Conditions | Yield |
---|---|
In water Electrolysis; anodic oxidation of 3.6 n chloride soln.;; |
potassium chlorate
Conditions | Yield |
---|---|
In water Electrolysis; | |
Electrolysis; acidic electrolyte; | |
Electrolysis; alk. electrolyte, max. current efficiency 60-65 %; |
Conditions | Yield |
---|---|
In water equilibrium reaction; examination at different temperatures;; | |
In water equilibrium reaction; examination at different temperatures;; | |
In water equilibrium reaction; examination at different temperatures;; | |
In water | |
In water concd. CaCl2 soln. as by-product; stepwise concg.;; |
chlorine dioxide
potassium carbonate
A
potassium chlorate
B
potassium chlorite
Conditions | Yield |
---|---|
In water byproducts: H2O; | |
In water byproducts: H2O; |
Conditions | Yield |
---|---|
Electrolysis; electrolysis of NaCl, addn. of K2CO3 to obtained NaClO3; | |
Electrolysis; electrolysis of NaCl, addn. of K2CO3 to obtained NaClO3; |
Conditions | Yield |
---|---|
With oxygen Addn. of O2 to introduced Cl2 does not increase yield.; |
Conditions | Yield |
---|---|
chlorination and treating obtd. soln. with KCl; | |
chlorination and treating obtd. soln. with KCl; |
perchloric acid monohydrate
A
potassium chlorate
Conditions | Yield |
---|---|
With 0.1n-KOH In neat (no solvent) byproducts: chlorine oxides, Cl2, O2; neutralisation of just melting HClO4*H2O with 0.1n KOH; yield of KClO3 much lower than expected from hydrolysis of Cl2O6; The products do not contain HCl;; |
Conditions | Yield |
---|---|
With potassium permanganate; water In water byproducts: MnO2; | |
With KMnO4; H2O In water byproducts: MnO2; |
chlorine dioxide
A
potassium chlorate
B
potassium chlorite
Conditions | Yield |
---|---|
With potassium hydroxide In not given byproducts: KClO3, H2O; | |
With potassium hydroxide In water addn. of a KOH soln. to a ClO2 soln. containing CO2 and protected from light;; multiple evaporation in the vac. at 45 - 50 °C until KClO3 pptd.; pptn. of K2CO3 with alc.; evaporation in the cold and in the vac.; adding alc. (95 %) to the residue; filtration; evaporation of the filtrate in the cold and in the vac.;; | |
With potassium hydroxide In water addn. of a KOH soln. to a ClO2 soln. containing CO2 and protected from light;; multiple evaporation in the vac. at 45 - 50 °C until KClO3 pptd.; pptn. of K2CO3 with alc.; fractionated crystn. in the vac.;; |
Conditions | Yield |
---|---|
With potassium hydroxide In not given byproducts: H2O; ClO2 contents max. 2% Cl2; crystn. at -8-5°C, grad of purification: 80%; | |
With potassium hydroxide In not given byproducts: H2O; ClO2 contents max. 2% Cl2; crystn. at -8-5°C, grad of purification: 80%; |
chlorine dioxide
A
potassium chlorate
B
potassium chlorite
Conditions | Yield |
---|---|
In water byproducts: H2O; dild. soln.;; | |
In water byproducts: H2O; | |
In water |
potassium permanganate
chlorine dioxide
potassium chlorate
chlorite
potassium chlorate
Conditions | Yield |
---|---|
With potassium hydroxide; manganese(IV) oxide In not given | |
With KOH; manganese(IV) oxide In not given |
Conditions | Yield |
---|---|
Electrolysis; | |
Electrolysis; |
Conditions | Yield |
---|---|
Electrolysis; perchlorate formation decreases at higher temps.; | |
Electrolysis; perchlorate formation decreases at higher temps.; |
Conditions | Yield |
---|---|
Electrolysis; effect of cathode substance; | |
Electrolysis; effect of cathode substance; |
Conditions | Yield |
---|---|
With hydrogenchloride byproducts: Cl2; Electrolysis; |
Conditions | Yield |
---|---|
Electrolysis; electrolysis of NaCl, addn. of KCl to obtained NaClO3; | |
Electrolysis; electrolysis of NaCl, addn. of KCl to obtained NaClO3; |
Conditions | Yield |
---|---|
at 95-98 °C; | |
at 95-98 °C; |
Conditions | Yield |
---|---|
