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Diethylenetriaminepentaacetic acid, also known as DTPA, is a synthetic chelating agent characterized by its ability to form stable complexes with metal ions. It is a versatile compound with a wide range of applications across various industries due to its unique properties.

67-43-6

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67-43-6 Hazards Identification

Pictogram(s):

Signal:

Danger

GHS Hazard Statements:

H319: Causes serious eye irritation [Warning Serious eye damage/eye irritation]
H332: Harmful if inhaled [Warning Acute toxicity, inhalation]
H360D: May damage the unborn child [Danger Reproductive toxicity]
H373: Causes damage to organs through prolonged or repeated exposure [Warning Specific target organ toxicity, repeated exposure]

Precautionary Statement Codes:

P203, P260, P261, P264+P265, P271, P280, P304+P340, P305+P351+P338, P317, P318, P319, P337+P317, P405, and P501

Hazard Classes and Categories:

Repr. 1B
Acute Tox. 4
STOT RE 2
Eye Irrit. 2
Eye Irrit. 2 (100%)
Acute Tox. 4 (63.03%)
Repr. 2 (77.06%)
STOT RE 2 (39.2%)

Hazards Summary:

The calcium salt causes fetal death and teratogenic effects in mice (thought to be associated with the chelation of essential divalent cations such as zinc); [REPROTOX] Causes convulsions and chronic pulmonary edema in intraperitoneal lethal-dose studies of rats (LD50 = 587 mg/kg); [RTECS] An eye irritant; [Acros Organics MSDS] See Edetic acid.

67-43-6 Usage

Uses

Used in Medical Imaging:
Diethylenetriaminepentaacetic acid is used as a chelating agent and serves as a magnetic resonance imaging (MRI) contrasting agent. It enhances the quality of MRI images by forming a complex with a gadolinium ion, which aids in visualizing internal structures more clearly.
Used in Environmental Remediation:
DTPA is employed for the treatment of radioactive materials, such as plutonium, americium, and other actinides. Its chelating properties enable it to bind with these radioactive elements, facilitating their safe disposal and containment.
Used in Agrochemical Industry:
Diethylenetriaminepentaacetic acid is an active component of manganese and zinc fertilizers used in the agrochemical industry. It helps improve the uptake of these essential nutrients by plants, promoting healthy growth and crop yields.
Used in Chemical Production:
DTPA acts as a color inhibitor and is utilized in the production of acrylon, a key component in the synthesis of various polymers and resins.
Used in Personal Care Products:
Diethylenetriaminepentaacetic acid is also used in soaps and other personal care products as a water softener. Its chelating properties help to prevent the formation of soap scum and improve the overall performance of these products.

Production Methods

Pentetic acid is a pentaacetic acid triamine formed during the preparation of the amino carboxylic acid and its salt.

Pharmaceutical Applications

Pentetic acid is mainly used as a chelating agent in the preparation of imaging and contrast agents for radionuclide and magnetic resonance imaging.It is also used as a carrier excipient for neutron-capture isotopes in, for example, radiotherapy.Pentetic acid–isotope complexes have also been considered as model active substances in scintigraphic imaging studies.Pentetic acid has been used to chelate metal ions to reduce formation of reactive oxygen species during lyophilization.

Safety Profile

Moderately toxic by intraperitoneal route. When heated to decomposition it emits toxic fumes of NOx.

Safety

Pentetic acid is used in intrathecal and intravenous injection preparations. The pure form of pentetic acid is moderately toxic by the intraperitoneal route. LD50 (mouse, IP): 0.54 g/kg LD50 (mouse, oral): 4.84 g/kg

storage

The activity of pentetic acid as a chelating agent may cause unwanted effects in formulations containing metal ions. The desired chelate may be displaced by other ions from the formulation.

Purification Methods

Crystallise DTPA from water. Dry under vacuum or at 110o. [Bielski & Thomas J Am Chem Soc 109 7761 1987, NMR: Wenzel et al. Anal Chem 54 615 1982, Beilstein 4 IV 2454.]

Incompatibilities

The activity of pentetic acid as a chelating agent may cause unwanted effects in formulations containing metal ions. The desired chelate may be displaced by other ions from the formulation.

Regulatory Status

Included in the FDA Inactive Ingredients Database (intrathecal and intravenous injections). Included in intravenous and intra-articular injections licensed in the UK.

