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Usage

Uses

Used in Chemical Synthesis:
Glycine, N-(carboxymethyl)-N-2-(carboxymethyl)aminoethylis used as a building block in chemical synthesis for the production of various compounds and polymers. Its carboxymethyl groups allow for easy functionalization and modification, making it a valuable component in the synthesis of complex molecules.
Used in Pharmaceutical Industry:
Glycine, N-(carboxymethyl)-N-2-(carboxymethyl)aminoethylis used as a pharmaceutical intermediate for the development of drugs with potential therapeutic applications. Its unique structure and functional groups enable the design of novel drug candidates with improved pharmacological properties.
Used in Cosmetics Industry:
Glycine, N-(carboxymethyl)-N-2-(carboxymethyl)aminoethylis used as an active ingredient in cosmetic formulations for its moisturizing and conditioning properties. Its ability to form complexes with other molecules makes it suitable for use in hair and skin care products to improve their performance and efficacy.
Used in Environmental Applications:
Glycine, N-(carboxymethyl)-N-2-(carboxymethyl)aminoethylis used in environmental applications for its ability to chelate metal ions and remove pollutants from water and soil. Its chelating properties make it a promising candidate for use in wastewater treatment and soil remediation processes.
Used in Research and Development:
Glycine, N-(carboxymethyl)-N-2-(carboxymethyl)aminoethylis used as a research tool in various scientific fields, including biochemistry, materials science, and nanotechnology. Its unique structure and properties make it an interesting subject for study and potential applications in cutting-edge research.

InChI:InChI=1/C8H14N2O6/c11-6(12)3-9-1-2-10(4-7(13)14)5-8(15)16/h9H,1-5H2,(H,11,12)(H,13,14)(H,15,16)

Upstream product

• 717-28-2 2-oxo-1,4-piperazinediacetic acid 
• 60-00-4 ethylenediaminetetraacetic acid 
• 4685-14-7 Paraquat 
• 139-33-3 edetate disodium 

Relevant academic research and scientific papers

Facile and Selective Conversion of Ethylenediaminetetraacetate to Ethylenediamine-N,N,N'-triacetate on a Cobalt Complex

Ethylenediaminetetraacetatocobaltate(III) is converted to aqua(ethylenediamine-N,N,N'-triacetato)cobalt(III) selectively in a 1 mol dm-3 K2CO3 aqueous solution at room temperature in the presence of PbO2.This reaction could be a simple and versatile procedure to obtain ed3a-type ligands.

Efficient Photoreduction of Methylviologen Sensitized by Chlorophyll Derivatives and Hydrogen Evolution by Visible Light

The photoreduction of methylviologen sensitized by chlorophyll derivatives and porphines was investigated using EDTA as a reducing agent.The quantum yield of the photoreduction depends greatly on the kind of central metal ion of chlorophyll derivatives and porphines.Zn-chlorophyll-a and Zn-tetraphyenylporphine show a high quantum efficiency amounting 0.4, which is higher than that of chlorophyll-a.

The iron(III)-catalyzed oxidation of EDTA in aqueous solution

At temperatures above 100 deg C iron(III) oxidizes coordinated EDTA to ethylenediaminetriacetic acid in aqueous solution in the absence of molecular oxygen.The reaction proceeds with an activation energy of 28.6 kcal/mol, and its rate is directly proportional to the concentration of Fe(III) and inversely proportional to pH.At 125 deg C, the halflife of Fe(III) in the presence of excess EDTA is about 3 h at pH 9.3, but increases to >70 h at pH 5.4.The reaction is stoichiometric and no other reaction products or by-products were detected by nmr, gc, and gc - mass spectroscopy.In the presence of oxygen iron catalyzes quantitative oxidation of ethylenediamine-N,N,N',N'-tetraacetic acid (EDTA) to ethylenediaminetriacetic acid.The copper(II)-EDTA chelate undergoes a similar reaction but higher temperatures (>/=170 deg C) are required.Iron(III) also oxidizes nitrilotriacetic acid (NTA) to iminodiacetic acid (IDA) and glycine.The hydrolyzed species Fe(OH)EDTA is shown to be the reactive intermediate, and the well-known (Fe-EDTA)2O(4-) μ-oxo dimer is shown not to exist at elevated temperatures (above 100 deg C).Probable mechanisms are proposed for these reactions and comparisons are made with earlier work.