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DAPI

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Identification
Molecular formula
C16H15N5
CAS number
28718-90-3
IUPAC name
N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide;methanesulfonate
State
State

At room temperature, DAPI is typically in solid form. It is stable and can be stored as a powder for long periods.

Melting point (Celsius)
300.00
Melting point (Kelvin)
573.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
350.38g/mol
Molar mass
350.3790g/mol
Density
1.3300g/cm3
Appearence

DAPI (4′,6-diamidino-2-phenylindole) appears as a yellow solid powder. It is often used in research laboratories for staining DNA, where it exhibits a bright blue fluorescence when bound to DNA, making it extremely useful for fluorescence microscopy applications.

Comment on solubility

Solubility of N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide Methanesulfonate

The solubility of N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide methanesulfonate can be characterized by a few key factors:

  • Polarity: This compound is likely to be polar due to the presence of the imidazolium ion, which enhances its interaction with polar solvents.
  • Solvent Interaction: It is expected to dissolve well in water, given that methanesulfonate anions are often soluble in polar solvents.
  • Temperature Dependency: The solubility may increase with temperature, as is common with many ionic compounds and salts.
  • Applications: The solubility profile is particularly important for applications in biological systems, where the compound may need to remain soluble to be effective.

In conclusion, the solubility of this compound is influenced by its polar nature and the environment in which it is placed, making it a versatile compound in various chemical applications.

Interesting facts

Exploring N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide Methanesulfonate

N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide methanesulfonate is a fascinating compound, drawing interest from both chemists and researchers. Here are some interesting facts about this unique chemical:

  • Imidazolium Ion Structure: This compound includes an imidazolium ion, known for its stability and propensity to engage in hydrogen bonding. The presence of nitrogen atoms in the ring structure plays a crucial role in its reactivity and interactions.
  • Diverse Applications: Imidazolium-based compounds are widely utilized in various fields, including catalysis, material science, and as ionic liquids. Their unique properties make them suitable for applications ranging from electrochemistry to solvents in organic synthesis.
  • Biological Activity: Compounds related to this one have been studied for their potential biological activities, including antimicrobial and anti-inflammatory effects. Such properties make them of considerable interest in medicinal chemistry.
  • Designing New Compounds: Researchers often modify imidazolium salts to create new derivatives for specific applications. The versatility of this compound allows for tailored functionalization, aiding in the development of innovative materials.

Notably, the methanesulfonate counterion contributes significantly to the compound's properties. It enhances solubility in polar solvents and can influence the overall stability of the imidazolium structure. As such, understanding the behavior of this compound at the molecular level offers insights into its future applications.

In conclusion, N-[2-(1,5-dimethylimidazol-1-ium-1-yl)ethyl]acetamide methanesulfonate serves as an excellent example of how intricate molecular design can lead to substances with varied applications across scientific disciplines. As we continue to explore its potential, this compound may unlock new pathways in chemistry and biochemistry.