Check Digit Verification of cas no

The CAS Registry Mumber 67-43-6 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 6 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 67-43:
(4*6)+(3*7)+(2*4)+(1*3)=56
56 % 10 = 6
So 67-43-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H13N3.5C2H4O2/c5-1-3-7-4-2-6;5*1-2(3)4/h7H,1-6H2;5*1H3,(H,3,4)

67-43-6 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (D0504)  Diethylenetriaminepentaacetic Acid  >98.0%(T)

  • 67-43-6

  • 25g

  • 111.00CNY

  • Detail
  • TCI America

  • (D0504)  Diethylenetriaminepentaacetic Acid  >98.0%(T)

  • 67-43-6

  • 500g

  • 467.00CNY

  • Detail
  • Alfa Aesar

  • (A10926)  Diethylenetriaminepentaacetic acid, 98+%   

  • 67-43-6

  • 50g

  • 238.0CNY

  • Detail
  • Alfa Aesar

  • (A10926)  Diethylenetriaminepentaacetic acid, 98+%   

  • 67-43-6

  • 250g

  • 383.0CNY

  • Detail
  • Alfa Aesar

  • (A10926)  Diethylenetriaminepentaacetic acid, 98+%   

  • 67-43-6

  • 1000g

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (A10926)  Diethylenetriaminepentaacetic acid, 98+%   

  • 67-43-6

  • 5000g

  • 3101.0CNY

  • Detail
  • Alfa Aesar

  • (31418)  Diethylenetriaminepentaacetic acid, 98%   

  • 67-43-6

  • 50g

  • 222.0CNY

  • Detail
  • Alfa Aesar

  • (31418)  Diethylenetriaminepentaacetic acid, 98%   

  • 67-43-6

  • 1kg

  • 1015.0CNY

  • Detail
  • Sigma

  • (32319)  Diethylenetriaminepentaaceticacid  for complexometry, ≥99.0%

  • 67-43-6

  • 32319-100G-F

  • 620.10CNY

  • Detail
  • USP

  • (1505506)  Penteticacid  United States Pharmacopeia (USP) Reference Standard

  • 67-43-6

  • 1505506-100MG

  • 4,662.45CNY

  • Detail

67-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name pentetic acid

1.2 Other means of identification

Product number -
Other names 9-Propylamino-phenanthren

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Ion exchange agents,Processing aids, not otherwise listed,Processing aids, specific to petroleum production,Surface active agents
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:67-43-6 SDS

67-43-6Synthetic route

formaldehyd
50-00-0

formaldehyd

sodium cyanide
143-33-9

sodium cyanide

1,5-diamino-3-azapentane
111-40-0

1,5-diamino-3-azapentane

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

Conditions
ConditionsYield
With aqueous alkali
diethylenetriaminepentaacetic acid, Ga(III)-salt, dianion
119088-94-7

diethylenetriaminepentaacetic acid, Ga(III)-salt, dianion

2-(HO)-5-(SO3H)C6H3CHNC2H4NHC2H4NHC2H4NCHC6H3-2-(OH)-5-(SO3H)
139701-37-4

2-(HO)-5-(SO3H)C6H3CHNC2H4NHC2H4NHC2H4NCHC6H3-2-(OH)-5-(SO3H)

Ga(N(CHC6H3-2-O-5-SO3))CH2NHC2H4NHC2H4NCH(C6H3-2-O-5-SO3)

Ga(N(CHC6H3-2-O-5-SO3))CH2NHC2H4NHC2H4NCH(C6H3-2-O-5-SO3)

B

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

Conditions
ConditionsYield
In water-d2 competition was followed by H-NMR spectroscopy, at 25 ° C;; aq. soln. of known pH evapd. to dryness, residue dissolved in equal amt. of D2O, left until equilibrium was reached (5 weeks);
diethylenetriaminepentaacetic acid, Ga(III)-salt, dianion
119088-94-7

diethylenetriaminepentaacetic acid, Ga(III)-salt, dianion

(CH3)C(CH2NCHC6H3(SO3)(O))3(6-)

(CH3)C(CH2NCHC6H3(SO3)(O))3(6-)

A

{Ga(saltames)}(3-)

{Ga(saltames)}(3-)

