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Deschloroketamine hydrochloride

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Identification
Molecular formula
C14H22ClNO2
CAS number
6740-88-1
IUPAC name
(4-piperidin-1-ium-1-ylcyclohexyl) butanoate;chloride
State
State

At room temperature, Deschloroketamine hydrochloride is in a solid state.

Melting point (Celsius)
235.00
Melting point (Kelvin)
508.15
Boiling point (Celsius)
608.00
Boiling point (Kelvin)
881.15
General information
Molecular weight
285.79g/mol
Molar mass
285.8470g/mol
Density
1.1000g/cm3
Appearence

Deschloroketamine hydrochloride typically appears as a crystalline solid. It is often white but can also have subtle variations in color depending on purity and environmental conditions.

Comment on solubility

Solubility of (4-piperidin-1-ium-1-ylcyclohexyl) butanoate;chloride

The solubility of (4-piperidin-1-ium-1-ylcyclohexyl) butanoate;chloride is influenced by several factors that stem from its unique structure. Given its ionic nature due to the presence of the chloride component, it demonstrates some interesting solubility characteristics:

  • Polar Solvents: This compound is likely to be more soluble in polar solvents, particularly water, because of the ionic interactions that can occur.
  • Non-Polar Solvents: In contrast, it may have limited solubility in non-polar solvents due to lack of suitable interactions.
  • Temperature Dependence: Solubility could increase with temperature, a common trait for many ionic compounds; thus, heating the solution might enhance dissolution.
  • Structural Impact: The bulky cyclohexyl group can affect solubility, possibly introducing steric hindrance that can impede solvation in some environments.

In summary, while (4-piperidin-1-ium-1-ylcyclohexyl) butanoate;chloride exhibits significant solubility in polar solvents due to its ionic nature, its solubility in non-polar environments is likely limited. Overall, it is essential to consider both the chemical structure and the solvent type to predict solubility accurately.

Interesting facts

Interesting Facts about (4-piperidin-1-ium-1-ylcyclohexyl) butanoate; chloride

(4-piperidin-1-ium-1-ylcyclohexyl) butanoate; chloride is an intriguing compound that falls into the category of quaternary ammonium salts. These unique substances are recognized for their diverse applications across various fields, including pharmaceuticals and organic synthesis.

Key Features

  • Quaternary Structure: This compound features a quaternary nitrogen atom, which means that it has four substituents. This configuration is significant because it enhances both its solubility and reactivity in various solvents.
  • Pharmaceutical Potential: Compounds with piperidine structures are widely researched due to their presence in many bioactive molecules. They can act as intermediates in drug synthesis, leading to important therapeutic agents.
  • Versatile Applications: It is utilized in various fields, including:
    • Surface active agents
    • Antiseptic formulations
    • Biochemical probes
  • Ion Exchange Properties: The presence of a chloride counterion allows the compound to have ionic character, making it a candidate for ion exchange applications, which are pivotal in water purification and separation processes.

As emphasized by researchers, “The versatility of quaternary ammonium compounds in both chemistry and medicine cannot be overstated.” Their structural complexity allows for intriguing interactions with biological systems, which can lead to substantial advancements in therapeutic treatments and understanding of biochemical pathways.

In conclusion, (4-piperidin-1-ium-1-ylcyclohexyl) butanoate; chloride not only serves as a fascinating study in chemical structure and reactivity but also highlights the intersection of organic chemistry and applied scientific research, showcasing the essential role that such compounds play in modern chemistry.

Synonyms
BUTYRIC ACID, 4-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE
1702-16-5
Butanoic acid, 4-(1-piperidinyl)cyclohexyl ester, hydrochloride