Tag: M.W=250-300

Sinru, Lin published the artcileAscending water electrode studies of metal extractants 4-acyl-5-pyrazolones and selected tervalent lanthanide ions, Formula: C12H9F3N2O2, the main research area is acylpyrazolone polarog ascending water electrode; water ascending stationary electrode acylpyrazolone; pyrazolone acyl polarog dichloroethane water; phenylmethyltrifluoroacetylpyrazolone polarog dichloroethane water; phenylmethylbenzoylpyrazolone polarog dichloroethane water; lanthanide acylpyrazolone polarog ascending water; complex lanthanide acylpyrazolone polarog.

The polarog. and chhronopotentiometric behavior of the chelating extractants 1-phenyl-3-methyl-4-trifluoroacetyl-5-pyrazolone and 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone in the dichloroethane-aqueous systems were characterized at the ascending H2O electrode and the stationary H2O electrode. The nature of the phase transfer processes both in the absence and presence of tervalent lanthanide metal ions was elucidated. Self-adduct and mixed ligand chelate formations were deduced (the latter when trioctylphosphine oxide is present). The reversibility, transfer coefficients, and transfer rate constants of the ligand anions were also deduced. This electrochem. approach is shown to provide novel insights into solvent extraction processes.

Analytical Chemistry published new progress about Electrodes. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Formula: C12H9F3N2O2.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Hasany, S. M. published the artcileExtraction of group Ib, IIb and III-VA elements with 1-phenyl-3-methyl-4-trifluoroacetyl-pyrazolon-5, Application In Synthesis of 1691-93-6, the main research area is IB extraction pyrazolone masking effect; IIB extraction pyrazolone masking effect; IIA extraction pyrazolone masking effect; IVA extraction pyrazolone masking effect; VA extraction pyrazolone masking effect; pyrazolone extraction Group IB IIB.

The extraction of group IB, IIB and IIIA-VA elements with 1-phenyl-3-methyl-4-trifluoroacetyl-pyrazolone-5 in CHCl3 was studied as a function of pH. The stripping of metal ions into solutions of KCN, HClO4 and appropriate pH buffers was studied. The masking effects of cyanide, citrate, iodide, thiosulfate and thiourea on the extraction were examined Selective group and individual separations are proposed on the basis of pH control, masking effects and back-extraction

Journal of Radioanalytical Chemistry published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Application In Synthesis of 1691-93-6.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Hasany, S. M. published the artcileExtraction of Group VIII elements with 1-phenyl-3-methyl-4-trifluoroacetylpyrazol-5-one, Name: 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, the main research area is Group 8 extraction separation; phenylmethylfluoroacetylpyrazolone extraction Group 8; fluoroacetylpyrazolone extraction Group 8; pyrazolone phenylmethylfluoroacetyl extraction Group 8; iron extraction separation; nickel extraction separation; palladium extraction separation; rhodium extraction separation; cobalt extraction separation.

The extraction of Group VIII elements with 1-phenyl-3-methyl-4-trifluoacetyl-pyrazol-5-one from aqueous solutions in CHCl3 was studied as a function of pH. Fe(III), Ni(II), Pd(II), and Rh(III) show partial extraction whereas Co(II) is extracted quant. The effect of citrate, cyanide, fluoride, iodide, thiosulfate and thiourea on the extraction of metal ions was investigated. Back-extraction studies were carried out to strip metal ions from the organic phase into appropriate aqueous solutions Based on these findings some useful anal. separations were proposed and a few of their possible applications are discussed.

Journal of Radioanalytical Chemistry published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Name: 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Huang, Chunhui published the artcileThe extraction of lanthanides with halogen substituted 4-acylpyrazolones, HPLC of Formula: 1691-93-6, the main research area is lanthanide extraction acylpyrazolone halogen derivative.