B

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

Conditions
ConditionsYield
In water-d2 competition reaction followed by H-NMR spectroscopy, at 25 ° C at pH 7.5; aq. soln. of known pH evapd. to dryness in vacuo, residue dissolved in equal volume of D2O, and left until equilibrium left (12 weeks);;
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

diethylenetriaminepentaacetic dianhydride
23911-26-4

diethylenetriaminepentaacetic dianhydride

Conditions
ConditionsYield
With pyridine; acetic anhydride at 80℃; for 24h;99%
With pyridine; acetic anhydride at 65℃; for 3h;97%
With pyridine; acetic anhydride In acetonitrile at 60℃; for 4h; Solvent; Temperature; Large scale;97%
uranyl nirate hexahydrate

uranyl nirate hexahydrate

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

UO2(diethylenetriaminepentaacetate) * H2O

UO2(diethylenetriaminepentaacetate) * H2O

Conditions
ConditionsYield
In water equimolar amts., pH=2-4 (pptn.); elem. anal.;99%
gadolinium(III) oxide

gadolinium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

1-deoxy-1-(methylamino)-D-glucitol
6284-40-8

1-deoxy-1-(methylamino)-D-glucitol

gadopentate dimeglumine

gadopentate dimeglumine

Conditions
ConditionsYield
Stage #1: diethylenetriaminopentaacetic acid; 1-deoxy-1-(methylamino)-D-glucitol In water for 0.0333333h; Sonication; Green chemistry;
Stage #2: gadolinium(III) oxide In water for 0.3h; Sonication; Green chemistry;
98%
methanol
67-56-1

methanol

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

methyl 5,8,11,-tris(2-methoxy-2-oxoethyl)-3-oxo-2-oxa-5,8,11-triazatridecan-13-oate
96121-82-3

methyl 5,8,11,-tris(2-methoxy-2-oxoethyl)-3-oxo-2-oxa-5,8,11-triazatridecan-13-oate

Conditions
ConditionsYield
With thionyl chloride In methanol for 4h; Heating;95%
With thionyl chloride for 16h;84%
3-azidopropylamine
88192-19-2

3-azidopropylamine

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C20H35N11O8

C20H35N11O8

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere;95%
ethanol
64-17-5

ethanol

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

pentaethyl diethylenetriamine-N,N,N',N'',N''-pentaacetate
51992-77-9

pentaethyl diethylenetriamine-N,N,N',N'',N''-pentaacetate

Conditions
ConditionsYield
Stage #1: ethanol; diethylenetriaminopentaacetic acid; sulfuric acid for 24h; Heating / reflux;
Stage #2: With sodium hydrogencarbonate In ethanol; water
91%
With sulfonic acid Heating;79%
With sulfuric acid for 20h; Esterification; Heating;78%
With sulfuric acid for 20h; Reflux; Inert atmosphere;76%
With hydrogenchloride at 20 - 78℃; for 48h; Large scale;20 kg
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

copper-diethylenetriaminepentaacetic acid complex
142198-25-2, 55187-64-9, 1118093-19-8

copper-diethylenetriaminepentaacetic acid complex

Conditions
ConditionsYield
With copper(II) carbonate In water for 18h;90%
3K(1+)*{IrCl6}(3-)*3H2O=K3{IrCl6}*3H2O

3K(1+)*{IrCl6}(3-)*3H2O=K3{IrCl6}*3H2O

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

iridium(III) pentachloro(diethylenetriaminepenta-acetate) pentahydrate

iridium(III) pentachloro(diethylenetriaminepenta-acetate) pentahydrate

Conditions
ConditionsYield
In water boiled for 3-4 h; cooled, filtered off, filtrate evapd., treated with ethanol; elem. anal.;90%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

1-aminooctadecane
124-30-1

1-aminooctadecane

1,11-bis(octadecylamino)-1,11-dioxo-6-aza-3,6,9-tris(carboxymethyl)undecane
135546-68-8

