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7782-68-5

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7782-68-5 Usage

Physical Properties

White stable crystalline solid; rhombohedral crystals; occurs in two forms: the normal HIO3, and pyroiodic acid HI3O8.

Uses

Different sources of media describe the Uses of 7782-68-5 differently. You can refer to the following data:
1. Aqueous solutions of iodic acid serve as strong oxidizing agents. The acid also is used in redox titrations.
2. Iodic acid is used in analytical chemistry laboratories to standardize solutions of both weak and strong bases using methyl red or methyl orange as the indicator. It acts as a key starting material to synthesize sodium or potassium iodate, thereby increasing the iodine content of salt.
3. A strong acid in analytical chemistry.

Preparation

Different sources of media describe the Preparation of 7782-68-5 differently. You can refer to the following data:
1. Iodic acid may be prepared by the reaction of sulfuric acid with barium iodate. The solution is filtered to remove barium sulfate and then crystallized to obtain iodic acid: Ba(IO3)2 + H2SO4 → BaSO4 + 2HIO3 It also may be produced by oxidation of iodine with concentrated nitric acid: 3I2 + 10HNO3 → 6HIO3 + 10NO + 2H2O Also, iodic acid may be obtained by oxidation of iodine with chlorine in dilute acidic solutions: I2 + 5Cl2 + 6H2O → 2HIO3 + 10HCl Another method of preparation involves oxidation of iodine with hydrogen peroxide: I2 + 5H2O2 → 2HIO3 + 4H2O It also may be prepared by treating hypoiodous acid with a base: 3HIO + 2OHˉ → HIO3 + 2H2O + Iˉ Hypoiodous acid may be obtained by alkaline hydrolysis of iodine at pH 12: I2 + H2O → HIO + H+ + Iˉ Iodic acid dehydrates to iodine pentaoxide when heated at 180°C: 2HIO3 → I2H5 + H2O Iodic acid is a relatively weak monoprotic acid, the Ka value at 25°C is 1.6 x 10–1. Several species have been detected in concentrated aqueous solutions, which include IO3ˉ, H+, HIO3, (HIO3)2 and (HIO3)3. Its solution turns blue litmus red and then bleaches the litmus paper because of its strong oxidizing properties. When heated with potassium iodate, potassium hydrogen iodate is formed: HIO3 + KIO3 → KH(IO3)2 An aqueous solution of iodic acid is a strong oxidizing agent. It liberates iodine from iodides: IO3ˉ + 5Iˉ + 6H+ → 3I2 + 3H2O or, HIO3 + 5HI → 3I2 + 3H2O In an aqueous solution, iodic acid oxidizes hydrogen sulfide to sulfur: 2HIO3 + 5H2S → I2 + 6H2O + 5S The solid iodic acid reacts vigorously with sulfur, phosphorus and other nonmetals.
2. Iodic acid may be prepared by the reaction of sulfuric acid with bariumiodate. The solution is filtered to remove barium sulfate and then crystallizedto obtain iodic acid: Ba(IO3)2 + H2SO4 → BaSO4 + 2HIO3 It also may be produced by oxidation of iodine with concentrated nitric acid: 3I2 + 10HNO3 → 6HIO3 + 10NO + 2H2O Also, iodic acid may be obtained by oxidation of iodine with chlorine in diluteacidic solutions: I2 + 5Cl2 + 6H2O → 2HIO3 + 10HCl Another method of preparation involves oxidation of iodine with hydrogenperoxide: I2 + 5H2O2 → 2HIO3 + 4H2O It also may be prepared by treating hypoiodous acid with a base: 3HIO + 2OHˉ → HIO3 + 2H2O + Iˉ Hypoiodous acid may be obtained by alkaline hydrolysis of iodine at pH 12: I2 + H2O → HIO + H+ + Iˉ Iodic acid dehydrates to iodine pentaoxide when heated at 180°C: 2HIO3 → I2H5 + H2O Iodic acid is a relatively weak monoprotic acid, the Ka value at 25°C is 1.6x10-1. Several species have been detected in concentrated aqueous solutions,which include IO3-, H+, HIO3, (HIO3)2 and (HIO3)3. Its solution turns blue lit-mus red and then bleaches the litmus paper because of its strong oxidizingproperties. When heated with potassium iodate, potassium hydrogen iodate is formed: HIO3 + KIO3 → KH(IO3)2 An aqueous solution of iodic acid is a strong oxidizing agent. It liberates iodine from iodides: IO3ˉ + 5Iˉ + 6H+ → 3I2 + 3H2O or, HIO3 + 5HI → 3I2 + 3H2O In an aqueous solution, iodic acid oxidizes hydrogen sulfide to sulfur: 2HIO3 + 5H2S → I2 + 6H2O + 5S The solid iodic acid reacts vigorously with sulfur, phosphorus and other non-metals.

