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11065-66-0

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11065-66-0 Usage

Description

[N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-) is a complex chemical compound that features a copper atom in a 3+ oxidation state. [N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-) is characterized by its unique coordination structure, where the copper ion is bonded to four nitrogen and six oxygen atoms derived from two glycine ligands. The ligands are attached to the copper atom through their carboxymethyl and amino groups, creating a stable coordination complex. [N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-) is of significant interest in the fields of chemical research and catalysis due to its distinctive structural properties and potential applications in synthetic and analytical chemistry.

Uses

Used in Chemical Research:
[N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-) is utilized as a catalyst in chemical research for its ability to facilitate various chemical reactions. Its unique coordination structure allows it to participate in a wide range of reactions, making it a valuable tool for chemists working on the development of new compounds and materials.
Used in Analytical Chemistry:
In analytical chemistry, [N,N-bis[2-[bis(carboxymethyl)amino]ethyl]glycinato(5-)]cuprate(3-) is employed as a reagent for the detection and analysis of specific substances. Its coordination properties enable it to selectively interact with certain compounds, making it a useful tool for identifying and quantifying these substances in complex mixtures.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, the compound's unique coordination structure and potential for use in synthetic chemistry suggest that it may also have applications in the pharmaceutical industry. It could potentially be used in the development of new drugs or as a component in drug delivery systems, taking advantage of its ability to form stable complexes with other molecules.
Used in Environmental Applications:
Similarly, while not explicitly stated in the materials, the compound's coordination properties could also make it useful in environmental applications, such as the removal of heavy metals from contaminated water or soil. Its ability to form stable complexes with metal ions could be harnessed to facilitate the cleanup of polluted environments.

Check Digit Verification of cas no

The CAS Registry Mumber 11065-66-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,1,0,6 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 11065-66:
(7*1)+(6*1)+(5*0)+(4*6)+(3*5)+(2*6)+(1*6)=70
70 % 10 = 0
So 11065-66-0 is a valid CAS Registry Number.

11065-66-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [copper(II)(diethylene triamine pentaacetate)](3-)

1.2 Other means of identification

Product number -
Other names [Cu(DTPA(-5H))](3-)

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:11065-66-0 SDS

11065-66-0Downstream Products

11065-66-0Relevant articles and documents

Synthesis and characterization of novel heterobinuclear mercury(II)-DTPA-M(II) complexes: Electrocatalytic and sensor applications

Mishra, Govind Krishna,Krishna, Vijay,Prakash, Rajiv

, p. 124 - 128 (2009/12/06)

Hg(II) metal complex is synthesized using octadentate ligand diethylene triamine penta acetic acid (DTPA) and the interaction of second metal ions viz. Cu(II), Pb(II), Mg(II) and Ca(II) is studied for the formation of novel heterobinuclear complexes. Hete

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