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2-(2-Undecyl-4,5-dihydroimidazol-1-yl)ethanol

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Identification
Molecular formula
C16H32N2O
CAS number
7365-45-9
IUPAC name
2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol
State
State

At room temperature, 2-(2-Undecyl-4,5-dihydroimidazol-1-yl)ethanol is typically in a liquid state due to its low melting point and relatively high boiling point. It transitions from a solid to a liquid near typical ambient temperatures.

Melting point (Celsius)
48.00
Melting point (Kelvin)
321.15
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.15
General information
Molecular weight
268.44g/mol
Molar mass
268.4420g/mol
Density
0.9601g/cm3
Appearence

2-(2-Undecyl-4,5-dihydroimidazol-1-yl)ethanol typically appears as a clear to pale yellow liquid. It is an amphiphilic compound containing both a hydrophilic imidazole moiety and a hydrophobic undecyl chain, which may contribute to its solubility properties in various solvents.

Comment on solubility

Solubility of 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol

The solubility of 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol can be considered through various factors. Understanding its behavior in different solvents is crucial for applications in both scientific and industrial contexts.

  • Polar Solvents: Due to the presence of the hydroxyl group (-OH) in its structure, this compound tends to be more soluble in polar solvents such as water and alcohols. The ability of the -OH group to form hydrogen bonds enhances solvation.
  • Nonpolar Solvents: While the compound has a hydrophobic tail from the undecyl group, its overall solubility in nonpolar solvents may be limited. However, some degree of solubility could still be observed due to the balance between hydrophilic and hydrophobic parts of the molecule.
  • Temperature Effects: Solubility might also vary with temperature; generally, an increase in temperature can enhance solubility in most solvents, particularly for organic compounds.

In summary, the solubility of 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol is significantly influenced by solvent polarity and temperature. Understanding these properties is essential for its effective utilization in various chemical processes.

Interesting facts

Interesting Facts About 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol

2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol is a fascinating compound that highlights the interactions between structure and function in chemical substances. Here are some key points that underscore its uniqueness:

  • Structural Diversity: The compound contains an imidazole ring, which is known for its presence in many biologically active molecules, including histidine, an essential amino acid in protein synthesis.
  • Long Hydrocarbon Chain: The undecyl group contributes to significant hydrophobic characteristics, making it an intriguing candidate for studies in lipid bilayer interactions and micelle formation.
  • Potential Applications: This compound's structural properties suggest potential applications in the fields of surfactants, antifungal agents, and even as additives in pharmaceuticals. Its hydrophilicity and hydrophobicity balance can influence solubility and bioavailability.
  • Biochemical Interactions: The presence of the hydroxyl (-OH) group enables the compound to participate in hydrogen bonding, which may facilitate its interaction with biomolecules such as enzymes and receptors.
  • Research Implications: Studies involving 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol could provide insights into the synthesis of new materials or drugs that leverage its unique chemical properties for enhanced efficacy.

In the words of a notable chemist, "It is not simply the molecules themselves, but the way they interact and integrate into larger systems that creates chemistry's magic." Thus, the exploration of this compound may lead to a deeper understanding of both foundational chemistry and potential applications that impact everyday life.

As research continues, the role of 2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol in various scientific domains looks promising, encouraging further investigation and innovation.

Synonyms
4,5-Dihydro-2-undecyl-1H-imidazole-1-ethanol
136-99-2
Lauryl hydroxyethyl imidazoline
2-Undecyl-2-imidazoline-1-ethanol
2-(2-undecyl-4,5-dihydroimidazol-1-yl)ethanol
1H-Imidazole-1-ethanol, 4,5-dihydro-2-undecyl-
Nalcamine G-11
HSDB 5622
UNII-0B4PCW98KD
1-(2-HYDROXYETHYL)-2-UNDECYLIMIDAZOLINE
54117-59-8
MACKAZOLINE 95L
1-Hydroxyethyl-2-undecylimidazoline
EINECS 205-271-0
NALCAMINE G 11
2-Imidazoline-1-ethanol, 2-undecyl-
0B4PCW98KD
1-(2-hydroxyethyl)-2-undecyl-2-imidazoline
DTXSID0059667
HYDROXYETHYLLAURYLGLYOXALIDINE
2-UNDECYL-1-(2-HYDROXYETHYL)-2-IMIDAZOLINE
1-(2-HYDROXYETHYL)-2-UNDECYLIMIDAZOLINE [HSDB]
Nalcamine G11
Maybridge1_000110
2Undecyl2imidazoline1ethanol
MixCom1_000198
SCHEMBL768833
2Imidazoline1ethanol, 2undecyl
1Hydroxyethyl2undecylimidazoline
CHEMBL4454230
DTXCID0034354
2-undecyl hydroxyethyl imidazoline
CCG-54334
4,5Dihydro2undecyl1Himidazole1ethanol
1HImidazole1ethanol, 4,5dihydro2undecyl
DB-312533
1-(2-Hyrdoxyethyl)-2-undecyl-2-imidazoline
NS00013830
LAURYL HYDROXYETHYL IMIDAZOLINE [INCI]
SR-01000643437-1
BRD-K70791121-001-01-6
Q27236564
2-(2-undecyl-4,5-dihydro-1H-imidazol-1-yl)ethan-1-ol