Chemical Properties

colorless, rhomb crystal(s) or white, crystal(s) powder(s); darkens on exposure to light; it is a moderately strong acid; used in analytical chemistry and in medicine [HAW93] [MER06]

Physical properties

Iodic acid, HIO3, can be obtained as a white solid. It dissolves in water very well, but it also exists in the pure state, as opposed to chloric acid or bromic acid. Iodic acid contains iodine in the oxidation state+5 and it is one of the most stable oxo-acids of the halogens in its pure state. When iodic acid is carefully heated, it dehydrates to iodine pentoxide. On subsequent heating, the iodine pentoxide further decomposes, giving a mixture of iodine, oxygen and lower oxides of iodine. Iodic acid can be produced by oxidizing I2 with chlorine in an aqueous solution. Iodic acid can be used to synthesize sodium or potassium iodate salts (which are used in salt as a source of iodine in the human body.

Definition

iodic acid: Any of various oxoacids of iodine, such as iodic(V) acid and iodic(VII) acid. When used without an oxidation state specifled, the term usually refers to iodic(V) acid (HIO3).

General Description

Iodic acid is the hydrated form of I2O5. Reaction of iodic acid with hydrogen iodide has been described by electrolytic dissociation theory. Combustion of mixture of chromic, iodic, sulfuric and phosphoric acids has been proposed. Its Raman spectra have been recorded. Vibrational assignment of IO3- has been evaluated.

Hazard

Toxic by ingestion, strong irritant to eyes and skin.

Purification Methods

Dissolve iodic acid in the minimum volume of hot dilute HNO3, filter and evaporate in a vacuum desiccator until crystals are formed. Collect the crystals and wash them with a little cold H2O and dry them in air in the dark. It is soluble in H2O: 269g/100mL at 20o and 295g/100mL at 40o. It is soluble in dilute EtOH and darkens on exposure to light. It is converted to HIO3.I2O5 on heating at 70o, but at 220o complete conversion to HIO3 occurs. [Lamb et al. J Am Chem Soc 42 1636 1920, Bray & Caulkins J Am Chem Soc 53 44 1931.]

Check Digit Verification of cas no

The CAS Registry Mumber 7782-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7782-68:
(6*7)+(5*7)+(4*8)+(3*2)+(2*6)+(1*8)=135
135 % 10 = 5
So 7782-68-5 is a valid CAS Registry Number.
InChI:InChI=1/Hg.2HIO3/c;2*2-1(3)4/h;2*(H,2,3,4)/p-2

