S-ethylisothiourea hydrochloride | Solubility of Things

Identification

Molecular formula

C₃H₉ClN₂S

CAS number

541-22-0

IUPAC name

[N'-(2-sulfanylethyl)carbamimidoyl]ammonium;chloride

State

At room temperature, S-ethylisothiourea hydrochloride is typically found in a solid state. Its crystalline form adds to its stability under standard conditions, making it suitable for various chemical reactions and processes.

Melting point (Celsius)

140.00

Melting point (Kelvin)

413.15

Boiling point (Celsius)

210.00

Boiling point (Kelvin)

483.15

General information

Molecular weight

138.62g/mol

Molar mass

138.6190g/mol

Density

1.2020g/cm³

Appearence

S-ethylisothiourea hydrochloride appears as a white crystalline powder. It is known for its solid and dry consistency, making it a distinct compound used in certain scientific applications.

Comment on solubility

Solubility of N'-(2-sulfanylethyl)carbamimidoyl;ammonium;chloride

The solubility of N'-(2-sulfanylethyl)carbamimidoyl;ammonium;chloride can be influenced by several factors, making it an interesting compound to study.

Generally, this compound is expected to exhibit moderate solubility in polar solvents, primarily water, due to its ionic nature. The presence of ammonium and chloride ions often contributes to solubility because:

Hydrogen bonding: The ability of ammonium groups to engage in hydrogen bonding with water molecules enhances solubility.
Ion-dipole interactions: The interaction between polar solvent molecules and ions increases solubility in ionic compounds.

However, it’s important to note some solubility limitations:

Temperature dependence: Solubility may vary with temperature, with higher temperatures generally leading to increased solubility.
Concentration effects: At higher concentrations, solubility can decrease due to saturation and potential precipitation of the compound.

Overall, while N'-(2-sulfanylethyl)carbamimidoyl;ammonium;chloride is likely to be soluble in water, the specifics can vary based on environmental conditions. Understanding these solubility parameters is crucial for its applications in various fields.

Interesting facts

Interesting Facts about N'-(2-sulfanylethyl)carbamimidoyl Ammonium Chloride

N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride is a fascinating compound that showcases the unique intersection of sulfur chemistry and ammonium compounds. Here are some noteworthy aspects of this intriguing compound:

Sulfur's Role: The presence of the sulfanyl (thiol) group in this compound introduces specific chemical properties. Sulfur is renowned for its ability to form strong bonds with carbon, which significantly contributes to the compound's stability.
Biological Relevance: Compounds containing sulfanyl groups are often found in biological systems. They can play essential roles in enzymatic reactions, cellular signaling, and protecting cells from oxidative stress.
Versatile Applications: Due to its unique structure, N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride can have potential applications in medicinal chemistry, particularly in the development of new therapeutic agents that may inhibit specific biological pathways.
Ammonium Feature: The ammonium portion of this compound contributes to its possible solubility properties and reactivity, making it an interesting subject for investigations related to ion exchange and coordination chemistry.

As we explore this compound further, scientists may uncover new synthetic routes and potential uses in various fields such as pharmaceuticals, materials science, and biochemistry. With ongoing research, the understanding of compounds like N'-(2-sulfanylethyl)carbamimidoyl ammonium chloride continues to evolve, opening doors to innovative solutions in science.