Electrolysis; electrolysis of CaCl2 and addn. of KCl to obtained Ca(ClO3)2; | |
Electrolysis; electrolysis of CaCl2 and addn. of KCl to obtained Ca(ClO3)2; |
Conditions | Yield |
---|---|
addn. of Ca(OH)2 to soln. remained after crystn. of bulk of KClO3; Calciumoxychloride can be pptd. by cooling soln., causing negligible chlorate loss.; | |
addn. of Ca(OH)2 to soln. remained after crystn. of bulk of KClO3; Calciumoxychloride can be pptd. by cooling soln., causing negligible chlorate loss.; |
potassium chlorate
Conditions | Yield |
---|---|
In water byproducts: O2; Irradiation (UV/VIS); U.V. light; | 100% |
In water byproducts: O2; Irradiation (UV/VIS); U.V. light; | 100% |
In neat (no solvent) Kinetics; byproducts: O2, NO2, ((C4H9)2NCO)2(CH2)6; sample heating at 5 K/min from up to 620°C; thermosonimetry and TG, high temp. microscopy; |
potassium chlorate
Conditions | Yield |
---|---|
In water hot soln. of KClO3 (0.0018 mol) added to hot soln. of Co(NH3)6Cl3 (0.0018 mol); cooled (4 d); crystals filtered off; dried in air; elem. anal.; | 99% |
Conditions | Yield |
---|---|
In water hot soln. of KClO3 (0.0012 mol) added to hot soln. of Co(NH3)6Br3 (0.0012 mol); cooled (3 d); crystals filtered off; dried in air; elem. anal.; | 99% |
potassium chlorate
hypochlorite
Conditions | Yield |
---|---|
With H In not given redn. of a boiling KClO3-soln. (1g in 100ml) by a foil of Pd, laden with hydrogen with addn. of 10ml 25% H2SO4;; | 94% |
With H In not given redn. of a boiling KClO3-soln. (1g in 100ml) by a foil of Pd, laden with hydrogen with addn. of 10ml 25% H2SO4;; | 94% |
With H redn. by hydrogen (Pd satd. with H);; |
potassium chlorate
tetraphenylantimony(V) chloride
tetraphenylantimony chlorate
Conditions | Yield |
---|---|
In water mixt. of Ph4SbCl and KClO3 in H2O was kept for 24 h at 12°C; solvent removed; recrystd. (acetone); elem. anal.; | 89% |
Conditions | Yield |
---|---|
In water anion exchange in aq. soln.; molar ratio (C5H5Ni(P(C4H9-n)3)2)(1+)Cl(1-):KClO3 = 1:3; between O°C and room temp.; product dissolved in benzene; recrystn. from hexane or benzene/hexane in the presence of P(C4H9-n)3; | 87% |
In water |
Conditions | Yield |
---|---|
In neat (no solvent) refluxing at 170 to 190°C for 3 h;; distillation;; | 80% |
potassium chlorate
Conditions | Yield |
---|---|
In water byproducts: KNO3; Co complex dissolved in H2O; KClO3 dissolved in H2O at room temp.; two solns. mixed; crystd. for 0.5 h; crystals collected by drawing off the mother liquor; air dried; elem. anal.; | 80% |
potassium chlorate
trans-dichlorobis(ethylenediamine)cobalt(III) chloride
trans-dichlorobis(ethylenediamine)cobalt(III) chlorate
Conditions | Yield |
---|---|
In water mixing aqueous solns. of cobalt compd. and chlorate salt for 0.5 h; drawing off mother liquor, air drying, elem. anal.; | 80% |
Conditions | Yield |
---|---|
In water byproducts: KCl; a soln. of Co-complex and KClO3 in water were mixed, allowed to stand for 1 d at room temp.; crystals were collected and dried in air; elem. anal.; | 80% |
potassium chlorate
hydrazine carboxamide
A
carbon dioxide
B
nitrogen
C
ammonia
Conditions | Yield |
---|---|
With hydrogenchloride | A n/a B 66% C n/a |
potassium chlorate
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: O2, KCl; heating;; | 66% |
In neat (no solvent) byproducts: O2, KCl; heating;; | 66% |
silica gel In neat (no solvent) various m,ixing proportions were investigated; 15 % SiO2 results the greatest yield of KClO4;; | 59% |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: O2; 1.5 mol KI/ mol KClO3; start at 350-400°C; violent reaction under formation of O2; mechanism discussed;; product mixture;; | A 65% B n/a |
Conditions | Yield |
---|---|
With potassium iodide molar ratio of KI:KIO3 = 1.5:1; | 65% |
With KI molar ratio of KI:KIO3 = 1.5:1; | 65% |
