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S-(2-Aminoethyl) ethanethioate

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Identification
Molecular formula
C4H9NOS
CAS number
673-10-5
IUPAC name
S-(2-aminoethyl) ethanethioate
State
State

State at Room Temperature: S-(2-Aminoethyl) ethanethioate is a solid at room temperature.

Melting point (Celsius)
178.00
Melting point (Kelvin)
451.15
Boiling point (Celsius)
237.00
Boiling point (Kelvin)
510.15
General information
Molecular weight
121.19g/mol
Molar mass
121.1930g/mol
Density
1.1320g/cm3
Appearence

Appearance: S-(2-Aminoethyl) ethanethioate typically presents as a crystalline solid. The compound can be characterized by a white or off-white color. Its appearance may vary depending on purity and method of preparation.

Comment on solubility

Solubility of S-(2-aminoethyl) ethanethioate

S-(2-aminoethyl) ethanethioate, with its unique structure, exhibits interesting solubility characteristics that are essential for its applications in various chemical processes. Understanding its solubility can provide insights into its behavior in different environments.

Key Points on Solubility

  • Water Solubility: S-(2-aminoethyl) ethanethioate is generally considered soluble in water due to the presence of both amino and thioate functional groups, which can interact with water molecules through hydrogen bonding.
  • Solvent Compatibility: This compound may also dissolve in polar organic solvents, enhancing its versatility in various chemical reactions.
  • Influence of pH: The solubility characteristics can change with pH levels, particularly because of the ionizable amine group, which could either promote or hinder solubility depending on the environment.
  • Practical Applications: The solubility profile of S-(2-aminoethyl) ethanethioate is critical for its use in biological systems and pharmaceuticals, where solubility impacts bioavailability and efficacy.

In summary, the solubility of S-(2-aminoethyl) ethanethioate plays a pivotal role in its functionality and usability. Its ability to dissolve in water and polar solvents, coupled with the influence of pH, makes it a compound of considerable interest in the field of chemical science.

Interesting facts

Interesting Facts about S-(2-aminoethyl) ethanethioate

S-(2-aminoethyl) ethanethioate, commonly known in scientific communities as a derivative of thioester, showcases unique properties and potential applications. This compound captures attention due to its intriguing structural features and versatile functionality. Here are some fascinating insights:

  • Biochemical Activity: S-(2-aminoethyl) ethanethioate is known to participate in numerous biochemical reactions, especially in the realm of organic synthesis. Its functional groups may contribute to reaction mechanisms that are beneficial in drug discovery and development.
  • Role in Cellular Processes: Research suggests that this compound could play a role in cellular signaling or as a precursor in metabolic pathways, highlighting its importance in biological systems.
  • Chemical Behavior: The presence of both amino and thioester functional groups allows for interesting reactivity, making this compound a useful candidate in various synthetic methodologies.
  • Applications in Research: As a thioester, S-(2-aminoethyl) ethanethioate could be explored for creating complex organic structures, offering a pathway for developing new materials or pharmaceuticals.
  • Potential Toxicity: Like many sulfur-containing compounds, caution is warranted. Some thioesters can present challenges in terms of toxicity and environmental impact, thus necessitating thorough research.

In summary, S-(2-aminoethyl) ethanethioate exemplifies the intricate nature of chemical compounds, where its various applications and interactions within biological systems underline its significance. Continued studies into this compound could unveil further mysteries and unlock new avenues in chemical science.

Synonyms
S-acetylcysteamine
6197-31-5
S-(2-aminoethyl) ethanethioate
S-Acetylthioethanolamine
1-[(2-aminoethyl)sulfanyl]ethan-1-one
CHEBI:17853
Ethanethioic acid, S-(2-aminoethyl) ester
S-Acetylcysteamin
thioacetic acid S-(2-aminoethyl) ester
C03537
SCHEMBL5597124
SCHEMBL8375300
SCHEMBL9019537
CHEMBL1190273
DTXSID90274859
YBWLIIDAKFNRBL-UHFFFAOYSA-N
AKOS006334232
EN300-6497871
Q27102663