7782-68-5 Well-known Company Product Price

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  • Detail
  • Alfa Aesar

  • (87681)  Iodic acid, ACS, 99.5%   

  • 7782-68-5

  • 50g

  • 759.0CNY

  • Detail
  • Alfa Aesar

  • (87681)  Iodic acid, ACS, 99.5%   

  • 7782-68-5

  • 250g

  • 2825.0CNY

  • Detail
  • Alfa Aesar

  • (A11925)  Iodic acid, 99%   

  • 7782-68-5

  • 50g

  • 314.0CNY

  • Detail
  • Alfa Aesar

  • (A11925)  Iodic acid, 99%   

  • 7782-68-5

  • 100g

  • 535.0CNY

  • Detail
  • Alfa Aesar

  • (A11925)  Iodic acid, 99%   

  • 7782-68-5

  • 250g

  • 1144.0CNY

  • Detail
  • Alfa Aesar

  • (A11925)  Iodic acid, 99%   

  • 7782-68-5

  • 1000g

  • 3634.0CNY

  • Detail
  • Sigma-Aldrich

  • (58060)  Iodicacid  puriss. p.a., ACS reagent, ≥99.5% (RT)

  • 7782-68-5

  • 58060-25G-F

  • 1,172.34CNY

  • Detail
  • Sigma-Aldrich

  • (58060)  Iodicacid  puriss. p.a., ACS reagent, ≥99.5% (RT)

  • 7782-68-5

  • 58060-100G-F

  • 2,294.37CNY

  • Detail
  • Sigma-Aldrich

  • (221929)  Iodicacid  ACS reagent, ≥99.5%

  • 7782-68-5

  • 221929-50G

  • 1,420.38CNY

  • Detail

7782-68-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name iodic acid

1.2 Other means of identification

Product number -
Other names trioxoiodic(V) acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7782-68-5 SDS

7782-68-5Synthetic route

water
7732-18-5

water

iodine
7553-56-2

iodine

A

oxygen
80937-33-3

oxygen

B

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In water oxidn. of I2 in H2O by ozone at 70°C for 2.5 h;; evapn. under vacuum at 40, then at 20°C, drying over KOH;;A n/a
B 95%
With tetrachloromethane In tetrachloromethane byproducts: COCl2, Cl(1-); oxidn. of I2 in CCl4 by ozone;; contamination with Cl(1-);;
water
7732-18-5

water

iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In hydrogenchloride byproducts: HClO4, Cl2; Electrolysis; porous anode clay-cell filled with solid I2 and 0.7n HCl; cathode cell filled with 2n-HNO3; cathode: copper tube covered with Ag and Au; anode: platinum cylinder; 20h at 15 Amp.; current yield: 85%;; evaporation and heating 24 h to 100 - 120°C; crystn.;;95%
With chlorine; silver(l) oxide In water byproducts: AgCl; pptn. of Cl(1-) with Ag2O in boiling soln.;; filtration of AgCl; evapn. of HIO3 soln.;;
In water Electrochem. Process; iodine as anode electrolysed at low current density and elevated temp. in air-tight anode space with dild. aq. HIO3-soln.; cathode space filled with dild. aq. H2SO4;;
water
7732-18-5

water

iodine trichloride
865-44-1

iodine trichloride

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In ethanol shaking of solid, moistened ICl3 containing no ICl moistened with C2H5OH and mixed with pieces of glass;; washing with ethanol;;14.29%
In ethanol shaking of solid, moistened ICl3 containing no ICl moistened with C2H5OH and mixed with pieces of glass;; washing with ethanol;;
periodic acid

periodic acid

glycerol
56-81-5

glycerol

iodic acid
7782-68-5

iodic acid

periodic acid

periodic acid

ethylene glycol
107-21-1

ethylene glycol

A

formaldehyd
50-00-0

formaldehyd

B

iodic acid
7782-68-5

iodic acid

iodobenzene
591-50-4

iodobenzene

sulfuric acid
7664-93-9

sulfuric acid

lead (IV)-oxide-anode

lead (IV)-oxide-anode

A

iodic acid
7782-68-5

iodic acid

B

(2E)-but-2-enedioic acid
110-17-8

(2E)-but-2-enedioic acid

C

p-benzoquinone
106-51-4

p-benzoquinone

Conditions
ConditionsYield
bei der elektrolytischen Oxydation mit Diaphragma;
1-chloro-2-iodyl-ethene

