit, indicating saturation where the solution can no longer dissolve additional amounts of the compound.

Overall, the solubility characteristics of 2-[dithiocarboxy(methyl)amino]acetic acid highlight the importance of molecular structure and environmental conditions in determining how well a compound dissolves. As such, this compound could be particularly useful in specific applications where solubility is a critical factor.

Interesting facts

Interesting Facts about 2-[Dithiocarboxy(methyl)amino]acetic Acid

2-[Dithiocarboxy(methyl)amino]acetic acid is a unique and intriguing compound with diverse applications in both organic chemistry and biochemistry. Here are some fascinating insights into this multifaceted compound:

  • Functional Groups: This compound features both dithiocarboxy and amino functional groups, giving it interesting reactivity characteristics. The presence of sulfur in the dithiocarboxy group often leads to unique bonding and interaction possibilities in various chemical environments.
  • Biological Relevance: Due to its amino acid structure, it may be implicated in synthetic pathways related to amino acids or peptides, potentially influencing biological systems or serving as a precursor for biologically active compounds.
  • Synthetic Versatility: The compound can be synthesized through a variety of methods, making it an appealing target for chemists looking to explore new synthetic pathways and create novel derivatives.
  • Potential Applications: Investigating its role in metal ion chelation is promising, as compounds with dithiocarboxy groups are known for their ability to bind to metal ions—an essential feature in many catalytic processes or in medicinal chemistry.

In summary, 2-[dithiocarboxy(methyl)amino]acetic acid not only showcases the exciting interactions of its constituent elements but also serves as an important compound in various fields of scientific research. As researchers continue to explore its properties and functions, its potential applications could offer further innovations in chemistry and biochemistry.

Synonyms
N-(Dithiocarboxy)sarcosine
40520-03-4
Sarcosine-N-dithiocarbamate
2-[dithiocarboxy(methyl)amino]acetic acid
Sarcosine dithiocarbamate
Sarcosinedithiocarbamate
N-(mercaptocarbonothioyl)-N-methylglycine diammoniate
N-(Dithiocarboxy)-N-methylglycine
Glycine, N-(dithiocarboxy)-N-methyl-
N-methyl-N-(sulfanylcarbonothioyl)glycine
2-(dithiocarboxy(methyl)amino)acetic acid
SDTC
SCHEMBL1537715
DTXSID90960927
ALBB-024033
STK663868
AKOS006273179
[Methyl(sulfanylcarbothioyl)amino]acetic acid #
H34314
glycine, N-(mercaptothioxomethyl)-N-methyl-, diammonium salt