With iodine In water heating an aq. suspension of I2 with KClO3 and some drops concd. HNO3; |
Conditions | Yield |
---|---|
In neat (no solvent) below -20°C;; passing ClO3F over KI; cooling at -183°C; distillation at -183 - 130°C in vacuum;; | 60% |
In neat (no solvent) below -20°C;; passing ClO3F over KI; cooling at -183°C; distillation at -183 - 130°C in vacuum;; | 60% |
potassium chlorate
hydrazonium sulfate
A
hydrogen azide
B
ammonia
Conditions | Yield |
---|---|
In not given yield is higher in presence of solid Ag2SO4; | A 22% B 48% |
In not given yield is higher in presence of solid Ag2SO4; | A 22% B 48% |
potassium chlorate
fluorine
A
perchloryl fluoride
C
chlorine dioxide
D
chlorine monofluoride
E
chlorine
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: O2; transport reaction: passing F2-N2 mixture over KClO3 at 25 - 60°C;; washing with NaOH; passing ClO3F through Na2S2O3 soln.; drying over NaOH and P2O5;; | A 45% B n/a C n/a D n/a E n/a |
Conditions | Yield |
---|---|
In not given multiple evapn. with ambient concd. HNO3; nearly no KClO4 is obtained using fuming HNO3;; | 30% |
In not given multiple evapn. using ambient concd. or water-free HNO3; nearly no KClO4 is formed, if fuming HNO3 is used;; | 30% |
In not given multiple evapn. with ambient concd. HNO3; nearly no KClO4 is obtained using fuming HNO3;; | 30% |
Conditions | Yield |
---|---|
With alkali | 25% |
With alkali | 25% |
Conditions | Yield |
---|---|
In not given boiling until yellow color disappears;; | 15% |
In not given boiling until yellow color disappears;; | 15% |
Conditions | Yield |
---|---|
In not given | 11% |
In not given | 11% |
In not given |
potassium chlorate
Conditions | Yield |
---|---|
In sulfuric acid addition of a solution of KClO3 in H2O (0.70 M ClO3(1-)) to a solution of the decaborate (0.20 M B10H10(2-)) in aq. H2SO4 (0.5 M H(1+)) and stirring at 25°C, 7 days;; filtration of ((C2H5)3NH)(B20H18);; | 8% |
In hydrogenchloride addition of a solution of KClO3 in H2O (0.70 M ClO3(1-)) to a solution of the decaborate (0.20 M B10H10(2-)) in aq. HCl (0.5 M H(1+)) and stirring at 25°C, 7 days;; filtration of ((C2H5)3NH)(B20H18);; | 8% |
In sulfuric acid addition of a solution of KClO3 in H2O (0.50 M ClO3(1-)) to a solution of the decaborate (0.20 M B10H10(2-)) in aq. H2SO4 (0.5 M H(1+)) and stirring at 25°C, 7 days;; filtration of ((C2H5)3NH)(B20H18);; | 5% |
Conditions | Yield |
---|---|
decompn. of Nh4Cl with heating KClO3; | >99 |
decompn. of Nh4Cl with heating KClO3; | |
decompn. of Nh4Cl with heating KClO3; | >99 |
decompn. of Nh4Cl with heating KClO3; |
Conditions | Yield |
---|---|
by ignition of the mixture; |
Conditions | Yield |
---|---|
With methyllithium 550 kg Cr2O3, 225 kg Al powder, 50-55 kg KClO3 and 50-55 kg lime put into Fe covering cylinder; | 80-85 |
Conditions | Yield |
---|---|
In melt byproducts: Cl2; melting of educts;; | |
In melt byproducts: Cl2; melting of educts;; |
Conditions | Yield |
---|---|
In water heating of Cr2O3 in KClO3 soln.;; |
Conditions | Yield |
---|---|
With water In not given in weakly acidic 0.1 n KCl soln., at 60-70°C; | |
With H2O In not given in weakly acidic 0.1 n KCl soln., at 60-70°C; |
Conditions | Yield |
---|---|
A n/a B 0% | |
A n/a B 0% |
Conditions | Yield |
---|---|
byproducts: KCl; gentle glowing; leaching off KCl from the cooled melt (water); hydrated BaO2; |
IUPAC Name: potassium chlorate
Synonyms of Potassium chlorate (CAS NO.3811-04-9): Anforstan ; Berthollet salt ;Chlorate de potassium ;Chloric acid potassium salt (1:1) ;Potassium oxymuriate
CAS NO: 3811-04-9
Molecular Formula: ClKO3
Molecular Weight: 122.55
Molecular Structure:
EINECS: 223-289-7
H bond acceptors: 3
H bond donors: 1
Freely Rotating Bonds: 0
Polar Surface Area: 54.37 Å2
Melting point: 356 °C(lit.)
