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Bethanechol chloride

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Identification
Molecular formula
C7H8ClNO2
CAS number
590-63-6
IUPAC name
dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium;chloride
State
State

At room temperature, Bethanechol chloride is typically in a solid state.

Melting point (Celsius)
214.50
Melting point (Kelvin)
487.70
Boiling point (Celsius)
383.15
Boiling point (Kelvin)
656.30
General information
Molecular weight
236.20g/mol
Molar mass
236.2040g/mol
Density
1.1579g/cm3
Appearence

Bethanechol chloride appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of Dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium Chloride

The solubility of dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium;chloride (C7H8ClNO2) can be described with careful consideration of its molecular structure and interactions with solvents. This compound is a quaternary ammonium salt, which tends to exhibit unique solubility characteristics due to its ionization properties. Here are some key points to consider:

  • Polar Nature: The presence of the chloride ion suggests that dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium chloride is likely to be soluble in polar solvents such as water due to its ionic nature.
  • Organic Solvents: It may also exhibit solubility in a variety of organic solvents, particularly those with a polar character, enhancing its applications in organic synthesis and pharmaceutical formulations.
  • Temperature Dependence: As with many chemical compounds, solubility may increase with temperature; therefore, one might expect better solubility in heated solutions.
  • pH Sensitivity: The solubility can also be influenced by the pH of the solution, as changes can affect the ionization state of the ammonium group.

In summary, while the precise solubility values for dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium chloride in various solvents would require empirical measurement, we can anticipate that its ionic character will play a significant role in determining its solubility properties in different environments.

Interesting facts

Interesting Facts about Dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium Chloride

Dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium chloride, often abbreviated as DMPTPAC, is a fascinating compound with a variety of applications in fields ranging from pharmaceuticals to chemical research. Here are some intriguing insights into this compound:

  • Structural Complexity: The unique structure of DMPTPAC, featuring a phenyltetralin moiety, plays a crucial role in its biological activity. The presence of bulky organic groups contributes to the compound's ability to interact with biological targets.
  • Biological Significance: Compounds like DMPTPAC have shown promise in pharmacological studies, potentially serving as candidates for drug development or as research tools.
  • Ammonium Functionality: The dimethylammonium group is a key feature that enhances the solubility and stability of the molecule in a variety of contexts, making it a useful intermediate in synthetic organic chemistry.
  • Chloride Ion Role: The chloride component plays a pivotal role in stabilizing the ammonium salt form, thereby influencing the compound's reactivity and overall behavior in solution.
  • Psychoactive Research: The phenyltetralin structure is of particular interest in neuropharmacology, as it bears resemblance to known psychoactive substances, warranting further exploration into its effects on the central nervous system.

In summary, Dimethyl-[3-(1-phenyltetralin-1-yl)propyl]ammonium chloride is much more than just a chemical compound. Its intricate structure and potential applications underline the significance of studying such compounds in the pursuit of new therapeutic agents and understanding complex biochemical systems.

Synonyms
10565-84-1
Naphthalene, 1,2,3,4-tetrahydro-1-(3-dimethylaminopropyl)-1-phenyl-, hydrochloride
LU 3-023
1-Naphthalenepropylamine, 1,2,3,4-tetrahydro-N,N-dimethyl-1-phenyl-, hydrochloride
Propylamine, N,N-dimethyl-3-(1,2,3,4-tetrahydro-1-phenylnaphthyl)-, hydrochloride