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7790-99-0

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7790-99-0 Usage

Chemical Properties

dark red or brown solid and/or liquid

Physical properties

Colorless gas; mold-like pungent odor; melting point 6.45°C; sublimes at4.77°C; supercools to a colorless liquid that boils at 4.5°C; liquid density2.8g/mL at 6°C; soluble in water.

Uses

Different sources of media describe the Uses of 7790-99-0 differently. You can refer to the following data:
1. Iodine monochloride is used to estimate theiodine values of fats and oils and as a topicalanti-infective (Merck 1996).
2. For determination of iodine absorption number of fatsIodine monochloride is used as a catalyst in organic synthesis. It is the source of electrophilic iodine in the synthesis of certain aromatic iodides. It is used to determine the iodine value of a substance.
3. In Wijs' solution (iodine monochloride in glacial acetic acid), used to determine iodine values of fats and oils.

Preparation

Iodine monochloride is prepared by the action of liquid or dry chlorine on astoichiometric quantity of solid iodine. Aqueous solutions of ICl are preparedby passing chlorine gas into a suspension of iodine in moderately stronghydrochloric acid: 5I2 + 4HCl + 3Cl2 → 10ICl + 2H2 Alternatively, iodine monochloride may be made by oxidation of iodine withiodic acid in strong hydrochloric acid solution: 2I2 + HIO3 + 2HCl → 2ICl + 3HIO

General Description

Black crystals or a reddish brown oily liquid with a pungent odor. Melting point 27°C (alpha form) or 14°C (beta form). Corrosive to metals and tissue.

Air & Water Reactions

Reacts with air to form iodine pentaoxide (I2O5), which decomposes into iodine (I2) and oxygen (O2) with heat beginning at 275°C and proceeding rapidly at 350°C. Soluble in water; reacts with water or steam to produce toxic and corrosive fumes [Lewis].

Reactivity Profile

Iodine monochloride is moderately explosive when heated [Lewis]. Reacts with rubber and many organic materials. Enflames (after a period of delay) with aluminum foil [Mellor 2:119(1946-1947)]. Reacts dangerously with other active metals. Reacts vigorously with cadmium sulfide, lead sulfide, silver sulfide, and zinc sulfide [Mellor 2, Supp. 1:502(1956)]. Combines very exothermically with phosphorus trichloride [Mellor 2, Supp. 1:502(1956)]. Forms Iodine pentaoxide in air which reacts explosively when warmed with carbon, sulfur, sugar, resin, or powdered combustible elements [Mellor 8: 841(1946-1947)].

Health Hazard

Different sources of media describe the Health Hazard of 7790-99-0 differently. You can refer to the following data:
1. Iodine monochloride is highly corrosive tothe skin. Contact with the skin causes burns and dark patches. Upon contact, washimmediately with 15-20% HCl. Vapors areirritating to the skin, eyes, and mucous mem branes. The compound is moderate to highlytoxic by an oral route. The lethal dose in ratsis 59 mg/kg (NIOSH 1986).
2. TOXIC; inhalation, ingestion or contact (skin, eyes) with vapors, dusts or substance may cause severe injury, burns or death. Reaction with water or moist air will release toxic, corrosive or flammable gases. Reaction with water may generate much heat that will increase the concentration of fumes in the air. Fire will produce irritating, corrosive and/or toxic gases. Runoff from fire control or dilution water may be corrosive and/or toxic and cause pollution.

Fire Hazard

Non-combustible, substance itself does not burn but may decompose upon heating to produce corrosive and/or toxic fumes. Vapors may accumulate in confined areas (basement, tanks, hopper/tank cars etc.). Substance will react with water (some violently), releasing corrosive and/or toxic gases and runoff. Contact with metals may evolve flammable hydrogen gas. Containers may explode when heated or if contaminated with water.

Purification Methods

Purify it by repeated fractional crystallisation from its melt at low temperatures. The black crystals melt to a red-brown liquid. [Cornog & Karges Inorg Synth I 165 1939.]

