Product Name

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  • Name

    Iodine

  • EINECS 231-442-4
  • CAS No. 7553-56-2
  • Article Data2682
  • CAS DataBase
  • Density 3.835 g/cm3
  • Solubility 0.3 g/L (20 °C) in water
  • Melting Point 113 °C(lit.)
  • Formula I2
  • Boiling Point 184.35 °C at 760 mmHg
  • Molecular Weight 253.809
  • Flash Point
  • Transport Information UN 2056 3/PG 2
  • Appearance Grey to purple solid
  • Safety 26-61-25-23
  • Risk Codes 36/37/38-50-20/21
  • Molecular Structure Molecular Structure of 7553-56-2 (Iodine)
  • Hazard Symbols HarmfulXn, DangerousN
  • Synonyms 7553-56-2
  • PSA 0.00000
  • LogP 1.77140

Synthetic route

sodium iodide
7681-82-5

sodium iodide

iodine
7553-56-2

iodine

Conditions
ConditionsYield
With phosgene In acetone at 20℃; for 0.25h; Reagent/catalyst;100%
With Fe3+-montmorillonite; propionic acid at 25℃; for 6h;
With propionic acid; K 10-montmorillonite; FeCl3; mixture of, dried at 120 degrees C, grounded at 25℃; for 6h;
hydrogen iodide
10034-85-2

hydrogen iodide

A

hydrogen
1333-74-0

hydrogen

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
Kinetics; Irradiation (UV/VIS); in glass vessel or uviol vessel, wavelenght higher than 2540Å;;A 100%
B 100%
Kinetics; Irradiation (UV/VIS); at room temperature, in quartz vessel; equilibrium; wavelenght lower than 2540Å;;A 92.3%
B 92.3%
995 °C; part of a Mg-S-I water splitting cycle;A 31%
B 31%
niobocene dichloride
12793-14-5

niobocene dichloride

triiodo hexafluoroarsenate
59555-19-0

triiodo hexafluoroarsenate

A

(η5-C5H5)2niobium(V)(Cl2) hexafluoroarsenate

(η5-C5H5)2niobium(V)(Cl2) hexafluoroarsenate

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In liquid sulphur dioxide under Ar; recrystn. (SO2), elem. anal.;A 99%
B n/a
molybdenum(VI) oxide

molybdenum(VI) oxide

magnesium iodide

magnesium iodide

A

magnesium oxide * molybdenum dioxide

magnesium oxide * molybdenum dioxide

B

iodine
7553-56-2

iodine

C

magnesium oxide

magnesium oxide

Conditions
ConditionsYield
In neat (no solvent, solid phase) vac.; equimolar ratio, heating (200°C 20 d, 800°C 30 d); XRD;A n/a
B 98.5%
C n/a
bis(pyridine)iodine(I) tetrachloroplatinate(II)

bis(pyridine)iodine(I) tetrachloroplatinate(II)

A

{Pt(pyridinium)2Cl4}

{Pt(pyridinium)2Cl4}

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: pyridine; heated at 130°C; washed with acetone-water (5:1), dried in vac.; elem. anal.;A 94%
B 96.5%
dimethoxy disulfide
28752-21-8

dimethoxy disulfide

A

iodine
7553-56-2

iodine

B

sulfur
7704-34-9

sulfur

Conditions
ConditionsYield
With hydrogenchloride byproducts: H2O, H2S, SO2; in presence of KI;A 90%
B n/a
With HCl byproducts: H2O, H2S, SO2; in presence of KI;A 90%
B n/a
bis(pyridine)iodine(I) tetrabromoplatinate(II)

bis(pyridine)iodine(I) tetrabromoplatinate(II)

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In neat (no solvent, solid phase) byproducts: pyridine; heated at 120°C; washed with acetone-water (5:1), dried in vac.; elem. anal.;A 85%
B 72.7%
iodide
14362-44-8

iodide

iodine
7553-56-2

iodine

Conditions
ConditionsYield
With ammonium peroxosulfate; iron(III) In hydrogenchloride byproducts: SO4(2-); Irradiation (UV/VIS); at 22°C with UV irradiation for 15 min; subsequent stirring in daylight for 20 min; mechanism discussed;;80.2%
With ammonium peroxosulfate; iron(III) In hydrogenchloride byproducts: SO4(2-); at 22°C in daylight for 35 min;;73.9%
With ammonium peroxosulfate; iron(III) In hydrogenchloride byproducts: SO4(2-); at 22°C in the dark for 15 min; subsequent stirring in daylight for 20 min;;69.6%
bismuth (III) nitrate pentahydrate

