220000
Iminodiacetic acid
98%, for peptide synthesis
Sinônimo(s):
2,2′-Azanediyldiacetic acid, Diglycine, IMDA
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About This Item
Fórmula linear:
HN(CH2COOH)2
Número CAS:
Peso molecular:
133.10
Beilstein:
878499
Número CE:
Número MDL:
Código UNSPSC:
12352106
ID de substância PubChem:
NACRES:
NA.22
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Nome do produto
Iminodiacetic acid, 98%
Nível de qualidade
Ensaio
98%
Formulário
solid
pf
243 °C (dec.) (lit.)
aplicação(ões)
peptide synthesis
cadeia de caracteres SMILES
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)
chave InChI
NBZBKCUXIYYUSX-UHFFFAOYSA-N
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Descrição geral
Iminodiacetic acid is a versatile chelating agent widely used in metal extraction and waste water treatment.
Aplicação
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.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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)
Chromatographic separation of proteins on metal immobilized iminodiacetic acid-bound molded monolithic rods of macroporous poly (glycidyl methacrylate-co-ethylene dimethacrylate)
Luo Q, et al.
Journal of Chromatography A, 926(2), 255-264 (2001)
AGET ATRP of methyl methacrylate catalyzed by FeCl3/iminodiacetic acid in the presence of air
Zhang L, et al.
Polymer, 49(13-14), 3054-3059 (2008)
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)
Hong-Ming Yang et al.
Analytical biochemistry, 432(2), 134-138 (2012-10-03)
Highly efficient protein immobilization is extremely crucial for solid-phase immunoassays. We present a strategy for oriented immobilization of functionally intact immunoglobulin G (IgG) on a polystyrene microtiter plate via iminodiacetic acid (IDA)-Ni(2+) and ZZ-His protein interaction. We immobilized a ZZ-EAP
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 220000-500G | 4061838776174 |
| 220000-25G | 4061838776167 |
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