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Atomfair N-Methyliminodiacetic acid MIDA C5H9NO4
Description N-Methyliminodiacetic Acid (CAS 4408-64-4) is a high-purity organic compound with the molecular formula C5H9NO4. This white crystalline solid is widely utilized as a versatile chelating agent and intermediate in organic synthesis, pharmaceutical research, and coordination chemistry. With an IUPAC name of 2-[carboxymethyl(methyl)amino]acetic acid , it features both carboxylic acid and tertiary amine functional groups, enabling strong metal ion binding capabilities. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied with comprehensive analytical documentation including1H NMR and FTIR spectra. Suitable for use in buffer preparation, catalyst systems, and as a precursor for specialty chemicals. Packaged under…
Description
Description
N-Methyliminodiacetic Acid (CAS 4408-64-4) is a high-purity organic compound with the molecular formula C5H9NO4. This white crystalline solid is widely utilized as a versatile chelating agent and intermediate in organic synthesis, pharmaceutical research, and coordination chemistry. With an IUPAC name of 2-[carboxymethyl(methyl)amino]acetic acid, it features both carboxylic acid and tertiary amine functional groups, enabling strong metal ion binding capabilities. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied with comprehensive analytical documentation including 1H NMR and FTIR spectra. Suitable for use in buffer preparation, catalyst systems, and as a precursor for specialty chemicals. Packaged under inert atmosphere in amber glass bottles to ensure stability.
- CAS No: 4408-64-4
- Molecular Formula: C5H9NO4
- Molecular Weight: 147.13
- Exact Mass: 147.05315777
- Monoisotopic Mass: 147.05315777
- IUPAC Name: 2-[carboxymethyl(methyl)amino]acetic acid
- SMILES: CN(CC(=O)O)CC(=O)O
- Synonyms: N-METHYLIMINODIACETIC ACID, 4408-64-4, Methyliminodiacetic acid, Glycine, N-(carboxymethyl)-N-methyl-, SH1YP5H4NA
Application
N-Methyliminodiacetic acid serves as a key building block in pharmaceutical synthesis, particularly for ??-lactam antibiotics. Its chelating properties make it valuable in metal ion sequestration applications and as a ligand in homogeneous catalysis. Researchers employ this compound in the development of novel coordination complexes for catalytic systems and as a buffer component in biochemical studies.
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