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Carbamylcholine chloride

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Identification
Molecular formula
C11H18ClNO
CAS number
56-72-4
IUPAC name
(3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride
State
State

At room temperature, carbamylcholine chloride is a solid.

Melting point (Celsius)
214.00
Melting point (Kelvin)
487.15
Boiling point (Celsius)
100.00
Boiling point (Kelvin)
373.15
General information
Molecular weight
197.71g/mol
Molar mass
197.7140g/mol
Density
1.0440g/cm3
Appearence

Carbamylcholine chloride appears as a white crystalline solid. It is highly hydrophilic and readily dissolves in water, forming a clear solution.

Comment on solubility

Solubility of (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride

The solubility characteristics of (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride can provide insights into its potential applications and behavior in various environments. Generally, quaternary ammonium compounds like this one exhibit a degree of solubility in polar solvents. Here are some key points to consider:

  • Solvent Polarity: This compound is likely to be more soluble in water and other polar solvents due to the presence of ammonium groups.
  • Temperature Dependency: Solubility tends to increase with rising temperature, making it essential to consider thermal conditions in practical applications.
  • Concentration Limits: When dissolved, the effective concentration may influence solubility, often leading to saturation points, which can vary significantly based on the specific solvent used.
  • pH Sensitivity: The solubility can also be affected by the pH of the solution, especially if the compound possesses weakly acidic or basic functional groups.

To summarize, understanding the solubility of (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride is crucial for its successful utilization in various chemical processes, formulations, or applications. Engaging in further studies can elucidate its solubility profile under different conditions, ultimately guiding its practical implementations.

Interesting facts

Interesting Facts About (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride

The compound (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride is a fascinating example of a quaternary ammonium salt that possesses unique biological and chemical properties. Here, we delve into some intriguing aspects of this compound:

  • Biological Significance: Quaternary ammonium compounds like this one are often used for their antimicrobial properties. They are known to effectively kill bacteria and fungi, making them valuable in disinfectants and antiseptics.
  • Structure and Function: The specific structure of this compound, with its phenyl and hydroxy groups, contributes to its solubility and reactivity. The presence of the hydroxy group can enhance intermolecular interactions, making it interesting for various applications in organic synthesis.
  • Applications in Industry: This compound may be utilized in the formulation of personal care products, including hair conditioners and skin care due to its conditioning properties. The ability to modify its molecular structure offers chemists tools to tailor its functionality for specific uses.
  • Quaternary Ammonium Chemistry: Quaternary ammonium salts are significant in the field of organic chemistry due to their diverse reactivity patterns. Research is ongoing to discover new applications and uses for these compounds in pharmaceuticals and advanced materials.
  • Research Potential: This compound’s structure presents numerous avenues for further research, particularly in drug development where modifications can lead to enhanced bioactivity or reduced toxicity. Scientists continue to explore such compounds to uncover novel therapeutic agents.

In conclusion, the compound (3-hydroxy-3-phenyl-pentyl)-dimethyl-ammonium;chloride serves as an excellent representative of the diverse world of quaternary ammonium compounds, combining unique structural features with potential applications across various fields.

Synonyms
alpha-(2-(Dimethylamino)ethyl)-alpha-ethylbenzyl alcohol hydrochloride
13064-13-6
BENZYL ALCOHOL, alpha-(2-(DIMETHYLAMINO)ETHYL)-alpha-ETHYL-, HYDROCHLORIDE