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IMINODIACETIC ACID
Кат. №: 56781-250G
Производитель: Sigma-Aldrich
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IMINODIACETIC ACID
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Кат. №: 56781-250G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Main image
Печать
IMINODIACETIC ACID
Кат. №: 56781-250G
Производитель: Sigma-Aldrich
Кол-во:
Фасовка:
Цена по запросу
Товар оформляется под заказ
Description Application Iminodiacetic acid (IDA) can be used as a tridentate ligand to chelate metal ions.[1] Some of the common applications of IDA include: • Synthesis of N-methyliminodiacetic acid (MIDA), which is an essential precursor for the synthesis of highly versatile MIDA boronates for cross coupling reactions.[2] • Synthesis of metal complexes of iminodiacetic acid with a radionuclide, especially 99mTc are as radiotracers for cholescintigraphy scans and for radiopharmaceutical applications.[3][4] • Synthesis of lanthanide hybrid frameworks via self-assembly of lanthanide ions (Ln3+) with iminodiacetic acid under hydrothermal conditions.[5] • Preparation of a thermosensitive macroporous protein-imprinted hydrogel for the recognition of protein by metal coordinate interaction.[6] • Synthesis of IDA functionalized styrene-divinyl benzene co-polymeric beads for the removal of heavy metal ions like Cd(II), Cr(VI), Ni(II) and Pb(II) from their aqueous solutions.[7] Packaging 1 kg in poly bottle 50, 250 g in poly bottle
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Chemical Biology, Chemical Synthesis, Glycine Derivatives, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More... Quality Level
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Description Application Iminodiacetic acid (IDA) can be used as a tridentate ligand to chelate metal ions.[1] Some of the common applications of IDA include: • Synthesis of N-methyliminodiacetic acid (MIDA), which is an essential precursor for the synthesis of highly versatile MIDA boronates for cross coupling reactions.[2] • Synthesis of metal complexes of iminodiacetic acid with a radionuclide, especially 99mTc are as radiotracers for cholescintigraphy scans and for radiopharmaceutical applications.[3][4] • Synthesis of lanthanide hybrid frameworks via self-assembly of lanthanide ions (Ln3+) with iminodiacetic acid under hydrothermal conditions.[5] • Preparation of a thermosensitive macroporous protein-imprinted hydrogel for the recognition of protein by metal coordinate interaction.[6] • Synthesis of IDA functionalized styrene-divinyl benzene co-polymeric beads for the removal of heavy metal ions like Cd(II), Cr(VI), Ni(II) and Pb(II) from their aqueous solutions.[7] Packaging 1 kg in poly bottle 50, 250 g in poly bottle
Related Categories
Chemical Biology, Chemical Synthesis, Glycine Derivatives, Peptide Synthesis and Peptide Chemistry, Unnatural Amino Acids & Derivatives More... Quality Level
Дорогой клиент, на сайте внедрена нейросеть для сбора информации о товаре. Это может привести к незначительным расхождениям в характеристиках продукции.