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150-39-0

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  • China Biggest factory Supply High Quality N-(2-Hydroxyethyl)ethylenediaminetriacetic acid 150-39-0

    Cas No: 150-39-0

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150-39-0 Usage

Chemical Properties

Crystalline

Uses

Different sources of media describe the Uses of 150-39-0 differently. You can refer to the following data:
1. Chelating compound.
2. N-(2-Hydroxyethyl)ethylenediaminetriacetic acid is a chelating agent.

Purification Methods

Crystallise HEDTA from warm H2O, after filtering, by addition of 95% EtOH and allowing to cool. The crystals, collected on a sintered-glass funnel, are washed three times with cold absolute EtOH, then again crystallised from H2O. After leaching with cold H2O, the crystals are dried at 100o under vacuum. [Spedding et al. J Am Chem Soc 78 34 1956, Beilstein 4 IV 2449.]

Check Digit Verification of cas no

The CAS Registry Mumber 150-39-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,5 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 150-39:
(5*1)+(4*5)+(3*0)+(2*3)+(1*9)=40
40 % 10 = 0
So 150-39-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H18N2O7/c13-4-3-11(5-8(14)15)1-2-12(6-9(16)17)7-10(18)19/h13H,1-7H2,(H,14,15)(H,16,17)(H,18,19)/p-1

150-39-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Hydroxyethyl)Ethylenediaminetriacetic Acid

1.2 Other means of identification

Product number -
Other names 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:150-39-0 SDS

150-39-0Synthetic route

formaldehyd
50-00-0

formaldehyd

sodium cyanide
143-33-9

sodium cyanide

2-(2-Aminoethylamino)ethanol
111-41-1

2-(2-Aminoethylamino)ethanol

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Conditions
ConditionsYield
With sodium hydroxide
Fe(3+)*3ClO4(1-)*7H2O=[Fe(ClO4)3]*7H2O

Fe(3+)*3ClO4(1-)*7H2O=[Fe(ClO4)3]*7H2O

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

[Fe(III)(N-hydroxyethyl-ethylenediamine triacetate)(H2O)]

[Fe(III)(N-hydroxyethyl-ethylenediamine triacetate)(H2O)]

Conditions
ConditionsYield
In water a ligand (0.01 mol) was suspended in water; the Fe-contg. compd. (0.01 mol) was added with stirring; acetone was added; the crystals were pptd. overnighnt being placed in a refrigerator; elem. anal.;89%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

vanadium(III) chloride
7718-98-1

vanadium(III) chloride

sodium carbonate
497-19-8

sodium carbonate

{N'-(2-hydroxyethyl)ethylenediamine-N,N,N'-triacetato}aquavanadium(III)*2H2O

{N'-(2-hydroxyethyl)ethylenediamine-N,N,N'-triacetato}aquavanadium(III)*2H2O

Conditions
ConditionsYield
In water under N2; ligand in H2O neutralized with Na2CO3; anhydrous VCl3 added, soln. stirred for a few minutes; crystals collected, washed with cold water and acetone; elem. anal.;85%
malachite

malachite

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

[(N-(2-hydroxyethyl)-N'-carboxymethyl-1,2-ethylenediamine-N,N'-diacetato)copper(II) hydrate]
205673-75-2

[(N-(2-hydroxyethyl)-N'-carboxymethyl-1,2-ethylenediamine-N,N'-diacetato)copper(II) hydrate]

Conditions
ConditionsYield
In water byproducts: CO2, CuO; N-(2-hydroxyethyl)-1,2-ethylenediamine-N,N,N'-triacetic acid and Cu2CO3(OH)2 in water heated in a Kitasato-flask (t<50 °C), stirred at reduced pressure to remove CO2, then heated at 60 °C, stirred 30 min, cooled to room temp.; filtered, slow evapn. of solvent in 3-4 wk, crystn., filtered, washed with cold water, air-dried, recrystn. from hot water; elem. anal.;85%
samarium(III) carbonate

samarium(III) carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Sm(3+)*C10H15N2O7(3-)*5H2O=Sm(C10H15N2O7)*5H2O

