methylammonium carbonate
potassium oxalate monohydrate
Conditions | Yield |
---|---|
With amalgamated potassium at 360℃; |
methylammonium carbonate
A
potassium oxalate monohydrate
Conditions | Yield |
---|---|
With potassium hydride at 80℃; |
Conditions | Yield |
---|---|
In not given neutralisation; | |
In not given neutralisation; |
potassium hydrogenoxalate
potassium carbonate
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In not given neutralisation; | |
In not given neutralisation; |
Conditions | Yield |
---|---|
In not given neutralisation; | |
In not given neutralisation; |
potassium hydrogenoxalate
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In not given neutralisation; | |
In not given neutralisation; |
Conditions | Yield |
---|---|
In neat (no solvent) Kinetics; 20°C, varying partial pressure of water and H2O2; |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In water prepn. by slow diffusion in H-shaped tube of aq. solns. contg. K2C2O4*H2O in one arm and (2-(2-pyridyl)imidazole)copper(II) nitrate in the other; diffusion is complete in one mo; elem. anal.; | 99% |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In water heating 0.05 mol soln. of sulfate in water at 90°C; addn. of 0.2 mol oxalate soln.; filtration at 10°C;; ppt. washed with water and at 50°C about 12 h dried;; | 97% |
In water heating 0.05 mol soln. of sulfate in water at 90°C; addn. of 0.2 mol oxalate soln.; filtration at 10°C;; ppt. washed with water and at 50°C about 12 h dried;; | 97% |
[ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2
potassium oxalate monohydrate
[(p-cymene)2Ru2(μ-η4-C2O4)]Cl2
Conditions | Yield |
---|---|
In methanol; chloroform at 20℃; for 18h; Reflux; | 96% |
[2,2]bipyridinyl
potassium oxalate monohydrate
[(copper(II)(nitrate)(2,2'-bipyridine)(H2O))2(μ-oxalate)]
Conditions | Yield |
---|---|
In water stirring (60°C, 1 h); filtn., recrystallization (water); elem. anal.; | 95% |
Conditions | Yield |
---|---|
In water at 20 - 90℃; for 24h; | 95% |
2,2'-biimidazole
potassium oxalate monohydrate
[Cu(2,2'-biimidazole)(oxalate)(H2O)]*H2O
Conditions | Yield |
---|---|
In water prepn. by slow diffusion in H-shaped tube of aq. solns. contg. K2C2O4*H2O in one arm and a mixt. of Cu(NO3)2*3H2O and 2,2'-biimidazole in the other; elem. anal.; | 90% |
4-amino-1,2,4-triazole
potassium oxalate monohydrate
nickel(II) oxalate dihydrate
Conditions | Yield |
---|---|
In water soln. (10 ml) of (C2H2N3)NH2 (2.00 mmol) added dropwise to soln. (10 ml)of Ni(C2O4)*2H2O (0.44 mmol) and K2C2O4*H2O (2.4 mmol); elem. anal.; | 90% |
4-amino-1,2,4-triazole
potassium oxalate monohydrate
cobalt(II) oxalate dihydrate
Conditions | Yield |
---|---|
In water soln. (10 ml) of (C2H2N3)NH2 (2.00 mmol) added dropwise to soln. (10 ml)of Co(C2O4)*2H2O (0.44 mmol) and K2C2O4*H2O (4.00 mmol); elem. anal.; | 90% |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide aq. soln. of K salt added to soln. of Zn compd. in DMF; evapd. slowly; elem. anal.; | 90% |
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide aq. soln. of K2C2O4*H2O added to a DMF soln. of Zn complex (1 equiv.); crystd., elem. anal.; | 90% |
Conditions | Yield |
---|---|