1-chloro-2-iodyl-ethene

water
7732-18-5

water

iodic acid
7782-68-5

iodic acid

meso-erythritol
909878-64-4

meso-erythritol

periodic acid

periodic acid

A

formaldehyd
50-00-0

formaldehyd

B

formic acid
64-18-6

formic acid

C

iodic acid
7782-68-5

iodic acid

tri-sec-butylborate

tri-sec-butylborate

hydrogen iodide
10034-85-2

hydrogen iodide

A

2-butyl iodide
513-48-4, 52152-71-3

2-butyl iodide

B

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
at 20℃;
tris-stearoyloxy-iodan

tris-stearoyloxy-iodan

water
7732-18-5

water

A

iodine
7553-56-2

iodine

B

iodic acid
7782-68-5

iodic acid

C

stearic acid
57-11-4

stearic acid

diethyl ether
60-29-7

diethyl ether

diiododioxycyanide
313677-30-4

diiododioxycyanide

sulfuric acid
7664-93-9

sulfuric acid

A

carbon dioxide
124-38-9

carbon dioxide

B

iodine
7553-56-2

iodine

C

iodic acid
7782-68-5

iodic acid

D

urea
57-13-6

urea

Conditions
ConditionsYield
at 0℃;
diethyl ether
60-29-7

diethyl ether

diiododioxycyanide
313677-30-4

diiododioxycyanide

water
7732-18-5

water

A

carbon dioxide
124-38-9

carbon dioxide

B

iodine
7553-56-2

iodine

C

iodic acid
7782-68-5

iodic acid

D

urea
57-13-6

urea

Conditions
ConditionsYield
at 0℃;
1-chloro-2-iodyl-ethene

1-chloro-2-iodyl-ethene

water
7732-18-5

water

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

iodic acid
7782-68-5

iodic acid

C

acetylene
74-86-2

acetylene

1-chloro-2-iodyl-ethene

1-chloro-2-iodyl-ethene

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

hydrogenchloride
7647-01-0

hydrogenchloride

B

iodic acid
7782-68-5

iodic acid

C

acetylene
74-86-2

acetylene

ethanol
64-17-5

ethanol

((Iodomethyl)sulfonyl)benzene
65492-21-9

((Iodomethyl)sulfonyl)benzene

sodium benzenesulfonate
873-55-2

sodium benzenesulfonate

A

2-Methyl-benzolsulfinsaeure

2-Methyl-benzolsulfinsaeure

B

hydrogen iodide
10034-85-2

hydrogen iodide

C

iodine
7553-56-2

iodine

D

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
at 200℃; im geschlossenen Rohr;
ethanol
64-17-5

ethanol

2-iodoso-4-nitrobenzoic acid
112391-34-1

2-iodoso-4-nitrobenzoic acid

furan-2,3,5(4H)-trione pyridine (1:1)

furan-2,3,5(4H)-trione pyridine (1:1)

A

2-iodo-4-nitrobenzoic acid
89459-38-1

2-iodo-4-nitrobenzoic acid

B

iodic acid
7782-68-5

iodic acid

C

4-nitro-benzoic acid
62-23-7

4-nitro-benzoic acid

water
7732-18-5

water

pyridine; compound with iodoform

pyridine; compound with iodoform

A

iodoform
75-47-8

iodoform

B

iodic acid
7782-68-5

iodic acid

C

pyridine hydriodide

pyridine hydriodide

hydrogen iodide
10034-85-2

hydrogen iodide

A

water
7732-18-5

water

B

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In neat (no solvent) decompn. by use of higher quantities of O3;;
hydrogen iodide
10034-85-2

hydrogen iodide

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In water alkaline solution;;
iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
With nitrogen trichloride In water
With chloride if lime In water
With hypochloric acid In not given oxidation;;
iodine
7553-56-2