Sm(3+)*C10H15N2O7(3-)*5H2O=Sm(C10H15N2O7)*5H2O

Conditions
ConditionsYield
With water In water in hot soln.; addn. of isopropanol with vigorous shaking then addn. of alcohol, washing (isopropanol), drying in air (24 h);80%
yttrium(III) carbonate

yttrium(III) carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Y(3+)*C10H15N2O7(3-)*6H2O=Y(C10H15N2O7)*6H2O

Y(3+)*C10H15N2O7(3-)*6H2O=Y(C10H15N2O7)*6H2O

Conditions
ConditionsYield
With water In water in hot soln.; addn. of isopropanol with vigorous shaking then addn. of alcohol, washing (isopropanol), drying in air (24 h);80%
neodymium carbonate

neodymium carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Nd(3+)*C10H15N2O7(3-)*6H2O=Nd(C10H15N2O7)*6H2O

Nd(3+)*C10H15N2O7(3-)*6H2O=Nd(C10H15N2O7)*6H2O

Conditions
ConditionsYield
With water In water in hot soln.; addn. of isopropanol with vigorous shaking then addn. of alcohol, washing (isopropanol), drying in air (24 h);80%
gadolinium(III) carbonate

gadolinium(III) carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Gd(3+)*C10H15N2O7(3-)*6H2O=Gd(C10H15N2O7)*6H2O

Gd(3+)*C10H15N2O7(3-)*6H2O=Gd(C10H15N2O7)*6H2O

Conditions
ConditionsYield
With water In water in hot soln.; addn. of isopropanol with vigorous shaking then addn. of alcohol, washing (isopropanol), drying in air (24 h);80%
europium(III) carbonate

europium(III) carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Eu(3+)*C10H15N2O7(3-)*5H2O=Eu(C10H15N2O7)*5H2O

Eu(3+)*C10H15N2O7(3-)*5H2O=Eu(C10H15N2O7)*5H2O

Conditions
ConditionsYield
With water In water in hot soln.; addn. of isopropanol with vigorous shaking then addn. of alcohol, washing (isopropanol), drying in air (24 h);80%
thorium(IV) nitrate pentahydrate

thorium(IV) nitrate pentahydrate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

sodium hydroxide
1310-73-2

sodium hydroxide

Th6(N-(2-hydroxoethyl)ethylenediaminetriacetate)

Th6(N-(2-hydroxoethyl)ethylenediaminetriacetate)

Conditions
ConditionsYield
In water for 48h; pH=8.4;72.1%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

water
7732-18-5

water

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

titanium tetrachloride
7550-45-0

titanium tetrachloride

(NH4)[Ti(O2)(N-(2-hydroxyethyl)ethylenediaminetriacetate)]·H2O

(NH4)[Ti(O2)(N-(2-hydroxyethyl)ethylenediaminetriacetate)]·H2O

Conditions
ConditionsYield
With ammonia at 20℃; for 48h; pH=2 - 5;65.2%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

water
7732-18-5

water

titanium tetrachloride
7550-45-0

titanium tetrachloride

[Ti((N-hydroxyethyl)ethylenediaminetriacetate)(H2O)]·2H2O

[Ti((N-hydroxyethyl)ethylenediaminetriacetate)(H2O)]·2H2O

Conditions
ConditionsYield
With ammonia at 20℃; for 72h; pH=3;55.9%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

4-Nitrophthalonitrile
31643-49-9

4-Nitrophthalonitrile

C18H20N4O7

C18H20N4O7

Conditions
ConditionsYield
With potassium carbonate In dimethyl sulfoxide at 50℃; for 48.25h; Inert atmosphere;55.45%
dysprosium(III) perchlorate

dysprosium(III) perchlorate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

water
7732-18-5

water

sodium hydroxide
1310-73-2

sodium hydroxide

{[Dy5(N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetate)4(H2O)10][Dy(H2O)7][Na(H2O)5]}(ClO4)7·(H2O)15

{[Dy5(N-(2-hydroxyethyl)ethylenediamine-N,N',N'-triacetate)4(H2O)10][Dy(H2O)7][Na(H2O)5]}(ClO4)7·(H2O)15

Conditions
ConditionsYield
at 80℃; for 1h; Reflux;50%
hafnium(IV) dichloride oxide octahydrate

hafnium(IV) dichloride oxide octahydrate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

