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Fluorescein diacetate

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Identification
Molecular formula
C21H21ClN2O4
CAS number
596-09-8
IUPAC name
diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium;chloride
State
State

At room temperature, fluorescein diacetate is a solid compound. It is generally stored in powdered form and is handled as such in laboratory settings. Its solid state facilitates ease of storage and handling.

Melting point (Celsius)
190.00
Melting point (Kelvin)
463.15
Boiling point (Celsius)
441.00
Boiling point (Kelvin)
714.15
General information
Molecular weight
476.96g/mol
Molar mass
476.9550g/mol
Density
1.3000g/cm3
Appearence

The compound typically appears as a pale yellow or yellow-orange powder. It may also be available in crystalline form. Its vibrant color is characteristic, and it is soluble in organic solvents but poorly soluble in water.

Comment on solubility

Solubility of Diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium; Chloride

The solubility of diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium chloride is influenced by several chemical and environmental factors. Here are some key points to consider:

  • Polarity: This compound contains both a quaternary ammonium group and a phenolic structure, which can affect its overall polarity. Typically, quaternary ammonium salts tend to be soluble in water, but the presence of bulky organic groups may hinder solubility.
  • Solvent Compatibility: Solubility is often greater in polar solvents like water or alcohols. However, due to the complex structure of this compound, solubility may vary when tested in non-polar solvents.
  • Temperature: Increased temperature usually enhances solubility for many compounds. The effect of temperature should be considered when attempting to dissolve this compound.
  • pH Levels: Altering the pH of the solution can also change the solubility of ionic compounds, potentially affecting solubility metrics.

As with many organic salts, one can expect that "the solubility characteristics of diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium chloride may reveal itself as a balance between hydrophilic and hydrophobic interactions, making it crucial to examine specific experimental conditions." Overall, while it may display appreciable solubility in aqueous systems, experimentation is essential to confirm its solubility properties accurately.

Interesting facts

Interesting Facts about Diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium Chloride

Diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium chloride is a fascinating compound with distinct characteristics that draw the attention of chemists and researchers alike. Below are some intriguing aspects of this compound:

  • Versatile Applications: Its unique structure allows it to participate in various chemical reactions, making it valuable in medicinal chemistry and material science.
  • Cromene Derivative Insights: The presence of the chromene moiety is significant, as chromenes are known for their vibrant fluorescence and potential applications in polymer science and as dyes.
  • Ammonium Salt Nature: As a quaternary ammonium compound, this compound showcases interesting properties related to its ionic structure, which can lead to enhanced solubility in polar solvents.
  • Biological Potential: Investigations have suggested that similar structures may exhibit pharmacological effects, such as antitumor or anti-inflammatory properties, indicating a promising path for drug development.
  • Research Opportunities: The compound invites in-depth studies related to its reactivity and potential functionalization, keeping the field of organic chemistry vibrant and continuous.

In conclusion, diisopropyl-[2-(3-methyl-4-oxo-2-phenyl-chromene-8-carbonyl)oxyethyl]ammonium chloride is more than just a chemical formula; it's a gateway to exploring innovative applications and understanding complex chemical interactions. As researchers delve into its properties, they can unlock new possibilities that contribute to advancements in various scientific domains.

Synonyms
Diisopropylamino 3-methylflavone-8-carboxylate hydrochloride
REC 1-0469
3468-06-2
4H-1-Benzopyran-8-carboxylic acid, 3-methyl-4-oxo-2-phenyl-, 2-(diisopropylamino)ethyl ester, hydrochloride