iodine

silver(I) acetate
563-63-3

silver(I) acetate

A

iodic acid
7782-68-5

iodic acid

B

silver(I) iodide

silver(I) iodide

Conditions
ConditionsYield
With water In water Kinetics; byproducts: CH3CO2H; mechanism investigated;;
nitrogen trichloride
10025-85-1

nitrogen trichloride

iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
With water In tetrachloromethane
perchloric acid
7601-90-3

perchloric acid

iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In water oxidation at 200 - 210°C;;
With water In perchloric acid storage at ambient temp.;;
In water at various temps. using aq. HClO4 in various concns.;; no periodic acid is formed;;
iodine
7553-56-2

iodine

periodic acid
13444-71-8

periodic acid

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In not given
dihydrogen peroxide
7722-84-1

dihydrogen peroxide

iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
With hydrogenchloride In not given in presence of HCl in acidic soln.;;
With hydrogen bromide In not given in presence of HBr in acididc soln.;;
water
7732-18-5

water

iodine(3+)

iodine(3+)

A

iodine
7553-56-2

iodine

B

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In water hydrolysis of I(3+) salts;;
perchloric acid
7601-90-3

perchloric acid

iodide
14362-44-8

iodide

iodic acid
7782-68-5

iodic acid

Conditions
ConditionsYield
In water Kinetics; reaction of iodide with aq. HClO4 at 135°C under formation of I2; oxidation of I2 at 200 - 210°C;;
bismuth (III) nitrate pentahydrate

bismuth (III) nitrate pentahydrate

nitric acid
7697-37-2

nitric acid

iodic acid
7782-68-5

iodic acid

Bismuth oxide iodate
1316858-53-3

Bismuth oxide iodate

Conditions
ConditionsYield
In water High Pressure; Bi(NO3)3, HIO3, HNO3 were heated in autoclave to 200°C, held for 1 week, cooled slowly, 6°C/h, to room temp.; filtered, washed with distilled water;99%
iodic acid
7782-68-5

iodic acid

periodic acid
10450-60-9

periodic acid

Conditions
ConditionsYield
In water Electrolysis; special apparatus with Pt wire net covered with PbO2 as anode and current intensity of 12 - 15A; 24h;; evapn. of anode soln. in vac. at 40 - 60°C not to dryness, addn. of some HNO3, further evapn.; crystn.; decantation of mother lye; dissolving H5IO6 in hot concd. HNO3 soln., filtration, recrystn., heating in desiccator over KOH to 40°C;;98%
In water Electrolysis; special apparatus with Pt wire net covered with PbO2 as anode and current intensity of 12 - 15A; 24h;; evapn. of anode soln. in purified air stream at 70 - 85°C; loss by partial formation of HIO3;;
In sulfuric acid Electrolysis; 50% HIO3 soln.; anode region: clay cell with MnO2 anode; cathode region: filled with 2n H2SO4 soln., Pt cathode; current yield: 0.39%;;
rubidium carbonate

rubidium carbonate

aluminum(III) nitrate nonahydrate

aluminum(III) nitrate nonahydrate

iodic acid
7782-68-5

iodic acid

Al(3+)*2Rb(1+)*6IO3(1-)*H(1+)

Al(3+)*2Rb(1+)*6IO3(1-)*H(1+)

Conditions
ConditionsYield
In water at 170℃; for 96h; High pressure;96%
bismuth (III) nitrate pentahydrate

bismuth (III) nitrate pentahydrate

hydrogen fluoride
7664-39-3

hydrogen fluoride

iodic acid
7782-68-5

iodic acid

potassium carbonate
584-08-7

potassium carbonate

KBi2(IO3)2F5

KBi2(IO3)2F5

Conditions
ConditionsYield
In water at 230℃; for 96h;95%
rubidium chloride

rubidium chloride

germanium dioxide

germanium dioxide

iodic acid
7782-68-5

iodic acid

2Rb(1+)*Ge(4+)*6(IO3)(1-)=Rb2Ge(IO3)6

2Rb(1+)*Ge(4+)*6(IO3)(1-)=Rb2Ge(IO3)6

Conditions
ConditionsYield
In water at 230℃; for 96h; High pressure;95%
cesium chloride