In water; N,N-dimethyl-formamide DMF soln. of Cu complex treated with 1 equiv. of K2C2O4*H2O in H2O; crystd. (air) at ambient temp. for 1 week, elem. anal.; | 90% |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In water byproducts: NaCl, KCl; an aq. soln. of Na2PdCl4 was added dropwise to an aq. soln. of Ru-complex and K2C2O4*H2O, 60 min; ppt. was filtered off, washed with water, air-dried; elem. anal.; | 89.8% |
Conditions | Yield |
---|---|
Stage #1: C34H49Cl4Ir3N4; silver trifluoromethanesulfonate In methanol at 20℃; for 3h; Darkness; Stage #2: potassium oxalate monohydrate In methanol for 8h; | 88% |
cis-dichlorobis(triethylphosphine)platinum(II)
potassium oxalate monohydrate
bis(triethylphosphine)(oxalato)platinum(II)
Conditions | Yield |
---|---|
In methanol; water Pt complex and potassium oxalate mixing in equal volumes of hot MeOH and water, concg., cooling, off-white crystals sepg.; purified by recrystn. from CH2Cl2/Et2O; identified by elem. anal., NMR, IR and UV spectra; | 85% |
piperazine
potassium oxalate monohydrate
(piperazine)copper(II) oxalate
Conditions | Yield |
---|---|
With air In water byproducts: K2Cu(oxalate)2*2H2O; Cu:ox:piperazine=1.10:10.86:11.61 reacted for 6 d; ppt. filtered; elem. anal.; | 85% |
pyrazine-2,3-diamine
bis[dichloro(pentamethylcyclopentadienyl)iridium(III)]
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In methanol at 20℃; for 3h; | 85% |
cis-dichlorobis(triethylphosphine)platinum(II)
potassium oxalate monohydrate
bis(triethylphosphine)(oxalato)platinum(II)
Conditions | Yield |
---|---|
In methanol; water byproducts: KCl; heated with stirring until all solids dissolved, further heated for 10 min; concd., cooled (several h), collected, washed (2xH2O), dried under vacuum for 12 h, recrystd. (CH2Cl2), filtered, Et2O added, several h at 25°C, crystd., cooled to -10°C for 16 h, collected, washed (Et2O), dried in vacuo (1 h), elem. anal.; | 84% |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In water byproducts: NaCl, KCl; an aq. soln. of Na2PdCl4 and MnCl2*4H2O was added dropwise to an aq. soln. of Ru-complex and K2C2O4*H2O, 60 min; ppt. was filtered off, washed with water, air-dried; elem. anal.; | 83.4% |
osmium(VIII) oxide
1,10-Phenanthroline
hydroxylamine hydrochloride
potassium oxalate monohydrate
Conditions | Yield |
---|---|
With HBr In water stirring at 70-80°C for 1 h, then cooling to 10°C, adjustment of pH to ca 4.5, then addn. of concd. HBr, boiling for 1.5 h, cooling to room temp., then addn. of a hot (70°C) aq. soln. of C12H8N2, stirring for 45 min at 25°C; filtration, drying in vac., washing with benzene, drying under P4O10 in vac. for 24 h, elem. anal.; | 83% |
Conditions | Yield |
---|---|
With polytetrafluoroethylene In water at 20 - 130℃; for 202h; Autoclave; | 83% |
potassium oxalate monohydrate
Conditions | Yield |
---|---|
With LiCl In water addn. of MnCl2 to mixt. of Ru-complex and LiCl (stirring), addn. of K2C2O4 (pptn. after few min); collection (filtration), washing (water, EtOH), drying in air; elem. anal.; | 81% |
4-aminopyridine
potassium oxalate monohydrate
cobalt(II) oxalate dihydrate
Conditions | Yield |
---|---|
In methanol; water react. MeOH soln. 4-ampy with aq. soln. Co(ox)*2H2O and K2(ox)*H2O; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water addn. of SnCl4 to 3.5-4 equiv. of K2C2O4 soln., heating to 70°C; EtOH addn., crystn. (cooling), filtration (ice-cold EtOH, ice-cold Et2O), recrystn. (aq. EtOH), drying (70°C); elem. anal.; | 80% |
Conditions | Yield |
---|---|