bismuth (III) nitrate pentahydrate

iodic acid
7782-68-5

iodic acid

A

2Bi(3+)*IO4(3-)*3IO3(1-)=Bi2(IO4)(IO3)3

2Bi(3+)*IO4(3-)*3IO3(1-)=Bi2(IO4)(IO3)3

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
With HNO3 or I2O5 or H5IO6 In water High Pressure; mixt. of Bi compd., HIO3, HNO3 (or I2O5 or H5IO6) and H2O was sealed in autoclave; heated to 215°C; held for 5 d; cooled at rate 10°C/h to room temp.; decanted; washed (EtOH, H2O); air-dried;A 75%
B n/a
C8H7ClN4O

C8H7ClN4O

but-3-en-1-amine hydrochloride
17875-18-2

but-3-en-1-amine hydrochloride

iodine
7553-56-2

iodine

Conditions
ConditionsYield
With triethylamine In ethanol for 4h;74%
iodine pentoxide
12029-98-0

iodine pentoxide

potassium chloride

potassium chloride

uranium(VI) trioxide

uranium(VI) trioxide

A

K2((UO2)3(IO3)4O2)

K2((UO2)3(IO3)4O2)

B

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In water High Pressure; UO2, I2O5, KCl, and water were heated in autoclave at 10°C/min to425°C, after 72 h autoclave was cooled over 24 h to 23°C; washed with MeOH and dried;A 73%
B n/a
N,N,N',N'-tetraethylthioamine
3768-61-4

N,N,N',N'-tetraethylthioamine

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In not given in acidic soln.;70%
In not given in acidic soln.;70%
N-trifluoroacetic-3-nitroaniline
25080-83-5

N-trifluoroacetic-3-nitroaniline

methyl iodide
74-88-4

methyl iodide

iodine
7553-56-2

iodine

Conditions
ConditionsYield
Stage #1: N-trifluoroacetic-3-nitroaniline With sodium hydride In tetrahydrofuran at 0℃; for 1h;
Stage #2: methyl iodide In tetrahydrofuran at 20℃;
66%
iodine pentoxide
12029-98-0

iodine pentoxide

water
7732-18-5

water

uranium(VI) trioxide

uranium(VI) trioxide

barium(II) chloride

barium(II) chloride

A

uranyl iodate monohydrate

uranyl iodate monohydrate

B

Ba((UO2)2(IO3)2O2)*H2O

Ba((UO2)2(IO3)2O2)*H2O

C

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In water High Pressure; UO2, I2O5, KCl, and water were heated in autoclave to 180°C, after 72 h autoclave was cooled at 9°C/h to 23°C; washed with MeOH and dried;A n/a
B 60%
C n/a
1,2-Diiodobenzene
615-42-9

1,2-Diiodobenzene

boron triiodide
13517-10-7

boron triiodide

A

iodine
7553-56-2

iodine

B

5,10-diiodo-5,10-dihydroboranthrene
24633-37-2

5,10-diiodo-5,10-dihydroboranthrene

Conditions
ConditionsYield
stirring mixt. of educts at 180°C for 5 h; I2 removed by sublimation at 60°C/0.1 Torr, sublimation of products;A n/a
B 56%
cyanogen iodide
506-78-5

cyanogen iodide

tertamethylammonium iodide
75-58-1

tertamethylammonium iodide

iodine
7553-56-2

iodine

Conditions
ConditionsYield
In neat (no solvent) at room temp.;38%
silver(I) iodide

silver(I) iodide

iodine
7553-56-2

iodine

Conditions
ConditionsYield
in presence of O3 at room temp.;2.8%
in presence of O3 at room temp.;2.8%
With manganese(IV) oxide at 370°C;
potassium iodate
7758-05-6

potassium iodate

A

iodine
7553-56-2

iodine

B

potassium iodide
7681-11-0

potassium iodide

Conditions
ConditionsYield
potassium polymanganite(IV) In solid byproducts: O2; mixt. of KIO3 and potassium polymanganate heated (400-600°C, 2h, air); X-ray diffraction;A 1%
B n/a
2-(iodomethyl)isoindoline-1,3-dione
203255-55-4

2-(iodomethyl)isoindoline-1,3-dione

iodine
7553-56-2

iodine

Conditions
ConditionsYield
Zerstzung bei Raumtemperatur;
2,4-dichloro-6-diiodomethyl-[1,3,5]triazine
30894-70-3

