CAS No.7553-56-2,Iodine Suppliers,MSDS download

: 7681-82-5
sodium iodide

: 7553-56-2
iodine

Conditions

Conditions	Yield
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;

: 10034-85-2
hydrogen iodide

A: 1333-74-0
hydrogen

B: 7553-56-2
iodine

Conditions

Conditions	Yield
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%

: 12793-14-5
niobocene dichloride

: 59555-19-0
triiodo hexafluoroarsenate

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

B: 7553-56-2
iodine

Conditions

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

...Expand

: molybdenum(VI) oxide

: magnesium iodide

A: magnesium oxide * molybdenum dioxide

B: 7553-56-2
iodine

C: magnesium oxide

Conditions

Conditions	Yield
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

...Expand

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

A: {Pt(pyridinium)2Cl4}

B: 7553-56-2
iodine

Conditions

Conditions	Yield
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%

: 28752-21-8
dimethoxy disulfide

A: 7553-56-2
iodine

B: 7704-34-9
sulfur

Conditions

Conditions	Yield
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)

: 16893-36-0, 83829-87-2, 84277-63-4
{Pt(2)Br2}

B: 7553-56-2
iodine

Conditions

Conditions	Yield
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%

: 14362-44-8
iodide

: 7553-56-2
iodine

Conditions

Conditions	Yield
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

: 7782-68-5
iodic acid

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

B: 7553-56-2
iodine

Conditions

Conditions	Yield
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

...Expand

: C8H7ClN4O

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

: 7553-56-2
iodine

Conditions

Conditions	Yield
With triethylamine In ethanol for 4h;	74%

: 12029-98-0
iodine pentoxide

: potassium chloride

: uranium(VI) trioxide

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

B: 7553-56-2
iodine

Conditions

Conditions	Yield
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

...Expand

: 3768-61-4
N,N,N',N'-tetraethylthioamine

: 7553-56-2
iodine

Conditions

Conditions	Yield
In not given in acidic soln.;	70%
In not given in acidic soln.;	70%

: 25080-83-5
N-trifluoroacetic-3-nitroaniline

: 74-88-4
methyl iodide

: 7553-56-2
iodine

Conditions

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

: 12029-98-0
iodine pentoxide

: 7732-18-5
water

: uranium(VI) trioxide

: barium(II) chloride

A: uranyl iodate monohydrate

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

C: 7553-56-2
iodine

Conditions

Conditions	Yield
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

...Expand

: 615-42-9
1,2-Diiodobenzene

: 13517-10-7
boron triiodide

A: 7553-56-2
iodine

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

Conditions

Conditions	Yield
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%

...Expand

: 506-78-5
cyanogen iodide

: 75-58-1
tertamethylammonium iodide

: 7553-56-2
iodine

Conditions

Conditions	Yield
In neat (no solvent) at room temp.;	38%

: silver(I) iodide

: 7553-56-2
iodine

Conditions

Conditions	Yield
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;

: 7758-05-6
potassium iodate

A: 7553-56-2
iodine

B: 7681-11-0
potassium iodide

Conditions

Conditions	Yield
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

: 203255-55-4
2-(iodomethyl)isoindoline-1,3-dione

: 7553-56-2
iodine

Conditions

Conditions	Yield
Zerstzung bei Raumtemperatur;

: 30894-70-3
2,4-dichloro-6-diiodomethyl-[1,3,5]triazine

: 7553-56-2
iodine

Conditions

Conditions	Yield
at 25℃;

: 64761-27-9
8-iodo-3,7-dihydro-purine-2,6-dione

: 7553-56-2
iodine

Conditions

Conditions	Yield
at 200℃; Abspaltung;

: 34058-26-9
5,7-Diiodoisatin

: 7664-93-9
sulfuric acid

: 7553-56-2
iodine

Conditions

Conditions	Yield
at 130℃; Zersetzung;

: 7664-93-9
sulfuric acid

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

: 7553-56-2
iodine

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

: 10034-85-2
hydrogen iodide

: 7553-56-2
iodine

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

: 10034-85-2
hydrogen iodide

: 7553-56-2
iodine

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

: 10034-85-2
hydrogen iodide

: 7553-56-2
iodine

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

: 7732-18-5
water

: 10034-85-2
hydrogen iodide

: 7553-56-2
iodine

...Expand

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

: 108-24-7
acetic anhydride

: 7553-56-2
iodine

: 7664-93-9
sulfuric acid

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

: 7553-56-2
iodine

Conditions

Conditions	Yield
at 150℃;

: 7446-09-5
sulfur dioxide

: 7732-18-5
water

: 7553-56-2
iodine

A: 7664-93-9
sulfuric acid

B: 10034-85-2
hydrogen iodide

Conditions

Conditions	Yield
0 - 25 °C; part of a Mg-S-I water splitting cycle;	A 100% B 100%

