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bis(4-aminophenyl) carbonate

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Identification
Molecular formula
C13H12N2O3
CAS number
5874-17-7
IUPAC name
bis(4-aminophenyl) carbonate
State
State

This compound is typically found as a solid at room temperature.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
446.00
Boiling point (Kelvin)
719.15
General information
Molecular weight
258.27g/mol
Molar mass
258.2730g/mol
Density
1.2900g/cm3
Appearence

Bis(4-aminophenyl) carbonate is typically a solid compound at room temperature. It may appear as a off-white or light-yellow powder or crystalline substance.

Comment on solubility

Solubility of Bis(4-aminophenyl) Carbonate

Bis(4-aminophenyl) carbonate, with the chemical formula C13H12N2O3, presents a unique solubility profile that is influenced by its chemical structure. Being an organic compound with polar amine groups, it tends to exhibit varying degrees of solubility in different solvents.

Here are some key points regarding the solubility of this compound:

  • Solvent Polarities: Bis(4-aminophenyl) carbonate is generally more soluble in polar organic solvents such as dimethyl sulfoxide (DMSO) and acetone due to the ability of these solvents to stabilize the amine groups through hydrogen bonding.
  • Water Solubility: This compound has limited solubility in water, primarily because of its hydrophobic aromatic rings. The presence of non-polar components can hinder interaction with water molecules.
  • Temperature Effects: Solubility can significantly increase with temperature; thus, heating the solvent might enhance the dissolution of bis(4-aminophenyl) carbonate.
  • pH Influence: The solubility may also be affected by the pH of the solution, given the amine functionalities, which can be protonated in acidic environments, potentially increasing solubility.

In summary, while bis(4-aminophenyl) carbonate shows some attractive solubility characteristics in specific solvents, its overall solubility can be classified as moderate, requiring careful selection of solvent conditions to optimize its use in various applications.

Interesting facts

Interesting Facts About Bis(4-Aminophenyl) Carbonate

Bis(4-aminophenyl) carbonate, often referred to as bis(4-AP) carbonate, is a fascinating compound with various applications in the field of materials science and organic chemistry. Here are some intriguing aspects:

  • Versatile Building Block: This compound serves as an important building block in the synthesis of advanced polymers. Its functional groups allow for various reactions that can lead to diverse polymeric materials.
  • Biodegradable Potential: With increasing interest in sustainable materials, bis(4-AP) carbonate presents an opportunity for developing biodegradable plastics, reducing environmental impact.
  • Enhanced Thermal Stability: The presence of carbonate groups in its structure contributes to enhanced thermal stability, making it a favorable candidate for applications that require materials to withstand heat without degrading.
  • Research Applications: Bis(4-AP) carbonate is often used in research to explore new ways to functionalize polymers, leading to innovative applications in coatings, adhesives, and drug delivery systems.
  • Health and Safety: While this compound is useful, it is essential to handle it with care, as some derivatives and by-products may pose health risks. Proper laboratory safety protocols should always be followed.

In summary, bis(4-aminophenyl) carbonate is more than just a compound; it embodies the intersection of chemistry and sustainable innovation. As research continues to progress, its full potential in both industry and academia is yet to be fully realized. As a chemist, exploring the modifications and applications of this compound offers a window into the future of material sciences!

Synonyms
Bis(4-aminophenyl) carbonate
4,4'-Diaminodiphenyl carbonate
CARBONIC ACID, BIS(p-AMINOPHENYL) ESTER
19363-39-4
GBN093K7XE
NSC 61487
NSC 80123
Phenol, 4-amino-, carbonate (2:1) (ester)
BRN 2944196
NSC-80123
UNII-GBN093K7XE
DTXSID40172972
NSC-61487
PHENOL, 4-AMINO-, 1,1'-CARBONATE
DTXCID0095463
RefChem:198468
NCIOpen2_004414
NCIOpen2_007988
4,4-Diaminodiphenyl carbonate
SCHEMBL2132487
NSC80123
DS-014617