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2-iminothiolane hydrochloride

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Identification
Molecular formula
C5H12ClN2OS
CAS number
4781-83-3
IUPAC name
3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium;chloride
State
State

At room temperature, 2-iminothiolane hydrochloride is typically in the solid state. It forms white to off-white crystals, which make it easy to handle and measure for laboratory use.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
184.60
Boiling point (Kelvin)
457.80
General information
Molecular weight
175.68g/mol
Molar mass
175.6800g/mol
Density
1.2810g/cm3
Appearence

2-Iminothiolane hydrochloride appears as a white to off-white crystalline powder. It is highly soluble in water and moist air sensitive, often used in biochemical conjugation to introduce sulfhydryl groups into proteins.

Comment on solubility

Solubility of 3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium chloride

The solubility of 3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium chloride can be influenced by several factors. As a quaternary ammonium compound with an organic moiety, its solubility profile often tends towards the following characteristics:

  • Water Solubility: Given the presence of a positively charged ammonium group and the anionic chloride, this compound is likely to exhibit good solubility in water.
  • Solvent Compatibility: It may also be soluble in polar organic solvents due to its charged and polar functional groups.
  • Temperature Effects: The solubility could increase with temperature, which is common for many ionic compounds.
  • pH Influence: The solubility may vary with changes in pH, especially since the compound has functional groups sensitive to protonation.

In specific scenarios, such as pharmaceutical applications, understanding the solubility of this compound is crucial – as it can impact its bioavailability and efficacy. Consequently, empirical solubility tests should be conducted to derive accurate data for practical applications.

Before utilizing this compound, it is essential to consider its solubility profile to ensure proper formulation and deployment in various environments.

Interesting facts

Exploring 3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium;chloride

The compound 3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium;chloride is a fascinating example of organic ammonium salts, which play vital roles in both biochemical pathways and industrial applications. Here are some intriguing aspects of this compound:

  • Dual Functionality: This compound features both oxamoyl and sulfanylethyl functional groups, which can impart unique biochemical properties. Oxamoyl groups are known for their ability to participate in hydrogen bonding, making them significant in molecular recognition processes.
  • Biological Relevance: Compounds with ammonium groups often mimic or influence biological molecules like amino acids or neurotransmitters, acting as crucial players in plant and animal physiology.
  • Potential Therapeutic Uses: Due to its structural characteristics, this compound may offer insights into the development of pharmaceuticals, especially in targeting specific enzymes or receptors in biological systems.
  • Synthesis Challenges: The synthesis of such compounds may involve complex organic reactions, highlighting the innovative methods chemists employ to construct multi-functional molecules.
  • Environmental Relevance: Investigating similar ammonium salts can provide information on their effects in ecological systems, as some can be used in fertilizers or as biodegradable agents in environmental applications.

In summary, 3-(oxamoylamino)propyl-(2-sulfanylethyl)ammonium;chloride exemplifies how chemical compounds can intertwine with biological functions and environmental chemistry. Its unique chemical structure opens doors to research that bridges the gap between synthetic chemistry and real-world applications.

Synonyms
(3-(2-Mercaptoethylamino)propyl)oxamide hydrochloride
24503-78-4
OXAMIDE, (3-((2-MERCAPTOETHYL)AMINO)PROPYL)-, MONOHYDROCHLORIDE
RefChem:367105