Conditions | Yield |
---|---|
In water | 95% |
trisodium nitrilotriacetate
Conditions | Yield |
---|---|
In water ligand salt added to a soln. of Re complex, stirred at 80°C for 2.5 h; evapd. (vac.), washed (CH2Cl2, CHCl3); elem. anal.; | 85.6% |
Conditions | Yield |
---|---|
In methanol; water to Cu-compd. in H2O Na-compd. and phenanthroline in H2O-CH3OH added, stirred, heated at reflux for 5 h, cooled to room temp.; filtered, stored for one week, elem. anal.; | 78% |
trisodium nitrilotriacetate
Conditions | Yield |
---|---|
In water aq. soln. of Na-salt (2 equiv.) added to aq. soln. of Cu-salt, aq. soln.of the rare-earth metal salt added dropwise, mixt. refluxed for 1 h; allowed to cool to room temp., soln. filtered, filtrate stored in desiccator over CaCl2 for 2 weeks; elem. anal.; | 65% |
Conditions | Yield |
---|---|
In methanol; water byproducts: CO; ligand salt added to a soln. of Re complex, stirred at 80°C for 19 h; chromd. (H2O, H2O/MeOH, MeOH), dried (N2), extd. (acetone), evapd. (vac.); elem. anal.; | 58.6% |
1,10-Phenanthroline
trisodium nitrilotriacetate
aqua(nitrilotriacetato)(1,10-phenanthroline)iron(III) monohydrate
Conditions | Yield |
---|---|
In methanol; water soln. 1,10-phenanthroline (1 mol) in MeOH added slowly to soln. FeCl3*6H2O (1 mol) in MeOH followed by aq. soln. sodium nitrilotriacetate (1 mol); slow evapn. at room temp. 3 wk; crystals filtered off; washed (H2O); dried in air; elem. anal.; | 25% |
trisodium nitrilotriacetate
Conditions | Yield |
---|---|
With triethanolamine |
trisodium nitrilotriacetate
copper hydroxide
Conditions | Yield |
---|---|
With H2O In water heating of an aq. soln. of Na3N(CH2COO)3 and an excess of Cu(OH)2;; filtration; concn. of filtrate; addn. of alc.;; |
trisodium nitrilotriacetate
diaqua(nitrilotriacetate)iron(III)
Conditions | Yield |
---|---|
In water reaction time: 20 min; pptn. washed with water, dried; elem. anal.; |
Conditions | Yield |
---|---|
With H2O2 In water |
Conditions | Yield |
---|---|
In perchloric acid La salt in aq. HClO4 mixed with aq. soln. of ligand (molar ratio 1:2, pH9.44); not isolated; detd. by (13)C NMR spectra; |
piperidine
3,5-Di-tert-butylcatechol
trisodium nitrilotriacetate
N,N-dimethyl-formamide
{piperidinium}2{Fe(N,N-bis(carboxymethyl)glycine)(3,5-di-tert-butylcatecholate)}*DMF
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide stoichiometric mixture of components, anaerobic conditions; elem. anal.; |
Conditions | Yield |
---|---|
With water In water reflux; filtration of hot soln.; crystn. by evapn.; washing (hot water); drying in air; | |
With water In water reflux; filtration of hot soln.; crystn. by evapn.; washing (hot water); drying in air; |
Conditions | Yield |
---|---|
With water In water reflux; filtration of hot soln.; crystn. by evapn.; washing (hot water); drying in air; | |
With water In water reflux; filtration of hot soln.; crystn. by evapn.; washing (hot water); drying in air; |
trisodium nitrilotriacetate
La(nitrilotriacetate(3-))
Conditions | Yield |
---|---|
In perchloric acid La salt in aq. HClO4 mixed with aq. soln. of ligand (molar ratio 1:1, pH3.66); not isolated; detd. by (13)C NMR spectra; |
trisodium nitrilotriacetate
Y(nitrilotriacetate(3-))
Conditions | Yield |
---|---|
In perchloric acid Y salt in aq. HClO4 mixed with aq. soln. of ligand (molar ratio 1:1, pH 9.32); not isolated; detd. by (13)C NMR spectra; |
water
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
B
Eu(ethylenediaminetetraacetate(4-))(nitrilotriacetate(3-))(4-)
