Conditions | Yield |
---|---|
absence of O2, 440-450°C; | 95% |
Conditions | Yield |
---|---|
In tetrahydrofuran-d8 at -80℃; for 0.5h; Catalytic behavior; Kinetics; Mechanism; Solvent; Temperature; Concentration; | A n/a B 95% |
Conditions | Yield |
---|---|
In benzene-d6 at -80℃; for 0.5h; Catalytic behavior; Solvent; Temperature; | A n/a B 95% |
Conditions | Yield |
---|---|
In benzene-d6 at -80℃; for 0.5h; Catalytic behavior; Kinetics; Solvent; Temperature; | A n/a B 95% |
Conditions | Yield |
---|---|
In benzene-d6 at -80℃; for 0.5h; Catalytic behavior; | A n/a B 95% |
Conditions | Yield |
---|---|
In (2)H8-toluene at -80℃; for 0.5h; Catalytic behavior; | A n/a B 95% |
Conditions | Yield |
---|---|
potassium hydroxide In solid byproducts: H2; 330 °C; with KOH (1:0.05) in N2 atmosphere, the heating rate 6 deg/min; | A 93% B n/a |
in aluminium block at 460-500°C; | A 79% B n/a |
With air In melt 460-500°C, in presence of air; | A 79% B 20% |
potassium oxalate
Conditions | Yield |
---|---|
With sawdust In not given oxidation at 240-250°C through 1-15 hours by air admission; | 80% |
With sawdust In not given oxidation at 240-250°C through 1-15 hours by air admission; | 80% |
With bran heating; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: K2CO3; 200°C;; | 72% |
In neat (no solvent) heating 2 % K amalgam up to boiling point of Hg;; | |
In neat (no solvent) byproducts: K2CO3; optimum temp. at 225°C, presence of O2;; small amt. of K2C2O4;; |
2-amino-N,N-dimethyl-3-phenylpropanamide
nitrobenzene
A
potassium oxalate
B
Potassium benzoate
C
dimethyl amine
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol at 50℃; Mechanism; flow of oxygen gas; | A 17% B 35% C 32% D n/a |
Conditions | Yield |
---|---|
With carbon monoxide; pyrographite High Pressure; 243 atm, 470°C 2,5 h; | 29% |
With CO; animal charcoal High Pressure; 243 atm, 470°C 2,5 h; | 29% |
(RS)-alanine N,N-dimethylamide
nitrobenzene
A
potassium formate
B
potassium oxalate
Conditions | Yield |
---|---|
With potassium tert-butylate In tert-butyl alcohol at 50℃; for 44h; anaerobic reaction; | A 20% B n/a C n/a |
acetoacetic acid methyl ester
A
potassium acetylsydnonate N-oxide
D
potassium oxalate
Conditions | Yield |
---|---|
Stage #1: acetoacetic acid methyl ester With potassium hydroxide In methanol at 23℃; Cooling; Inert atmosphere; Stage #2: With nitrogen(II) oxide In methanol at 23℃; under 1551.49 - 1965.21 Torr; | A 18% B n/a C n/a D n/a |
Conditions | Yield |
---|---|
In neat (no solvent) at 230 up to 240 °C;; | 17% |
In neat (no solvent) at 230 up to 240 °C;; | 17% |
Conditions | Yield |
---|---|
With carbon dioxide at 230-240°C in CO2 atmosphere; | A n/a B 17% |
With CO2; sand at 230-240°C in CO2 atmosphere; | A n/a B 17% |
carbon dioxide
carbon monoxide
potassium carbonate
A
potassium formate
B
potassium oxalate
C
potassium hydrogencarbonate
Conditions | Yield |
---|---|
In neat (no solvent) High Pressure; 2 h at 380°C; cooling, dissolution in water, addn. of HClO4; HPLC; | A 0% B 1% C 0.8% |
D
potassium oxalate
Conditions | Yield |
---|---|
In neat (no solvent) sample heating in N2 up to 700°C; DSC, XRD; | A n/a B n/a C 1% D n/a |
B
potassium oxalate
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With potassium hydroxide; oxygen at 180 - 280℃; | |
With potassium permanganate In not given in alkaline soln., effect of concns.,temp. react. time; | |
With KMnO4 In not given in alkaline soln., effect of concns.,temp. react. time; |