Check Digit Verification of cas no

The CAS Registry Mumber 7790-99-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,9 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7790-99:
(6*7)+(5*7)+(4*9)+(3*0)+(2*9)+(1*9)=140
140 % 10 = 0
So 7790-99-0 is a valid CAS Registry Number.
InChI:InChI=1/ClI/c1-2

7790-99-0 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Detail
  • Alfa Aesar

  • (39104)  Iodine monochloride   

  • 7790-99-0

  • 25g

  • 401.0CNY

  • Detail
  • Alfa Aesar

  • (39104)  Iodine monochloride   

  • 7790-99-0

  • 100g

  • 692.0CNY

  • Detail
  • Alfa Aesar

  • (39104)  Iodine monochloride   

  • 7790-99-0

  • 500g

  • 1894.0CNY

  • Detail
  • Alfa Aesar

  • (H31938)  Iodine monochloride, 1M soln. in dichloromethane   

  • 7790-99-0

  • 100ml

  • 716.0CNY

  • Detail
  • Alfa Aesar

  • (H31938)  Iodine monochloride, 1M soln. in dichloromethane   

  • 7790-99-0

  • 500ml

  • 2197.0CNY

  • Detail
  • Alfa Aesar

  • (44348)  Iodine monochloride, ACS   

  • 7790-99-0

  • 25g

  • 500.0CNY

  • Detail
  • Alfa Aesar

  • (44348)  Iodine monochloride, ACS   

  • 7790-99-0

  • 100g

  • 1574.0CNY

  • Detail
  • Alfa Aesar

  • (44348)  Iodine monochloride, ACS   

  • 7790-99-0

  • 500g

  • 7137.0CNY

  • Detail
  • Alfa Aesar

  • (42647)  Iodine monochloride, approx. 0.22N soln. in glacial acetic acid   

  • 7790-99-0

  • 500ml

  • 486.0CNY

  • Detail
  • Alfa Aesar

  • (42647)  Iodine monochloride, approx. 0.22N soln. in glacial acetic acid   

  • 7790-99-0

  • 1L

  • 576.0CNY

  • Detail
  • Alfa Aesar

  • (42647)  Iodine monochloride, approx. 0.22N soln. in glacial acetic acid   

  • 7790-99-0

  • 4L

  • 2301.0CNY

  • Detail
  • Fluka

  • (35071)  Wijssolution  volumetric, 0.1 M ICl

  • 7790-99-0

  • 35071-1L

  • 1,067.04CNY

  • Detail

7790-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Iodine monochloride

1.2 Other means of identification

Product number -
Other names IODINE MONOCHLORIDE

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:7790-99-0 SDS

7790-99-0Synthetic route

sodium chlorate

sodium chlorate

iodine
7553-56-2

iodine

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
With hydrogenchloride; sodium chloride In water at 25 - 27℃; for 19h;99.6%
With hydrogenchloride; sodium chloride In water at 20 - 50℃;
iodine
7553-56-2

iodine

chlorine
7782-50-5

chlorine

A

Iodine monochloride
7790-99-0

Iodine monochloride

B

iodine trichloride
865-44-1

iodine trichloride

Conditions
ConditionsYield
In neat (no solvent) passing dry chlorine over dry iodine;; distillation in stream of chlorine at 100-101.5°C;;A 85%
B n/a
In neat (no solvent) passing dry chlorine over dry iodine;; distillation at 100-101.5°C;;A 35%
B n/a
In neat (no solvent) excess of iodine;
In neat (no solvent)
iodine
7553-56-2

iodine

1,3-dichloro-[1,3,5]triazinane-2,4,6-trione
2782-57-2

1,3-dichloro-[1,3,5]triazinane-2,4,6-trione

A

cyanuric acid
108-80-5

cyanuric acid

B

triiodoisocyanuric acid
27694-85-5

triiodoisocyanuric acid

C

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
absence of moist, 24h, 180-230°C, every 30 min ICl removed,; removing of (HNCO)3: sublimation (220-230°C, 0.1 Torr), purity >99;A n/a
B 75.6%
C n/a
dichloroiodomethane
594-04-7

dichloroiodomethane

A

methylene chloride
74-87-3

methylene chloride

B

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
beim Erwaermen ueber den Zersetzungspunkt;
dichloroiodomethane
594-04-7

dichloroiodomethane

water
7732-18-5

water

A

methylene chloride
74-87-3

methylene chloride

B

Iodine monochloride
7790-99-0

Iodine monochloride

sulfuryl dichloride
7791-25-5

sulfuryl dichloride

iodine
7553-56-2

iodine

A

Iodine monochloride
7790-99-0

Iodine monochloride

B

iodine trichloride
865-44-1

iodine trichloride

Conditions
ConditionsYield
In not given in presence of AlCl3;;
tetrachloromethane
56-23-5