2,4-dichloro-6-diiodomethyl-[1,3,5]triazine

iodine
7553-56-2

iodine

Conditions
ConditionsYield
at 25℃;
8-iodo-3,7-dihydro-purine-2,6-dione
64761-27-9

8-iodo-3,7-dihydro-purine-2,6-dione

iodine
7553-56-2

iodine

Conditions
ConditionsYield
at 200℃; Abspaltung;
5,7-Diiodoisatin
34058-26-9

5,7-Diiodoisatin

sulfuric acid
7664-93-9

sulfuric acid

iodine
7553-56-2

iodine

Conditions
ConditionsYield
at 130℃; Zersetzung;
sulfuric acid
7664-93-9

sulfuric acid

2-iodo-1-(4-naphtho[1,2-d][1,2,3]triazol-2-yl-phenyl)-ethanone

2-iodo-1-(4-naphtho[1,2-d][1,2,3]triazol-2-yl-phenyl)-ethanone

iodine
7553-56-2

iodine

1-bromopyrrolidin-2-one
2401-40-3

1-bromopyrrolidin-2-one

hydrogen iodide
10034-85-2

hydrogen iodide

iodine
7553-56-2

iodine

(1R)-3-bromo-1,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-2,4-dione
128475-96-7

(1R)-3-bromo-1,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-2,4-dione

hydrogen iodide
10034-85-2

hydrogen iodide

iodine
7553-56-2

iodine

(1R)-3-iodo-1,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-2,4-dione

(1R)-3-iodo-1,8,8-trimethyl-3-aza-bicyclo[3.2.1]octane-2,4-dione

hydrogen iodide
10034-85-2

hydrogen iodide

iodine
7553-56-2

iodine

3-imino-2-phenyl-3H-indole
6339-33-9

3-imino-2-phenyl-3H-indole

water
7732-18-5

water

hydrogen iodide
10034-85-2

hydrogen iodide

iodine
7553-56-2

iodine

2,3,4,5-tetraiodo-1H-pyrrole
87-58-1

2,3,4,5-tetraiodo-1H-pyrrole

acetic anhydride
108-24-7

acetic anhydride

iodine
7553-56-2

iodine

sulfuric acid
7664-93-9

sulfuric acid

(3S)-cis-3,6-bis-(2,5-diiodo-1(3)H-imidazol-4-ylmethyl)-piperazine-2,5-dione

(3S)-cis-3,6-bis-(2,5-diiodo-1(3)H-imidazol-4-ylmethyl)-piperazine-2,5-dione

iodine
7553-56-2

iodine

Conditions
ConditionsYield
at 150℃;
sulfur dioxide
7446-09-5

sulfur dioxide

water
7732-18-5

water

iodine
7553-56-2

iodine

A

sulfuric acid
7664-93-9

sulfuric acid

B

hydrogen iodide
10034-85-2

hydrogen iodide

Conditions
ConditionsYield
0 - 25 °C; part of a Mg-S-I water splitting cycle;A 100%
B 100%
bromine
7726-95-6

bromine

iodine
7553-56-2

iodine

cadmium(II) sulphide

cadmium(II) sulphide

cadmium(II) iodide

cadmium(II) iodide

Conditions
ConditionsYield
In gas100%
In solid100%
In further solvent(s) with I2 dissolved in organic solvents;100%
bismuth
7440-69-9

bismuth

iodine
7553-56-2

iodine

bismuth(III) iodide
7787-64-6

bismuth(III) iodide

Conditions
ConditionsYield
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
In melt passing a stream of I2/inert gas into molten Bi with formation of volatile BiI3; description of the aparatus given;;100%
thallium

thallium

iodine
7553-56-2

iodine

thallium(I) iodide

thallium(I) iodide

Conditions
ConditionsYield
In neat (no solvent) in vac., for 0% excess Tl at 540°C, for 1% excess Tl at 500, 540°C, for 2, 5, 10, 20% excess Tl at 450, 500, 540°C; sublimed, elem. anal., IR, XRD;100%
In neat (no solvent) in vac., for 20% excess Tl at 400°C; sublimed, elem. anal., IR, XRD;99.1%
In neat (no solvent) in vac., for 0% excess Tl at 500°C; sublimed, elem. anal., IR, XRD;98.9%
lithium borohydride