Equilibrium extraction behavior for a series of representative tervalent lanthanide ions, La, Pr, Eu, and Yb, using chloroform solutions containing halogenated derivatives of 4-acyl-1-phenyl-3-methyl-5-pyrazolone were studied. These lanthanides are extracted as simple chelates, LnL3. The equilibrium constants of these extraction reactions were calculated The relationships between the acid dissociation constants, Ka, determined by a 2-phase titration method, distribution constants, KDR, and the extraction equilibrium constants, Kex, are discussed.

Solvent Extraction and Ion Exchange published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, HPLC of Formula: 1691-93-6.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Matsui, Masakazu published the artcile4-Acyl-5-pyrazolones as an analytical reagent. II. Applicability of halogen substituted 4-acyl-5-pyrazolones to the solvent extraction of metals, Formula: C12H9F3N2O2, the main research area is pyrazolone haloacyl extraction agent; europium extraction haloacylpyrazolone; substituent effect extraction haloacylpyrazolone.

Several 4-halogenated acyl derivatives of 1-aryl-3-methyl-5-pyrazolone were synthesized from 1-aryl-3-methyl-5-pyrazolone and the chlorinated acetyl chloride or perfluoroacyl anhydride, and their effectiveness as the solvent extracting agent of metals was evaluated. The placement of the halogen atom into the 4-acetyl group strengthened the acidity of the pyrazolones remarkably. A linear relations was established between the dissociation constant of 1-aryl derivatives and the Hammet σ constant The derivatives had an extremely large extraction constant for Eu chelates, and for example, the pH value at half extraction by 0.02 M of 1-tolyl-3-methyl-4-trifluoroacetyl-5-pyrazolone decreased to 1.1 when n-octanol was used as the extracting solvent.

Bulletin of the Institute for Chemical Research, Kyoto University published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Formula: C12H9F3N2O2.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Umetani, S. published the artcileAdduct formation properties of some polydentate phosphine oxides in the synergistic extraction of metals with 4-acyl-5-pyrazolone derivatives, Synthetic Route of 1691-93-6, the main research area is extraction transition metal pyrazolone adduct; acrylpyrazolone extraction transition metal synergism; phosphoryl compound extraction synergism pyrazolone.

Some bi- and tridentate phosphine oxide compounds were synthesized and liquid-liquid extraction equilibrium of metal ions with 4-acyl-5-pyrazolone derivatives and the neutral phosphine oxide compounds were investigated. Bis(diphenylphosphinyl)methane was found to be a very powerful ligand in the synergistic extraction of rare earths, alk. earths and the divalent metals such as Co(II), Ni(II), Zn(II) and Cd(II). The composition of the extracted species were determined by a graphical method. The adduct formation constants between the acylpyrazolone chelates and the neutral ligands were determined and discussed in terms of the mol. structure.

Process Metallurgy published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Synthetic Route of 1691-93-6.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Sujatha, S. published the artcileSynergistic solvent extraction of trivalent lanthanides by mixtures of 1-phenyl-3-methyl-4-trifluoroacetyl-pyrazolone-5 and neutral oxo-donors, Application of 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, the main research area is extraction synergism lanthanide fluoroacetylpyrazolone sulfoxide; adduct formation extraction lanthanide diketone complex; ethylhexyl sulfoxide adduct lanthanide fluoroacetylpyrazolone complex; phenylphosphine oxide adduct lanthanide fluoroacetylpyrazolone complex.

The synergistic solvent extraction of Nd3+, Eu3+, or Lu3+ by 3-methyl-1-phenyl-4-trifluoroacetyl-5-pyrazolone (HL) in the presence of neutral oxo-donors (D) in CHCl3 was studied by using radioactive tracers. The aqueous Ln3+ ions are present as various forms of chloroacetate complexes. Equilibrium extraction constants were determined for Ln3+ by HL in mixtures containing bis(2-ethylhexyl) sulfoxide (B2EHSO) or Ph3PO. Adduct formation constants were calculated for LnL3.D and LnL3.2D in the CHCl3 phase. Addition of B2EHSO or Ph3PO increases the Lu-Eu separation factor, while B2EHSO addition decreases the Eu-Nd separation factor (but Ph3PO addition causes a moderate increase).