HfHEDTA

HfHEDTA

Conditions
ConditionsYield
With hydrogenchloride In water for 3h; pH=5;45%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

4-(2-(2-oxomorpholin-4-yl)ethyl)piperazine-2,6-dione

4-(2-(2-oxomorpholin-4-yl)ethyl)piperazine-2,6-dione

Conditions
ConditionsYield
Stage #1: N-(2-hydroxyethyl)ethylenediaminetriacetic acid With formamide at 110℃; under 22.5023 Torr; for 1.5h;
Stage #2: at 150 - 160℃; for 5h; Inert atmosphere;
39%
potassium metavanadate

potassium metavanadate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

water
7732-18-5

water

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

K[VO(O2)(N-[2-(2-oxomorpholine-4-yl)ethyl]iminodiacetato(2-))]

K[VO(O2)(N-[2-(2-oxomorpholine-4-yl)ethyl]iminodiacetato(2-))]

Conditions
ConditionsYield
With KOH In ethanol; water ice-cooled aq. KVO3 soln. and H2O2 mixed, organic ligand added whilst stirring, pH adjusted to 3.0 with 2 M KOH, ethanol added dropwise, crystals formed in 2 weeks; washed with cooled ethanol, dried over silica gel at 5°C, elem. anal.;31.5%
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

1,2-diamino-benzene
95-54-5

1,2-diamino-benzene

N-(2-Hydroxyethyl)-N,N',N'-tris(2-benzylimidazolylmethyl)-1,2-diaminoethane tetrahydrochloride
123994-30-9

N-(2-Hydroxyethyl)-N,N',N'-tris(2-benzylimidazolylmethyl)-1,2-diaminoethane tetrahydrochloride

Conditions
ConditionsYield
With hydrogenchloride 1.) 175 deg C - 190 deg C, 70 min, 2.) 20 deg C, 24 h; Yield given. Multistep reaction;
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

N-(2-Hydroxyethyl)-N,N',N'-tris(2-benzylimidazolylmethyl)-1,2-diaminoethane
102651-58-1

N-(2-Hydroxyethyl)-N,N',N'-tris(2-benzylimidazolylmethyl)-1,2-diaminoethane

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 2.) conc. HCl / 1.) 175 deg C - 190 deg C, 70 min, 2.) 20 deg C, 24 h
2: 41 percent / conc. NH4OH
View Scheme
ruthenium(III) chloride trihydrate

ruthenium(III) chloride trihydrate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Na{Ru(hedta)(H2O)}*4H2O

Na{Ru(hedta)(H2O)}*4H2O

Conditions
ConditionsYield
With hydrogenchloride In ethanol RuCl3*3H2O reduced by refluxing in hot EtOH and HCl, addn. of N-(2-hydroxyethyl)ethylenediaminetriacetic acid; pretreated with a Zn/Hg reduction step (to reduce Ru(III));
europium(III) carbonate

europium(III) carbonate

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

europium(III) N-(2-hydroxyethyl)ethylenediaminetriacetate*2H2O
77461-02-0

europium(III) N-(2-hydroxyethyl)ethylenediaminetriacetate*2H2O

Conditions
ConditionsYield
In not given heating (30 min); filtration, pptn. (isopropanol), drying in air (24 h);
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

vanadyl
20644-97-7

vanadyl

oxo (N'-(2-hydroxy ethyl) ethylene diamine N,N,N' triacetato) vanadate (IV) (1-)
62560-22-9, 754942-28-4

oxo (N'-(2-hydroxy ethyl) ethylene diamine N,N,N' triacetato) vanadate (IV) (1-)

Conditions
ConditionsYield
In water reaction in an acidic solution;;
In water reaction in an acidic solution;;
N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

titanium(III)

titanium(III)

N-(2-hydroxyethyl)-ethylenediaminetriacetatoaquotitanium(III)
75431-40-2, 732977-43-4

N-(2-hydroxyethyl)-ethylenediaminetriacetatoaquotitanium(III)

Conditions
ConditionsYield
In further solvent(s) mixt. of excess of soln. of HEDTA in aq. LiCl and soln. of Ti(3+) in aq. LiCl;
dysprosium((III) oxide

dysprosium((III) oxide

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Dy(3+)*C10H15N2O7(3-)*8H2O=Dy(C10H15N2O7)*8H2O

