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1H-imidazol-5-ylmethanol

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Identification
Molecular formula
C4H6N2O
CAS number
5118-13-8
IUPAC name
1H-imidazol-5-ylmethanol
State
State

1H-imidazol-5-ylmethanol is a solid at room temperature. It is stable under normal temperatures and pressures, and it is typically stored in tightly sealed containers to prevent contamination or degradation.

Melting point (Celsius)
88.00
Melting point (Kelvin)
361.10
Boiling point (Celsius)
287.50
Boiling point (Kelvin)
560.70
General information
Molecular weight
112.12g/mol
Molar mass
112.1170g/mol
Density
1.3420g/cm3
Appearence

1H-imidazol-5-ylmethanol typically appears as a white to off-white crystalline solid. It may come in finely divided powder form or as small crystal aggregates. The compound is often used in research and development settings, where appearance is less critical than purity or functional group presence.

Comment on solubility

Solubility of 1H-imidazol-5-ylmethanol (C4H6N2O)

The solubility of 1H-imidazol-5-ylmethanol is an intriguing aspect of its chemical behavior. This compound displays a notable degree of solubility in various solvents, making it quite versatile in different environments. Here are some important points regarding its solubility:

  • Polar Solvents: 1H-imidazol-5-ylmethanol is readily soluble in polar solvents such as water and methanol due to the presence of its hydroxymethyl group, which can form hydrogen bonds with solvent molecules.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents is significantly lower. This is largely because the imidazole ring and hydroxymethyl group can better interact with polar environments than with non-polar ones.
  • Temperature Dependence: The solubility may also vary with temperature; typically, an increase in temperature can enhance solubility, allowing for more efficient dissolution in solvents.

In practical applications, such as pharmaceuticals and chemical synthesis, the solubility of 1H-imidazol-5-ylmethanol can influence its utilization and effectiveness. Understanding its solubility profile is crucial, as it affects reaction kinetics, bioavailability, and the overall behavior of the compound in biochemical systems.

Ultimately, the solubility characteristics of 1H-imidazol-5-ylmethanol demonstrate the intricate relationship between molecular structure and solvent interaction, presenting opportunities for innovative applications in various scientific fields.

Interesting facts

Interesting Facts about 1H-imidazol-5-ylmethanol

1H-imidazol-5-ylmethanol is a fascinating organic compound with numerous applications in both scientific research and industrial processes. Here are some notable aspects of this compound:

  • Structure and Significance: 1H-imidazol-5-ylmethanol contains the imidazole ring, which is a key component in many biologically active molecules, including histamine and various alkaloids.
  • Role in Synthesis: The presence of a hydroxymethyl group makes 1H-imidazol-5-ylmethanol a valuable building block for synthesizing diverse chemical entities, facilitating the development of new pharmaceuticals.
  • Pharmaceutical Applications: This compound is investigated for its potential therapeutic effects. Its structural similarities to other biologically active compounds enable it to be explored in drug discovery.
  • Catalytic Properties: 1H-imidazol-5-ylmethanol may function as a catalyst in certain chemical reactions, enhancing efficiency while reducing unwanted byproducts.
  • Research Potential: Ongoing studies focus on understanding how modifications to this compound can influence reactivity and selectivity in organic reactions.

In summary, 1H-imidazol-5-ylmethanol is a versatile compound with potential across multiple fields, from pharmaceuticals to synthetic chemistry. As research progresses, it will undoubtedly reveal more of its secrets that can contribute to advancements in science and technology.

Synonyms
822-55-9
IMIDAZOLE-4-METHANOL
(1H-Imidazol-4-yl)methanol
4-(Hydroxymethyl)imidazole
1H-Imidazole-4-methanol
1H-imidazol-5-ylmethanol
1H-Imidazol-4-ylmethanol
1H-Imidazole-5-methanol
(3H-Imidazol-4-yl)-methanol
(1H-imidazol-4-yl)-methanol
4(5)-(Hydroxymethyl)imidazole
4-imidazolemethanol
4-HYDROXYMETHYLIMIDAZOLE
(1H-imidazol-5-yl)methanol
CHEBI:28182
5-(hydroxymethyl)imidazole
4-IMIDAZOLYLMETHANOL
QD0132T507
DTXSID40231619
IMIDAZOLE-4(OR 5)-METHANOL
NSC-39016
4(5)-Hydroxymethylimidazole
1H-Imidazol-4-ylmethanol; 4-(Hydroxymethyl)imidazole; 4-Imidazolylmethanol; 4-Methylol-1H-imidazole
UNII-QD0132T507
1H-Imidazole-4-methanol (9CI)
MZ0
4-imidazole methanol
5-hydroxymethylimidazole
4-hydroxymethyl imidazole
4-Methylol-1H-imidazole
Lopac-H-1877
C05562
1H-imidazol-4-yl-methanol
imidazole, 4-hydroxymethyl-
Lopac0_000603
1H-Imidazol-4-ylmethanol #
4(5)-Hydroxymethyl imidazole
4-(hydroxymethyl)-1H-imidazole
CHEMBL1397797
imidazole, 4(5)-hydroxymethyl-
DTXCID20154110
MFCD00266718
AKOS005258761
AKOS015951052
4(5)-(Hydroxymethyl)imidazole, 97%
CCG-204692
PB24669
SDCCGSBI-0050585.P002
NCGC00015502-01
NCGC00015502-02
NCGC00015502-03
NCGC00015502-04
NCGC00015502-05
NCGC00093363-02
AC-23132
AS-58725
PD034373
DB-032007
CS-0008531
EN300-50616
H67433
W10530
AB-131/25126047
Q27103551
Z234898057
628-579-0