lithium borohydride

iodine
7553-56-2

iodine

diborane
14452-61-0

diborane

Conditions
ConditionsYield
Kinetics; byproducts: H2, LiI; Interaction of initial cryst. materials in molar ratio LiBH4:I2 = 1.50 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;100%
byproducts: H2, LiI; Interaction of initial cryst. materials in molar ratio LiBH4:I2 = 1.35 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;99.5%
Kinetics; byproducts: H2, LiI; Interaction of initial cryst. materials in molar ratio LiBH4:I2 = 2.0 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;99.8%
Kinetics; byproducts: H2, LiI; Interaction of initial cryst. materials in molar ratio LiBH4:I2 = 2.5 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;95.4%
byproducts: H2, HI; Grinding of initial materials (molar ratio = 1) while being cooled withliq. N2, thorough mixing, transferring of mixt. to a thermographic ampoule and heating in vac. or N2.; Sepn. of gas mixt. by fractional condensation. Detn. of composition after the thermography by gas volumetric anal.;
sodium tetrahydroborate
16940-66-2

sodium tetrahydroborate

iodine
7553-56-2

iodine

diborane
14452-61-0

diborane

Conditions
ConditionsYield
byproducts: H2, NaI; Interaction of initial cryst. materials in molar ratio NaBH4:I2 = 1.35 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;100%
byproducts: H2, NaI; Interaction of initial cryst. materials in molar ratio NaBH4:I2 = 1.5 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;97.7%
Kinetics; byproducts: H2, NaI; Interaction of initial cryst. materials in molar ratio NaBH4:I2 = 2.5 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;94%
Kinetics; byproducts: H2, NaI; Interaction of initial cryst. materials in molar ratio NaBH4:I2 = 2.0 under mechanical activation with a vibration ball mill (dry N2, atm. pressure, 25°C).; Detn. of gas phase formed by infrared and mass spectroscopy, and gas volumetric anal.;88.7%
byproducts: H2, HI; Grinding of initial materials (molar ratio = 1) while being cooled withliq. N2, thorough mixing, transferring of mixt. to a thermographic ampoule and heating in vac. or N2.; Sepn. of gas mixt. by fractional condensation. Detn. of composition after the thermography by gas volumetric anal.;
tellurium

tellurium

iodine
7553-56-2

iodine

tungsten(VI) chloride
13283-01-7

tungsten(VI) chloride

1,4-diiodo-cyclo-hexatellurium(2+) bis(hexachlorotungstate(-))

1,4-diiodo-cyclo-hexatellurium(2+) bis(hexachlorotungstate(-))

Conditions
ConditionsYield
In neat (no solvent) Ar atmosphere, sealed ampoule, formation of black melt at 300°C, tube furnace (150°C), crystn. (3 months);100%
cis-I(CO)2(CH3NC)2W.tplbond.CNEt2

cis-I(CO)2(CH3NC)2W.tplbond.CNEt2

iodine
7553-56-2

iodine

(I)3(CO)(CH3NC)2W.tplbond.CNEt2

(I)3(CO)(CH3NC)2W.tplbond.CNEt2

Conditions
ConditionsYield
In dichloromethane first at -30°c, than at room temp. for 10min stirring, reducing of the soln., adding Et2O/pentane; drying at 25°C (vacuo), elem. anal.;100%
cis-{(PhCH2)2Co(III)(2,2'-bipyridine)2}ClO4

cis-{(PhCH2)2Co(III)(2,2'-bipyridine)2}ClO4

iodine
7553-56-2

iodine

cis-benzyl iodo bis(2,2'-bipyridyl) cobalt(III) perchlorate

cis-benzyl iodo bis(2,2'-bipyridyl) cobalt(III) perchlorate

B

iodomethylbenzene
620-05-3

iodomethylbenzene

Conditions
ConditionsYield
In tetrachloromethane Kinetics; Irradiation (UV/VIS); Kinetics of the reaction of Co(H2CC6H5)2(bipy)2ClO4 with I2 under irradiation with light at 517 nm is investigated.; PhCh2I and Co(H2CC6H5)I(bipy)2ClO4 are the main products.;A n/a
B 100%
trans-(CH3)2Co(11-hydroxy-2,3,9,10-tetramethyl-1,4,8,11-tetraazaundeca-1,3,8,10-tetraen-1-olate)

trans-(CH3)2Co(11-hydroxy-2,3,9,10-tetramethyl-1,4,8,11-tetraazaundeca-1,3,8,10-tetraen-1-olate)

iodine
7553-56-2

iodine

A

methane
34557-54-5

methane

B

ethane
74-84-0

ethane

C

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
In tetrachloromethane Irradiation (UV/VIS); Irradiation at 509 nm in CCl4; Estimation of the quantum yield of the photochemical reaction. Yield of the products estimated by g.l.c.;A 0.02%
B <1
C 100%
trans-(CH3)2Co(11-hydroxy-2,3,9,10-tetramethyl-1,4,8,11-tetraazaundeca-1,3,8,10-tetraen-1-olate)

trans-(CH3)2Co(11-hydroxy-2,3,9,10-tetramethyl-1,4,8,11-tetraazaundeca-1,3,8,10-tetraen-1-olate)

iodine
7553-56-2

iodine

trans-methyl iodo cobalt (III) 3,9-dimethyl-4,8-diazaundecane-3,8-diene-2,10-dione dioximate

trans-methyl iodo cobalt (III) 3,9-dimethyl-4,8-diazaundecane-3,8-diene-2,10-dione dioximate