cesium chloride

germanium dioxide

germanium dioxide

iodic acid
7782-68-5

iodic acid

2Cs(1+)*Ge(4+)*6(IO3)(1-)=Cs2Ge(IO3)6

2Cs(1+)*Ge(4+)*6(IO3)(1-)=Cs2Ge(IO3)6

Conditions
ConditionsYield
In water at 230℃; for 96h; High pressure;95%
potassium chloride

potassium chloride

germanium dioxide

germanium dioxide

iodic acid
7782-68-5

iodic acid

2K(1+)*Ge(4+)*6(IO3)(1-)=K2Ge(IO3)6

2K(1+)*Ge(4+)*6(IO3)(1-)=K2Ge(IO3)6

Conditions
ConditionsYield
In water at 230℃; for 96h; High pressure;95%
iodic acid
7782-68-5

iodic acid

caesium carbonate
534-17-8

caesium carbonate

Cs2(I3O8)(IO3), β, monoclinic

Cs2(I3O8)(IO3), β, monoclinic

Conditions
ConditionsYield
In water High Pressure; Cs2CO3, HIO3 and H2O mixed, placed in autoclave, heated to 220°C,held for 2 d, cooled to room temp. at 10°C/h; filtered off, washed with water, dried at 80°C;94%
gallium(III) nitrate nonahydrate

gallium(III) nitrate nonahydrate

iodic acid
7782-68-5

iodic acid

potassium carbonate
584-08-7

potassium carbonate

Ga(3+)*2K(1+)*6IO3(1-)*H(1+)

Ga(3+)*2K(1+)*6IO3(1-)*H(1+)

Conditions
ConditionsYield
In water at 170℃; for 96h; High pressure;94%
5,5-difluoro-1,3,7,9-tetramethyl-10-(4-(prop-2-yn-1-yloxy)phenyl)-5H-4λ4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-5-uide

5,5-difluoro-1,3,7,9-tetramethyl-10-(4-(prop-2-yn-1-yloxy)phenyl)-5H-4λ4-dipyrrolo[1,2-c:2',1'-f][1,3,2]diazaborinin-5-uide

iodine
7553-56-2

iodine

iodic acid
7782-68-5

iodic acid

4,4-difluoro-2,6-diiodo-1,3,5,7-tetramethyl-8-(4-propargyloxyphenyl)-4-bora-3a,4a-diaza-s-indacene

4,4-difluoro-2,6-diiodo-1,3,5,7-tetramethyl-8-(4-propargyloxyphenyl)-4-bora-3a,4a-diaza-s-indacene

Conditions
ConditionsYield
In ethanol at 60℃; for 2h; Inert atmosphere;94%
rubidium carbonate

rubidium carbonate

iodic acid
7782-68-5

iodic acid

rubidium iodate
13446-76-9

rubidium iodate

Conditions
ConditionsYield
In water at 230℃; for 83h; Autoclave;93%
In water quantitative reaction of a saturated soln. of iodic acid with Rb2CO3; pptd.; washed with ice cold water; filtered; dried;
zinc(II) nitrate hexahydrate

zinc(II) nitrate hexahydrate

hydrogen fluoride
7664-39-3

hydrogen fluoride

iodic acid
7782-68-5

iodic acid

ZnIO3F

ZnIO3F

Conditions
ConditionsYield
With potassium carbonate at 220℃; for 96h; Autoclave;92%
iodic acid
7782-68-5

