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Diethylenetriaminepentaacetic acid, 99%

Catalog Number
ACM67436-3
Product Name
Diethylenetriaminepentaacetic acid, 99%
Structure
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CAS
67-43-6
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Synonyms
FT-0083201; Pentetic acid, United States Pharmacopeia (USP) Reference Standard; Detarex; Hamp-Ex Acid; NSC-759314; NCGC00261116-01; Diethylenetriaminepentaacetic acid. (Note-The sodium salts are named as follows: pentetate monosodium (1 Na ion); NSC759314; NSC7340; AN-DTPA;
IUPAC Name
2-[bis[2-[bis(carboxymethyl)amino]ethyl]amino]acetic acid;
Molecular Weight
393.349g/mol
Molecular Formula
C14H23N3O10;
Canonical SMILES
C(CN(CC(=O)O)CC(=O)O)N(CCN(CC(=O)O)CC(=O)O)CC(=O)O;
InChI
InChI=1S/C14H23N3O10/c18-10(19)5-15(1-3-16(6-11(20)21)7-12(22)23)2-4-17(8-13(24)25)9-14(26)27/h1-9H2,(H,18,19)(H,20,21)(H,22,23)(H,24,25)(H,26,27);
InChI Key
QPCDCPDFJACHGM-UHFFFAOYSA-N;
Storage
The activity of pentetic acid as a chelating agent may cause
unwanted effects in formulations containing metal ions. The desired
chelate may be displaced by other ions from the formulation.-20°C
Complexity
481
Covalently-Bonded Unit Count
1
EC Number
200-652-8
Exact Mass
393.138g/mol
H-Bond Acceptor
13
H-Bond Donor
5
Heavy Atom Count
27
Monoisotopic Mass
393.138g/mol
NSC Number
759314
Other Experimental
White crystalline solid. MP 230 deg C (decomposes). Slightly soluble in cold water; insoluble in hot water. /Diethylenetriamine pentaacetic acid/;MW: 393.35 /Diethylenetriamine pentaacetic acid/;
Rotatable Bond Count
16
Topological Polar Surface Area
196A^2
UNII
7A314HQM0I
Application
Diethylenetriaminepentaacetic acid, 99%, serves primarily as a chelating agent, binding with metal ions to form stable complexes. This characteristic enables its use in a variety of applications. In the medical field, it is utilized as a contrasting agent in magnetic resonance imaging (MRI), enhancing image clarity by forming a complex with gadolinium ions. Additionally, it assists in the treatment of radioactive materials, such as plutonium and americium. In the agricultural industry, it acts as a key ingredient in manganese and zinc fertilizers. The compound is also employed as a color inhibitor in acrylon production and functions as a water softener in soaps. Furthermore, it serves as a carrier excipient for neutron-capture isotopes in radiotherapy and has applications in scintigraphic imaging studies. It can also reduce the formation of reactive oxygen species during lyophilization. Despite its varied uses, Diethylenetriaminepentaacetic acid remains an essentially odorless, white crystalline solid. Visit our Titration Center to learn more about its broad applications.
January 23, 2025

Exceptional Chelating Agent for Research Applications

Diethylenetriaminepentaacetic acid, 99%, is outstanding for chelating metal ions in our research. We effectively used it in MRI imaging, enhancing contrast significantly. Its versatility in radiotherapy and agriculture is impressive, offering reliable and consistent results.

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