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N-Acetylcysteamine

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Identification
Molecular formula
C4H9NOS
CAS number
35395-40-9
IUPAC name
N-(2-sulfanylethyl)acetamide
State
State

At room temperature, N-Acetylcysteamine is typically in a liquid state, although it may also be found as a solid at lower temperatures due to its melting point being slightly above average room temperature.

Melting point (Celsius)
55.50
Melting point (Kelvin)
328.70
Boiling point (Celsius)
254.50
Boiling point (Kelvin)
527.70
General information
Molecular weight
119.18g/mol
Molar mass
119.1830g/mol
Density
1.1470g/cm3
Appearence

N-Acetylcysteamine appears as a colorless to pale yellow liquid at room temperature. It is often described as having a characteristic amine-like odor.

Comment on solubility

Solubility of N-(2-sulfanylethyl)acetamide

N-(2-sulfanylethyl)acetamide exhibits interesting solubility characteristics that can be quite significant in its applications. Understanding its solubility profile helps in predicting how the compound will behave in various environments, which is crucial for both laboratory and industrial settings.

Solubility Attributes

  • Solvent Compatibility: N-(2-sulfanylethyl)acetamide is generally soluble in polar solvents, such as water and alcohols, due to the presence of the amide functional group, which promotes hydrogen bonding.
  • Temperature Dependence: The solubility may increase with temperature, a common trait for many organic compounds, leading to enhanced interactions with solvents.
  • pH Influence: The solubility can also be affected by the pH of the solution, as the ionization of functional groups can enhance solubility in aqueous environments.

In practical terms, it is often stated that “a compound’s solubility can dictate its reactivity and bioavailability.” Therefore, knowledge of the solubility of N-(2-sulfanylethyl)acetamide is vital for anyone working with this compound, particularly in pharmaceuticals and chemical synthesis, where the right conditions can lead to successful reactions and product formulation.

Conclusion

In summary, considering the solubility of N-(2-sulfanylethyl)acetamide in various solvents and conditions can provide valuable insights into its potential uses and applications in different fields of research and industry.

Interesting facts

Interesting Facts about N-(2-sulfanylethyl)acetamide

N-(2-sulfanylethyl)acetamide, often simply referred to as a derivative of acetamide, is an intriguing compound that finds its significance in various fields of research and application.

Key Characteristics

  • Biological Activity: This compound is noted for its potential biological applications. Compounds with similar structures have been studied for their effects on various biological systems, including antimicrobial and antifungal properties.
  • Synthetic Utility: N-(2-sulfanylethyl)acetamide can serve as an important building block in organic synthesis. Chemists often use it to create more complex molecules.
  • Research Interest: There is ongoing research examining the compound's role in medicinal chemistry, particularly in the design of novel therapeutic agents.

Chemical Behavior

The presence of the sulfanyl (thiol) group within the molecule contributes to *unique reactivity and properties*. This means that it can participate in various chemical reactions that might not be possible for other amide compounds. For instance, it may engage in thiol-exchange reactions, offering pathways to create new materials or functionalities.

Applications in Science and Industry

Some notable applications include:

  • **Pharmaceuticals:** Investigated for use as intermediates in the synthesis of drugs.
  • **Agriculture:** Potential development in pesticide formulations.
  • **Material Science:** The thiol group may contribute to properties desirable in the development of polymers and other materials.

In summary, N-(2-sulfanylethyl)acetamide serves not just as a simple compound, but as a *gateway to innovative solutions* in various scientific arenas. By understanding its properties and potential, researchers can unravel new avenues for its application.

Synonyms
N-Acetylcysteamine
1190-73-4
N-(2-Mercaptoethyl)acetamide
2-Acetamidoethanethiol
Acetylcysteamine
Acetamide, N-(2-mercaptoethyl)-
N-(2-Sulfanylethyl)acetamide
N-Acetylmercaptoethylamine
Cysteamine, N-acetyl-
N-Acetyl cysteamin
Cysteamine,N-acetyl
N-Acetyl cysteamine
Ethanethiol, 2-(acetylamino)-
N-Acetyl cysteamin [German]
NSC 38835
NSH3F3JX85
BRN 1743117
N-acetyl-beta-mercaptoethylamine
ACETAMIDE, N-(beta-MERCAPTOETHYL)-
NSC-38835
thiol N-acetyl-beta-mercaptoethylamine
CHEBI:74410
DTXSID90152289
4-04-00-01607 (Beilstein Handbook Reference)
N-ACETYL-.BETA.-MERCAPTOETHYLAMINE
TNA-mercaptoethylamine
DTXCID8074780
Acetamide, N-(2-mercaptoethyl)-(8CI,9CI)
683-054-3
MFCD00037831
Acetamide, N-(.beta.-mercaptoethyl)-
n-(2-mercaptoethyl)-acetamide
N-Acetylcysteamine, 95%
UNII-NSH3F3JX85
2-acetylaminoethyl mercaptan
WLN: SH2MV1
SCHEMBL474178
N-(2-mercapto-ethyl)-acetamide
Acetamide N-(2-mercaptoethyl)-
N-(2-Sulfanylethyl)acetamide #
WLZ2883
~{N}-(2-sulfanylethyl)ethanamide
NSC38835
AKOS006223010
AT13754
AS-60537
SY117216
EN300-211454
Q27144656
W0K