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Pine Oil Quaternary Ammonium Chloride

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Identification
Molecular formula
C15H27ClNO2
CAS number
34590-94-8
IUPAC name
2-(1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium;chloride
State
State

The compound is typically in a liquid state at room temperature.

Melting point (Celsius)
22.00
Melting point (Kelvin)
295.15
Boiling point (Celsius)
110.00
Boiling point (Kelvin)
383.15
General information
Molecular weight
269.80g/mol
Molar mass
269.8040g/mol
Density
1.0750g/cm3
Appearence

Pine Oil Quaternary Ammonium Chloride usually appears as a colorless to pale yellow liquid, depending on its concentration and purity. The liquid has a characteristic odor reminiscent of pine.

Comment on solubility

Solubility of 2-(1,4-Dioxaspiro[4.5]decan-3-yl)piperidin-1-ium Chloride

The solubility of 2-(1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium chloride presents intriguing characteristics that can be explored from various perspectives. This compound, characterized by its unique structure, shows a tendency to exhibit solubility in both polar and non-polar solvents.

Factors Influencing Solubility

  • Polarity: The presence of the piperidine moiety contributes to its solubility in water due to its ability to engage in hydrogen bonding.
  • Complex Structure: The dioxaspiro ring may enhance solubility in organic solvents, thanks to its larger hydrophobic area.
  • Ionization: As a quaternary ammonium salt (due to the chloride ion), it is likely to be highly soluble in polar solvents, especially in aqueous solutions.

This compound is particularly fascinating because it may exemplify a balance between hydrophilicity and lipophilicity, making it versatile in various chemical environments. Generally, the solubility of ionic compounds like chlorides is favored in polar solvents, where the solvent's capability to stabilize ionic interactions can be observed.

In summary, the solubility of 2-(1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium chloride highlights the significance of molecular structure and solvent interactions, paving the way for diverse applications in chemical sciences.

Interesting facts

Interesting Facts about 2-(1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium chloride

The compound 2-(1,4-dioxaspiro[4.5]decan-3-yl)piperidin-1-ium chloride is a fascinating example of the intersection between organic chemistry and medicinal research. Here are some intriguing points to consider:

  • Structural Complexity: This compound features a spirocyclic structure, which is notable for its unique geometric configuration. The spiro center indicates that the compound has a complex ring system that can greatly influence its chemical behavior and biological activity.
  • Potential Applications: Compounds like this one may exhibit pharmacological properties. Their unique structures can lead to various interactions with biological targets, making them potential candidates for drug development.
  • Quaternary Ammonium: The presence of the piperidinium ion indicates that this compound is a quaternary ammonium salt, often associated with antimicrobial and antiseptic properties. This class of compounds has significant applications in both medicinal and industrial chemistry.
  • Research Context: Researchers are continually investigating the reactivity and efficacy of spirocyclic compounds in various contexts, including their role in developing new therapeutic agents.

The study of such compounds exemplifies the beauty and complexity of chemistry, where even a small change in structure can yield vastly different properties and functionalities. As Dr. Antoine Lavoisier famously stated, "Nothing is lost, nothing is created, everything is transformed," which holds true in the intricate world of chemical reactions and compound interactions.

Synonyms
2-(2-Piperidyl)-1,4-dioxaspiro(4.5)decane hydrochloride
7553-32-4
1,4-DIOXASPIRO(4.5)DECANE, 2-(2-PIPERIDYL)-, HYDROCHLORIDE