Journal of Chemical Engineering of Japan published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Application of 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Umetani, Shigeo published the artcileMixed-ligand chelate extraction of lanthanides with 1-phenyl-3-methyl-4-(trifluoroacetyl)-5-pyrazolone and some phosphine oxide compounds, HPLC of Formula: 1691-93-6, the main research area is lanthanide extraction phosphine oxide pyrazolone.

Mixed-ligand chelate extraction was studied for La, Pr, Eu, Ho, and Yb into CHCl3 with 1-phenyl-3-methyl-4-(trifluoroacetyl)-5-pyrazolone (HPMTFP) and with 1 of 3 phosphine oxide compounds (TOPO, octylphenyl(N,N-diisobutylcarbamoylmethyl)phosphine oxide (CMPO), and methylenebis(diphenylphosphine oxide) (MBDPO)). Lanthanide ions are extracted from a 0.1 M NaClO4 as Ln(PMTFP)3(TOPO)2 and Ln(PMTFP)3(CMPO), resp. In the extraction of lanthanides with the mixture of HPMTFP and MBDPO, the extracted species are Ln(PMTFP)3(MBDPO) or Ln(PMTFP)2(ClO4)(MBDPO)2 in the absence or presence of NaClO4, resp. The extraction constants of these systems do not increase monotonically with at. number but have a maximum at Eu or Ho.

Inorganic Chemistry published new progress about Extraction. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, HPLC of Formula: 1691-93-6.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Umetani, Shigeo published the artcileLiquid-liquid distribution of 4-acyl-3-methyl-1-phenyl-5-pyrazolones and their zinc complexes, Safety of 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, the main research area is acylmethylphenylpyrazolone partition aqueous cyclohexane; zinc acylmethylphenylpyrazolone partition aqueous cyclohexane.

The distribution of 8 4-acyl-3-methyl-1-phenyl-5-pyrazolones and their Zn complexes between aqueous and cyclohexane phases was investigated. The acid dissociation constants and partition constants of the extractants were discussed in terms of a substituent effect. Two series of examined reagents in which one has an aromatic substituent at the 4-position of 5-pyrazolone, and the other an aliphatic one give similar extraction constants Since their acid dissociation constants are essentially the same, a relationship, log PMA = 2 log PHA + constant, is postulated. The extraction constant of a fluorinated reagent which has a considerably small pKa value is also similar to that of the reagents having aliphatic substituents.

Bulletin of the Chemical Society of Japan published new progress about Ionization. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Safety of 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics

Umetani, Shigeo published the artcileThe solvent extraction of divalent metals with 1-phenyl-3-methyl-4-trifluoroacetylpyrazol-5-one and TOPO as the group separation and concentration methods of trace metals, Recommanded Product: 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, the main research area is divalent metal separation water analysis.

The synergistic extraction of divalent metals with 1-phenyl-3-methyl-4-(trifluoroacetyl)pyrazol-5-one (I) [1691-93-6] and trioctylphosphine oxide (II) [78-50-2] was studied for cyclohexane solutions containing 0.02-0.05M I and 0.01M II. Extraction >98% was obtained for Cu, Mn, Zn, Co, Pb, Cd, Fe, and Ni as divalent ions in aqueous solutions buffered to pH 1.5-2.8. The VO2+ extraction was incomplete. At pH 2.4-4 a quant. extraction was obtained for Ca, Mg, Sr, and Ba. The method is suitable for group separation and concentration of trace metals from natural waters, especially for emission spectroscopy.

Bulletin of the Institute for Chemical Research, Kyoto University published new progress about Divalent metals. 1691-93-6 belongs to class pyrazoles-derivatives, name is 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one, and the molecular formula is C12H9F3N2O2, Recommanded Product: 5-Methyl-2-phenyl-4-(2,2,2-trifluoroacetyl)-1H-pyrazol-3(2H)-one.

Referemce:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics