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Merck

420352

Sigma-Aldrich

Ethylenediamine diacetate

98%

Sinónimos:

Ethanediammonium diacetate

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About This Item

Fórmula lineal:
NH2CH2CH2NH2 · 2CH3COOH
Número de CAS:
Peso molecular:
180.20
Beilstein/REAXYS Number:
5444394
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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assay

98%

mp

118-120 °C (lit.)

functional group

amine
carboxylic acid

SMILES string

CC(O)=O.CC(O)=O.NCCN

InChI

1S/C2H8N2.2C2H4O2/c3-1-2-4;2*1-2(3)4/h1-4H2;2*1H3,(H,3,4)

InChI key

SAXQBSJDTDGBHS-UHFFFAOYSA-N

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Application

  • Catalytic Synthesis: Utilization of Ethylenediamine Diacetate as an effective catalyst for synthesizing specific thioxothiazolidin-4-one, important for organic chemists and pharmacological studies aiming at new drug development (S Holota, A Lozynskyi, Y Konechnyi, Y Shepeta, 2021).
  • Reaction of New Amides: Exploration of reactions between new N-(2,2-Dichloro-1-cyanoethenyl)amides and aliphatic amines facilitated by Ethylenediamine Diacetate, relevant for medicinal chemistry and synthesis (OV Shablykin, SA Chumachenko, 2021).
  • Microwave-Assisted Organic Synthesis: Application of Ethylenediamine Diacetate in microwave-assisted synthesis processes, which is valuable for accelerating chemical reactions in drug synthesis and material processing (P Martín-Acosta, G Feresin, A Tapia, 2016).

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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    Ethylenediamine diacetate (EDDA)-catalyzed one-pot synthesis of tetrahydroquinolines by domino Knoevenagel/hetero Diels-Alder reactions from 1, 3-dicarbonyls.
    Lee YR and Hung TV.
    Tetrahedron, 67(49), 9627-9634 (2011)
    Euan Pyle et al.
    Cell chemical biology, 25(7), 840-848 (2018-04-24)
    The role of membrane lipids in modulating eukaryotic transporter assembly and function remains unclear. We investigated the effect of membrane lipids in the structure and transport activity of the purine transporter UapA from Aspergillus nidulans. We found that UapA exists
    Efficient and general method for the synthesis of benzopyrans by ethylenediamine diacetate-catalyzed reactions of resorcinols with α, β-unsaturated aldehydes. One step synthesis of biologically active (?)-confluentin and (?)-daurichromenic acid.
    Lee YR, et al.
    Tetrahedron Letters, 46(44), 7539-7543 (2005)
    Shima Shahsavari et al.
    International journal of radiation biology, 96(4), 502-509 (2019-12-13)
    Purpose: Early and accurate imaging of glioblastoma is of great value in staging, metastatic detection, treatment management and prognosis. The human epidermal growth factor receptor 2 (HER2) plays an essential role in the tumorigenesis and tumor progression in cancer. The
    Kusum Vats et al.
    Journal of labelled compounds & radiopharmaceuticals, 60(9), 431-438 (2017-05-26)
    Targeted delivery of chemotherapeutic drug at the tumor site enhances the efficacy with minimum systemic exposure. Towards this, drugs conjugated with peptides having affinity towards a particular molecular target are recognized as affective agents for targeted chemotherapy. Thus, in the

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