N-(2-Acetamido)iminodiacetic Acid丨CAS 26239-55-4

N-(2-Acetamido)iminodiacetic Acid丨CAS 26239-55-4
Product Introduction:
Catalog No.: SS118373
CAS No.: 26239-55-4
Assay: 99.0% to 101.0%
Product Name: N-(2-Acetamido)iminodiacetic acid
Molecular Formula: C6H10N2O5
Molecular Weight: 190.15
Synonym(s): N-(Carbamoylmethyl)iminodiacetic acid; N-(2-Amino-2-oxoethyl)-N-(carboxymethyl)-glycine; ADA
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Technical Parameters
Description

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Specifications

 

Appearance White crystalline powder
Assay 99.0% to 101.0%
Water Content 0.5% max
Loss on drying 1% max
Melt point 209 to 218℃
pH (0.01M H2O) 1.5 to 3.0
Solubility (9% in 1M NaOH) Colorless, clear
Heavy metal (Pb) 0.0005% max
Ultraviolet absorbance (300nm, 9% in 1M NaOH) 0.08 max
Ultraviolet absorbance (260nm, 0.05M in H2O heat) 0.20 max
Ultraviolet absorbance (280nm, 0.05M in H2O heat) 0.05 max
   

 

 


 

Applications

 

1. Chelating Agent

Functions similarly to other aminopolycarboxylic acids (like EDTA), forming stable complexes with metal ions such as Ca²⁺, Mg²⁺, Fe³⁺, and Cu²⁺.

Used in:

Metal ion sequestration in analytical and industrial chemistry

Water treatment to reduce hardness or remove trace metals

Soil and agriculture to enhance micronutrient availability

2. Medical and Diagnostic Use

Utilized as a chelating moiety in the synthesis of radiopharmaceutical agents, especially for:

Diagnostic imaging (e.g., MRI contrast agents)

Radiolabeled compounds in nuclear medicine

Offers improved biocompatibility and target specificity due to the presence of the acetamido group.

3. Analytical Chemistry

Employed in titration and complexometric analysis to determine metal concentrations in water, soil, food, and biological samples.

4. Pharmaceutical and Biochemical Research

May serve as a chelating scaffold or ligand in the development of:

Metal-dependent enzyme inhibitors

Drug delivery vehicles involving metal complexes

 

Benefits

 

1. Strong Metal Binding Capability

Coordinates with a broad range of metal ions, enhancing solubility, stability, and bioavailability of metal complexes.

2. Selective Chelation

The acetamido group introduces additional hydrogen bonding potential and electronic modulation, allowing more controlled binding in complex environments.

3. Improved Biocompatibility

The molecular structure offers low toxicity and enhanced biodegradability compared to some traditional chelators.

4. Versatile Reactivity

Amenable to derivatization and conjugation with other bioactive or functional molecules for custom applications in medical imaging or therapy.

5. Useful in Controlled Metal Delivery

Helps control the release of essential metal ions (like iron or zinc) in nutritional, pharmaceutical, or agronomic applications.

 

Conclusion

 

N-(2-Acetamido)iminodiacetic acid (CAS 26239-55-4) is a specialized chelating agent with applications in radiopharmaceuticals, diagnostics, environmental analysis, and metal ion management. Its ability to form stable, selective complexes, combined with its biocompatible structure, makes it a valuable alternative to conventional chelators like EDTA in both research and applied sciences.

 

 

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