All Photos(2)
Synonym(s):
2,2′-Azanediyldiacetic acid, Diglycine, IMDA
Linear Formula:
HN(CH2COOH)2
CAS Number:
Molecular Weight:
133.10
Beilstein/REAXYS Number:
878499
EC Number:
MDL number:
UNSPSC Code:
12352106
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
assay
98%
form
solid
mp
243 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
OC(=O)CNCC(O)=O
InChI
1S/C4H7NO4/c6-3(7)1-5-2-4(8)9/h5H,1-2H2,(H,6,7)(H,8,9)
InChI key
NBZBKCUXIYYUSX-UHFFFAOYSA-N
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General description
Iminodiacetic acid is a versatile chelating agent widely used in metal extraction and waste water treatment.
Application
Iminodiacetic acid can be used:
- In the preparation of iminodiacetic acid (IDA)-type adsorbent for protein purification.
- As a catalyst along with iron (FeCl3) complexes for methyl methacrylate (MMA) polymerization.
- In the preparation of chelating resins with glycidyl methacrylate for the selective removal and recovery of metal ions from industrial waste water.
- As a reagent for the preparation of pinene-derived iminodiacetic acid (PIDA), which is in turn used as a ligand for the synthesis of diastereoselective oxiranyl C(sp3) boronates from the corresponding olefins.
- In the surface functionalization of multi-walled carbon nanotubes (MWCNTs) which is further utilized as a sorbent for the separation of heavy metal ions.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis of chelating resins with iminodiacetic acid and its wastewater treatment application
Wang C-C, et al.
Journal of Applied Polymer Science, 84(7), 1353-1362 (2002)
Preparation of iminodiacetic acid functionalized multi-walled carbon nanotubes and its application as sorbent for separation and preconcentration of heavy metal ions
Wang J, et al.
Journal of Hazardous Materials, 186(2-3), 1985-1992 (2011)
Iminodiacetic acid modified kenaf fiber for waste water treatment
Razak MA, et al.
International Journal of Biological Macromolecules, 112, 754-760 (2018)
Áine Moyna et al.
Journal of chromatography. A, 1249, 155-163 (2012-07-06)
Capillary housed laurylmethacrylate-co-ethylene dimethacrylate (LMA-co-EDMA) polymer monoliths were fabricated, functionalised with varying amounts of vinyl azlactone, followed by immobilisation of iminodiacetic acid (IDA), forming a range of acetyl-iminodiacetic acid (AIDA) functionalised monoliths, applied to the chelation ion chromatographic separation of
Zeina Mehyou et al.
Talanta, 87, 168-173 (2011-11-22)
A simple protocol to obtain Cu(II)-IDA (iminodiacetic acid)-modified capillaries was developed for immobilized metal ion affinity chromatography (IMAC). It consisted in the synthesis of IDA-silane used for a one-step coating of fused silica capillaries. The approach prevented the hydrolysis of
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