B

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
In tetrachloromethane Kinetics; byproducts: C2H6, CH4; Irradiation (UV/VIS); Kinetics of the reaction of Co(CH3)2(H3CCNOHC(CH3)NC3H6NC(CH3)CNOCH3) with I2 under irradiation with light at 517 nm is investigated.; MeI and Co(CH3)I(H3CCNOHC(CH3)NC3H6NC(CH3)CNOCH3) are the main products, C2H6 and CH4 are byproducts.;A n/a
B 100%
CoMe(pyridine)(dimethylglyoxime(-1H))2
23642-14-0

CoMe(pyridine)(dimethylglyoxime(-1H))2

iodine
7553-56-2

iodine

A

iodobisdimethylglyoximepyridine cobalt(III)

iodobisdimethylglyoximepyridine cobalt(III)

B

methyl iodide
74-88-4

methyl iodide

Conditions
ConditionsYield
In tetrachloromethane Kinetics; Irradiation (UV/VIS); Kinetics of the reaction of Co(CH3)(H3CCNOHONCCH3)2(C5H5N) with I2 under irradiation with light at 517 nm is investigated.; MeI and CoI(H3CCNOHONCCH3)2(C5H5N) are the products.;A n/a
B 100%
[CoEt(dimethylglyoximate(1-))2(pyridine)]

[CoEt(dimethylglyoximate(1-))2(pyridine)]

iodine
7553-56-2

iodine

A

iodobisdimethylglyoximepyridine cobalt(III)

iodobisdimethylglyoximepyridine cobalt(III)

B

ethyl iodide
75-03-6

ethyl iodide

Conditions
ConditionsYield
In tetrachloromethane Kinetics; Irradiation (UV/VIS); Kinetics of the reaction of Co(C2H5)(H3CCNOHONCCH3)2(C5H5N) with I2 under irradiation with light at 517 nm is investigated.; MeI and CoI(H3CCNOHONCCH3)2(C5H5N) are the products.;A n/a
B 100%
(η4-2,5-bis(trimethylsilyl)-3,4-cyclopentacyclopentadienone)(η5-cyclopentadienyl)cobalt

(η4-2,5-bis(trimethylsilyl)-3,4-cyclopentacyclopentadienone)(η5-cyclopentadienyl)cobalt

iodine
7553-56-2

iodine

(η4-2-iodo-5-trimethylsilyl-3,4-cyclopentacyclopentadienone)(η5-cyclopentadienyl)cobalt

(η4-2-iodo-5-trimethylsilyl-3,4-cyclopentacyclopentadienone)(η5-cyclopentadienyl)cobalt

Conditions
ConditionsYield
With sodium thiosulfate In acetone addn. of iodine to a soln. of Co-compd., stirring at room temp. for 1 h, change of colour from brown-red to red on addn. of aq. Na2S2O3; extg. the aq. layer with CH2Cl2, drying over Na2SO4, filtration, evapn., chromy. (Al2O3, ethyl acetate), elem. anal.;100%
Pt2I2(CO)2(P-tert.-Bu2Ph2)2
118714-49-1

Pt2I2(CO)2(P-tert.-Bu2Ph2)2

iodine
7553-56-2

iodine

PtPtI2(CO)(P-t-Bu2Ph)
19618-88-3

PtPtI2(CO)(P-t-Bu2Ph)