Boiling point: 400 °C
Density: 2,32 g/cm3
Storage temp.: 2-8 °C
Water Solubility: 73 g/L (20 °C )
Sensitive: Hygroscopic
Appearance: colourless crystals or colourless to white crystalline powder
Stability: Stability Strong oxidizer - contact with combustible material may cause fire. Mixtures with combustible material may be shock-sensitive. Incompatible with organics, combustible materials, strong reducing agents
Product Categories of Potassium chlorate (CAS NO.3811-04-9): Inorganic Chemicals;Inorganics;Inorganic Salts;Potassium;Synthetic Reagents;Metal and Ceramic Science;Potassium Salts;Salts;Essential Chemicals;Reagent Grade;Routine Reagents;ACS GradeSynthetic Reagents;Analytical Reagents for General Use;O-P, Puriss p.a. ACS;Puriss p.a. ACS
SMILES: [K+].[O-]Cl(=O)=O
InChI: InChI=1/ClHO3.K/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1
InChIKey: VKJKEPKFPUWCAS-REWHXWOFAC
Std. InChI: InChI=1S/ClHO3.K/c2-1(3)4;/h(H,2,3,4);/q;+1/p-1
Std. InChIKey: VKJKEPKFPUWCAS-UHFFFAOYSA-M
Potassium chlorate (CAS NO.3811-04-9) is used as an oxidizing agent, to prepare oxygen, as a disinfectant, in safety matches, and in explosives and fireworks. It is also used in cultivation, forcing the blossoming stage of a Longan tree, causing it to produce fruit in warmer climates.
In industry, Potassium chlorate (CAS NO.3811-04-9) is produced by the electrolysis of a sodium chloride solution to form sodium chlorate, which is reacted with potassium chloride to precipitate potassium chlorate. The resultant sodium chloride is returned to the mother liquor for electrolysis. Besides, it can also be produced on a smaller scale by the thermal disproportionation of a hypochlorite to its respective chlorate and chloride by boiling, then adding KCl. This reaction should be done in a fume hood due to the production of chlorine and chlorine dioxide gas.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
dog | LDLo | oral | 1200mg/kg (1200mg/kg) | "Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 1, Pg. 242, 1955. | |
guinea pig | LDLo | intraperitoneal | 1800mg/kg (1800mg/kg) | BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: COMA LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | Journal of Pharmacology and Experimental Therapeutics. Vol. 35, Pg. 1, 1929. |
guinea pig | LDLo | oral | 7500mg/kg (7500mg/kg) | BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: COMA LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | Journal of Pharmacology and Experimental Therapeutics. Vol. 35, Pg. 1, 1929. |
human | LDLo | unreported | 429mg/kg (429mg/kg) | Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 21, Pg. 169, 1886. | |
rabbit | LDLo | oral | 2gm/kg (2000mg/kg) | Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 21, Pg. 169, 1886. | |
rat | LD50 | oral | 1870mg/kg (1870mg/kg) | American Industrial Hygiene Association Journal. Vol. 30, Pg. 470, 1969. | |
rat | LDLo | intraperitoneal | 1500mg/kg (1500mg/kg) | BEHAVIORAL: CHANGES IN MOTOR ACTIVITY (SPECIFIC ASSAY) BEHAVIORAL: COMA LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES | Journal of Pharmacology and Experimental Therapeutics. Vol. 35, Pg. 1, 1929. |
Reported in EPA TSCA Inventory.
