Potassium formate supplier

Name
Potassium formate
EINECS 209-677-9
CAS No. 590-29-4
Article Data193
CAS DataBase
Density 1.560 g/mL at 20 °C
Solubility H₂O: 1 M at 20 °C, clear, colorless
Melting Point 165-168 °C
Formula CH₂KO₂
Boiling Point 100.6 °C at 760 mmHg
Molecular Weight 84.116
Flash Point 29.9 °C
Transport Information
Appearance white crystalline solid
Safety 37/39-26
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Formicacid, potassium salt (8CI,9CI);Potassium formate (6CI);EcoForm PF 75;
PSA 40.13000
LogP -0.99800

Synthetic route

: C21H37N2O3PRu

A: 863971-63-5
carbonylhydrido[6-(di-tert-butylphosphinomethylene)-2-(N,N-diethylaminomethyl)-1,6-dihydropyridine]ruthenium(II)

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium tert-butylate at 25℃; for 0.0833333h;	A 100% B 97 %Spectr.

: 124-38-9
carbon dioxide

: C21H34N2O3PRu(1-)*K(1+)

A: C21H35N2O3PRu

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
With hydrogen In dimethylsulfoxide-d6 at 120℃; under 750.075 Torr; for 1h;	A 98% B 15%

...Expand

: 201230-82-2
carbon monoxide

: potassium hydroxide

: 590-29-4
potassium formate

Conditions

Conditions	Yield
In water 1 h, 160°C, 20 atm CO-pressure;	97.8%
In water 1 h, 160°C, 20 atm CO-pressure;	97.8%
in presence of enough water, methanol, ethanol, acetone or ether;

: potassium sulfate

: barium sulfide

: 201230-82-2
carbon monoxide

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With water In water byproducts: BaSO4, H2S; 150-160°C under pressure;	97%
With H2O In water byproducts: BaSO4, H2S; 150-160°C under pressure;	97%

...Expand

: potassium sulfate

: 201230-82-2
carbon monoxide

: barium(II) hydroxide

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With water In water byproducts: BaSO4; 150-160°C under pressure;	97%
With H2O In water byproducts: BaSO4; 150-160°C under pressure;	97%

...Expand

: 298-14-6
potassium hydrogencarbonate

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With hydrogen In water at 100℃; under 30003 Torr; for 10h; Temperature; Pressure; Autoclave;	96.8%
With nickel; hydrogen In water at 200℃; under 45004.5 Torr; for 2h; Green chemistry;	92.1%
With hydrogen; palladium In water with Pd -black,30-60 atm,70-95°C,24 h;	70%

: 67-56-1
methanol

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With [carbonylchlorohydrido{bis[2-(diphenylphosphinomethyl)ethyl]amino}ethylamino] ruthenium(II); potassium hydrogencarbonate; potassium hydroxide In water at 150℃; for 20h; Catalytic behavior; Reagent/catalyst; Temperature; Time; Autoclave; Inert atmosphere;	92%
With C12H16IrN4O2(1+)*BF4(1-); potassium hydroxide In water at 115℃; for 15h; Catalytic behavior; Reagent/catalyst; Temperature; Schlenk technique; Inert atmosphere;

: potassium cyanide

A: 7664-41-7
ammonia

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
	A 73.3% B 85.1%
	A 73.3% B 85.1%
With water In water at b.p.;in concd. soln.;

: potassium fluoride

: 18296-01-0
triethylsilyl formate

A: 358-43-0
triethylsilyl fluoride

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
at 20℃; for 0.25h; Schlenk technique; Inert atmosphere; Glovebox;	A n/a B 85%

...Expand

: 584-08-7
potassium carbonate

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With nickel; hydrogen In water at 200℃; under 45004.5 Torr; for 2h; Green chemistry;	76.6%

: 1333-74-0
hydrogen

: 298-14-6
potassium hydrogencarbonate

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With palladium In not given 60 atm, 70°C;	75%
With Pd black In not given 60 atm, 70°C;	75%
With palladium In not given 60 atm, 70°C;	75%
In water 4h, 350°C, 380 atm;	11%
In water 4h, 350°C, 380 atm;	11%

: C14H10N5O8(1-)*K(1+)

A: 590-29-4
potassium formate

B: 126865-59-6
4-[N-(4'-methoxyphenyl)amino]-5,7-dinitro-2,1,3-benzoxadiazole

Conditions

Conditions	Yield
With water at 90℃; for 1h;	A n/a B 73%

: C13H8N5O7(1-)*K(1+)

A: 97346-17-3
4,6-dinitro-7-phenylaminobenzofurazan

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
With water at 90℃; for 1h;	A 72% B n/a

: 124-38-9
carbon dioxide

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium tetrafluoroborate; 1,2,3-trimethylbenzimidazoline In dimethylsulfoxide-d6 at 50℃; under 1794.37 Torr; for 18h; Reagent/catalyst; Solvent; Pressure; Temperature;	66%
With potassium fluoride; carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II); Dimethylphenylsilane In acetonitrile at 60℃; under 760.051 Torr; for 4h; Catalytic behavior; Temperature; Reagent/catalyst; Solvent;	55%
With C23H19ClN7ORu(1+)*Cl(1-); hydrogen; potassium hydroxide In tetrahydrofuran; water at 20 - 130℃; under 11400.8 Torr; for 25h; Catalytic behavior; Reagent/catalyst; Autoclave; Schlenk technique;	5.8%

: 617-86-7
triethylsilane

: 124-38-9
carbon dioxide

A: 597-52-4
Triethylsilanol

B: 994-49-0
hexaethyl disiloxane

C: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium fluoride; dodecacarbonyl-triangulo-triruthenium In water at 80℃; under 5171.62 Torr; for 13h; Inert atmosphere; Autoclave; Green chemistry;	A n/a B n/a C 60%

...Expand

: 75-46-7
trifluoromethan

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium hydroxide at 140℃; under 2585.81 Torr; for 24h;	55%

: 124491-96-9
(RS)-alanine N,N-dimethylamide

: 98-95-3
nitrobenzene

A: 590-29-4
potassium formate

B: 583-52-8
potassium oxalate

C K2CO3: K2CO3

Conditions

Conditions	Yield
With potassium tert-butylate In tert-butyl alcohol at 50℃; for 44h; anaerobic reaction;	A 20% B n/a C n/a

...Expand

: 124-38-9
carbon dioxide

: 201230-82-2
carbon monoxide

: 584-08-7
potassium carbonate

A: 590-29-4
potassium formate

B: 583-52-8
potassium oxalate

C: 298-14-6
potassium hydrogencarbonate

Conditions

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%

...Expand

: 67-66-3
chloroform

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium hydroxide

: 544-17-2
calcium diformate

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium sulfate
With potassium sulfate

: 107-31-3
Methyl formate

A: 67-56-1
methanol

B: 590-29-4
potassium formate

Conditions

Conditions	Yield
With potassium hydroxide at 25℃; Mechanism; carbonyl carbon, carbonyl oxygen and nucleophile oxygen isotope effect;

: 530-27-8
D-gulopyranose

A: 590-29-4
potassium formate

B: potassium D-lyxonate

Conditions

Conditions	Yield
With potassium hydroxide; oxygen; sodium anthraquinone-2-sulfonate; dihydrogen peroxide at 19.9℃; under 750.06 Torr; for 48.6111h; Mechanism; Product distribution; Thermodynamic data; different reaction times, O2 concentrations, absence and presence of catalyst; activation energy;
With potassium hydroxide; oxygen at 19.9℃; under 750.06 Torr;

: 201230-82-2
carbon monoxide

: 590-29-4
potassium formate

Conditions

Conditions	Yield
With KRu; hydrogen heterogeneous reaction in an UHV/high pressure reactor system;

: 154-58-5
1,5-anhydro-D-glucitol

A: 590-29-4
potassium formate

B: arabinoate

Conditions

Conditions	Yield
With potassium hydroxide; oxygen; sodium anthraquinone-2-sulfonate; dihydrogen peroxide at 29.9℃; under 750.06 Torr; Mechanism; Product distribution; Thermodynamic data; different reaction times, O2 concentrations, absence and presence of catalyst; activation energy;

: 133-99-3, 490-37-9, 2152-98-9, 4482-75-1, 5965-66-2, 13299-27-9, 13360-52-6, 14641-93-1, 15548-43-3, 16462-44-5, 16984-36-4, 16984-38-6, 20869-27-6, 22688-72-8, 27452-49-9, 29276-55-9, 30608-12-9, 34481-13-5, 37169-60-1, 37169-64-5, 64234-01-1, 64234-02-2, 75281-88-8, 80446-85-1, 84413-57-0, 92344-56-4, 93221-87-5, 93301-77-0, 94799-29-8, 100427-98-3, 100428-00-0, 101312-82-7, 102046-24-2, 102046-25-3, 109432-00-0, 109432-02-2, 109432-04-4, 109432-08-8, 135268-49-4, 138231-26-2, 140461-59-2, 145414-22-8, 145414-26-2, 146339-75-5, 146339-76-6, 149116-55-2
lactose

A: 530-27-8
D-gulopyranose

B: 590-29-4
potassium formate

C: 82563-97-1
4-deoxy-D-glycero-2,3-hexodiulose

D: 136208-72-5
potassium O-β-D-galactopyranosyl-(1->3)-D-arabinonate

Conditions

Conditions	Yield
With potassium hydroxide; oxygen at 19.9℃; under 750.06 Torr; for 48.6111h;

...Expand

: 133-99-3, 490-37-9, 2152-98-9, 4482-75-1, 5965-66-2, 13299-27-9, 13360-52-6, 14641-93-1, 15548-43-3, 16462-44-5, 16984-36-4, 16984-38-6, 20869-27-6, 22688-72-8, 27452-49-9, 29276-55-9, 30608-12-9, 34481-13-5, 37169-60-1, 37169-64-5, 64234-01-1, 64234-02-2, 75281-88-8, 80446-85-1, 84413-57-0, 92344-56-4, 93221-87-5, 93301-77-0, 94799-29-8, 100427-98-3, 100428-00-0, 101312-82-7, 102046-24-2, 102046-25-3, 109432-00-0, 109432-02-2, 109432-04-4, 109432-08-8, 135268-49-4, 138231-26-2, 140461-59-2, 145414-22-8, 145414-26-2, 146339-75-5, 146339-76-6, 149116-55-2
lactose

A: 530-27-8
D-gulopyranose

B: 590-29-4
potassium formate

C: 136208-72-5
potassium O-β-D-galactopyranosyl-(1->3)-D-arabinonate

Conditions

Conditions	Yield
With potassium hydroxide; oxygen; sodium anthraquinone-2-sulfonate; dihydrogen peroxide at 19.9℃; under 750.06 Torr; for 48.6111h; Mechanism; Rate constant; Product distribution; different reaction times, O2 concentrations, absence and presence of catalyst;
With potassium hydroxide; oxygen; sodium anthraquinone-2-sulfonate; dihydrogen peroxide at 19.9℃; under 750.06 Torr; for 48.6111h; Thermodynamic data; different reaction times, O2 concentrations, absence and presence of catalyst; activation energy;

...Expand

: 133-99-3, 490-37-9, 2152-98-9, 4482-75-1, 5965-66-2, 13299-27-9, 13360-52-6, 14641-93-1, 15548-43-3, 16462-44-5, 16984-36-4, 16984-38-6, 20869-27-6, 22688-72-8, 27452-49-9, 29276-55-9, 30608-12-9, 34481-13-5, 37169-60-1, 37169-64-5, 64234-01-1, 64234-02-2, 75281-88-8, 80446-85-1, 84413-57-0, 92344-56-4, 93221-87-5, 93301-77-0, 94799-29-8, 100427-98-3, 100428-00-0, 101312-82-7, 102046-24-2, 102046-25-3, 109432-00-0, 109432-02-2, 109432-04-4, 109432-08-8, 135268-49-4, 138231-26-2, 140461-59-2, 145414-22-8, 145414-26-2, 146339-75-5, 146339-76-6, 149116-55-2
lactose

A: 590-29-4
potassium formate

B: arabinoate

Conditions

Conditions	Yield
With potassium hydroxide; oxygen at 29.9℃; under 750.06 Torr;

: 2-Nitro-4-aci-nitro-1,1-dimethoxy-1,4-dihydro-naphthalinkalium

A: 124-38-9
carbon dioxide

B: 590-29-4
potassium formate

C: 18718-46-2
2,4-Dinitronaphthol-(1)-kalium

Conditions

Conditions	Yield
at 157 - 180℃; Product distribution; Thermodynamic data; ΔH of the decomposition;

...Expand

: C8H9N2O6(1-)*K(1+)

A: 124-38-9
carbon dioxide

B: 590-29-4
potassium formate

C: 14314-69-3
potassium 2,4-dinitrophenolate

Conditions

Conditions	Yield
at 112 - 120℃; Product distribution; Thermodynamic data; ΔH of the decomposition;

...Expand

: C9H11N2O7(1-)*K(1+)

A: 124-38-9
carbon dioxide

B: 590-29-4
potassium formate

C: 14314-69-3
potassium 2,4-dinitrophenolate

Conditions

Conditions	Yield
at 115 - 156℃; Product distribution; Thermodynamic data; ΔH of the decomposition;

...Expand

: 24962-55-8
4-hydroxybenzaldehyde 4-methylbenzenesulfonate ester

: 590-29-4
potassium formate

: 51804-15-0
4-carboxyphenyl 4-methylbenzenesulfonate

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	98%
With dichloro(1,5-cyclooctadiene)palladium(II); N-Methyldicyclohexylamine; dtbpf; 9-methyl-9H-fluorene-9-carbonyl chloride; bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate In 1,4-dioxane at 80℃; for 18h; Reagent/catalyst; Inert atmosphere;	99 %Spectr.

: 590-29-4
potassium formate

: 79917-90-1
1-butyl-3-methylimidazolium chloride

: 497144-87-3
1-butyl-3-methylimidazolium formate

Conditions

Conditions	Yield
In water Green chemistry;	97.9%
In water at 25℃;	90.5%
In methanol at 20℃; for 24h;

: 590-29-4
potassium formate

: 100-44-7
benzyl chloride

: 104-57-4
benzyl formate

Conditions

Conditions	Yield
Silica D22; tetramethlyammonium chloride at 150℃; for 2h; Mechanism; other alkyl halides, other alkali salts, other catalyst;	97%
Silica D22; tetramethlyammonium chloride at 150℃; for 2h;	97%
Amberlyst A27 In toluene at 95℃; for 15h; Product distribution; other catalysts (ion exchange resins);	97 % Chromat.
With Amberlyst A27 In toluene at 95℃; for 20h;	100.0 % Chromat.
With graphene oxide-supported quaternary ammonium salt at 80℃; for 8h;

: 3058-39-7
4-iodobenzonitrile

: 590-29-4
potassium formate

: 619-65-8
4-cyanobenzoic Acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	97%

: 590-29-4
potassium formate

: 104-88-1
4-chlorobenzaldehyde

: 619-66-9
4-Carboxybenzaldehyde

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In diethylene glycol dimethyl ether at 120℃; for 18h; Inert atmosphere;	97%

: (E)-3-(3-bromo-4-fluorobenzylidene)isobenzofuran-1(3H)-one

: 590-29-4
potassium formate

: (Z)-2-fluoro-5-((3-oxoisobenzofuran-1(3H)-ylidene)methyl)benzoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	96%

: 338-65-8
1-chloro-2,2-difluoroethane

: 590-29-4
potassium formate

: 1137875-58-1
2,2-difluoroethyl formate

Conditions

Conditions	Yield
at 125℃; for 5.5h;	96%

: 590-29-4
potassium formate

: 583-52-8
potassium oxalate

Conditions

Conditions	Yield
absence of O2, 440-450°C;	95%

: 590-29-4
potassium formate

: 99-73-0
para-bromophenacyl bromide

: 10536-76-2
p-bromophenacyl formate

Conditions

Conditions	Yield
With Tris(3,6-dioxaheptyl)amine In acetonitrile for 0.25h; Heating;	95%

: 51934-41-9
4-iodobenzoic acid ethyl ester

: 590-29-4
potassium formate

: 713-57-5
terephthalic acid monoethyl ester

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	95%
Stage #1: potassium formate With acetic anhydride; N-ethyl-N,N-diisopropylamine In N,N-dimethyl-formamide at 20℃; Stage #2: 4-iodobenzoic acid ethyl ester With tris(dibenzylideneacetone)dipalladium (0); lithium chloride In N,N-dimethyl-formamide at 80℃; for 22h;	81%

: 623-00-7
4-bromobenzenecarbonitrile

: 590-29-4
potassium formate

: 619-65-8
4-cyanobenzoic Acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	95%

: 22966-09-2
(2E)-3-(4-bromophenyl)-1-phenylprop-2-en-1-one

: 590-29-4
potassium formate

: 20118-38-1
4-[(1E)-3-oxo-3-phenylprop-1-en-1-yl]benzoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	95%

: 5798-75-4
Ethyl 4-bromobenzoate

: 590-29-4
potassium formate

: 713-57-5
terephthalic acid monoethyl ester

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	95%

: 10CH4O*4Nb(2+)*14Cl(1-)*2Nb(3+)

: 590-29-4
potassium formate

: [K(methanol)]4[Nb6Cl12(formate)6]