ethylene glycol
A
Glyoxal
B
potassium hydrogene glycolate
C
potassium oxalate
D
potassium glyoxylate
Conditions | Yield |
---|---|
With potassium hydroxide; gold at 23℃; Mechanism; electrooxidation pathways on var. metal electrodes, var. electrode potentials; other polyols; |
A
N,N'-di(p-tolyl)acetamidine
B
potassium oxalate
N,N'-dimethyl-N,N'-dinitroso-oxamide
A
diazomethane
B
potassium oxalate
1,2-Dithiooxalsaeure-S,S-dimethylester
A
methylthiol
B
potassium oxalate
Conditions | Yield |
---|---|
With potassium hydroxide |
Conditions | Yield |
---|---|
With potassium hydroxide |
S1,S2-Diphenylethanebis(thioate)
A
potassium thiophenolate
B
potassium oxalate
potassium tetrachloroplatinate(II)
potassium oxalate
Conditions | Yield |
---|---|
In water at 95℃; for 1h; Product distribution / selectivity; | 98% |
Conditions | Yield |
---|---|
Stage #1: cis-diaminediiodoplatinum(II) With silver nitrate In water for 8h; Stage #2: potassium oxalate In water | 98% |
potassium oxalate
4-Methylbenzyl chloride
bis((4-methylphenyl)methyl)oxalate
Conditions | Yield |
---|---|
Stage #1: potassium oxalate; 4-Methylbenzyl chloride In N,N-dimethyl acetamide at 50℃; for 0.25h; Stage #2: With sodium dodecyl-sulfate; potassium hydroxide In N,N-dimethyl acetamide at 50 - 110℃; for 6h; pH=9 - 11; Reagent/catalyst; | 95% |
cis-dichlorobis(2,2′-bipyridine)ruthenium(II)
potassium oxalate
{RuC2O4(bpy)2}
Conditions | Yield |
---|---|
In ethanol; water for 2.03333h; Heating / reflux; | 94% |
In methanol; water refluxed for 5 h under inert atm.; evapd. in vacuo, residue was recrystd. from MeOH; (1)H NMR spectral data; | 83% |
potassium oxalate
potassium trifluoro(oxalato)manganate(III) monohydrate
Conditions | Yield |
---|---|
With HF In water MnO(OH) was dissolved in 40% HF and the soln. was warmed at 100°C for 5 min; the soln. was filtered, filtrate was cooled to room temp., soln. of K2C2O4 was added, then EtOH was added, ppt. was filtered off, washed with EtOH, dried in vac.; elem.anal.; | 94% |
potassium oxalate
Conditions | Yield |
---|---|
In water byproducts: KCl; heating to 130 °C in an autoclave for 2.5h;; evapn. on a water bath, crystn.; mother liquor retreated to enhance the yield;; | 90% |
potassium oxalate
Conditions | Yield |
---|---|
In water AgNO3 was slowly added at room temp. to soln. of Pt-complex in water, filtered, K2C2O4 was added, stirred for 24 h at 20°C; exts. with CH2Cl2, evapd. in stream in air, dried in air at 20°C; | 90% |
Conditions | Yield |
---|---|
In methanol; water a soln. of borate in methanol was reacted with Cu-salt in methanol for 30 min at 25°C, then the soln. was reacted with K-salt in water under stirring for 15 min at 25°C; filtered, slow concd.; elem. anal.; | 90% |
Conditions | Yield |
---|---|
In methanol; water a soln. of borate in methanol was reacted with Cu-salt in methanol for 30 min at 25°C, then the soln. was reacted with K-salt in water under stirring for 15 min at 25°C; filtered, slow concd.; elem. anal.; | 90% |
[1,1'-bis(diphenylphosphino)ferrocene]platinum(II) chloride
chloroform
water
potassium oxalate
Conditions | Yield |
---|---|
In water soln. of K-salt in water was added to suspn. of Pt-complex in water, heated under reflux for ca. 3 h; filtered, washed with water, dried in vac., crystd. from CHCl3-n-pentane; elem. anal.; | 87% |
Conditions | Yield |
---|---|
In water at 95℃; for 1.25h; Product distribution / selectivity; | 86% |