tetrachloromethane

iodine
7553-56-2

iodine

A

1,1,2,2-tetrachloroethylene
127-18-4

1,1,2,2-tetrachloroethylene

B

trichloroiodomethane
594-22-9

trichloroiodomethane

C

hexachloroethane
67-72-1

hexachloroethane

D

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
In tetrachloromethane other Radiation; γ-radiation of I2 soln. in CCl4; yield depends on concn. of I2 and on dose of radiation;;
tetrachloromethane
56-23-5

tetrachloromethane

iodine
7553-56-2

iodine

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
In tetrachloromethane other Radiation; γ-radiation of I2 soln. in CCl4 saturated with air;;
iodine
7553-56-2

iodine

mercury dichloride

mercury dichloride

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
In water
iodine
7553-56-2

iodine

mercury dichloride

mercury dichloride

A

Iodine monochloride
7790-99-0

Iodine monochloride

B

mercury(II) iodide

mercury(II) iodide

Conditions
ConditionsYield
In water 6h heating to 250°C in sealed tube;;
In water 6h heating to 250°C in sealed tube;;
In not given at heating to 250°C in sealed tube; molar rate = 1:1;;
Conditions
ConditionsYield
In gaseous matrix byproducts: CH3; reaction of in situ generated Cl atoms (by microwave discharge from Cl2/He or Cl2/Ne mixt., Cl atom beam velocity 1150-1950 m/s) with alkyl iodide according to: S. M. A. Hoffmann, D. J. Smith, R. Grice, Mol. Phys. 49 (1983) 621; mass spectroscopy;
hydrogenchloride
7647-01-0

hydrogenchloride

cadmium(II) sulphide

cadmium(II) sulphide

A

sulfuric acid
7664-93-9

sulfuric acid

B

Iodine monochloride
7790-99-0

Iodine monochloride

C

cadmium(II) chloride
10108-64-2

cadmium(II) chloride

Conditions
ConditionsYield
With potassium iodate In not given byproducts: S, KCl, H2O; oxidation with KIO3 in presence of HCl;;
With KIO3 In not given byproducts: S, KCl, H2O; oxidation with KIO3 in presence of HCl;;
zinc sulfide

zinc sulfide

A

sulfuric acid
7664-93-9

sulfuric acid

B

potassium chloride

potassium chloride

C

Iodine monochloride
7790-99-0

Iodine monochloride

D

zinc(II) chloride
7646-85-7

zinc(II) chloride

Conditions
ConditionsYield
With hydrogenchloride; potassium iodate In not given byproducts: S, H2O; oxidation with KIO3; HCl-concentration: 65 vol.% HCl;;
zinc sulfide

zinc sulfide

A

potassium chloride

potassium chloride

B

Iodine monochloride
7790-99-0

Iodine monochloride

C

zinc(II) chloride
7646-85-7

zinc(II) chloride

Conditions
ConditionsYield
With hydrogenchloride; potassium iodate In not given byproducts: S, H2O; oxidation with KIO3; HCl-concentration: < 15 vol.% HCl;;
chloride
16887-00-6

chloride

iodonium-ion

iodonium-ion

A

Iodine monochloride
7790-99-0

Iodine monochloride

B

lead(II) chloride

lead(II) chloride

Conditions
ConditionsYield
In diethyl ether; water Electrochem. Process;
iodide
14362-44-8

iodide

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
With hydrogenchloride; cerium (IV) sulfate In hydrogenchloride strongly acidic solution;;
In hydrogenchloride
iodide
14362-44-8

iodide

chlorine
7782-50-5

chlorine

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
In neat (no solvent) byproducts: metal chloride; formation from metal iodides and liquid Cl2;;
iodide
14362-44-8

iodide

Iodine monochloride
7790-99-0

Iodine monochloride

Conditions
ConditionsYield
In not given acidic soln.; ClO3(1-) : I(1-) = 1 : 3;;
Conditions
ConditionsYield
In gaseous matrix byproducts: C2H5; reaction of in situ generated Cl atoms (by microwave discharge from Cl2/He or Cl2/Ne mixt., Cl atom beam velocity 1150-1950 m/s) with alkyl iodide according to: S. M. A. Hoffmann, D. J. Smith, R. Grice, Mol. Phys. 49 (1983) 621; mass spectroscopy;
Conditions
ConditionsYield
In gaseous matrix byproducts: C3H7; reaction of in situ generated Cl atoms (by microwave discharge from Cl2/He or Cl2/Ne mixt., Cl atom beam velocity 1150-1950 m/s) with alkyl iodide according to: S. M. A. Hoffmann, D. J. Smith, R. Grice, Mol. Phys. 49 (1983) 621; mass spectroscopy;
Iodine monochloride
7790-99-0

Iodine monochloride

triphenylbismuthane
603-33-8

triphenylbismuthane

diphenylbismuth(III) chloride
5153-28-6

diphenylbismuth(III) chloride

Conditions
ConditionsYield
In diethyl ether byproducts: C6H5I;100%
In diethyl ether byproducts: C6H5I;100%
byproducts: C6H5I;
Iodine monochloride
7790-99-0

Iodine monochloride

sodium sulfate
7757-82-6

sodium sulfate

sodium chloride
7647-14-5

sodium chloride

Conditions
ConditionsYield
evaporated, with excess of ICl;100%
evaporated, with excess of ICl;100%
tris(2,4-pentanedionato)ruthenium(III)
31378-26-4, 31378-27-5, 14284-93-6

tris(2,4-pentanedionato)ruthenium(III)

Iodine monochloride
7790-99-0

Iodine monochloride

ruthenium tris-γ-chloroacetylacetonate

ruthenium tris-γ-chloroacetylacetonate

Conditions
ConditionsYield
In benzene immediate reaction;100%
In benzene100%
Iodine monochloride
7790-99-0

Iodine monochloride

(Me3Si)3C(SnMe2Cl)
71084-86-1

(Me3Si)3C(SnMe2Cl)

trichloro(tris(trimethylsilyl)methyl)stannane
71084-75-8

trichloro(tris(trimethylsilyl)methyl)stannane

Conditions
ConditionsYield
In tetrachloromethane Ar-atmosphere; dropwise addn. of excess ICl to Sn-compd., stirring for 1h; solvent removal, recrystn. (hexane);99%
C25H27NO8PdS

C25H27NO8PdS

Iodine monochloride
7790-99-0

Iodine monochloride

C25H27ClINO8PdS

C25H27ClINO8PdS

Conditions
ConditionsYield
In dichloromethane for 0.0833333h; Inert atmosphere;99%
Iodine monochloride
7790-99-0

Iodine monochloride

TsiSnMe3
28830-25-3

TsiSnMe3

(Me3Si)3C(SnMe2Cl)
71084-86-1

(Me3Si)3C(SnMe2Cl)

Conditions
ConditionsYield
In tetrachloromethane; dichloromethane solution of ICl (1.32 mmol) in CCl4 was added dropwise (0,5 h) to a stirred solution of tin compound (1.26 mmol) in 1/4 CH2Cl2/CCl4 at room temperature; reaction was monitored by (1)H-NMR spectroscopy; solvent was removed under reduced pressure; pink residue kept under vacuum for 3 h; product was identified by comparison of its spectra with an authentic sample;98%
Iodine monochloride
7790-99-0

Iodine monochloride

(Me3Si)2C(SnMe3)2
60950-96-1

(Me3Si)2C(SnMe3)2

(Me3Si)2C(SnMe2Cl)2
60739-99-3

(Me3Si)2C(SnMe2Cl)2

Conditions
ConditionsYield
In tetrachloromethane solution of ICl (2.5 mmol) in CCl4 was added (stirring) to a solution of tin compound (1.02 mmol); progress of reaction was monitored by (1)H-NMR spectroscopy;; solvent was removed, residue kept under vacuum for 3 h;;98%
caesium cobalt(III)bis(1,2-dicarboilide)

caesium cobalt(III)bis(1,2-dicarboilide)

Iodine monochloride
7790-99-0

Iodine monochloride

caesium 3,3'-commo-bis(decahydro-8-iodo-1,2-dicarba-3-cobalta-closo-dodecaborate)(1-)
84913-27-9

caesium 3,3'-commo-bis(decahydro-8-iodo-1,2-dicarba-3-cobalta-closo-dodecaborate)(1-)

Conditions
ConditionsYield
In ethanol under N2 atm. ICl was added to soln. Cs(3,3'-Co(1,2-C2B9H11)2) in EtOH and refluxed for 10 h; Na2SO3 in water was added and refluxed for 5 min, soln. was concd., ppt.was filtered off, washed with water andpetroleum ether, and dried in va cuo; elem. anal.;98%
Iodine monochloride
7790-99-0

Iodine monochloride

(Me3Si)3C(SnMe2Cl)
71084-86-1

(Me3Si)3C(SnMe2Cl)

dichloro(methyl)(tris(trimethylsilyl)methyl)stannane
71084-87-2

dichloro(methyl)(tris(trimethylsilyl)methyl)stannane

Conditions
ConditionsYield
In tetrachloromethane Ar-atmosphere; dropwise addn. of ICl to equimolar amt. of Sn-compd.; solvent removal (after 30 min), recrystn. (hexane);98%
cesium carba-closo-dodecaborate

cesium carba-closo-dodecaborate

Iodine monochloride
7790-99-0

Iodine monochloride

cesium 2,3,4,5,6,7,8,9,10,11,12-undecaiodocarba-closo-dodecaborate

cesium 2,3,4,5,6,7,8,9,10,11,12-undecaiodocarba-closo-dodecaborate

Conditions
ConditionsYield
In 1,1,2,2-tetrachloroethane at 150℃; for 72h; Inert atmosphere; Schlenk technique;98%
triphenyl[(E)-1,1,1-trifluorotridec-2-en-2-yl]germane

triphenyl[(E)-1,1,1-trifluorotridec-2-en-2-yl]germane

Iodine monochloride
7790-99-0

Iodine monochloride

dichlorophenyl[(E)-1,1,1-trifluorotridec-2-en-2-yl]germane

dichlorophenyl[(E)-1,1,1-trifluorotridec-2-en-2-yl]germane

Conditions
ConditionsYield
In chloroform at 50℃; for 4h; Inert atmosphere;98%
In chloroform Inert atmosphere; Heating;98%
C25H27Br2NO8PdS

C25H27Br2NO8PdS

Iodine monochloride
7790-99-0

Iodine monochloride

C25H27BrClNO8PdS

C25H27BrClNO8PdS

Conditions
ConditionsYield
In dichloromethane for 0.166667h; Inert atmosphere;98%
C27H27BN2OSi
1449074-41-2

C27H27BN2OSi

Iodine monochloride
7790-99-0

Iodine monochloride

C19H16BIN2O
1449074-52-5

C19H16BIN2O

Conditions
ConditionsYield
Stage #1: C27H27BN2OSi; Iodine monochloride In dichloromethane at -78℃; for 18h; Inert atmosphere;
Stage #2: With 2-methyl-but-2-ene In dichloromethane at 20℃; for 0.0833333h; Inert atmosphere;
98%
ethoxy(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane
213900-42-6

ethoxy(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane

Iodine monochloride
7790-99-0

Iodine monochloride

chloro(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane
113629-70-2

chloro(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane

Conditions
ConditionsYield
In tetrachloromethane Ar-atmosphere; dropwise addn. of ICl to equimolar amt. of Sn-compd., stirring for 1 h; solvent removal, recrystn. (hexane);96%
trimethyl(trifluorsilyl)stannane
126087-12-5

trimethyl(trifluorsilyl)stannane

Iodine monochloride
7790-99-0

Iodine monochloride

A

chlorotrifluorosilane
14049-36-6

chlorotrifluorosilane

B

trimethylstannyl iodide
811-73-4

trimethylstannyl iodide

Conditions
ConditionsYield
A 96%
B n/a
chloro(diphenyl)(tris(trimethylsilyl)methyl)stannane
73056-68-5

chloro(diphenyl)(tris(trimethylsilyl)methyl)stannane

Iodine monochloride
7790-99-0

Iodine monochloride

trichloro(tris(trimethylsilyl)methyl)stannane
71084-75-8

trichloro(tris(trimethylsilyl)methyl)stannane

Conditions
ConditionsYield
In tetrachloromethane Ar-atmosphere; addn. of slight excess of ICl to Sn-compd., stirring overnight; solvent removal, recrystn. (hexane);96%
(1,2,3,4-tetrakis(carbomethoxy)-1,3-pentadienyl)palladium(II)(8-(methylthio)quinoline)

(1,2,3,4-tetrakis(carbomethoxy)-1,3-pentadienyl)palladium(II)(8-(methylthio)quinoline)

Iodine monochloride
7790-99-0

Iodine monochloride

C22H21ClINO8PdS

C22H21ClINO8PdS

Conditions
ConditionsYield
In dichloromethane for 0.0833333h; Inert atmosphere;96%
ethoxy(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane
213900-42-6

ethoxy(dimethyl)(tris(dimethylphenylsilyl)methyl)stannane

Iodine monochloride
7790-99-0

Iodine monochloride

dichloro(methyl)(tris(dimethylphenylsilyl)methyl)stannane
213900-43-7

dichloro(methyl)(tris(dimethylphenylsilyl)methyl)stannane

Conditions
ConditionsYield
In tetrachloromethane Ar-atmosphere; dropwise addn. of excess ICl to Sn-compd., stirring for 3h; solvent removal, recrystn. (hexane);95%
C63H50ClO2OsP3(1+)*Cl(1-)

C63H50ClO2OsP3(1+)*Cl(1-)

Iodine monochloride
7790-99-0

Iodine monochloride

C63H50ClIO2OsP3(2+)*2Cl2I(1-)

C63H50ClIO2OsP3(2+)*2Cl2I(1-)

Conditions
ConditionsYield
In dichloromethane at 20℃; for 3h;95%
C26H29NO8PdS

C26H29NO8PdS

Iodine monochloride
7790-99-0

Iodine monochloride

C26H29ClINO8PdS

C26H29ClINO8PdS

Conditions
ConditionsYield
In dichloromethane for 0.0833333h; Inert atmosphere;95%
tetramethylammonium ammine-undecahydro-closo-doedecaborate

tetramethylammonium ammine-undecahydro-closo-doedecaborate

iodine
7553-56-2

iodine

Iodine monochloride
7790-99-0

Iodine monochloride

tetramethlyammonium chloride
75-57-0

tetramethlyammonium chloride

B12H2I11N(2-)*H(1+)*C4H12N(1+)

B12H2I11N(2-)*H(1+)*C4H12N(1+)

Conditions
ConditionsYield
Stage #1: tetramethylammonium ammine-undecahydro-closo-doedecaborate; iodine In dichloromethane at 20 - 80℃; for 3h; Sealed tube;
Stage #2: Iodine monochloride In dichloromethane at 300℃; for 5h; Sealed tube;
Stage #3: tetramethlyammonium chloride In water
95%
(η5-C5Me5)Co(Et2C2B4H4)

(η5-C5Me5)Co(Et2C2B4H4)

Iodine monochloride
7790-99-0

Iodine monochloride

(C5Me5)Co(2,3-Et2C2B4H-4,5,6-I3)

(C5Me5)Co(2,3-Et2C2B4H-4,5,6-I3)

Conditions
ConditionsYield
In dichloromethane under N2; Co complex dissolved in dry CH2Cl2 at 0°C, ICl in CH2Cl2 added dropwise, stirred at 0°C for 2 h, then at room temp. for 4 h; satd. aq. soln. of sodium thiosulfate added, aq. layer sepd., washed with CH2Cl2, the combined org. materials washed with concd. aq. NaCl, driedover MgSO4, evapd.; elem. anal.;94%
3-iodo-1,2-dicarba-closo-dodecaborane
137495-63-7

3-iodo-1,2-dicarba-closo-dodecaborane

Iodine monochloride
7790-99-0

Iodine monochloride

3,4,5,7,8,9,10,11,12-nonaiodo-1,2-dicarba-closo-dodecaborane
634917-31-0

3,4,5,7,8,9,10,11,12-nonaiodo-1,2-dicarba-closo-dodecaborane

Conditions
ConditionsYield
With NaHSO3; Zn; triflic acid In further solvent(s) N2, triflic acid, ICl, borane heated at 90°C for 3 d, allowed to cool to room temp., cold water, aq. NaHSO3 added, ppt. filtered, dissolved (ethyl acetate), Zn added; filtered, solvent evapd. (vac.), recrystd. (ethyl acetate); elem. anal.;94%
2-methoxy-3-(trimethylsilyl)phenylboronic acid
1257792-97-4