iodic acid

caesium carbonate
534-17-8

caesium carbonate

Cs2I4O11, β

Cs2I4O11, β

Conditions
ConditionsYield
In water High Pressure; Cs2CO3 and HIO3 in water were heated in Teflon-lined autoclave to 220°C for 4 days; cooled slowly at 6°C/h, ppt. was filtered and washed with water and EtOH;91%
iodic acid
7782-68-5

iodic acid

lithium carbonate
554-13-2

lithium carbonate

titanium(IV) oxide

titanium(IV) oxide

lithium hexaiodatotitanate

lithium hexaiodatotitanate

Conditions
ConditionsYield
In water High Pressure; Li2CO3, TiO2, HIO3 and H2O placed in autoclave, heated to 230°C for 4 d, cooled to room temp. at 6°C/h; washed with H2O, EtOH;91%
thallium(I) carbonate

thallium(I) carbonate

iodic acid
7782-68-5

iodic acid

thallium(I,III) iodate

thallium(I,III) iodate

Conditions
ConditionsYield
In water byproducts: I2; High Pressure; combining of Tl2CO3 and HIO3 with H2O; placing in Teflon-lined autoclave; sealing; heating to 230°C for 4 ds; slow cooling to room temp. at 6°C/h; decanting; filtration, washing with H2O and acetone;90%
barium(II) chloride dihydrate
10361-37-2

barium(II) chloride dihydrate

water
7732-18-5

water

germanium dioxide

germanium dioxide

iodic acid
7782-68-5

iodic acid

6IO3(1-)*Ge(4+)*Ba(2+)*H2O

6IO3(1-)*Ge(4+)*Ba(2+)*H2O

Conditions
ConditionsYield
at 230℃; for 96h; High pressure;90%
barium(II) chloride dihydrate
10361-37-2

barium(II) chloride dihydrate

hydrogen fluoride
7664-39-3

hydrogen fluoride

vanadia

vanadia

iodic acid
7782-68-5

iodic acid

FI2O8V(2-)*Ba(2+)

FI2O8V(2-)*Ba(2+)

Conditions
ConditionsYield
In water at 220℃; for 48h; High pressure; Autoclave;90%
rubidium carbonate

rubidium carbonate

gallium(III) nitrate nonahydrate

gallium(III) nitrate nonahydrate

iodic acid
7782-68-5

iodic acid

Ga(3+)*2Rb(1+)*6IO3(1-)*H(1+)

Ga(3+)*2Rb(1+)*6IO3(1-)*H(1+)

Conditions
ConditionsYield
In water at 170℃; for 96h; High pressure;90%
cerium(IV) oxide

cerium(IV) oxide

lanthanum(III) oxide

lanthanum(III) oxide

iodic acid
7782-68-5

iodic acid

La0.3Ce9(IO3)36

La0.3Ce9(IO3)36

Conditions
ConditionsYield
With sulfuric acid at 230℃; for 72h; Autoclave; High pressure;90%
stannous fluoride

stannous fluoride

iodic acid
7782-68-5

iodic acid

2IO3(1-)*Sn(4+)*2F(1-)

2IO3(1-)*Sn(4+)*2F(1-)

Conditions
ConditionsYield
With ammonium fluoride-hydrogen fluoride at 250℃; for 72h; Autoclave;90%
barium(II) chloride dihydrate
10361-37-2

barium(II) chloride dihydrate

iodic acid
7782-68-5

iodic acid

titanium(IV) oxide

titanium(IV) oxide

6IO3(1-)*Ba(2+)*Ti(4+)

6IO3(1-)*Ba(2+)*Ti(4+)

Conditions
ConditionsYield
With hydrogen fluoride In water at 220℃; for 72h; Autoclave;90%
iodic acid
7782-68-5

iodic acid

potassium carbonate
584-08-7

potassium carbonate

zirconium(IV) oxide
7440-67-7

zirconium(IV) oxide

potassium zirconium iodate,

potassium zirconium iodate,

Conditions
ConditionsYield
In water at 230℃; for 4h; Autoclave; High pressure;89%
indium(III) nitrate monohydrate

indium(III) nitrate monohydrate

iodic acid
7782-68-5

iodic acid

silver nitrate

silver nitrate

6IO3(1-)*3Ag(1+)*In(3+)

