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Structure of 4408-64-4
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N-Methyliminodiacetic acid features a methyl-substituted imino backbone that enhances solubility and metal-chelating efficiency. This derivative integrates readily into coordination complexes, offering improved stability in aqueous systems compared to unsubstituted analogs. The molecule’s polar carboxylate groups enable strong binding to transition metals, making it valuable for purification and catalytic applications.
N-Methyliminodiacetic acid serves as a versatile bifunctional building block in synthetic chemistry, enabling efficient chelation and coordination in metal complexation. Its methylated iminodiacetic framework provides enhanced lipophilicity and metabolic stability compared to parent analogs, facilitating applications in radiolabeling agents and pharmaceutical intermediates. The molecule exhibits robust bench stability, tolerates diverse reaction conditions, and simplifies purification due to its polar yet crystalline nature—ideal for use in peptide conjugation, macrocyclic ligand synthesis, and the construction of targeted therapeutics.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: