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158135

Sigma-Aldrich

1,2-Diaminopropane-N,N,N′,N′-tetraacetic acid

≥98%

Synonym(s):

Propylenediamine-N,N,N′,N′-tetraacetic acid

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About This Item

Linear Formula:
(HO2CCH2)2NCH(CH3)CH2N(CH2CO2H)2
CAS Number:
4408-81-5
Molecular Weight:
306.27
Beilstein:
2223855
EC Number:
224-559-7
MDL number:
MFCD00004286
UNSPSC Code:
12352116
PubChem Substance ID:
24849720
NACRES:
NA.22

Assay

≥98%

form

powder

mp

241 °C (dec.) (lit.)

SMILES string

CC(CN(CC(O)=O)CC(O)=O)N(CC(O)=O)CC(O)=O

InChI

1S/C11H18N2O8/c1-7(13(5-10(18)19)6-11(20)21)2-12(3-8(14)15)4-9(16)17/h7H,2-6H2,1H3,(H,14,15)(H,16,17)(H,18,19)(H,20,21)

InChI key

XNCSCQSQSGDGES-UHFFFAOYSA-N

Application

Employed in organometallic ligation.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H319

Precautionary Statements

P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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S H Koenig et al.
Magnetic resonance in medicine, 2(2), 159-168 (1985-04-01)
Since contrast in magnetic resonance imaging (MRI) is so sensitive to the magnetic relaxation rates of tissue protons, the use of paramagnetic ions to alter contrast in a tissue-specific fashion is an alluring prospect. The influence of these ions on
Journal of the Chemical Society. Chemical Communications, 381-381 (1993)
T P Ryan et al.
Chemical research in toxicology, 3(4), 384-390 (1990-07-01)
ADR-529 [(+)-1,2-bis(3,5-dioxopiperazin-1-yl)propane], a nonpolar, cyclic analogue of EDTA, protects against anthracycline cardiotoxicity in vivo. The protective mechanism presumably involves chelation of iron by a hydrolysis product of ADR-529, thus preventing the formation of reactive iron/oxygen species which can damage membrane
Bin Liu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(5), 1115-1121 (2010-10-12)
The eight-coordinate (enH2)[YIII(pdta)(H2O)](2)·10H2O (en=ethylenediamine and H4pdta=1,3-propylenediamine-N,N,N',N'-tetraacetic acid) was synthesized, meanwhile its molecular and crystal structures were determined by single-crystal X-ray diffraction technology. The interaction between [Y(III)(pdta)(H2O)]2(2-) and bovine serum albumin (BSA) was investigated by UV-vis and fluorescence spectra. The results
Carsten K Schmidt et al.
Environmental pollution (Barking, Essex : 1987), 131(1), 107-124 (2004-06-24)
Aminopolycarboxylic acids, such as ethylenediaminetetraacetic acid (EDTA), nitrilotriacetic acid (NTA), diethylenetriaminepentaacetic acid (DTPA), 1,3-propylenediaminetetraacetic acid (1,3-PDTA), beta-alaninediacetic acid (beta-ADA), and methylglycinediacetic acid (MGDA), are used in large quantities in a broad range of industrial applications and domestic products in order
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