Conditions

Conditions	Yield
In methanol for 10h;	94%

: 590-29-4
potassium formate

A: 583-52-8
potassium oxalate

B: 584-08-7
potassium carbonate

Conditions

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%

: 623-03-0
4-Cyanochlorobenzene

: 590-29-4
potassium formate

: 619-65-8
4-cyanobenzoic Acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In diethylene glycol dimethyl ether at 120℃; for 18h; Inert atmosphere;	93%

: 60811-21-4
1-bromo-3-chloro-4-fluorobenzene

: 590-29-4
potassium formate

: 403-16-7
3-chloro-4-fluorobenzoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	93%

: 590-29-4
potassium formate

: 52287-51-1
6-bromo-1,4-benzodioxane

: 4442-54-0
2,3-dihydro-1,4-benzodioxin-6-carboxylic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	93%

: 7335-27-5
ethyl 4-chlorobenzoate

: 590-29-4
potassium formate

: 713-57-5
terephthalic acid monoethyl ester

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In diethylene glycol dimethyl ether at 120℃; for 18h; Inert atmosphere;	93%

: 104-92-7
1-bromo-4-methoxy-benzene

: 590-29-4
potassium formate

: 100-09-4
4-methoxybenzoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	92%

: 590-29-4
potassium formate

: 64697-40-1
1-methyl-3-octylimidazol-3-ium chloride

: C12H23N2(1+)*CHO2(1-)

Conditions

Conditions	Yield
In water at 25℃;	91.2%

: 491862-84-1
1-fluoro-3-iodo-5-methylbenzene

: 590-29-4
potassium formate

: 518070-19-4
3-fluoro-5-methylbenzoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	91%

: 584-12-3
2-bromofuran

: 590-29-4
potassium formate

: 88-14-2
2-furanoic acid

Conditions

Conditions	Yield
With [PhCOPd(PtBu3)I]; dtbpf In 2-methyltetrahydrofuran at 80℃; for 18h; Inert atmosphere;	91%

Potassium formate Consensus Reports

Reported in EPA TSCA Inventory.

Potassium formate Specification

The IUPAC name of thisa chemical is potassium formate. With the CAS registry number 590-29-4, it is also named as Formic acid potassium salt. The product's categories are Alphabetical Biological Buffers; Biological Buffers; BioUltra Buffers; Buffer Solutions Protein Structural Analysis; Inorganic Salts; Optimization Reagents Synthetic Reagents; Potassium; X-Ray Crystallography. It is white crystalline solid which should be sealed in the container and stored in dry place.

The other characteristics of this product can be summarized as: (1)ACD/LogP: -0.54; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): -2.3; (4)ACD/LogD (pH 7.4): -3.94; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 1; (8)ACD/KOC (pH 7.4): 1; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 0; (12)Enthalpy of Vaporization: 22.69 kJ/mol; (13)Vapour Pressure: 36.5 mmHg at 25°C; (14)Exact Mass: 83.961361; (15)MonoIsotopic Mass: 83.961361; (16)Topological Polar Surface Area: 40.1; (17)Heavy Atom Count: 4; (18)Complexity: 13.5.

Uses of Potassium formate: It is an intermediate in the formate potash process for the production of potassium. It has also been studied as a potential environmentally-friendly deicing salt for use on roads. In addition, it can react with chloroacetonitrile to get formyloxy-acetonitrile. This reaction needs reagent KI and solvent tetrahydrothiophene 1,1-dioxide at temperature of 100 °C. The reaction time is 4.0 hours. The yield is 76%.

When you are using this chemical, please be cautious about it as the following:
It is irritating to eyes, respiratory system and skin. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. If you want to contact this product, you must wear suitable gloves and eye/face protection.

People can use the following data to convert to the molecule structure.
1. SMILES:[K+].[O-]C=O
2. InChI:InChI=1/CH2O2.K/c2-1-3;/h1H,(H,2,3);/q;+1/p-1
3. InChIKey:WFIZEGIEIOHZCP-REWHXWOFAK

The following are the toxicity data which has been tested.

Organism	Test Type	Route	Reported Dose (Normalized Dose)	Effect	Source
mouse	LD50	intravenous	95mg/kg (95mg/kg)		Zeitschrift fuer Ernaehrungswissenschaft. Vol. 9, Pg. 332, 1969.
mouse	LD50	oral	5500mg/kg (5500mg/kg)		Zeitschrift fuer Ernaehrungswissenschaft. Vol. 9, Pg. 332, 1969.

Product Name

Potassium formate

Synthetic route

Potassium formate Consensus Reports

Potassium formate Specification

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