...Expand

: 7726-95-6
bromine

: 7553-56-2
iodine

: cadmium(II) sulphide

: cadmium(II) iodide

Conditions

Conditions	Yield
In gas	100%
In solid	100%
In further solvent(s) with I2 dissolved in organic solvents;	100%

...Expand

: 7440-69-9
bismuth

: 7553-56-2
iodine

: 7787-64-6
bismuth(III) iodide

Conditions

Conditions	Yield
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

: 7553-56-2
iodine

: thallium(I) iodide

Conditions

Conditions	Yield
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

: 7553-56-2
iodine

: 14452-61-0
diborane

Conditions

Conditions	Yield
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.;

: 16940-66-2
sodium tetrahydroborate

: 7553-56-2
iodine

: 14452-61-0
diborane

Conditions

Conditions	Yield
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

: 7553-56-2
iodine

: 13283-01-7
tungsten(VI) chloride

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

Conditions

Conditions	Yield
In neat (no solvent) Ar atmosphere, sealed ampoule, formation of black melt at 300°C, tube furnace (150°C), crystn. (3 months);	100%

...Expand

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

: 7553-56-2
iodine

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

Conditions

Conditions	Yield
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

: 7553-56-2
iodine

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

B: 620-05-3
iodomethylbenzene

Conditions

Conditions	Yield
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%

...Expand

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

: 7553-56-2
iodine

A: 34557-54-5
methane

B: 74-84-0
ethane

C: 74-88-4
methyl iodide

Conditions

Conditions	Yield
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%

...Expand

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

: 7553-56-2
iodine

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

B: 74-88-4
methyl iodide

Conditions

Conditions	Yield
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%

...Expand

: 23642-14-0
CoMe(pyridine)(dimethylglyoxime(-1H))2

: 7553-56-2
iodine

A: iodobisdimethylglyoximepyridine cobalt(III)

B: 74-88-4
methyl iodide

Conditions

Conditions	Yield
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%

...Expand

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

: 7553-56-2
iodine

A: iodobisdimethylglyoximepyridine cobalt(III)

B: 75-03-6
ethyl iodide

Conditions

Conditions	Yield
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%

...Expand

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

: 7553-56-2
iodine

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

Conditions

Conditions	Yield
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%

: 118714-49-1
Pt2I2(CO)2(P-tert.-Bu2Ph2)2

: 7553-56-2
iodine

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

Conditions

Conditions	Yield
In not given react. (N2, CO or Ar); elem. anal.;	100%

: 7553-56-2
iodine

: 617-85-6
triethylantimony

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

Conditions

Conditions	Yield
In dichloromethane elem. anal.;	100%

: 7782-49-2
selenium

: 7784-36-3
arsenic pentafluoride

: 13637-84-8
fluorosulfonylchloride

: 7446-09-5
sulfur dioxide

: 7553-56-2
iodine

: (diselenium tetraiodine)(AsF6)2*SO2

Conditions

Conditions	Yield
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 %

...Expand

: 7782-49-2
selenium

: 7784-36-3
arsenic pentafluoride

: 7446-09-5
sulfur dioxide

: 7553-56-2
iodine

: (diselenium tetraiodine)-(AsF6)2

Conditions

Conditions	Yield
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 %

...Expand

: 38573-93-2, 34208-81-6
anti-2-norbornene-7-yl-trimethyl tin

: 7553-56-2
iodine

: 811-73-4
trimethylstannyl iodide

Conditions

Conditions	Yield
In methanol	100%
In methanol	100%
In dimethyl sulfoxide	88%

: 7553-56-2
iodine

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

: β-Methoxycarbonyl-ethyldi-n-butyl-iodstannan

Conditions

Conditions	Yield
In tetrachloromethane byproducts: CH3(CH2)3I;	100%

: 136835-13-7
benzimidazolin-2-ylidene(chloro)gold

: 7553-56-2
iodine

: (benzimidazolin-2-ylidene)triiodogold

Conditions

Conditions	Yield
In dichloromethane protective gas: argon; stirring mixture (20 h/room temp.);; pptn.; filtration; washing (CH2Cl2); drying; elem. anal.;;	100%

: 165751-19-9
((C6H5)2PC5H4)Mo(CO)3Mn(CO)5

: 7553-56-2
iodine

: [(η5-C5H4PPh2)Mo(CO)3I]

Conditions

Conditions	Yield
In not given	100%

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

: 7553-56-2
iodine

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

Conditions

Conditions	Yield
In nitromethane-d3 not isolated, monitored by NMR;	100%

: 7553-56-2
iodine

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

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

Conditions

Conditions	Yield
In tetrachloromethane room temp.;	100%

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

: 7553-56-2
iodine

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

Conditions

Conditions	Yield
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%

: 192053-32-0
tetra(supersilyl)dialane

: 7553-56-2
iodine

: 217202-48-7
disupersilyl aluminum iodide

Conditions

Conditions	Yield
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)

: 7553-56-2
iodine

A: 591-50-4
iodobenzene

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

Conditions

Conditions	Yield
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%

...Expand