Conditions
ConditionsYield
In not given react. (N2, CO or Ar); elem. anal.;100%
iodine
7553-56-2

iodine

triethylantimony
617-85-6

triethylantimony

triethylstibine di-iodide
25088-65-7, 58116-52-2

triethylstibine di-iodide

Conditions
ConditionsYield
In dichloromethane elem. anal.;100%
selenium
7782-49-2

selenium

arsenic pentafluoride
7784-36-3

arsenic pentafluoride

fluorosulfonylchloride
13637-84-8

fluorosulfonylchloride

sulfur dioxide
7446-09-5

sulfur dioxide

iodine
7553-56-2

iodine

(diselenium tetraiodine)(AsF6)2*SO2

(diselenium tetraiodine)(AsF6)2*SO2

Conditions
ConditionsYield
byproducts: AsF3; SO2 and AsF5 were condensed into Se and I2; after 16 h no insoluble material was observed; condensed SO2ClF into the soln.; react. time 3 h; slowly (ca.20 h) condension; cooling; crystn.; washing; removed volatile materials by evacuation; subjected to vac. for <0.2 h; elem. anal.;100%
byproducts: AsF3; SO2 and AsF5 were condensed onto Se and I2; after 16 h no insoluble material was observed; condensation of SO2ClF onto the soln.; react. time 7 h; slowly (ca.20 h) condensation of solvent; cooling; crystn.; washing; removal of volatile material by evacuation; elem. anal.;104 %
selenium
7782-49-2

selenium

arsenic pentafluoride
7784-36-3

arsenic pentafluoride

sulfur dioxide
7446-09-5

sulfur dioxide

iodine
7553-56-2

iodine

(diselenium tetraiodine)-(AsF6)2

(diselenium tetraiodine)-(AsF6)2

Conditions
ConditionsYield
AsF5 was condensed onto a mixture of Se and I2 in liq. SO2; react. time 4 h; slowly (ca.20 h) condensation of solvent; crystn.; after 16 h removal of volatile material by evacuation; elem. anal.; X-ray diffraction;100%
AsF5 was condensed onto a mixture of Se and I2 in liq. SO2; react. time 6 h; slowly (ca.20 h) condensation; crystn.; after 16 h removal of volatile materials by evacuation; elem. anal.; X-ray diffraction;106 %
anti-2-norbornene-7-yl-trimethyl tin
38573-93-2, 34208-81-6

anti-2-norbornene-7-yl-trimethyl tin

iodine
7553-56-2

iodine

trimethylstannyl iodide
811-73-4

trimethylstannyl iodide

Conditions
ConditionsYield
In methanol100%
In methanol100%
In dimethyl sulfoxide88%
iodine
7553-56-2

iodine

methyl 3-(tri-n-butylstannyl)propionate
19464-44-9

methyl 3-(tri-n-butylstannyl)propionate

β-Methoxycarbonyl-ethyldi-n-butyl-iodstannan

β-Methoxycarbonyl-ethyldi-n-butyl-iodstannan

Conditions
ConditionsYield
In tetrachloromethane byproducts: CH3(CH2)3I;100%
benzimidazolin-2-ylidene(chloro)gold
136835-13-7

benzimidazolin-2-ylidene(chloro)gold

iodine
7553-56-2

iodine

(benzimidazolin-2-ylidene)triiodogold

(benzimidazolin-2-ylidene)triiodogold

Conditions
ConditionsYield
In dichloromethane protective gas: argon; stirring mixture (20 h/room temp.);; pptn.; filtration; washing (CH2Cl2); drying; elem. anal.;;100%
((C6H5)2PC5H4)Mo(CO)3Mn(CO)5
165751-19-9

((C6H5)2PC5H4)Mo(CO)3Mn(CO)5

iodine
7553-56-2

iodine

[(η5-C5H4PPh2)Mo(CO)3I]

[(η5-C5H4PPh2)Mo(CO)3I]

Conditions
ConditionsYield
In not given100%
{Ru(C5H3(OH)(P(C6H5)3))(C5H5)}(1+)*PF6(1-)={Ru(C5H3(OH)(P(C6H5)3))(C5H5)}PF6

{Ru(C5H3(OH)(P(C6H5)3))(C5H5)}(1+)*PF6(1-)={Ru(C5H3(OH)(P(C6H5)3))(C5H5)}PF6

iodine
7553-56-2

iodine

{Ru(C5H5)(C5H3OP(C6H5)3)I}(1+)*PF6(1-)={Ru(C5H5)(C5H3OP(C6H5)3)I}(PF6)

{Ru(C5H5)(C5H3OP(C6H5)3)I}(1+)*PF6(1-)={Ru(C5H5)(C5H3OP(C6H5)3)I}(PF6)

Conditions
ConditionsYield
In nitromethane-d3 not isolated, monitored by NMR;100%
iodine
7553-56-2

iodine

bis[2,4,6-tris[bis(trimethylsilyl)methyl]phenyl]distilbene
201533-93-9

bis[2,4,6-tris[bis(trimethylsilyl)methyl]phenyl]distilbene

[((Si(CH3)3)2CH)3C6H2]SbI2
201533-95-1

[((Si(CH3)3)2CH)3C6H2]SbI2

Conditions
ConditionsYield
In tetrachloromethane room temp.;100%
μ-carbido-bis(phthalocyaninato(2-)iron(IV))

