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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

Quality Level

100

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)

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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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
Journal of the Chemical Society. Chemical Communications, 381-381 (1993)
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
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
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
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