2-methoxy-3-(trimethylsilyl)phenylboronic acid

Iodine monochloride
7790-99-0

Iodine monochloride

3-iodo-2-methoxyphenylboronic acid
1257793-14-8

3-iodo-2-methoxyphenylboronic acid

Conditions
ConditionsYield
In chloroform (Ar); stirring stoich. mixt. of boronic acid deriv. and ICl in CHCl3 at 0°C for 12 h; concg., addn. of diethyl ether, addn. of aq. Na2S2O3, separating organicphase, evapn., filtration, washing with CHCl3, elem. anal.;94%
iron pentacarbonyl
13463-40-6

iron pentacarbonyl

Iodine monochloride
7790-99-0

Iodine monochloride

benzyltrimethylammonium iodide
4525-46-6

benzyltrimethylammonium iodide

sulfur
7704-34-9

sulfur

(BTMA)2[Fe4S4I3Cl]

(BTMA)2[Fe4S4I3Cl]

Conditions
ConditionsYield
Stage #1: iron pentacarbonyl; Iodine monochloride; benzyltrimethylammonium iodide; sulfur In tetrahydrofuran at -60℃; Inert atmosphere; Schlenk technique;
Stage #2: In tetrahydrofuran for 23h; Inert atmosphere; Schlenk technique; Reflux;
94%
C35H43BN2O3Si

C35H43BN2O3Si

Iodine monochloride
7790-99-0

Iodine monochloride

C27H32BIN2O3

C27H32BIN2O3

Conditions
ConditionsYield
Stage #1: C35H43BN2O3Si; Iodine monochloride In dichloromethane at -78℃; for 18h; Inert atmosphere;
Stage #2: With 2-methyl-but-2-ene In dichloromethane at 20℃; for 0.0833333h; Inert atmosphere;
94%
Cs(1+)*C5H25B22N2(1-)

Cs(1+)*C5H25B22N2(1-)

Iodine monochloride
7790-99-0

Iodine monochloride

trimethylamine hydrochloride
593-81-7

trimethylamine hydrochloride

C3H9N*C5H13B22I12N2(1-)*H(1+)

C3H9N*C5H13B22I12N2(1-)*H(1+)

Conditions
ConditionsYield
Stage #1: Cs(1+)*C5H25B22N2(1-); Iodine monochloride With trifluorormethanesulfonic acid at 50℃; for 24h;
Stage #2: trimethylamine hydrochloride In water for 12h;
94%
C56H62B2N2SSi

C56H62B2N2SSi

Iodine monochloride
7790-99-0

Iodine monochloride

C53H53B2IN2S

C53H53B2IN2S

Conditions
ConditionsYield
In tetrahydrofuran at 20℃; for 5h; Inert atmosphere;94%

7790-99-0Relevant articles and documents

Hoffmann, S. M. A.,Smith, D. J.,Gonzales Urenna, A.,Grice, R.

, p. 99 - 102 (1984)

Swift, E. H.

, p. 894 - 894 (1930)

Cornog, J.,Karges, R. A.

, p. 1882 - 1882 (1932)

Method for preparing hexafluorobutadiene from iodine and chlorine

-

Paragraph 0034-0035; 0045-0046; 0056-0057, (2017/08/27)

The invention relates to a method for preparing hexafluorobutadiene from iodine and chlorine. The method comprises the following steps: preparing a metal coordinated ionic liquid solvent, and reacting iodine with chlorine to prepare iodine monochloride; reacting iodine monochloride with chlorotrifluoroethylene in the presence of the metal coordinated ionic liquid solvent to prepare 1,2-dichloro-2-iodo-1,1,2-trifluoroethane; carrying out a reaction on the 1,2-dichloro-2-iodo-1,1,2-trifluoroethane in the presence of the metal coordinated ionic liquid solvent under the catalysis of zinc powder to obtain 1,2,3,4-tetrachloro-1,1,2,3,4,4-hexafluorobutane; and reacting the 1,2,3,4-tetrachloro-1,1,2,3,4,4-hexafluorobutane with zinc powder in the presence of the metal coordinated ionic liquid solvent to generate hexafluorobutadiene.

Stabilizing aqueous solution of iodine chloride by adding sodium chloride

-

Page/Page column 3, (2011/02/19)

This invention relates generally to non-ionic X-ray contrast agents. It further relates to the preparation of iodine chloride, a key reagent in the synthesis of non-ionic X-ray contrast agents such as iodixanol and iohexol. In particular, the iodine chloride is produced in a reaction involving iodine, sodium chlorate, and hydrochloric acid as the starting materials. The instant invention relates to a method of stabilizing aqueous iodine chloride solutions by adding about one to about four molar equivalents of sodium chloride relative to sodium chlorate to an aqueous reaction mixture of sodium chlorate, hydrochloric acid, and iodine.

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