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ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE is a chemical compound derived from ethylenediamine and acetoacetic acid, characterized by its chelating and complexing properties. It is known for its ability to form stable complexes with metal ions, making it a versatile agent in various industrial applications. ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE is also utilized as a reagent in organic synthesis and as a stabilizer in polymers, while its corrosive and hazardous nature necessitates careful handling.

1471-94-9

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1471-94-9 Usage

Uses

Used in Pharmaceutical Industry:
ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE is used as a chelating agent for the stabilization of metal ions in pharmaceutical formulations, enhancing the efficacy and safety of certain drugs.
Used in Agriculture:
In the agricultural sector, ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE serves as a complexing agent, facilitating the absorption and distribution of essential nutrients and trace elements in fertilizers and plant growth regulators.
Used in Cosmetics Industry:
ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE is employed as a stabilizer in cosmetic products, improving the shelf life and performance of formulations by preventing the oxidation and degradation of active ingredients.
Used in Chemical Processes:
As a reagent in organic synthesis, ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE is utilized for the production of various chemical compounds, contributing to the development of new materials and substances with specific properties and applications.
Used in Polymer Industry:
ETHYLENEDIAMINE-N,N'-BIS-ACETOACETAMIDE functions as a stabilizer in polymers, enhancing their resistance to degradation and improving their overall performance in various applications, such as plastics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 1471-94-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 1 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1471-94:
(6*1)+(5*4)+(4*7)+(3*1)+(2*9)+(1*4)=79
79 % 10 = 9
So 1471-94-9 is a valid CAS Registry Number.

1471-94-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxo-N-[2-(3-oxobutanoylamino)ethyl]butanamide

1.2 Other means of identification

Product number -
Other names Ethylenediaminebisacetoacetamide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1471-94-9 SDS

1471-94-9Downstream Products

1471-94-9Relevant articles and documents

A facile synthesis of N,N′-oligomethylenebis(4,5-dihydrofuran-3- carboxamide)s using manganese(III)-based radical cyclization of N,N′-oligomethylenebis(3-oxobutanamide)s with 1,1-diarylethenes

Chowdhury, Firoz Alam,Nishino, Hiroshi

, p. 1337 - 1344 (2005)

The reaction of N,N′-oligomethylenebis(3-oxobutanamide)s with 1,1-diarylethenes in the presence of manganese(III) acetate in acetic acid at 100° produced N,N′-oligomethylenebis(2-methyl-5,5-diaryl-4,5- dihydrofuran-3-carboxamide)s. Similarly, the reaction of 3-oxobutanamidoethyl 3-oxobutanoate or N,N′-(3,6-dioxaoctamethylene)bis(3-oxobutanamide) with 1,1-diphenylethene gave (2-methyl-5,5-diphenyl-4,5-dihydrofuran-3-amido)ethyl 2-methyl-5,5-diphenyl-4,5-dihydrofuran-3-carboxylate or N,N′-(3,6-dioxa- octamethylene)bis(2-methyl-5,5-diphenyl-4,5-dihydrofuran-3-carboxamide) in moderate yields.

Synthesis of cool white light emitting novel dysprosium (Dy3+) complexes with tetradentate β-ketoamide and heterocyclic auxiliary ligands

Punia, Monika,Khatkar, Satyender Pal,Taxak, Vinod Bala,Dhankhar, Priyanka,Boora Doon, Priti

, p. 1209 - 1219 (2021)

To improve current multiphase white light emitting diodes (WLEDs), a novel series of five complexes consisting of one binary and four ternary complexes that emitted cool white light was successfully synthesized using a chelating tetradentate ligand and auxiliary ligands, i.e. 5,6-dimethyl-1,10-phenanthroline, 1,10-phenanthroline, 4,4′-dimethyl-2,2′-bipyridyl, and 2,2′-bipyridyl. The series was examined structurally using elemental analysis, Fourier transform infrared spectroscopy, energy dispersive X-ray analysis, ultraviolet–visible spectroscopy, and proton nuclear magnetic resonance spectroscopy. These complexes had the appropriate thermal stability required for the generation of white organic LEDs (WOLEDs). Dysprosium (III) (Dy3+) ion complexes demonstrated the characteristic emission peaks of blue colour at 482 nm and yellow colour at 572 nm, respectively, when excited using near ultraviolet light. Band gap, refractive index, and decay lifetime of the optimized samples were recorded as 2.68 eV, 2.12, and 1.601 ms, respectively. Correlated colour temperature value (7875 K), Commission International de l'Eclairage coordinates (0.300, 0.294), and colour purity (21.04 × 10?2) of the optimized complex were near to those of white illuminants as defined by the National Television System Committee. These complexes had promise as commercial LEDs for the advanced optoelectronics devices, especially as WOLEDs for illumination applications.

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