420352
Ethylenediamine diacetate
98%
Synonym(s):
Ethanediammonium diacetate
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About This Item
Linear Formula:
NH2CH2CH2NH2 · 2CH3COOH
CAS Number:
Molecular Weight:
180.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5444394
Assay:
98%
Quality Level
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
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
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)
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)
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