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Clobenpropit

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Identification
Molecular formula
C16H22ClINO
CAS number
156293-15-9
IUPAC name
[3-(4-chlorophenyl)-3-hydroxy-hex-5-enyl]-trimethyl-ammonium;iodide
State
State

At room temperature, Clobenpropit exists as a solid. It’s stable under standard conditions and should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
157.00
Melting point (Kelvin)
430.15
Boiling point (Celsius)
318.00
Boiling point (Kelvin)
591.15
General information
Molecular weight
346.91g/mol
Molar mass
346.9080g/mol
Density
1.2046g/cm3
Appearence

Clobenpropit appears as a white to off-white crystalline powder that is not hygroscopic. Its appearance can vary slightly depending on the form and purity of the sample. It is typically a solid under normal laboratory conditions and has a fine granular texture.

Comment on solubility

Solubility of [3-(4-chlorophenyl)-3-hydroxy-hex-5-enyl]-trimethyl-ammonium;iodide

The solubility of the compound [3-(4-chlorophenyl)-3-hydroxy-hex-5-enyl]-trimethyl-ammonium;iodide can be understood through several key factors:

  • Polar vs. Non-Polar: This compound has significant polar characteristics due to the quaternary ammonium structure. As a result, it tends to be more soluble in polar solvents such as water compared to non-polar solvents.
  • Ionization: The presence of the iodide counterion encourages ion-dipole interactions, enhancing solubility in aqueous solutions.
  • Hydrophilic Groups: The hydroxy group introduces additional hydrophilicity, promoting solubility in water and other polar solvents, while the 4-chlorophenyl group may contribute some hydrophobic characteristics.

In summary, this compound is expected to be relatively soluble in water due to its ionic nature and polar functional groups, making it suitable for various applications in aqueous environments.

Interesting facts

Interesting Facts about [3-(4-chlorophenyl)-3-hydroxy-hex-5-enyl]-trimethyl-ammonium;iodide

This compound, known for its intriguing structure and potential applications, offers several points of interest for chemists and chemical enthusiasts alike:

  • Quaternary Ammonium Compound: The presence of the trimethylammonium group in its structure classifies it as a quaternary ammonium compound. Such compounds are notable for their role as disinfectants, surfactants, and phase transfer catalysts.
  • Biological Activity: The unique structure of this compound may exhibit interesting biological properties. Compounds with similar configurations have shown potential as antimicrobial agents or in modulating biological activities, making them a topic of interest in medicinal chemistry.
  • Reactivity: Due to the presence of the hydroxyl group, the compound is expected to participate in various chemical reactions. This characteristic can lead to the synthesis of other derivatives, expanding its chemical toolkit.
  • Halogen Incorporation: The incorporation of a chlorine atom (from the 4-chlorophenyl group) can impart distinctive reactivity and stability to the compound. Halogens are often utilized in organic synthesis to introduce additional functional groups or modify physical properties.
  • Potential Uses: The dual functional groups in this compound establish it as a candidate for diverse applications. It might find a role in dyes, herbicides, or in the development of ion-exchange materials.
  • Structural Complexity: Its multi-faceted design represents the complexity often seen in organic chemistry, where variations in structure can lead to significant differences in reactivity and properties.

In conclusion, the compound's combination of a quaternary ammonium structure with aromatic and hydroxy functionalities opens the door to both established and innovative chemical pathways. Its unique characteristics serve as an excellent illustration of how small variations in molecular structure can lead to a wide array of applications and functions in organic chemistry.

Synonyms
2238-73-5
(3-(p-Chlorophenyl)-3-hydroxy-5-hexenyl)trimethylammonium iodide
AMMONIUM, (3-(p-CHLOROPHENYL)-3-HYDROXY-5-HEXENYL)TRIMETHYL-, IODIDE
DTXSID60945029
3-(4-Chlorophenyl)-3-hydroxy-N,N,N-trimethylhex-5-en-1-aminium iodide