1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea

Identification

Molecular formula

C₁₅H₁₄N₄O₅

CAS number

70288-86-7

IUPAC name

1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea

State

This compound is typically found in a solid state at room temperature, appearing as a crystalline powder.

Melting point (Celsius)

230.00

Melting point (Kelvin)

503.15

Boiling point (Celsius)

405.00

Boiling point (Kelvin)

678.15

General information

Molecular weight

364.35g/mol

Molar mass

364.3480g/mol

Density

1.6700g/cm³

Appearence

This compound appears as a solid, often found in the form of crystalline powder. The color can vary depending on purity but is generally an off-white to pale yellow.

Comment on solubility

Solubility of 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea

The solubility of 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea is an important consideration for its applications in various chemical processes and formulations. Here are some key points regarding its solubility:

Solvent Dependence: The solubility of this compound can significantly vary depending on the solvent used. It is typically more soluble in polar solvents such as water due to the presence of hydroxyl groups that can form hydrogen bonds.
Temperature Influence: Increased temperature generally enhances solubility for many organic compounds. Thus, raising the temperature can aid in dissolving 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea.
pH Sensitivity: The solubility may also be affected by the pH of the solution. In more alkaline solutions, the compound may ionize, leading to increased solubility.
Complexation Potential: The presence of functional groups may allow this compound to form complexes with metal ions, further influencing its solubility profile.

In summary, the solubility of 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea is multifaceted, dependent on factors such as solvent choice, temperature, pH, and potential complexation. Understanding these dynamics is essential for optimizing its use in various chemical applications.

Interesting facts

Interesting Facts about 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea

1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea is an intriguing chemical compound that showcases the fascinating interplay between structure and function in organic chemistry. Here are some key points that highlight its significance:

Dual Functionality: This compound features dual functional groups which contribute to its potential applications in both medicinal and industrial chemistry.
Origins in Dye Chemistry: The presence of phenyl groups indicates its historical significance in dye chemistry, particularly in azo dyes and more complex dye structures.
Potential as a Drug: Derivatives of this compound may possess pharmacological properties, especially with its dihydroxyamino substituents, which are often related to antioxidant activities.
Synthetic Variability: The ability to modify the peripheral substituents opens the door for synthetic chemists to design new compounds with varying activities and properties.
Research Interest: There is ongoing research into its application as a phenolic resin precursor, which could lead to advancements in the material sciences.

As a compound rich in functional groups and structural complexity, 1,3-bis[[4-(dihydroxyamino)phenyl]imino]urea embodies the essence of organic synthesis, illustrating how variations in molecular structure can lead to a diverse array of chemical behaviors and applications. Such compounds often serve as a foundation for further developments in both academic research and commercial industries.