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S-Acetylthioethylammonium chloride

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Identification
Molecular formula
C4H10ClNS
CAS number
7464-52-8
IUPAC name
2-acetylsulfanylethylammonium;chloride
State
State

At room temperature, S-Acetylthioethylammonium chloride is in a solid state. It often forms crystalline powders which are stable under standard conditions.

Melting point (Celsius)
194.00
Melting point (Kelvin)
467.00
Boiling point (Celsius)
276.00
Boiling point (Kelvin)
549.00
General information
Molecular weight
155.67g/mol
Molar mass
155.6650g/mol
Density
1.2550g/cm3
Appearence

S-Acetylthioethylammonium chloride typically appears as a white to off-white crystalline powder. It is generally odorless and its appearance can vary slightly based on purity and form.

Comment on solubility

Solubility of 2-acetylsulfanylethylammonium chloride

The solubility of 2-acetylsulfanylethylammonium chloride can be influenced by several factors such as temperature, solvent type, and the inherent properties of the compound itself. In general, ammonium salts, like the one in question, tend to exhibit good solubility in polar solvents, primarily due to their ionic nature. Here are some key points regarding the solubility of this compound:

  • Polar Solvents: This compound is likely to be soluble in water, as chlorides of ammonium salts typically dissolve well due to the interactions between water molecules and the ionic constituents.
  • Temperature Dependence: The solubility of 2-acetylsulfanylethylammonium chloride may increase with temperature, a common trait observed in many salts.
  • Effect of pH: The solubility may also be influenced by the pH of the solution, with acidic or basic conditions affecting the compound’s ionization and solubility.

In summary, one can expect 2-acetylsulfanylethylammonium chloride to be readily soluble in water, which makes it a useful compound in various applications that require solutions of ammonium salts. An important takeaway is that understanding the solubility properties of such compounds is crucial for their effective utilization in chemical processes.

Interesting facts

Interesting Facts About 2-Acetylsulfanylethylammonium Chloride

2-Acetylsulfanylethylammonium chloride is a fascinating compound that plays a notable role in various chemical processes and applications.

Chemical Structure and Properties

This compound consists of an acetyl group attached to a sulfanyl group which enhances its reactivity with other chemicals. The key features of this compound include:

  • Ammonium Ion: The presence of an ammonium ion indicates that this compound may exhibit basic properties, which can lead to interesting interactions in solution.
  • Chloride Ion: The chloride ion acts as a counterion that can influence the solubility and stability of the compound in different media.

Applications

2-Acetylsulfanylethylammonium chloride has various applications in the field of chemistry:

  • Synthetic Chemistry: It can be utilized as a building block in the synthesis of more complex organic molecules.
  • Pharmaceuticals: This compound may have potential uses in drug design and development, particularly for compounds that require sulfanyl functionalities.

Safety and Handling

When working with 2-acetylsulfanylethylammonium chloride, it is essential to consider safety precautions:

  • Always wear protective eyewear and gloves.
  • Handle under a fume hood to avoid inhalation of any gases or vapors that may be released during reactions.

As a new or seasoned chemistry student, understanding the attributes and potential applications of compounds like 2-acetylsulfanylethylammonium chloride can greatly enhance your chemical knowledge and experimentational acumen.

Quote: "Every molecule has a story to tell, and understanding it unlocks the mysteries of matter."

Synonyms
Thioacetic acid S-2-aminoethyl ester hydrochloride
2-acetylsulfanylethylazanium;chloride
S-Acetylcysteamine hydrochloride
S-Acetyl-2-mercaptoethylamine hydrochloride
S-(2-Aminoethyl)ethanethioate hydrochloride
Ethanethiol, 2-amino-, acetate, hydrochloride
Ethanethioic acid, S-(2-aminoethyl)ester, hydrochloride
ACETIC ACID, THIO-, S-2-AMINOETHYL ESTER, HYDROCHLORIDE
Thioacetic acid S-(2-amino-ethyl) esterhydrochloride