μ-carbido-bis(phthalocyaninato(2-)iron(IV))

iodine
7553-56-2

iodine

0.34[(C32H16N8)Fe]2C*0.66[(C32H16N8)Fe]2C(1+)*0.66I3(1-)=([(C32H16N8)Fe]2C)(I3)066

0.34[(C32H16N8)Fe]2C*0.66[(C32H16N8)Fe]2C(1+)*0.66I3(1-)=([(C32H16N8)Fe]2C)(I3)066

Conditions
ConditionsYield
In further solvent(s) excess of I2, stirring in chloronaphthalene (60-70°C, 1 h); cooling, collection (filtration), washing (EtOH), drying (vac.); elem. anal.;100%
tetra(supersilyl)dialane
192053-32-0

tetra(supersilyl)dialane

iodine
7553-56-2

iodine

disupersilyl aluminum iodide
217202-48-7

disupersilyl aluminum iodide

Conditions
ConditionsYield
In pentane Ar-atmosphere; stirring (40°C, 3 h); detd. by NMR spectroscopy;100%
In pentane all manipulations with exclusion of air and moisture; soln. of compds. heated at 40°C for 3 h; controlled by NMR; volatiles evapd. by oil pump; elem. anal.;
phenyl bis(trifluoroacetate)

phenyl bis(trifluoroacetate)

iodine
7553-56-2

iodine

A

iodobenzene
591-50-4

iodobenzene

B

Tl(1+)*Tl(3+)*4CF3COO(1-)=Tl2(CF3COO)4

Tl(1+)*Tl(3+)*4CF3COO(1-)=Tl2(CF3COO)4

Conditions
ConditionsYield
In acetonitrile soln. of iodine addn. to soln. of Tl-compd., mixing, standing (dark, 220h, room temperature), evacuation (under Ar, room temperature, then wate r bath, distillation of I-compd.), product remaining in solid residue;A 99%
B 100%
tellurium

tellurium

iodine
7553-56-2

iodine

aluminium(III) iodide
7784-23-8

aluminium(III) iodide

TeI3(1+)*AlI4(1-)=TeI3[AlI4]
165602-57-3

TeI3(1+)*AlI4(1-)=TeI3[AlI4]

Conditions
ConditionsYield
In neat (no solvent) Ar atm.; molar ratio Te:I2:AlI3 1:2:1, heating (150-200°C, several hours);100%

Iodine History

 Iodine was discovered by Bernard Courtois in 1811. Charles Bernard Desormes (1777–1862) and Nicolas Clément (1779–1841), to continue research. He also gave some of the substance to Joseph Louis Gay-Lussac (1778–1850), a well-known chemist at that time, and to physicist André-Marie Ampère (1775–1836). On 29 November 1813, Dersormes and Clément made public Courtois’s discovery. On December 6, Gay-Lussac announced that the new substance was either an element or a compound of oxygen. Ampère had given some of his sample to Humphry Davy (1778–1829). Davy did some experiments on the substance and noted its similarity to chlorine. Davy sent a letter dated December 10 to the Royal Society of London stating that he had identified a new element. element.

Iodine Consensus Reports

Reported in EPA TSCA Inventory.

Iodine Standards and Recommendations

OSHA PEL: CL 0.1 ppm
ACGIH TLV: CL 0.1 ppm
DFG MAK: 0.1 ppm (1.1 mg/m3)

Iodine Analytical Methods

For occupational chemical analysis use OSHA: #ID-177 or NIOSH: Iodine, 6005.

Iodine Specification

Iodine (CAS NO.7553-56-2), its Synonyms are Actomar; Diiodine; Eranol; Ethanolic solution of iodine; Iodine Tincture. It is violet-black crystals with a metallic luster and a sharp odor. It forms compounds with most elements, but is less reactive than the other halogens, which displace it from iodides. Iodine exhibits some metallic-like properties. It dissolves readily in chloroform, carbon tetrachloride, or carbon disulphide to form beautiful purple solutions. It is only slightly soluble in water. Iodine compounds are important in organic chemistry and very useful in medicine and photography.

