Skip to main content

Cyclohexanol

ADVERTISEMENT
Identification
Molecular formula
C6H12O
CAS number
108-93-0
IUPAC name
(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;iodide
State
State

At room temperature, cyclohexanol is a viscous liquid or can be found as a solid depending on the ambient temperature, and it typically has a camphor-like odor.

Melting point (Celsius)
25.93
Melting point (Kelvin)
299.08
Boiling point (Celsius)
161.64
Boiling point (Kelvin)
434.79
General information
Molecular weight
100.16g/mol
Molar mass
100.1580g/mol
Density
1.0200g/cm3
Appearence

Cyclohexanol appears as a colorless, viscous liquid or sticky solid with a camphor-like odor.

Comment on solubility

Solubility Overview

The compound (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium iodide is an intriguing ionic compound. Its solubility can be influenced by a variety of factors due to its structure and the presence of the iodide ion. Here are some key points to consider:

  • Ionic Character: The iodide (I-) component typically increases solubility in polar solvents, particularly water.
  • Ammonium Group: The triethylammonium group contributes to solubility by enhancing interactions with water molecules, supporting dissolution.
  • Hydrophobic Portions: The cyclohexyl and phenyl groups introduce hydrophobic characteristics that may limit solubility in purely aqueous environments.
  • Temperature Dependency: As with many ionic compounds, solubility may increase with temperature, making it beneficial to test solubility at various temperatures.

In summary, while the ionic nature of (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium iodide suggests reasonable solubility in polar solvents, the presence of large hydrophobic groups could lead to variability. When exploring its practical applications, one must consider both the solute characteristics and the solvent environment for optimal results.

Interesting facts

Interesting Facts about (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;iodide

This compound belongs to a fascinating class of quaternary ammonium salts, which are known for their versatility and unique properties. Comprising a triethylammonium cation and an iodide anion, it presents a synergy of different molecular features that can lead to exciting applications in various fields.

Chemical Significance

  • Quaternary Ammonium Salts: The presence of the triethylammonium group contributes to the compound's ability to act as a phase transfer catalyst, facilitating reactions between reactants in different phases.
  • Hydroxyl Group: The -OH functional group provides potential for hydrogen bonding, which can significantly affect the compound's reactivity and interactions with biological systems.
  • Cyclohexyl and Phenyl Groups: These bulky groups enhance the compound's hydrophobic character, making it a potential candidate for applications in drug delivery and formulations.

Application Potential

The unique structure of this compound opens doors to various industrial and research applications, including:

  • Biological Studies: Due to its quaternary ammonium nature, this compound could serve as a model system for exploring membrane interactions.
  • Pharmaceutical Development: Compounds with similar structures are often tested for their efficacy as antimicrobial agents or in transporting drugs across biological barriers.
  • Catalysis: The ability to influence reaction pathways through phase transfer catalysis can position this compound as a valuable tool in organic synthesis.

Future Research Directions

Scientists are exploring various avenues to enhance the applications of this compound, including:

  • Modification of Functional Groups: Altering the substituents on the aromatic or alicyclic rings could lead to compounds with tailored properties.
  • Combination with Other Compounds: Investigating its behavior in mixed systems may reveal synergistic effects when combined with other catalysts or drugs.

In conclusion, the compound (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;iodide showcases a rich structural diversity, making it a point of interest for not only chemists but also those in pharmaceuticals and materials science. The ongoing exploration of its chemical and biological properties could pave the way for innovative discoveries and advancements.

Synonyms
Tridihexethyl iodide
Tridihexethide
Trihexethyl iodide
Claviton
Tridihexide
Propethonum iodide
125-99-5
Ioduro de tridihexetilo
Iodure de tridihexethyl
Tridihexethyli iodidum
Propethonium iodide
(3-Cyclohexyl-3-hydroxy-3-phenylpropyl)triethylammonium iodide
7Y7FXO7GQP
1-Cyclohexyl-3-diethylamino-1-phenyl-1-propanol ethiodide
3-Diethylamino-1-cyclohexyl-1-phenyl-1-propanol ethiodide
3-Diethylamino-1-phenyl-1-cyclohexyl-1-propanol ethiodide
CHEBI:9704
alpha-(2-Diethylaminoethyl)-alpha-phenylcyclohexanemethanol ethiodide
DTXSID00875351
3-cyclohexyl-N,N,N-triethyl-3-hydroxy-3-phenylpropan-1-aminium iodide
tridihexAthyl (cation)
RefChem:933377
A03AB08
DTXCID901013473
Benzenepropanaminium, gamma-cyclohexyl-N,N,N-triethyl-gamma-hydroxy-, iodide (1:1)
204-762-7
Tridihexethyl iodide [INN]
(3-cyclohexyl-3-hydroxy-3-phenylpropyl)-triethylazanium;iodide
Tridihexethyli iodidum [INN-Latin]
EINECS 204-762-7
UNII-7Y7FXO7GQP
Iodure de tridihexethyl [INN-French]
Ioduro de tridihexetilo [INN-Spanish]
921 C
gamma-Cyclohexyl-N,N,N-triethyl-gamma-hydroxybenzenepropanaminium iodide
SCHEMBL249851
CHEMBL2107686
TRIDIHEXETHYL IODIDE [MI]
VFEDLMLHAGASHB-UHFFFAOYSA-M
TRIDIHEXETHYL IODIDE [WHO-DD]
AMMONIUM, (3-CYCLOHEXYL-3-HYDROXY-3-PHENYLPROPYL)TRIETHYL-, IODIDE
Benzenepropanaminium, gamma-cyclohexyl-N,N,N-triethyl-gamma-hydroxy-, iodide
NS00079191
C07862
Q27108477
BENZENEPROPANAMINIUM, .GAMMA.-CYCLOHEXYL-N,N,N-TRIETHYL-.GAMMA.-HYDROXY-, IODIDE (1:1)