234877
亚氨二乙酸钠 二元 水合物
98%
别名:
亚氨基二乙酸 二钠盐 水合物
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关于此项目
线性分子式:
C4H5NO4Na2 · xH2O
化学文摘社编号:
分子量:
177.07 (anhydrous basis)
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
亚氨二乙酸钠 二元 水合物, 98%
InChI
1S/C4H7NO4.2Na.H2O/c6-3(7)1-5-2-4(8)9;;;/h5H,1-2H2,(H,6,7)(H,8,9);;;1H2/q;2*+1;/p-2
SMILES string
O.[Na+].[Na+].[O-]C(=O)CNCC([O-])=O
InChI key
YSBGCHXLMBAKPV-UHFFFAOYSA-L
assay
98%
form
solid
functional group
amine
Quality Level
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Application
Sodium iminodiacetate dibasic hydrate (Iminodiacetic acid disodium salt monohydrate) has been used in the preparation of:
- different iminodiacetic acid-agarose supports, useful for selective adsorption of large proteins
- N-(o-hydroxybenzyl) iminodiacetic acid (multidentante ligand)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
New multidentate ligands. XVII. Chelating tendencies of N-(o-hydroxybenzyl) iminodiacetic acid (H3L).
Harris WR, et al.
Inorganic Chemistry, 14(5), 974-978 (1975)
Benevides C C Pessela et al.
Journal of chromatography. A, 1055(1-2), 93-98 (2004-11-25)
A strategy to selectively adsorb large proteins on immobilized metal ion affinity chromatography supports is presented. It is based on the fact that large proteins have a large surface that permits the long distance interaction with groups placed quite far
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