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:1:2, pH 8.99); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
water
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
B
Eu(ethylenediaminetetraacetate(4-))(nitrilotriacetate(3-))(4-)
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:10:10, pH 7.40); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
water
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:1:20, pH 7.40); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
water
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:1:2, pH 7.03); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. soln. of ligand (molar ratio 1:1, pH3.60); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. soln. of ligand (molar ratio 1:50, pH 5.00-9.00); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
La(ethylenediaminetetraacetate(4-))(nitrilotriacetate(3-))(4-)
Conditions | Yield |
---|---|
In perchloric acid La salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:1:1, pH 9.64-11.12); not isolated; detd. by (13)C NMR spectra; |
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
Eu(ethylenediaminetetraacetate(4-))(nitrilotriacetate(3-))(4-)
Conditions | Yield |
---|---|
In perchloric acid Eu salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetate and nitrilotriacetate (molar ratio 1:1:2, pH 11.50 or molar ratio 1:1:20, pH 9.03-11.50 or molar ratio 1:10:10, pH 8.99-11.50); not isolated; detd. by time-resolved laser fluorescence spectroscopy andEXAFS spectra; |
trisodium nitrilotriacetate
ethylene diamine tetraacetic acid tetrasodium salt
Y(ethylenediaminetetraacetate(4-))(nitrilotriacetate(3-))(4-)
Conditions | Yield |
---|---|
In perchloric acid Y salt in aq. HClO4 mixed with aq. solns. of ethylenediaminetetraacetateand nitrilotriacetate (molar ratio 1:1:1, pH 9.60-11.12); not isolated; detd. by (13)C NMR spectra; |
trisodium nitrilotriacetate
Ga(N(CH2COO)3)(H2O)2=Ga(N(CH2COO)3)*2H2O
Conditions | Yield |
---|---|
In water mixing solns. of Ga-salt and org. compd., mixed soln. heating (water bath), pptn.; ppt. sepn., washing (water slightly acidified to pH 3 with nitric acid),drying to const. weight in thermostat at 50-60°C; elem. anal.; d erivatographic anal.; |
Conditions | Yield |
---|---|
In water In(ClO4)3 mixed with Na3N(CH2COO)3 (1:2); |
trisodium nitrilotriacetate
Conditions | Yield |
---|---|
In water |
trisodium nitrilotriacetate
Conditions | Yield |
---|---|
In water at 80℃; for 0.5h; |
MF: C6H6NNa3O6
MW: 257.08
EINECS: 225-768-6
Mol File: 5064-31-3.mol
CAS DataBase Reference: 5064-31-3(CAS DataBase Reference)
NIST Chemistry Reference: 5064-31-3(NIST)
Synonyms:NITRILOTRIACETIC ACID, TRI NA SALT;NITRILOTRIACETIC ACID TRISODIUM SALT;N,N-BIS[CARBOXYMETHYL]GLYCINE TRISODIUM SALT;NTA TRISODIUM SALT;TRIGLYCOLLAMIC ACID TRISODIUM SALT;TRISODIUM NITRILOTRIACETATE;cheeloxnta-14,-na3;chemcolox365powder
The structure of SODIUM NITRILOTRIACETATE(5064-31-3) is:
1. | or-rat:emb 495 µg/plate | JJATDK JAT, Journal of Applied Toxicology. 1 (1981),190. | ||
2. | orl-rat LD50:1100 mg/kg | TXAPA9 Toxicology and Applied Pharmacology. 18 (1971),398. | ||
3. | ipr-rat LD50:254 mg/kg | TXAPA9 Toxicology and Applied Pharmacology. 18 (1971),398. | ||
4. | orl-mus LD50:681 mg/kg | NCILB* Progress Report for Contract No. NIH-NCI-E-C-72-3252, Submitted to the National Cancer Institute by Litton Bionetics, Inc. (Bethesda, MD) NIH-NCI-E-C-72-3252 . | ||
5. | orl-mky LD50:750 mg/kg | TXAPA9 Toxicology and Applied Pharmacology. 18 (1971),398. |
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