1,11-bis(octadecylamino)-1,11-dioxo-6-aza-3,6,9-tris(carboxymethyl)undecane

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 50℃;90%
nickel(II) dichloride hydrate

nickel(II) dichloride hydrate

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

[Ni2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*6H2O

[Ni2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*6H2O

Conditions
ConditionsYield
With Na2CO3 In water aq. soln. of pentacarboxylic acid treated with Na2CO3; aq. soln. of metal salt added dropwise at room temp. with stirring; mixt. stirred for 12 h; soln. slowly concd. on steam bath; added dropwise into acetone; ppt. filtered off; washed with acetone; dried under vac.; recrystd.; elem. anal.;89%
europium(III) oxide

europium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

water
7732-18-5

water

cadmium(II) acetate dihydrate
5743-04-4

cadmium(II) acetate dihydrate

[Eu2Cd2(diethylenetriaminepentaacetic acid)2(H2O)4](H2O)4

[Eu2Cd2(diethylenetriaminepentaacetic acid)2(H2O)4](H2O)4

Conditions
ConditionsYield
at 170℃; for 168h; Autoclave;88%
3K(1+)*{IrCl6}(3-)*3H2O=K3{IrCl6}*3H2O

3K(1+)*{IrCl6}(3-)*3H2O=K3{IrCl6}*3H2O

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

iridium(III) trichloro(diethylenetriaminepenta-acetate) trihydrate

iridium(III) trichloro(diethylenetriaminepenta-acetate) trihydrate

Conditions
ConditionsYield
In water heated under N2 in an autoclave at a pressure of 20 atm and 150°C for 6 h; cooled, filtered off, filtrate evapd., treated with ethanol; elem. anal.;86%
copper(II) chloride hydrate

copper(II) chloride hydrate

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

[Cu2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

[Cu2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

Conditions
ConditionsYield
With Na2CO3 In water aq. soln. of pentacarboxylic acid treated with Na2CO3; aq. soln. of metal salt added dropwise at room temp. with stirring; mixt. stirred for 12 h; soln. slowly concd. on steam bath; added dropwise into acetone; ppt. filtered off; washed with acetone; dried under vac.; recrystd.; elem. anal.;86%
chromium dichloride

chromium dichloride

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

[Cr2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

[Cr2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

Conditions
ConditionsYield
With Na2CO3 In water aq. soln. of pentacarboxylic acid treated with Na2CO3; aq. soln. of metal salt added dropwise at room temp. with stirring; mixt. stirred for 12 h; soln. slowly concd. on steam bath; added dropwise into acetone; ppt. filtered off; washed with acetone; dried under vac.; recrystd.; elem. anal.;85%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

N-[2-(2,6-dioxo-4-morpholinyl)ethyl]-N-[3-(2,6-dioxo-4-morpholinyl)propyl]
127902-41-4

N-[2-(2,6-dioxo-4-morpholinyl)ethyl]-N-[3-(2,6-dioxo-4-morpholinyl)propyl]

Conditions
ConditionsYield
With pyridine; acetic anhydride at 60℃; for 24h; Inert atmosphere;85%
gadolinium(III) oxide

gadolinium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

2Na(1+)*Gd(3+)*N(CH2COO)(CH2CH2N(CH2COO)2)2(5-)*H2O*7H2O=Na2{GdN(CH2COO)(CH2CH2N(CH2COO)2)2*H2O}*7H2O

2Na(1+)*Gd(3+)*N(CH2COO)(CH2CH2N(CH2COO)2)2(5-)*H2O*7H2O=Na2{GdN(CH2COO)(CH2CH2N(CH2COO)2)2*H2O}*7H2O

Conditions
ConditionsYield
In water Gd2O3 and diethylenetriaminepentaacetic acid soln. was stirred at 368 K for 6,5 h, NaOH was slowly added at room temp. to pH 7 with stirring; after filtration mixt. was concd. in vac. and pptd. with acetone; recrystn. from hot H2O/acetone; elem. anal.;84%
morpholine
110-91-8

morpholine

gadolinium(III) oxide

gadolinium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

gadopentate dimorpholine

gadopentate dimorpholine

Conditions
ConditionsYield
Stage #1: morpholine; diethylenetriaminopentaacetic acid In water for 0.0333333h; Sonication; Green chemistry;
Stage #2: gadolinium(III) oxide In water for 0.3h; Sonication; Green chemistry;
84%
cobalt(II) chloride hydrate

cobalt(II) chloride hydrate

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

[Co2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*11H2O

[Co2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*11H2O

Conditions
ConditionsYield
With Na2CO3 In water aq. soln. of pentacarboxylic acid treated with Na2CO3; aq. soln. of metal salt added dropwise at room temp. with stirring; mixt. stirred for 12 h; soln. slowly concd. on steam bath; added dropwise into acetone; ppt. filtered off; washed with acetone; dried under vac.; recrystd.; elem. anal.;83%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

