158186
Ethylenediamine-N,N′-diacetic acid
≥98%
Synonym(s):
EDDA, N,N′-Ethylenediglycine
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About This Item
Linear Formula:
HOOCCH2NHCH2CH2NHCH2COOH
CAS Number:
Molecular Weight:
176.17
Beilstein:
1778355
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
≥98%
mp
224 °C (dec.) (lit.)
SMILES string
OC(=O)CNCCNCC(O)=O
InChI
1S/C6H12N2O4/c9-5(10)3-7-1-2-8-4-6(11)12/h7-8H,1-4H2,(H,9,10)(H,11,12)
InChI key
IFQUWYZCAGRUJN-UHFFFAOYSA-N
Application
Ethylenediamine-N,N′-diacetic acid (EDDA) is a chelating agent that can be used to synthesize:
- Binary and ternary copper(II) complexes with potent proteasome inhibitory properties.
- Pd(EDDA) complexes which can coordinate with amino acids, peptides, or DNA units.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Zhiwen Yuan et al.
Biodegradation, 19(1), 41-52 (2007-04-04)
Ethylenediaminetetraacetic acid (EDTA) and nitrilotriacetic acid (NTA) are widely used anthropogenic chelating agents for control of metal speciation and are ubiquitous in natural waters and wastewaters. This is the first report of systematic measurement of the growth yields of a
Structural characterization, ROS-inductive and proteasome inhibitory properties of ternary and binary copper (II) complexes of N2- and N2O2-ligands.
Chan CW, et al.
Inorgorganica Chimica Acta, 450, 202-210 (2016)
Tomokazu Yoshimura et al.
Journal of colloid and interface science, 339(1), 230-235 (2009-08-18)
Three anionic homologues of a novel partially fluorinated carboxylate-type anionic gemini surfactant, N,N'-di(3-perfluoroalkyl-2-hydroxypropyl)-N,N'-diacetic acid ethylenediamine (2C(n)(F) edda, where n represents the number of carbon atoms in the fluorocarbon chain (4, 6, and 8)) were synthesized. In these present gemini surfactants
Katarina Norén et al.
Journal of colloid and interface science, 319(2), 416-428 (2007-12-25)
The adsorption of amino acids onto mineral surfaces plays an important role in a wide range of areas, e.g., low-temperature aqueous geochemistry, bone formation and protein-bone interactions. In this work, the adsorption of three alpha aminoacids (sarcosine, MIDA and EDDA)
Pornthep Sompornpisut et al.
Biophysical journal, 95(11), 5349-5361 (2008-08-05)
We present an approach for incorporating solvent accessibility data from electron paramagnetic resonance experiments in the structural refinement of membrane proteins through restrained molecular dynamics simulations. The restraints have been parameterized from oxygen (PiO(2)) and nickel-ethylenediaminediacetic acid (PiNiEdda) collision frequencies
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