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Salmeterol

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Identification
Molecular formula
C25H37NO4
CAS number
89365-50-4
IUPAC name
4-[2-[6-[[2-(3,4-dihydroxyphenyl)-2-hydroxy-ethyl]amino]hexylamino]-1-hydroxy-ethyl]benzene-1,2-diol
State
State

At room temperature, Salmeterol is in a solid state.

Melting point (Celsius)
113.50
Melting point (Kelvin)
386.65
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
603.77g/mol
Molar mass
603.7680g/mol
Density
1.1658g/cm3
Appearence

Salmeterol is a white to off-white crystalline powder.

Comment on solubility

Solubility of 4-[2-[6-[[2-(3,4-dihydroxyphenyl)-2-hydroxy-ethyl]amino]hexylamino]-1-hydroxy-ethyl]benzene-1,2-diol

The solubility of the compound with the formula C25H37NO4 can be evaluated considering several key factors:

  • Polarity: Due to the presence of multiple hydroxyl (–OH) groups, the compound exhibits significant polarity, which can influence its solubility in polar solvents like water.
  • Hydrogen Bonding: The ability to form hydrogen bonds with water molecules increases its solubility in aqueous environments.
  • Alkyl Chains: The hydrophobic nature of the hydrocarbon segments may limit the overall solubility in polar solvents, suggesting a more complex solubility profile.
  • Solvent Interaction: The interaction with different solvents is crucial; it's likely to be more soluble in organic solvents than in water.

In summary, while the compound has functional groups that enhance solubility in polar solvents, its extensive alkyl chains may restrict solubility in highly polar media. Therefore, testing in various solvents is essential to determine its specific solubility characteristics.

Interesting facts

Interesting Facts about 4-[2-[6-[[2-(3,4-dihydroxyphenyl)-2-hydroxy-ethyl]amino]hexylamino]-1-hydroxy-ethyl]benzene-1,2-diol

This compound is a fascinating example of how complex organic chemistry can weave together different functional groups to achieve unique properties. Its structure reveals a rich interplay between aromatic rings, amino groups, and hydroxy functionalities, making it a subject of interest in both biochemical research and pharmaceutical applications.

Biological Significance

  • Potential Therapeutic Applications: Due to its ability to mimic naturally occurring biological molecules, this compound can have significant implications for drug development, particularly in targeting metabolic disorders.
  • Antioxidant Properties: The presence of multiple hydroxy groups suggests potential antioxidant capabilities, allowing it to combat oxidative stress in biological systems.

Chemical Structure Insights

The intricate configuration of this compound features:

  • Aromatic Compounds: The benzene derivative provides a stable backbone for the molecule, contributing to its structural integrity.
  • Amine Functionalities: The presence of amino groups indicates possible interactions with biological targets, enhancing its role in medicinal chemistry.
  • Hydroxy Groups: Essential for solubility and reactivity, these groups can also participate in hydrogen bonding, affecting the compound's overall properties.

Applications in Research

In research settings, this compound may serve as a valuable tool for:

  • Studying Enzyme Reactions: Its structure may mimic substrates or inhibitors, providing insights into enzyme mechanisms.
  • Investigating Cell Signaling Pathways: The compound’s complex framework allows scientists to explore its role in cellular processes.

Overall, the unique characteristics of 4-[2-[6-[[2-(3,4-dihydroxyphenyl)-2-hydroxy-ethyl]amino]hexylamino]-1-hydroxy-ethyl]benzene-1,2-diol present ample opportunities for innovative research and application in fields ranging from medicinal chemistry to biology. As we explore compounds of this nature, we unveil the intricate connections between structure and function that drive the molecular landscape of life.

Synonyms
HEXOPRENALINE
3215-70-1
Ipradol
Esoprenalina
Hexoprenalino
Hexoprenalinum
Esoprenalina [DCIT]
Hexoprenaline [INN:BAN]
Hexoprenalinum [INN-Latin]
St-1512
Hexoprenalino [INN-Spanish]
hexoprenalina
Ipradol (TN)
UNII-G9L6B3W684
1,2-Benzenediol, 4,4'-(1,6-hexanediylbis(imino(1-hydroxy-2,1-ethanediyl)))bis-
Hexoprenaline (INN)
St1512
G9L6B3W684
HEXOPRENALINE [MI]
HEXOPRENALINE [INN]
HEXOPRENALINE [WHO-DD]
3215-70-1(free base)
DTXSID7048322
1,12-Bis(3,4-dihydroxyphenyl)-3,10-diaza-1,12-dodecandiol
alpha,alpha'-(Hexamethylenebis(iminomethylene))bis(3,4-dihydroxybenzylalcohol)
Hexoprenalinum (INN-Latin)
1,2-Benzenediol,4,4'-[1,6-hexanediylbis[imino(1-hydroxy-2,1-ethanediyl)]]bis-
Hexoprenalino (INN-Spanish)
NCGC00167522-01
Hexoprenalin
4-(2-((6-((2-(3,4-dihydroxyphenyl)-2-hydroxyethyl)amino)hexyl)amino)-1-hydroxyethyl)benzene-1,2-diol
4-{2-[(6-{[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino}hexyl)amino]-1-hydroxyethyl}benzene-1,2-diol
4-[2-[6-[[2-(3,4-dihydroxyphenyl)-2-hydroxyethyl]amino]hexylamino]-1-hydroxyethyl]benzene-1,2-diol
SCHEMBL121449
CHEMBL1589896
DTXCID5028297
R03AC06
R03CC05
AKOS040746895
DB08957
DA-74116
FH158621
HY-121185
NS00003917
D08039
Q4134964
BRD-A33894669-065-01-9