Safety Information for Potassium chlorate (CAS NO.3811-04-9):
Hazard Codes: OXnN
Risk Statements: 9-20/22-51/53
R9: Explosive when mixed with combustible material.
R20/22: Harmful by inhalation and if swallowed.
R51/53: Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Safety Statements: 13-16-27-61
S13: Keep away from food, drink and animal foodstuffs.
S16: Keep away from sources of ignition.
S27: Take off immediately all contaminated clothing.
S61: Avoid release to the environment. Refer to special instructions / safety data sheets.
RIDADR: UN 1485 5.1/PG 2
WGK Germany: 2
RTECS: FO0350000
HazardClass: 5.1
PackingGroup: II
Moderately toxic to humans by an unspecified route. Moderately toxic experimentally by ingestion and intraperitoneal routes. A gastrointestinal tract and kidney irritant. Can cause hemolysis of red blood cells and methemoglobinemia. Toxic dose to a human is about 5 g.
A powerful oxidizer and very reactive material. It has been the cause of many industrial explosions. May explode on heating. Explosive reactions with ammonium chloride, aqua regia + ruthenium, sulfur dioxide solutions in ether or ethanol. Reacts with fluorine to form the explosive gas fluorine perchlorate.
Forms sensitive explosive mixtures with agricultural materials (e.g., peat, powdered sulfur, sawdust, thiuram), aluminum + antimony trisulfide powders, arsenic trisulfide, carbon, charcoal + potassium nitrate + sulfur, charcoal + sulfur, cyanides, cyanoguanidine, hydrocarbons, manganese dioxide + traces of organic matter, manganese dioxide + potassium hydroxide, metal + wood, metal phosphides (e.g., tricopper diphosphide, trimercury tetraphosphide), metal phosphinates (e.g., barium phosphinate), finely divided metals (e.g., aluminum, copper, magnesium, zinc, germanium, titanium, zirconium, steel, chromium), metal phosphides (e.g., tricopper diphosphide, trimercury tetraphosphide), metal sulfides (e.g., antimony trisulfide, silver sulfide), metal thiocyanates (e.g., ammonium thiocyanate, barium thiocyanate), nitric acid + organic materials, powdered nonmetals (e.g., arsenic, carbon, phosphorus, sulfur, boron), reducing agents (e.g., calcium hydride, strontium hydride, sodium phosphinate, calcium phosphinate, barium phosphinate), sugars (e.g., glucose), sulfur, sulfur + metal derivatives (e.g., cobalt, cobalt oxide, copper nitride, copper sulfate, copper chlorate), sulfuric acid, sodium amide, tannic acid.
Violent reaction or ignition with NH3, NH4Cl, NH4+ salts, ammonium sulfate, Sb2S3, As, barium hypophosphite, BaS, calcium hypophosphite, CaS, charcoal, Cu3P2, fabrics, gallic acid, hydrogen iodide, lactose, (Mg + CuSO4 (anhydrous) + NH4NO3 + H2O), MnO2, dinickel trioxide, dibasic organic acids, organic matter, NaNH2, sugar + sulfuric acid, sucrose, SO2, H2SO4, thiocyanates, thorium dicarbide, sodium amide, fabrics, KOH, metal hypophosphites.
When heated to decomposition it emits very toxic fumes of Cl− and K2O. Used in the manufacture of soap, glass, and pottery. See also CHLORATES.
DOT Classification: 5.1; Label: Oxidizer
General Information: As in any fire, wear a self-contained breathing apparatus in pressure-demand, MSHA/NIOSH (approved or equivalent), and full protective gear. Strong oxidizer. Contact with other material may cause fire. Use water spray to keep fire-exposed containers cool.
Extinguishing Media: Use water spray, dry chemical, carbon dioxide, or chemical foam.
Handling: Remove contaminated clothing and wash before reuse. Use spark-proof tools and explosion proof equipment. Avoid breathing dust, vapor, mist, or gas. Avoid contact with skin and eyes.
Storage: Keep away from heat, sparks, and flame. Do not store near combustible materials. Store in a cool, dry place. Store in a tightly closed container. Keep away from strong acids.
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