Physical properties about Iodine are: 
(1)ACD/LogP: 2.064; (2)ACD/LogD (pH 5.5): 2.06; (3)ACD/LogD (pH 7.4): 2.06; (4)ACD/BCF (pH 5.5): 21.82; (5)ACD/BCF (pH 7.4): 21.82; (6)Index of Refraction: 1.788 ; (7)Molar Refractivity: 27.988 cm3; (8)Molar Volume: 66.188 cm3; (9)Polarizability: 11.095 10-24cm3; (10)Surface Tension: 54.8499984741211 dyne/cm; (11)Density: 3.835 g/cm3 ; (12)Enthalpy of Vaporization: 41.57 kJ/mol; (13)Boiling Point: 184.35 °C at 760 mmHg; (14)Vapour Pressure: 0.490000009536743 mmHg at 25°C

Preparation of Iodine: 
Iodine can be produced from iodates:
IO3- + 3SO2 + 3H2O → I- + 3SO42- + 6H-
IO3- + I- + 6H+ → 3I2 + 3H2O
Iodine can also be produced from brine. This process consists of cleaning the solution (of clays and other materials), adding sulfuric acid to a pH <2.5 followed by treatment with gaseous chlorine:
2I- + Cl2 → I2 + 2Cl-
after which the Iodine is recovered by a countercurrent air blow out step. process.

Uses of Iodine:
Iodine (CAS NO.7553-56-2) is used for the manufacture of organic compounds, for the manufacture of potassium iodide and sodium iodide, and for the manufacture of other inorganic compounds. Iodine is used as a catalyst in the chlorination of organic compounds and in analytical chemistry for determination of the iodine numbers of oils. Iodine for medicinal, photographic, and pharmaceutical purposes is usually in the form of alkali iodides, prepared through the agency of ferrous iodide. It is also used for the manufacture of dyes and as a germicide. Simple iodine derivatives of hydrocarbons, such as iodoform (CHI3), have an antiseptic action. Organic compounds containing iodine have been used as rubber emulsifiers, chemical antioxidants, and dyes and pigments.

Safety information of Iodine:
When you are using this chemical, please be cautious about it as the following:
1. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice;
2. Avoid release to the environment. Refer to special instructions safety data sheet;
3. Avoid contact with eyes;
4. Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer);

You can still convert the following datas into molecular structure:
(1)InChI=1S/I2/c1-2;
(2)InChIKey=PNDPGZBMCMUPRI-UHFFFAOYSA-N;
(3)SmilesII

The toxicity data of Iodine is as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
dog LDLo intravenous 40mg/kg (40mg/kg)   "Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 76, 1959.
dog LDLo oral 800mg/kg (800mg/kg)   "Abdernalden's Handbuch der Biologischen Arbeitsmethoden." Vol. 4, Pg. 1289, 1935.
human LDLo oral 28mg/kg (28mg/kg) GASTROINTESTINAL: "HYPERMOTILITY, DIARRHEA"

GASTROINTESTINAL: OTHER CHANGES
"Toxicology of Drugs and Chemicals," Deichmann, W.B., New York, Academic Press, Inc., 1969Vol. -, Pg. 330, 1969.
man LDLo unreported 29mg/kg (29mg/kg)   "Poisoning; Toxicology, Symptoms, Treatments," 2nd ed., Arena, J.M., Springfield, IL, C.C. Thomas, 1970Vol. 2, Pg. 73, 1970.
mouse LD50 oral 22gm/kg (22000mg/kg)   Drugs of the Future. Vol. 4, Pg. 876, 1979.
mouse LD50 subcutaneous > 8650mg/kg (8650mg/kg)   Drugs in Japan Vol. -, Pg. 1226, 1990.
rabbit LD50 oral 10gm/kg (10000mg/kg)   Drugs of the Future. Vol. 4, Pg. 876, 1979.
rabbit LDLo subcutaneous 175mg/kg (175mg/kg)   "Handbook of Toxicology," 4 vols., Philadelphia, W.B. Saunders Co., 1956-59Vol. 5, Pg. 76, 1959.
rat LCLo inhalation 137ppm/1H (137ppm) BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY)

SENSE ORGANS AND SPECIAL SENSES: LACRIMATION: EYE
National Technical Information Service. Vol. OTS0555278,
rat LD50 oral 14gm/kg (14000mg/kg)   Drugs of the Future. Vol. 4, Pg. 876, 1979.
rat LD50 subcutaneous 10500mg/kg (10500mg/kg)   Drugs in Japan Vol. -, Pg. 1226, 1990.
women TDLo oral 26mg/kg/1Y-I (26mg/kg) ENDOCRINE: EVIDENCE OF THYROID HYPERFUNCTION Postgraduate Medical Journal. Vol. 62, Pg. 661, 1986.
 

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