acetic anhydride
108-24-7

acetic anhydride

diethylenetriaminepentaacetic dianhydride
23911-26-4

diethylenetriaminepentaacetic dianhydride

Conditions
ConditionsYield
With pyridine at 65℃; for 24h;83%
In pyridine at 80℃;
With pyridine at 65℃; for 24h;
With pyridine In pyridine at 65℃; for 24h;
manganese(II) chloride hydrate

manganese(II) chloride hydrate

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

[Mn2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

[Mn2(diethylenetriaminepentaacetic acid(-2H))(H2O)6]Cl2*10H2O

Conditions
ConditionsYield
With Na2CO3 In water aq. soln. of pentacarboxylic acid treated with Na2CO3; aq. soln. of metal salt added dropwise at room temp. with stirring; mixt. stirred for 12 h; soln. slowly concd. on steam bath; added dropwise into acetone; ppt. filtered off; washed with acetone; dried under vac.; recrystd.; elem. anal.;82%
holmium(III) oxide

holmium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

water
7732-18-5

water

methylamine
74-89-5

methylamine

C28H36Ho2N6O20(4-)*4CH5N*4H(1+)*12H2O

C28H36Ho2N6O20(4-)*4CH5N*4H(1+)*12H2O

Conditions
ConditionsYield
Stage #1: holmium(III) oxide; diethylenetriaminopentaacetic acid In water for 15h; Reflux;
Stage #2: water; methylamine pH=6;
78.96%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C11(13)CH13NO4
1271786-89-0

C11(13)CH13NO4

C25(13)CH34N4O13
1271786-92-5

C25(13)CH34N4O13

Conditions
ConditionsYield
With dmap; 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide77%
(2R)-N-amino-2-[(tert-butoxy)carbonylamino]-3-(4-phenylphenyl)propanamide 2,2,2-trifluoroacetic acid
919528-69-1

(2R)-N-amino-2-[(tert-butoxy)carbonylamino]-3-(4-phenylphenyl)propanamide 2,2,2-trifluoroacetic acid

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

trifluoroacetic acid
76-05-1

trifluoroacetic acid

2-({2-[({N-[(2R)-2-amino-3-(4-phenylphenyl)-propanoylamino]carbamoyl}methyl){2-[bis(carboxymethyl)amino]ethyl}amino]ethyl}(carboxymethyl)amino)acetic acid trifluoroacetic acid salt

2-({2-[({N-[(2R)-2-amino-3-(4-phenylphenyl)-propanoylamino]carbamoyl}methyl){2-[bis(carboxymethyl)amino]ethyl}amino]ethyl}(carboxymethyl)amino)acetic acid trifluoroacetic acid salt

Conditions
ConditionsYield
Stage #1: (2R)-N-amino-2-[(tert-butoxy)carbonylamino]-3-(4-phenylphenyl)propanamide 2,2,2-trifluoroacetic acid; diethylenetriaminopentaacetic acid With HBTU; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; for 0.75h;
Stage #2: trifluoroacetic acid With chlorotriisopropylsilane In dichloromethane at 20℃; for 4h;
73%
(guanidinium)3[tetraperoxoniobate]

(guanidinium)3[tetraperoxoniobate]

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

water
7732-18-5

water

dihydrogen peroxide
7722-84-1

dihydrogen peroxide

[guanidinium]3[Nb2(O2)4(OOCCH2NO(C2H4NO(CH2COO)2)2)]*3H2O

[guanidinium]3[Nb2(O2)4(OOCCH2NO(C2H4NO(CH2COO)2)2)]*3H2O

Conditions
ConditionsYield
With nitric acid In water dissolving of (guanidinium)3(Nb(O2)4) in water, addn. of 35 wt% H2O2 soln., addn. of HOOCCH2N(C2H4N(CH2COOH)2)2 with stirring; adjusting of pH to 3 with nitric acid; gentle heating for a few minites at 70°C; addn. of EtOH, pptn. for 24 h at 5°C; filtration, washing with ethanol, drying in air; elem. anal.;70%
gadolinium(III) oxide

gadolinium(III) oxide

diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

water
7732-18-5

water

cadmium(II) acetate dihydrate
5743-04-4

cadmium(II) acetate dihydrate

[Gd2Cd2(diethylenetriaminepentaacetic acid)2(H2O)4](H2O)4

[Gd2Cd2(diethylenetriaminepentaacetic acid)2(H2O)4](H2O)4

Conditions
ConditionsYield
at 170℃; for 168h; Autoclave;69.5%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C32H17N9Zn