With sulfur dioxide In water at 95℃; for 1h; Product distribution / selectivity; | 78% |
In water byproducts: CO2, KCl; treatment of K2(PtCl6) with excessive K2C2O4 in boiling aq. soln.;; | |
In water byproducts: CO2, KCl; treatment of K2(PtCl6) with excessive K2C2O4 in boiling aq. soln.;; |
potassium oxalate
A
bis(4-nitrophenyl)acenaphthenequinonediimine
B
zinc(II) oxalate
Conditions | Yield |
---|---|
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min; | A 85% B n/a |
[ZnCl2(bis(3,5-dichlorophenyl)acenaphthenequinonediimine)]
potassium oxalate
A
bis(3,5-dichlorophenyl)acenaphthenequinonediimine
B
zinc(II) oxalate
Conditions | Yield |
---|---|
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min; | A 85% B n/a |
potassium oxalate
A
bis(3-trifluoromethylphenyl)acenaphthenequinonediimine
B
zinc(II) oxalate
Conditions | Yield |
---|---|
In dichloromethane; water Zn complex was suspended in CH2Cl2 and soln. potassium oxalate in water was added, shaked for 5 min; | A 85% B n/a |
potassium oxalate
Conditions | Yield |
---|---|
In water silver nitrate added to metal complex soln. (2:1 molar ratio), stirred for 20 h at room temp., filtered, evapd.; extd. (CH2Cl2), dried (vac.), elem. anal.; | 85% |
1,10-Phenanthroline
4,4′-( pyridine-2,6-diyl)dibenzoic acid
potassium oxalate
Conditions | Yield |
---|---|
With sodium hydroxide In water at 160℃; for 72h; | 85% |
potassium oxalate
Conditions | Yield |
---|---|
In dimethyl sulfoxide to Ru complex in DMSO K2(ox) was added and refluxed for 1 h; EtOH was added, ppt. was filtered, washed with cold EtOH and Et2O, and vac.-dried at room temp.; elem. anal.; | 84% |
[InCl3(C5H3N(C2H3NOH)2)(CH3OH)]
potassium oxalate
Conditions | Yield |
---|---|
With H2O In methanol; water byproducts: KCl; stirring (1 h, 25°C); filtn., solvent removal, extracting (MeOH); elem. anal.; | 80% |
potassium oxalate
[Ru(1,4,7-trithiacyclononane)(DMSO-S)(η2-oxalate)]
Conditions | Yield |
---|---|
In methanol addn. of potassium oxalate to stirred soln. of ruthenim compd. in methanol, refluxing for 1 h; cooling, filtration, washing with methanol, ether, drying in vac., elem.anal.; | 78% |
potassium oxalate
Conditions | Yield |
---|---|
In ethanol; water for 4h; Reflux; | 78% |
Conditions | Yield |
---|---|
In water at 110℃; for 48h; | 78% |
Conditions | Yield |
---|---|
In water High Pressure; mixt. placed in Teflon vessel, sonicated for 5 min, sealed in stainless steel autoclave; hydrothermally treated at 120°C for 35 h, cooleddown to room temp. for 18 h; ppt. washed with water, dried in vac.; elem. anal.; | 75% |
MF: C2K2O4
MW: 166.22
EINECS: 209-506-8
Synonyms:DI-POTASSIUM OXALATE; dipotassiumethanedioate; Ethanedioicacid, dipotassiumsalt; oxalicacid,dipotassiumsalt;potassiumneutraloxalate;potassiumoxalate(k2c2o4);Potassium Oxalate Anhydrous;Potassium oxalate
POTASSIUM OXALATE's structure:
Potassium oxalate(583-52-8) gives basic aqueous solutions. Reacts as a base to neutralize acids in reactions that generate heat, but less than is generated by neutralization of the bases in reactivity group 10. Can serve as a reducing agent in reactions that generate carbon dioxide.
|
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
women | LDLo | oral | 1gm/kg (1000mg/kg) | CARDIAC: ARRHYTHMIAS (INCLUDING CHANGES IN CONDUCTION) VASCULAR: SHOCK GASTROINTESTINAL: OTHER CHANGES | Medecine Legale et Dommage Corporel. Vol. 4, Pg. 178, 1971. |
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