In methanol; water MeOH soln. of (C2H2N3)NH2 (2.5 mmol) layered onto aq. soln. of K2Cu(C2O4)2*2H2O (0.5 mmol) and K2C2O4*H2O (0.33 mmol); kept (2 wk); washed with cold H2O and Et2O; dried in air; elem. anal.; | 80% |
Conditions | Yield |
---|---|
In methanol; water aq. soln. of K oxalate added to MeOH-H2O soln. of NC5H4CHCHC5H4N and Mn salt (molar ratio 1:1:3); ppt. collected; elem. anal.; | 80% |
[Pd(C,N-κ2-C6H4CH=NC6H3-2,6-i-Pr2)(μ-Cl)]2
potassium oxalate monohydrate
C40H44N2O4Pd2
Conditions | Yield |
---|---|
Stage #1: [Pd(C,N-κ2-C6H4CH=NC6H3-2,6-i-Pr2)(μ-Cl)]2 With silver nitrate In acetonitrile at 20℃; for 15h; Darkness; Stage #2: potassium oxalate monohydrate In dichloromethane; water at 20℃; for 16h; Schlenk technique; | 80% |
[(C6F5)2Pt(μ-PPh2)2Pt(CH3CN)2]
tetrabutylammonium perchlorate
potassium oxalate monohydrate
Conditions | Yield |
---|---|
In acetone at 20℃; for 20h; | 77% |
Conditions | Yield |
---|---|
In water molar ratio Zr:oxalic acid:K2C2O4=1:3:1, pH-adjustment to 1.5 (0.1 M KOH), stirring at 80°C for 12 h; filtration, crystn. (closed vessel, room temp., 2 months), collection (filtration), washing (cold water), drying (vac., 6 h); elem. anal.; | 75% |
Conditions | Yield |
---|---|
In ethanol; water ligand added to Cu salt in H2O/EtOH 80:20 v/v, gently refluxed for 15 min, treated with K2Ox*H2O while stirring; evapd. at room temp., elem. anal.; | 75% |
The IUPAC name of Ethanedioic acid,potassium salt, hydrate (1:2:1) is dipotassium oxalate hydrate. With the CAS registry number 6487-48-5, it is also named as Ethanedioic acid, dipotassium salt, monohydrate. Besides, it is white crystals or powder, which should be stored at room temperature. And it is stable and hygroscopic. Moreover, the product is soluble in water and incompatible with strong oxidizing agents. In addition, this chemical is harmful in contact with skin and if swallowed. You should avoid contact with skin and eyes when use it.
The other characteristics of this product can be summarized as: (1)EINECS: 209-506-8; (2)ACD/LogP: -1.19; (3)# of Rule of 5 Violations: 0; (4)ACD/LogD (pH 5.5): -5.7; (5)ACD/LogD (pH 7.4): -5.94; (6)ACD/BCF (pH 5.5): 1; (7)ACD/BCF (pH 7.4): 1; (8)ACD/KOC (pH 5.5): 1; (9)ACD/KOC (pH 7.4): 1; (10)H bond acceptors: 4; (11)H bond donors: 2; (12)Freely Rotating Bonds: 1; (13)Density: 2.13 g/mL at 25 °C; (14)Flash Point: 188.8 °C; (15)Melting point: 356 °C; (16)Water solubility: 364 g/L at 20 °C; (17)Enthalpy of Vaporization: 67.15 kJ/mol; (18)Boiling Point: 365.1 °C at 760 mmHg; (19)Vapour Pressure: 2.51E-06 mmHg at 25 °C.
Preparation and usages: please neutralize Potassium hydroxide or Potassium carbonate with the solution of Oxalic acid or Potassium hydrogen oxalate. And then you would get the crystals of Ethanedioic acid,potassium salt, hydrate (1:2:1) afer cooling. Besides, this chemical can be used to make drug and bleacher. It also can be used as analytical reagents. Additionally, it is used in preventing of blood coagulation, pharmaceutical industry and film printing.
People can use the following data to convert to the molecule structure.
(1)SMILES:[K+].[K+].[O-]C(=O)C([O-])=O.O
(2)InChI:InChI=1/C2H2O4.2K.H2O/c3-1(4)2(5)6;;;/h(H,3,4)(H,5,6);;;1H2/q;2*+1;/p-2
(3)InChIKey:QCPTVXCMROGZOL-NUQVWONBAS
(4)Std. InChI:InChI=1S/C2H2O4.2K.H2O/c3-1(4)2(5)6;;;/h(H,3,4)(H,5,6);;;1H2/q;2*+1;/p-2
(5)Std. InChIKey:QCPTVXCMROGZOL-UHFFFAOYSA-L
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