C32H17N9Zn

C46H38N12O9Zn

C46H38N12O9Zn

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃; for 26h;63.63%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C40H31N9OZn

C40H31N9OZn

C54H52N12O10Zn

C54H52N12O10Zn

Conditions
ConditionsYield
With triethylamine In N,N-dimethyl-formamide at 20℃; for 26h;63.51%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C36H26N8O4Si

C36H26N8O4Si

C64H68N14O22Si

C64H68N14O22Si

Conditions
ConditionsYield
With dmap In dimethyl sulfoxide at 20℃; for 3h;62.51%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C32H21N9

C32H21N9

C46H42N12O9

C46H42N12O9

Conditions
ConditionsYield
With dmap In dimethyl sulfoxide at 20℃; for 3h;62.42%
diethylenetriaminopentaacetic acid
67-43-6

diethylenetriaminopentaacetic acid

C37H25FeN9O2

C37H25FeN9O2

C50H44FeN12O11

C50H44FeN12O11

Conditions
ConditionsYield
With sodium carbonate In N,N-dimethyl-formamide at 20℃; for 3h;62.4%

67-43-6Relevant academic research and scientific papers

Lightening Agents and/or Dyes that Contain Aldehyde(s)

-

, (2010/12/29)

Agents for dyeing and/or lightening keratin fibers, in particular human hair, containing, relative to the weight thereof, 0.001 to 15 wt. % of at least one aldehyde of the formula (I): wherein X represents —CH(R2)—SO2—Y—R1, —CR3R4R5, or wherein Y represents —CH(CHO)— or —CH2— or a chemical bond, and wherein each of R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 independently represents —H or —CN or —F or —Cl or —Br or —I or —CHO or —NH2 or —NO2 or —CF3 or —CCl3 or —CF2CF3 or —CCl2CCl3 or an optionally substituted (C1-C6) alkyl group or a hydroxyalkyl group or a polyhydroxyalkyl group or an optionally substituted (C1-C6) alkylene group, and wherein the agent contains no oxidation dye precursors of developer and coupler type.

Imaging of Enzyme Activity

-

, (2008/06/13)

This invention relates to biochemistry and magnetic resonance imaging.

Imaging thrombus with glycoprotein llb/llla antagonists

-

, (2008/06/13)

This invention relates to a method of using a radiolabeled small molecule antagonist of the platelet IIb/IIIa receptor for the diagnosis of arterial and venous thrombi.

Process for producing an amide compound

-

, (2008/06/13)

There is disclosed a process for producing an amide compound, which process is characterized in that a compound having an amino group are reacted with a polyaminopolycarboxylic acid anhydride in the presence of the polyaminopolycarboxylic acid.

Use of small molecule radioligands to discover inhibitors of amyloid-beta peptide production and for diagnostic imaging

-

, (2008/06/13)

This invention relates to a method of using radiolabelled and/or radiopharmaceutical small molecule inhibitors of beta-amyloid peptide production for the diagnosis of neurological and other disorders involving APP processing and beta-amyloid production. Furthermore, radiolabelled small molecule inhibitors identified by the methods of the present invention would be useful in the diagnosis of neurological disorders, such as Alzheimer's disease, which involve elevated levels of Aβ peptides.

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.

Water-soluble Hexadentate Schiff-base Ligands as Sequestrating Agents for Iron(III) and Gallium(III)

Evans, Dennis F.,Jakubovic, David A.

, p. 2927 - 2934 (2007/10/02)

Complexes of FeIII and GaIII with hexadentate Schiff-base ligands have been characterised in aqueous solution.They were prepared by the condensation of salicylaldehydes, containing a sulphonate or trimethylammonium group, with polyamines in the presence of the metal ions.These complexes have stabilities, at physiological pH, similar to those of the hydroxamic acid siderophore complexes.The kinetics of the displacement of FeIII from III(edta)>(1-) (edta = ethylenediamine-N,N,N',N'-tetra-acetate) by two of these ligands has been studied.

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