Skip to main content

Cycrimine hydrochloride

ADVERTISEMENT
Identification
Molecular formula
C21H36ClNO
CAS number
77-39-4
IUPAC name
(3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;chloride
State
State

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

Melting point (Celsius)
177.00
Melting point (Kelvin)
450.15
Boiling point (Celsius)
465.00
Boiling point (Kelvin)
738.15
General information
Molecular weight
343.98g/mol
Molar mass
343.9600g/mol
Density
1.0023g/cm3
Appearence

Cycrimine hydrochloride typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;chloride

This compound, recognized as a quaternary ammonium salt, has distinctive solubility characteristics primarily influenced by its structural features. Understanding its solubility can be summarized in several key aspects:

  • Polarity: The presence of multiple functional groups, such as the hydroxy and ammonium groups, enhances the polarity of the molecule. This increase in polarity often leads to improved solubility in polar solvents, such as water.
  • Ionic Interactions: As a salt, the chloride component can readily dissociate in polar solvents, further facilitating its solubility due to ionic hydration.
  • Hydrogen Bonding: The hydroxy group offers opportunities for hydrogen bonding with water molecules, which can enhance solubility even more.

On the flip side, the bulky cyclohexyl and phenyl groups may impart some hydrophobic characteristics, potentially limiting solubility in strictly polar environments. Hence, the solubility of this compound can be summarized as:

  • Generally soluble in polar solvents like water.
  • Possibly less soluble in nonpolar solvents due to hydrophobic character.

In conclusion, understanding the balance of hydrophilic and hydrophobic interactions in (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;chloride is crucial in predicting its solubility behavior. Test conditions and solvent choices will play a critical role in its solubility profile.

Interesting facts

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

This unique compound is not just a mouthful but also a significant participant in various chemical reactions and applications. It belongs to the class of quaternary ammonium salts, which are well-known for their wide-ranging uses in both industrial and research settings.

Key Characteristics:

  • Ion Pairing: As a quaternary ammonium compound, this salt can form ion pairs that affect solubility and reactivity. The presence of the chloride ion contributes to its overall stability in solution.
  • Biological Applications: Such compounds often exhibit antimicrobial properties, making them of great interest in pharmaceuticals and biochemistry. Researchers investigate their potential as disinfectants and antiseptics.
  • Chemical Versatility: The structure of this compound allows it to react with various substrates, making it a candidate for use in synthesis and catalysis.

Noteworthy Differences:

Compared to other ammonium salts, the presence of the bulky cyclohexyl and phenyl groups enhances the hydrophobic character of the molecule. This influences:

  • Phase Separation: It can affect how the compound interacts with water and organic solvents.
  • Biocompatibility: The distinct chemical structure may lead to varying degrees of compatibility with biological systems.

A quote from renowned chemist Linus Pauling resonates when discussing compounds like this: "The nature of the chemical bond is the most important scientific problem of our time." In the case of (3-cyclohexyl-3-hydroxy-3-phenyl-propyl)-triethyl-ammonium;chloride, understanding its bonding and structural nuances can open doors to innovative applications in materials science and therapeutics.

In summary, this compound exemplifies the fascinating interplay between structure and function within the world of chemistry, showcasing the importance of molecular design in developing new and useful chemical entities.

Synonyms
Tridihexethyl chloride
4310-35-4
Pathilon
Pathilon chloride
(3-Cyclohexyl-3-hydroxy-3-phenylpropyl)triethylammonium chloride
UNII-25YK75CYMX
EINECS 224-323-3
25YK75CYMX
CHEBI:9703
DTXSID4023701
3-cyclohexyl-N,N,N-triethyl-3-hydroxy-3-phenylpropan-1-aminium chloride
DTXCID103701
AMMONIUM, (3-CYCLOHEXYL-3-HYDROXY-3-PHENYLPROPYL)TRIETHYL-, CHLORIDE
Tridihexethyl chloride [USP:INN:BAN]
Benzenepropanaminium, gamma-cyclohexyl-N,N,N-triethyl-gamma-hydroxy-, chloride
TRIDIHEXETHYL CHLORIDE (MART.)
TRIDIHEXETHYL CHLORIDE [MART.]
Tridihexethyl chloride (USP:INN:BAN)
TRIDIHEXETHYL IODIDE TRIDIHEXETHYL CHLORIDE
224-323-3
Tridihexethyl (Chloride)
Pathilon (TN)
TRIDIHEXETHYL CHLORIDE (200 MG)
(3-cyclohexyl-3-hydroxy-3-phenylpropyl)-triethylazanium;chloride
NCGC00017006-01
MLS002154119
Tridihexethyl chloride (BAN)
SCHEMBL100471
4310-35-4 (chloride)
CHEMBL1200771
Tridihexethyl chloride(200 mg)
HY-B1806A
XJGONMZLEDGBRM-UHFFFAOYSA-M
HMS1571A06
HMS2098A06
HMS2233A09
HMS3373K12
HMS3715A06
Tox21_110733
TRIDIHEXETHYL CHLORIDE [VANDF]
AKOS040754253
CCG-221042
TRIDIHEXETHYL CHLORIDE [WHO-DD]
Benzenepropanaminium, .gamma.-cyclohexyl-N,N,N-triethyl-.gamma.-hydroxy-, chloride
SMR001233426
CAS-4310-35-4
DB-247007
TRIDIHEXETHYL CHLORIDE [ORANGE BOOK]
CS-0013848
NS00083217
D00723
SR-01000838833
SR-01000838833-2
Q27108476
TRIDIHEXETHYL IODIDE TRIDIHEXETHYL CHLORIDE [MI]