62554-97-6

Usage

Uses

Used in Water Treatment:
2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is used as a chelating agent for water treatment processes. It helps in binding and removing metal ions, thereby improving water quality and preventing the formation of scale and corrosion.
Used in Metal Extraction:
In the metal extraction industry, 2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is used as a chelating agent to selectively bind and extract specific metal ions from ores or other sources. This enhances the efficiency of metal recovery and purification processes.
Used in Analytical Chemistry:
2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is utilized as a chelating agent in analytical chemistry for the separation, detection, and quantification of metal ions. Its ability to form stable complexes with various metal ions aids in accurate and precise analysis.
Used in Cleaning Products:
2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is used as a chelating agent in the formulation of cleaning products. It enhances the effectiveness of detergents by sequestering metal ions that can interfere with the cleaning process, leading to improved cleaning performance.
Used in Medical Diagnostic Procedures:
In the medical field, 2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is used in certain diagnostic procedures. Its chelating properties allow for the binding and detection of specific metal ions, aiding in the diagnosis of various conditions.
Used in Chelation Therapy for Heavy Metal Poisoning:
2,2'-[1,2-ethanediylbis(iminocarbonyl)]bisbenzoic acid is employed as a chelating agent in chelation therapy for the treatment of heavy metal poisoning. It binds to and helps remove toxic metal ions from the body, reducing their harmful effects and promoting recovery.

Upstream product

• 85-44-9 phthalic anhydride 
• 107-15-3 ethylenediamine 
• 607-26-1 N,N'-ethylenediphthalimide 

Relevant academic research and scientific papers

Spectral studies of dimeric copper(II) complexes of acid amide derivatives as models for type III copper enzymes

Dimeric (hydrated and anhydrated) complexes of Cu(II) with N,N'-bis(3-carboxy-1-oxo-2-prop-2-enyl)ethylenediamine (BCOPENH2, A) and N,N'-bis(2-carboxy-1-oxo-phenylenyl)ethylenediamine (BCOPHENH2, B) have been prepared and characerised by elemental analysis, magnetic susceptibility measurements, EPR, thermal and spectral (IR, UV/Vis) studies. EPR parameters and magnetic behaviour indicates that the complexes are antiferromagnetic in nature and most likely adopt the typical carboxylate cage structure. Interesting amide bonding patterns have been observed and various EPR parameters have been evaluated on the basis of these studies, tentative probable structures of the complexes have been proposed.

Synthesis and studies on metal coordination with a novel carboxyamide ligand

Novel complexes of Co(II), Ni(II), Cu(II) and Pd(II) with the new ligand [N,N′-bis(2-carboxy-1-oxo-phenelenyl)ethylenediamine] (H2L) have been synthesized and characterized on the basis of elemental analyses, magnetic susceptibility, thermal, infrared, electronic, 1H NMR and EPR spectral studies. Infrared and 1H NMR spectra show that H2L acts as a binegative tetradentate ligand. Coordination occurs through deprotonated carboxylate oxygens and nondeprotonated amido nitrogens in all the complexes. Electronic spectral studies and magnetic moment values suggest N2O2 coordination around each metal centre with strong field square planar chromophores. The probable structures of the complexes have been assigned on the basis of spectral studies. The complex formation between M(II) [M(II) = Mn(II), Co(II), Ni(II), Cu(II) and Zn(II)] and (L2-) has also been studied potentiometrically in 75% aqueous DMF at 25°C in 0.1 M NaClO4. The stability constants were found to follow the order: Mn(II) Zn(II).