Dy(3+)*C10H15N2O7(3-)*8H2O=Dy(C10H15N2O7)*8H2O

Conditions
ConditionsYield
With water In water
erbium(III) oxide

erbium(III) oxide

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Er(3+)*C10H15N2O7(3-)*6H2O=Er(C10H15N2O7)*6H2O

Er(3+)*C10H15N2O7(3-)*6H2O=Er(C10H15N2O7)*6H2O

Conditions
ConditionsYield
With water In water
europium(III) oxide

europium(III) oxide

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

Eu(3+)*C10H15N2O7(3-)*7H2O=Eu(C10H15N2O7)*7H2O

Eu(3+)*C10H15N2O7(3-)*7H2O=Eu(C10H15N2O7)*7H2O

Conditions
ConditionsYield
With water In water
gadolinium(III) oxide

gadolinium(III) oxide

N-(2-hydroxyethyl)ethylenediaminetriacetic acid
150-39-0

N-(2-hydroxyethyl)ethylenediaminetriacetic acid

gadolinium N-(2-hydroxyethyl)ethylenediaminetriacetic acid aquo complex

gadolinium N-(2-hydroxyethyl)ethylenediaminetriacetic acid aquo complex

Conditions
ConditionsYield
With water In water

150-39-0Downstream Products

150-39-0Related news

Reaction of Np(VI) with N-(2-Hydroxyethyl)ethylenediaminetriacetic acid in perchloric acid solutions09/29/2019

The stoichiometry of the reaction Np(VI) + H3hedta [hedta is N-(2-hydroxyethyl)ethylenediaminetriacetate, HEDTA, anion] in a 0.05 M HClO4 solution was studied by spectrophotometry. With Np(VI) in excess, 1 mol of HEDTA reduces 4 mol of Np(VI) to Np(V). In 0.125–1.0 M HClO4 solutions (the ionic ...detailed

Synthesis, properties, and crystal structure of the tin(IV) complex with N-(2-hydroxyethyl)ethylenediaminetriacetic acid [Sn(μ-Hedtra)(μ-OH)SnCl3(H2O)] · 3H2O09/28/2019

The binuclear tin(IV) complex with N-(2-hydroxyethyl)ethylenediamine-N,N′,N′-triacetic acid (H4Hedtra) is synthesized. The compound is characterized by elemental analysis, thermogravimetry, and IR spectroscopy. An X-ray diffraction analysis of complex Sn(μ-Hedtra)(μ-OH)SnCl3(H2O)] · 3H2O (I...detailed

150-39-0Relevant articles and documents

Imaging of Enzyme Activity

-

, (2008/06/13)

This invention relates to biochemistry and magnetic resonance imaging.

Polypeptide derivatives

-

, (2008/06/13)

A biologically active peptide selected from growth factors, peptide hormones, interferons and cytokines and analogues and derivatives thereof, and bearing at least one chelating group linked to an amino group of said peptide, the chelating group being capable of complexing a detectable element and such amino group having no significant binding affinity to target receptors, are complexed with a detectable element and are useful as a pharmaceutical, e.g. a radiopharmaceutical for in vivo imaging of target tissues or for therapy.

Manganese (II) chelate manufacture

-

, (2008/06/13)

The process of this invention for preparing Mn(II) chelate comprises forming the Mn(II) chelate by mixing manganese(II) oxide (insoluble) with an aqueous suspension comprising a molar equivalent or molar excess of the insoluble protonated chelating compound at a temperature of from 20° to 50° C. When the reaction is carried out with a protonated chelating agent in the absence of base, a precipitate of the protonated Mn(II) chelate is formed. A low osmolarity Mn(II) chelate solution can be formed from the precipitates by dissolving them in an aqueous solution of base. When the initial chelate forming reaction is carried out in a solution containing a molar equivalent or excess of sodium hydroxide, a low osmolarity solution of the Mn(II) chelate is directly formed with most chelating agents. Preferred chelating compounds for this process include DPDP, DTPA, DCTA, EDTP, DOTA, DOXA, DO3A and EDTA. The Mn(II) chelate precipitates and low osmolarity solutions formed by the above processes are also aspects of this invention.

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