58145-14-5

Usage

Uses

Used in Industrial Processes:
2-[bis(2-aminoethyl)amino]ethanol is used as a chelating agent for [its ability to sequester metal ions], which is crucial in various industrial processes to prevent metal-induced degradation and improve product quality.
Used in Detergent Production:
In the detergent industry, 2-[bis(2-aminoethyl)amino]ethanol is used as a chelating agent for [its capacity to bind metal ions], which helps to prevent the formation of insoluble metal salts that can reduce detergent effectiveness.
Used in Agrochemicals:
2-[bis(2-aminoethyl)amino]ethanol is utilized as a chelating agent in agrochemicals for [its ability to stabilize metal-containing active ingredients], thereby enhancing their performance and reducing environmental impact.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2-[bis(2-aminoethyl)amino]ethanol is used as a building block for [its role in the synthesis of complex molecules], contributing to the development of new drugs and therapeutic agents.
Used in Chemical Synthesis:
2-[bis(2-aminoethyl)amino]ethanol is employed as a versatile building block in chemical synthesis for [its structural properties that facilitate the creation of a wide range of complex molecules], finding applications in various chemical products and materials.

InChI:InChI=1/C6H17N3O/c7-1-3-9(4-2-8)5-6-10/h10H,1-8H2

Upstream product

• 75-21-8 oxirane 
• 2851-60-7 N,N'-bis(salicylidene)diethylenetriamine 
• 111-40-0 3-azapentane-1,5-diamine 

Downstream Products

• 1293980-12-7 C₂₅H₃₃N₃O₂ 
• 1293980-13-8 C₂₅H₃₁N₃O₂P⁽¹⁺⁾*Cl^(1-) 
• 1293980-14-9 C₂₅H₃₀N₃O₂P 
• 1293980-15-0 C₂₅H₃₀N₃O₃P 
• 1293980-16-1 C₃₅H₄₉N₃O₆ 
• 1293980-17-2 C₃₆H₅₁N₃O₈S 
• 1293980-18-3 C₃₃H₄₂N₄O 
• 1293980-20-7 C₃₃H₃₉N₄OP 

Relevant academic research and scientific papers

A mitochondria-targeting fluorescent Fe3+ probe and its application in labile Fe3+ monitoring via imaging and flow cytometry

The biogenesis of heme and iron-sulfur cluster in mitochondria is closely associated with the intracellular iron homeostasis. In this study, a mitochondria-targeting probe with the reversible turn-on fluorescent response to Fe3+ was developed for mitochondrial labile Fe3+ monitoring by modifying spirolactam rhodamine with a chelator. With this probe, the mitochondrial labile Fe3+ fluctuation in adherent cells upon ferric citrate incubation was visualzied via confocal imaging, and the flow cytometric assay for mitochondrial Fe3+ in suspension cells, which is difficult to be monitored via confocal imaging, was also developed. Moreover, the labile Fe3+ drop in mitochondria of K562 cells undergoing the DMSO-stimulated erythroid differentiation was observed for the first time.

Reversible FRET Fluorescent Probe for Ratiometric Tracking of Endogenous Fe3+in Ferroptosis

A reversible fluorescent probe DRhFe is devised by linking spirolactam rhodamine and dansylamide through an Fe3+ ionophore N2-hydroxyethyldiethylenetriamine, where Fe3+ chelation generating rhodamine B can switch intramolecular fluorescence resonance energy transfer for ratiometric Fe3+ sensing. Probe DRhFe exhibits an Fe3+-specific emission shift from 483 to 576 nm, and this ratiometric response has been successfully applied to monitor labile Fe3+ fluctuations in cells undergoing ferroptosis.

A turn-on fluorescent Fe3+ sensor derived from an anthracene-bearing bisdiene macrocycle and its intracellular imaging application

Integrating N2-hydroxyethyldiethylenetriamine with anthracene gives a [2+2] macrocycle fluorescent sensor. This sensor displays an instant/reversible turn-on response specific to Fe3+, which allows facile visualization of the Fe3+/Fe2+ transition and intracellular Fe3+ imaging. the Partner Organisations 2014.

First synthesis of P-chirogenic prophosphatranes

Syntheses are reported for the novel P-chirogenic bicyclic prophosphatranes P(RNCH2CH2)2N(OCH2CH2) - (8) in which the two R groups [i.e., 1-methylenenaphthyl and 1,2-methoxybenzyl (8)] and in its corresponding phosphine oxide (9) are different. Also synthesized was the transannulated protonated phosphatrane cation in the salt [HP(RNCH2CH2)3N]Cl in which the three R groups [i.e., 1-methylenenaphthyl, 1,2-methoxybenzyl, and (S)-1-phenethyl (14)] are different, and also in its corresponding deprotonated prophosphatrane form P(RNCH2CH2)3N (15). Good analytical resolution of racemic 9 is reported, whereas only partial resolution was achieved for diastereomeric 14.