6IO3(1-)*3Ag(1+)*In(3+)

Conditions
ConditionsYield
With nitric acid In water at 230℃; for 72h; Autoclave;89%
aluminum(III) nitrate nonahydrate

aluminum(III) nitrate nonahydrate

iodic acid
7782-68-5

iodic acid

potassium carbonate
584-08-7

potassium carbonate

Al(3+)*2K(1+)*6IO3(1-)*H(1+)

Al(3+)*2K(1+)*6IO3(1-)*H(1+)

Conditions
ConditionsYield
In water at 170℃; for 96h; High pressure;86%
iodic acid
7782-68-5

iodic acid

caesium carbonate
534-17-8

caesium carbonate

Cs2I4O11

Cs2I4O11

Conditions
ConditionsYield
With Nb2O5 In water High Pressure; hydrothermal react.; mixt. Cs2CO3, HIO3, Nb2O5 (1:28.5:1.9 mol) in H2O loaded into Teflon-lined autoclave; gradually heated to 220°C and held for 4 d; cooled slowly (6°C/h) to room temp.; decanted; product washed (H2O, EtOH); manual sepn.; TGA;85%
barium(II) chloride dihydrate
10361-37-2

barium(II) chloride dihydrate

iodic acid
7782-68-5

iodic acid

titanium(IV) oxide

titanium(IV) oxide

6IO3(1-)*Ba(2+)*Ti(4+)

6IO3(1-)*Ba(2+)*Ti(4+)

Conditions
ConditionsYield
With hydrogen fluoride In water at 220℃; for 72h; Autoclave;85%
lanthanum(III) oxide

lanthanum(III) oxide

iodic acid
7782-68-5

iodic acid

lanthanum iodate

lanthanum iodate

Conditions
ConditionsYield
In water High Pressure; La2O3 and HIO3 in water were heated in Teflon-lined autoclave to 220°C for 4 days; cooled slowly at 6°C/h, ppt. was filtered and washed with water and EtOH;83%
rubidium carbonate

rubidium carbonate

iodic acid
7782-68-5

iodic acid

2Rb(1+)*I3O8(1-)*IO3(1-)*2HIO3*H2O=Rb2(I3O8)(IO3)(HIO3)2(H2O)

2Rb(1+)*I3O8(1-)*IO3(1-)*2HIO3*H2O=Rb2(I3O8)(IO3)(HIO3)2(H2O)

Conditions
ConditionsYield
In water High Pressure; Rb2CO3, HIO3 and H2O mixed, placed in autoclave, heated to 220°C,held for 2 d, cooled to room temp. at 10°C/h; filtered off, washed with water, dried at 60°C;82%

7782-68-5Relevant articles and documents

Scott, A.,Arbuckle, W.

, p. 302 - 302 (1901)

Bray, W. C.,Caulkins, A. L.

, p. 44 - 44 (1931)

Kinetics of iodous acid disproportionation

Schmitz, Guy,Furrow, Stanley D.

supporting information, p. 525 - 530 (2013/07/26)

The iodous acid disproportionation is autocatalytic, and it is not easy to measure the rate constant of the step 2IO2H → IO 3- + IOH + H+ separately. Hg(II) was used previously to suppress the autocatalytic pathway, but this method presents difficulties discussed in this work. A more effective method is the use of crotonic acid, an effective IOH scavenger. It suppresses side reactions, and a purely second-order rate law is obtained. The rate constant decreases from 5 to 0.2 M-1 s-1 when the sulfuric acid concentration increases from 0.08 to 0.60 M. The observed decrease could be explained if IO 2- reacts faster than IO2H. This may have consequences for the mechanism of the oscillating Bray-Liebhafsky reaction.

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