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32319

Sigma-Aldrich

Diethylenetriaminepentaacetic acid

for complexometry, ≥99.0%

Synonym(s):

(Carboxymethylimino)bis(ethylenenitrilo)tetraacetic acid, N,N-Bis(2-[bis(carboxymethyl)amino]ethyl)glycine, DETAPAC, DTPA, Penta(carboxymethyl)diethylenetriamine, Pentetic acid

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About This Item

Linear Formula:
[(HOOCCH2)2NCH2CH2]2NCH2COOH
CAS Number:
Molecular Weight:
393.35
Beilstein:
1810219
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:
NACRES:
NA.21

grade

for complexometry

Assay

≥99.0% (KT)
≥99.0%

ign. residue

≤0.05% (as SO4)

loss

≤0.1% loss on drying, 20°C, HV

mp

219-220 °C (lit.)

anion traces

chloride (Cl-): ≤1000 mg/kg
sulfate (SO42-): ≤200 mg/kg

cation traces

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤10 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤500 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

SMILES string

OC(=O)CN(CCN(CC(O)=O)CC(O)=O)CCN(CC(O)=O)CC(O)=O

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

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General description

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Application

  • Grafting nanocellulose with diethylenetriaminepentaacetic acid: Development of a novel paper additive for enhancing recycled OCC pulp fibers by functionalizing nanocellulose with DTPA (Li et al., 2022).
  • Controlling multivalency and multimodality: Study on up to pentamodal dendritic platforms based on DTPA cores, illustrating DTPA′s role in multivalency and drug delivery systems (Pulido et al., 2014).
  • Adsorption of Hg (II) ions by DTPA-modified cellulose: Exploration of a DTPA-modified cellulose adsorbent for removing mercury ions from aqueous solutions (Li et al., 2019).
  • DTPA-functionalized multi-walled carbon nanotubes/titanium oxide-PVDF nanofiber membrane: Study on the effective separation of oil/water mixtures using a DTPA-functionalized membrane (Venkatesh et al., 2021).

Other Notes

Complexing agent for the chelation of iron in solution

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Repr. 1B - STOT RE 2 Inhalation

Target Organs

Respiratory Tract

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

392.0 °F - closed cup

Flash Point(C)

200 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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J.R. Bowyer
Febs Letters, 172, 239-239 (1984)
Sébastien Leguay et al.
Inorganic chemistry, 51(23), 12638-12649 (2012-11-17)
Complexation of trivalent actinides with DTPA (diethylenetriamine pentaacetic acid) was studied as a function of pcH and temperature in (Na,H)Cl medium of 0.1 M ionic strength. Formation constants of both complexes AnHDTPA(-) and AnDTPA(2-) (where An stands for Am, Cm
Janice S C Chew-Harris et al.
Annals of clinical biochemistry, 50(Pt 1), 39-46 (2012-11-07)
It is well known that plasma creatinine concentration is affected by muscle mass, while some studies have suggested cystatin C is affected by body mass index (BMI). Our aim was to assess the effects of lean versus fat mass on
Vincent Cutillas et al.
Antimicrobial agents and chemotherapy, 59(1), 310-316 (2014-10-29)
Clinical studies have shown that integrase strand transfer inhibitors (INSTIs) can be used effectively against HIV-1 infection. To date, no resistance substitution has been found in INSTI-naive patients treated with the new integrase inhibitor dolutegravir (DTG). In a recent selection
Yang Song et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(24), 9725-9730 (2009-06-06)
The reactions of glutathione (GSH) with polychlorinated biphenyl (PCB) quinones having different degrees of chlorination on the quinone ring were examined. EPR spectroscopy and MS revealed 2 types of reactions yielding different products: (i) a nonenzymatic, nucleophilic displacement of chlorine

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