126736-75-2 Usage
Uses
Used in Chemical Industry:
PHENYLENEETHYLENETRIAMINE PENTAACETIC ACID is used as a precursor for bifunctional chelating agents for its ability to form stable complexes with metal ions, which is essential in various chemical processes and applications.
Used in Water Treatment:
PHENYLENEETHYLENETRIAMINE PENTAACETIC ACID is used as a chelating agent in water treatment processes to bind and remove metal ions, improving water quality and preventing issues related to metal contamination.
Used in Agriculture:
In agriculture, PHENYLENEETHYLENETRIAMINE PENTAACETIC ACID is used as a chelating agent to enhance the uptake of nutrients by plants, particularly micronutrients that are essential for plant growth and development.
Used in Pharmaceuticals:
PHENYLENEETHYLENETRIAMINE PENTAACETIC ACID is used as a chelating agent in the pharmaceutical industry to improve the solubility and stability of metal-containing drugs, as well as to facilitate drug delivery and enhance therapeutic efficacy.
Used in Environmental Remediation:
PHENYLENEETHYLENETRIAMINE PENTAACETIC ACID is employed in environmental remediation efforts to remove heavy metals from contaminated soil and water, mitigating the harmful effects of metal pollution on ecosystems and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 126736-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,7,3 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 126736-75:
(8*1)+(7*2)+(6*6)+(5*7)+(4*3)+(3*6)+(2*7)+(1*5)=142
142 % 10 = 2
So 126736-75-2 is a valid CAS Registry Number.
126736-75-2Relevant academic research and scientific papers
Gouin, Sebastien G.,Gestin, Jean-Francois,Monrandeau, Laurence,Segat-Dioury, Fabienne,Meslin, Jean Claude,Deniaud, David
, p. 454 - 461 (2005)
We wish to report the synthesis and metal complexation properties of new radionuclide chelating agents for use in nuclear medicine. The strategy includes the facile preparation of rigid analogues of DTPA and TTHA possessing an aromatic ring. The aromatic